Ricardo A Maselli

Title(s)Professor, Neurology
SchoolUniversity of California, Davis
Address1515 Newton Ct
CA 95616
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. to make corrections and additions.
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    1. Atypical Case of POEMS Presented as Demyelinating Polyneuropathy With Motor Conduction Block. J Clin Neuromuscul Dis. 2021 Dec 01; 23(2):116-118. Guo SY, Duffy AO, Maselli RA, Xiong G. PMID: 34808659; PMCID: PMC8601671.
      View in: PubMed   Mentions:
    2. Dominant and recessive congenital myasthenic syndromes caused by SYT2 mutations. Muscle Nerve. 2021 08; 64(2):219-224. Maselli RA, Wei DT, Hodgson TS, Sampson JB, Vazquez J, Smith HL, Pytel P, Ferns M. PMID: 34037996.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    3. Recessive congenital myasthenic syndrome caused by a homozygous mutation in SYT2 altering a highly conserved C-terminal amino acid sequence. Am J Med Genet A. 2020 07; 182(7):1744-1749. Maselli RA, van der Linden H, Ferns M. PMID: 32250532.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    4. Phenotypic Differences in 2 Unrelated Cases Carrying Identical DOK7 Mutations. J Clin Neuromuscul Dis. 2019 Sep; 21(1):30-34. Bissay V, Maselli RA. PMID: 31453852.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    5. 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. Rudell JB, Maselli RA, Yarov-Yarovoy V, Ferns MJ. PMID: 30994901; PMCID: PMC6687949.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    6. 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. Maselli RA, Vázquez J, Schrumpf L, Arredondo J, Lara M, Strober JB, Pytel P, Wollmann RL, Ferns M. PMID: 29441694; PMCID: PMC6014458.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    7. A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5. Ann N Y Acad Sci. 2018 02; 1413(1):119-125. Maselli RA, Arredondo J, Vázquez J, Chong JX, Bamshad MJ, Nickerson DA, Lara M, Ng F, Lo VL, Pytel P, McDonald CM. PMID: 29377152; PMCID: PMC6252105.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    8. Congenital Myasthenic Syndrome due to DOK7 mutations in a family from Chile. Eur J Transl Myol. 2017 06 27; 27(3):6832. Bevilacqua JA, Lara M, Díaz J, Campero M, Vázquez J, Maselli RA. PMID: 29118959; PMCID: PMC5658635.
      View in: PubMed   Mentions: 4  
    9. 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. Maselli RA, Arredondo J, Vázquez J, Chong JX, University of Washington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Lara M, Ng F, Lo VL, Pytel P, McDonald CM. PMID: 28544784; PMCID: PMC5541137.
      View in: PubMed   Mentions: 13  Translation:Humans
    10. Effect of 3,4-diaminopyridine at the murine neuromuscular junction. Muscle Nerve. 2017 02; 55(2):223-231. Ng F, Lee DC, Schrumpf LA, Mazurek ME, Lee Lo V, Gill SK, Maselli RA. PMID: 27251582.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    11. 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. 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. PMID: 26662952.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    12. 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. Ram S, Devapriya IA, Fenton G, Mcvay L, Nguyen DV, Tassone F, Maselli RA, Hagerman RJ. PMID: 25388402; PMCID: PMC4427531.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    13. Choline Acetyltransferase Mutations Causing Congenital Myasthenic Syndrome: Molecular Findings and Genotype-Phenotype Correlations. Hum Mutat. 2015 Sep; 36(9):881-93. Arredondo J, Lara M, Gospe SM, Mazia CG, Vaccarezza M, Garcia-Erro M, Bowe CM, Chang CH, Mezei MM, Maselli RA. PMID: 26080897; PMCID: PMC4537391.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    14. Defective fast inactivation recovery of Nav 1.4 in congenital myasthenic syndrome. Ann Neurol. 2015 May; 77(5):840-50. Arnold WD, Feldman DH, Ramirez S, He L, Kassar D, Quick A, Klassen TL, Lara M, Nguyen J, Kissel JT, Lossin C, Maselli RA. PMID: 25707578; PMCID: PMC4510994.