Keith Hyland - Publications

Affiliations: 
Baylor University, Waco, TX 
Area:
Neuroscience Biology

70 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Shoffner J, Trommer B, Thurm A, Farmer C, Langley WA, Soskey L, Rodriguez AN, D'Souza P, Spence SJ, Hyland K, Swedo SE. CSF concentrations of 5-methyltetrahydrofolate in a cohort of young children with autism. Neurology. PMID 27178705 DOI: 10.1212/Wnl.0000000000002766  0.52
2016 Lim YY, Tapawan SJC, Pang AYW, Hyland K, Tay SKH. Secondary Cerebral Folate Deficiency Comorbidity in Neuronal Ceroid Lipofuscinosis Journal of Pediatric Neurology. 14: 78-81. DOI: 10.1055/s-0036-1583275  0.52
2015 Yeo TW, Lampah DA, Kenangalem E, Tjitra E, Price RN, Weinberg JB, Hyland K, Granger DL, Anstey NM. Impaired systemic tetrahydrobiopterin bioavailability and increased dihydrobiopterin in adult falciparum malaria: association with disease severity, impaired microvascular function and increased endothelial activation. Plos Pathogens. 11: e1004667. PMID 25764397 DOI: 10.1371/journal.ppat.1004667  0.52
2015 Rubach MP, Mukemba J, Florence S, Lopansri BK, Hyland K, Volkheimer AD, Yeo TW, Anstey NM, Weinberg JB, Mwaikambo ED, Granger DL. Impaired systemic tetrahydrobiopterin bioavailability and increased oxidized biopterins in pediatric falciparum malaria: association with disease severity. Plos Pathogens. 11: e1004655. PMID 25764173 DOI: 10.1371/journal.ppat.1004655  0.52
2015 Mercimek-Mahmutoglu S, Sidky S, Hyland K, Patel J, Donner EJ, Logan W, Mendoza-Londono R, Moharir M, Raiman J, Schulze A, Siriwardena K, Yoon G, Kyriakopoulou L. Prevalence of inherited neurotransmitter disorders in patients with movement disorders and epilepsy: a retrospective cohort study. Orphanet Journal of Rare Diseases. 10: 12. PMID 25758715 DOI: 10.1186/S13023-015-0234-9  0.52
2014 Mercimek-Mahmutoglu S, Cordeiro D, Cruz V, Hyland K, Struys EA, Kyriakopoulou L, Mamak E. Novel therapy for pyridoxine dependent epilepsy due to ALDH7A1 genetic defect: L-arginine supplementation alternative to lysine-restricted diet. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 18: 741-6. PMID 25127453 DOI: 10.1016/J.Ejpn.2014.07.001  0.52
2014 D'Aco KE, Bearden D, Watkins D, Hyland K, Rosenblatt DS, Ficicioglu C. Severe 5,10-methylenetetrahydrofolate reductase deficiency and two MTHFR variants in an adolescent with progressive myoclonic epilepsy. Pediatric Neurology. 51: 266-70. PMID 25079578 DOI: 10.1016/j.pediatrneurol.2014.04.005  0.52
2014 Sparks SE, Wassif CA, Goodwin H, Conley SK, Lanham DC, Kratz LE, Hyland K, Gropman A, Tierney E, Porter FD. Decreased cerebral spinal fluid neurotransmitter levels in Smith-Lemli-Opitz syndrome Journal of Inherited Metabolic Disease. 37: 415-420. PMID 24500076 DOI: 10.1007/s10545-013-9672-5  0.52
2014 Rognum IJ, Tran H, Haas EA, Hyland K, Paterson DS, Haynes RL, Broadbelt KG, Harty BJ, Mena O, Krous HF, Kinney HC. Serotonin metabolites in the cerebrospinal fluid in sudden infant death syndrome. Journal of Neuropathology and Experimental Neurology. 73: 115-22. PMID 24423636 DOI: 10.1097/NEN.0000000000000034  0.52
2014 Blau N, Hyland K, Hoffmann GF. Defects in catabolism of biogenic amines Congenital Neurotransmitter Disorders: a Clinical Approach. 93-99.  0.52
