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Ricardo A Maselli, MD

Title(s)Professor, Neurology
SchoolUniversity of California, Davis
Phone530-754-5011
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help.
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    1. Bissay V, Maselli RA. Phenotypic Differences in 2 Unrelated Cases Carrying Identical DOK7 Mutations. J Clin Neuromuscul Dis. 2019 Sep; 21(1):30-34. PMID: 31453852.
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    2. Rudell JB, Maselli RA, Yarov-Yarovoy V, Ferns MJ. Pathogenic effects of agrin V1727F mutation are isoform specific and decrease its expression and affinity for HSPGs and LRP4. Hum Mol Genet. 2019 08 15; 28(16):2648-2658. PMID: 30994901.
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    3. Maselli RA, Vázquez J, Schrumpf L, Arredondo J, Lara M, Strober JB, Pytel P, Wollmann RL, Ferns M. Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A. Mol Genet Genomic Med. 2018 05; 6(3):434-440. PMID: 29441694.
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    4. Maselli RA, Arredondo J, Vázquez J, Chong JX, Bamshad MJ, Nickerson DA, Lara M, Ng F, Lo VL, Pytel P, McDonald CM. A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5. Ann N Y Acad Sci. 2018 02; 1413(1):119-125. PMID: 29377152.
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    5. Bevilacqua JA, Lara M, Díaz J, Campero M, Vázquez J, Maselli RA. Congenital Myasthenic Syndrome due to DOK7 mutations in a family from Chile. Eur J Transl Myol. 2017 06 27; 27(3):6832. PMID: 29118959.
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    6. Maselli RA, Arredondo J, Vázquez J, Chong JX, Bamshad MJ, Nickerson DA, Lara M, Ng F, Lo VL, Pytel P, McDonald CM. Presynaptic congenital myasthenic syndrome with a homozygous sequence variant in LAMA5 combines myopia, facial tics, and failure of neuromuscular transmission. Am J Med Genet A. 2017 Aug; 173(8):2240-2245. PMID: 28544784.
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    7. Ng F, Lee DC, Schrumpf LA, Mazurek ME, Lee Lo V, Gill SK, Maselli RA. Effect of 3,4-diaminopyridine at the murine neuromuscular junction. Muscle Nerve. 2017 02; 55(2):223-231. PMID: 27251582.
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    8. Burns TM, Smith GA, Allen JA, Amato AA, Arnold WD, Barohn R, Benatar M, Bird SJ, Bromberg M, Chahin N, Ciafaloni E, Cohen JA, Corse A, Crum BA, David WS, Dimberg E, Sousa EA, Donofrio PD, Dyck PJ, Engel AG, Ensrud ER, Ferrante M, Freimer M, Gable KL, Gibson S, Gilchrist JM, Goldstein JM, Gooch CL, Goodman BP, Gorelov D, Gospe SM, Goyal NA, Guidon AC, Guptill JT, Gutmann L, Gutmann L, Gwathmey K, Harati Y, Harper CM, Hehir MK, Hobson-Webb LD, Howard JF, Jackson CE, Johnson N, Jones SM, Juel VC, Kaminski HJ, Karam C, Kennelly KD, Khella S, Khoury J, Kincaid JC, Kissel JT, Kolb N, Lacomis D, Ladha S, Larriviere D, Lewis RA, Li Y, Litchy WJ, Logigian E, Lou JS, MacGowen DJ, Maselli R, Massey JM, Mauermann ML, Mathews KD, Meriggioli MN, Miller RG, Moon JS, Mozaffar T, Nations SP, Nowak RJ, Ostrow LW, Pascuzzi RM, Peltier A, Ruzhansky K, Richman DP, Ross MA, Rubin DI, Russell JA, Sachs GM, Salajegheh MK, Saperstein DS, Scelsa S, Selcen D, Shaibani A, Shieh PB, Silvestri NJ, Singleton JR, Smith BE, So YT, Solorzano G, Sorenson EJ, Srinivasen J, Tavee J, Tawil R, Thaisetthawatkul P, Thornton C, Trivedi J, Vernino S, Wang AK, Webb TA, Weiss MD, Windebank AJ, Wolfe GI. Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine. Muscle Nerve. 2016 Feb; 53(2):165-8. PMID: 26662952.