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    15. 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. Arredondo J, Lara M, Ng F, Gochez DA, Lee DC, Logia SP, Nguyen J, Maselli RA. PMID: 24281389; PMCID: PMC4024244.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    16. Exome sequencing detection of two untranslated GFPT1 mutations in a family with limb-girdle myasthenia. Clin Genet. 2014 Feb; 85(2):166-71. Maselli RA, Arredondo J, Nguyen J, Lara M, Ng F, Ngo M, Pham JM, Yi Q, Stajich JM, McDonald K, Hauser MA, Wollmann RL. PMID: 23488891.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    17. Animal models of antimuscle-specific kinase myasthenia. Ann N Y Acad Sci. 2012 Dec; 1274:140-7. Richman DP, Nishi K, Ferns MJ, Schnier J, Pytel P, Maselli RA, Agius MA. PMID: 23252909; PMCID: PMC3915870.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    18. Synaptic basal lamina-associated congenital myasthenic syndromes. Ann N Y Acad Sci. 2012 Dec; 1275:36-48. Maselli RA, Arredondo J, Ferns MJ, Wollmann RL. PMID: 23278576.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansAnimalsCells
    19. 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. Richman DP, Yu Y, Lee TT, Tseng PY, Yu WP, Maselli RA, Tang CY, Chen TY. PMID: 22790975; PMCID: PMC3508202.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansAnimalsCells
    20. LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z-) agrin. Hum Genet. 2012 Jul; 131(7):1123-35. Maselli RA, Fernandez JM, Arredondo J, Navarro C, Ngo M, Beeson D, Cagney O, Williams DC, Wollmann RL, Yarov-Yarovoy V, Ferns MJ. PMID: 22205389; PMCID: PMC4795461.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansCells
    21. Acute severe animal model of anti-muscle-specific kinase myasthenia: combined postsynaptic and presynaptic changes. Arch Neurol. 2012 Apr; 69(4):453-60. Richman DP, Nishi K, Morell SW, Chang JM, Ferns MJ, Wollmann RL, Maselli RA, Schnier J, Agius MA. PMID: 22158720; PMCID: PMC3915865.
      View in: PubMed   Mentions: 14     Fields:    Translation:AnimalsCells
    22. Protection of human muscle acetylcholinesterase from soman by pyridostigmine bromide. Muscle Nerve. 2011 Apr; 43(4):591-5. Maselli RA, Henderson JD, Ng J, Follette D, Graves G, Wilson BW. PMID: 21404290.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    23. Congenital myasthenic syndrome associated with epidermolysis bullosa caused by homozygous mutations in PLEC1 and CHRNE. Clin Genet. 2011 Nov; 80(5):444-51. Maselli RA, Arredondo J, Cagney O, Mozaffar T, Skinner S, Yousif S, Davis RR, Gregg JP, Sivak M, Konia TH, Thomas K, Wollmann RL. PMID: 21175599.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    24. Mutations in MUSK causing congenital myasthenic syndrome impair MuSK-Dok-7 interaction. Hum Mol Genet. 2010 Jun 15; 19(12):2370-9. Maselli RA, Arredondo J, Cagney O, Ng JJ, Anderson JA, Williams C, Gerke BJ, Soliven B, Wollmann RL. PMID: 20371544; PMCID: PMC2876883.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansAnimalsCells
    25. Mutations in LAMB2 causing a severe form of synaptic congenital myasthenic syndrome. J Med Genet. 2009 Mar; 46(3):203-8. Maselli RA, Ng JJ, Anderson JA, Cagney O, Arredondo J, Williams C, Wessel HB, Abdel-Hamid H, Wollmann RL. PMID: 19251977; PMCID: PMC2643050.
      View in: PubMed   Mentions: 47     Fields:    Translation:HumansCells
    26. Variable phenotypes associated with mutations in DOK7. Muscle Nerve. 2008 Apr; 37(4):448-56. Anderson JA, Ng JJ, Bowe C, McDonald C, Richman DP, Wollmann RL, Maselli RA. PMID: 18161030.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    27. Abnormal nerve conduction features in fragile X premutation carriers. Arch Neurol. 2008 Apr; 65(4):495-8. Soontarapornchai K, Maselli R, Fenton-Farrell G, Tassone F, Hagerman PJ, Hessl D, Hagerman RJ. PMID: 18413472; PMCID: PMC2888466.