2013 Goyal M, Fequiere PR, McGrath TM, Hyland K. Seizures with decreased levels of pyridoxal phosphate in cerebrospinal fluid. Pediatric Neurology. 48: 227-31. PMID 23419474 DOI: 10.1016/j.pediatrneurol.2012.11.006  0.52
2012 Farook MF, DeCuypere M, Hyland K, Takumi T, LeDoux MS, Reiter LT. Altered serotonin, dopamine and norepinepherine levels in 15q duplication and Angelman syndrome mouse models. Plos One. 7: e43030. PMID 22916201 DOI: 10.1371/Journal.Pone.0043030  0.52
2012 Friedman J, Roze E, Abdenur JE, Chang R, Gasperini S, Saletti V, Wali GM, Eiroa H, Neville B, Felice A, Parascandalo R, Zafeiriou DI, Arrabal-Fernandez L, Dill P, Eichler FS, ... ... Hyland K, et al. Sepiapterin reductase deficiency: a treatable mimic of cerebral palsy. Annals of Neurology. 71: 520-30. PMID 22522443 DOI: 10.1002/Ana.22685  0.52
2012 O'Leary RE, Shih JC, Hyland K, Kramer N, Asher YJ, Graham JM. De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine. European Journal of Medical Genetics. 55: 349-53. PMID 22365943 DOI: 10.1016/j.ejmg.2012.01.007  0.52
2012 Hyland K, Hyland L. Deficiencies of Tetrahydrobiopterin, Tyrosine Hydroxylase and Aromatic L-Amino Acid Decarboxylase Primer On the Autonomic Nervous System. 427-430. DOI: 10.1016/B978-0-12-386525-0.00087-1  0.52
2011 Horvath GA, Selby K, Poskitt K, Hyland K, Waters PJ, Coulter-Mackie M, Stockler-Ipsiroglu SG. Hemiplegic migraine, seizures, progressive spastic paraparesis, mood disorder, and coma in siblings with low systemic serotonin. Cephalalgia : An International Journal of Headache. 31: 1580-6. PMID 22013141 DOI: 10.1177/0333102411420584  0.52
2011 Veerapandiyan A, Winchester SA, Gallentine WB, Smith EC, Kansagra S, Hyland K, Mikati MA. Electroencephalographic and seizure manifestations of pyridoxal 5'-phosphate-dependent epilepsy. Epilepsy & Behavior : E&B. 20: 494-501. PMID 21292558 DOI: 10.1016/j.yebeh.2010.12.046  0.52
2010 Hyland K, Shoffner J, Heales SJ. Cerebral folate deficiency. Journal of Inherited Metabolic Disease. 33: 563-70. PMID 20668945 DOI: 10.1007/S10545-010-9159-6  0.52
2010 Allen GF, Neergheen V, Oppenheim M, Fitzgerald JC, Footitt E, Hyland K, Clayton PT, Land JM, Heales SJ. Pyridoxal 5'-phosphate deficiency causes a loss of aromatic L-amino acid decarboxylase in patients and human neuroblastoma cells, implications for aromatic L-amino acid decarboxylase and vitamin B(6) deficiency states. Journal of Neurochemistry. 114: 87-96. PMID 20403077 DOI: 10.1111/J.1471-4159.2010.06742.X  0.52
2010 Shoffner J, Hyams L, Langley GN, Cossette S, Mylacraine L, Dale J, Ollis L, Kuoch S, Bennett K, Aliberti A, Hyland K. Fever plus mitochondrial disease could be risk factors for autistic regression. Journal of Child Neurology. 25: 429-34. PMID 19773461 DOI: 10.1177/0883073809342128  0.52
2009 Samaco RC, Mandel-Brehm C, Chao HT, Ward CS, Fyffe-Maricich SL, Ren J, Hyland K, Thaller C, Maricich SM, Humphreys P, Greer JJ, Percy A, Glaze DG, Zoghbi HY, Neul JL. Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities. Proceedings of the National Academy of Sciences of the United States of America. 106: 21966-71. PMID 20007372 DOI: 10.1073/pnas.0912257106  0.52
