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Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis
Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis
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Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosis

Bodemer, C. ; Bourrat, E. ; Mazereeuw-Hautier, J. ; Boralevi, F. ; Barbarot, S. ; Bessis, D. ; Blanchet-Bardon, C. ; Bourdon-Lanoy, E. ; Stalder, J.-F. ; Ribet, V. ; Guerrero, D. ; Sibaud, V.

British journal of dermatology (1951), 2011-11, Vol.165 (5), p.1087-1094 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009
Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009
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Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009

Oji, Vinzenz, MD ; Tadini, Gianluca, MD ; Akiyama, Masashi, MD, PhD ; Blanchet Bardon, Claudine, MD ; Bodemer, Christine, MD, PhD ; Bourrat, Emmanuelle, MD ; Coudiere, Philippe, PharmD ; DiGiovanna, John J., MD ; Elias, Peter, MD ; Fischer, Judith, MD, PhD ; Fleckman, Philip, MD ; Gina, Michal, MD ; Harper, John, MD, FCRCP, FRCPCH ; Hashimoto, Takashi, MD ; Hausser, Ingrid, PhD ; Hennies, Hans Christian, PhD ; Hohl, Daniel, MD, PhD ; Hovnanian, Alain, MD, PhD ; Ishida-Yamamoto, Akemi, MD, PhD ; Jacyk, Witold K., MD ; Leachman, Sancy, MD, PhD ; Leigh, Irene, MD, FRCP, FMedSci ; Mazereeuw-Hautier, Juliette, MD, PhD ; Milstone, Leonard, MD ; Morice-Picard, Fanny, MD ; Paller, Amy S., MS, MD ; Richard, Gabriele, MD, FACMG ; Schmuth, Matthias, MD ; Shimizu, Hiroshi, MD, PhD ; Sprecher, Eli, MD, PhD ; Van Steensel, Maurice, MD, PhD ; Taïeb, Alain, MD ; Toro, Jorge R., MD ; Vabres, Pierre, MD ; Vahlquist, Anders, MD, PhD ; Williams, Mary, MD ; Traupe, Heiko, MD

Journal of the American Academy of Dermatology, 2010-10, Vol.63 (4), p.607-641 [Periódico revisado por pares]

New York, NY: Mosby, Inc

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3
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2
Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2
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Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

Lefèvre, Caroline ; Audebert, Stéphanie ; Jobard, Florence ; Bouadjar, Bakar ; Lakhdar, Hakima ; Boughdene-Stambouli, Omar ; Blanchet-Bardon, Claudine ; Heilig, Roland ; Foglio, Mario ; Weissenbach, Jean ; Lathrop, Mark ; Prud'homme, Jean-François ; Fischer, Judith

Human molecular genetics, 2003-09, Vol.12 (18), p.2369-2378 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity
Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity
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Connexin30 mutations responsible for hidrotic ectodermal dysplasia cause abnormal hemichannel activity

Essenfelder, Guilherme Munhoz ; Bruzzone, Roberto ; Lamartine, Jérôme ; Charollais, Anne ; Blanchet-Bardon, Claudine ; Barbe, Michael T. ; Meda, Paolo ; Waksman, Gilles

Human molecular genetics, 2004-08, Vol.13 (16), p.1703-1714 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Oral liarozole vs. acitretin in the treatment of ichthyosis: a phase II/III multicentre, double-blind, randomized, active-controlled study
Oral liarozole vs. acitretin in the treatment of ichthyosis: a phase II/III multicentre, double-blind, randomized, active-controlled study
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Oral liarozole vs. acitretin in the treatment of ichthyosis: a phase II/III multicentre, double-blind, randomized, active-controlled study

Verfaille, C.J. ; Vanhoutte, F.P. ; Blanchet-Bardon, C. ; Van Steensel, M.A. ; Steijlen, P.M.

British journal of dermatology (1951), 2007-05, Vol.156 (5), p.965-973 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
Mutations in GJB6 cause hidrotic ectodermal dysplasia
Mutations in GJB6 cause hidrotic ectodermal dysplasia
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Mutations in GJB6 cause hidrotic ectodermal dysplasia

Laoudj, Dalila ; Christianson, Arnold L ; Kelsell, David P ; Callouet, Edwige ; Hand, Colette ; Pitaval, Amandine ; Lamartine, Jérôme ; Radhakrishna, Uppala ; Rouleau, Guy A ; Waksman, Gilles ; Antonarakis, Stylianos ; Kibar, Zoha ; Munhoz Essenfelder, Guilherme ; Zonana, Jonathan ; Blanchet-Bardon, Claudine ; Fraser, Clarke ; Lanneluc, Isabelle ; Lemaître, Gilles ; Hayflick, Susan J ; Der Kaloustian, Vazken

Nature genetics, 2000-10, Vol.26 (2), p.142-144 [Periódico revisado por pares]

London: Nature Publishing Group

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7
Ainhum and "African acral keratoderma": three cases
Ainhum and "African acral keratoderma": three cases
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Ainhum and "African acral keratoderma": three cases

Koudoukpo, C ; Bourrat, E ; Rausky, J ; Yédomon, H ; Bagot, M ; Blanchet-Bardon, C ; Petit, A

Annales de dermatologie et de vénéréologie, 2015-03, Vol.142 (3), p.170-175 [Periódico revisado por pares]

France

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8
Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity
Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity
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Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity

Fischer, Judith ; Faure, Alexandra ; Bouadjar, Bakar ; Blanchet-Bardon, Claudine ; Karaduman, Aysen ; Thomas, Isabelle ; Emre, Serap ; Cure, Susan ; Özgüc, Meral ; Weissenbach, Jean ; Prud'homme, Jean-François

American journal of human genetics, 2000-03, Vol.66 (3), p.904-913 [Periódico revisado por pares]

Chicago, IL: Elsevier Inc

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9
Evidence of a marked 25-hydroxyvitamin D deficiency in patients with congenital ichthyosis
Evidence of a marked 25-hydroxyvitamin D deficiency in patients with congenital ichthyosis
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Evidence of a marked 25-hydroxyvitamin D deficiency in patients with congenital ichthyosis

Ingen-Housz-Oro, S ; Boudou, P ; Bergot, C ; Ibrahim, F ; Souberbielle, JC ; Dubertret, L ; Blanchet-Bardon, C

Journal of the European Academy of Dermatology and Venereology, 2006-09, Vol.20 (8), p.947-952 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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10
Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome
Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome
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Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome

Blanchet-Bardon, Claudine ; Bouadjar, Bakar ; Stalder, Jean-François ; Cure, Susan ; Prud'Homme, Jean-François ; Lefèvre, Caroline ; Jobard, Florence ; Hoffmann, Aude ; Fischer, Judith

Journal of investigative dermatology, 2001-12, Vol.117 (6), p.1657-1661 [Periódico revisado por pares]

Danvers, MA: Elsevier Inc

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