Biblio

10 resultats trouvés
Filtres: Auteur is Bourrat, Emmanuelle  [Clear All Filters]
A
Melki I, Devilliers H, Gitiaux C, Bondet V, Duffy D, Charuel J-L, Miyara M, Bokov P, Kheniche A, Kwon T et al..  2020.  Anti-MDA5 juvenile idiopathic inflammatory myopathy: a specific subgroup defined by differentially enhanced interferon-alpha signalling. RHEUMATOLOGY. 59:1927-1937.
B
Dreyfus I, Pauwels C, Bourrat E, Bursztejn A-C, Maruani A, Chiaverini C, Maza A, Mallet S, Bessis D, Barbarot S et al..  2015.  Burden of Inherited Ichthyosis: A French National Survey. ACTA DERMATO-VENEREOLOGICA. 95:326-331.
E
Phan C, Beauchet A, Burztejn A-C, Severino-Freire M, Mazereeuw-Hautier J, Barbarot S, Girard C, Lasek A, Reguiai Z, Abasq C et al..  2019.  Evaluation of Children with Psoriasis from the BiPe Cohort: Are Patients Using Biotherapies in Real Life Eligible for Phase III Clinical Studies? PEDIATRIC DRUGS. 21:169-175.
F
Dreyfus I, Bourrat E, Maruani A, Bessis D, Chiaverini C, Vabres P, Ezzedine K, Mazereeuw-Hautier J.  2014.  Factors Associated with Impaired Quality of Life in Adult Patients Suffering from Ichthyosis. ACTA DERMATO-VENEREOLOGICA. 94:344-346.
G
Ballin N, Hotz A, Bourrat E, Kuesel J, Oji V, Bouadjar B, Brognoli D, Hickman G, Heinz L, Vabres P et al..  2019.  Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4. HUMAN MUTATION. 40:2318-2333.
M
Thomas AC, Zeng Z, Riviere J-B, O'Shaughnessy R, Al-Olabi L, St-Onge J, Atherton DJ, Aubert H, Bagazgoitia L, Barbarot S et al..  2016.  Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis. JOURNAL OF INVESTIGATIVE DERMATOLOGY. 136:770-778.
O
Chiaverini C, Roger C, Fontas E, Bourrat E, Bourdon-Lanoy E, Labreze C, Mazereeuw J, Vabres P, Bodemer C, Lacour J-P.  2016.  Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial. ORPHANET JOURNAL OF RARE DISEASES. 11:31.
P
Brun J, Chiaverini C, Devos C, Leclerc-Mercier S, Mazereeuw J, Bourrat E, Maruani A, Mallet S, Abasq C, Phan A et al..  2017.  Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex. ORPHANET JOURNAL OF RARE DISEASES. 12:119.
R
Jordan M, Carmignac V, Sorlin A, Kuentz P, Albuisson J, Borradori L, Bourrat E, Boute O, Bukvic N, Bursztejn A-C et al..  2020.  Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation. JOURNAL OF INVESTIGATIVE DERMATOLOGY. 140:1106+.
T
Bessis D, Bigorre M, Malissen N, Captier G, Chiaverini C, Abasq C, Barbarot S, Boccara O, Bourrat E, Fertit HEl et al..  2017.  The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literature. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY. 76:478-487.