Year |
Citation |
Score |
2013 |
Shin JY, Méndez-López I, Wang Y, Hays AP, Tanji K, Lefkowitch JH, Schulze PC, Worman HJ, Dauer WT. Lamina-associated polypeptide-1 interacts with the muscular dystrophy protein emerin and is essential for skeletal muscle maintenance. Developmental Cell. 26: 591-603. PMID 24055652 DOI: 10.1016/J.Devcel.2013.08.012 |
0.309 |
|
2012 |
Ash DB, Papadimitriou D, Hays AP, Dimauro S, Hirano M. A novel mutation in PNPLA2 leading to neutral lipid storage disease with myopathy. Archives of Neurology. 69: 1190-2. PMID 22964912 DOI: 10.1001/Archneurol.2011.2600 |
0.321 |
|
2012 |
Rong L, Yan S, Hays A, Gooch C, Schmidt AM. RAGE-Dependent Signaling in Peripheral Neurons and Macrophages Regulates Peripheral Nerve Repair (IN1-2.004) Neurology. 78. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In1-2.004 |
0.322 |
|
2010 |
Hays AP. Utility of skin biopsy to evaluate peripheral neuropathy. Current Neurology and Neuroscience Reports. 10: 101-7. PMID 20425234 DOI: 10.1007/S11910-010-0094-6 |
0.351 |
|
2009 |
Souayah N, Ajroud-Driss S, Sander HW, Brannagan TH, Hays AP, Chin RL. Small fiber neuropathy following vaccination for rabies, varicella or Lyme disease. Vaccine. 27: 7322-5. PMID 19808027 DOI: 10.1016/J.Vaccine.2009.09.077 |
0.302 |
|
2009 |
Ostlund C, Guan T, Figlewicz DA, Hays AP, Worman HJ, Gerace L, Schirmer EC. Reduction of a 4q35-encoded nuclear envelope protein in muscle differentiation. Biochemical and Biophysical Research Communications. 389: 279-83. PMID 19716805 DOI: 10.1016/J.Bbrc.2009.08.133 |
0.321 |
|
2009 |
Chen IH, Mitsumoto H, Vonsattel JP, Hays AP. Amyotrophic lateral sclerosis and neurosarcoidosis: a case report. Muscle & Nerve. 39: 234-8. PMID 19127576 DOI: 10.1002/Mus.21159 |
0.317 |
|
2008 |
Hirano M, Angelini C, Montagna P, Hays AP, Tanji K, Mitsumoto H, Gordon PH, Naini AB, DiMauro S, Rowland LP. Amyotrophic lateral sclerosis with ragged-red fibers. Archives of Neurology. 65: 403-6. PMID 18332255 DOI: 10.1001/Archneurol.2007.65 |
0.345 |
|
2008 |
Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaño P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, et al. X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1. American Journal of Human Genetics. 82: 208-13. PMID 18179901 DOI: 10.1016/J.Ajhg.2007.09.013 |
0.309 |
|
2007 |
Mitsumoto H, Ulug AM, Pullman SL, Gooch CL, Chan S, Tang MX, Mao X, Hays AP, Floyd AG, Battista V, Montes J, Hayes S, Dashnaw S, Kaufmann P, Gordon PH, et al. Quantitative objective markers for upper and lower motor neuron dysfunction in ALS. Neurology. 68: 1402-10. PMID 17452585 DOI: 10.1212/01.Wnl.0000260065.57832.87 |
0.305 |
|
2007 |
Huang S, Liang J, Zheng M, Li X, Wang M, Wang P, Vanegas D, Wu D, Chakraborty B, Hays AP, Chen K, Chen SG, Booth S, Cohen M, Gambetti P, et al. Inducible overexpression of wild-type prion protein in the muscles leads to a primary myopathy in transgenic mice. Proceedings of the National Academy of Sciences of the United States of America. 104: 6800-5. PMID 17420473 DOI: 10.1073/Pnas.0608885104 |
0.327 |
|
2006 |
De Sousa EA, Hays AP, Chin RL, Sander HW, Brannagan TH. Characteristics of patients with sensory neuropathy diagnosed with abnormal small nerve fibres on skin biopsy. Journal of Neurology, Neurosurgery, and Psychiatry. 77: 983-5. PMID 16844956 DOI: 10.1136/Jnnp.2006.091074 |
0.374 |
|
2006 |
Gordon PH, Cheng B, Katz IB, Pinto M, Hays AP, Mitsumoto H, Rowland LP. The natural history of primary lateral sclerosis. Neurology. 66: 647-53. PMID 16534101 DOI: 10.1212/01.Wnl.0000200962.94777.71 |
0.322 |
|
2006 |
Keller CE, Hays AP, Rowland LP, Moghadaszadeh B, Beggs AH, Bhagat G. Adult-onset nemaline myopathy and monoclonal gammopathy. Archives of Neurology. 63: 132-4. PMID 16401746 DOI: 10.1001/Archneur.63.1.132 |
0.322 |
|
2006 |
