| Year |
Citation |
Score |
| 2010 |
Schwartz E, Chambers R. Wilhelm Caspari, 1872-1944. Science (New York, N.Y.). 105: 613. PMID 17788559 DOI: 10.1126/science.105.2737.613 |
0.164 |
|
| 2007 |
SCHWARTZ E, LEIBOWITZ H. Local nasal therapy with pyribenzamine in seasonal and nonseasonal hay fever. The Journal of Allergy. 20: 269-72. PMID 18145263 DOI: 10.1016/0021-8707(49)90040-4 |
0.193 |
|
| 2007 |
SCHWARTZ E, WOLF J. Histamine antagonists; a comparative study of their effect on histamine and allergic skin wheals. The Journal of Allergy. 20: 32-49. PMID 18104339 DOI: 10.1016/0021-8707(49)90081-7 |
0.186 |
|
| 2004 |
SCHWARTZ E, LEVIN L, LEIBOWITZ H, REICHER J, KELLY JF, WALLMAN M, FEINBLATT TM. Oral cortisone therapy in ragweed hay fever. The Journal of Allergy. 23: 32-8. PMID 14907275 DOI: 10.1016/0021-8707(52)90071-3 |
0.19 |
|
| 2004 |
BLEIER AH, SCHWARTZ E. Cortisone in treating Stevens-Johnson syndrome. Report of a case. American Journal of Ophthalmology. 34: 618-20. PMID 14819194 DOI: 10.1016/0002-9394(51)90311-X |
0.196 |
|
| 2003 |
SCHWARTZ E, KALTER HH. Right aortic arch versus mediastinal tumors and densities: diagnostic problems. Diseases of the Chest. 28: 91-7. PMID 14391168 DOI: 10.1378/chest.28.1.91 |
0.17 |
|
| 2002 |
SCHWARTZ E, GLUCK R. Disappearance of tuberculosis in patient treated with antituberculosis drugs for pulmonary tuberculosis coexisting with bronchogenic carcinoma. Diseases of the Chest. 31: 465-7. PMID 13414592 DOI: 10.1378/chest.31.4.465 |
0.188 |
|
| 2002 |
KALTER HH, LEIBOWITZ S, SCHWARTZ E. Ambulatory treatment of tuberculous intrathoracic lymphadenitis. Diseases of the Chest. 30: 508-12. PMID 13365499 DOI: 10.1378/chest.30.5.508 |
0.182 |
|
| 2002 |
Wanless IR, Sweeney G, Dhillon AP, Guido M, Piga A, Galanello R, Gamberini MR, Schwartz E, Cohen AR. Lack of progressive hepatic fibrosis during long-term therapy with deferiprone in subjects with transfusion-dependent beta-thalassemia. Blood. 100: 1566-9. PMID 12176871 DOI: 10.1182/Blood-2002-01-0306 |
0.35 |
|
| 2000 |
Keller MA, Delgrosso K, Surrey S, Schwartz E. Identification of the nucleotide change (CAC → CGC) responsible for Hb P-Galveston [β117(G19)His → Arg] Hemoglobin. 24: 165-167. PMID 10870891 |
0.527 |
|
| 1998 |
SCHWARTZ E, LEIBOWITZ S. Tuberculin tine test. The American Review of Respiratory Disease. 88: 97. PMID 13987367 DOI: 10.1164/arrd.1963.88.1.97 |
0.176 |
|
| 1998 |
Yussim E, Schwartz E, Sidi Y, Ehrenfeld M. Acute renal failure precipitated by non-steroidal anti-inflammatory drugs (NSAIDs) in multiple myeloma. American Journal of Hematology. 58: 142-4. PMID 9625583 DOI: 10.1002/(SICI)1096-8652(199806)58:2<142::AID-AJH10>3.0.CO;2-D |
0.181 |
|
| 1998 |
Cui Z, Reilly MP, Surrey S, Schwartz E, McKenzie SE. -245 bp of 5'-flanking region from the human platelet factor 4 gene is sufficient to drive megakaryocyte-specific expression in vivo Blood. 91: 2326-2333. PMID 9516130 DOI: 10.1182/Blood.V91.7.2326.2326_2326_2333 |
0.615 |
|
| 1998 |
Norris CF, Pricop L, Millard SS, Taylor SM, Surrey S, Schwartz E, Salmon JE, McKenzie SE. A naturally occurring mutation in Fc gamma RIIA: a Q to K127 change confers unique IgG binding properties to the R131 allelic form of the receptor. Blood. 91: 656-62. PMID 9427722 |
0.544 |
|
| 1998 |
McKenzie SE, Taylor SM, Reilly MP, Surrey S, Schwartz E. Immune-mediated Thrombocytopenia is More Severe in Human FcγRIIa Transgenic Mice than in Wild-type Mice • 782 Pediatric Research. 43: 136-136. DOI: 10.1203/00006450-199804001-00803 |
0.566 |
|
| 1998 |
Norris CF, Pricop L, Millard SS, Taylor SM, Surrey S, Schwartz E, Salmon JE, McKenzie SE. A Naturally Occurring Mutation in FcγRIIA: A Q to K127 Change Confers Unique IgG Binding Properties to the R131 Allelic Form of the Receptor Blood. 91: 656-662. DOI: 10.1182/Blood.V91.2.656 |
0.577 |
|
| 1997 |
Tamary H, Surrey S, Augustine J, Shalmon L, Schwartz E, Rappaport EF. Molecular analysis of a compound heterozygote for hypoprothrombinemia and dysprothrombinemia (-G 7248/7249 and ARG 340 TRP). Blood Coagulation & Fibrinolysis : An International Journal in Haemostasis and Thrombosis. 8: 337-43. PMID 9351523 DOI: 10.1097/00001721-199709000-00003 |
0.58 |
|
| 1997 |
Baranovskaya S, Shevtsov S, Maksimova S, Kuzmin A, Schwartz E. The mutations and VNTRs in the phenylalanine hydroxylase gene of phenylketonuria in St Petersburg. Journal of Inherited Metabolic Disease. 19: 705. PMID 8892033 DOI: 10.1007/BF01799853 |
0.301 |
|
| 1997 |
McKenzie SE, Subudhi SK, Cassel DL, Malladi P, Surrey S, Schwartz E. #644 c-kit gene promoter region polymorphism in a family with congenital hypoplastic anemia Journal of Pediatric Hematology/Oncology. 19: 383. DOI: 10.1097/00043426-199707000-00092 |
0.606 |
|
| 1996 |
Trifillis P, Adachi K, Yamaguchi T, Schwartz E, Surrey S. Expression studies of delta-globin gene alleles associated with reduced hemoglobin A2 levels in Greek Cypriots. The Journal of Biological Chemistry. 271: 26931-8. PMID 8900178 DOI: 10.1074/Jbc.271.43.26931 |
0.613 |
|
| 1996 |
Adachi K, Pang J, Reddy LR, Bradley LE, Chen Q, Trifillis P, Schwartz E, Surrey S. Polymerization of three hemoglobin A2 variants containing Val6 and inhibition of hemoglobin S polymerization by hemoglobin A2. The Journal of Biological Chemistry. 271: 24557-63. PMID 8798718 DOI: 10.1074/Jbc.271.40.24557 |
