(Q33922326)

30 July 2017

1 reference

title

Congenital fibre type disproportion a time-locked diagnosis: a clinical and morphological follow-up study (English)

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30 July 2017

0 references

Fons John Marie Gabreëls

series ordinal

2

object named as

Gabreëls FJ

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30 July 2017

Bartholomeus MG

1

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30 July 2017

ter Laak HJ

series ordinal

3

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30 July 2017

van Engelen BG

series ordinal

4

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30 July 2017

publication date

1 June 2000

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Clinical Neurology and Neurosurgery

30 July 2017

published in

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30 July 2017

volume

102

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30 July 2017

issue

2

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30 July 2017

page(s)

97-101

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Congenital fibre type disproportion myopathy. A histological diagnosis with an uncertain clinical outlook

30 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Type I fiber atrophy and nemaline bodies.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Clinical variability in congenital fiber type disproportion.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Congenital fibre type disproportion

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Congenital fibre type disproportion with unusual clinico-pathologic manifestations

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

The spectrum of the so-called rigid spine syndrome: nosological considerations and report of three female cases

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Sequential muscle biopsy changes in a case of congenital myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Minicores and congential fibre type disproportion observed in a family

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Postnatal centralization of muscle fibre nuclei in centronuclear myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Centronuclear myopathy and type-1 hypotrophy without central nuclei. Distinct nosologic entities?

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Limb-girdle muscular dystrophy: clinical and pathologic reevaluation

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Lobulated fibers in neuromuscular diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

Single-fiber electromyography in neuromuscular disorders: correlation of muscle histochemistry, single-fiber electromyography, and clinical findings

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2800%2900066-4

7 January 2021

10.1016/S0303-8467(00)00066-4

Identifiers

DOI

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30 July 2017

1 reference