Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

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Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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name

Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

@en

Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

@nl

type

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label

Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

@en

Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

@nl

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Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

@en

Infantile-onset Pompe disease with neonatal debut: A case report and literature review.

@nl

P1476

Infantile-onset Pompe disease with neonatal debut: A case report and literature review

@en

P2093

Luis Albajara

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Luis García Guereta

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Mar García Romero

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Marta Cabrera

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Miguel Saenz de Pipaon

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Miriam Martínez

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Rita M Regojo

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P275

Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International

P2860

Recombinant human acid [alpha]-glucosidase: major clinical benefits in infantile-onset Pompe disease

2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy: the Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC).

The impact of antibodies on clinical outcomes in diseases treated with therapeutic protein: lessons learned from infantile Pompe disease.

Pompe disease: literature review and case series

Adult and infantile glycogenosis type II in one family, explained by allelic diversity.

Infantile Pompe disease: A case report and review of the Chinese literature

Atypical immunologic response in a patient with CRIM-negative Pompe disease.

Pompe's disease.

The genotype-phenotype correlation in Pompe disease.

c.1437G>A intron 9 substitution on acid α-glucosidase gene associated with classic infantile-onset Pompe disease phenotype.

P304

e9186

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scholarly article

case report

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10.1097/MD.0000000000009186

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P407

English

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P478

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María L Couce

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ScienceSource

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2017-12-01T00:00:00Z

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29390460

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P921

hypertrophic cardiomyopathy

glycogen storage disease II

Anzim

ventricular fibrillation

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5758162

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