Factor XIII deficiency diagnosis: Challenges and tools.

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Factor XIII deficiency diagnosis: Challenges and tools.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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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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Factor XIII deficiency diagnosis: Challenges and tools.

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Factor XIII deficiency diagnosis: Challenges and tools.

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Factor XIII deficiency diagnosis: Challenges and tools.

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Factor XIII deficiency diagnosis: Challenges and tools.

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Factor XIII deficiency diagnosis: Challenges and tools.

@en

Factor XIII deficiency diagnosis: Challenges and tools.

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P1476

Factor XIII deficiency diagnosis: Challenges and tools.

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P2093

A Shapiro

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P2860

Factor XIII: novel structural and functional aspects.

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

Novel aspects of factor XIII deficiency.

Arg77His and Trp187Arg are the most common mutations causing FXIII deficiency in Iran.

Measurement of factor XIII activity in plasma.

Factor XIII deficiency: an update.

Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms.

The burden and management of FXIII deficiency.

Inhibitors of Factor XIII/13 in older patients.

Morbidity and mortality in a large number of Iranian patients with severe congenital factor XIII deficiency.

P304

3-11

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scholarly article

P356

10.1111/IJLH.12756

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P433

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P478

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P50

Flora Peyvandi

Majid Naderi

Mehran Karimi

P577

2017-10-13T00:00:00Z

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P698

29027765

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