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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 7, 1998
[Treatment of acne]P Delanoë, Y de Prost
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 1, 1994
[Hereditary epidermolysis bullosa: towards classification and genetic counseling based upon identification of molecular defects]A Hovnanian, Y de Prost
Annales De Dermatologie Et De Venereologie|February 1, 1979
[Pathology of the polymorphonuclears in dermatology. Methods of investigation. Clinical pictures (author's transl)]Y de Prost, R Touraine
The British Journal of Dermatology|May 23, 2018
Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of KIT. A prospective studyC Meni, S Georgin-Lavialle, L Le Saché de Peufeilhoux, et al.
The British Journal of Dermatology|September 18, 2008
Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndromeM Halabi-Tawil, F M Ruemmele, S Fraitag, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
La Revue Du Praticien|January 5, 2002
[Management of atopic dermatitis]D Hamel-Teillac, Y de Prost
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 1, 1995
[Treatment of atopic dermatitis]D Teillac-Hamel, Y de Prost
American Journal of Human Genetics|August 27, 1998
Deletions within COL7A1 exons distant from consensus splice sites alter splicing and produce shortened polypeptides in dominant dystrophic epidermolysis bullosaA Sakuntabhai, N Hammami-Hauasli, C Bodemer, et al.
The Journal of Investigative Dermatology|April 1, 1995
DNA-based prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa in six pregnancies at risk for recurrenceA Hovnanian, L Hilal, C Blanchet-Bardon, et al.
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