Slonim AE, Bulone L, Minikes J, Hays AP, Shanske S, Tsujino S, DiMauro S. Benign course of glycogen storage disease type IIb in two brothers: nature or nurture? Muscle & Nerve. 33: 571-4. PMID 16320310 DOI: 10.1002/Mus.20473 |
0.327 |
|
2005 |
Madrid RE, Kubisch C, Hays AP. Early-onset toe walking in rippling muscle disease due to a new caveolin-3 gene mutation. Neurology. 65: 1301-3. PMID 16247063 DOI: 10.1212/01.Wnl.0000180963.85963.73 |
0.302 |
|
2005 |
Brannagan TH, Hays AP, Chin SS, Sander HW, Chin RL, Magda P, Green PH, Latov N. Small-fiber neuropathy/neuronopathy associated with celiac disease: skin biopsy findings. Archives of Neurology. 62: 1574-8. PMID 16216941 DOI: 10.1001/Archneur.62.10.1574 |
0.37 |
|
2005 |
Renaud S, Hays AP, Brannagan TH, Sander HW, Edgar M, Weimer LH, Olarte MR, Dalakas MC, Xiang Z, Danon MJ, Latov N. Gene expression profiling in chronic inflammatory demyelinating polyneuropathy. Journal of Neuroimmunology. 159: 203-14. PMID 15652421 DOI: 10.1016/J.Jneuroim.2004.10.021 |
0.315 |
|
2004 |
Rong LL, Yan SF, Wendt T, Hans D, Pachydaki S, Bucciarelli LG, Adebayo A, Qu W, Lu Y, Kostov K, Lalla E, Yan SD, Gooch C, Szabolcs M, Trojaborg W, ... Hays AP, et al. RAGE modulates peripheral nerve regeneration via recruitment of both inflammatory and axonal outgrowth pathways. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 18: 1818-25. PMID 15576485 DOI: 10.1096/Fj.04-1900Com |
0.335 |
|
2004 |
Rong LL, Trojaborg W, Qu W, Kostov K, Yan SD, Gooch C, Szabolcs M, Hays AP, Schmidt AM. Antagonism of RAGE suppresses peripheral nerve regeneration. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 18: 1812-7. PMID 15576484 DOI: 10.1096/Fj.04-1899Com |
0.346 |
|
2004 |
Leung CL, He CZ, Kaufmann P, Chin SS, Naini A, Liem RK, Mitsumoto H, Hays AP. A pathogenic peripherin gene mutation in a patient with amyotrophic lateral sclerosis. Brain Pathology (Zurich, Switzerland). 14: 290-6. PMID 15446584 DOI: 10.1111/J.1750-3639.2004.Tb00066.X |
0.345 |
|
2004 |
Chin RL, Latov N, Sander HW, Hays AP, Croul SE, Magda P, Brannagan TH. Sensory CIDP presenting as cryptogenic sensory polyneuropathy. Journal of the Peripheral Nervous System : Jpns. 9: 132-7. PMID 15363060 DOI: 10.1111/J.1085-9489.2004.09302.X |
0.396 |
|
2004 |
Kaufmann P, Pullman SL, Shungu DC, Chan S, Hays AP, Del Bene ML, Dover MA, Vukic M, Rowland LP, Mitsumoto H. Objective tests for upper motor neuron involvement in amyotrophic lateral sclerosis (ALS). Neurology. 62: 1753-7. PMID 15159473 DOI: 10.1212/Wnl.63.10.1988 |
0.325 |
|
2004 |
Tay SK, Akman HO, Chung WK, Pike MG, Muntoni F, Hays AP, Shanske S, Valberg SJ, Mickelson JR, Tanji K, DiMauro S. Fatal infantile neuromuscular presentation of glycogen storage disease type IV. Neuromuscular Disorders : Nmd. 14: 253-60. PMID 15019703 DOI: 10.1016/J.Nmd.2003.12.006 |
0.37 |
|
2004 |
Lee G, Jeong Y, Wirguin I, Hays AP, Willison HJ, Latov N. Induction of human IgM and IgG anti-GM1 antibodies in transgenic mice in response to lipopolysaccharides from Campylobacter jejuni. Journal of Neuroimmunology. 146: 63-75. PMID 14698848 DOI: 10.1016/J.Jneuroim.2003.10.045 |
0.314 |
|
2004 |
He CZ, Hays AP. Expression of peripherin in ubiquinated inclusions of amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 217: 47-54. PMID 14675609 DOI: 10.1016/J.Jns.2003.08.016 |
0.328 |
|
2003 |
Portlock CS, Boland P, Hays AP, Antonescu CR, Rosenblum MK. Nemaline myopathy: a possible late complication of Hodgkin's disease therapy. Human Pathology. 34: 816-8. PMID 14506646 DOI: 10.1016/S0046-8177(03)00242-9 |
0.334 |
|
2003 |
Chin RL, Sherman WH, Sander HW, Hays AP, Latov N. Etanercept (Enbrel) therapy for chronic inflammatory demyelinating polyneuropathy. Journal of the Neurological Sciences. 210: 19-21. PMID 12736082 DOI: 10.1016/S0022-510X(03)00010-8 |
0.3 |
|
2003 |