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    9. Ram S, Devapriya IA, Fenton G, Mcvay L, Nguyen DV, Tassone F, Maselli RA, Hagerman RJ. Axonal neuropathy in female carriers of the fragile X premutation with fragile x-associated tremor ataxia syndrome. Muscle Nerve. 2015 Aug; 52(2):234-9. PMID: 25388402.
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    10. Arredondo J, Lara M, Gospe SM, Mazia CG, Vaccarezza M, Garcia-Erro M, Bowe CM, Chang CH, Mezei MM, Maselli RA. Choline Acetyltransferase Mutations Causing Congenital Myasthenic Syndrome: Molecular Findings and Genotype-Phenotype Correlations. Hum Mutat. 2015 Sep; 36(9):881-93. PMID: 26080897.
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    11. Arnold WD, Feldman DH, Ramirez S, He L, Kassar D, Quick A, Klassen TL, Lara M, Nguyen J, Kissel JT, Lossin C, Maselli RA. Defective fast inactivation recovery of Nav 1.4 in congenital myasthenic syndrome. Ann Neurol. 2015 May; 77(5):840-50. PMID: 25707578.
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    12. Arredondo J, Lara M, Ng F, Gochez DA, Lee DC, Logia SP, Nguyen J, Maselli RA. COOH-terminal collagen Q (COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal lamina. Hum Genet. 2014 May; 133(5):599-616. PMID: 24281389.
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    13. Maselli RA, Arredondo J, Nguyen J, Lara M, Ng F, Ngo M, Pham JM, Yi Q, Stajich JM, McDonald K, Hauser MA, Wollmann RL. Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia. Clin Genet. 2014 Feb; 85(2):166-71. PMID: 23488891.
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    14. Richman DP, Nishi K, Ferns MJ, Schnier J, Pytel P, Maselli RA, Agius MA. Animal models of antimuscle-specific kinase myasthenia. Ann N Y Acad Sci. 2012 Dec; 1274:140-7. PMID: 23252909.
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    15. Maselli RA, Arredondo J, Ferns MJ, Wollmann RL. Synaptic basal lamina-associated congenital myasthenic syndromes. Ann N Y Acad Sci. 2012 Dec; 1275:36-48. PMID: 23278576.
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    16. Richman DP, Yu Y, Lee TT, Tseng PY, Yu WP, Maselli RA, Tang CY, Chen TY. Dominantly inherited myotonia congenita resulting from a mutation that increases open probability of the muscle chloride channel CLC-1. Neuromolecular Med. 2012 Dec; 14(4):328-37. PMID: 22790975.
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    17. 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. Hum Genet. 2012 Jul; 131(7):1123-35. PMID: 22205389.
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    18. 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. Arch Neurol. 2012 Apr; 69(4):453-60. PMID: 22158720.
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    19. Maselli RA, Henderson JD, Ng J, Follette D, Graves G, Wilson BW. Protection of human muscle acetylcholinesterase from soman by pyridostigmine bromide. Muscle Nerve. 2011 Apr; 43(4):591-5. PMID: 21404290.
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    20. Maselli RA, Arredondo J, Cagney O, Mozaffar T, Skinner S, Yousif S, Davis RR, Gregg JP, Sivak M, Konia TH, Thomas K, Wollmann RL. Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE. Clin Genet. 2011 Nov; 80(5):444-51. PMID: 21175599.
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    21. 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. Hum Mol Genet. 2010 Jun 15; 19(12):2370-9. PMID: 20371544.
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    22. 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. J Med Genet. 2009 Mar; 46(3):203-8. PMID: 19251977.
