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Robert L. Wollmann, MD PhD - Publications

Affiliations: 
Pathology University of Chicago, Chicago, IL 
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33 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
2013 Hanna N, Bouhenni R, Gupta B, Abu-Amero KK, Wollmann R, Edward DP. Histopathologic changes in the extraocular muscle in centronuclear myopathy with a Dynamin 2 mutation. Ophthalmic Genetics. 34: 83-6. PMID 22924779 DOI: 10.3109/13816810.2012.716487  0.314
2012 Maselli RA, Arredondo J, Ferns MJ, Wollmann RL. Synaptic basal lamina-associated congenital myasthenic syndromes. Annals of the New York Academy of Sciences. 1275: 36-48. PMID 23278576 DOI: 10.1111/J.1749-6632.2012.06807.X  0.314
2012 Maselli RA, Fernandez JM, Arredondo J, Navarro C, Ngo M, Beeson D, Cagney O, Williams DC, Wollmann RL, Yarov-Yarovoy V, Ferns MJ. LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin. Human Genetics. 131: 1123-35. PMID 22205389 DOI: 10.1007/S00439-011-1132-4  0.344
2012 Richman DP, Nishi K, Morell SW, Chang JM, Ferns MJ, Wollmann RL, Maselli RA, Schnier J, Agius MA. Acute severe animal model of anti-muscle-specific kinase myasthenia: combined postsynaptic and presynaptic changes. Archives of Neurology. 69: 453-60. PMID 22158720 DOI: 10.1001/Archneurol.2011.2200  0.304
2011 Ghadge GD, Wollmann R, Baida G, Traka M, Roos RP. The L-coding region of the DA strain of Theiler's murine encephalomyelitis virus causes dysfunction and death of myelin-synthesizing cells. Journal of Virology. 85: 9377-84. PMID 21752920 DOI: 10.1128/Jvi.00178-11  0.32
2010 Maselli RA, Arredondo J, Cagney O, Ng JJ, Anderson JA, Williams C, Gerke BJ, Soliven B, Wollmann RL. Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction. Human Molecular Genetics. 19: 2370-9. PMID 20371544 DOI: 10.1093/Hmg/Ddq110  0.318
2009 Maselli RA, Ng JJ, Anderson JA, Cagney O, Arredondo J, Williams C, Wessel HB, Abdel-Hamid H, Wollmann RL. Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome. Journal of Medical Genetics. 46: 203-8. PMID 19251977 DOI: 10.1136/Jmg.2008.063693  0.346
2008 Traka M, Wollmann RL, Cerda SR, Dugas J, Barres BA, Popko B. Nur7 is a nonsense mutation in the mouse aspartoacylase gene that causes spongy degeneration of the CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 11537-49. PMID 18987190 DOI: 10.1523/Jneurosci.1490-08.2008  0.342
2008 Baida G, Popko B, Wollmann RL, Stavrou S, Lin W, Tretiakova M, Krausz TN, Roos RP. A subgenomic segment of Theiler's murine encephalomyelitis virus RNA causes demyelination. Journal of Virology. 82: 5879-86. PMID 18400855 DOI: 10.1128/Jvi.02432-07  0.323
2008 Anderson JA, Ng JJ, Bowe C, McDonald C, Richman DP, Wollmann RL, Maselli RA. Variable phenotypes associated with mutations in DOK7. Muscle & Nerve. 37: 448-56. PMID 18161030 DOI: 10.1002/Mus.20944  0.312
2007 Chen XJ, Levedakou EN, Millen KJ, Wollmann RL, Soliven B, Popko B. Proprioceptive sensory neuropathy in mice with a mutation in the cytoplasmic Dynein heavy chain 1 gene. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 14515-24. PMID 18160659 DOI: 10.1523/Jneurosci.4338-07.2007  0.321
2007 Groshong JS, Spencer MJ, Bhattacharyya BJ, Kudryashova E, Vohra BP, Zayas R, Wollmann RL, Miller RJ, Gomez CM. Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome. The Journal of Clinical Investigation. 117: 2903-12. PMID 17853947 DOI: 10.1172/Jci30383  0.303
2004 Vohra BP, Groshong JS, Maselli RA, Verity MA, Wollmann RL, Gomez CM. Focal caspase activation underlies the endplate myopathy in slow-channel syndrome. Annals of Neurology. 55: 347-52. PMID 14991812 DOI: 10.1002/Ana.10823  0.317
2003 Maselli RA, Wan J, Dunne V, Graves M, Baloh RW, Wollmann RL, Jen J. Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2. Neurology. 61: 1743-8. PMID 14694040 DOI: 10.1212/01.Wnl.0000099748.41130.9A  0.325
2003 Maselli RA, Dunne V, Pascual-Pascual SI, Bowe C, Agius M, Frank R, Wollmann RL. Rapsyn mutations in myasthenic syndrome due to impaired receptor clustering. Muscle & Nerve. 28: 293-301. PMID 12929188 DOI: 10.1002/Mus.10433  0.339
2003 Maselli RA, Chen D, Mo D, Bowe C, Fenton G, Wollmann RL. Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Muscle & Nerve. 27: 180-7. PMID 12548525 DOI: 10.1002/Mus.10300  0.338
