Skip to content
The industry
Pathologies
Care
Training
Research
Menu
en
fr
Presentation of the sector
Missions
Gouvernance
Centres of Reference for Rare Diseases
Find a specialist
Research/diagnostic laboratories
Patient associations
Scientific societies
Others French Healthcare Networks for Rare diseases
Partners
Primary amyloidosis and others immunoglobulin deposition diseases
Bradykinin-mediated angioedema
Acquired And Inherited Aplastic Anemia
Autoimmune cytopenias
Primary immunodeficiency
Histiocytosis
Castleman disease
Mastocytosis
Thrombotic microangiopathy
Chronic neutropenia
LGL proliferation
Hypereosinophilic syndrome
Expert opinion RCP
Orphanet Emergency / Disability files
Therapeutic patient education programs
Transition from Pediatric to Adult Service
Find a specialist
MOOC MaRIH
University qualification « Immunohematology and Internal Medicine »
UQ « MAT and other immunological diseases of hemostasis »
Clinical quizzes
MaRIH magazines
Ongoing clinical trials
MaRIH Research Grant
Gammapathies Monoclonales De Signification Clinique (MGCS) : Atteintes Cutanées
Acquired and inherited aplastic anemia
Diamond-Blackfan anemia
Paroxysmal nocturnal hemoglobinuria
Fanconi anemia
Autoimmune hemolytic anemia
Immune thrombocytopenic purpura
Evans syndrome
Histiocytosis
Maladie d’Erdheim-Chester
Request for expert opinion on genomic RCP
Close
The industry
Presentation of the sector
Missions
Gouvernance
Centres of Reference for Rare Diseases
Find a specialist
Research/diagnostic laboratories
Patient associations
Scientific societies
Others French Healthcare Networks for Rare diseases
Partners
Pathologies
Primary amyloidosis and others immunoglobulin deposition diseases
Gammapathies Monoclonales De Signification Clinique (MGCS) : Atteintes Cutanées
Bradykinin-mediated angioedema
Acquired And Inherited Aplastic Anemia
Acquired and inherited aplastic anemia
Diamond-Blackfan anemia
Paroxysmal nocturnal hemoglobinuria
Fanconi anemia
Autoimmune cytopenias
Autoimmune hemolytic anemia
Immune thrombocytopenic purpura
Evans syndrome
Primary immunodeficiency
Histiocytosis
Histiocytosis
Maladie d’Erdheim-Chester
Castleman disease
Mastocytosis
Thrombotic microangiopathy
Chronic neutropenia
LGL proliferation
Hypereosinophilic syndrome
Care
Expert opinion RCP
Request for expert opinion on genomic RCP
Orphanet Emergency / Disability files
Therapeutic patient education programs
Transition from Pediatric to Adult Service
Find a specialist
Training
MOOC MaRIH
University qualification « Immunohematology and Internal Medicine »
UQ « MAT and other immunological diseases of hemostasis »
Clinical quizzes
MaRIH magazines
Research
Ongoing clinical trials
MaRIH Research Grant
Home
Agenda
RARE 2023: les rencontres des maladies rares
RARE 2023: les rencontres des maladies rares
Ajouter à mon calendrier