0.566 |
|
| 1996 |
Bauman WA, Zhong YG, Schwartz E. Vitamin D deficiency in veterans with chronic spinal cord injury. Metabolism: Clinical and Experimental. 44: 1612-6. PMID 8786732 DOI: 10.1016/0026-0495(95)90083-7 |
0.213 |
|
| 1996 |
Norris CF, Surrey S, Bunin GR, Schwartz E, Buchanan GR, McKenzie SE. Relationship between Fc receptor IIA polymorphism and infection in children with sickle cell disease. The Journal of Pediatrics. 128: 813-9. PMID 8648541 DOI: 10.1016/S0022-3476(96)70334-7 |
0.578 |
|
| 1996 |
Schwartz E. Book Review Genes, Blood, and Courage: A boy called Immortal Sword By David G. Nathan. 276 pp. Cambridge, Mass., Harvard University Press, 1995. $24.95. 0-674-34473-1 The New England Journal of Medicine. 334: 1066-1066. DOI: 10.1056/Nejm199604183341617 |
0.377 |
|
| 1995 |
Schwartz E, Dabezies MA, Krevsky B. Hydrogen peroxide injury to the colon. Digestive Diseases and Sciences. 40: 1290-1. PMID 7781449 DOI: 10.1007/BF02065540 |
0.17 |
|
| 1994 |
Reilly AF, Norris CF, Surrey S, Bruchak FJ, Rappaport EF, Schwartz E, McKenzie SE. Genetic diversity in human Fc receptor II for immunoglobulin G: Fcgamma receptor IIA ligand-binding polymorphism Clinical and Diagnostic Laboratory Immunology. 1: 640-644. PMID 8556514 |
0.523 |
|
| 1994 |
Tamary H, Surrey S, Kirschmann H, Shalmon L, Zaizov R, Schwartz E, Rappaport EF. Systematic use of automated fluorescence-based sequence analysis of amplified genomic DNA for rapid detection of point mutations. American Journal of Hematology. 46: 127-33. PMID 8172179 DOI: 10.1002/Ajh.2830460213 |
0.613 |
|
| 1994 |
Reilly AF, Surrey S, Rappaport EF, Schwartz E, McKenzie SE. Variation in human FCGR2C gene copy number Immunogenetics. 40: 456. PMID 7959956 DOI: 10.1007/Bf00177829 |
0.6 |
|
| 1994 |
Asakura T, Mattiello JA, Obata K, Asakura K, Reilly MP, Tomassini N, Schwartz E, Ohene-Frempong K. Partially oxygenated sickled cells: sickle-shaped red cells found in circulating blood of patients with sickle cell disease. Proceedings of the National Academy of Sciences of the United States of America. 91: 12589-93. PMID 7809083 DOI: 10.1073/Pnas.91.26.12589 |
0.367 |
|
| 1994 |
Allen RJ, Brunberg J, Schwartz E, Schaefer AM, Jackson G. MRI characterization of cerebral dysgenesis in maternal PKU. Acta Paediatrica (Oslo, Norway : 1992). Supplement. 407: 83-5. PMID 7766967 DOI: 10.1111/J.1651-2227.1994.TB13460.X |
0.187 |
|
| 1994 |
Kim H, Dugan N, Silber J, Martin M, Schwartz E, Ohene-Frempong K, Cohen A. Erythrocytapheresis therapy to reduce iron overload in chronically transfused patients with sickle cell disease. Blood. 83: 1136-1142. DOI: 10.1182/Blood.V83.4.1136.Bloodjournal8341136 |
0.376 |
|
| 1994 |
Fortina P, Parrella T, Sartore M, Gottardi E, Gabutti V, Delgrosso K, Mansfield E, Rappaport E, Schwartz E, Camaschella C. Interaction of rare illegitimate recombination event and a poly A addition site mutation resulting in a severe form of alpha thalassemia. Blood. 83: 3356-3362. DOI: 10.1182/Blood.V83.11.3356.3356 |
0.451 |
|
| 1993 |
Cassel DL, Keller MA, Surrey S, Schwartz E, Schreiber AD, Rappaport EF, McKenzie SE. Differential expression of Fc gamma RIIA, Fc gamma RIIB and Fc gamma RIIC in hematopoietic cells: analysis of transcripts. Molecular Immunology. 30: 451-60. PMID 8464427 DOI: 10.1016/0161-5890(93)90113-P |
0.6 |
|
| 1993 |
Trifillis P, Kyrri A, Kalogirou E, Kokkofitou A, Ioannou P, Schwartz E, Surrey S. Analysis of delta-globin gene mutations in Greek cypriots. Blood. 82: 1647-51. PMID 8364213 DOI: 10.1182/Blood.V82.5.1647.1647 |
0.626 |
|
| 1993 |
Keller MA, Cassel DL, Rappaport EF, McKenzie SE, Schwartz E, Surrey S. Fluorescence-based RT PCR analysis: determination of the ratio of soluble to membrane-bound forms of Fc gamma RIIA transcripts in hematopoietic cell lines. Pcr Methods and Applications. 3: 32-8. PMID 8220183 DOI: 10.1101/Gr.3.1.32 |
0.599 |
|
| 1993 |
Horiuchi K, Stephens MJ, Adachi K, Asakura T, Schwartz E, Ohene-Frempong K. Image analysis studies of the degree of irreversible deformation of sickle cells in relation to cell density and Hb F level. British Journal of Haematology. 85: 356-64. PMID 7506569 DOI: 10.1111/J.1365-2141.1993.Tb03179.X |
0.354 |
|
| 1992 |
Fortina P, Dotti G, Conant R, Monokian G, Parrella T, Hitchcock W, Rappaport E, Schwartz E, Surrey S. Detection of the most common mutations causing beta-thalassemia in Mediterraneans using a multiplex amplification refractory mutation system (MARMS). Pcr Methods and Applications. 2: 163-6. PMID 1477672 DOI: 10.1101/Gr.2.2.163 |
0.627 |
|
| 1992 |
Fortina P, Conant R, Parrella T, Rappaport E, Scanlin T, Schwartz E, Robertson JM, Surrey S. Fluorescence-based, multiplex allele-specific PCR (MASPCR) detection of the delta F508 deletion in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. Molecular and Cellular Probes. 6: 353-6. PMID 1382222 DOI: 10.1016/0890-8508(92)90013-N |
0.602 |
|
| 1992 |
McKenzie SE, Keller MA, Cassel DL, Schreiber AD, Schwartz E, Surrey S, Rappaport EF. Characterization of the 5'-flanking transcriptional regulatory region of the human Fc gamma receptor gene, Fc gamma RIIA. Molecular Immunology. 29: 1165-74. PMID 1382218 DOI: 10.1016/0161-5890(92)90052-Y |
