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101. Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency

102. Genetic diagnosis of primary immunodeficiencies: A survey of the French national registry

105. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations

109. Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

110. Outcome after failure of allogeneic hematopoietic stem cell transplantation in children with acute leukemia: a study by the société Francophone de greffe de moelle et de thérapie cellulaire (SFGM-TC)

111. A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations

115. Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases

116. Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome

117. Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability

120. Kinesin-1 controls mast cell degranulation and anaphylaxis through PI3K-dependent recruitment to the granular Slp3/Rab27b complex

123. Polymerase ε1 mutation in a human syndrome with facial dysmorphism, immunodeficiency, livedo, and short stature ('FILS syndrome')

124. X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene

126. Alemtuzumab as First Line Treatment in Children with Familial Lymphohistiocytosis

127. Rab27a

129. Germline TIM-3 Mutations Characterize Sub-Cutaneous Panniculitis T-Cell Lymphomas with Hemophagocytic Lymphohistiocytic Syndrome

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