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    23. Anderson JA, Ng JJ, Bowe C, McDonald C, Richman DP, Wollmann RL, Maselli RA. Variable phenotypes associated with mutations in DOK7. Muscle Nerve. 2008 Apr; 37(4):448-56. PMID: 18161030.
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    24. Soontarapornchai K, Maselli R, Fenton-Farrell G, Tassone F, Hagerman PJ, Hessl D, Hagerman RJ. Abnormal nerve conduction features in fragile X premutation carriers. Arch Neurol. 2008 Apr; 65(4):495-8. PMID: 18413472.
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    25. Hagerman RJ, Coffey SM, Maselli R, Soontarapornchai K, Brunberg JA, Leehey MA, Zhang L, Gane LW, Fenton-Farrell G, Tassone F, Hagerman PJ. Neuropathy as a presenting feature in fragile X-associated tremor/ataxia syndrome. Am J Med Genet A. 2007 Oct 01; 143A(19):2256-60. PMID: 17726686.
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    26. Denning L, Anderson JA, Davis R, Gregg JP, Kuzdenyi J, Maselli RA. High throughput genetic analysis of congenital myasthenic syndromes using resequencing microarrays. PLoS One. 2007 Sep 19; 2(9):e918. PMID: 17878953.
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    27. Maselli R, Dris H, Schnier J, Cockrell J, Wollmann R. Congenital myasthenic syndrome caused by two non-N88K rapsyn mutations. Clin Genet. 2007 Jul; 72(1):63-5. PMID: 17594401.
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    28. Navedo MF, Lasalde-Dominicci JA, Báez-Pagán CA, Díaz-Pérez L, Rojas LV, Maselli RA, Staub J, Schott K, Zayas R, Gomez CM. Novel beta subunit mutation causes a slow-channel syndrome by enhancing activation and decreasing the rate of agonist dissociation. Mol Cell Neurosci. 2006 May-Jun; 32(1-2):82-90. PMID: 16624571.
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    29. Dunne V, Maselli RA. Common founder effect of rapsyn N88K studied using intragenic markers. J Hum Genet. 2004; 49(7):366-9. PMID: 15252722.
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    30. Vohra BP, Groshong JS, Maselli RA, Verity MA, Wollmann RL, Gomez CM. Focal caspase activation underlies the endplate myopathy in slow-channel syndrome. Ann Neurol. 2004 Mar; 55(3):347-52. PMID: 14991812.
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    31. 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. 2003 Dec 23; 61(12):1743-8. PMID: 14694040.
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    32. 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. 2003 Sep; 28(3):293-301. PMID: 12929188.
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    33. Maselli RA, Books W, Dunne V. Effect of inherited abnormalities of calcium regulation on human neuromuscular transmission. Ann N Y Acad Sci. 2003 Sep; 998:18-28. PMID: 14592859.
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    34. Añor S, Lipsitz D, Williams DC, Tripp L, Willits N, Maselli R, LeCouteur RA. Evaluation of jitter by stimulated single-fiber electromyography in normal dogs. J Vet Intern Med. 2003 Jul-Aug; 17(4):545-50. PMID: 12892306.
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    35. Dunne V, Maselli RA. Identification of pathogenic mutations in the human rapsyn gene. J Hum Genet. 2003; 48(4):204-7. PMID: 12730725.
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    36. 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. 2003 Feb; 27(2):180-7. PMID: 12548525.
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    37. 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. J Neurosci. 2002 Aug 01; 22(15):6447-57. PMID: 12151524.
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    38. Gomez CM, Maselli RA, Vohra BP, Navedo M, Stiles JR, Charnet P, Schott K, Rojas L, Keesey J, Verity A, Wollmann RW, Lasalde-Dominicci J. Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms. Ann Neurol. 2002 Jan; 51(1):102-12. PMID: 11782989.
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    39. Maselli RA, Kong DZ, Bowe CM, McDonald CM, Ellis WG, Agius MA, Gomez CM, Richman DP, Wollmann RL. Presynaptic congenital myasthenic syndrome due to quantal release deficiency. Neurology. 2001 Jul 24; 57(2):279-89. PMID: 11468313.
