Ricardo Maselli

Title(s)Professor, Neurology
SchoolSchool of Medicine
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. Adeno-Associated Virus Type 9-Mediated Gene Therapy of Choline Acetyltransferase-Deficient Mice. Hum Gene Ther. 2024 Feb; 35(3-4):123-131. Lin CV, Thomas CAD, Huynh TL, Wei DT, Young JN, Aivazian AS, McInnes A, Xu J, Cook SE, Vazquez J, Maselli RA. PMID: 38299967.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    2. Intravenous immunoglobulin is safe and effective in controlling pre-existing paraneoplastic neuromuscular diseases in cancer patients treated with immune checkpoint inhibitors: two case reports and literature review. Front Oncol. 2023; 13:1199195. Xiong G, Young RB, Chow H, Maverakis E, Maselli RA, Richman DP, Li T. PMID: 37465116; PMCID: PMC10350685.
      View in: PubMed   Mentions:
    3. 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:    Fields:    Translation:Humans
    4. 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: 6     Fields:    Translation:HumansCells
    5. 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: 7     Fields:    Translation:HumansCells
    6. 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: 1     Fields:    Translation:Humans
    7. 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: 7     Fields:    Translation:HumansCells
    8. 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: 4     Fields:    Translation:HumansCells
    9. 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: 4     Fields:    Translation:HumansCells
    10. 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: 10  
    11. 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: 17     Fields:    Translation:Humans
    12. 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: 6     Fields:    Translation:AnimalsCells
    13. 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
    14. 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: 3     Fields:    Translation:HumansCells
    15. 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: 12     Fields:    Translation:HumansCells
    16. 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: 35     Fields:    Translation:HumansCells
    17. 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: 18     Fields:    Translation:HumansAnimalsCells
    18. 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: 9     Fields:    Translation:HumansCells
    19. 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
    20. 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: 16     Fields:    Translation:HumansAnimalsCells
    21. 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: 9     Fields:    Translation:HumansAnimalsCells
    22. 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: 45     Fields:    Translation:HumansCells
    23. 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: 16     Fields:    Translation:AnimalsCells
    24. 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
    25. 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: 20     Fields:    Translation:HumansCells
    26. 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: 38     Fields:    Translation:HumansAnimalsCells
    27. 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: 51     Fields:    Translation:HumansCells
    28. 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: 17     Fields:    Translation:Humans
    29. 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: 41     Fields:    Translation:HumansCells
    30. 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: 32     Fields:    Translation:Humans
    31. 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
    32. 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: 12     Fields:    Translation:HumansCells
    33. 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: 4     Fields:    Translation:HumansAnimalsCells
    34. 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: 2     Fields:    Translation:HumansCells
    35. 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
    36. 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
    37. 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: 19     Fields:    Translation:HumansCells
    38. 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
    39. 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
    40. 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: 13     Fields:    Translation:Humans
    41. 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: 17     Fields:    Translation:HumansCells
    42. 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: 22     Fields:    Translation:AnimalsCells
    43. 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: 21     Fields:    Translation:HumansAnimalsCells
    44. 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: 5     Fields:    Translation:HumansCells
    45. 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: 5     Fields:    Translation:HumansCells
    46. 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: 15     Fields:    Translation:Humans
    47. 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: 3     Fields:    Translation:HumansAnimalsCells
    48. 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
    49. 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
    50. 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
    51. 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
    52. 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
    53. 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
    54. 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
    55. 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
    56. 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: 4     Fields:    Translation:HumansCells
    57. 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: 31     Fields:    Translation:AnimalsCells
    58. 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
    59. 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
    60. 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
    61. 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: 21     Fields:    Translation:HumansCells
    62. 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: 2     Fields:    Translation:Humans
    63. 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
    64. 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
    65. 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
    66. 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: 43     Fields:    Translation:HumansCells
    67. 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
    68. 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
    69. 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
    70. 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: 7     Fields:    Translation:AnimalsCells
    71. 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
    72. 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.
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    73. Single motor unit H-reflex in motor neuron disorders. Muscle Nerve. 1992 Jun; 15(6):656-60. Soliven B, Maselli RA. PMID: 1508230.
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    74. 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.
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    75. 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.
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    76. 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.
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    77. 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.
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    78. 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.
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    79. Inflammation at the neuromuscular junction in myasthenia gravis. Neurology. 1991 Sep; 41(9):1497-504. Maselli RA, Richman DP, Wollmann RL. PMID: 1891103.
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    80. 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.
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    81. 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.
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    82. 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: 11     Fields:    Translation:Humans
    83. 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.
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    84. Episodic nocturnal wanderings in non-epileptic young patients. Sleep. 1988 Apr; 11(2):156-61. Maselli RA, Rosenberg RS, Spire JP. PMID: 3381056.
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    85. 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.
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    86. 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.
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    87. 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.
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    88. 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.
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    89. 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.
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    90. 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.
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    91. 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: 8     Fields:    Translation:HumansCTClinical Trials
    92. 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: 25     Fields:    Translation:HumansCTClinical Trials