Detalhe da pesquisa
1.
Dermatoscopic and clinical features of congenital or congenital-type nail matrix nevi: A multicenter prospective cohort study by the International Dermoscopy Society.
J Am Acad Dermatol
; 87(3): 551-558, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35104588
2.
Biologics combined with conventional systemic agents for the treatment of children with severe psoriasis. Real-life data from the BiPe cohorts and a practice survey among French and Italian pediatric dermatologists.
Dermatol Ther
; 35(11): e15828, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36107157
3.
Switching biologics in children with psoriasis: Results from the BiPe cohort.
Pediatr Dermatol
; 39(1): 35-41, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34888920
4.
Cutaneous lipomas and macrocephaly as early signs of PTEN hamartoma tumor syndrome.
Pediatr Dermatol
; 37(5): 839-843, 2020 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-32657433
5.
Biallelic pathogenic variants in the lanosterol synthase gene LSS involved in the cholesterol biosynthesis cause alopecia with intellectual disability, a rare recessive neuroectodermal syndrome.
Genet Med
; 21(9): 2025-2035, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30723320
6.
Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE.
Acta Derm Venereol
; 98(2): 251-255, 2018 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29110021
7.
A prospective study of risk for Sturge-Weber syndrome in children with upper facial port-wine stain.
J Am Acad Dermatol
; 72(3): 473-80, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25592619
8.
Papular and annular fixed urticarial eruption: a characteristic skin manifestation in patients with relapsing polychondritis.
J Am Acad Dermatol
; 65(6): 1161-6, 2011 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-21596456
9.
Balloon cell nevus: histologic and dermoscopic features.
J Am Acad Dermatol
; 72(2): e55-6, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25592363
10.
iPSC reprogramming of fibroblasts from a patient with a Rothmund-Thomson syndrome RTS.
Stem Cell Res
; 45: 101807, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32416578
11.
Cytokine Signature in Schnitzler Syndrome: Proinflammatory Cytokine Production Associated to Th Suppression.
Front Immunol
; 11: 588322, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33324407
12.
A 9-year-old child with methemoglobinemia.
Clin Chem
; 60(8): 1126-7, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-25070976
13.
Polyhexamethylenebiguanide hydrochloride exposure and erythema multiforme in a physician.
Int J Occup Med Environ Health
; 19(1): 81-2, 2006.
Artigo
em Inglês
| MEDLINE | ID: mdl-16881604
14.
Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes.
Eur J Hum Genet
; 20(5): 584-7, 2012 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-22258527
15.
Effectiveness of anti-IL1 in Schnitzler's syndrome.
Joint Bone Spine
; 74(5): 509-10, 2007 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17921021