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    40. Maselli RA, Bakshi N. AAEM case report 16. Botulism. American Association of Electrodiagnostic Medicine. Muscle Nerve. 2000 Jul; 23(7):1137-44. PMID: 10883013.
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    41. Lee EK, Maselli RA, Ellis WG, Agius MA. Morvan's fibrillary chorea: a paraneoplastic manifestation of thymoma. J Neurol Neurosurg Psychiatry. 1998 Dec; 65(6):857-62. PMID: 9854961.
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    42. Gomez CM, Maselli R, Williams JM, Bhattacharyya BB, Wollmann RL, Day JW. Genetic manipulation of AChR responses suggests multiple causes of weakness in slow-channel syndrome. Ann N Y Acad Sci. 1998 May 13; 841:167-80. PMID: 9668235.
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    43. Agius MA, Maselli RA, Zhu S, Fairclough RH, Lin MY, Ellis W. Rhodamine-labeled alpha-bungarotoxin allows visualization of end plates in congenital end plate acetylcholinesterase deficiency (CEAD). Ann N Y Acad Sci. 1998 May 13; 841:207-9. PMID: 9668242.
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    44. Maselli RA, Agius M, Lee EK, Bakshi N, Mandler RN, Ellis W. Morvan's fibrillary chorea. Electrodiagnostic and in vitro microelectrode findings. Ann N Y Acad Sci. 1998 May 13; 841:497-500. PMID: 9668281.
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    45. Agius MA, Zhu S, Lee EK, Aarli JA, Kirvan C, Fairclough RH, Maselli R. Antibodies to AChR, synapse-organizing proteins, titin, and other muscle proteins in Morvan's fibrillary chorea. Ann N Y Acad Sci. 1998 May 13; 841:522-4. PMID: 9668285.
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    46. Maselli RA. Electrodiagnosis of disorders of neuromuscular transmission. Ann N Y Acad Sci. 1998 May 13; 841:696-711. PMID: 9668317.
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    47. Maselli RA. Pathogenesis of human botulism. Ann N Y Acad Sci. 1998 May 13; 841:122-39. PMID: 9668232.
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    48. Richman DP, Agius MA, Kirvan CA, Gomez CM, Fairclough RH, Dupont BL, Maselli RA. Antibody effector mechanisms in myasthenia gravis. The complement hypothesis. Ann N Y Acad Sci. 1998 May 13; 841:450-65. PMID: 9668274.
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    49. Bakshi N, Maselli RA. Absence of F waves in heat stroke. Muscle Nerve. 1998 Feb; 21(2):263-4. PMID: 9466611.
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    50. Bakshi N, Maselli RA, Gospe SM, Ellis WG, McDonald C, Mandler RN. Fulminant demyelinating neuropathy mimicking cerebral death. Muscle Nerve. 1997 Dec; 20(12):1595-7. PMID: 9390675.
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    51. 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. 1997 Oct; 20(10):1284-95. PMID: 9324085.
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    52. 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. J Neurosci. 1997 Jun 01; 17(11):4170-9. PMID: 9151734.
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    53. Maselli RA. End-plate electromyography: use of spectral analysis of end-plate noise. Muscle Nerve. 1997 Jan; 20(1):52-8. PMID: 8995583.
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    54. Sheikh FS, Maselli R. Unsuspected V nerve lesion resulting from perineural cancer spread detected by blink reflex. Muscle Nerve. 1996 Dec; 19(12):1623-5. PMID: 8941282.
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    55. Mandler RN, Maselli RA. Stimulated single-fiber electromyography in wound botulism. Muscle Nerve. 1996 Sep; 19(9):1171-3. PMID: 8761277.
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    56. Gomez CM, Maselli R, Gammack J, Lasalde J, Tamamizu S, Cornblath DR, Lehar M, McNamee M, Kuncl RW. A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome. Ann Neurol. 1996 Jun; 39(6):712-23. PMID: 8651643.
