F. Morice-Picard: search on Z-Library

51

High dose pulsed corticosteroid therapy combined with Methotrexate for Severe Alopecia Areata of Childhood

Chong, J H, Taïeb, A, Morice-Picard, F, Dutkiewicz, A S, Léauté-Labrèze, C, Boralevi, F

Journal:

Journal of the European Academy of Dermatology and Venereology

Year:

2017

Language:

english

File:

PDF, 231 KB

english, 2017

52

ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient

Petre, J, Lasseaux, E, Ged, C, Arveiler, B, Taïeb, A, Morice-Picard, F

Journal:

Journal of the European Academy of Dermatology and Venereology

Year:

2017

Language:

english

File:

PDF, 254 KB

english, 2017

53

617 Cole disease: Role of ENPP1 in regulation of pigmentation and epidermal differentiation

Nesmond, S., Bochner, R., Sarig, O., Pain, C., Bergeron, V., rambert, J., Morice-Picard, F., Sprecher, E., Taieb, A., Cario-Andre, M.

Journal:

The Journal of Investigative Dermatology

Year:

2017

Language:

english

File:

PDF, 246 KB

english, 2017

54

Focal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patients

Lee, Beom Hee, Morice-Picard, Fanny, Boralevi, Franck, Chen, Brenden, Desnick, Robert J.

Journal:

Journal of Human Genetics

Year:

2017

Language:

english

File:

PDF, 686 KB

english, 2017

55

The Burden Of Albinism: Creation Of A Questionnaire

Ezzedine, K, Morice-Picard, F, Gliksohn, A, Bodemer, C, Taieb, C

Journal:

Value in Health

Year:

2017

Language:

english

File:

PDF, 58 KB

english, 2017

56

Mosaic NRASopathy n a child with giant melanocytic congenital naevus, epidermal hamartoma and bilateral nephroblastomatosis: clinical implication for follow-up

Maridet, C, Morice-Picard, F, Gros, A, Crivelli, L, de la Fouchardière, A, Vergier, B, Taïeb, A

Journal:

Journal of the European Academy of Dermatology and Venereology

Year:

2018

Language:

english

File:

PDF, 390 KB

english, 2018

57

Effects of the Staphylococcus aureus and Staphylococcus epidermidis Secretomes Isolated from the Skin Microbiota of Atopic Children on CD4+ T Cell Activation

Laborel-Préneron, Emeline, Bianchi, Pascale, Boralevi, Franck, Lehours, Philippe, Fraysse, Frédérique, Morice-Picard, Fanny, Sugai, Motoyuki, Sato'o, Yusuke, Badiou, Cédric, Lina, Gérard, Schmitt, Ann

Journal:

PLoS ONE

Year:

2015

Language:

english

File:

PDF, 1.67 MB

english, 2015

58

Epidermolysis bullosa simplex generalized severe induces a Th17 response and is improved by Apremilast treatment

Castela, E., Tulic, M. K., Rozières, A., Bourrat, E., Nicolas, J.-F., Kanitakis, J., Vabres, P., Bessis, D., Mazereeuw, J., Morice-Picard, F., Baty, D., Berard, F., Lacour, J.-P., Passeron, T., Chiave

Journal:

British Journal of Dermatology

Year:

2018

Language:

english

File:

PDF, 790 KB

english, 2018

59

Pigmentation Abnormalities in Nucleotide Excision Repair Disorders: Evidence and Hypotheses

Kasraian, Zeinab, Trompezinski, Sandra, Cario-André, Muriel, Morice-Picard, Fanny, Ged, Cécile, Jullie, Marie-Laure, Taieb, Alain, Rezvani, Hamid Reza

Journal:

Pigment Cell & Melanoma Research

Year:

2018

Language:

english

File:

PDF, 674 KB

english, 2018

60

Mosaic mutations in FGFR3 and FGFR2 are associated with naevoid acanthosis nigricans or RAVEN (round and velvety epidermal naevus)

Larsabal, M., Cogrel, O., Caumont, C., Jegou, M-H, Taïeb, A, Morice-Picard, F.

