Suchergebnisse - "Hadj-Rabia, S"

PubPharm (186)

1

Mosaic GJB2 mutation A88V leading to diffuse neonatal hyperkeratosis and porokeratotic hamartoma

enthalten in: Journal of the European Academy of Dermatology and Venereology : JEADV | 2023

von Letertre, O. | Jullie, M. | Reboul, M. | +6

2

Management of sirolimus treatment for tumours associated with Kasabach-Merritt phenomenon

enthalten in: Journal of the European Academy of Dermatology and Venereology : JEADV | 2022

von Labonnelie, A. | Soupre, V. | Maruani, A. | +3

3

Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation

enthalten in: Journal of the European Academy of Dermatology and Venereology : JEADV | 2022

von Leclerc-Mercier, S. | Mercier, S. | Bellon, N. | +5

4

Skin biopsy is helpful in the diagnosis of hereditary fibrosing POIKiloderma with tendon contractures, myopathy and pulmonary fibrosis, due to FAM111B mutation

enthalten in: Journal of the European Academy of Dermatology and Venereology | 2022

von Leclerc‐Mercier, S. | Mercier, S. | Bellon, N. | +5

5

Development and co-construction of a therapeutic patient education program for albinism

enthalten in: Annales de dermatologie et de venereologie | 2021

von Dufresne, H. | de Longcamp, A. | Compain, S. | +11

6

The association of Greig syndrome and mastocytosis reveals the involvement of the hedgehog pathway in advanced mastocytosis

enthalten in: Blood | 2021

von Polivka, L. | Parietti, V. | Bruneau, J. | +27

7

Management of albinism : French guidelines for diagnosis and care

enthalten in: Journal of the European Academy of Dermatology and Venereology : JEADV | 2021

von Moreno-Artero, E. | Morice-Picard, F. | Bremond-Gignac, D. | +9

8

Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations

enthalten in: The British journal of dermatology | 2021

von Hérissé, A. | Charlesworth, A. | Bellon, N. | +6

9

Immunological and virological profile of children with chilblain-like lesions and SARS-CoV-2

enthalten in: Journal of the European Academy of Dermatology and Venereology : JEADV | 2021

von Fertitta, L. | Welfringer-Morin, A. | Ouedrani, A. | +9

10

The challenging management of a series of 43 infants with Netherton syndrome : unexpected complications and novel mutations

enthalten in: The British journal of dermatology | 2021

von Bellon, N. | Hadj-Rabia, S. | Moulin, F. | +11

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