Respiratory involvement in inherited primary muscle conditions. - Wikidata - wikimedia - TriplyDB

Respiratory involvement in inherited primary muscle conditions.

Respiratory involvement in inherited primary muscle conditions.

http://www.wikidata.org/entity/Q36596271

about

Emery-Dreifuss muscular dystrophy: a test case for precision medicine.Diaphragm Dysfunction: Diagnostic Approaches and Management Strategies Phosphofructo-1-kinase deficiency leads to a severe cardiac and hematological disorder in addition to skeletal muscle glycogenosis Results of a two-year pilot study of clinical outcome measures in collagen VI- and laminin alpha2-related congenital muscular dystrophies.Consensus statement on standard of care for congenital muscular dystrophies.Neuromuscular disease and anesthesia.Muscle-Derived Proteins as Serum Biomarkers for Monitoring Disease Progression in Three Forms of Muscular Dystrophy.Gene therapy in monogenic congenital myopathies.Utility Of diaphragm ultrasound in myopathy.The neurology of acutely failing respiratory mechanics.Comparison of sitting and supine forced vital capacity in collagen VI-related dystrophy and laminin α2-related dystrophy.Physiology of respiratory disturbances in muscular dystrophies.

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Respiratory involvement in inherited primary muscle conditions.

http://www.wikidata.org/entity/Q36596271

description

2006 nî lūn-bûn

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2006年の論文

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2006年論文

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2006年論文

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Respiratory involvement in inherited primary muscle conditions.

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Respiratory involvement in inherited primary muscle conditions.

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Respiratory involvement in inherited primary muscle conditions.

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JNNP.2005.078881

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Journal of Neurology, Neurosurgery and Psychiatry

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Respiratory involvement in inherited primary muscle conditions.

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Kinnear WJ

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Shahrizaila N

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Wills AJ

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P2860

Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy

Emery-Dreifuss syndrome

Unusual type of benign x-linked muscular dystrophy

Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome 1p35-36.

Clinical and metabolic correction of pompe disease by enzyme therapy in acid maltase-deficient quail

Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI

Mitochondrial DNA and disease

Bethlem myopathy: a slowly progressive congenital muscular dystrophy with contractures

Melas: an original case and clinical criteria for diagnosis

Ventilatory support in facioscapulohumeral muscular dystrophy

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