2009 Gunasekera RS, Hyland K. In vivo regulation of phenylalanine hydroxylase in the genetic mutant hph-1 mouse model. Molecular Genetics and Metabolism. 98: 264-72. PMID 19560382 DOI: 10.1016/j.ymgme.2009.05.007  0.52
2009 Rosenberg EH, Struys EA, Hyland K, Plecko B, Waters PJ, Mercimek-Mahmutoglu S, Stockler-Ipsiroglu S, Gallagher RC, Scharer G, Van Hove JL, Jakobs C, Salomons GS. Mutation detection in DNA isolated from cerebrospinal fluid and urine: Clinical utility and pitfalls of multiple displacement amplification. Molecular Genetics and Metabolism. 97: 312-4. PMID 19501531 DOI: 10.1016/J.Ymgme.2009.05.002  0.52
2009 Parikh S, Hyland K, Lachhwani DK. Vitamins, not surgery: spinal fluid testing in hemispheric epilepsy. Pediatric Neurology. 40: 477-9. PMID 19433287 DOI: 10.1016/j.pediatrneurol.2009.01.007  0.52
2009 Gallagher RC, Van Hove JL, Scharer G, Hyland K, Plecko B, Waters PJ, Mercimek-Mahmutoglu S, Stockler-Ipsiroglu S, Salomons GS, Rosenberg EH, Struys EA, Jakobs C. Folinic acid-responsive seizures are identical to pyridoxine-dependent epilepsy. Annals of Neurology. 65: 550-6. PMID 19142996 DOI: 10.1002/Ana.21568  0.52
2009 Willoughby RE, Opladen T, Maier T, Rhead W, Schmiedel S, Hoyer J, Drosten C, Rupprecht CE, Hyland K, Hoffmann GF. Tetrahydrobiopterin deficiency in human rabies Journal of Inherited Metabolic Disease. 32: 65-72. PMID 18949578 DOI: 10.1007/s10545-008-0949-z  0.52
2009 Allen RP, Connor JR, Hyland K, Earley CJ. Abnormally increased CSF 3-Ortho-methyldopa (3-OMD) in untreated restless legs syndrome (RLS) patients indicates more severe disease and possibly abnormally increased dopamine synthesis. Sleep Medicine. 10: 123-8. PMID 18226951 DOI: 10.1016/j.sleep.2007.11.012  0.52
2008 Willoughby RE, Roy-Burman A, Martin KW, Christensen JC, Westenkirschner DF, Fleck JD, Glaser C, Hyland K, Rupprecht CE. Generalised cranial artery spasm in human rabies. Developments in Biologicals. 131: 367-75. PMID 18634498  0.52
2008 Hyland K. Clinical utility of monoamine neurotransmitter metabolite analysis in cerebrospinal fluid. Clinical Chemistry. 54: 633-41. PMID 18310141 DOI: 10.1373/Clinchem.2007.099986  0.52
2008 Ormazabal A, Oppenheim M, Serrano M, García-Cazorla A, Campistol J, Ribes A, Ruiz A, Moreno J, Hyland K, Clayton P, Heales S, Artuch R. Pyridoxal 5'-phosphate values in cerebrospinal fluid: reference values and diagnosis of PNPO deficiency in paediatric patients. Molecular Genetics and Metabolism. 94: 173-7. PMID 18294893 DOI: 10.1016/J.Ymgme.2008.01.004  0.52
2008 Horvath GA, Stockler-Ipsiroglu SG, Salvarinova-Zivkovic R, Lillquist YP, Connolly M, Hyland K, Blau N, Rupar T, Waters PJ. Autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia: evidence of a phenotypic continuum between dominant and recessive forms. Molecular Genetics and Metabolism. 94: 127-31. PMID 18276179 DOI: 10.1016/J.Ymgme.2008.01.003  0.52
2008 Moretti P, Peters SU, Del Gaudio D, Sahoo T, Hyland K, Bottiglieri T, Hopkin RJ, Peach E, Min SH, Goldman D, Roa B, Bacino CA, Scaglia F. Brief report: autistic symptoms, developmental regression, mental retardation, epilepsy, and dyskinesias in CNS folate deficiency. Journal of Autism and Developmental Disorders. 38: 1170-7. PMID 18027081 DOI: 10.1007/S10803-007-0492-Z  0.52