Alaedini A, Sander HW, Hays AP, Latov N. Antiganglioside antibodies in multifocal acquired sensory and motor neuropathy. Archives of Neurology. 60: 42-6. PMID 12533087 DOI: 10.1001/Archneur.60.1.42 |
0.415 |
|
2002 |
Alaedini A, Green PH, Sander HW, Hays AP, Gamboa ET, Fasano A, Sonnenberg M, Lewis LD, Latov N. Ganglioside reactive antibodies in the neuropathy associated with celiac disease. Journal of Neuroimmunology. 127: 145-8. PMID 12044986 DOI: 10.1016/S0165-5728(02)00102-9 |
0.354 |
|
2002 |
Salviati L, Sacconi S, Rasalan MM, Kronn DF, Braun A, Canoll P, Davidson M, Shanske S, Bonilla E, Hays AP, Schon EA, DiMauro S. Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease. Archives of Neurology. 59: 862-5. PMID 12020273 DOI: 10.1001/Archneur.59.5.862 |
0.325 |
|
2001 |
Trojaborg W, Weimer LH, Hays AP. Electrophysiologic studies in critical illness associated weakness: myopathy or neuropathy--a reappraisal. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 112: 1586-93. PMID 11514240 DOI: 10.1016/S1388-2457(01)00572-7 |
0.383 |
|
2001 |
Dabby R, Lange DJ, Trojaborg W, Hays AP, Lovelace RE, Brannagan TH, Rowland LP. Inclusion body myositis mimicking motor neuron disease. Archives of Neurology. 58: 1253-6. PMID 11493165 DOI: 10.1001/Archneur.58.8.1253 |
0.396 |
|
2001 |
Vu TH, Hays AP, Tanji K, Younger D, Gundersen GG, Eastwood A, Braun CW, DiMauro S, Bonilla E. Myopathy with tubulin-reactive crystalline inclusions. Neurology. 57: 149-52. PMID 11445649 DOI: 10.1212/Wnl.57.1.149 |
0.319 |
|
2000 |
Dynes GJ, Schwimer CJ, Staugaitis SM, Doyle JJ, Hays AP, Mitsumoto H. Amyotrophic lateral sclerosis with multiple sclerosis: a clinical and pathological report. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group On Motor Neuron Diseases. 1: 349-53. PMID 11464854 DOI: 10.1080/146608200750139837 |
0.339 |
|
2000 |
Dabby R, Weimer LH, Hays AP, Olarte M, Latov N. Antisulfatide antibodies in neuropathy: clinical and electrophysiologic correlates. Neurology. 54: 1448-52. PMID 10751255 DOI: 10.1212/Wnl.54.7.1448 |
0.389 |
|
2000 |
Rosoklija GB, Dwork AJ, Younger DS, Karlikaya G, Latov N, Hays AP. Local activation of the complement system in endoneurial microvessels of diabetic neuropathy. Acta Neuropathologica. 99: 55-62. PMID 10651028 DOI: 10.1007/Pl00007406 |
0.341 |
|
1999 |
Shimada A, Lange DJ, Hays AP. Amyotrophic lateral sclerosis in an adult following acute paralytic poliomyelitis in early childhood. Acta Neuropathologica. 97: 317-21. PMID 10090681 DOI: 10.1007/S004010050991 |
0.359 |
|
1998 |
Younger DS, Rosoklija G, Hays AP. Diabetic peripheral neuropathy. Seminars in Neurology. 18: 95-104. PMID 9562671 DOI: 10.1055/S-2008-1040865 |
0.379 |
|
1997 |
Brannagan TH, Hays AP, Lange DJ, Trojaborg W. The role of quantitative electromyography in inclusion body myositis. Journal of Neurology, Neurosurgery, and Psychiatry. 63: 776-9. PMID 9416815 DOI: 10.1136/Jnnp.63.6.776 |
0.365 |
|
1997 |
Younger DS, Calabrese LH, Hays AP. Granulomatous angiitis of the nervous system. Neurologic Clinics. 15: 821-34. PMID 9367966 DOI: 10.1016/S0733-8619(05)70349-2 |
0.331 |
|
1997 |
Gordon PH, Rowland LP, Younger DS, Sherman WH, Hays AP, Louis ED, Lange DJ, Trojaborg W, Lovelace RE, Murphy PL, Latov N. Lymphoproliferative disorders and motor neuron disease: an update. Neurology. 48: 1671-8. PMID 9191785 DOI: 10.1212/Wnl.48.6.1671 |
0.391 |
|
1997 |
Corbo M, Abouzahr MK, Latov N, Iannaccone S, Quattrini A, Nemni R, Canal N, Hays AP. Motor nerve biopsy studies in motor neuropathy and motor neuron disease. Muscle & Nerve. 20: 15-21. PMID 8995578 DOI: 10.1002/(Sici)1097-4598(199701)20:1<15::Aid-Mus2>3.0.Co;2-K |
0.373 |
|
1996 |
Gordon PH, Hays AP, Rowland LP, Dickoff DJ, Schotland DL, Rosenberg RN, Wolfe DE, Lange DJ, Lovelace RE. Erroneous diagnosis corrected after 28 years. Not spinal muscular atrophy with ophthalmoplegia but minicore myopathy. Archives of Neurology. 53: 1194-6. PMID 8912497 DOI: 10.1001/Archneur.1996.00550110146028 |