      View in: PubMed   Mentions: 36     Fields:    Translation:HumansCells
    28. Neuropathy as a presenting feature in fragile X-associated tremor/ataxia syndrome. Am J Med Genet A. 2007 Oct 01; 143A(19):2256-60. Hagerman RJ, Coffey SM, Maselli R, Soontarapornchai K, Brunberg JA, Leehey MA, Zhang L, Gane LW, Fenton-Farrell G, Tassone F, Hagerman PJ. PMID: 17726686.
      View in: PubMed   Mentions: 26  Translation:Humans
    29. High throughput genetic analysis of congenital myasthenic syndromes using resequencing microarrays. PLoS One. 2007 Sep 19; 2(9):e918. Denning L, Anderson JA, Davis R, Gregg JP, Kuzdenyi J, Maselli RA. PMID: 17878953; PMCID: PMC1975473.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    30. Congenital myasthenic syndrome caused by two non-N88K rapsyn mutations. Clin Genet. 2007 Jul; 72(1):63-5. Maselli R, Dris H, Schnier J, Cockrell J, Wollmann R. PMID: 17594401.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    31. 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. Navedo MF, Lasalde-Dominicci JA, Báez-Pagán CA, Díaz-Pérez L, Rojas LV, Maselli RA, Staub J, Schott K, Zayas R, Gomez CM. PMID: 16624571; PMCID: PMC4636114.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansAnimalsCells
    32. Common founder effect of rapsyn N88K studied using intragenic markers. J Hum Genet. 2004; 49(7):366-369. Dunne V, Maselli RA. PMID: 15252722.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    33. Focal caspase activation underlies the endplate myopathy in slow-channel syndrome. Ann Neurol. 2004 Mar; 55(3):347-52. Vohra BP, Groshong JS, Maselli RA, Verity MA, Wollmann RL, Gomez CM. PMID: 14991812.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    34. Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2. Neurology. 2003 Dec 23; 61(12):1743-8. Maselli RA, Wan J, Dunne V, Graves M, Baloh RW, Wollmann RL, Jen J. PMID: 14694040.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    35. Rapsyn mutations in myasthenic syndrome due to impaired receptor clustering. Muscle Nerve. 2003 Sep; 28(3):293-301. Maselli RA, Dunne V, Pascual-Pascual SI, Bowe C, Agius M, Frank R, Wollmann RL. PMID: 12929188.
      View in: PubMed   Mentions: 14     Fields:    Translation:HumansCells
    36. Effect of inherited abnormalities of calcium regulation on human neuromuscular transmission. Ann N Y Acad Sci. 2003 Sep; 998:18-28. Maselli RA, Books W, Dunne V. PMID: 14592859.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    37. Evaluation of jitter by stimulated single-fiber electromyography in normal dogs. J Vet Intern Med. 2003 Jul-Aug; 17(4):545-50. Añor S, Lipsitz D, Williams DC, Tripp L, Willits N, Maselli R, LeCouteur RA. PMID: 12892306.
      View in: PubMed   Mentions: 1     Fields:    Translation:AnimalsCells
    38. Identification of pathogenic mutations in the human rapsyn gene. J Hum Genet. 2003; 48(4):204-7. Dunne V, Maselli RA. PMID: 12730725.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    39. Choline acetyltransferase mutations in myasthenic syndrome due to deficient acetylcholine resynthesis. Muscle Nerve. 2003 Feb; 27(2):180-7. Maselli RA, Chen D, Mo D, Bowe C, Fenton G, Wollmann RL. PMID: 12548525.
      View in: PubMed   Mentions: 13     Fields:    Translation:HumansCells
    40. Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome. J Neurosci. 2002 Aug 01; 22(15):6447-57. Gomez CM, Maselli RA, Groshong J, Zayas R, Wollmann RL, Cens T, Charnet P. PMID: 12151524; PMCID: PMC6758155.
