Alain Hovnanian
University of Paris
283 Papers
1.5K Citations
Alain Hovnanian is an academic researcher from University of Paris. The author has contributed to research in topics: Netherton syndrome & Medicine. The author has an hindex of 67, co-authored 256 publications. Previous affiliations of Alain Hovnanian include Paris Diderot University & Necker-Enfants Malades Hospital.
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Papers
No association between HLA-B and cutaneous reactions to sulphonamides in human immunodeficiency virus-infected patients.
Zulma G. Vitezica,Zulma G. Vitezica,Pierre Wolkenstein,C. Lonjou,C. Lonjou,M. Eliaszewicz,X. Sicard,X. Sicard,J.-C. Roujeau,Alain Hovnanian,Alain Hovnanian +10 more
TL;DR: The presence in PC-2 of structurally abnormal, premature teeth and possibly adult teeth suggests that K17-expressing keratinocytes play an important role in odontogenesis and tooth eruption: this is an area for further study.
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Mutational founder effect in recessive dystrophic epidermolysis bullosa families from Southern Tunisia.
Ahlem Sabrine Ben Brick,Nadia Laroussi,Hela Mesrati,Rym Kefi,Mbarka Bchetnia,Khaled Lasram,Nizar Ben Halim,Lilia Romdhane,Houyem Ouragini,Salaheddine Marrakchi,Mohamed Samir Boubaker,Mounira Meddeb Cherif,Daniele Castiglia,Alain Hovnanian,Alain Hovnanian,Sonia Abdelhak,Hamida Turki +16 more
TL;DR: The molecular investigation of 15 patients belonging to 14 nuclear families from the city of Sfax in Southern Tunisia, with clinical features of RDEB-SG complicated by squamous cell carcinoma in 3 patients, identified two novel mutations, p.Val769LeufsX1 and p.Ala2297SerfsX91, which should provide a rapid molecular diagnosis tool for mutation screening in RdeB patients from Southern Tunisia and possibly from other Mediterranean populations sharing the same genetic background.
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Patent
Mutations in spink5 responsible for netherton's syndrome and atopic diseases
Alain Hovnanian,Stephane Chavanas,William O.C.M. Cookson,Miriam F Moffat,Andrew Walley +4 more
- 02 Mar 2001
TL;DR: In this paper, the SPINK5 gene was identified as a susceptibility gene for atopic disease in general and was used as a source of genetic screens, therapeutic products and Nucleic acids and proteins corresponding to mutant versions of the gene.
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Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
Y. Capri,P. Vanlieferinghen,B. Boeuf,P. Dechelotte,Alain Hovnanian,Alain Hovnanian,B. Lecomte +6 more
TL;DR: Le diagnostic moleculaire avait cependant permis de proposer un diagnostic prenatal and une interruption mediale de grossesse des fœtus atteints dans le syndrome de Netherton.
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•Journal Article
Hematopoietic and mesenchymal cell transplantation after myeloablative and non-myeloablative conditioning for recessive dystrophic and junctional epidermolysis bullosa (RDEB, JEB)
Jakub Tolar,John A. McGrath,Douglas R. Keene,Kristen P. Hook,Mark J. Osborn,Megan J. Riddle,S. Kavand,Maria K. Hordinsky,David T. Woodley,Mei Chen,Alain Hovnanian,Katsuto Tamai,Bruce R. Blazar,John E. Wagner +13 more
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