Literature DB >> 1848688

Corticosteroid-responsive dominantly inherited neuropathy in childhood.

S J Bird1, J T Sladky.   

Abstract

We describe three children with corticosteroid-responsive inflammatory demyelinating polyneuropathy from families with dominantly inherited neuropathy. There were atypical clinical, electrophysiologic, and pathologic characteristics that suggested a coexistent inflammatory demyelinating neuropathy and that should alert the clinician to the possibility of an associated acquired, potentially treatable disorder.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1848688     DOI: 10.1212/wnl.41.3.437

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  11 in total

Review 1.  Chronic inflammatory demyelinative polyneuropathy.

Authors:  Gérard Said
Journal:  J Neurol       Date:  2002-03       Impact factor: 4.849

2.  Inflammatory demyelinating CNS disorder in a case of X-linked Charcot-Marie-Tooth disease: positive response to natalizumab.

Authors:  Jochen H Weishaupt; Claudia Ganser; Mathias Bähr
Journal:  J Neurol       Date:  2012-03-13       Impact factor: 4.849

3.  Reversible inflammatory neuropathy superimposed on Charcot-Marie-Tooth type 1A disease.

Authors:  José Gazulla; Carmen Almárcegui; José Berciano
Journal:  Neurol Sci       Date:  2017-11-21       Impact factor: 3.307

4.  Immunological study of hereditary motor and sensory neuropathy type 1a (HMSN1a).

Authors:  C M Gabriel; N A Gregson; N W Wood; R A C Hughes
Journal:  J Neurol Neurosurg Psychiatry       Date:  2002-02       Impact factor: 10.154

5.  A novel GJB1 frameshift mutation produces a transient CNS symptom of X-linked Charcot-Marie-Tooth disease.

Authors:  Hideya Sakaguchi; Satoshi Yamashita; Akiko Miura; Tomoo Hirahara; En Kimura; Yasushi Maeda; Tadashi Terasaki; Teruyuki Hirano; Makoto Uchino
Journal:  J Neurol       Date:  2010-09-21       Impact factor: 4.849

Review 6.  [The role of the immune system in hereditary demyelinating neuropathies].

Authors:  M Mäurer; K V Toyka; R Martini
Journal:  Nervenarzt       Date:  2005-06       Impact factor: 1.214

Review 7.  Role of immune cells in animal models for inherited neuropathies: facts and visions.

Authors:  Mathias Mäurer; Igor Kobsar; Martin Berghoff; Christoph D Schmid; Stefano Carenini; Rudolf Martini
Journal:  J Anat       Date:  2002-04       Impact factor: 2.610

Review 8.  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

9.  Chronic inflammatory demyelinating polyneuropathy or hereditary motor and sensory neuropathy? Diagnostic value of morphological criteria.

Authors:  A A Gabreëls-Festen; F J Gabreëls; J E Hoogendijk; P A Bolhuis; P J Jongen; H M Vingerhoets
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

10.  Occurrence of active demyelinating lesions in children with hereditary motor and sensory neuropathy (HMSN) type I.

Authors:  A Vital; C Vital; J Julien; D Fontan
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.