Zobrazeno 1 - 10
of 49
pro vyhledávání: '"L, Sillard"'
Treatment of keloids with laser-assisted topical steroid delivery: a retrospective study of 23 cases
Autor:
M. Cavalié, Philippe Bahadoran, Thierry Passeron, Jean-Philippe Lacour, Henri Montaudié, L. Sillard
Publikováno v:
Dermatologic Therapy. 28:74-78
Topical or intralesional corticosteroids are referred to as gold standard treatments for keloids. Recent studies showed that ablative fractional laser (AFL) treatment facilitates delivery of topical drug deeply into the skin by creating vertical chan
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 141:279-284
Resume Introduction L’histiocytofibrome (HF) est une tumeur benigne tres frequente survenant le plus souvent sur les membres inferieurs des adultes, essentiellement des femmes. Il existe toutefois des HF atypiques, se comportant comme des tumeurs l
Autor:
Mathilde Cailliez, Philippe Bahadoran, Jean Paul Ortonne, Jean-Philippe Lacour, Christine Chiaverini, Robert Ballotti, Hee Young Kang, Etienne Bérard, Patrick Niaudet, L. Sillard, Geneviève Guest
Publikováno v:
Journal of the American Academy of Dermatology. 68:e111-e116
Background Patients with infantile nephropathic cystinosis have progressive accumulation of cystine in tissues leading to delayed extrarenal complications. No simple tool is available to evaluate the level of body cystine accumulation. Objective We s
Autor:
Ortonne Jp, Philippe Bahadoran, Jean-Philippe Lacour, F. Le Duff, L. Sillard, Thierry Passeron, W. Bayoumi, E. Fontas
Publikováno v:
British Journal of Dermatology. 166:208-211
Summary Background The treatment of vitiligo remains unsatisfactory. Objectives To assess in patients with vitiligo the effect of a laser dermabrasion in addition to the association of topical steroids and ultraviolet (UV) B in difficult-to-treat are
Autor:
Thierry Passeron, Damien Giacchero, F. Le Duff, E. Fontas, Jean-Philippe Lacour, L. Sillard, Ortonne Jp
Publikováno v:
British Journal of Dermatology. 163:188-192
Summary Background The 308-nm excimer laser and 308-nm excimer lamp have both been shown to be effective in treating vitiligo but a direct comparison has never been performed. Objectives To test the equivalence of these two devices for treating nonse
Publikováno v:
Annales de Dermatologie et de Vénéréologie. 137:48-52
Resume Introduction La mucinose papuleuse generalisee est une affection rare, de pathogenie encore obscure et de traitement difficile. Nous en rapportons un cas resistant au traitement par corticoides et controle par des immunoglobulines intraveineus
Autor:
F. Mantoux, Jean-Claude Larrouy, Jean-Philippe Lacour, L. Sillard, Véronique Hofman, Philippe Bahadoran, Thierry Passeron
Publikováno v:
European Journal of Dermatology. 23:121-123
ejd.2012.1907 Auteur(s) : Laura Sillard1, Frederic Mantoux1, Jean-Claude Larrouy1, Veronique Hofman2, Thierry Passeron1, Jean-Philippe Lacour1, Philippe Bahadoran1,3,4 pbahador@unice.fr 1 Dermatology department, Archet Hospital, 151 route Saint Antoi
Autor:
L. Evesque, B. Moreau, L. Sillard, E. Arno, Anne-Laure Couderc, V. Queyrel, Olivier Guérin, A. Gary
Publikováno v:
European Geriatric Medicine. 3:317-319
A.L. Couderc *, L. Evesque , V. Queyrel , L. Sillard , A. Gary , E. Arno , B. Moreau , O. Guerin a Department of Gerontology, Cimiez Hospital, University Hospital (CHU) of Nice, Nice, France Department of Gastro-Enterology, Archet Hospital, CHU of Ni
Publikováno v:
Annales de dermatologie et de venereologie. 141(4)
Histiocytoma (HC) is a very common benign tumour generally seen in the lower limbs of adults, particularly women. There are, however, atypical forms of HC that behave like locally aggressive tumours, occasionally with relapse or even metastasis. Here
Autor:
Pierre Cochat, Christine Chiaverini, E. Fontas, Jean Paul Ortonne, Niaudet P, Michel Foulard, François Xavier Bernard, Kazumasa Wakamatsu, Mauro Picardo, Shosuke Ito, Robert Ballotti, Guest G, Enrica Flori, Mathilde Cailliez, Stefania Briganti, Corinne Antignac, Etienne Bérard, L. Sillard
Publikováno v:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology. 26(9)
Cystinosis is a rare autosomal recessive disease characterized by cystine crystal accumulation leading to multiorgan dysfunctions and caused by mu- tation in CTNS. CTNS encodes cystinosin, a cystine/H symporter that exports cystine out of the lysosom