      View in: PubMed   Mentions: 21     Fields:    Translation:AnimalsCells
    41. Novel delta subunit mutation in slow-channel syndrome causes severe weakness by novel mechanisms. Ann Neurol. 2002 Jan; 51(1):102-12. 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. PMID: 11782989; PMCID: PMC4841278.
      View in: PubMed   Mentions: 15     Fields:    Translation:HumansAnimalsCells
    42. Presynaptic congenital myasthenic syndrome due to quantal release deficiency. Neurology. 2001 Jul 24; 57(2):279-89. Maselli RA, Kong DZ, Bowe CM, McDonald CM, Ellis WG, Agius MA, Gomez CM, Richman DP, Wollmann RL. PMID: 11468313.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    43. AAEM case report 16. Botulism. American Association of Electrodiagnostic Medicine. Muscle Nerve. 2000 Jul; 23(7):1137-44. Maselli RA, Bakshi N. PMID: 10883013.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    44. Morvan's fibrillary chorea: a paraneoplastic manifestation of thymoma. J Neurol Neurosurg Psychiatry. 1998 Dec; 65(6):857-62. Lee EK, Maselli RA, Ellis WG, Agius MA. PMID: 9854961; PMCID: PMC2170383.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    45. 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. Gomez CM, Maselli R, Williams JM, Bhattacharyya BB, Wollmann RL, Day JW. PMID: 9668235.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansAnimalsCells
    46. 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. Agius MA, Maselli RA, Zhu S, Fairclough RH, Lin MY, Ellis W. PMID: 9668242.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    47. Morvan's fibrillary chorea. Electrodiagnostic and in vitro microelectrode findings. Ann N Y Acad Sci. 1998 May 13; 841:497-500. Maselli RA, Agius M, Lee EK, Bakshi N, Mandler RN, Ellis W. PMID: 9668281.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    48. 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. Agius MA, Zhu S, Lee EK, Aarli JA, Kirvan C, Fairclough RH, Maselli R. PMID: 9668285.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    49. Electrodiagnosis of disorders of neuromuscular transmission. Ann N Y Acad Sci. 1998 May 13; 841:696-711. Maselli RA. PMID: 9668317.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    50. Pathogenesis of human botulism. Ann N Y Acad Sci. 1998 May 13; 841:122-39. Maselli RA. PMID: 9668232.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    51. Antibody effector mechanisms in myasthenia gravis. The complement hypothesis. Ann N Y Acad Sci. 1998 May 13; 841:450-65. Richman DP, Agius MA, Kirvan CA, Gomez CM, Fairclough RH, Dupont BL, Maselli RA. PMID: 9668274.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansAnimalsCells
    52. Absence of F waves in heat stroke. Muscle Nerve. 1998 Feb; 21(2):263-4. Bakshi N, Maselli RA. PMID: 9466611.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    53. Fulminant demyelinating neuropathy mimicking cerebral death. Muscle Nerve. 1997 Dec; 20(12):1595-7. Bakshi N, Maselli RA, Gospe SM, Ellis WG, McDonald C, Mandler RN. PMID: 9390675.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    54. Cluster of wound botulism in California: clinical, electrophysiologic, and pathologic study. Muscle Nerve. 1997 Oct; 20(10):1284-95. Maselli RA, Ellis W, Mandler RN, Sheikh F, Senton G, Knox S, Salari-Namin H, Agius M, Wollmann RL, Richman DP. PMID: 9324085.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    55. Slow-channel transgenic mice: a model of postsynaptic organellar degeneration at the neuromuscular junction. J Neurosci. 1997 Jun 01; 17(11):4170-9. Gomez CM, Maselli R, Gundeck JE, Chao M, Day JW, Tamamizu S, Lasalde JA, McNamee M, Wollmann RL. PMID: 9151734; PMCID: PMC6573568.
