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E K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Kunz

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E K, Kropf S, Schoenfeld A, Feistner H, Jakubiczka S, Marimastat Kunz WS, Scherlach C, Tempelmann C, Mawrin C, Dengler R, Schreiber F, Goertler M, Vielhaber S: Sonography of your median nerve in CMT1A, CMT2A, CMTX, and HNPP. Muscle Nerve 2013, 47:385?95. fifty three. Zaidman CM, Al-Lozi M, Pestronk A: Peripheral nerve measurement in normals and clients with polyneuropathy: an ultrasound research. Muscle Nerve 2009, forty:960?sixty six. fifty four. Kaku DA, Parry GJ, Malamut R, Lupski JR, Garcia CA: Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy affiliated using a segmental duplication of chromosome 17. Neurology 1806?808, 1993:forty three. fifty five. Garcia CA, Malamut RE, England JD, Parry GS, Liu P, Lupski JR: Clinical variability in two pairs of identical twins with all the Charcot-Marie-Tooth illness type 1A duplication. Neurology 2090?093, 1995:forty five. 56. Silander K, Meretoja P, Nelis E, Timmerman V, Van Broeckhoven C, Aula P, Savontaus ML: A de novo duplication in 17p11.two and also a novel mutation in the Po gene in two Dejerine-Sottas syndrome clients. Hum Mutat 1996, 8:304?10. 57. Plante-Bordeneuve V, Parman Y, Guiochon-Mantel A, Alj Y, Deymeer F, Serdaroglu P, Eraksoy M, Mentioned G: The array of chronic demyelinating neuropathy of infancy: a clinico- pathological and genetic study of fifteen unrelated cases. J Neurol 2001, 248:795?03. fifty eight. Meggouh F, De Visser M, Arts WF, De Coo RI, Van Schaik IN, Baas PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/12711626 F: Early onset neuropathy in a compound kind of Charcot-Marie-Tooth disorder. Ann Neurol 2005, fifty seven:589?ninety one. 59. Hodapp JA, Carter GT, Lipe HP, Michelson SJ, Kraft GH, Fowl TD: Double problems in hereditary neuropathy: concomitant mutations during the PMP-22 gene and an additional gene produce novel phenotypes. Arch Neurol 2006, 63:112?17. sixty. Chanson JB, Echaniz-Laguna A, Blanc F, Lacour A, Ballonzoli L, Kremer S, Namer IJ, Lannes B, Tranchant C, Vermersch P, De Seze J: Central nervous procedure abnormalities in sufferers with PMP22 gene mutations: a future review. J Neurol Neurosurg Psychiatry 2013, 84:392?ninety seven. 61. Uncini A, Di Guglielmo G, Di Muzio A, Gambi D, Sabatelli M, Mignogna T, Tonali P, Marzella R, Finelli P, Archidiacono N, Rocchi M: Differential electrophysiological functions of neuropathies involved with 17p11.two deletion and duplication. Muscle mass Nerve 1995, eighteen:628?35. 62. Lewis RA, Krajewski K, Tate B, Shy ME: Motor Device Quantity Estimation (MUNE) of Proximal and Distal Extremity Muscle tissues in CMT1A, CMTX, and CMT2. Neurology 2000, 54(Suppl three):A70. 63. Gabreels-Festen AA, Bolhuis PA, Hoogendijk JE, Valentijn LJ, Eshuis EJ, Gabreels FJ: Charcot-Marie-Tooth illness type 1A: morphological phenotype of your 17p duplication vs . PMP22 issue mutations. Acta Neuropathol 1995, 90:645?49. sixty four. Fabrizi GM, Simonati A, Morbin M, Cavallaro T, Taioli F, Benedetti MD, Edomi P, Rizzuto N: Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy kind 1A with the 17p11.2p12 duplication: a cross- sectional morphometric and immunohistochemical review in twenty cases. Muscle mass Nerve 1998, 21:869?seventy seven. sixty five. Gabreels-Festen AA, Joosten EM, Gabreels FJ, Jennekens FG, Janssen-van Kempen TW: Early morphological functions in dominantly inherited demyelinating motor and sensory neuropathy (HMSN type I). J Neurol Sci 1992, 107:a hundred forty five?fifty four. 66. Smith TW, Bhawan PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/9547713 J, Keller RB, DeGirolami U: Charcot-Marie-Tooth disorder linked with hypertrophic neuropathy: a neuropathologic research of two cases. J Neuropathol Exp Neurol 1980, 39:420?forty. 67. Valentijn LJ, Baas F, Zorn I, Hensels GW, De Visser M, Bolhuis PA: Alternatively sized duplic.

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