Literature DB >> 3239958

Myopathy with unique ultrastructural feature in Marinesco-Sjögren syndrome.

C A Sewry1, T Voit, V Dubowitz.   

Abstract

We have investigated 3 children aged 6, 3, and 2 years, from 2 families, with the clinical features of Marinesco-Sjögren syndrome. Muscle biopsy specimens from all 3 were abnormal and showed small vacuoles and slight variation in fiber size. Electron microscopy revealed vacuolation and membranous whorls and, in particular, a unique dense membranous structure associated with nuclei. These cases emphasize the involvement of muscle in Marinesco-Sjögren syndrome and the importance of electron microscopy in differential diagnosis.

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Year:  1988        PMID: 3239958     DOI: 10.1002/ana.410240416

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  11 in total

1.  Myopathy is a prominent feature in Marinesco-Sjögren syndrome: A muscle computed tomography study.

Authors:  Ibrahim Mahjneh; Anna-Kaisa Anttonen; Mirja Somer; Anders Paetau; Anna-Elina Lehesjoki; Hannu Somer; Bjarne Udd
Journal:  J Neurol       Date:  2005-09-15       Impact factor: 4.849

Review 2.  Ataxia.

Authors:  Umar Akbar; Tetsuo Ashizawa
Journal:  Neurol Clin       Date:  2015-02       Impact factor: 3.806

Review 3.  Neuropathology of Charcot-Marie-Tooth and related disorders.

Authors:  J Michael Schröder
Journal:  Neuromolecular Med       Date:  2006       Impact factor: 3.843

4.  Myopathy in Marinesco-Sjögren syndrome: an ultrastructural study.

Authors:  Y Goto; A Komiyama; Y Tanabe; Y Katafuchi; E Ohtaki; I Nonaka
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

Review 5.  BiP and its nucleotide exchange factors Grp170 and Sil1: mechanisms of action and biological functions.

Authors:  Julia Behnke; Matthias J Feige; Linda M Hendershot
Journal:  J Mol Biol       Date:  2015-02-16       Impact factor: 5.469

6.  Sil1-Mutant Mice Elucidate Chaperone Function in Neurological Disorders.

Authors:  Stephan Buchkremer; José Andrés González Coraspe; Joachim Weis; Andreas Roos
Journal:  J Neuromuscul Dis       Date:  2016-05-27

7.  GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical Studies.

Authors:  Kristoffer Haugarvoll; Stefan Johansson; Carlos E Rodriguez; Helge Boman; Bjørn Ivar Haukanes; Ove Bruland; Francisco Roque; Inge Jonassen; Maria Blomqvist; Wenche Telstad; Jan-Eric Månsson; Per Morten Knappskog; Laurence A Bindoff
Journal:  PLoS One       Date:  2017-01-04       Impact factor: 3.240

8.  SIL1, the endoplasmic-reticulum-localized BiP co-chaperone, plays a crucial role in maintaining skeletal muscle proteostasis and physiology.

Authors:  Viraj P Ichhaporia; Jieun Kim; Kanisha Kavdia; Peter Vogel; Linda Horner; Sharon Frase; Linda M Hendershot
Journal:  Dis Model Mech       Date:  2018-05-10       Impact factor: 5.758

9.  Mutations in INPP5K, Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment.

Authors:  Manuela Wiessner; Andreas Roos; Christopher J Munn; Ranjith Viswanathan; Tamieka Whyte; Dan Cox; Benedikt Schoser; Caroline Sewry; Helen Roper; Rahul Phadke; Chiara Marini Bettolo; Rita Barresi; Richard Charlton; Carsten G Bönnemann; Osório Abath Neto; Umbertina C Reed; Edmar Zanoteli; Cristiane Araújo Martins Moreno; Birgit Ertl-Wagner; Rolf Stucka; Christian De Goede; Tamiris Borges da Silva; Denisa Hathazi; Margherita Dell'Aica; René P Zahedi; Simone Thiele; Juliane Müller; Helen Kingston; Susanna Müller; Elizabeth Curtis; Maggie C Walter; Tim M Strom; Volker Straub; Kate Bushby; Francesco Muntoni; Laura E Swan; Hanns Lochmüller; Jan Senderek
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

10.  In-depth phenotyping of lymphoblastoid cells suggests selective cellular vulnerability in Marinesco-Sjögren syndrome.

Authors:  Laxmikanth Kollipara; Stephan Buchkremer; José Andrés González Coraspe; Denisa Hathazi; Jan Senderek; Joachim Weis; René P Zahedi; Andreas Roos
Journal:  Oncotarget       Date:  2017-07-28
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