(Q72817805)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8326329%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

title

Exercise intolerance and recurrent myoglobinuria as the only expression of Xp21 Becker type muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8326329%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference

1 reference

C Doriguzzi

1

1 reference

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29 October 2019

L Palmucci

2

1 reference

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29 October 2019

T Mongini

3

1 reference

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29 October 2019

L Chiadò-Piat

4

1 reference

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29 October 2019

G Restagno

5

1 reference

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29 October 2019

M Ferrone

6

1 reference

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29 October 2019

publication date

1 May 1993

1 reference

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29 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8326329%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

volume

240

1 reference

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29 October 2019

issue

5

1 reference

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29 October 2019

page(s)

269-271

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00838159

29 October 2019

exact match

0 references

cites work

The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion

1 reference

12 December 2020

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

1 reference

12 December 2020

Body building and myoglobinuria: report of three cases.

1 reference

12 December 2020

Improved diagnosis of Becker muscular dystrophy by dystrophin testing

1 reference

12 December 2020

Myoglobinuria and carnitine palmityl transferase deficiency in father and son.

1 reference

12 December 2020

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies

1 reference

12 December 2020

Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification

1 reference

12 December 2020

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications

1 reference

12 December 2020

Metabolic causes of myoglobinuria

1 reference

12 December 2020

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

12 December 2020

Use of DNA probes in detecting carriers of Duchenne muscular dystrophy: selected case studies

1 reference

12 December 2020

Fatal rhabdomyolysis complicating general anaesthesia in a child with Becker muscular dystrophy

1 reference

12 December 2020

Dystrophin: the protein product of the Duchenne muscular dystrophy locus

1 reference

12 December 2020

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

1 reference

12 December 2020

Feline muscular dystrophy with dystrophin deficiency

1 reference

12 December 2020

[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]

1 reference

12 December 2020

Dilating cardiomyopathy as the expression of Xp21 Becker type muscular dystrophy

1 reference

12 December 2020

Body building and rhabdomyolysis

1 reference

12 December 2020

X chromosome-linked muscular dystrophy (mdx) in the mouse

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00838159

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8326329%20AND%20SRC:MED&resulttype=core&format=json

29 October 2019

1 reference