0.633 |
|
| 1992 |
Fortina P, Conant R, Monokian G, Dotti G, Parrella T, Hitchcock W, Kant J, Scanlin T, Rappaport E, Schwartz E, Surrey S. Non-radioactive detection of the most common mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex allele-specific polymerase chain reaction Human Genetics. 90: 375-378. PMID 1282898 DOI: 10.1007/Bf00220462 |
0.603 |
|
| 1992 |
Cohen AR, Martin MB, Silber JH, Kim HC, Ohene-Frempong K, Schwartz E. A modified transfusion program for prevention of stroke in sickle cell disease. Blood. 79: 1657-1661. DOI: 10.1182/Blood.V79.7.1657.Bloodjournal7971657 |
0.374 |
|
| 1991 |
Schwartz E, Lee BS. Braccio da Gamba Jama: the Journal of the American Medical Association. 266: 1360. PMID 1880863 DOI: 10.1001/Jama.1991.03470100052025 |
0.306 |
|
| 1991 |
Cornelius AS, Campbell D, Schwartz E, Poncz M. Elevated common acute lymphoblastic leukemia antigen expression in pediatric immune thrombocytopenic purpura. The American Journal of Pediatric Hematology/Oncology. 13: 57-61. PMID 1827572 DOI: 10.1097/00043426-199121000-00014 |
0.344 |
|
| 1991 |
Trifillis P, Ioannou P, Schwartz E, Surrey S. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence-based DNA sequence analysis. Blood. 78: 3298-305. PMID 1742490 DOI: 10.1182/Blood.V78.12.3298.Bloodjournal78123298 |
0.629 |
|
| 1991 |
Ballas SK, Talacki CA, Adachi K, Schwartz E, Surrey S, Rappaport E. The Xmn I site (-158, C----T) 5' to the G gamma gene: correlation with the Senegalese haplotype and G gamma globin expression. Hemoglobin. 15: 393-405. PMID 1724976 DOI: 10.3109/03630269108998859 |
0.619 |
|
| 1991 |
Fortina P, Delgrosso K, Werner E, Haines K, Rappaport E, Schwartz E, Surrey S. A greater than 200 kb deletion removing the entire beta-like globin gene cluster in a family of Irish descent. Hemoglobin. 15: 23-41. PMID 1717405 DOI: 10.3109/03630269109072482 |
0.626 |
|
| 1991 |
Trifillis P, Ioannou P, Schwartz E, Surrey S. Identification of four novel delta-globin gene mutations in Greek Cypriots using polymerase chain reaction and automated fluorescence- based DNA sequence analysis Blood. 78: 3298-3305. DOI: 10.1182/blood.v78.12.3298.3298 |
0.351 |
|
| 1991 |
Manno C, Hedberg K, Kim H, Bunin G, Nicolson S, Jobes D, Schwartz E, Norwood W. Comparison of the hemostatic effects of fresh whole blood, stored whole blood, and components after open heart surgery in children Blood. 77: 930-936. DOI: 10.1182/Blood.V77.5.930.Bloodjournal775930 |
0.364 |
|
| 1990 |
Cohen A, Martin M, Mizanin J, Konkle DF, Schwartz E. Vision and hearing during deferoxamine therapy. The Journal of Pediatrics. 117: 326-30. PMID 2380834 DOI: 10.1016/S0022-3476(05)80556-6 |
0.354 |
|
| 1990 |
Heidenreich R, Eisman R, Surrey S, Delgrosso K, Bennett JS, Schwartz E, Poncz M. Organization of the gene for platelet glycoprotein IIb. Biochemistry. 29: 1232-44. PMID 2322558 DOI: 10.1021/Bi00457A020 |
0.623 |
|
| 1990 |
Cohen AR, Martin M, Schwartz E. Current Treatment of Cooley's Anemia Annals of the New York Academy of Sciences. 612: 286-292. PMID 2291556 DOI: 10.1111/J.1749-6632.1990.Tb24316.X |
0.317 |
|
| 1990 |
Talacki CA, Rappaport E, Schwartz E, Surrey S, Ballas SK. Beta-globin gene cluster haplotypes in Hb C heterozygotes. Hemoglobin. 14: 229-40. PMID 2228698 DOI: 10.3109/03630269009002261 |
0.617 |
|
| 1990 |
Ramachandran B, Rappaport EF, Surrey S, Poncz M, Schwartz E. Polymerase chain reaction (PCR) for detection of PstI polymorphism in the human PF4 gene. Nucleic Acids Research. 18: 5919. PMID 1977142 DOI: 10.1093/Nar/18.19.5919 |
0.6 |
|
| 1990 |
Eisman R, Surrey S, Ramachandran B, Schwartz E, Poncz M. Structural and functional comparison of the genes for human platelet factor 4 and PF4alt. Blood. 76: 336-44. PMID 1695112 DOI: 10.1182/Blood.V76.2.336.336 |
0.644 |
|
| 1990 |
Month SR, Wood RW, Trifillis PT, Orchowski PJ, Sharon B, Ballas SK, Surrey S, Schwartz E. Analysis of 5' flanking regions of the gamma globin genes from major African haplotype backgrounds associated with sickle cell disease. The Journal of Clinical Investigation. 85: 364-70. PMID 1688883 DOI: 10.1172/Jci114447 |
0.643 |
|
| 1990 |
Eisman R, Surrey S, Ramachandran B, Schwartz E, Poncz M. Structural and functional comparison of the genes for human platelet factor 4 and PF4alt Blood. 76: 336-344. DOI: 10.1182/blood.v76.2.336.bloodjournal762336 |
0.61 |
|
| 1990 |
Gumucio D, Lockwood W, Weber J, Saulino A, Delgrosso K, Surrey S, Schwartz E, Goodman M, Collins F. The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors Blood. 75: 756-761. DOI: 10.1182/blood.v75.3.756.756 |
0.584 |
|
| 1990 |
Adachi K, Kim J, Asakura T, Schwartz E. Characterization of two types of fetal hemoglobin: alpha 2G gamma 2 and alpha 2A gamma 2 Blood. 75: 2070-2075. DOI: 10.1182/Blood.V75.10.2070.2070 |
0.376 |
|
| 1990 |
FORTINA P, DELGROSSO K, HAINES K, RAPPAPORT E, WERNER E, SCHWARTZ E, SURREY S. Mapping of Deletional Forms of ?- and ???-Thalassemia Annals of the New York Academy of Sciences. 612: 480-484. DOI: 10.1111/J.1749-6632.1990.Tb24337.X |
0.556 |
|
| 1990 |
