Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement.

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Two Brothers with Atypical UNC13D-Related Hemophagocytic Lymphohistiocytosis Characterized by Massive Lung and Brain Involvement.

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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

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2017年學術文章

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2017年學術文章

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Two Brothers with Atypical UNC ...... ve Lung and Brain Involvement.

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Two Brothers with Atypical UNC ...... ve Lung and Brain Involvement.

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Two Brothers with Atypical UNC ...... ve Lung and Brain Involvement.

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Two Brothers with Atypical UNC ...... ve Lung and Brain Involvement.

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Two Brothers with Atypical UNC ...... ve Lung and Brain Involvement.

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Two Brothers with Atypical UNC ...... ve Lung and Brain Involvement.

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Two Brothers with Atypical UNC ...... ive Lung and Brain Involvement

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Carol Saunders

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Caterina Cancrini

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Emilia Cirillo

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Giuliana Giardino

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Laura Papetti

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Maia De Luca

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Roberta Romano

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P2860

Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11

Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis

Hemophagocytic Lymphohistiocytosis in Children: Pathogenesis and Treatment

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11

Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases

Familial hemophagocytic lymphohistiocytosis may present during adulthood: clinical and genetic features of a small series.

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

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1892

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scholarly article

case report

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10.3389/FIMMU.2017.01892

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P478

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Claudio Pignata

Massimiliano Valeriani

Paolo Palma

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2017-12-21T00:00:00Z

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29312353

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5742579

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