      View in: PubMed   Mentions: 23     Fields:    Translation:AnimalsCells
    56. End-plate electromyography: use of spectral analysis of end-plate noise. Muscle Nerve. 1997 Jan; 20(1):52-8. Maselli RA. PMID: 8995583.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCellsPHPublic Health
    57. Unsuspected V nerve lesion resulting from perineural cancer spread detected by blink reflex. Muscle Nerve. 1996 Dec; 19(12):1623-5. Sheikh FS, Maselli R. PMID: 8941282.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    58. Stimulated single-fiber electromyography in wound botulism. Muscle Nerve. 1996 Sep; 19(9):1171-3. Mandler RN, Maselli RA. PMID: 8761277.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    59. A beta-subunit mutation in the acetylcholine receptor channel gate causes severe slow-channel syndrome. Ann Neurol. 1996 Jun; 39(6):712-23. Gomez CM, Maselli R, Gammack J, Lasalde J, Tamamizu S, Cornblath DR, Lehar M, McNamee M, Kuncl RW. PMID: 8651643.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    60. Single fiber electromyography of extraocular muscles: a sensitive method for the diagnosis of ocular myasthenia gravis. Muscle Nerve. 1995 Sep; 18(9):943-7. Rivero A, Crovetto L, Lopez L, Maselli R, Nogués M. PMID: 7643873.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    61. Function and ultrastructure of the neuromuscular junction in post-polio syndrome. Ann N Y Acad Sci. 1995 May 25; 753:129-37. Maselli RA, Wollmann R, Roos R. PMID: 7611622.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    62. Hypertrophic peripheral neuropathy due to leprosy: MR features. J Comput Assist Tomogr. 1994 Nov-Dec; 18(6):995-6. Benedetti PF, Anderson MW, Maselli R, Rogero GW. PMID: 7962819.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    63. Pathophysiology of myasthenia gravis and Lambert-Eaton syndrome. Neurol Clin. 1994 May; 12(2):285-303. Maselli RA. PMID: 8041343.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    64. Neuromuscular transmission in amyotrophic lateral sclerosis. Muscle Nerve. 1993 Nov; 16(11):1193-203. Maselli RA, Wollman RL, Leung C, Distad B, Palombi S, Richman DP, Salazar-Grueso EF, Roos RP. PMID: 8105377.
      View in: PubMed   Mentions: 32     Fields:    Translation:HumansCells
    65. Effector mechanisms of myasthenic antibodies. Ann N Y Acad Sci. 1993 Jun 21; 681:264-73. Richman DP, Wollmann RL, Maselli RA, Gomez CM, Corey AL, Agius MA, Fairclough RH. PMID: 8357166.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    66. Analysis of neuromuscular transmission failure induced by anticholinesterases. Ann N Y Acad Sci. 1993 Jun 21; 681:402-4. Maselli RA, Leung C. PMID: 8395155.
      View in: PubMed   Mentions: 2     Fields:    Translation:AnimalsCells
    67. Single motor unit H-reflex in motor neuron disorders. Muscle Nerve. 1993 May; 16(5):565-6. Trontelj JV. PMID: 8515766.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    68. Analysis of anticholinesterase-induced neuromuscular transmission failure. Muscle Nerve. 1993 May; 16(5):548-53. Maselli RA, Leung C. PMID: 8390609.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    69. 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. Besser R, Wessler I, Gutmann L. PMID: 1298266.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    70. Intrafamilial heterogeneity in hereditary motor neuron disease. Neurology. 1992 Aug; 42(8):1488-92. Appelbaum JS, Roos RP, Salazar-Grueso EF, Buchman A, Iannaccone S, Glantz R, Siddique T, Maselli R. PMID: 1641141.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    71. Single motor unit H-reflex in motor neuron disorders. Muscle Nerve. 1992 Jun; 15(6):656-60. Soliven B, Maselli RA. PMID: 1508230.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    72. Neuromuscular transmission as a function of motor unit size in patients with prior poliomyelitis. Muscle Nerve. 1992 Jun; 15(6):648-55. Maselli RA, Cashman NR, Wollman RL, Salazar-Grueso EF, Roos R. PMID: 1324424.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    73. In vitro microelectrode study of neuromuscular transmission in a case of botulism. Muscle Nerve. 1992 Mar; 15(3):273-6. Maselli RA, Burnett ME, Tonsgard JH. PMID: 1313544.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    74. Experimental allergic neuritis in the SJL/J mouse: dysfunction of peripheral nerve without clinical signs. J Neuroimmunol. 1991 Dec; 35(1-3):247-59. Dieperink ME, O'Neill A, Maselli R, Stefansson K. PMID: 1955568.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    75. Anconeus muscle: a human muscle preparation suitable for in-vitro microelectrode studies. Muscle Nerve. 1991 Dec; 14(12):1189-92. Maselli RA, Mass DP, Distad BJ, Richman DP. PMID: 1662771.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansCells
    76. 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. Maselli RA, Soliven BC. PMID: 1662770.
