Literature DB >> 2747736

Longitudinal conduction studies in hereditary motor and sensory neuropathy type 1.

E P Roy1, L Gutmann, J E Riggs.   

Abstract

Motor conduction studies were performed serially in 10 patients, ages 10-62 years, with clinical and electrophysiological criteria of hereditary motor and sensory neuropathy type 1 (HMSN-1) over periods of 11-19 years. Median nerve conduction velocity (MNCV) and distal motor latency showed no significant change on serial studies. Mean median compound muscle action potential (CMAP) amplitude values, however, decreased 66% in 8 patients. Observed clinical progression in HMSN-1, over prolonged periods of time, was not associated with MNCV slowing. However, CMAP amplitude reduction, reflecting progressive axonal loss, correlated with clinical deterioration.

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Year:  1989        PMID: 2747736     DOI: 10.1002/mus.880120110

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  5 in total

1.  Ultralate cerebral potentials in a patient with hereditary motor and sensory neuropathy type I indicate preserved C-fibre function.

Authors:  J Lankers; A Frieling; K Kunze; B Bromm
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-07       Impact factor: 10.154

2.  Hereditary motor and sensory neuropathy type I and type II.

Authors:  A Sghirlanzoni; D Pareyson; V Scaioli; R Marazzi; L Pacini
Journal:  Ital J Neurol Sci       Date:  1990-10

3.  Clinical disease severity and axonal dysfunction in hereditary motor and sensory neuropathy Ia.

Authors:  Camiel Verhamme; Ivo N van Schaik; Johannes H T M Koelman; Rob J de Haan; Marinus Vermeulen; Marianne de Visser
Journal:  J Neurol       Date:  2004-12       Impact factor: 4.849

Review 4.  Dejerine-Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients.

Authors:  Anneke Gabreëls-Festen
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

5.  Comparison between clinical disabilities and electrophysiological values in Charcot-Marie-Tooth 1A patients with PMP22 duplication.

Authors:  Young Hwa Kim; Hwa Kyung Chung; Kee Duk Park; Kyoung-Gyu Choi; Seung-Min Kim; Il-Nam Sunwoo; Young-Chul Choi; Jeong-Geun Lim; Kwang Woo Lee; Kwang-Kuk Kim; Dong Kuk Lee; In Soo Joo; Ki-Han Kwon; Seok Beom Gwon; Jae Hyeon Park; Dae-Seong Kim; Seung Hyun Kim; Woo-Kyung Kim; Bum Chun Suh; Sang-Beom Kim; Nam-Hee Kim; Eun Hee Sohn; Ok-Joon Kim; Hyun Sook Kim; Jung Hee Cho; Sa-Yoon Kang; Chan-Ik Park; Jiyoung Oh; Jong Hyu Shin; Ki Wha Chung; Byung-Ok Choi
Journal:  J Clin Neurol       Date:  2012-06-29       Impact factor: 3.077

  5 in total

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