Related references
Note: Only part of the references are listed.Diagnostic evaluation of patients with suspected haemophagocytic lymphohistiocytosis
Kai Lehmberg et al.
BRITISH JOURNAL OF HAEMATOLOGY (2013)
The American College of Rheumatology 1990 criteria for the classification of vasculitis: Introduction
Gene G. Hunder et al.
ARTHRITIS AND RHEUMATISM (2010)
Efficacy of Traditional and Biologic Agents in Different Clinical Phenotypes of Adult-Onset Still's Disease
Stefano Franchini et al.
ARTHRITIS AND RHEUMATISM (2010)
The American college of rheumatology 1990 criteria for the classification of polyarteritis nodosa
Robert W. Lightfoot et al.
ARTHRITIS AND RHEUMATISM (2010)
Primary and secondary hemophagocytic lymphohistiocytosis: clinical features, pathogenesis and therapy
Sumit Gupta et al.
EXPERT REVIEW OF CLINICAL IMMUNOLOGY (2010)
Familial Hemophagocytic Lymphohistiocytosis Type 5 (FHL-5) Is Caused by Mutations in Munc18-2 and Impaired Binding to Syntaxin 11
Udo zur Stadt et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Macrophage Activation Syndrome in Juvenile Systemic Lupus Erythematosus A Multinational Multicenter Study of Thirty-Eight Patients
Alessandro Parodi et al.
ARTHRITIS AND RHEUMATISM (2009)
Nationwide survey of hemophagocytic lymphohistiocytosis in Japan
Eiichi Ishii et al.
INTERNATIONAL JOURNAL OF HEMATOLOGY (2007)
HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis
Jan-Inge Henter et al.
PEDIATRIC BLOOD & CANCER (2007)
Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2
Johannes Jung et al.
BLOOD (2006)
Characteristics and long-term outcome of 15 episodes of systemic lupus erythematosus-associated hemophagocytic syndrome
Olivier Lambotte et al.
MEDICINE (2006)
Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11
U zur Stadt et al.
HUMAN MOLECULAR GENETICS (2005)
Modern management of children with haemophagocytic lymphohistiocytosis
GE Janka et al.
BRITISH JOURNAL OF HAEMATOLOGY (2004)
The GLADEL multinational Latin American prospective inception cohort of 1,214 patients with systemic lupus erythematosus - Ethnic and disease heterogeneity among Hispanics
BA Pons-Estel et al.
MEDICINE (2004)
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3)
J Feldmann et al.
CELL (2003)
Morbidity and mortality in systemic lupus erythematosus during a 10-year period -: A comparison of early and late manifestations in a cohort of 1,000 patients
R Cervera et al.
MEDICINE (2003)
Classification criteria for Sjogren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group
C Vitali et al.
ANNALS OF THE RHEUMATIC DISEASES (2002)
Proposal for a new set of classification criteria for adult-onset Still disease
B Fautrel et al.
MEDICINE (2002)
Reactive haemophagocytic syndrome in children with inflammatory disorders.: A retrospective study of 24 patients
JL Stéphan et al.
RHEUMATOLOGY (2001)
Macrophage activation syndrome: a potentially fatal complication of rheumatic disorders
S Sawhney et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2001)
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome
G Ménasché et al.
NATURE GENETICS (2000)
Share Paper
