Literature DB >> 22172417

Muscle imaging in congenital myopathies.

Susana Quijano-Roy1, Robert Y Carlier, Dirk Fischer.   

Abstract

Congenital myopathies are a genetically heterogeneous group of early-onset myopathies classified according to the predominant histopathological findings in skeletal muscle. During the past years, considerable overlap between different pathological and genetic forms of congenital myopathies has been discovered. In contrast, the pattern of involved muscles seen on muscle imaging is often more specific, providing useful additional information in the differential diagnosis of these diseases. Therefore, muscle imaging can help to target the most appropriate genetic investigations. The aim of this review is to give a comprehensive up-to-date overview of the muscle imaging findings that have recently been described in different genetic congenital myopathies.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22172417     DOI: 10.1016/j.spen.2011.10.003

Source DB:  PubMed          Journal:  Semin Pediatr Neurol        ISSN: 1071-9091            Impact factor:   1.636


  16 in total

1.  Value of structured reporting in neuromuscular disorders.

Authors:  Francesco Alessandrino; Lara Cristiano; Claudia Maria Cinnante; Tommaso Tartaglione; Simonetta Gerevini; Tommaso Verdolotti; Giovanna Stefania Colafati; Emanuele Ghione; Raimondo Vitale; Lorenzo Peverelli; Claudia Brogna; Angela Berardinelli; Maurizio Moggio; Eugenio M Mercuri; Anna Pichiecchio
Journal:  Radiol Med       Date:  2019-03-09       Impact factor: 3.469

2.  Characterization and genetic diagnosis of centronuclear myopathies in seven Chinese patients.

Authors:  Yan Zhao; Zhe Zhao; Hongrui Shen; Qi Bing; Jing Hu
Journal:  Neurol Sci       Date:  2018-09-19       Impact factor: 3.307

3.  SEPN1-related myopathy in three patients: novel mutations and diagnostic clues.

Authors:  Anna Ardissone; Cinzia Bragato; Flavia Blasevich; Elio Maccagnano; Franco Salerno; Claudia Gandioli; Lucia Morandi; Marina Mora; Isabella Moroni
Journal:  Eur J Pediatr       Date:  2016-01-16       Impact factor: 3.183

4.  Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3).

Authors:  Barbara Joureau; Josine Marieke de Winter; Stefan Conijn; Sylvia J P Bogaards; Igor Kovacevic; Albert Kalganov; Malin Persson; Johan Lindqvist; Ger J M Stienen; Thomas C Irving; Weikang Ma; Michaela Yuen; Nigel F Clarke; Dilson E Rassier; Edoardo Malfatti; Norma B Romero; Alan H Beggs; Coen A C Ottenheijm
Journal:  Ann Neurol       Date:  2018-02-06       Impact factor: 10.422

5.  Sporadic late-onset nemaline myopathy: clinical, pathology and imaging findings in a single center cohort.

Authors:  Mauro Monforte; Guido Primiano; Gabriella Silvestri; Massimiliano Mirabella; Marco Luigetti; Cristina Cuccagna; Enzo Ricci; Serenella Servidei; Giorgio Tasca
Journal:  J Neurol       Date:  2018-01-22       Impact factor: 4.849

6.  Whole-body muscle MRI to detect myopathies in non-extrapyramidal bent spine syndrome.

Authors:  Mickaël Ohana; Marie-Christine Durand; Catherine Marty; Jean-Philippe Lazareth; Thierry Maisonobe; Dominique Mompoint; Robert-Yves Carlier
Journal:  Skeletal Radiol       Date:  2014-05-31       Impact factor: 2.199

7.  Soft-Tissue Abnormalities Associated with Treatment-Resistant and Treatment-Responsive Clubfoot: Findings of MRI Analysis.

Authors:  Daniel K Moon; Christina A Gurnett; Hyuliya Aferol; Marilyn J Siegel; Paul K Commean; Matthew B Dobbs
Journal:  J Bone Joint Surg Am       Date:  2014-08-06       Impact factor: 5.284

Review 8.  [Imaging of primary muscular diseases : What do neurologists expect from radiologists?]

Authors:  M P Wattjes; A Fischmann; D Fischer
Journal:  Radiologe       Date:  2017-12       Impact factor: 0.635

9.  In vivo characterization of skeletal muscle function in nebulin-deficient mice.

Authors:  Charlotte Gineste; Augustin C Ogier; Isabelle Varlet; Zaynab Hourani; Monique Bernard; Henk Granzier; David Bendahan; Julien Gondin
Journal:  Muscle Nerve       Date:  2020-01-21       Impact factor: 3.217

10.  Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohort.

Authors:  Michela Catteruccia; Fabiana Fattori; Valentina Codemo; Lucia Ruggiero; Lorenzo Maggi; Giorgio Tasca; Chiara Fiorillo; Marika Pane; Angela Berardinelli; Margherita Verardo; Cinzia Bragato; Marina Mora; Lucia Morandi; Claudio Bruno; Lucio Santoro; Elena Pegoraro; Eugenio Mercuri; Enrico Bertini; Adele D'Amico
Journal:  Neuromuscul Disord       Date:  2013-02-08       Impact factor: 4.296

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