Journal:

British Journal of Dermatology

Year:

2018

Language:

english

File:

PDF, 819 KB

english, 2018

61

Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis

Hotz, A, Oji, V, Bourrat, E, Jonca, N, Mazereeuw-Hautier, J, Betz, R, Blume-Peytavi, U, Stieler, K, Morice-Picard, F, Schönbuchner, I, Markus, S, Schlipf, N, Fischer, J

Journal:

Acta Dermato Venereologica

Year:

2016

Language:

english

File:

PDF, 2.79 MB

english, 2016

62

Dermatological manifestations in cardiofaciocutaneous syndrome: A prospective multicentric study of 45 mutation-positive patients

Bessis, D., Morice-Picard, F., Bourrat, E., Abadie, C., Aouinti, S., Baumann, C., Best, M., Bursztejn, A.-C., Capri, Y., Chiaverini, C., Coubes, C., Giuliano, F., Hadj-Rabia, S., Jacquemont, M.-L., La

Journal:

British Journal of Dermatology

Year:

2018

Language:

english

File:

PDF, 816 KB

english, 2018

63

Erratum

Hotz, A, Oji, V, Bourrat, E, Jonca, N, Mazereeuw-Hautier, J, Betz, R, Blume-Peytavi, U, Stieler, K, Morice-Picard, F, Schönbuchner, I, Markus, S, Schlipf, N, Fischer, J

Journal:

Acta Dermato Venereologica

Year:

2016

File:

PDF, 86 KB

2016

64

Dermatological manifestations in Noonan syndrome: A prospective multicentric study of 129 mutation-positive patients

Bessis, D., Miquel, J., Bourrat, E., Chiaverini, C., Morice-Picard, F., Abadie, C., Manna, F., Baumann, C., Best, M., Blanchet, P., Bursztejn, A.-C., Capri, Y., Coubes, C., Giuliano, F., Guillaumont,

Journal:

British Journal of Dermatology

Year:

2018

Language:

english

File:

PDF, 1.40 MB

english, 2018

65

Dermatological manifestations in cardiofaciocutaneous syndrome

Bessis, D., Morice-Picard, F., Bourrat, E., Abadie, C., Aouinti, S., Baumann, C., Best, M., Bursztejn, A.-C., Capri, Y., Chiaverini, C., Coubes, C., Giuliano, F., Hadj-Rabia, S., Jacquemont, M.-L., La

Journal:

British Journal of Dermatology

Year:

2019

File:

PDF, 76 KB

2019

66

Acanthosis nigricans nævoïde associé aux mutations FGFR3 et FGFR2

Larsabal, M., Cogrel, O., Caumont, C., Jegou, M.-H., Taïeb, A., Morice-picard, F.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

Language:

french

File:

PDF, 298 KB

french, 2018

67

Dermatological manifestations in cardiofaciocutaneous syndrome

Bessis, D., Morice-Picard, F., Bourrat, E., Abadie, C., Aouinti, S., Baumann, C., Best, M., Bursztejn, A.-C., Capri, Y., Chiaverini, C., Coubes, C., Giuliano, F., Hadj-Rabia, S., Jacquemont, M.-L., La

Journal:

British Journal of Dermatology

Year:

2019

Language:

english

File:

PDF, 76 KB

english, 2019

68

Isolated straight hair nevus in a White child

Rault, Lucie, Morice-Picard, Fanny, Svahn, Isabelle, Gontier, Etienne, Eyraud, Alexia, Taïeb, Alain

Journal:

Pediatric Dermatology

Year:

2019

File:

PDF, 471 KB

2019

69

Isolated straight hair nevus in a White child

Rault, Lucie, Morice-Picard, Fanny, Svahn, Isabelle, Gontier, Etienne, Eyraud, Alexia, Taïeb, Alain

Journal:

Pediatric Dermatology

Year:

2019

Language:

english

File:

PDF, 471 KB

english, 2019

70

297 Identification of mutations in SDR9C7 in three patients with autosomal recessive congenital ichthyosis

Mazereeuw-Hautier, J., Severino-Freire, M., Texier, H., Vincent, M., Aubert, H., Morice-Picard, F., Jonca, N.

Journal:

The Journal of Investigative Dermatology

Year:

2019

Language:

english

File:

PDF, 196 KB

english, 2019

71

Identification et caractérisation de deux nouvelles mutations du gène SPINK5 associées à une forme atténuée du syndrome de Netherton

Casassa, E.A., Morice-Picard, F., Pichery, M., Zaafouri, S., Reynier, M., Boralevi, F., Mazereeuw-Hautier, J., Jonca, N.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

Language:

french

File:

PDF, 241 KB

french, 2018

72

Syndrome KID : une génodermatose menaçant le pronostic vital

Godillot, C.-M., Michaud, V., Boralevi, F., Labreze, C., Guigonis, V., Severino-Freire, M., Onnis, G., Morice-Picard, F., Mazereeuw-Hautier, J.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

Language:

french

File:

PDF, 166 KB

french, 2018

73

Génétique en dermatologie

Morice-Picard, F.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2019

File:

PDF, 1.80 MB

2019

74

Hereditary mucoepithelial dysplasia results from heterozygous variants at p.Arg557 mutational hotspot in SREBF1, encoding a transcription factor involved in cholesterol homeostasis