0.339 |
|
1996 |
Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39: 507-20. PMID 8619529 DOI: 10.1002/Ana.410390413 |
0.307 |
|
1996 |
Van den Berg L, Hays AP, Nobile-Orazio E, Kinsella LJ, Manfredini E, Corbo M, Rosoklija G, Younger DS, Lovelace RE, Trojaborg W, Lange DE, Goldstein S, Delfiner JS, Sadiq SA, Sherman WH, et al. Anti-MAG and anti-SGPG antibodies in neuropathy. Muscle & Nerve. 19: 637-43. PMID 8618562 DOI: 10.1002/(Sici)1097-4598(199605)19:5<637::Aid-Mus12>3.0.Co;2-K |
0.377 |
|
1996 |
Younger DS, Rosoklija G, Hays AP, Trojaborg W, Latov N. Diabetic peripheral neuropathy: a clinicopathologic and immunohistochemical analysis of sural nerve biopsies. Muscle & Nerve. 19: 722-7. PMID 8609922 DOI: 10.1002/(Sici)1097-4598(199606)19:6<722::Aid-Mus6>3.0.Co;2-C |
0.323 |
|
1996 |
Abouzahr MK, Lange DJ, Latov N, Olarte M, Rowland LP, Hays AP, Corbo M. Diagnostic biopsy of the motor nerve to the gracilis muscle: Clinical pearl Neurosurgical Focus. 1. DOI: 10.3171/Foc.1996.1.6.10 |
0.373 |
|
1996 |
Latov N, Brannagan T, Rowland LP, Sherman WH, Hays AP, Lange DJ, Trojaborg W, Younger DS. Reply from the Authors: SGPG in ALS Neurology. 46: 1196-1196. DOI: 10.1212/Wnl.46.4.1196 |
0.394 |
|
1995 |
Rowland LP, Sherman WL, Hays AP, Lange DJ, Latov N, Trojaborg W, Younger DS. Autopsy-proven amyotrophic lateral sclerosis, Waldenström's macroglobulinemia, and antibodies to sulfated glucuronic acid paragloboside. Neurology. 45: 827-9. PMID 7723980 DOI: 10.1212/Wnl.45.4.827 |
0.356 |
|
1995 |
Wirguin I, Rosoklija G, Trojaborg W, Hays AP, Latov N. Axonal degeneration accompanied by conduction block induced by toxin mediated immune reactivity to GM1 ganglioside in rat nerves. Journal of the Neurological Sciences. 130: 17-21. PMID 7650526 DOI: 10.1016/0022-510X(94)00270-X |
0.338 |
|
1995 |
McAlarney T, Pastores GM, Hays AP, Latov N. Antisulfatide antibody and neuropathy in a patient with Gaucher's disease. Neurology. 45: 1622-3. PMID 7644066 DOI: 10.1212/Wnl.45.8.1622 |
0.362 |
|
1995 |
Trojaborg W, Hays AP, van den Berg L, Younger DS, Latov N. Motor conduction parameters in neuropathies associated with anti-MAG antibodies and other types of demyelinating and axonal neuropathies. Muscle & Nerve. 18: 730-5. PMID 7540258 DOI: 10.1002/Mus.880180709 |
0.393 |
|
1994 |
Younger DS, Dalmau J, Inghirami G, Sherman WH, Hays AP. Anti-Hu-associated peripheral nerve and muscle microvasculitis. Neurology. 44: 181-3. PMID 8290066 DOI: 10.1212/Wnl.44.1.181-A |
0.362 |
|
1994 |
Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE. Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. Neurology. 44: 721-7. PMID 8164833 DOI: 10.1212/Wnl.44.4.721 |
0.324 |
|
1994 |
Burns SM, Lange DJ, Jaffe I, Hays AP. Axonal neuropathy in eosinophilia-myalgia syndrome. Muscle & Nerve. 17: 293-8. PMID 8107705 DOI: 10.1002/Mus.880170306 |
0.383 |
|
1994 |
Apostolski S, Sadiq SA, Hays A, Corbo M, Suturkova-Milosevic L, Chaliff P, Stefansson K, LeBaron RG, Ruoslahti E, Hays AP. Identification of Gal(beta 1-3)GalNAc bearing glycoproteins at the nodes of Ranvier in peripheral nerve. Journal of Neuroscience Research. 38: 134-41. PMID 8078098 DOI: 10.1002/Jnr.490380203 |
0.323 |
|
1994 |
Thomas FP, Lebo RV, Rosoklija G, Ding XS, Lovelace RE, Latov N, Hays AP. Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome. Acta Neuropathologica. 87: 91-7. PMID 7511317 DOI: 10.1007/Bf00386259 |
0.342 |
|
1993 |
Corbo M, Quattrini A, Latov N, Hays AP. Localization of GM1 and Gal(beta 1-3)GalNAc antigenic determinants in peripheral nerve. Neurology. 43: 809-14. PMID 7682302 DOI: 10.1212/Wnl.43.4.809 |
0.363 |
|
1992 |
Santoro M, Uncini A, Corbo M, Staugaitis SM, Thomas FP, Hays AP, Latov N. Experimental conduction block induced by serum from a patient with anti-GM1 antibodies. Annals of Neurology. 31: 385-90. PMID 1586139 DOI: 10.1002/Ana.410310407 |