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    57. Rivero A, Crovetto L, Lopez L, Maselli R, Nogués M. Single fiber electromyography of extraocular muscles: a sensitive method for the diagnosis of ocular myasthenia gravis. Muscle Nerve. 1995 Sep; 18(9):943-7. PMID: 7643873.
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    58. Maselli RA, Wollmann R, Roos R. Function and ultrastructure of the neuromuscular junction in post-polio syndrome. Ann N Y Acad Sci. 1995 May 25; 753:129-37. PMID: 7611622.
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    59. Benedetti PF, Anderson MW, Maselli R, Rogero GW. Hypertrophic peripheral neuropathy due to leprosy: MR features. J Comput Assist Tomogr. 1994 Nov-Dec; 18(6):995-6. PMID: 7962819.
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    60. Maselli RA. Pathophysiology of myasthenia gravis and Lambert-Eaton syndrome. Neurol Clin. 1994 May; 12(2):285-303. PMID: 8041343.
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    61. Maselli RA, Wollman RL, Leung C, Distad B, Palombi S, Richman DP, Salazar-Grueso EF, Roos RP. Neuromuscular transmission in amyotrophic lateral sclerosis. Muscle Nerve. 1993 Nov; 16(11):1193-203. PMID: 8105377.
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    62. Richman DP, Wollmann RL, Maselli RA, Gomez CM, Corey AL, Agius MA, Fairclough RH. Effector mechanisms of myasthenic antibodies. Ann N Y Acad Sci. 1993 Jun 21; 681:264-73. PMID: 8357166.
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    63. Maselli RA, Leung C. Analysis of neuromuscular transmission failure induced by anticholinesterases. Ann N Y Acad Sci. 1993 Jun 21; 681:402-4. PMID: 8395155.
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    64. Trontelj JV. Single motor unit H-reflex in motor neuron disorders. Muscle Nerve. 1993 May; 16(5):565-6. PMID: 8515766.
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    65. Maselli RA, Leung C. Analysis of anticholinesterase-induced neuromuscular transmission failure. Muscle Nerve. 1993 May; 16(5):548-53. PMID: 8390609.
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    66. Besser R, Wessler I, Gutmann L. Analysis of the organophosphate-induced electromyographic response to repetitive nerve stimulation: two types of end-plate depolarization account for the two most common patterns of decrement. Muscle Nerve. 1992 Dec; 15(12):1369-71. PMID: 1298266.
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    67. Appelbaum JS, Roos RP, Salazar-Grueso EF, Buchman A, Iannaccone S, Glantz R, Siddique T, Maselli R. Intrafamilial heterogeneity in hereditary motor neuron disease. Neurology. 1992 Aug; 42(8):1488-92. PMID: 1641141.
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    68. Soliven B, Maselli RA. Single motor unit H-reflex in motor neuron disorders. Muscle Nerve. 1992 Jun; 15(6):656-60. PMID: 1508230.
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    69. Maselli RA, Cashman NR, Wollman RL, Salazar-Grueso EF, Roos R. Neuromuscular transmission as a function of motor unit size in patients with prior poliomyelitis. Muscle Nerve. 1992 Jun; 15(6):648-55. PMID: 1324424.
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    70. Maselli RA, Burnett ME, Tonsgard JH. In vitro microelectrode study of neuromuscular transmission in a case of botulism. Muscle Nerve. 1992 Mar; 15(3):273-6. PMID: 1313544.
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    71. Dieperink ME, O'Neill A, Maselli R, Stefansson K. Experimental allergic neuritis in the SJL/J mouse: dysfunction of peripheral nerve without clinical signs. J Neuroimmunol. 1991 Dec; 35(1-3):247-59. PMID: 1955568.
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    72. Maselli RA, Mass DP, Distad BJ, Richman DP. Anconeus muscle: a human muscle preparation suitable for in-vitro microelectrode studies. Muscle Nerve. 1991 Dec; 14(12):1189-92. PMID: 1662771.
