Literature DB >> 12401454

A short protocol for muscle MRI in children with muscular dystrophies.

Eugenio Mercuri1, Anna Pichiecchio, Serena Counsell, Joanna Allsop, Claudio Cini, Heinz Jungbluth, Carla Uggetti, Graeme Bydder.   

Abstract

The use of muscle magnetic resonance imaging in patients with muscular dystrophies or congenital myopathies has been limited. We describe the development of a short protocol to be used in young patients with neuromuscular disorders. The protocol includes transverse T1-weighted spin echo sequence images of thighs and calves. The total scanning time is less than 30 minutes, and can be easily applied to patients over the age of 4 years without any need for sedation. Although only the leg muscles are imaged, the images obtained can still help to identify specific patterns of muscle involvement and provide additional help in the differential diagnosis of muscle disorders with overlapping clinical features.

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Year:  2002        PMID： 12401454     DOI： 10.1016/s1090-3798(02)90617-3

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN： 1090-3798            Impact factor:   3.140


  39 in total

1.  MRI in the assessment of muscular pathology: a comparison between limb-girdle muscular dystrophies, hyaline body myopathies and myotonic dystrophies.

Authors:  R Stramare; V Beltrame; R Dal Borgo; L Gallimberti; A C Frigo; E Pegoraro; C Angelini; L Rubaltelli; G P Feltrin
Journal:  Radiol Med       Date:  2010-02-22       Impact factor: 3.469

2.  Magnetic resonance imaging of leg muscles in patients with myotonic dystrophies.

Authors:  Stojan Peric; Ruzica Maksimovic; Bojan Banko; Milica Durdic; Bogdan Bjelica; Ivo Bozovic; Yunus Balcik; Jovan Pesovic; Dusanka Savic-Pavicevic; Vidosava Rakocevic-Stojanovic
Journal:  J Neurol       Date:  2017-07-29       Impact factor: 4.849

3.  Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.

Authors:  Maria J Melià; Akatsuki Kubota; Saida Ortolano; Juan J Vílchez; Josep Gámez; Kurenai Tanji; Eduardo Bonilla; Lluís Palenzuela; Israel Fernández-Cadenas; Anna Pristoupilová; Elena García-Arumí; Antoni L Andreu; Carmen Navarro; Michio Hirano; Ramon Martí
Journal:  Brain       Date:  2013-03-29       Impact factor: 13.501

4.  Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity.

Authors:  Mickael Tordjman; Ivana Dabaj; Pascal Laforet; Adrien Felter; Ana Ferreiro; Moustafa Biyoukar; Bruno Law-Ye; Edmar Zanoteli; Claudia Castiglioni; John Rendu; Christophe Beroud; Alexandre Chamouni; Pascale Richard; Dominique Mompoint; Susana Quijano-Roy; Robert-Yves Carlier
Journal:  Eur Radiol       Date:  2018-05-25       Impact factor: 5.315

5.  Texture analysis using T1-weighted images for muscles in Charcot-Marie-Tooth disease patients and volunteers.

Authors:  Ji Hyun Lee; Young Cheol Yoon; Hyun Su Kim; Jae-Hun Kim; Byung-Ok Choi
Journal:  Eur Radiol       Date:  2020-10-30       Impact factor: 5.315

6.  Adult onset glycogen storage disease type II (adult onset Pompe disease): report and magnetic resonance images of two cases.

Authors:  Andrew Del Gaizo; Sima Banerjee; Michael Terk
Journal:  Skeletal Radiol       Date:  2009-12       Impact factor: 2.199

7.  Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing.

Authors:  Mariacristina Scoto; Thomas Cullup; Sebahattin Cirak; Shu Yau; Adnan Y Manzur; Lucy Feng; Thomas S Jacques; Glenn Anderson; Stephen Abbs; Caroline Sewry; Heinz Jungbluth; Francesco Muntoni
Journal:  Eur J Hum Genet       Date:  2013-02-27       Impact factor: 4.246

8.  Late-onset Pompe disease: a genetic-radiological correlation on cerebral vascular anomalies.

Authors:  A Pichiecchio; S Sacco; P De Filippi; E Caverzasi; S Ravaglia; S Bastianello; C Danesino
Journal:  J Neurol       Date:  2017-08-30       Impact factor: 4.849

9.  Bioimpedance Analysis as a Method to Evaluate the Proportion of Fatty and Muscle Tissues in Progressive Myopathy in Pompe Disease.

Authors:  Agnieszka Różdżyńska-Świątkowska; Elżbieta Jurkiewicz; Anna Tylki-Szymańska
Journal:  JIMD Rep       Date:  2015-08-08

10.  Local restoration of dystrophin expression with the morpholino oligomer AVI-4658 in Duchenne muscular dystrophy: a single-blind, placebo-controlled, dose-escalation, proof-of-concept study.

Authors:  Maria Kinali; Virginia Arechavala-Gomeza; Lucy Feng; Sebahattin Cirak; David Hunt; Carl Adkin; Michela Guglieri; Emma Ashton; Stephen Abbs; Petros Nihoyannopoulos; Maria Elena Garralda; Mary Rutherford; Caroline McCulley; Linda Popplewell; Ian R Graham; George Dickson; Matthew J A Wood; Dominic J Wells; Steve D Wilton; Ryszard Kole; Volker Straub; Kate Bushby; Caroline Sewry; Jennifer E Morgan; Francesco Muntoni
Journal:  Lancet Neurol       Date:  2009-08-25       Impact factor: 44.182
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