Schwartz E. Helminthic Infections Among Peace Corps Volunteers in Nepal Jama: the Journal of the American Medical Association. 263: 373. DOI: 10.1001/jama.1990.03440030056016 |
0.178 |
|
| 1989 |
Cohen AR, Mizanin J, Schwartz E. Rapid removal of excessive iron with daily, high-dose intravenous chelation therapy. The Journal of Pediatrics. 115: 151-5. PMID 2738783 DOI: 10.1016/S0022-3476(89)80353-1 |
0.357 |
|
| 1989 |
Kim HC, Alavi A, Russell MO, Schwartz E. Differentiation of bone and bone marrow infarcts from osteomyelitis in sickle cell disorders. Clinical Nuclear Medicine. 14: 249-54. PMID 2706866 DOI: 10.1097/00003072-198904000-00002 |
0.343 |
|
| 1989 |
TALACKI CA, LARNER J, SCHWARTZ E, SURREY S, RAPPAPORT EF, BALLAS SK. The Effect of Alpha Thalassemia on the Clinical Course of Hemoglobin SC Disease Annals of the New York Academy of Sciences. 565: 365-366. DOI: 10.1111/J.1749-6632.1989.Tb24189.X |
0.586 |
|
| 1989 |
BALLAS SK, LARNER J, SMITH ED, SURREY S, SCHWARTZ E, RAPPAPORT EF. Rheological Properties of SickleErythrocytes in the Steady State Predict the Frequency and Severity of the Sickle Cell Painful Crisis Annals of the New York Academy of Sciences. 565: 363-364. DOI: 10.1111/J.1749-6632.1989.Tb24188.X |
0.549 |
|
| 1988 |
Mouallem M, Friedman E, Pauzner R, Schwartz E, Rubinstein E. Rickettsiosis-associated hyponatremia. Infection. 15: 315-6. PMID 3692602 DOI: 10.1007/BF01647728 |
0.23 |
|
| 1988 |
Manno CS, Cohen AR, Schwartz E, Day DL. Sickle cell anemia and cholelithiasis Pediatric Radiology. 18: 178-179. PMID 3353155 DOI: 10.1007/Bf02387571 |
0.356 |
|
| 1988 |
Fortina P, Delgrosso K, Rappaport E, Poncz M, Ballas SK, Schwartz E, Surrey S. A large deletion encompassing the entire alpha-like globin gene cluster in a family of northern European extraction. Nucleic Acids Research. 16: 11223-35. PMID 2905048 DOI: 10.1093/Nar/16.23.11223 |
0.626 |
|
| 1988 |
Burk C, Ingram C, Weiner M, Rappaport EF, Schwartz E, Poncz M. A Taq 1 polymorphism for the human platelet glycoprotein IIIa gene (GP3A). Nucleic Acids Research. 16: 7216. PMID 2900503 DOI: 10.1093/Nar/16.14.7216 |
0.403 |
|
| 1988 |
Sharon B, Poncz M, Surrey S, Schwartz E. Non-random association of the Rsa I polymorphic site 5' to the beta-globin gene with major sickle cell haplotypes. Hemoglobin. 12: 115-24. PMID 2898459 DOI: 10.3109/03630268808998018 |
0.631 |
|
| 1988 |
Schwartz E, Cohen A, Surrey S. Overview of the beta thalassemias: genetic and clinical aspects. Hemoglobin. 12: 551-64. PMID 2463234 DOI: 10.3109/03630268808991644 |
0.641 |
|
| 1988 |
Zimrin AB, Eisman R, Vilaire G, Schwartz E, Bennett JS, Poncz M. Structure of platelet glycoprotein IIIa. A common subunit for two different membrane receptors. The Journal of Clinical Investigation. 81: 1470-5. PMID 2452834 DOI: 10.1172/Jci113478 |
0.428 |
|
| 1988 |
Surrey S, Delgrosso K, Malladi P, Schwartz E. A single-base change at position -175 in the 5'-flanking region of the G gamma-globin gene from a black with G gamma-beta+ HPFH. Blood. 71: 807-10. PMID 2449926 DOI: 10.1182/Blood.V71.3.807.807 |
0.637 |
|
| 1987 |
Molho M, Katz I, Schwartz E, Shemesh Y, Sadeh M, Wolf E. Familial bilateral paralysis of diaphragm. Adult onset. Chest. 91: 466-7. PMID 3816327 DOI: 10.1378/CHEST.91.3.466 |
0.196 |
|
| 1987 |
Poncz M, Sutton M, Delgrosso K, Schwartz E, Surrey S. DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2). Nucleic Acids Research. 15: 5169-79. PMID 3601670 DOI: 10.1093/Nar/15.13.5169 |
0.644 |
|
| 1987 |
Piomelli S, Lerner N, Cohen A, Schwartz E, Nathan D, Wolfe L, Weatherall D, Nienhuis A. Bone marrow transplantation for thalassemia. The New England Journal of Medicine. 317: 964. PMID 3306390 DOI: 10.1056/NEJM198710083171516 |
0.198 |
|
| 1987 |
Poncz M, Surrey S, LaRocco P, Weiss MJ, Rappaport EF, Conway TM, Schwartz E. Cloning and characterization of platelet factor 4 cDNA derived from a human erythroleukemic cell line. Blood. 69: 219-23. PMID 3098319 |
0.569 |
|
| 1987 |
Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF. The xerocytosis of Hb SC disease. Blood. 69: 124-30. PMID 2947642 DOI: 10.1182/Blood.V69.1.124.Bloodjournal691124 |
0.615 |
|
| 1987 |
Guzzo C, Weiner M, Rappaport E, Larocco P, Surrey S, Poncz M, Schwartz E. An Eco R1 polymorphism of a human platelet factor 4 (PF4) gene Nucleic Acids Research. 15: 380. PMID 2881257 DOI: 10.1093/Nar/15.1.380 |
0.597 |
|
| 1987 |
Poncz M, Surrey S, LaRocco P, Weiss M, Rappaport E, Conway T, Schwartz E. Cloning and characterization of platelet factor 4 cDNA derived from a human erythroleukemic cell line Blood. 69: 219-223. DOI: 10.1182/Blood.V69.1.219.219 |
0.607 |
|
| 1987 |
Ohene-Frempong K, Rappaport E, Schwartz E. Thalassemia Syndromes: Recent Advances Hematology/Oncology Clinics of North America. 1: 503-519. DOI: 10.1016/S0889-8588(18)30666-X |
0.375 |
|
| 1986 |
Hoyt RW, Scarpa N, Wilmott RW, Cohen A, Schwartz E. Pulmonary function abnormalities in homozygous beta-thalassemia. The Journal of Pediatrics. 109: 452-5. PMID 3746533 DOI: 10.1016/S0022-3476(86)80116-0 |
0.365 |
|
| 1986 |
Reisner Y, Ben-Bassat I, Douer D, Kaploon A, Schwartz E, Ramot B. Demonstration of clonable alloreactive host T cells in a primate model for bone marrow transplantation. Proceedings of the National Academy of Sciences of the United States of America. 83: 4012-5. PMID 3520563 DOI: 10.1073/Pnas.83.11.4012 |