2007 Tay SK, Poh KS, Hyland K, Pang YW, Ong HT, Low PS, Goh DL. Unusually mild phenotype of AADC deficiency in 2 siblings. Molecular Genetics and Metabolism. 91: 374-8. PMID 17533144 DOI: 10.1016/j.ymgme.2007.04.006  0.52
2007 Hyland K. Inherited disorders affecting dopamine and serotonin: critical neurotransmitters derived from aromatic amino acids. The Journal of Nutrition. 137: 1568S-1572S; discuss. PMID 17513427  0.52
2007 Lam AAJ, Hyland K, Heales SJR. Tetrahydrobiopterin availability, nitric oxide metabolism and glutathione status in the hph-1 mouse; implications for the pathogenesis and treatment of tetrahydrobiopterin deficiency states Journal of Inherited Metabolic Disease. 30: 256-262. PMID 17242981 DOI: 10.1007/s10545-006-0502-x  0.52
2006 Hogg RJ, Lee J, Nardelli N, Julian BA, Cattran D, Waldo B, Wyatt R, Jennette JC, Sibley R, Hyland K, Fitzgibbons L, Hirschman G, Donadio JV, Holub BJ. Clinical trial to evaluate omega-3 fatty acids and alternate day prednisone in patients with IgA nephropathy: report from the Southwest Pediatric Nephrology Study Group. Clinical Journal of the American Society of Nephrology : Cjasn. 1: 467-74. PMID 17699247 DOI: 10.2215/CJN.01020905  0.52
2006 Friedman J, Hyland K, Blau N, MacCollin M. Dopa-responsive hypersomnia and mixed movement disorder due to sepiapterin reductase deficiency. Neurology. 67: 2032-5. PMID 17159114 DOI: 10.1212/01.Wnl.0000247274.21261.B4  0.52
2006 Lin FY, Gascon GG, Hyland K, Chugani H, Chugani D. Transient nonketotic hyperglycinemia and defective serotonin metabolism in a child with neonatal seizures. Journal of Child Neurology. 21: 900-3. PMID 17005111 DOI: 10.1177/08830738060210101001  0.52
2006 Earley CJ, Hyland K, Allen RP. Circadian changes in CSF dopaminergic measures in restless legs syndrome. Sleep Medicine. 7: 263-8. PMID 16564215 DOI: 10.1016/j.sleep.2005.09.006  0.52
2005 Neul JL, Maricich SM, Islam M, Barrish J, Smith EO, Bottiglieri T, Hyland K, Humphreys P, Percy A, Glaze D. Spinal fluid 5-methyltetrahydrofolate levels are normal in Rett syndrome. Neurology. 64: 2151-2. PMID 15985595 DOI: 10.1212/01.Wnl.0000166032.58239.6C  0.52
2005 Demos MK, Waters PJ, Vallance HD, Lillquist Y, Makhseed N, Hyland K, Blau N, Connolly MB. 6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemia. Annals of Neurology. 58: 164-7. PMID 15984017 DOI: 10.1002/Ana.20532  0.52
2005 McPhee SWJ, Francis J, Janson CG, Serikawa T, Hyland K, Ong EO, Raghavan SS, Freese A, Leone P. Effects of AAV-2-mediated aspartoacylase gene transfer in the tremor rat model of Canavan disease Molecular Brain Research. 135: 112-121. PMID 15857674 DOI: 10.1016/j.molbrainres.2004.12.007  0.52
2005 Moretti P, Sahoo T, Hyland K, Bottiglieri T, Peters S, del Gaudio D, Roa B, Curry S, Zhu H, Finnell RH, Neul JL, Ramaekers VT, Blau N, Bacino CA, Miller G, et al. Cerebral folate deficiency with developmental delay, autism, and response to folinic acid. Neurology. 64: 1088-90. PMID 15781839 DOI: 10.1212/01.Wnl.0000154641.08211.B7  0.52
2005 Wang CH, Li SH, Weisel RD, Fedak PW, Hung A, Li RK, Rao V, Hyland K, Cherng WJ, Errett L, Leclerc Y, Bonneau D, Latter DA, Verma S. Tetrahydrobiopterin deficiency exaggerates intimal hyperplasia after vascular injury. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 289: R299-304. PMID 15774769 DOI: 10.1152/ajpregu.00269.2004  0.52
