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Publications by Alain Fischer
Gene Therapy of Primary T Cell Immunodeficiencies
Gene
Medicine
Genetics
Hematologically Important Mutations: Leukocyte Adhesion Deficiency (First Update)
Blood Cells, Molecules, and Diseases
Molecular Medicine
Hematology
Molecular Biology
Cell Biology
Infections Fongiques Et Granulomatose Septique Chronique
Medecine/Sciences
Biochemistry
Medicine
Genetics
Molecular Biology
Human Adenylate Kinase 2 Deficiency Causes a Profound Hematopoietic Defect Associated With Sensorineural Deafness
Nature Genetics
Genetics
A Human Severe Combined Immunodeficiency (SCID) Condition With Increased Sensitivity to Ionizing Radiations and Impaired V(D)J Rearrangements Defines a New DNA Recombination/Repair Deficiency
Journal of Experimental Medicine
Medicine
Allergy
Immunology
AIRE Deficiency in Thymus of 2 Patients With Omenn Syndrome
Journal of Clinical Investigation
Medicine
Partial T and B Lymphocyte Immunodeficiency and Predisposition to Lymphoma in Patients With Hypomorphic Mutations in Artemis
Journal of Clinical Investigation
Medicine
Munc18-2 Deficiency Causes Familial Hemophagocytic Lymphohistiocytosis Type 5 and Impairs Cytotoxic Granule Exocytosis in Patient NK Cells
Journal of Clinical Investigation
Medicine
A Hypermorphic IκBα Mutation Is Associated With Autosomal Dominant Anhidrotic Ectodermal Dysplasia and T Cell Immunodeficiency
Journal of Clinical Investigation
Medicine
Primary Immunodeficiencies: 2009 Update
Journal of Allergy and Clinical Immunology
Allergy
Immunology
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