0.244 |
|
| 1985 |
Cohen A, Mizanin J, Schwartz E. Treatment of iron overload in Cooley's anemia. Annals of the New York Academy of Sciences. 445: 274-81. PMID 3860130 DOI: 10.1111/J.1749-6632.1985.Tb17197.X |
0.338 |
|
| 1985 |
Tanaka Y, Kelleher JF, Schwartz E, Asakura T, Shelton J, Shelton JR, Schroeder WA. Oxygen binding and stability properties of hb Santa ana (β88 leu→pro) Hemoglobin. 9: 157-169. PMID 3839771 DOI: 10.3109/03630268508996997 |
0.365 |
|
| 1984 |
Liebhaber SA, Rappaport EF, Cash FE, Ballas SK, Schwartz E, Surrey S. Hemoglobin I mutation encoded at both alpha-globin loci on the same chromosome: concerted evolution in the human genome. Science (New York, N.Y.). 226: 1449-51. PMID 6505702 DOI: 10.1126/Science.6505702 |
0.63 |
|
| 1984 |
Adachi K, Vonk H, Reilly MP, Adachi H, Schroeder WA, Schwartz E, Asakura T. Relationship between tetramer-dimer assembly and the stability of Hb Malmö (α2β297Gln) Biochimica Et Biophysica Acta. 790: 132-140. PMID 6487633 DOI: 10.1016/0167-4838(84)90216-4 |
0.362 |
|
| 1984 |
Cohen A, Martin M, Schwartz E. Depletion of excessive liver iron stores with desferrioxamine. British Journal of Haematology. 58: 369-73. PMID 6477838 DOI: 10.1111/J.1365-2141.1984.Tb06096.X |
0.348 |
|
| 1984 |
Cohen AR, Schmidt JM, Martin MB, Barnsley W, Schwartz E. Clinical trial of young red cell transfusions The Journal of Pediatrics. 104: 865-868. PMID 6374083 DOI: 10.1016/S0022-3476(84)80482-5 |
0.38 |
|
| 1984 |
Rappaport EF, Schwartz E, Poncz M, Surrey S. Frequent occurrence of a zeta-globin-region deletion in American blacks accounts for a previously-described restriction site polymorphism. Biochemical and Biophysical Research Communications. 125: 817-23. PMID 6097249 DOI: 10.1016/0006-291X(84)90612-0 |
0.634 |
|
| 1984 |
Semenza GL, Delgrosso K, Poncz M, Malladi P, Schwartz E, Surrey S. The silent carrier allele: beta thalassemia without a mutation in the beta-globin gene or its immediate flanking regions. Cell. 39: 123-8. PMID 6091904 DOI: 10.1016/0092-8674(84)90197-1 |
0.736 |
|
| 1984 |
Cohen A, Witzleben C, Schwartz E. Treatment of iron overload. Seminars in Liver Disease. 4: 228-38. PMID 6091277 DOI: 10.1055/S-2008-1041773 |
0.326 |
|
| 1984 |
Semenza GL, Delgrosso K, Surrey S, Malladi P, Schwartz E, Ponca M. THE SILENT CARRIER ALLELE: β-THALASSEMIA WITHOUT A MUTATION IN THE β-GLOBIN GENE REGION Pediatric Research. 18: 248A-248A. DOI: 10.1203/00006450-198404001-00931 |
0.726 |
|
| 1984 |
Semenza GL, Malladi P, Poncz M, Delgrosso K, Schwartz E, Surrey S. DETECTION OF A NOVEL DNA POLYMORPHISM IN THE β-GLOBIN CLUSTER AND EVIDENCE FOR SITE-SPECIFIC RECOMBINATION Pediatric Research. 18: 225A-225A. DOI: 10.1203/00006450-198404001-00794 |
0.719 |
|
| 1984 |
Russell MO, Goldberg HI, Hodson A, Kim HC, Halus J, Reivich M, Schwartz E. Effect of transfusion therapy on arteriographic abnormalities and on recurrence of stroke in sickle cell disease Blood. 63: 162-169. DOI: 10.1182/Blood.V63.1.162.Bloodjournal631162 |
0.355 |
|
| 1983 |
Greenberg J, Ohene-Frempong K, Halus J, Way C, Schwartz E. Trial of low doses of aspirin as prophylaxis insickle cell disease The Journal of Pediatrics. 102: 781-784. PMID 6842340 DOI: 10.1016/S0022-3476(83)80258-3 |
0.351 |
|
| 1983 |
Deitch S, Chadwick D, Coleman T, O‘Hare D, Sokoloff B, Sterne G, Wagner V, Sgroi S, Schwartz E, Felitto H, Grundfast K. Gonorrhea in Prepubertal Children Journal of Urology. 130: 1257-1257. DOI: 10.1016/S0022-5347(17)51804-2 |
0.19 |
|
| 1982 |
Poncz M, Colman N, Herbert V, Schwartz E, Cohen A. Congenital folate malabsorption. The Journal of Pediatrics. 99: 828-9. PMID 7299568 DOI: 10.1016/S0022-3476(81)80430-1 |
0.322 |
|
| 1982 |
Cohen A, Martin M, Schwartz E. Response to long-term deferoxamine therapy in thalassemia. The Journal of Pediatrics. 99: 689-94. PMID 7299539 DOI: 10.1016/S0022-3476(81)80385-X |
0.357 |
|
| 1982 |
Poncz M, Solowiejczyk D, Harpel B, Mory Y, Schwartz E, Surrey S. Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes. Hemoglobin. 6: 27-36. PMID 7068433 DOI: 10.3109/03630268208996930 |
0.638 |
|
| 1982 |
Schmidt WF, Asakura T, Schwartz E. Effect of cetiedil on cation and water movements in erythrocytes. The Journal of Clinical Investigation. 69: 589-94. PMID 7061704 DOI: 10.1172/JCI110485 |
0.228 |
|
| 1982 |
Poncz M, Solowiejczyk D, Ballantine M, Schwartz E, Surrey S. "Nonrandom" DNA sequence analysis in bacteriophage M13 by the dideoxy chain-termination method. Proceedings of the National Academy of Sciences of the United States of America. 79: 4298-302. PMID 6956859 DOI: 10.1073/Pnas.79.14.4298 |
0.586 |
|
| 1982 |
Balsley JF, Rappaport E, Schwartz E, Surrey S. The gamma-delta-beta-globin gene region in G gamma-beta +-hereditary persistence of fetal hemoglobin. Blood. 59: 828-31. PMID 6174163 DOI: 10.1182/Blood.V59.4.828.828 |
0.632 |
|
| 1982 |
Graziano J, Piomelli S, Seaman C, Wang T, Cohen A, Kelleher JJ, Schwartz E. A simple technique for preparation of young red cells for transfusion from ordinary blood units. Blood. 59: 865-868. DOI: 10.1182/Blood.V59.4.865.Bloodjournal594865 |