      View in: PubMed   Mentions: 4     Fields:    Translation:AnimalsCells
    77. Inflammation at the neuromuscular junction in myasthenia gravis. Neurology. 1991 Sep; 41(9):1497-504. Maselli RA, Richman DP, Wollmann RL. PMID: 1891103.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    78. Sympathetic skin responses are decreased and lymphocyte beta-adrenergic receptors are increased in progressive multiple sclerosis. Ann Neurol. 1990 Apr; 27(4):366-72. Karaszewski JW, Reder AT, Maselli R, Brown M, Arnason BG. PMID: 2162144.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansCells
    79. Electrophysiologic studies on locked-in patients: heterogeneity of findings. Electroencephalogr Clin Neurophysiol. 1989 Nov; 73(5):419-26. Towle VL, Maselli R, Bernstein LP, Spire JP. PMID: 2479520.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    80. Comparison of sympathetic skin response with quantitative sudomotor axon reflex test in diabetic neuropathy. Muscle Nerve. 1989 May; 12(5):420-3. Maselli RA, Jaspan JB, Soliven BC, Green AJ, Spire JP, Arnason BG. PMID: 2725569.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    81. Effects of a monoclonal anti-acetylcholine receptor antibody on the avian end-plate. J Physiol. 1989 Apr; 411:271-83. Maselli RA, Nelson DJ, Richman DP. PMID: 2614725; PMCID: PMC1190524.
      View in: PubMed   Mentions: 3     Fields:    Translation:AnimalsCells
    82. Episodic nocturnal wanderings in non-epileptic young patients. Sleep. 1988 Apr; 11(2):156-61. Maselli RA, Rosenberg RS, Spire JP. PMID: 3381056.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    83. In vitro blockade of neuromuscular transmission by monoclonal anti-acetylcholine receptor antibodies. Ann N Y Acad Sci. 1988; 540:523-4. Maselli RA, Jow B, Richman DP, Nelson DJ. PMID: 2849901.
      View in: PubMed   Mentions:    Fields:    Translation:AnimalsCells
    84. Blood lymphocyte beta-adrenergic receptors in multiple sclerosis. Ann N Y Acad Sci. 1988; 540:585-8. Arnason BG, Brown M, Maselli R, Karaszewski J, Reder A. PMID: 2849904.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    85. Sympathetic skin response in diabetic neuropathy. Muscle Nerve. 1987 Oct; 10(8):711-6. Soliven B, Maselli R, Jaspan J, Green A, Graziano H, Petersen M, Spire JP. PMID: 2825012.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    86. Late denervation in patients with antecedent paralytic poliomyelitis. N Engl J Med. 1987 Jul 02; 317(1):7-12. Cashman NR, Maselli R, Wollmann RL, Roos R, Simon R, Antel JP. PMID: 3587319.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    87. Post-poliomyelitis syndrome: evidence of ongoing denervation in symptomatic and asymptomatic patients. Birth Defects Orig Artic Ser. 1987; 23(4):237-9. Cashman NR, Maselli R, Wollmann RL, Roos R, Simon R, Antel JP. PMID: 3620621.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    88. Edrophonium: an aid in the diagnosis of acute organophosphate poisoning. Ann Neurol. 1986 May; 19(5):508-10. Maselli R, Jacobsen JH, Spire JP. PMID: 3717911.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    89. Clinical studies with an aldose reductase inhibitor in the autonomic and somatic neuropathies of diabetes. Metabolism. 1986 Apr; 35(4 Suppl 1):83-92. Jaspan JB, Towle VL, Maselli R, Herold K. PMID: 3083212.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCTClinical Trials
    90. 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. Jaspan J, Maselli R, Herold K, Bartkus C. PMID: 6137601.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCTClinical Trials
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