Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

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Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

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2015 nî lūn-bûn

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2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

2015年论文

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2015年论文

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Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

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Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

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type

Item

label

Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

@ast

Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

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Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

@ast

Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

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P1476

Congenital Parvovirus B19 Infection: Persistent Viremia and Red Blood Cell Aplasia

@en

P2093

Amélie Collins

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Chia-Ling Nhan-Chang

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Christiana R Farkouh

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Jennifer A Rathe

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Jennifer M Duchon

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Lynn L Simpson

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Natalie Neu

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Russell S Miller

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Sruti S Nadimpalli

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Vasudeva M Kamath

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P2860

Human parvovirus B19.

Parvovirus B19-induced perturbation of human megakaryocytopoiesis in vitro.

Neurologic manifestations associated with parvovirus B19 infection.

Advances in human B19 erythrovirus biology

Parvovirus B19.

Intravenous immunoglobulin therapy for pure red cell aplasia related to human parvovirus b19 infection: a retrospective study of 10 patients and review of the literature.

Advances in the biology, diagnosis and host-pathogen interactions of parvovirus B19.

Resistance to parvovirus B19 infection due to lack of virus receptor (erythrocyte P antigen).

Gestational and fetal outcomes in B19 maternal infection: a problem of diagnosis.

Congenital human parvovirus b19 infection with persistent viremia.

P304

ofv049

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P31

scholarly article

P356

10.1093/OFID/OFV049

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P433

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P478

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P50

Adam J Ratner

P577

2015-04-15T00:00:00Z

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P5875

277629907

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P698

26288800

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P921

birth defect

P932

4539735

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