0.373 |
|
| 1981 |
Cohen A, Cohen IJ, Schwartz E. Scurvy and altered iron stores in thalassemia major. The New England Journal of Medicine. 304: 158-60. PMID 7442735 DOI: 10.1056/Nejm198101153040307 |
0.36 |
|
| 1981 |
Asakura T, Ohnishi ST, Adachi K, Ozguc M, Hashimoto K, Devlin MT, Schwartz E. Effect of piracetam on sickle erythrocytes and sickle hemoglobin. Biochimica Et Biophysica Acta. 668: 397-405. PMID 7236716 DOI: 10.1016/0005-2795(81)90173-2 |
0.364 |
|
| 1981 |
Asakura T, Adachi K, Schwartz E, Wiley J. Molecular stability of Hb Philly (alpha 2 beta 2 35(Cl) Tyr leads to Phe). Rhe relationship of hemoglobin stability to ligand state as defined by heat and mechanical shaking tests. Hemoglobin. 5: 177-90. PMID 7216817 DOI: 10.3109/03630268108996923 |
0.389 |
|
| 1981 |
Schmidt WF, Poncz M, Russell MO, Schwartz E. Unusual manifestations of chronic granulomatous disease. American Journal of Diseases of Children (1960). 135: 376-7. PMID 7211803 DOI: 10.1001/Archpedi.1981.02130280066023 |
0.352 |
|
| 1981 |
Poncz M, Colman N, Herbert V, Schwartz E, Cohen AR. Therapy of congenital folate malabsorption. The Journal of Pediatrics. 98: 76-9. PMID 6969796 DOI: 10.1016/S0022-3476(81)80541-0 |
0.314 |
|
| 1981 |
Poncz M, Groenberg J, Russell MO, Schwartz E, Cohen AR. 852 THROMBOCYTOSIS IN PATIENTS WITH SICKLE CELL ANEMIA AND PNEUMONIA Pediatric Research. 15: 584-584. DOI: 10.1203/00006450-198104001-00877 |
0.362 |
|
| 1981 |
Bender JW, Saral R, Schwartz E. 788 Eosinophilia After Bone Marrow Transplantation Pediatric Research. 15: 573-573. DOI: 10.1203/00006450-198104001-00812 |
0.307 |
|
| 1981 |
Cohen A, Schwartz E. 669 Aps-Spr Abstract Submissions-Players And Strategies Pediatric Research. 15: 552-552. DOI: 10.1203/00006450-198104001-00682 |
0.335 |
|
| 1980 |
Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E, Surrey S. Alpha-gene deletions in black newborn infants with Hb Bart's. Blood. 56: 931-3. PMID 7426755 DOI: 10.1182/Blood.V56.5.931.Bloodjournal565931 |
0.624 |
|
| 1980 |
Cohen A, Markenson AL, Schwartz E. Transfusion requirements and splenectomy in thalassemia major. The Journal of Pediatrics. 97: 100-2. PMID 7381628 DOI: 10.1016/S0022-3476(80)80144-2 |
0.356 |
|
| 1980 |
Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E. Linkage of alpha G-Philadelphia to alpha-thalassemia in African-Americans . Proceedings of the National Academy of Sciences of the United States of America. 77: 4885-9. PMID 6933536 DOI: 10.1073/Pnas.77.8.4885 |
0.614 |
|
| 1980 |
Surrey S, Ohene-Frempong K, Rappaport E, Atwater J, Schwartz E. alpha Thalassemia and the expression of hemoglobin G-Philadelphia. Annals of the New York Academy of Sciences. 344: 62-72. PMID 6930883 DOI: 10.1111/J.1749-6632.1980.Tb33649.X |
0.614 |
|
| 1980 |
Cohen A, Schwartz E. Decreasing Iron Stores During Intensive Chelation Therapy Annals of the New York Academy of Sciences. 344: 405-408. PMID 6930880 DOI: 10.1111/J.1749-6632.1980.Tb33679.X |
0.336 |
|
| 1980 |
Asakura T, Ohnishi ST, Adachi K, Ozguc M, Hashimoto K, Singer M, Russell MO, Schwartz E. Effect of cetiedil on erythrocyte sickling: new type of antisickling agent that may affect erythrocyte membranes. Proceedings of the National Academy of Sciences of the United States of America. 77: 2955-9. PMID 6930678 DOI: 10.1073/Pnas.77.5.2955 |
0.357 |
|
| 1980 |
Kim HC, Friedman S, Asakura T, Schwartz E. Inclusions in red blood cells containing Hb S or Hb C. British Journal of Haematology. 44: 547-54. PMID 6246916 DOI: 10.1111/J.1365-2141.1980.Tb08708.X |
0.415 |
|
| 1980 |
Ohene-Frempong K, Schwartz E. Clinical features of thalassemia. Pediatric Clinics of North America. 27: 403-20. PMID 6155656 DOI: 10.1016/S0031-3955(16)33858-5 |
0.347 |
|
| 1980 |
Adachi K, Kinney TR, Schwartz E, Asakura T. Molecular stability and function of Hb C-Harlem. Hemoglobin. 4: 1-26. PMID 6153380 DOI: 10.3109/03630268009042370 |
0.341 |
|
| 1980 |
Cohen A, Schwartz E. Iron chelation therapy in sickle cell anemia. American Journal of Hematology. 7: 69-76. PMID 507048 DOI: 10.1002/Ajh.2830070109 |
0.362 |
|
| 1980 |
Adachi K, Asakura T, Schwartz E. Aggregation of hemoglobin S and hemoglobin CHarlem with nonsickle hemoglobin in concentrated phosphate buffer Blood. 55: 494-500. DOI: 10.1182/Blood.V55.3.494.Bloodjournal553494 |
0.349 |
|
| 1979 |
Rubin RN, Ballas SK, Atwater J, Burka ER, Adachi K, Asakura T, Schwartz E. Hemoglobin Potomac: clinical picture, biosynthesis and stability. Hemoglobin. 2: 447-51. PMID 721612 DOI: 10.3109/03630267809007079 |
0.349 |
|
| 1979 |
Lau PW, Hung C, Minakata K, Schwartz E, Asakura T. Spin-label studies of membrane-associated denatured hemoglobin in normal and sickle cells. Biochimica Et Biophysica Acta. 552: 499-508. PMID 221019 DOI: 10.1016/0005-2736(79)90194-9 |
0.332 |
|
| 1978 |
Surrey S, Chambers JS, Muni D, Schwartz E. Restriction endonuclease analysis of human globin genes in cellular DNA. Biochemical and Biophysical Research Communications. 83: 1125-31. PMID 708430 DOI: 10.1016/0006-291X(78)91512-7 |
0.62 |
|
| 1978 |
Friedman S, Back B, Delivoria-Papadopoulos M, Atwater J, Asakura T, Schwartz E. A simple test for detection of sickle hemoglobin in the neonatal period. American Journal of Clinical Pathology. 70: 85-88. PMID 696677 DOI: 10.1093/Ajcp/70.1.85 |
