Detalhe da pesquisa
1.
Pathophysiology and management of sensitive skin: position paper from the special interest group on sensitive skin of the International Forum for the Study of Itch (IFSI).
J Eur Acad Dermatol Venereol
; 34(2): 222-229, 2020 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-31660659
2.
The impact of atopic dermatitis on sexual health.
J Eur Acad Dermatol Venereol
; 33(2): 428-432, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30160809
3.
Sensitive skin can be small fibre neuropathy: results from a case-control quantitative sensory testing study.
Br J Dermatol
; 179(5): 1157-1162, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30113701
4.
Development and validation of a new tool to assess the Burden of Sensitive Skin (BoSS).
J Eur Acad Dermatol Venereol
; 32(12): 2217-2223, 2018 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-30022546
5.
Sensitive skin in France: a study on prevalence, relationship with age and skin type and impact on quality of life.
J Eur Acad Dermatol Venereol
; 32(5): 791-795, 2018 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-29397030
6.
Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis.
Clin Genet
; 91(2): 333-338, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27103078
7.
Evaluation of the effects on cutaneous sensitivity of a face emulsion containing sclareolide in women presenting with sensitive skin through quantitative sensory testing.
J Eur Acad Dermatol Venereol
; 36(1): e74-e75, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34487370
8.
Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic test.
Clin Genet
; 89(6): 700-7, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-26757139
9.
Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management.
Clin Genet
; 89(4): 501-506, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26497935
10.
Clinical spectrum of eye malformations in four patients with Mowat-Wilson syndrome.
Am J Med Genet A
; 167(7): 1587-92, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25899569
11.
[New treatments and therapeutic perspectives in atopic dermatitis]. / Nouveaux traitements et perspectives thérapeutiques dans la dermatite atopique.
Ann Dermatol Venereol
; 147(6-7): 466-474, 2020.
Artigo
em Francês
| MEDLINE | ID: mdl-32303389
12.
Real-life study of anti-itching effects of a cream containing menthoxypropanediol, a TRPM8 agonist, in atopic dermatitis patients.
J Eur Acad Dermatol Venereol
; 33(2): e67-e69, 2019 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-30067875
13.
Unexpected diagnosis of a SHH nonsense variant causing a variable phenotype ranging from familial coloboma and Intellectual disability to isolated microcephaly.
Clin Genet
; 94(1): 182-184, 2018 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29498412
14.
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.
Nat Genet
; 28(4): 365-70, 2001 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-11479539
15.
Take a Swipe at Actinide Bioavailability: Application of a New In Vitro Method.
Health Phys
; 124(6): 495-507, 2023 06 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37022177
16.
Homozygous SMN1 exons 1-6 deletion: pitfalls in genetic counseling and general recommendations for spinal muscular atrophy molecular diagnosis.
Am J Med Genet A
; 158A(7): 1735-41, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22678974
17.
What do French patients and geneticists think about prenatal and preimplantation diagnoses in Marfan syndrome?
Prenat Diagn
; 32(13): 1318-23, 2012 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-23147988
18.
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France.
Arch Pediatr
; 29(4): 253-257, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35351343
19.
Image Gallery: Erythroderma revealing a nonbullous bullous pemphigoid.
Br J Dermatol
; 175(5): e136-e137, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27790691
20.
Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type I.
Clin Genet
; 77(3): 258-65, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19817772