Hadj-Rabia S - Search Results

1

A toxic palmitoylation of Cdc42 enhances NF-κB signaling and drives a severe autoinflammatory syndrome.

Bekhouche B, Tourville A, Ravichandran Y, Tacine R, Abrami L, Dussiot M, Khau-Dancasius A, Boccara O, Khirat M, Mangeney M, Dingli F, Loew D, Boëda B, Jordan P, Molina TJ, Bellon N, Fraitag S, Hadj-Rabia S, Blanche S, Puel A, Etienne-Manneville S, van der Goot FG, Cherfils J, Hermine O, Casanova JL, Bodemer C, Smahi A, Delon J. Bekhouche B, et al. J Allergy Clin Immunol. 2020 Nov;146(5):1201-1204.e8. doi: 10.1016/j.jaci.2020.03.020. Epub 2020 Apr 10. J Allergy Clin Immunol. 2020. PMID: 32283203 No abstract available.

2

[Prenatal diagnosis in dermatology].

Hadj-Rabia S, Bodemer C, De Prost Y, Lyonnet S. Hadj-Rabia S, et al. Ann Dermatol Venereol. 1999 Dec;126(12):981-91. Ann Dermatol Venereol. 1999. PMID: 10648978 Review. French. No abstract available.

3

[Anhidrotic ectodermal dysplasia and Incontinentia pigmenti: pieces of the same puzzle].

Hadj-Rabia S, Smahi A, Bodemer C. Hadj-Rabia S, et al. Ann Dermatol Venereol. 2002 Mar;129(3):277-80. Ann Dermatol Venereol. 2002. PMID: 11988680 Free article. French. No abstract available.

4

Osteopetrosis, lymphedema, anhidrotic ectodermal dysplasia, and immunodeficiency in a boy and incontinentia pigmenti in his mother.

Dupuis-Girod S, Corradini N, Hadj-Rabia S, Fournet JC, Faivre L, Le Deist F, Durand P, Döffinger R, Smahi A, Israel A, Courtois G, Brousse N, Blanche S, Munnich A, Fischer A, Casanova JL, Bodemer C. Dupuis-Girod S, et al. Pediatrics. 2002 Jun;109(6):e97. doi: 10.1542/peds.109.6.e97. Pediatrics. 2002. PMID: 12042591

5

Late recurrence of inflammatory first-stage lesions in incontinentia pigmenti: an unusual phenomenon and a fascinating pathologic mechanism.

Bodak N, Hadj-Rabia S, Hamel-Teillac D, de Prost Y, Bodemer C. Bodak N, et al. Arch Dermatol. 2003 Feb;139(2):201-4. doi: 10.1001/archderm.139.2.201. Arch Dermatol. 2003. PMID: 12588226

6

Clinical study of 40 cases of incontinentia pigmenti.

Hadj-Rabia S, Froidevaux D, Bodak N, Hamel-Teillac D, Smahi A, Touil Y, Fraitag S, de Prost Y, Bodemer C. Hadj-Rabia S, et al. Arch Dermatol. 2003 Sep;139(9):1163-70. doi: 10.1001/archderm.139.9.1163. Arch Dermatol. 2003. PMID: 12975158

7

Skin markers of occult spinal dysraphism in children: a review of 54 cases.

Guggisberg D, Hadj-Rabia S, Viney C, Bodemer C, Brunelle F, Zerah M, Pierre-Kahn A, de Prost Y, Hamel-Teillac D. Guggisberg D, et al. Arch Dermatol. 2004 Sep;140(9):1109-15. doi: 10.1001/archderm.140.9.1109. Arch Dermatol. 2004. PMID: 15381552 Review.

8

Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: a tight junction disease.

Hadj-Rabia S, Baala L, Vabres P, Hamel-Teillac D, Jacquemin E, Fabre M, Lyonnet S, De Prost Y, Munnich A, Hadchouel M, Smahi A. Hadj-Rabia S, et al. Gastroenterology. 2004 Nov;127(5):1386-90. doi: 10.1053/j.gastro.2004.07.022. Gastroenterology. 2004. PMID: 15521008

9

Three severe cases of EBS Dowling-Meara caused by missense and frameshift mutations in the keratin 14 gene.

Titeux M, Mazereeuw-Hautier J, Hadj-Rabia S, Prost C, Tonasso L, Fraitag S, de Prost Y, Hovnanian A, Bodemer C. Titeux M, et al. J Invest Dermatol. 2006 Apr;126(4):773-6. doi: 10.1038/sj.jid.5700154. J Invest Dermatol. 2006. PMID: 16439965 Free article.

10

Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus.

Bal E, Baala L, Cluzeau C, El Kerch F, Ouldim K, Hadj-Rabia S, Bodemer C, Munnich A, Courtois G, Sefiani A, Smahi A. Bal E, et al. Hum Mutat. 2007 Jul;28(7):703-9. doi: 10.1002/humu.20500. Hum Mutat. 2007. PMID: 17354266

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