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    73. Maselli RA, Soliven BC. Analysis of the organophosphate-induced electromyographic response to repetitive nerve stimulation: paradoxical response to edrophonium and D-tubocurarine. Muscle Nerve. 1991 Dec; 14(12):1182-8. PMID: 1662770.
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    74. Maselli RA, Richman DP, Wollmann RL. Inflammation at the neuromuscular junction in myasthenia gravis. Neurology. 1991 Sep; 41(9):1497-504. PMID: 1891103.
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    75. Karaszewski JW, Reder AT, Maselli R, Brown M, Arnason BG. Sympathetic skin responses are decreased and lymphocyte beta-adrenergic receptors are increased in progressive multiple sclerosis. Ann Neurol. 1990 Apr; 27(4):366-72. PMID: 2162144.
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    76. Towle VL, Maselli R, Bernstein LP, Spire JP. Electrophysiologic studies on locked-in patients: heterogeneity of findings. Electroencephalogr Clin Neurophysiol. 1989 Nov; 73(5):419-26. PMID: 2479520.
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    77. Maselli RA, Jaspan JB, Soliven BC, Green AJ, Spire JP, Arnason BG. Comparison of sympathetic skin response with quantitative sudomotor axon reflex test in diabetic neuropathy. Muscle Nerve. 1989 May; 12(5):420-3. PMID: 2725569.
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    78. Maselli RA, Nelson DJ, Richman DP. Effects of a monoclonal anti-acetylcholine receptor antibody on the avian end-plate. J Physiol. 1989 Apr; 411:271-83. PMID: 2614725.
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    79. Maselli RA, Rosenberg RS, Spire JP. Episodic nocturnal wanderings in non-epileptic young patients. Sleep. 1988 Apr; 11(2):156-61. PMID: 3381056.
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    80. Maselli RA, Jow B, Richman DP, Nelson DJ. In vitro blockade of neuromuscular transmission by monoclonal anti-acetylcholine receptor antibodies. Ann N Y Acad Sci. 1988; 540:523-4. PMID: 2849901.
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    81. Arnason BG, Brown M, Maselli R, Karaszewski J, Reder A. Blood lymphocyte beta-adrenergic receptors in multiple sclerosis. Ann N Y Acad Sci. 1988; 540:585-8. PMID: 2849904.
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    82. Soliven B, Maselli R, Jaspan J, Green A, Graziano H, Petersen M, Spire JP. Sympathetic skin response in diabetic neuropathy. Muscle Nerve. 1987 Oct; 10(8):711-6. PMID: 2825012.
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    83. Cashman NR, Maselli R, Wollmann RL, Roos R, Simon R, Antel JP. Late denervation in patients with antecedent paralytic poliomyelitis. N Engl J Med. 1987 Jul 02; 317(1):7-12. PMID: 3587319.
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    84. Cashman NR, Maselli R, Wollmann RL, Roos R, Simon R, Antel JP. Post-poliomyelitis syndrome: evidence of ongoing denervation in symptomatic and asymptomatic patients. Birth Defects Orig Artic Ser. 1987; 23(4):237-9. PMID: 3620621.
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    85. Maselli R, Jacobsen JH, Spire JP. Edrophonium: an aid in the diagnosis of acute organophosphate poisoning. Ann Neurol. 1986 May; 19(5):508-10. PMID: 3717911.
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    86. Jaspan JB, Towle VL, Maselli R, Herold K. Clinical studies with an aldose reductase inhibitor in the autonomic and somatic neuropathies of diabetes. Metabolism. 1986 Apr; 35(4 Suppl 1):83-92. PMID: 3083212.
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    87. Jaspan J, Maselli R, Herold K, Bartkus C. Treatment of severely painful diabetic neuropathy with an aldose reductase inhibitor: relief of pain and improved somatic and autonomic nerve function. Lancet. 1983 Oct 01; 2(8353):758-62. PMID: 6137601.
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