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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 16, 2007
[Multifocal infection due to Mycobacterium intracellulare: first case of interferon gamma receptor partial dominant deficiency in tropical French territory]M Muszlak, A Chapgier, R Barry Harivelo, et al.
Human Genetics|January 5, 2007
A gene responsible for Ghosal hemato-diaphyseal dysplasia maps to chromosome 7q33-34B Isidor, N Dagoneau, C Huber, et al.
British Journal of Haematology|July 27, 2005
Transient familial haemophagocytic lymphohistiocytosis reactivation post-CD34 haematopoietic stem cell transplantationH Almousa, M Ouachée-Chardin, C Picard, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 15, 2019
Cutaneous granulomas with primary immunodeficiency in children: a report of 17 new patients and a review of the literatureS Leclerc-Mercier, D Moshous, B Neven, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 27, 2021
Investigation of primary immune deficiency after severe bacterial infection in children: A population-based study in western FranceC Flatrès, J M Roué, C Picard, et al.
The British Journal of Dermatology|November 6, 2009
Place of human amniotic membrane immunoblotting in the diagnosis of autoimmune bullous dermatosesS Grootenboer-Mignot, V Descamps, C Picard-Dahan, et al.
Clinical and Experimental Immunology|December 18, 2014
Value of allohaemagglutinins in the diagnosis of a polysaccharide antibody deficiencyH Schaballie, F Vermeulen, B Verbinnen, et al.
Tissue Antigens|February 9, 2011
Linkage disequilibrium between HLA-G*0104 and HLA-E*0103 alleles in Tswa PygmiesJ Di Cristofaro, D C Julie, S Buhler, et al.
European Journal of Biochemistry|October 6, 1998
Antiproliferative effects of SR31747A in animal cell lines are mediated by inhibition of cholesterol biosynthesis at the sterol isomerase stepC Labit-Le Bouteiller, M F Jamme, M David, et al.
Immunogenetics|May 10, 2000
Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group BW Wiszniewski, M C Fondaneche, N Lambert, et al.
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