Detalhe da pesquisa
1.
The association of Greig syndrome and mastocytosis reveals the involvement of the hedgehog pathway in advanced mastocytosis.
Blood
; 138(23): 2396-2407, 2021 12 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34424959
2.
The challenging management of a series of 43 infants with Netherton syndrome: unexpected complications and novel mutations.
Br J Dermatol
; 184(3): 532-537, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-32479644
3.
Management of albinism: French guidelines for diagnosis and care.
J Eur Acad Dermatol Venereol
; 35(7): 1449-1459, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-34042219
4.
Development and co-construction of a therapeutic patient education program for albinism.
Ann Dermatol Venereol
; 148(4): 246-250, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34217528
5.
Genotypic and Phenotypic Analysis of 34 Cases of Inherited Junctional Epidermolysis Bullosa caused by COL17A1 Mutations.
Br J Dermatol
; 2020 Sep 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32911566
6.
Multidisciplinary consensus recommendations from a European network for the diagnosis and practical management of patients with incontinentia pigmenti.
J Eur Acad Dermatol Venereol
; 34(7): 1415-1424, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32678511
7.
[Off-label drugs in childhood psoriasis]. / Prescriptions hors AMM (autorisation de mise sur le marché) dans le psoriasis de l'enfant.
Ann Dermatol Venereol
; 147(6-7): 429-438, 2020.
Artigo
em Francês
| MEDLINE | ID: mdl-32299624
8.
Management of congenital ichthyoses: European guidelines of care, part two.
Br J Dermatol
; 180(3): 484-495, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29897631
9.
Dermatological manifestations in cardiofaciocutaneous syndrome: a prospective multicentric study of 45 mutation-positive patients.
Br J Dermatol
; 180(1): 172-180, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30141192
10.
Management of congenital ichthyoses: European guidelines of care, part one.
Br J Dermatol
; 180(2): 272-281, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30216406
11.
Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.
Br J Dermatol
; 180(6): 1438-1448, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30417923
12.
Long-term evolving profile of childhood autoimmune blistering diseases: Retrospective study on 38 children.
J Eur Acad Dermatol Venereol
; 33(6): 1158-1163, 2019 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-30702174
13.
Biological treatments for paediatric psoriasis : a retrospective observational study on biological drug survival in daily practice in childhood psoriasis.
J Eur Acad Dermatol Venereol
; 33(10): 1984-1992, 2019 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-30883928
14.
Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of KIT. A prospective study.
Br J Dermatol
; 179(4): 925-932, 2018 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-29787623
15.
Topical pimecrolimus for paediatric cutaneous mastocytosis.
Clin Exp Dermatol
; 43(5): 559-565, 2018 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-29460435
16.
Hydatidosis: Preparation and evaluation of radiolabeled antigens and antibodies.
Exp Parasitol
; 187: 67-74, 2018 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29499179
17.
Mosaic GJB2 mutation A88V leading to diffuse neonatal hyperkeratosis and porokeratotic hamartoma.
J Eur Acad Dermatol Venereol
; 37(6): e801-e803, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36734293
18.
[Psoriatic arthritis in France, from infants to the elderly: Findings from two cross-sectional, multicenter studies]. / Rhumatisme psoriasique en France, du nourrisson à la personne âgée : données de deux études transversales multicentriques.
Ann Dermatol Venereol
; 145(1): 13-20, 2018 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-29146007
19.
Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype study.
Clin Genet
; 92(5): 477-486, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-28105635
20.
Management of sirolimus treatment for tumours associated with Kasabach-Merritt phenomenon.
J Eur Acad Dermatol Venereol
; 36(7): e586-e588, 2022 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-35285089