2002 Gomez CM, Maselli RA, Groshong J, Zayas R, Wollmann RL, Cens T, Charnet P. Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 6447-57. PMID 12151524 DOI: 10.1523/Jneurosci.22-15-06447.2002  0.325
2001 Zhu X, Hadhazy M, Groh ME, Wheeler MT, Wollmann R, McNally EM. Overexpression of gamma-sarcoglycan induces severe muscular dystrophy. Implications for the regulation of Sarcoglycan assembly. The Journal of Biological Chemistry. 276: 21785-90. PMID 11287429 DOI: 10.1074/Jbc.M101877200  0.309
2000 Wong K, Armstrong RC, Gyure KA, Morrison AL, Rodriguez D, Matalon R, Johnson AB, Wollmann R, Gilbert E, Le TQ, Bradley CA, Crutchfield K, Schiffmann R. Foamy cells with oligodendroglial phenotype in childhood ataxia with diffuse central nervous system hypomyelination syndrome. Acta Neuropathologica. 100: 635-46. PMID 11078215 DOI: 10.1007/S004010000234  0.315
1998 Hack AA, Ly CT, Jiang F, Clendenin CJ, Sigrist KS, Wollmann RL, McNally EM. Gamma-sarcoglycan deficiency leads to muscle membrane defects and apoptosis independent of dystrophin. The Journal of Cell Biology. 142: 1279-87. PMID 9732288 DOI: 10.1083/Jcb.142.5.1279  0.322
1997 Bhattacharyya BJ, Day JW, Gundeck JE, Leonard S, Wollmann RL, Gomez CM. Desensitization of mutant acetylcholine receptors in transgenic mice reduces the amplitude of neuromuscular synaptic currents. Synapse (New York, N.Y.). 27: 367-77. PMID 9372559 DOI: 10.1002/(Sici)1098-2396(199712)27:4<367::Aid-Syn10>3.0.Co;2-P  0.301
1997 Maselli RA, Ellis W, Mandler RN, Sheikh F, Senton G, Knox S, Salari-Namin H, Agius M, Wollmann RL, Richman DP. Cluster of wound botulism in California: clinical, electrophysiologic, and pathologic study. Muscle & Nerve. 20: 1284-95. PMID 9324085 DOI: 10.1002/(Sici)1097-4598(199710)20:10<1284::Aid-Mus11>3.0.Co;2-3  0.338
1997 Dowling J, Yang Y, Wollmann R, Reichardt LF, Fuchs E. Developmental expression of BPAG1-n: insights into the spastic ataxia and gross neurologic degeneration in dystonia musculorum mice. Developmental Biology. 187: 131-42. PMID 9242412 DOI: 10.1006/Dbio.1997.8567  0.307
1997 Gomez CM, Maselli R, Gundeck JE, Chao M, Day JW, Tamamizu S, Lasalde JA, McNamee M, Wollmann RL. Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 4170-9. PMID 9151734 DOI: 10.1523/Jneurosci.17-11-04170.1997  0.352
1997 Gómez RM, Rinehart JE, Wollmann R, Roos RP. Theiler's murine encephalomyelitis virus-induced cardiac and skeletal muscle disease. Journal of Virology. 70: 8926-33. PMID 8971022 DOI: 10.1128/Jvi.70.12.8926-8933.1996  0.339
1996 Gomez CM, Bhattacharyya BB, Charnet P, Day JW, Labarca C, Wollmann RL, Lambert EH. A transgenic mouse model of the slow-channel syndrome. Muscle & Nerve. 19: 79-87. PMID 8538674 DOI: 10.1002/(Sici)1097-4598(199601)19:1<79::Aid-Mus11>3.0.Co;2-Z  0.336
1995 Maselli RA, Wollmann R, Roos R. Function and Ultrastructure of the Neuromuscular Junction in Post‐Polio Syndrome Annals of the New York Academy of Sciences. 753: 129-137. PMID 7611622 DOI: 10.1111/J.1749-6632.1995.Tb27539.X  0.341
1991 Maselli RA, Richman DP, Wollmann RL. Inflammation at the neuromuscular junction in myasthenia gravis. Neurology. 41: 1497-504. PMID 1891103 DOI: 10.1212/Wnl.41.9.1497  0.304
1987 Cashman NR, Maselli R, Wollmann RL, Roos R, Simon R, Antel JP. Late denervation in patients with antecedent paralytic poliomyelitis. The New England Journal of Medicine. 317: 7-12. PMID 3587319 DOI: 10.1056/Nejm198707023170102  0.322
1986 Kohrman MH, Picchietti DL, Wollmann R, Chelmicka-Schorr EE. A variant of Fukuyama congenital muscular dystrophy in a non-Japanese child. Pediatric Neurology. 2: 290-293. PMID 3508701 DOI: 10.1016/0887-8994(86)90023-8  0.311
1984 Roos RP, Wollmann R. DA strain of Theiler's murine encephalomyelitis virus induces demyelination in nude mice. Annals of Neurology. 15: 494-9. PMID 6732198 DOI: 10.1002/Ana.410150516  0.306
1984 Gomez CM, Wollmann RL, Richman DP. Induction of the morphologic changes of both acute and chronic experimental myasthenia by monoclonal antibody directed against acetylcholine receptor. Acta Neuropathologica. 63: 131-43. PMID 6610275 DOI: 10.1007/Bf00697195  0.31
1983 Lukes SA, Wollmann R, Stefannson K. Meningeal Sarcomatosis and Multiple Astrocytomas Jama Neurology. 40: 179-182. PMID 6830462 DOI: 10.1001/Archneur.1983.04050030073016  0.305
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