Morice-Picard, Fanny, Michaud, Vincent, Lasseaux, Eulalie, Rezvani, Hamid Reza, Plaisant, Claudio, Bessis, Didier, Leauté-Labrèze, Christine, Arveiler, Benoit, Taieb, Alain, Trimouille, Aurélien, Bora

Journal:

The Journal of Investigative Dermatology

Year:

2019

File:

PDF, 11.89 MB

2019

75

Identification et caractérisation de deux nouvelles mutations du gène SPINK5 associées à une forme atténuée du syndrome de Netherton

Casassa, E.A., Morice-Picard, F., Pichery, M., Zaafouri, S., Reynier, M., Boralevi, F., Mazereeuw-Hautier, J., Jonca, N.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

File:

PDF, 241 KB

2018

76

Syndrome KID : une génodermatose menaçant le pronostic vital

Godillot, C.-M., Michaud, V., Boralevi, F., Labreze, C., Guigonis, V., Severino-Freire, M., Onnis, G., Morice-Picard, F., Mazereeuw-Hautier, J.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

File:

PDF, 166 KB

2018

77

Génétique en dermatologie

Morice-Picard, F.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2019

File:

PDF, 1.80 MB

2019

78

Hétérozygotie composite de KRT85 associée à une forme récessive d’hypotrichose

Amico, S., Morice-Picard, F., Taieb, A.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

File:

PDF, 292 KB

2018

79

Incontinentia pigmenti chez le garçon et mosaïcisme cutané

Chambelland, A., Chiaverini, C., Aubert, H., Bourrat, E., Morice-Picard, F., Puzenat, E., Lacour, J.-P.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2018

File:

PDF, 165 KB

2018

80

Ichtyose congénitale autosomique récessive associées à des mutations du gène SDR9C7

Mazereeuw-Hautier, J., Severino Freire, M., Texier, H., Vincent, M., Aubert, H., Morice-Picard, F., Jonca, N.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2019

File:

PDF, 321 KB

2019

81

Enseignements de l’essai TOTEM évaluant le tasélisib, inhibiteur de la PI3 K, dans les syndromes hypertrophiques liés à PIK3CA

Luu, M., Vabres, P., Devilliers, H., Loffroy, R., Carpentier, M., Maurer, A., Yousfi, M., Fleck, C., Phan, A., Martin, L., Morice-Picard, F., Petit, F., Willems, M., Bessis, D., Jacquemont, M.-L., Mar

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2019

File:

PDF, 120 KB

2019

82

Improvement of epidermal covering on AEC patients with severe skin erosions by PRIMA-1MET/APR-246

Aberdam, Edith, Roux, Lauriane N., Secrétan, Philippe-Henri, Boralevi, Franck, Schlatter, Joël, Morice-Picard, Fanny, Sol, Stefano, Bodemer, Christine, Missero, Caterina, Cisternino, Salvatore, Aberda

Journal:

Cell Death and Disease

Year:

2020

Language:

english

File:

PDF, 3.43 MB

english, 2020

83

Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA

Angelini, ChloÃ©, Thibaud, Marie, Aladjidi, Nathalie, Bessou, Pierre, Cabasson, SÃ©bastien, Colson, Cindy, Espil-Taris, Caroline, Goizet, Cyril, Husson, Marie, Morice-Picard, Fanny, De Sandre-Giovanno

Journal:

Neuropediatrics

Year:

2020

File:

PDF, 2.15 MB

2020

84

A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies

Michaud, Vincent, Fiore, Mathieu, Coste, Valentine, Huguenin, Yoann, Bordet, Jean-Claude, Plaisant, Claudio, Lasseaux, Eulalie, Morice-Picard, Fanny, Arveiler, Benoit

Journal:

Platelets

Year:

2020

Language:

english

File:

PDF, 1.56 MB

english, 2020

85

Morice-Picard, F., Labreze, C., Michaud, V., Bessis, D., Lasseaux, E., Taieb, A., Trimouille, A., Boralevi, F.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2020

File:

PDF, 34 KB

2020

86

Dufresne, H., Compain, S., de Longcamp, A., Morice-Picard, F., DeladriÃ¨re, E., Bekel, L., Godot, C., Rateaux, M., Godeau, M., Jouanne, B., Bodemer, C., Bremond-Gignac, D., Robert, M., Hadj-Rabia, S.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2020

File:

PDF, 39 KB

2020

87

Syndrome de Wells et cutis laxa acquiseÂ : une association atypique

Bouquerel, M.M., Dequidt, L., Jullie, M.-L., Gibier, J.-B., Lefevre, G., Dezoteux, F., Morice-Picard, F., Trimouille, A., Doutre, M.-S.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2020

File:

PDF, 1.38 MB

2020

88

Aberdam, E., Roux, L.N., Secretan, P.-H., Boralevi, F., Schlatter, J., Morice-Picard, F., Sol, S., Bodemer, C., Missero, C., Cisternino, S., Aberdam, D., Hadj-Rabia, S.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2020

File:

PDF, 175 KB

2020

89

RÃ©cidive conjonctivale dâun syringocystadÃ©nocarcinome papillifÃ¨re sur syndrome de Schimmelpenning associÃ© aux mutations post-zygotiques HRAS et BRAF

Dupont, A., Pacaud, A., Saunier, V., Caumont, C., Jullie, M.-L., TaÃ¯eb, A., Morice-Picard, F., Dousset, L.