0.389 |
|
1992 |
Rowland LP, Sherman WH, Latov N, Lange DJ, McDonald TD, Younger DS, Murphy PL, Hays AP, Knowles D. Amyotrophic lateral sclerosis and lymphoma: bone marrow examination and other diagnostic tests. Neurology. 42: 1101-2. PMID 1579233 DOI: 10.1212/Wnl.42.5.1101 |
0.323 |
|
1992 |
Lange DJ, Trojaborg W, Latov N, Hays AP, Younger DS, Uncini A, Blake DM, Hirano M, Burns SM, Lovelace RE. Multifocal motor neuropathy with conduction block: is it a distinct clinical entity? Neurology. 42: 497-505. PMID 1549208 DOI: 10.1212/Wnl.42.3.497 |
0.377 |
|
1992 |
Quattrini A, Corbo M, Dhaliwal SK, Sadiq SA, Lugaresi A, Oliveira A, Uncini A, Abouzahr K, Miller JR, Lewis L, Estes D, Cardo L, Hays AP, Latov N. Anti-sulfatide antibodies in neurological disease: binding to rat dorsal root ganglia neurons. Journal of the Neurological Sciences. 112: 152-159. PMID 1469427 DOI: 10.1016/0022-510X(92)90145-B |
0.414 |
|
1992 |
Corbo M, Quattrini A, Lugaresi A, Santoro M, Latov N, Hays AP. Patterns of reactivity of human anti-GM1 antibodies with spinal cord and motor neurons. Annals of Neurology. 32: 487-93. PMID 1456733 DOI: 10.1002/Ana.410320402 |
0.359 |
|
1992 |
Hirano M, Ott BR, Raps EC, Minetti C, Lennihan L, Libbey NP, Bonilla E, Hays AP. Acute quadriplegic myopathy: a complication of treatment with steroids, nondepolarizing blocking agents, or both. Neurology. 42: 2082-7. PMID 1436516 DOI: 10.1212/Wnl.42.11.2082 |
0.36 |
|
1992 |
Corbo M, Hays AP. Peripherin and neurofilament protein coexist in spinal spheroids of motor neuron disease. Journal of Neuropathology and Experimental Neurology. 51: 531-7. PMID 1381416 DOI: 10.1097/00005072-199209000-00008 |
0.337 |
|
1992 |
Thomas FP, Lovelace RE, Ding XS, Sadiq SA, Petty GW, Sherman WH, Latov N, Hays AP. Vasculitic neuropathy in a patient with cryoglobulinemia and anti-MAG IGM monoclonal gammopathy. Muscle & Nerve. 15: 891-8. PMID 1379693 DOI: 10.1002/Mus.880150805 |
0.382 |
|
1992 |
Diaz-Arrastia R, Younger DS, Hair L, Inghirami G, Hays AP, Knowles DM, Odel JG, Fetell MR, Lovelace RE, Rowland LP. Neurolymphomatosis: a clinicopathologic syndrome re-emerges. Neurology. 42: 1136-41. PMID 1340762 DOI: 10.1212/Wnl.42.6.1136 |
0.358 |
|
1991 |
Younger DS, Rowland LP, Latov N, Hays AP, Lange DJ, Sherman W, Inghirami G, Pesce MA, Knowles DM, Powers J. Lymphoma, motor neuron diseases, and amyotrophic lateral sclerosis. Annals of Neurology. 29: 78-86. PMID 1996882 DOI: 10.1002/Ana.410290114 |
0.39 |
|
1991 |
Sadiq SA, van den Berg LH, Thomas FP, Kilidireas K, Hays AP, Latov N. Human monoclonal antineurofilament antibody cross-reacts with a neuronal surface protein. Journal of Neuroscience Research. 29: 319-25. PMID 1920532 DOI: 10.1002/Jnr.490290307 |
0.322 |
|
1991 |
Cafferty MS, Lovelace RE, Hays AP, Servidei S, Dimauro S, Rowland LP. Polyglucosan body disease. Muscle & Nerve. 14: 102-7. PMID 1847989 DOI: 10.1002/Mus.880140203 |
0.392 |
|
1991 |
McDonald TD, Medori R, Younger DS, Chang HW, Minetti C, Uncini A, Bonilla E, Hays AP, Lovelace RE. Becker muscular dystrophy or spinal muscular atrophy?--Dystrophin studies resolve conflicting results of electromyography and muscle biopsy. Neuromuscular Disorders : Nmd. 1: 195-200. PMID 1822794 DOI: 10.1016/0960-8966(91)90024-M |
0.344 |
|
1991 |
Thomas FP, Trojaborg W, Nagy C, Santoro M, Sadiq SA, Latov N, Hays AP. Experimental autoimmune neuropathy with anti-GM1 antibodies and immunoglobulin deposits at the nodes of Ranvier. Acta Neuropathologica. 82: 378-83. PMID 1767631 DOI: 10.1007/Bf00296548 |
0.402 |
|
1991 |
Lugaresi A, Corbo M, Thomas FP, Miyatani N, Ariga T, Yu RK, Hays AP, Latov N. Identification of glycoconjugates which are targets for anti-Gal(beta 1-3)GalNAc autoantibodies in spinal motor neurons. Journal of Neuroimmunology. 34: 69-76. PMID 1716641 DOI: 10.1016/0165-5728(91)90100-L |
