Lista de obras -

Alitretinoin reduces erythema in inherited ichthyosis.

artículo científico publicado en 2018

Burden of inherited ichthyosis: a French national survey

artículo científico publicado en 2015

Burnlike scars: A sign suggestive of KLHL24-related epidermolysis bullosa simplex

artículo científico publicado en 2018

COVID-19 Lockdown induced acral dermatosis in children

artículo científico publicado en 2020

Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndrome

artículo científico publicado en 2003

Childhood chronic prurigo: Interest in patch tests and delayed-reading skin prick tests to environmental allergens

artículo científico publicado en 2017

Clinical Profile of Methotrexate-resistant Juvenile Localised Scleroderma

scientific article published on 01 May 2019

Clinical and Therapeutic Aspects of Linear Psoriasis: A Study of 30 Cases

artículo científico publicado en 2018

Corkscrew hair: a new dermoscopic sign for diagnosis of tinea capitis in black children

artículo científico publicado en 2011

Cyclic AMP promotes a peripheral distribution of melanosomes and stimulates melanophilin/Slac2-a and actin association

artículo científico publicado en 2004

Cystinosin is a melanosomal protein that regulates melanin synthesis

artículo científico publicado en 2012

Dennie-Morgan fold plus dark circles: suspect atopy at first sight.

artículo científico publicado en 2015

Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation

scientific article published on 18 January 2019

Dermatological spectrum of hand, foot and mouth disease from classical to generalized exanthema.

artículo científico publicado en 2014

Dermoscopy of eccrine angiomatous hamartoma: The spitzoid pattern

scientific article published on 18 September 2018

Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment

scientific article published on 02 December 2018

First clinical description of an infant with interleukin-36-receptor antagonist deficiency successfully treated with anakinra

artículo científico publicado en 2013

Flexural agminated eruptive nevi in Langerhans cell histiocytosis

artículo científico publicado en 2013

Genotypic and Phenotypic Analysis of 34 Cases of Inherited Junctional Epidermolysis Bullosa caused by COL17A1 Mutations

scientific article published on 10 September 2020

Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations

scientific article published on 04 January 2021

IQoL-32: a new ichthyosis-specific measure of quality of life

artículo científico publicado en 2013

Inversa Dystrophic Epidermolysis Bullosa Is Caused by Missense Mutations at Specific Positions of the Collagenic Domain of Collagen Type VII

artículo científico publicado en 2010

Ivermectin safety in infants and children under 15 kg treated for scabies: a multicentric observational study

scientific article published on 29 September 2019

Lethal form of keratitis-ichthyosis-deafness syndrome caused by the GJB2 mutation p.Ser17Phe

artículo científico publicado en 2014

Microphthalmia-associated transcription factor regulates RAB27A gene expression and controls melanosome transport

artículo científico publicado en 2008

Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing

artículo científico publicado en 2017

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis. ⬇️

artículo científico publicado en 2016

Multiple neonatal Staphylococcal cold abscesses in large skin folds: a benign neonatal skin infection

Nd:YAG Laser Treatment for Multiple Cutaneous Glomangiomas: Report of 3 Cases

artículo científico publicado en 2011

Non-accidental injury or congenital infection?

artículo científico publicado en 2017

Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial.

artículo científico publicado en 2016

PLACK syndrome resulting from a new homozygous insertion mutation in CAST.

artículo científico publicado en 2017

Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex

artículo científico publicado en 2017

Papular, profuse, and precocious keratosis pilaris.

artículo científico publicado en 2011

Pigmented macules of bony prominences (PMBP): A distinct presentation in patients with red hair

artículo científico publicado en 2016

Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study

artículo científico publicado en 2008

Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation

artículo científico publicado en 2019

Scabies polymerase chain reaction with standardized dry swab sampling: an easy tool for cluster diagnosis of human scabies

artículo científico publicado en 2019

Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results From the French National Paediatric Cohort CONAPE.

artículo científico publicado en 2017

Skin Patterns Associated with Upper Airway Infantile Haemangiomas: A Retrospective Multicentre Study

artículo científico publicado en 2016

Spectrum of Clinical Responses to Therapies in Infantile Bullous Pemphigoid

artículo científico publicado en 2016

The H syndrome: two novel mutations affecting the same amino acid residue of hENT3.

artículo científico publicado en 2009

The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literature

artículo científico publicado en 2016

Therapeutic patient education in atopic dermatitis: worldwide experiences.

