Hadj-Rabia S - Search Results

1

Evaluation of Children with Psoriasis from the BiPe Cohort: Are Patients Using Biotherapies in Real Life Eligible for Phase III Clinical Studies?

Phan C, Beauchet A, Burztejn AC, Severino-Freire M, Mazereeuw-Hautier J, Barbarot S, Girard C, Lasek A, Reguiai Z, Abasq C, Sassolas B, Droitcourt C, Perrussel M, Hadj-Rabia S, Mallet S, Phan A, Lacour JP, Bourrat E, Aubin F, Mahé E; Groupe de Recherche de la Société Française de Dermatologie Pédiatrique, and the Groupe de Recherche sur le Psoriasis de la Société Française de Dermatologie. Phan C, et al. Paediatr Drugs. 2019 Jun;21(3):169-175. doi: 10.1007/s40272-019-00335-9. Paediatr Drugs. 2019. PMID: 31155692 Clinical Trial.

2

[Hereditary cholestasis, an unusual etiology of pruritus in the infant].

Mahé E, Lacaille F, Hadj-Rabia S, Bodemer C, De Prost Y, Hamel-Teillac D. Mahé E, et al. Ann Dermatol Venereol. 2004 Dec;131(12):1092-4. doi: 10.1016/s0151-9638(04)93847-1. Ann Dermatol Venereol. 2004. PMID: 15692445 French.

3

[Fabry disease. Role of the dermatologist and therapeutic advance].

Mahé E, Hadj-Rabia S, Chauveau D, De Prost Y. Mahé E, et al. Ann Dermatol Venereol. 2005 Feb;132(2):171-6. doi: 10.1016/s0151-9638(05)79234-6. Ann Dermatol Venereol. 2005. PMID: 15798573 Review. French. No abstract available.

4

[What is your diagnosis? Annular hypopigmented skin lesions in a 6-year-old child].

Marrou K, Mahé E, Hadj-Rabia S, Fraitag S, Flageul B, Buffet P, de Prost Y. Marrou K, et al. Arch Pediatr. 2005 Jul;12(7):1145-7. doi: 10.1016/j.arcped.2005.03.056. Arch Pediatr. 2005. PMID: 16021684 French. No abstract available.

5

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.

6

Subcutaneous fat necrosis of the newborn: a systematic evaluation of risk factors, clinical manifestations, complications and outcome of 16 children.

Mahé E, Girszyn N, Hadj-Rabia S, Bodemer C, Hamel-Teillac D, De Prost Y. Mahé E, et al. Br J Dermatol. 2007 Apr;156(4):709-15. doi: 10.1111/j.1365-2133.2007.07782.x. Br J Dermatol. 2007. PMID: 17493069

7

Propranolol for treatment of ulcerated infantile hemangiomas.

Saint-Jean M, Léauté-Labrèze C, Mazereeuw-Hautier J, Bodak N, Hamel-Teillac D, Kupfer-Bessaguet I, Lacour JP, Naouri M, Vabres P, Hadj-Rabia S, Nguyen JM, Stalder JF, Barbarot S; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Saint-Jean M, et al. J Am Acad Dermatol. 2011 May;64(5):827-32. doi: 10.1016/j.jaad.2010.12.040. Epub 2011 Feb 25. J Am Acad Dermatol. 2011. PMID: 21353332

8

Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C.

Hadj-Rabia S, Oriot D, Soufir N, Dufresne H, Bourrat E, Mallet S, Poulhalon N, Ezzedine K, Grandchamp B, Taïeb A, Catteau B, Sarasin A, Bodemer C. Hadj-Rabia S, et al. Br J Dermatol. 2013 May;168(5):1109-13. doi: 10.1111/bjd.12183. Br J Dermatol. 2013. PMID: 23278166

9

Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity.

Hadj-Rabia S, Callewaert BL, Bourrat E, Kempers M, Plomp AS, Layet V, Bartholdi D, Renard M, De Backer J, Malfait F, Vanakker OM, Coucke PJ, De Paepe AM, Bodemer C. Hadj-Rabia S, et al. Orphanet J Rare Dis. 2013 Feb 25;8:36. doi: 10.1186/1750-1172-8-36. Orphanet J Rare Dis. 2013. PMID: 23442826 Free PMC article.

10

Propranolol-resistant infantile haemangiomas.

Caussé S, Aubert H, Saint-Jean M, Puzenat E, Bursztejn AC, Eschard C, Mahé E, Maruani A, Mazereeuw-Hautier J, Dreyfus I, Miquel J, Chiaverini C, Boccara O, Hadj-Rabia S, Stalder JF, Barbarot S; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Caussé S, et al. Br J Dermatol. 2013 Jul;169(1):125-9. doi: 10.1111/bjd.12417. Br J Dermatol. 2013. PMID: 23659587

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