0.34 |
|
1990 |
Hays AP, Roxas A, Sadiq SA, Vallejos H, D'Agati V, Thomas FP, Torres R, Sherman WH, Bailey-Braxton D, Hays AG. A monoclonal IgA in a patient with amyotrophic lateral sclerosis reacts with neurofilaments and surface antigen on neuroblastoma cells. Journal of Neuropathology and Experimental Neurology. 49: 383-98. PMID 2362186 DOI: 10.1097/00005072-199007000-00003 |
0.383 |
|
1990 |
Younger DS, Rowland LP, Latov N, Sherman W, Pesce M, Lange DJ, Trojaborg W, Miller JR, Lovelace RE, Hays AP. Motor neuron disease and amyotrophic lateral sclerosis: relation of high CSF protein content to paraproteinemia and clinical syndromes. Neurology. 40: 595-9. PMID 2320231 DOI: 10.1212/Wnl.40.4.595 |
0.369 |
|
1990 |
Uncini A, Lange DJ, Lovelace RE, Solomon M, Hays AP. Long-duration polyphasic motor unit potentials in myopathies: a quantitative study with pathological correlation. Muscle & Nerve. 13: 263-7. PMID 2320048 DOI: 10.1002/Mus.880130315 |
0.35 |
|
1990 |
Thomas FP, Vallejos U, Foitl DR, Miller JR, Barrett R, Fetell MR, Knowles DM, Latov N, Hays AP. B cell small lymphocytic lymphoma and chronic lymphocytic leukemia with peripheral neuropathy: two cases with neuropathological findings and lymphocyte marker analysis. Acta Neuropathologica. 80: 198-203. PMID 2167605 DOI: 10.1007/Bf00308924 |
0.332 |
|
1990 |
Sadiq SA, Thomas FP, Kilidireas K, Protopsaltis S, Hays AP, Lee KW, Romas SN, Kumar N, van den Berg L, Santoro M. The spectrum of neurologic disease associated with anti-GM1 antibodies. Neurology. 40: 1067-72. PMID 2162499 DOI: 10.1212/Wnl.40.7.1067 |
0.384 |
|
1990 |
Santoro M, Thomas FP, Fink ME, Lange DJ, Uncini A, Wadia NH, Latov N, Hays AP. IgM deposits at nodes of Ranvier in a patient with amyotrophic lateral sclerosis, anti-GM1 antibodies, and multifocal motor conduction block. Annals of Neurology. 28: 373-7. PMID 2132741 DOI: 10.1002/Ana.410280312 |
0.385 |
|
1990 |
Thomas FP, Thomas JE, Sadiq SA, van den Berg LH, Roelofs RI, Latov N, Hays AP. Human monoclonal IgM anti-Gal(beta 1-3)GalNAc autoantibodies bind to the surface of bovine spinal motoneurons. Journal of Neuropathology and Experimental Neurology. 49: 89-95. PMID 1689771 DOI: 10.1097/00005072-199003000-00001 |
0.323 |
|
1990 |
Srinivasan J, Hays AP, Thomas FP, Sadiq SA, Barth KH, Liem R, Mena MA, DeYebenes JG, Latov N. Autoantigens in human neuroblastoma cells. Journal of Neuroimmunology. 26: 43-50. PMID 1688443 DOI: 10.1016/0165-5728(90)90118-7 |
0.348 |
|
1989 |
Younger DS, Hays AP, Uncini A, Lange DJ, Lovelace RE, DiMauro S. Recurrent myoglobinuria and HIV seropositivity: incidental or pathogenic association? Muscle & Nerve. 12: 842-3. PMID 2608081 DOI: 10.1002/Mus.880121009 |
0.326 |
|
1989 |
Trojaborg W, Galassi G, Hays AP, Lovelace RE, Alkaitis M, Latov N. Electrophysiologic study of experimental demyelination induced by serum of patients with IgM M proteins and neuropathy. Neurology. 39: 1581-6. PMID 2479887 DOI: 10.1212/Wnl.39.12.1581 |
0.381 |
|
1989 |
Thomas FP, Adapon PH, Goldberg GP, Latov N, Hays AP. Localization of neural epitopes that bind to IgM monoclonal autoantibodies (M-proteins) from two patients with motor neuron disease. Journal of Neuroimmunology. 21: 31-9. PMID 2461959 DOI: 10.1016/0165-5728(89)90156-2 |
0.383 |
|
1989 |
Hays AP, Roxas A, Sadiq SA, Vallejos H, DʼAgati V, Cadet JL, Suber F, Thomas FP, Torres R, Sherman WH, Bailey-Braxton P, Latov N. A MONOCLONAL IgAγ IN MOTOR NEURON DISEASE REACTS WITH NEUROFILAMENTS AND THE SURFACE OF NEUROBLASTOMA CELLS: 190 Journal of Neuropathology and Experimental Neurology. 48: 364. DOI: 10.1097/00005072-198905000-00196 |
0.32 |
|
1988 |
Webster C, Silberstein L, Hays AP, Blau HM. Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy. Cell. 52: 503-13. PMID 3342447 DOI: 10.1016/0092-8674(88)90463-1 |
