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Page 1
Search for ReCQL4 mutations in 39 patients genotyped for suspected Rothmund-Thomson/Baller-Gerold syndromes.
Piard J, Aral B, Vabres P, Holder-Espinasse M, Mégarbané A, Gauthier S, Capra V, Pierquin G, Callier P, Baumann C, Pasquier L, Baujat G, Martorell L, Rodriguez A, Brady AF, Boralevi F, González-Enseñat MA, Rio M, Bodemer C, Philip N, Cordier MP, Goldenberg A, Demeer B, Wright M, Blair E, Puzenat E, Parent P, Sznajer Y, Francannet C, DiDonato N, Boute O, Barlogis V, Moldovan O, Bessis D, Coubes C, Tardieu M, Cormier-Daire V, Sousa AB, Franques J, Toutain A, Tajir M, Elalaoui SC, Geneviève D, Thevenon J, Courcet JB, Rivière JB, Collet C, Gigot N, Faivre L, Thauvin-Robinet C. Piard J, et al. Among authors: boralevi f. Clin Genet. 2015 Mar;87(3):244-51. doi: 10.1111/cge.12361. Epub 2014 Mar 26. Clin Genet. 2015. PMID: 24635570
The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literature.
Bessis D, Bigorre M, Malissen N, Captier G, Chiaverini C, Abasq C, Barbarot S, Boccara O, Bourrat E, El Fertit H, Eschard C, Hubiche T, Lacour JP, Leboucq N, Mahé E, Mallet S, Marque M, Martin L, Mazereeuw-Hautier J, Milla N, Phan A, Plantin P, Picot MC, Puzenat E, Rigau V, Vabres P, Fraitag S, Boralevi F; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Bessis D, et al. Among authors: boralevi f. J Am Acad Dermatol. 2017 Mar;76(3):478-487. doi: 10.1016/j.jaad.2016.08.046. Epub 2016 Oct 11. J Am Acad Dermatol. 2017. PMID: 27742172 Review.
Nail Psoriasis: A Systematic Evaluation in 313 Children with Psoriasis.
Pourchot D, Bodemer C, Phan A, Bursztejn AC, Hadj-Rabia S, Boralevi F, Miquel J, Hubiche T, Puzenat E, Souillet AL, Kupfer I, Piram M, Beauchet A, Mahé E; Groupe de Recherche de la Société Française de Dermatologie Pédiatrique. Pourchot D, et al. Among authors: boralevi f. Pediatr Dermatol. 2017 Jan;34(1):58-63. doi: 10.1111/pde.13028. Epub 2016 Nov 22. Pediatr Dermatol. 2017. PMID: 27873356
Hereditary Mucoepithelial Dysplasia Results from Heterozygous Variants at p.Arg557 Mutational Hotspot in SREBF1, Encoding a Transcription Factor Involved in Cholesterol Homeostasis.
Morice-Picard F, Michaud V, Lasseaux E, Rezvani HR, Plaisant C, Bessis D, Leauté-Labrèze C, Arveiler B, Taieb A, Trimouille A, Boralevi F. Morice-Picard F, et al. Among authors: boralevi f. J Invest Dermatol. 2020 Jun;140(6):1289-1292.e2. doi: 10.1016/j.jid.2019.10.014. Epub 2019 Nov 29. J Invest Dermatol. 2020. PMID: 31790666 Free article. No abstract available.
LEKTI proteolytic processing in human primary keratinocytes, tissue distribution and defective expression in Netherton syndrome.
Bitoun E, Micheloni A, Lamant L, Bonnart C, Tartaglia-Polcini A, Cobbold C, Al Saati T, Mariotti F, Mazereeuw-Hautier J, Boralevi F, Hohl D, Harper J, Bodemer C, D'Alessio M, Hovnanian A. Bitoun E, et al. Among authors: boralevi f. Hum Mol Genet. 2003 Oct 1;12(19):2417-30. doi: 10.1093/hmg/ddg247. Epub 2003 Jul 29. Hum Mol Genet. 2003. PMID: 12915442
Clinical phenotype of scabies by age.
Boralevi F, Diallo A, Miquel J, Guerin-Moreau M, Bessis D, Chiavérini C, Plantin P, Hubiche T, Maruani A, Lassalle M, Boursault L, Ezzedine K; Groupe de Recherche Clinique en Dermatologie Pédiatrique. Boralevi F, et al. Pediatrics. 2014 Apr;133(4):e910-6. doi: 10.1542/peds.2013-2880. Epub 2014 Mar 31. Pediatrics. 2014. PMID: 24685953
Clinical and Therapeutic Aspects of Linear Psoriasis: A Study of 30 Cases.
Say M, Boralévi F, Lenormand C, Bursztejn AC, Estève E, Phan A, Bourrat E, Lacour JP, Richard MA, Acher A, Jullien D, Beneton N, Descamps V, Bodemer C, Lagaude M, Chiaverini C, Mahé E; Groupe de Recherche sur le Psoriasis de la Société Française de Dermatologie, and the Groupe de Recherche de la Société Française de Dermatologie Pédiatrique. Say M, et al. Among authors: boralevi f. Am J Clin Dermatol. 2018 Aug;19(4):609-615. doi: 10.1007/s40257-018-0354-9. Am J Clin Dermatol. 2018. PMID: 29594973
164 results