C. Philippe

Transforming growth factor-β stimulates arginase activity in macrophages. Implications for the regulation of macrophage cytotoxicity

V Boutard, R Havouis, Bruno Fouqueray et al. · The Journal of Immunology · 1995 · 185 citations

Rett‐like phenotypes: expanding the genetic heterogeneity to the <i><scp>KCNA2</scp></i> gene and first familial case of <i><scp>CDKL5</scp></i>‐related disease

Lila Allou, Sophie Julia, Daniel Amsallem et al. · Clinical Genetics · 2016 · 49 citations

Rett‐like Phenotypes, Genetics, Pathology +16

Linkage study in a large pedigree with Stickler syndrome: exclusion of COL2A1 as the mutant gene

Jacky Bonaventure, C. Philippe, Ghislaine Plessis et al. · Human Genetics · 1992 · 44 citations

Mutant Gene, Developmental Biology, Mendelian Disorder +9

Autosomal recessive <scp>IFT57</scp> hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia

Julien Thévenon, Laurence Duplomb, Shubha R. Phadke et al. · Clinical Genetics · 2016 · 25 citations · Full text

Developmental Biology, Mendelian Disorder, Short Stature +13

Incontinentia pigmenti (type 1) and X;5 translocation.

Pierre Bitoun, C. Philippe, Meriem Cherif et al. · PubMed · 1992 · 18 citations