(Q41289785)

29 September 2017

1 reference

title

Calf enlargement in neuromuscular diseases: a quantitative ultrasound study in 350 patients and review of the literature (English)

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29 September 2017

Reimers CD

1

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29 September 2017

Schlotter B

series ordinal

2

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29 September 2017

Eicke BM

series ordinal

3

1 reference

29 September 2017

Witt TN

series ordinal

4

1 reference

29 September 2017

publication date

1 November 1996

1 reference

Journal of the Neurological Sciences

29 September 2017

published in

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29 September 2017

volume

143

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29 September 2017

issue

1-2

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29 September 2017

page(s)

46-56

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[A new x-chromosomal muscular dystrophy]

29 September 2017

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Muscle hypertrophy secondary to the tethered cord syndrome

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Crural hypertrophy associated with centronuclear myopathy

7 January 2021

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Age changes in body composition revealed by computed tomography

7 January 2021

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Spinal muscular atrophy and hypertrophy of the calves

7 January 2021

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Computed tomography of muscle

7 January 2021

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A clinical and genetic study of chronic proximal spinal muscular atrophy

7 January 2021

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Calf hypertrophy and asymmetry in female carriers of X‐linked Duchenne muscular dystrophy: an over‐diagnosed clinical manifestation

7 January 2021

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Muscle hypertrophy in Duchenne muscular dystrophy. A pathological and morphometric study

7 January 2021

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Benign familial spinal muscular atrophy with hypertrophy of the calves

7 January 2021

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An unusual variant of Becker muscular dystrophy

7 January 2021

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Calf enlargement in hereditary motor and sensory neuropathy

7 January 2021

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Symptomatic sarcoidosis of skeletal muscle

7 January 2021

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A new type of hereditary distal myopathy with characteristic sarcoplasmic bodies and intermediate (skeletin) filaments

7 January 2021

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The spectrum and diagnosis of acid maltase deficiency.

7 January 2021

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A benign motor neuron disorder: delayed cramps and fasciculation after poliomyelitis or myelitis

7 January 2021

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Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

7 January 2021

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Benign spinal muscular atrophy arising in childhood and adolescence

7 January 2021

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Juvenile proximal spinal muscular atrophy with early hypertrophy of calves

7 January 2021

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

7 January 2021

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The quadriceps strength of healthy elderly people remeasured after eight years

7 January 2021

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Dominant inherited distal spinal muscular atrophy with atrophic and hypertrophic calves

7 January 2021

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Deficiency of skeletal muscle succinate dehydrogenase and aconitase. Pathophysiology of exercise in a novel human muscle oxidative defect

7 January 2021

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Centronuclear myopathy in old age

7 January 2021

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Dominantly inherited pseudohypertrophic muscular dystrophy with internalized capillaries

7 January 2021

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Congenital centronuclear (myotubular) myopathy. A clinical, pathological and genetic study in eight children.

7 January 2021

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Creatine phospholinase activity in spinal muscular atrophy.

7 January 2021

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Size and composition of the calf and quadriceps muscles in Duchenne muscular dystrophy. A tomographic and histochemical study

7 January 2021

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Atypical Myopathy With Myofibrillar Aggregates

7 January 2021

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Muscle hypertrophy with neuropathy

7 January 2021

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Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.

7 January 2021

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Distal and congenital myopathy with hypertrophy of the calves. Presence of mitochondrial anomalies

7 January 2021

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Centronuclear myopathy with unusual clinical picture

7 January 2021

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Hereditary Distal Myopathy With Onset in Infancy

7 January 2021

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Debrancher deficiency neuromuscular disorder with pseudohypertrophy in two brothers

7 January 2021

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Muscular pseudohypertrophy in an adult case with centronuclear myopathy

7 January 2021

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Neuromyotonia. A mild case

7 January 2021

1 reference

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Chronic proximal spinal muscular atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Hypertrophia musculorum vera in familial ataxia

7 January 2021

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[Congenital muscular dystrophy: clinical study of 17 patients]

7 January 2021

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Neurogenic muscle hypertrophy. Report of two cases

7 January 2021

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Anterior-horn cell degeneration and gross calf hypertrophy with adolescent onset. A new spinal muscular atrophy syndrome

7 January 2021

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The benign proximal spinal progressive muscular atrophies

7 January 2021

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Hypertrophia musculorum vera. Study of a family

7 January 2021

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Muscle acetylcholinesterase in a familial myopathic disease

7 January 2021

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Muscular ultrasound in idiopathic inflammatory myopathies of adults

7 January 2021

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Skeletal muscle sonography: a correlative study of echogenicity and morphology

7 January 2021

1 reference

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The spectrum of mild X-linked recessive muscular dystrophy.

7 January 2021

1 reference

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A comparison of anthropometry with computed tomography in limbs of young and aged men

7 January 2021

1 reference

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A case of myopathy associated with a dystrophin gene deletion and abnormal glycogen storage

7 January 2021

1 reference

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Department of Neurology, Northwestern University Medical School, Chicago, Illinois

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Hereditary motor and sensory neuropathy with calf muscle enlargement

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Late Infantile Acid Maltase Deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Studies on the carrier state in X-linked recessive (Duchenne) muscular dystrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Kugelberg-welander syndrome with dominant inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Hereditary motor and sensory neuropathy with calf hypertrophy is associated with 17p 11.2 duplication

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Distal myopathy with onset in early infancy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Benign infantile spinal muscular atrophy. A prospective study.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Neuronal type of Charcot-Marie-Tooth disease with a syndrome of continuous motor unit activity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Muscle hypertrophy and a syndrome of continuous motor unit activity in prednisone-responsive Guillain-Barré polyneuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Disseminated cysticercosis. New observations, including CT scan findings and experience with treatment by praziquantel

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Asymptomatic benign familial spinal muscular atrophy with hypertrophy of the calves and high creatine kinase levels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Size and strength of the quadriceps muscles of old and young women

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

The size and strength of the quadriceps muscles of old and young men.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

Isaacs' syndrome with muscle hypertrophy reversed by phenytoin therapy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900037-8

10.1016/S0022-510X(96)00037-8

7 January 2021

Identifiers

DOI

1 reference

29 September 2017

1 reference