Journal:

Annales de Dermatologie et de Vénéréologie

Year:

2020

File:

PDF, 288 KB

2020

90

Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage

Fayyad, Nour, Kobaisi, Farah, Beal, David, Mahfouf, Walid, Ged, CÃ©cile, Morice-Picard, Fanny, Fayyad-Kazan, Mohammad, Fayyad-Kazan, Hussein, Badran, Bassam, Rezvani, Hamid R., Rachidi, Walid

Journal:

Frontiers in Genetics

Year:

2020

File:

PDF, 1.36 MB

2020

High dose pulsed corticosteroid therapy combined with Methotrexate for Severe Alopecia Areata of Childhood

ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient

617 Cole disease: Role of ENPP1 in regulation of pigmentation and epidermal differentiation

Focal facial dermal dysplasia type 4: identification of novel CYP26C1 mutations in unrelated patients

The Burden Of Albinism: Creation Of A Questionnaire

Mosaic NRASopathy n a child with giant melanocytic congenital naevus, epidermal hamartoma and bilateral nephroblastomatosis: clinical implication for follow-up

Effects of the Staphylococcus aureus and Staphylococcus epidermidis Secretomes Isolated from the Skin Microbiota of Atopic Children on CD4+ T Cell Activation

Epidermolysis bullosa simplex generalized severe induces a Th17 response and is improved by Apremilast treatment

Pigmentation Abnormalities in Nucleotide Excision Repair Disorders: Evidence and Hypotheses

Mosaic mutations in FGFR3 and FGFR2 are associated with naevoid acanthosis nigricans or RAVEN (round and velvety epidermal naevus)

Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis

Dermatological manifestations in cardiofaciocutaneous syndrome: A prospective multicentric study of 45 mutation-positive patients

Erratum

Dermatological manifestations in Noonan syndrome: A prospective multicentric study of 129 mutation-positive patients

Dermatological manifestations in cardiofaciocutaneous syndrome

Acanthosis nigricans nævoïde associé aux mutations FGFR3 et FGFR2

Dermatological manifestations in cardiofaciocutaneous syndrome

Isolated straight hair nevus in a White child

Isolated straight hair nevus in a White child

297 Identification of mutations in SDR9C7 in three patients with autosomal recessive congenital ichthyosis

Identification et caractérisation de deux nouvelles mutations du gène SPINK5 associées à une forme atténuée du syndrome de Netherton

Syndrome KID : une génodermatose menaçant le pronostic vital

Génétique en dermatologie

Hereditary mucoepithelial dysplasia results from heterozygous variants at p.Arg557 mutational hotspot in SREBF1, encoding a transcription factor involved in cholesterol homeostasis

Identification et caractérisation de deux nouvelles mutations du gène SPINK5 associées à une forme atténuée du syndrome de Netherton

Syndrome KID : une génodermatose menaçant le pronostic vital

Génétique en dermatologie

Hétérozygotie composite de KRT85 associée à une forme récessive d’hypotrichose

Incontinentia pigmenti chez le garçon et mosaïcisme cutané

Ichtyose congénitale autosomique récessive associées à des mutations du gène SDR9C7

Enseignements de l’essai TOTEM évaluant le tasélisib, inhibiteur de la PI3 K, dans les syndromes hypertrophiques liés à PIK3CA

Improvement of epidermal covering on AEC patients with severe skin erosions by PRIMA-1MET/APR-246

Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA

A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies

Des variants hot-spot hÃ©tÃ©rozygotes de SREBF1Â responsables de la dysplasie mucoÃ©pithÃ©liale hÃ©rÃ©ditaire

Co-construction dâun programme dâÃ©ducation thÃ©rapeutique dÃ©diÃ© Ã lâalbinisme

Syndrome de Wells et cutis laxa acquiseÂ : une association atypique

Erosions chroniques du syndrome AECÂ : repositionnement topique dâune molÃ©cule anticancÃ©reuse

RÃ©cidive conjonctivale dâun syringocystadÃ©nocarcinome papillifÃ¨re sur syndrome de Schimmelpenning associÃ© aux mutations post-zygotiques HRAS et BRAF

Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage