Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis. - Wikidata - awgldk - TriplyDB

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

http://www.wikidata.org/entity/Q46509825

about

UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis Hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis: recent advances and controversies Towards the targeted management of Chediak-Higashi syndrome Hemophagocytic lymphohistiocytosis: review of etiologies and management Hemophagocytic syndrome in children and adults Hemophagocytic lymphohistiocytosis: an update on diagnosis and pathogenesis Hematopoetic stem cell transplantation in children Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports Hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis: a journey of a thousand miles begins with a single (big) step Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3 Hematopoietic stem cell transplantation in infants.Clinical presentation of hemophagocytic lymphohistiocytosis in adults is less typical than in children Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosis.Hemophagocytic Syndrome and Critical Illness: New Insights into Diagnosis and Management.STXBP2 mutations in children with familial haemophagocytic lymphohistiocytosis type 5 An intermediate alemtuzumab schedule reduces the incidence of mixed chimerism following reduced-intensity conditioning hematopoietic cell transplantation for hemophagocytic lymphohistiocytosis.Importance of hyperbilirubinemia in differentiation of primary and secondary hemophagocytic lymphohistiocytosis in pediatric cases.How I treat hemophagocytic lymphohistiocytosis.Chemoimmunotherapy for hemophagocytic lymphohistiocytosis: long-term results of the HLH-94 treatment protocol Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding.Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosis.A journey of hope: lessons learned from studies on rare diseases and orphan drugs.A Hemophagocytic Lymphohistiocytosis Case with Newly Defined UNC13D (c.175G>C; p.Ala59Pro) Mutation and a Rare Complication.Pre- and post-natal treatment of hemophagocytic lymphohistiocytosis.Reduced intensity conditioning and allogeneic stem cell transplantation in childhood malignant and nonmalignant diseases.Hematopoietic cell transplantation for correction of primary immunodeficiencies.The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis Familial haemophagocytic lymphohistiocytosis: advances in the genetic basis, diagnosis and management.Reduced-intensity conditioning haematopoietic cell transplantation for haemophagocytic lymphohistiocytosis: an important step forward.Reduced-intensity conditioning for allogeneic stem cell transplant in primary immune deficiencies.Risk for complications in patients with hemophagocytic lymphohistiocytosis who undergo hematopoietic stem cell transplantation: myeloablative versus reduced-intensity conditioning regimens.Lymphoma presenting as secondary HLH: a review with a tale of two cases.Hereditary and acquired hemophagocytic lymphohistiocytosis.Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis.Unrelated donor hematopoietic stem cell transplantation for the treatment of non-malignant genetic diseases: An alemtuzumab based regimen is associated with cure of clinical disease; earlier clearance of alemtuzumab may be associated with graft reje Hemophagocytic lymphohistiocytosis in infants: a single center experience from India.Perforin gene transfer into hematopoietic stem cells improves immune dysregulation in murine models of perforin deficiency A retrospective analysis of 56 children with hemophagocytic lymphohistiocytosis.Fludarabine-based reduced-intensity conditioning regimen for hematopoietic stem cell transplantation in primary hemophagocytic lymphohistiocytosis.

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P2860

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

http://www.wikidata.org/entity/Q46509825

description

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2005年学术文章

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2005年学术文章

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name

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

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Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

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type

label

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

@en

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

@nl

prefLabel

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

@en

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

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J.1365-2141.2005.05501.X

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British Journal of Haematology

P1476

Haematopoietic stem cell transplantation in haemophagocytic lymphohistiocytosis.

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P2093

Alexandra H Filipovich

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David Webb

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Gritta Janka

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Helmut Gadner

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Histiocyte Society

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Jacek Winiarski

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R Maarten Egeler

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Shinsaku Imashuku

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Stephan Ladisch

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P2860

Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

Six novel mutations in the PRF1 gene in children with haemophagocytic lymphohistiocytosis

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.

Unrelated 5/6-locus matched umbilical cord blood transplantation in a 23-month-old child with hemophagocytic lymphohistiocytosis.

Treatment of hemophagocytic lymphohistiocytosis with HLH-94 immunochemotherapy and bone marrow transplantation.

Cerebromeningeal haemophagocytic lymphohistiocytosis.

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

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

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622-630

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scholarly article

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10.1111/J.1365-2141.2005.05501.X

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5

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129

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Scott M Montgomery

Jan-Inge Henter

Franco Locatelli

AnnaCarin Horne

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2005-06-01T00:00:00Z

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7824436

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15916685

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