MYO-MRI diagnostic protocols in genetic myopathies

Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt

Standard

MYO-MRI diagnostic protocols in genetic myopathies. / Chardon, Jodi Warman; Díaz-Manera, Jordi; Tasca, Giorgio; Bönnemann, Carsten G.; Gómez-Andrés, David; Heerschap, Arend; Mercuri, Eugenio; Muntoni, Francesco; Pichiecchio, Anna; Ricci, Enzo; Walter, Maggie C.; Hanna, Michael; Jungbluth, Heinz; Morrow, Jasper M.; Torrón, Roberto Fernández; Udd, Bjarne; Vissing, John; Yousry, Tarek; Quijano-Roy, Susana; Straub, Volker; Carlier, Robert Y.; MYO-MRI Working Group.

I: Neuromuscular Disorders, Bind 29, Nr. 11, 11.2019, s. 827-841.

Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt

Harvard

Chardon, JW, Díaz-Manera, J, Tasca, G, Bönnemann, CG, Gómez-Andrés, D, Heerschap, A, Mercuri, E, Muntoni, F, Pichiecchio, A, Ricci, E, Walter, MC, Hanna, M, Jungbluth, H, Morrow, JM, Torrón, RF, Udd, B, Vissing, J, Yousry, T, Quijano-Roy, S, Straub, V, Carlier, RY & MYO-MRI Working Group 2019, 'MYO-MRI diagnostic protocols in genetic myopathies', Neuromuscular Disorders, bind 29, nr. 11, s. 827-841. https://doi.org/10.1016/j.nmd.2019.08.011

APA

Chardon, J. W., Díaz-Manera, J., Tasca, G., Bönnemann, C. G., Gómez-Andrés, D., Heerschap, A., Mercuri, E., Muntoni, F., Pichiecchio, A., Ricci, E., Walter, M. C., Hanna, M., Jungbluth, H., Morrow, J. M., Torrón, R. F., Udd, B., Vissing, J., Yousry, T., Quijano-Roy, S., ... MYO-MRI Working Group (2019). MYO-MRI diagnostic protocols in genetic myopathies. Neuromuscular Disorders, 29(11), 827-841. https://doi.org/10.1016/j.nmd.2019.08.011

Vancouver

Chardon JW, Díaz-Manera J, Tasca G, Bönnemann CG, Gómez-Andrés D, Heerschap A o.a. MYO-MRI diagnostic protocols in genetic myopathies. Neuromuscular Disorders. 2019 nov.;29(11):827-841. https://doi.org/10.1016/j.nmd.2019.08.011

Author

Chardon, Jodi Warman ; Díaz-Manera, Jordi ; Tasca, Giorgio ; Bönnemann, Carsten G. ; Gómez-Andrés, David ; Heerschap, Arend ; Mercuri, Eugenio ; Muntoni, Francesco ; Pichiecchio, Anna ; Ricci, Enzo ; Walter, Maggie C. ; Hanna, Michael ; Jungbluth, Heinz ; Morrow, Jasper M. ; Torrón, Roberto Fernández ; Udd, Bjarne ; Vissing, John ; Yousry, Tarek ; Quijano-Roy, Susana ; Straub, Volker ; Carlier, Robert Y. ; MYO-MRI Working Group. / MYO-MRI diagnostic protocols in genetic myopathies. I: Neuromuscular Disorders. 2019 ; Bind 29, Nr. 11. s. 827-841.

Bibtex

@article{e61643d7b4664624a4a309e123c38f2f,
title = "MYO-MRI diagnostic protocols in genetic myopathies",
abstract = "Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases.",
keywords = "Congenital myopathy, Inflammatory myopathy, Inherited myopathy, Limb girdle muscular dystrophy, Magnetic resonance imaging, Whole-body MRI",
author = "Chardon, {Jodi Warman} and Jordi D{\'i}az-Manera and Giorgio Tasca and B{\"o}nnemann, {Carsten G.} and David G{\'o}mez-Andr{\'e}s and Arend Heerschap and Eugenio Mercuri and Francesco Muntoni and Anna Pichiecchio and Enzo Ricci and Walter, {Maggie C.} and Michael Hanna and Heinz Jungbluth and Morrow, {Jasper M.} and Torr{\'o}n, {Roberto Fern{\'a}ndez} and Bjarne Udd and John Vissing and Tarek Yousry and Susana Quijano-Roy and Volker Straub and Carlier, {Robert Y.} and {MYO-MRI Working Group}",
year = "2019",
month = nov,
doi = "10.1016/j.nmd.2019.08.011",
language = "English",
volume = "29",
pages = "827--841",
journal = "Journal of Neuromuscular Diseases",
issn = "0960-8966",
publisher = "Elsevier",
number = "11",

}

RIS

TY - JOUR

T1 - MYO-MRI diagnostic protocols in genetic myopathies

AU - Chardon, Jodi Warman

AU - Díaz-Manera, Jordi

AU - Tasca, Giorgio

AU - Bönnemann, Carsten G.

AU - Gómez-Andrés, David

AU - Heerschap, Arend

AU - Mercuri, Eugenio

AU - Muntoni, Francesco

AU - Pichiecchio, Anna

AU - Ricci, Enzo

AU - Walter, Maggie C.

AU - Hanna, Michael

AU - Jungbluth, Heinz

AU - Morrow, Jasper M.

AU - Torrón, Roberto Fernández

AU - Udd, Bjarne

AU - Vissing, John

AU - Yousry, Tarek

AU - Quijano-Roy, Susana

AU - Straub, Volker

AU - Carlier, Robert Y.

AU - MYO-MRI Working Group

PY - 2019/11

Y1 - 2019/11

N2 - Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases.

AB - Whole-body magnetic resonance imaging has emerged as a useful imaging tool in diagnosing and characterizing the progression of myopathies and muscular dystrophies. Whole-body MRI indications and diagnostic efficacy are becoming better defined with the increasing number of cases, publications and discussions within multidisciplinary working groups. Advanced Whole-body MRI protocols are rapid, lower cost, and well-tolerated by patients. Accurate interpretation of muscle Whole-body MRI requires a detailed knowledge of muscle anatomy and differential pattern of involvement in muscle diseases. With the surge in recently identified novel genetic myopathies, Whole-body MRI will become increasingly useful for phenotypic validation of genetic variants of unknown significance. In addition, Whole-body MRI will be progressively used as a biomarker for disease progression and quantify response to therapy with the emergence of novel disease modifying treatments. This review outlines Whole-body MRI indications and updates refined protocols and provides a comprehensive overview of the diagnostic utility and suggested methodology of Whole-body MRI for pediatric and adult patients with muscle diseases.

KW - Congenital myopathy

KW - Inflammatory myopathy

KW - Inherited myopathy

KW - Limb girdle muscular dystrophy

KW - Magnetic resonance imaging

KW - Whole-body MRI

UR - http://www.scopus.com/inward/record.url?scp=85075535994&partnerID=8YFLogxK

U2 - 10.1016/j.nmd.2019.08.011

DO - 10.1016/j.nmd.2019.08.011

M3 - Review

C2 - 31727541

AN - SCOPUS:85075535994

VL - 29

SP - 827

EP - 841

JO - Journal of Neuromuscular Diseases

JF - Journal of Neuromuscular Diseases

SN - 0960-8966

IS - 11

ER -

ID: 240244705