2005 Gunasekera RS, Damodaran H, Rajakarunanayake Y, Hyland K. The significance of linearity of quantities in electrophoresed and blotted materials demonstrated by BandScan© - An analytical program 2005 Ieee Computational Systems Bioinformatics Conference, Workshops and Poster Abstracts. 277. DOI: 10.1109/CSBW.2005.132  0.52
2004 Pranzatelli MR, Hyland K, Tate ED, Arnold LA, Allison TJ, Soori GS. Evidence of cellular immune activation in children with opsoclonus-myoclonus: cerebrospinal fluid neopterin. Journal of Child Neurology. 19: 919-24. PMID 15704863 DOI: 10.1177/08830738040190120201  0.52
2004 Saunders-Pullman R, Blau N, Hyland K, Zschocke J, Nygaard T, Raymond D, Shanker V, Mohrmann K, Arnold L, Tabbal S, deLeon D, Ford B, Brin M, Chouinard S, Ozelius L, et al. Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test. Molecular Genetics and Metabolism. 83: 207-12. PMID 15542391 DOI: 10.1016/j.ymgme.2004.07.010  0.52
2004 Kweon GR, Marks JD, Krencik R, Leung EH, Schumacker PT, Hyland K, Kang UJ. Distinct mechanisms of neurodegeneration induced by chronic complex I inhibition in dopaminergic and non-dopaminergic cells. The Journal of Biological Chemistry. 279: 51783-92. PMID 15469939 DOI: 10.1074/Jbc.M407336200  0.52
2004 Hyland K, Kasim S, Egami K, Arnold LA, Jinnah HA. Tetrahydrobiopterin deficiency and dopamine loss in a genetic mouse model of Lesch-Nyhan disease. Journal of Inherited Metabolic Disease. 27: 165-78. PMID 15159647 DOI: 10.1023/B:BOLI.0000028728.93113.4d  0.52
2004 Assmann BE, Robinson RO, Surtees RAH, Bräutigam C, Heales SJR, Wevers RA, Zschocke J, Hyland K, Sharma R, Hoffmann GF. Infantile parkinsonism-dystonia and elevated dopamine metabolites in CSF Neurology. 62: 1872-1874. PMID 15159499 DOI: 10.1212/01.Wnl.0000126440.16612.51  0.52
2004 Pons R, Ford B, Chiriboga CA, Clayton PT, Hinton V, Hyland K, Sharma R, De Vivo DC. Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis. Neurology. 62: 1058-65. PMID 15079002 DOI: 10.1212/Wnl.62.7.1058  0.52
2004 Chang YT, Sharma R, Marsh JL, McPherson JD, Bedell JA, Knust A, Bräutigam C, Hoffmann GF, Hyland K. Levodopa-Responsive Aromatic L-Amino Acid Decarboxylase Deficiency Annals of Neurology. 55: 435-438. PMID 14991824 DOI: 10.1002/ana.20055  0.52
2004 Hyland K, Arnold LA. Deficiencies of Tetrahydrobiopterin, Tyrosine Hydroxylase, and Aromatic L-Amino Acid Decarboxylase Primer On the Autonomic Nervous System: Second Edition. 271-273. DOI: 10.1016/B978-012589762-4/50073-6  0.52
2003 Swoboda KJ, Saul JP, McKenna CE, Speller NB, Hyland K. Aromatic L-amino acid decarboxylase deficiency: overview of clinical features and outcomes. Annals of Neurology. 54: S49-55. PMID 12891654 DOI: 10.1002/ana.10631  0.52
2003 Hyland K, Gunasekara RS, Munk-Martin TL, Arnold LA, Engle T. The hph-1 mouse: a model for dominantly inherited GTP-cyclohydrolase deficiency. Annals of Neurology. 54: S46-8. PMID 12891653 DOI: 10.1002/ana.10695  0.52
2003 Hyland K. The lumbar puncture for diagnosis of pediatric neurotransmitter diseases. Annals of Neurology. 54: S13-7. PMID 12891649 DOI: 10.1002/Ana.10627  0.52