artículo científico publicado en 2013

Topical Corticosteroid Concerns Among Parents of Children with Psoriasis versus Atopic Dermatitis: A French Multicenter Cross-Sectional Study.

artículo científico

Topical ropivacaine for analgesia of aplasia cutis congenita in newborns with hereditary epidermolysis bullosa

artículo científico publicado en 2020

Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa

artículo científico publicado en 2016

Treatment of Severe Hailey-Hailey Disease With Apremilast

article published in 2018

Treatment of voluminous and complicated superficial slow-flow vascular malformations with sirolimus (PERFORMUS): protocol for a multicenter phase 2 trial with a randomized observational-phase design.

artículo científico publicado en 2018

Lista de obras de

Alitretinoin reduces erythema in inherited ichthyosis.

Burden of inherited ichthyosis: a French national survey

Burnlike scars: A sign suggestive of KLHL24-related epidermolysis bullosa simplex

COVID-19 Lockdown induced acral dermatosis in children

Characterization of the molecular defects in Rab27a, caused by RAB27A missense mutations found in patients with Griscelli syndrome

Childhood chronic prurigo: Interest in patch tests and delayed-reading skin prick tests to environmental allergens

Clinical Profile of Methotrexate-resistant Juvenile Localised Scleroderma

Clinical and Therapeutic Aspects of Linear Psoriasis: A Study of 30 Cases

Corkscrew hair: a new dermoscopic sign for diagnosis of tinea capitis in black children

Cyclic AMP promotes a peripheral distribution of melanosomes and stimulates melanophilin/Slac2-a and actin association

Cystinosin is a melanosomal protein that regulates melanin synthesis

Dennie-Morgan fold plus dark circles: suspect atopy at first sight.

Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation

Dermatological spectrum of hand, foot and mouth disease from classical to generalized exanthema.

Dermoscopy of eccrine angiomatous hamartoma: The spitzoid pattern

Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment

First clinical description of an infant with interleukin-36-receptor antagonist deficiency successfully treated with anakinra

Flexural agminated eruptive nevi in Langerhans cell histiocytosis

Genotypic and Phenotypic Analysis of 34 Cases of Inherited Junctional Epidermolysis Bullosa caused by COL17A1 Mutations

Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations

IQoL-32: a new ichthyosis-specific measure of quality of life

Inversa Dystrophic Epidermolysis Bullosa Is Caused by Missense Mutations at Specific Positions of the Collagenic Domain of Collagen Type VII

Ivermectin safety in infants and children under 15 kg treated for scabies: a multicentric observational study

Lethal form of keratitis-ichthyosis-deafness syndrome caused by the GJB2 mutation p.Ser17Phe

Microphthalmia-associated transcription factor regulates RAB27A gene expression and controls melanosome transport

Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis. ⬇️

Multiple neonatal Staphylococcal cold abscesses in large skin folds: a benign neonatal skin infection

Nd:YAG Laser Treatment for Multiple Cutaneous Glomangiomas: Report of 3 Cases

Non-accidental injury or congenital infection?

Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial.

PLACK syndrome resulting from a new homozygous insertion mutation in CAST.

Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex

Papular, profuse, and precocious keratosis pilaris.

Pigmented macules of bony prominences (PMBP): A distinct presentation in patients with red hair

Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study

Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation

Scabies polymerase chain reaction with standardized dry swab sampling: an easy tool for cluster diagnosis of human scabies

Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results From the French National Paediatric Cohort CONAPE.

Skin Patterns Associated with Upper Airway Infantile Haemangiomas: A Retrospective Multicentre Study

Spectrum of Clinical Responses to Therapies in Infantile Bullous Pemphigoid

The H syndrome: two novel mutations affecting the same amino acid residue of hENT3.

The scalp hair collar and tuft signs: A retrospective multicenter study of 78 patients with a systematic review of the literature

Therapeutic patient education in atopic dermatitis: worldwide experiences.

Topical Corticosteroid Concerns Among Parents of Children with Psoriasis versus Atopic Dermatitis: A French Multicenter Cross-Sectional Study.

Topical ropivacaine for analgesia of aplasia cutis congenita in newborns with hereditary epidermolysis bullosa

Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa

Treatment of Severe Hailey-Hailey Disease With Apremilast

Treatment of voluminous and complicated superficial slow-flow vascular malformations with sirolimus (PERFORMUS): protocol for a multicenter phase 2 trial with a randomized observational-phase design.