0.357 |
|
| 1978 |
Gill FM, Shapiro SS, Schwartz E. Severe congenital hypoprothrombinemia. The Journal of Pediatrics. 93: 264-6. PMID 671167 DOI: 10.1016/S0022-3476(78)80515-0 |
0.32 |
|
| 1978 |
Kinney TR, Friedman S, Cifuentes E, Kim HC, Schwartz E. Variations in globin synthesis in delta-beta-thalassaemia. British Journal of Haematology. 38: 15-22. PMID 638060 DOI: 10.1111/J.1365-2141.1978.Tb07103.X |
0.427 |
|
| 1978 |
Cohen A, Schwartz E. Iron chelation therapy with deferoxamine in Cooley anemia. The Journal of Pediatrics. 92: 643-7. PMID 633031 DOI: 10.1016/S0022-3476(78)80314-X |
0.342 |
|
| 1978 |
Cohen A, Schwartz E. Excretion of iron in response to deferoxamine in sickle cell anemia. The Journal of Pediatrics. 92: 659-62. PMID 633013 DOI: 10.1016/S0022-3476(78)80317-5 |
0.362 |
|
| 1978 |
Cohen AR, Markenson A, Schwartz E. 590 Transfusion Requirements And Splenectomy In Cooley'S Anemia Pediatric Research. 12: 462-462. DOI: 10.1203/00006450-197804001-00595 |
0.384 |
|
| 1977 |
Kim HC, Weierbach RG, Friedman S, Schwartz E. Globin biosynthesis in sickle cell, Hb SC, and Hb C diseases. The Journal of Pediatrics. 91: 13-20. PMID 874650 DOI: 10.1016/S0022-3476(77)80434-4 |
0.435 |
|
| 1977 |
Asakura T, Minakata K, Adachi K, Russell MO, Schwartz E. Denatured hemoglobin in sickle erythrocytes. The Journal of Clinical Investigation. 59: 633-40. PMID 845254 DOI: 10.1172/Jci108681 |
0.396 |
|
| 1977 |
Adachi K, Ghory PK, Asakura T, Schwartz E. A monomeric form of pyruvate kinase in human pyruvate kinase deficiency. Proceedings of the National Academy of Sciences of the United States of America. 74: 501-4. PMID 15247 DOI: 10.1073/Pnas.74.2.501 |
0.33 |
|
| 1977 |
Kim HC, Alavi A, Russell MO, Schwartz E. Scintigraphic Detection Of Bone And Bone Marrow In-Farcts In Sickle Cell Disorders Pediatric Research. 11: 473-473. DOI: 10.1203/00006450-197704000-00620 |
0.349 |
|
| 1977 |
Festa RS, Asakura T, Schwartz E. Abnormally Low P 50 In Patients With Malignancies Pediatric Research. 11: 471-471. DOI: 10.1203/00006450-197704000-00606 |
0.361 |
|
| 1977 |
Asner B, Friedman S, Atwater J, Schwartz E. THE OCCURRENCE OF 1–2% HB BART'S IN A HIGH PROPORTION OF BLACK NEONATES AS AN EXPRESSION OF α-THALASSEMIA Pediatric Research. 11: 467-467. DOI: 10.1203/00006450-197704000-00582 |
0.379 |
|
| 1977 |
Cifuentes E, Gill FM, Roth K, Schwartz E. Evaluation Of Anemia In Cystinosis Pediatric Research. 11: 454-454. DOI: 10.1203/00006450-197704000-00505 |
0.363 |
|
| 1977 |
Kim H, Weierbach R, Friedman S, Schwartz E. Detection of sickle alpha- or beta0-thalassemia by studies of globin biosynthesis Blood. 49: 785-792. DOI: 10.1182/Blood.V49.5.785.Bloodjournal495785 |
0.438 |
|
| 1977 |
Kim H, Weierbach R, Friedman S, Schwartz E. Detection of sickle alpha- or beta0-thalassemia by studies of globin biosynthesis Blood. 49: 785-792. DOI: 10.1182/blood.v49.5.785.785 |
0.347 |
|
| 1976 |
Friedman S, Ozsoylu S, Luddy R, Schwartz E. Heterozygous beta thalassaemia of unusual severity. British Journal of Haematology. 32: 65-77. PMID 1259927 DOI: 10.1111/J.1365-2141.1976.Tb01876.X |
0.44 |
|
| 1976 |
Friedman S, Schwartz E, Ahern E, Ahern V. Variations in globin chain synthesis in hereditary persistence of fetal haemoglobin. British Journal of Haematology. 32: 357-64. PMID 1252370 DOI: 10.1111/J.1365-2141.1976.Tb00939.X |
0.436 |
|
| 1976 |
Friedman S, Schwartz E. Hereditary persistence of foetal haemoglobin with β-chain synthesis in cis position ( G γ-β + -HPFH) in a negro family Nature. 259: 138-140. PMID 1246351 DOI: 10.1038/259138A0 |
0.424 |
|
| 1976 |
Russell MO, Goldberg HI, Reis L, Friedman S, Slater R, Reivich M, Schwartz E. Transfusion therapy for cerebrovascular abnormalities in sickle cell disease. The Journal of Pediatrics. 88: 382-7. PMID 1245948 DOI: 10.1016/S0022-3476(76)80251-X |
0.275 |
|
| 1976 |
Alter BP, Friedman S, Hobbins JC, Mahoney MJ, Sherman AS, McSweeney JF, Nathan DG, Schwartz E. Prenatal diagnosis of sickle-cell anemia and alpha G Philadelphia. Study of a Fetus also at risk for H b S/beta+-thalassemia. The New England Journal of Medicine. 294: 1040-1. PMID 3736 DOI: 10.1056/NEJM197605062941906 |
0.312 |
|
| 1976 |
Asakura T, Adachi K, Shapiro M, Friedman S, Schwartz E. Mechanical precipitation of hemoglobin köln. Biochimica Et Biophysica Acta. 412: 197-201. PMID 83 DOI: 10.1016/0005-2795(75)90034-3 |
0.394 |
|
| 1975 |
Friedman S, Schwartz E, Ahern V, Ahern E. Globin synthesis in the Jamaican Negro with beta-thalassaemia. British Journal of Haematology. 28: 505-13. PMID 4455302 DOI: 10.1111/J.1365-2141.1974.Tb06669.X |
0.361 |
|
| 1975 |
Kinney TR, Harris MB, Russell MO, Duckett J, Schwartz E. Priapism in association with sickle hemoglobinopathies in children. The Journal of Pediatrics. 86: 241-2. PMID 1111689 DOI: 10.1016/S0022-3476(75)80478-1 |
0.32 |
|
| 1974 |
Asakura T, Adachi K, Sono M, Friedman S, Schwartz E. Mechanical stability of hemoglobin subunits: an abnormality in betaS-subunits of sickle hemoglobin. Biochemical and Biophysical Research Communications. 57: 780-6. PMID 4827832 DOI: 10.1016/0006-291X(74)90614-7 |
0.36 |
