Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities.

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Andersen syndrome: an association of periodic paralysis, cardiac arrhythmia and dysmorphic abnormalities.

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2006 nî lūn-bûn

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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2006年學術文章

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Andersen syndrome: an associat ...... and dysmorphic abnormalities.

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Andersen syndrome: an associat ...... and dysmorphic abnormalities.

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Item

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Andersen syndrome: an associat ...... and dysmorphic abnormalities.

@en

Andersen syndrome: an associat ...... and dysmorphic abnormalities.

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Andersen syndrome: an associat ...... and dysmorphic abnormalities.

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Andersen syndrome: an associat ...... and dysmorphic abnormalities.

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P1476

Andersen syndrome: an associat ...... and dysmorphic abnormalities.

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P2093

Alberto A Gabbai

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Antonio C Antunes

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Célia H Tengan

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Gilberto M Manzano

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José R Bauab

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P2860

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

Functional and clinical characterization of KCNJ2 mutations associated with LQT7 (Andersen syndrome)

A calcium channel mutation causing hypokalemic periodic paralysis

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

Andersen‐Tawil syndrome: a model of clinical variability, pleiotropy, and genetic heterogeneity

Intermittent muscular weakness, extrasystoles, and multiple developmental anomalies. A new syndrome?

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.

The primary periodic paralyses: diagnosis, pathogenesis and treatment.

P304

582-584

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scholarly article

P356

10.1590/S0004-282X2006000400009

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P433

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P478

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Gilmar Fernandes do Prado

P577

2006-09-01T00:00:00Z

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P698

17119796

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