0.315 |
|
1988 |
Latov N, Hays AP, Yu RK, Ito H, Thomas FP. Antibodies to glycoconjugates in human motor neuron disease. Neurochemical Pathology. 8: 181-7. PMID 3253621 DOI: 10.1007/Bf03160145 |
0.37 |
|
1988 |
Younger DS, Chou S, Hays AP, Lange DJ, Emerson R, Brin M, Thompson H, Rowland LP. Primary lateral sclerosis. A clinical diagnosis reemerges. Archives of Neurology. 45: 1304-7. PMID 3196189 DOI: 10.1001/Archneur.1988.00520360022005 |
0.322 |
|
1988 |
Bonilla E, Samitt CE, Miranda AF, Hays AP, Salviati G, DiMauro S, Kunkel LM, Hoffman EP, Rowland LP. Duchenne muscular dystrophy: deficiency of dystrophin at the muscle cell surface. Cell. 54: 447-52. PMID 3042151 DOI: 10.1016/0092-8674(88)90065-7 |
0.342 |
|
1988 |
Lange DJ, Britton CB, Younger DS, Hays AP. The neuromuscular manifestations of human immunodeficiency virus infections. Archives of Neurology. 45: 1084-8. PMID 2845898 DOI: 10.1001/Archneur.1988.00520340038008 |
0.326 |
|
1988 |
Hays AP, Lee SS, Latov N. Immune reactive C3d on the surface of myelin sheaths in neuropathy. Journal of Neuroimmunology. 18: 231-44. PMID 2452830 DOI: 10.1016/0165-5728(88)90101-4 |
0.326 |
|
1988 |
Latov N, Hays AP, Donofrio PD, Liao J, Ito H, McGinnis S, Konstadoulakis M, Freddo L, Shy ME, Manoussos K. Monoclonal IgM with unique specificity to gangliosides GM1 and GD1b and to lacto-N-tetraose associated with human motor neuron disease. Neurology. 38: 763-8. PMID 2452383 DOI: 10.1212/Wnl.38.5.763 |
0.392 |
|
1987 |
Galassi G, Rowland LP, Hays AP, Hopkins LC, DiMauro S. High serum levels of creatine kinase: asymptomatic prelude to distal myopathy. Muscle & Nerve. 10: 346-50. PMID 3587269 DOI: 10.1002/Mus.880100411 |
0.32 |
|
1987 |
Hays AP, Latov N, Takatsu M, Sherman WH. Experimental demyelination of nerve induced by serum of patients with neuropathy and an anti-MAG IgM M-protein. Neurology. 37: 242-56. PMID 2433641 DOI: 10.1212/Wnl.37.2.242 |
0.33 |
|
1986 |
Hays AP, Shy ME, Latov N, Sherman WH, Cowen D. IMMUNOHISTOCHEMICAL BINDING OF HUMAN IgM TO MOTOR NERVE TERMINALS Journal of Neuropathology and Experimental Neurology. 45: 357. DOI: 10.1097/00005072-198605000-00128 |
0.328 |
|
1985 |
Freddo L, Hays AP, Sherman WH, Latov N. Axonal neuropathy in a patient with IgM M-protein reactive with nerve endoneurium. Neurology. 35: 1321-5. PMID 4022379 DOI: 10.1212/Wnl.35.9.1321 |
0.341 |
|
1985 |
Kaplan JG, Katzman R, Horoupian DS, Fuld PA, Mayeux R, Hays AP. Progressive dementia, visual deficits, amyotrophy, and microinfarcts. Neurology. 35: 789-96. PMID 4000480 DOI: 10.1212/Wnl.35.6.789 |
0.321 |
|
1985 |
Miranda AF, Shanske S, Hays AP, DiMauro S. Immunocytochemical analysis of normal and acid maltase-deficient muscle cultures. Archives of Neurology. 42: 371-3. PMID 3921010 DOI: 10.1001/Archneur.1985.04060040081017 |
0.351 |
|
1985 |
Takatsu M, Hays AP, Latov N, Abrams GM, Nemni R, Sherman WH, Nobile-Orazio E, Saito T, Freddo L. Immunofluorescence study of patients with neuropathy and IgM M proteins. Annals of Neurology. 18: 173-81. PMID 2412485 DOI: 10.1002/Ana.410180203 |
0.368 |
|
1984 |
Sherman WH, Olarte MR, McKiernan G, Sweeney K, Latov N, Hays AP. Plasma exchange treatment of peripheral neuropathy associated with plasma cell dyscrasia. Journal of Neurology, Neurosurgery, and Psychiatry. 47: 813-9. PMID 6470723 DOI: 10.1136/Jnnp.47.8.813 |
0.317 |
|
1984 |
Kushner MJ, Parrish M, Burke A, Behrens M, Hays AP, Frame B, Rowland LP. Nystagmus in motor neuron disease: clinicopathological study of two cases. Annals of Neurology. 16: 71-7. PMID 6465863 DOI: 10.1002/Ana.410160114 |
0.35 |
|
1984 |
Nobile-Orazio E, Hays AP, Latov N, Perman G, Golier J, Shy ME, Freddo L. Specificity of mouse and human monoclonal antibodies to myelin-associated glycoprotein. Neurology. 34: 1336-42. PMID 6207463 DOI: 10.1212/Wnl.34.10.1336 |
