(Q72338425)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

title

[Congenital muscular dystrophy] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

1 reference

F Vassella

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

M Mumenthaler

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

E Rossi

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

H Moser

4

1 reference

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26 October 2019

U Wiesmann

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

publication date

1 January 1967

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

Deutsche Zeitschrift fur Nervenheilkunde

26 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

volume

190

1 reference

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26 October 2019

issue

4

1 reference

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26 October 2019

page(s)

349-374

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6069208%20AND%20SRC:MED&resulttype=core&format=json

MUSCLE LACTATE DEHYDROGENASE PATTERNS IN TWO TYPES OF X-LINKED MUSCULAR DYSTROPHY

26 October 2019

cites work

1 reference

12 December 2020

Central core disease-an investigation of a rare muscle cell abnormality.

1 reference

12 December 2020

THE DIAGNOSTIC VALUE OF SERUM CREATINE KINASE IN NEUROMUSCULAR AND MUSCULAR DISEASE

1 reference

12 December 2020

Arthrogryposis multiplex congenita. Case due to disease of the anterior horn cells

1 reference

12 December 2020

[Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children.]

1 reference

12 December 2020

THE SIGNIFICANCE OF LACTATE DEHYDROGENASE ISOZYMES IN ABNORMAL HUMAN SKELETAL MUSCLE

1 reference

12 December 2020

Arthrogryposis Multiplex Congenita A Case of Neurogenic Origin

1 reference

12 December 2020

Congenital myopathy--A fifty-year follow-up.

1 reference

12 December 2020

A new congenital non-progressive myopathy

1 reference

12 December 2020

Clinical pathological conference: The Children's Medical Center, Boston, Mass

1 reference

12 December 2020

A Case of Congenital Defect of the Muscular System (Dystrophia muscularis congenita) and its Association with Congenital Talipes equino-varus

1 reference

12 December 2020

Hereditary non-progressive muscular dystrophy inducing arthrogryposis syndrome.

1 reference

12 December 2020

[Multiple congenital arthrogryposis]

1 reference

12 December 2020

1 reference

12 December 2020

AN UNUSUAL VARIETY OF MUSCULAR DYSTROPHY

1 reference

12 December 2020

Arthrogryposis multiplex due to congenital muscular dystrophy

1 reference

12 December 2020

Muscular hypotonia in infancy; diagnosis and differentiation

1 reference

12 December 2020

A case of arthrogryposis multiplex congenita with lesions in the nervous system

1 reference

12 December 2020

Congenital muscular dystrophy. A case report with autopsyfindings

1 reference

12 December 2020

The prognostic value of the muscle biopsy in the floppy infant.

1 reference

12 December 2020

THE HYPOTONIC INFANT. A REVIEW.

1 reference

12 December 2020

Experimental clubfoot and arthrogryposis multiplex congenita

1 reference

12 December 2020

NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY

1 reference

12 December 2020

[Two cases of familial congenital muscular dystrophy simulating Werdnig-Hoffman-Oppenheim disease]

1 reference

12 December 2020

Myotubular myopathy. Persistence of fetal muscle in an adolescent boy

1 reference

12 December 2020

Identifiers

1 reference