Poster Session 2: Inherited neuropathies
Friday July 23, 1999
GENETIC ANALYSIS OF A COHORT OF DUTCH PATIENTS SUSPECTED FOR HMSN. Baas F, Bienfait H, Hoogendijk JE, Vreijling J, Gabreëls-Festen A, de Visser M
AXONAL FORM OF CMT NEUROPATHY IN MORROCAN CONSANGUINEOUS FAMILIES: CLINICAL AND GENETIC HETEROGENEITY. Birouk N, Bouhouche A, Maisonobe T, Belaïdi H, Benomar A, Bouslam N, Kably B, Mellah S, Ouazzani R, Le Guern E, Chkili T
UNUSUAL ELECTROPHYSIOLOGICAL FINDINGS IN A FAMILY WITH CMTX. Gutierrez A, England JD, Ferer SS, Sumner AJ, Garcia CA, Warner LE, Lupski JR
DISTRIBUTION OF PMP22 IN DIFFERENT CMT1A AND HNPP GENOTYPES. Hanemann CO, D'Urso D, Gabreëls-Festen A, Müller HW
HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE IIC (HMSN IIC) IS GENETICALLY DISTINCT FROM HMSN IIA, IIB, AND IID. Nagamatsu M, Jenkins RB, Schaid DJ, Klein DM, Dyck PJ
SMALL FIBERS INVOLVEMENT IN FRIEDREICH ATAXIA. Nolano M, Crisci C, D'Addio G, Wendelschafer-Crabb G, Kennedy WR, Provitera V, Caruso G
MYELINATED FIBERS IN CHARCOT-MARIE-TOOTH DISEASE TYPE 1B WITH ARG98HIS MUTATION OF Po. Ohnishi A, Yamamoto T, Ikeda M
ABNORMALITIES OF IN VITRO MYELINATION IN ORGANOTYPIC CULTURES OF DORSAL ROOT GANGLIA (DRG) FROM A TRANSGENIC RAT MODEL OF CHARCOT-MARIE-TOOTH DISEASE TYPE 1A (CMT1A). Schenone A, Mancardi GL, Grandis M, Nave K, Sereda M, Levi G, Barbieri O, Abbruzzese M, Windebank AJ, Nobbio L
IDENTIFICATION OF DNA MUTATIONS IN ARCHIVAL SURAL NERVE BIOPSIES CONFIRMED BY BLOOD SAMPLES IN HMSN X: OCCASIONAL ASSOCIATION WITH BECKER'S MUSCULAR DYSTROPHY AND COLOR BLINDNESS. Schröder JM, Senderek J, Bergmann C, Hermanns B
LATE-ONSET FAMILIAL AMYLOIDOTIC POLYNEUROPATHY TYPE 1 (MET 30 TRANSTHYRETIN MUTATION) UNRELATED TO ENDEMIC FOCUS IN JAPAN: CLINICOPATHOLOGIC AND GENETIC FEATURES. Sobue G, Misu K, Hattori N, Nagamatsu M, Ikeda S, Ando Y, Nakazato M
AXO-GLIAL INTERACTIONS IN THE PMP22-RELATED NEUROPATHIES. Yamamoto T, Ohnishi A