85th ENMC International Workshop on Congenital Muscular Dystrophy. 6th International CMD Workshop. 1st Workshop of the Myo-Cluster Project 'GENRE'. 27-28th October 2000, Naarden, The Netherlands (Q77316172)

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scientific article published on 01 January 2002

Language	Label	Description	Also known as
English	85th ENMC International Workshop on Congenital Muscular Dystrophy. 6th International CMD Workshop. 1st Workshop of the Myo-Cluster Project 'GENRE'. 27-28th October 2000, Naarden, The Netherlands	scientific article published on 01 January 2002

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scholarly article

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4 December 2019

85th ENMC International Workshop on Congenital Muscular Dystrophy. 6th International CMD Workshop. 1st Workshop of the Myo-Cluster Project 'GENRE'. 27-28th October 2000, Naarden, The Netherlands (English)

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4 December 2019

Pascale Guicheney

2

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4 December 2019

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Francesco Muntoni

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4 December 2019

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1 January 2002

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4 December 2019

Neuromuscular Disorders

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4 December 2019

12

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4 December 2019

1

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4 December 2019

69-78

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4 December 2019

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

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Abnormal localization of laminin subunits in muscular dystrophies

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Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy

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Immunofluorescence study of a muscle biopsy from a 1-year-old patient with Walker-Warburg syndrome.

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Probing the Gene eXpression Database for candidate genes

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Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome.

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Human laminin M chain: epitope analysis of its monoclonal antibodies by immunoscreening of cDNA clones and tissue expression

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Immunogold and freeze etch electron microscopic studies of merosin localization in basal lamina of human skeletal muscle fibers

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7 January 2021

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Unusual laminin alpha2 processing in myoblasts from a patient with a novel variant of congenital muscular dystrophy

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Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings

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Merosin-positive congenital muscular dystrophy with mental retardation and cataracts: a new entity in two families

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Congenital muscular dystrophy with central and peripheral nervous system involvement in a Belgian patient.

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Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42.

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An early onset muscular dystrophy with diaphragmatic involvement, early respiratory failure and secondary alpha2 laminin deficiency unlinked to the LAMA2 locus on 6q22

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Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2.

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Congenital muscular dystrophy with secondary merosin deficiency and normal brain MRI: a novel entity?

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Binding of ADAM12, a marker of skeletal muscle regeneration, to the muscle-specific actin-binding protein, alpha -actinin-2, is required for myoblast fusion

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The cysteine-rich domain of human ADAM 12 supports cell adhesion through syndecans and triggers signaling events that lead to beta1 integrin-dependent cell spreading

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Identifiers

10.1016/S0960-8966(01)00209-7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11731288%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11731288%20AND%20SRC:MED&resulttype=core&format=json

4 December 2019

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