2003 Clayton PT, Surtees RAH, DeVile C, Hyland K, Heales SJR. Neonatal epileptic encephalopathy Lancet. 361: 1614. PMID 12747882 DOI: 10.1016/S0140-6736(03)13312-0  0.52
2003 Perera A, Hyland K, Nguyen HK, Kane RR. Synthesis of deuterium-labeled 3-O-methyldopa and 4-O-methyldopa Journal of Labelled Compounds and Radiopharmaceuticals. 46: 389-394. DOI: 10.1002/Jlcr.677  0.52
2002 Swoboda KJ, Hyland K. Diagnosis and treatment of neurotransmitter-related disorders. Neurologic Clinics. 20: 1143-61, viii. PMID 12616685 DOI: 10.1016/S0733-8619(02)00018-X  0.52
2002 Hyland K, Arnold LA. Value of lumbar puncture in the diagnosis of infantile epilepsy and folinic acid-responsive seizures. Journal of Child Neurology. 17: 3S48-55; discussion . PMID 12597055  0.52
2001 Earley CJ, Hyland K, Allen RP. CSF dopamine, serotonin, and biopterin metabolites in patients with restless legs syndrome Movement Disorders. 16: 144-149. PMID 11215576 DOI: 10.1002/1531-8257(200101)16:1<144::AID-MDS1009>3.0.CO;2-F  0.52
1999 Heales SJ, Canevari L, Brand MP, Clark JB, Land JM, Hyland K. Cerebrospinal fluid nitrite plus nitrate correlates with tetrahydrobiopterin concentration. Journal of Inherited Metabolic Disease. 22: 221-3. PMID 10384372 DOI: 10.1023/A:1005540828706  0.52
1998 Furukawa Y, Kish SJ, Bebin EM, Jacobson RD, Fryburg JS, Wilson WG, Shimadzu M, Hyland K, Trugman JM. Dystonia with motor delay in compound heterozygotes for GTP-cyclohydrolase I gene mutations. Annals of Neurology. 44: 10-6. PMID 9667588 DOI: 10.1002/Ana.410440107  0.52
1998 Brashear A, Butler IJ, Hyland K, Farlow MR, Dobyns WB. Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism. Annals of Neurology. 43: 521-6. PMID 9546335 DOI: 10.1002/Ana.410430417  0.52
1997 Chang YT, Hyland K, Mues G, Marsh JL. Human hair follicles as a peripheral source of tyrosine hydroxylase and aromatic L-amino acid decarboxylase mRNA Neuroscience Letters. 222: 210-212. PMID 9148252 DOI: 10.1016/S0304-3940(97)13380-8  0.52
1996 Brand MP, Hyland K, Engle T, Smith I, Heales SJ. Neurochemical effects following peripheral administration of tetrahydropterin derivatives to the hph-1 mouse. Journal of Neurochemistry. 66: 1150-6. PMID 8769878 DOI: 10.1046/J.1471-4159.1996.66031150.X  0.52
1995 Hyland K, Buist NR, Powell BR, Hoffman GF, Rating D, McGrath J, Acworth IN. Folinic acid responsive seizures: a new syndrome? Journal of Inherited Metabolic Disease. 18: 177-81. PMID 7564240 DOI: 10.1007/Bf00711760  0.52
1994 Bottiglieri T, Hyland K, Reynolds EH. The Clinical Potential of Ademetionine (S-Adenosylmethionine) in Neurological Disorders Drugs. 48: 137-152. PMID 7527320 DOI: 10.2165/00003495-199448020-00002  0.52
1993 Hyland K, Surtees RAH, Heales SJR, Bowron A, Howells DW, Smith I. Cerebrospinal Fluid Concentrations of Pterins and Metabolites of Serotonin and Dopamine in a Pediatric Reference Population Pediatric Research. 34: 10-14. PMID 7689195 DOI: 10.1203/00006450-199307000-00003  0.52
1986 Pinkerton CR, Smith I, Leeming RJ, Sarna G, Hyland K, Curzon G, Chessells JM. Biopterin and neurotransmitter amine metabolism in children with acute lymphoblastic leukemia receiving methotrexate therapy. The Journal of Pediatrics. 108: 470-4. PMID 2419534 DOI: 10.1016/S0022-3476(86)80904-0  0.52
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