Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports. (Q48768992)

15 February 2018

title

Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports. (English)

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15 February 2018

facioscapulohumeral muscular dystrophy

main subject

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5

Chinnery PF

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15 February 2018

author name string

Bushby KM

1

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15 February 2018

Pollitt C

2

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15 February 2018

Johnson MA

3

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15 February 2018

Rogers MT

4

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15 February 2018

publication date

1 December 1998

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15 February 2018

published in

Neuromuscular Disorders

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15 February 2018

volume

8

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15 February 2018

issue

8

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15 February 2018

page(s)

574-579

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15 February 2018

Genetic counselling in facioscapulohumeral muscular dystrophy

cites work

1 reference

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Locomotor problems in infantile facioscapulohumeral muscular dystrophy. Retrospective study of 9 patients.

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Facioscapulohumeral muscular dystrophy in early childhood

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7 January 2021

Facioscapulohumeral muscular dystrophy (FSHD): design of natural history study and results of baseline testing. FSH-DY Group

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7 January 2021

A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): implications for therapeutic trials. The FSH-DY Group

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Polymyositis with facioscapulohumeral distribution

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Inflammatory myopathy with facioscapulohumeral distribution

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Familial myopathies with restricted distribution, facial weakness and inflammatory changes in affected muscles

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7 January 2021

"Polymyositis" with involvement of facial and distal musculature. One form of the fascioscapulohumeral syndrome?

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7 January 2021

Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD

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7 January 2021

Diagnostic criteria for facioscapulohumeral muscular dystrophy

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Unexpected sarcolemmal complement membrane attack complex deposits on nonnecrotic muscle fibers in muscular dystrophies

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7 January 2021

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

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The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. I. Natural history

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A Japanese boy with myalgia and cramps has a novel in-frame deletion of the dystrophin gene

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Myalgia and cramps: dystrophinopathy with wide-ranging laboratory findings

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7 January 2021

Steroid-responsive myalgia in a patient with Becker muscular dystrophy

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7 January 2021

High-dose intravenous immunoglobulin exerts its beneficial effect in patients with dermatomyositis by blocking endomysial deposition of activated complement fragments

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A pilot trial of prednisone in facioscapulohumeral muscular dystrophy. FSH-DY Group.

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7 January 2021

10.1016/S0960-8966(98)00088-1

Identifiers

DOI

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15 February 2018

1 reference

15 February 2018