|
| 1974 |
Schwartz E, Gill FM. REGULATION OF HEMOGLOBIN SYNTHESIS IN β‐THALASSEMIA* Annals of the New York Academy of Sciences. 232: 33-39. PMID 4528708 DOI: 10.1111/J.1749-6632.1974.Tb20569.X |
0.313 |
|
| 1974 |
Asakura T, Onishi T, Friedman S, Schwartz E. Abnormal precipitation of oxyhemoglobin S by mechanical shaking. Proceedings of the National Academy of Sciences of the United States of America. 71: 1594-8. PMID 4525907 DOI: 10.1073/Pnas.71.5.1594 |
0.359 |
|
| 1974 |
Friedman S, Atwater J, Gill FM, Schwartz E. α-Thalassemia in Negro Infants Pediatric Research. 8: 955-959. PMID 4444865 DOI: 10.1203/00006450-197412000-00008 |
0.337 |
|
| 1974 |
Harris MB, Root RK, Schwartz E. METABOLIC AND FUNCTIONAL DEFECTS IN NEONATAL GRANULOCYTES |[lpar]|PMN|[rpar]| Pediatric Research. 8: 413-413. DOI: 10.1203/00006450-197404000-00440 |
0.332 |
|
| 1974 |
Wiley JS, Gill FM, Schwartz E. A New Form Of Congenital Hemolytic Anemia With Extreme Microcytosis And Calcium Leak Pediatric Research. 8: 411-411. DOI: 10.1203/00006450-197404000-00425 |
0.354 |
|
| 1974 |
Russell MO, Goldberg HI, Friedman S, Reivich M, Schwartz E. Improvement Of Cerebral Vascular Disease In Sickle Cell Anemia Following Transfusions Pediatric Research. 8: 408-408. DOI: 10.1203/00006450-197404000-00409 |
0.368 |
|
| 1974 |
Harris MB, Djerassi I, Schwartz E, Root RK. Polymorphonuclear Leukocytes Prepared by Continuous-Flow Filtration Leukapheresis: Viability and Function Blood. 44: 707-713. DOI: 10.1182/Blood.V44.5.707.707 |
0.349 |
|
| 1973 |
Gill F, Atwater J, Schwartz E. Hemoglobin Lepore trait: globin synthesis in bone marrow and peripheral blood. Science (New York, N.Y.). 178: 623-5. PMID 5086396 DOI: 10.1126/Science.178.4061.623 |
0.427 |
|
| 1973 |
Friedman S, Hamilton RW, Schwartz E. Beta-thalassemia in the American Negro. The Journal of Clinical Investigation. 52: 1453-9. PMID 4703230 DOI: 10.1172/jci107319 |
0.34 |
|
| 1973 |
Gill FM, Schwartz E. Synthesis of globin chains in sickle -thalassemia. The Journal of Clinical Investigation. 52: 709-14. PMID 4685090 DOI: 10.1172/Jci107232 |
0.438 |
|
| 1973 |
Gill FM, Schwartz E. Anemia in early infancy. Pediatric Clinics of North America. 19: 841-53. PMID 4628193 DOI: 10.1016/S0031-3955(16)32769-9 |
0.362 |
|
| 1973 |
Asakura T, Agarwal PL, Relman DA, McCray JA, Chance B, Schwartz E, Friedman S, Lubin B. Mechanical instability of the oxy-form of sickle haemoglobin. Nature. 244: 437-8. PMID 4582496 DOI: 10.1038/244437A0 |
0.353 |
|
| 1973 |
Gill FM, Schwartz E. Free α-Globin Pool in Human Bone Marrow Journal of Clinical Investigation. 52: 3057-3063. PMID 4127219 DOI: 10.1172/Jci107504 |
0.426 |
|
| 1973 |
Habib M, Watson V, Schwartz E. The effect of sodium cyanate on globin synthesis. Blood. 41: 635-639. DOI: 10.1182/Blood.V41.5.635.635 |
0.373 |
|
| 1972 |
Hamilton RW, Schwartz E, Atwater J, Erslev AJ. Acquired hemoglobin H disease. The New England Journal of Medicine. 285: 1217-21. PMID 5113710 DOI: 10.1056/Nejm197111252852202 |
0.423 |
|
| 1972 |
Schwartz E, Atwater J. α-Thalassemia in the American Negro Journal of Clinical Investigation. 51: 412-418. PMID 5061833 DOI: 10.1172/Jci106827 |
0.425 |
|
| 1972 |
Schwartz E. Hemoglobinopathies of clinical importance Pediatric Clinics of North America. 19: 889-905. PMID 4562934 DOI: 10.1016/S0031-3955(16)32772-9 |
0.358 |
|
| 1972 |
Friedman S, Oski FA, Schwartz E. Bone Marrow and Peripheral Blood Globin Synthesis in an American Black Family With Beta Thalassemia Blood. 39: 785-793. DOI: 10.1182/Blood.V39.6.785.785 |
0.423 |
|
| 1971 |
Gill FM, Schwartz E, Brent RL. Platelet transfusion as a diagnostic and therapeutic aid in the newborn Pediatric Research. 5: 409-409. DOI: 10.1203/00006450-197108000-00159 |
0.333 |
|
| 1970 |
Schwartz E, Kan YW, Nathan DG. Unbalanced globin chain synthesis in alpha-thalassemia heterozygotes. Annals of the New York Academy of Sciences. 165: 288-94. PMID 5260151 DOI: 10.1111/j.1749-6632.1969.tb27798.x |
0.281 |
|
| 1970 |
Lubin BH, Baehner RL, Schwartz E, Shohet SB, Nathan DG, Janeway CA. Hydrogen Peroxide Hemolysis: A Test for Biliary Obstruction Pediatric Research. 4: 476-477. DOI: 10.1203/00006450-197009000-00190 |
0.329 |
|
| 1969 |
Kan YW, Schwartz E, Nathan DG. Globin chain synthesis in the alpha thalassemia syndromes. The Journal of Clinical Investigation. 47: 2512-22. PMID 5775343 DOI: 10.1172/JCI105933 |
0.333 |
|
| 1969 |
Schwartz E. The silent carrier of beta thalassemia New England Journal of Medicine. 281: 1327-1333. PMID 5355437 DOI: 10.1056/Nejm196912112812403 |
0.424 |
|
| 1968 |
Rigolosi RS, Schwartz E, Glick SM. Occurrence of growth-hormone deficiency in acromegaly as a result of pituitary apoplexy. The New England Journal of Medicine. 279: 362-4. PMID 5662169 DOI: 10.1056/NEJM196808152790707 |
0.19 |
|
| 1968 |
Schwartz E. Therapy for blood disorders in infants and children Pediatric Clinics of North America. 15: 473-492. PMID 4968372 DOI: 10.1016/S0031-3955(16)32134-4 |
0.333 |
|
| 1968 |
Schwartz E, Gerald PS. Mouse hemoglobin: chain composition multiple electrophoretic bands. Experientia. 23: 763-5. PMID 4964917 DOI: 10.1007/BF02154164 |
0.221 |
|
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