(Q40442977)

20 September 2017

title

Occurrence of haemophagocytic lymphohistiocytosis at less than 1 year of age: analysis of 96 patients (English)

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20 September 2017

Shinsaku Imashuku

1

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20 September 2017

Ikuyo Ueda

2

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20 September 2017

Tomoko Teramura

3

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20 September 2017

Kanako Mori

4

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20 September 2017

Akira Morimoto

5

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20 September 2017

Masahiro Sako

6

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20 September 2017

Eiichi Ishii

7

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20 September 2017

publication date

25 February 2005

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European Journal of Pediatrics

20 September 2017

published in

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20 September 2017

volume

164

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20 September 2017

issue

5

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20 September 2017

page(s)

315-319

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Perforin defects of primary haemophagocytic lymphohistiocytosis in Japan

20 September 2017

cites work

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12 December 2020

Pathogenesis of haemophagocytic lymphohistiocytosis

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12 December 2020

Familial hemophagocytic lymphohistiocytosis

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12 December 2020

Intermittent hemophagocytic lymphohistiocytosis is a regular feature of lysinuric protein intolerance

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12 December 2020

Haemophagocytosis in hereditary fructose intolerance: a diagnostic dilemma.

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12 December 2020

Hemophagocytic syndrome presenting as acute hepatic failure in two infants: clinical overlap with neonatal hemochromatosis

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12 December 2020

Clinical features and treatment strategies of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis

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12 December 2020

Neonatal herpes simplex virus infection

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12 December 2020

Acute hemorrhagic, hepatic, and neurologic manifestations in juvenile rheumatoid arthritis: possible relationship to drugs or infection

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12 December 2020

Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society.

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12 December 2020

No mutations of SAP/SH2D1A/DSHP and perforin genes in patients with Epstein-Barr virus-associated hemophagocytic syndrome in Japan

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12 December 2020

Characteristic perforin gene mutations of haemophagocytic lymphohistiocytosis patients in Japan

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12 December 2020

Chronic active Epstein-Barr virus infection associated with mutations in perforin that impair its maturation

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12 December 2020

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

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12 December 2020

Biology and treatment of familial hemophagocytic lymphohistiocytosis: importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis

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12 December 2020

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

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12 December 2020

Advances in the management of hemophagocytic lymphohistiocytosis.

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12 December 2020

Low natural killer activity and central nervous system disease as a high-risk prognostic indicator in young patients with hemophagocytic lymphohistiocytosis.

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12 December 2020

Haemophagocytic lymphohistiocytosis: proposal of a diagnostic algorithm based on perforin expression

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12 December 2020

Localization of a gene for familial hemophagocytic lymphohistiocytosis at chromosome 9q21.3-22 by homozygosity mapping

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12 December 2020

Multiple sulphatase deficiency and haemophagocytic syndrome

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12 December 2020

Differential diagnosis of hemophagocytic syndrome: underlying disorders and selection of the most effective treatment

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12 December 2020

Enterovirus-associated haemophagocytic syndrome in a neonate

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12 December 2020

CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two children

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12 December 2020

Identification of novel MUNC13-4 mutations in familial haemophagocytic lymphohistiocytosis and functional analysis of MUNC13-4-deficient cytotoxic T lymphocytes

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12 December 2020

Perforin expression in cytotoxic lymphocytes from patients with hemophagocytic lymphohistiocytosis and their family members

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12 December 2020

Macrophage activation syndrome and reactive hemophagocytic lymphohistiocytosis: the same entities?

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12 December 2020

Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society

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12 December 2020

Prognosis for neonates with enterovirus hepatitis and coagulopathy.

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12 December 2020

HLH-94: a treatment protocol for hemophagocytic lymphohistiocytosis. HLH study Group of the Histiocyte Society

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12 December 2020

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).

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12 December 2020

10.1007/S00431-005-1636-9

Identifiers

DOI

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20 September 2017

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