(Q42480362)

1 November 2017

Autophagic vacuoles with sarcolemmal features delineate Danon disease and related myopathies (English)

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1 November 2017

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Kazuma Sugie

1

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1 November 2017

Satoru Noguchi

2

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1 November 2017

Yoshimichi Kozuka

3

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1 November 2017

Eri Arikawa-Hirasawa

4

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1 November 2017

Mikihito Tanaka

5

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1 November 2017

Chuanzhu Yan

6

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1 November 2017

Paul Saftig

7

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1 November 2017

Kurt von Figura

8

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1 November 2017

Michio Hirano

9

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1 November 2017

Satoshi Ueno

10

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1 November 2017

Ikuya Nonaka

11

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1 November 2017

Ichizo Nishino

12

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1 November 2017

1 June 2005

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Journal of Neuropathology & Experimental Neurology

1 November 2017

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1 November 2017

64

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1 November 2017

6

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1 November 2017

513-522

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

1 November 2017

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Lysosomal glycogen storage disease with normal acid maltase

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Clinicopathological features of genetically confirmed Danon disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Sarcolemmal indentation in cardiomyopathy with mental retardation and vacuolar myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

A novel form of autophagic vacuolar myopathy with late-onset and multiorgan involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Autophagic vacuolar myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Accumulation of autophagic vacuoles and cardiomyopathy in LAMP-2-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Disease model: LAMP-2 enlightens Danon disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Primary structure of dystrophin-related protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Type VI collagen anchors endothelial basement membranes by interacting with type IV collagen

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Lysosomal membrane proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

VAMP-7 mediates vesicular transport from endosomes to lysosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Dissection of autophagosome formation using Apg5-deficient mouse embryonic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Laminin-induced acetylcholine receptor clustering: an alternative pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

Characterization of Danon disease in a male patient and his affected mother

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F64.6.513

21 January 2018

Identifiers

DOI

10.1093/JNEN/64.6.513

1 reference

1 November 2017

1 reference