(Q35036499)

5 August 2017

1 reference

title

Autophagic vacuolar myopathies (English)

1 reference

5 August 2017

0 references

Ichizo Nishino

1

1 reference

5 August 2017

publication date

1 January 2003

1 reference

Current Neurology and Neuroscience Reports

5 August 2017

published in

1 reference

5 August 2017

volume

3

1 reference

5 August 2017

issue

1

1 reference

5 August 2017

page(s)

64-69

1 reference

https://scigraph.springernature.com/pub.10.1007/s11910-003-0040-y

5 August 2017

exact match

0 references

cites work

Lysosomal glycogen storage disease with normal acid maltase

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-003-0040-Y

Clinicopathological features of genetically confirmed Danon disease

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-003-0040-Y

Infantile autophagic vacuolar myopathy is distinct from Danon disease

21 January 2018

1 reference

12 December 2020

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).

1 reference

12 December 2020

X-linked myopathy with excessive autophagy: a new hereditary muscle disease

1 reference

12 December 2020

"Rimmed vacuole myopathy" sparing the quadriceps. A unique disorder in Iranian Jews

1 reference

12 December 2020

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy

1 reference

12 December 2020

Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filaments

1 reference

12 December 2020

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

1 reference

12 December 2020

Cell surface expression of lysosome-associated membrane protein-2 (lamp2) and CD63 as markers of in vivo platelet activation in malignancy

1 reference

12 December 2020

Gene locus for autosomal recessive distal myopathy with rimmed vacuoles maps to chromosome 9

1 reference

12 December 2020

Inclusion body myositis-like phenotype induced by transgenic overexpression of beta APP in skeletal muscle

1 reference

12 December 2020

Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy

1 reference

12 December 2020

Plasma membrane repair is mediated by Ca(2+)-regulated exocytosis of lysosomes

1 reference

12 December 2020

Impaired innervation of cultured human muscle overexpressing betaAPP experimentally and genetically: relevance to inclusion-body myopathies

1 reference

12 December 2020

Familial distal myopathy with rimmed vacuole and lamellar (myeloid) body formation

1 reference

12 December 2020

Hereditary inclusion body myopathy maps to chromosome 9p1-q1

1 reference

12 December 2020

10.1007/S11910-003-0040-Y

Identifiers

DOI

1 reference

5 August 2017

1 reference