0.31 |
|
1984 |
Nobile-Orazio E, Latov N, Hays AP, Takatsu M, Abrams GM, Sherman WH, Miller JR, Messito MJ, Saito T, Tahmoush A. Neuropathy and anti-MAG antibodies without detectable serum M-protein. Neurology. 34: 218-21. PMID 6198602 DOI: 10.1212/Wnl.34.2.218 |
0.32 |
|
1983 |
Nemni R, Galassi G, Latov N, Sherman WH, Olarte MR, Hays AP. Polyneuropathy in nonmalignant IgM plasma cell dyscrasia: a morphological study. Annals of Neurology. 14: 43-54. PMID 6311075 DOI: 10.1002/Ana.410140108 |
0.364 |
|
1983 |
Sherman WH, Latov N, Hays AP, Takatsu M, Nemni R, Galassi G, Osserman EF. Monoclonal IgM kappa antibody precipitating with chondroitin sulfate C from patients with axonal polyneuropathy and epidermolysis. Neurology. 33: 192-201. PMID 6296726 DOI: 10.1212/Wnl.33.2.192 |
0.304 |
|
1983 |
Hays AP, Nemni R, Takatsu M, Abrams GM, Latov N. Immunocytochemical studies of human peripheral nerve with serum Neurology. 33: 1531-1531. DOI: 10.1212/Wnl.33.11.1531-A |
0.306 |
|
1983 |
Hays AP, Takatsu M, Latov N, Sherman WH, Duffyy PE. 134 FOCAL DEMYELINATION OF CAT SCIATIC NERVE INDUCED BY INTRANEURAL INJECTION OF SERUM FROM PATIENTS WITH POLYNEUROPATHY AND MONOCLONAL IgM REACTIVE WITH MYELINASSOCIATED GLYCOPROTEIN Journal of Neuropathology and Experimental Neurology. 42: 349. DOI: 10.1097/00005072-198305000-00140 |
0.371 |
|
1982 |
Fetell MR, Smallberg G, Lewis LD, Lovelace RE, Hays AP, Rowland LP. A benign motor neuron disorder: delayed cramps and fasciculation after poliomyelitis or myelitis. Annals of Neurology. 11: 423-7. PMID 7103419 DOI: 10.1002/Ana.410110418 |
0.361 |
|
1982 |
Abrams GM, Latov N, Hays AP, Sherman W, Zimmerman EA. Immunocytochemical studies of human peripheral nerve with serum from patients with polyneuropathy and paraproteinemia. Neurology. 32: 821-6. PMID 6285225 DOI: 10.1212/Wnl.32.8.821 |
0.387 |
|
1982 |
DiMauro S, Miranda AF, Olarte M, Friedman R, Hays AP. Muscle phosphoglycerate mutase deficiency. Neurology. 32: 584-91. PMID 6283419 DOI: 10.1212/Wnl.32.6.584 |
0.325 |
|
1981 |
Hays AP, Hallett M, Delfs J, Morris J, Sotrel A, Shevchuk MM, DiMauro S. Muscle phosphofructokinase deficiency: abnormal polysaccharide in a case of late-onset myopathy. Neurology. 31: 1077-86. PMID 6943439 DOI: 10.1212/Wnl.31.9.1077 |
0.319 |
|
1981 |
Nemni R, Galassi G, Cohen M, Hays AP, Gould R, Singh N, Bressman S, Gamboa ET. Symmetric sarcoid polyneuropathy: analysis of a sural nerve biopsy. Neurology. 31: 1217-23. PMID 6287346 DOI: 10.1212/Wnl.31.10.1217 |
0.342 |
|
1980 |
Mauro SD, Trevisan C, Hays A. Disorders of lipid metabolism in muscle Muscle & Nerve. 3: 369-388. PMID 7421873 DOI: 10.1002/Mus.880030502 |
0.314 |
|
1980 |
DiMauro S, Miranda AF, Hays AP, Franck WA, Hoffman GS, Schoenfeldt RS, Singh N. Myoadenylate deaminase deficiency--muscle biopsy and muscle culture in a patient with gout. Journal of the Neurological Sciences. 47: 191-202. PMID 7411167 DOI: 10.1016/0022-510X(80)90003-9 |
0.311 |
|
1980 |
Agamanolis DP, Askari AD, Di Mauro S, Hays A, Kumar K, Lipton M, Raynor A. Muscle phosphofructokinase deficiency: two cases with unusual polysaccharide accumulation and immunologically active enzyme protein. Muscle & Nerve. 3: 456-67. PMID 6450324 DOI: 10.1002/Mus.880030602 |
0.367 |
|
1979 |
Willner J, DiMauro S, Eastwood A, Hays A, Roohi F, Lovelace R. Muscle carnitine deficiency. Genetic heterogeneity. Journal of the Neurological Sciences. 41: 235-246. PMID 438852 DOI: 10.1016/0022-510X(79)90042-X |
0.307 |
|
1979 |
DiMauro S, Hartwig GB, Hays A, Eastwood AB, Franco R, Olarte M, Chang M, Roses AD, Fetell M, Schoenfeldt RS, Stern LZ. Debrancher deficiency: neuromuscular disorder in 5 adults. Annals of Neurology. 5: 422-36. PMID 288318 DOI: 10.1002/Ana.410050504 |
0.355 |
|
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