List of works - Christine Chiaverini

Alitretinoin reduces erythema in inherited ichthyosis.

scientific article

Burden of inherited ichthyosis: a French national survey

scientific article published in March 2015

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

scientific article published on 25 March 2018

COVID-19 Lockdown induced acral dermatosis in children

scientific article published on 28 June 2020

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

scientific article

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

scientific article published on 21 September 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

scientific article published on 01 August 2018

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

scientific article published on 01 March 2011

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

scientific article

Cystinosin is a melanosomal protein that regulates melanin synthesis

scientific article published on 30 May 2012

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

scientific article

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.

scientific article published on April 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

scientific article published on 9 September 2013

Flexural agminated eruptive nevi in Langerhans cell histiocytosis

scientific article published in May 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

scientific article published on 7 March 2013

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

scientific article published on 17 June 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

scientific article published on 01 September 2014

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

scientific article

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

scientific article published on 2 February 2017

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

scientific article published on 14 January 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

scientific article published on 01 February 2011

Non-accidental injury or congenital infection?

scientific article published on 17 January 2017

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

scientific article published on 25 March 2016

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

scientific article published on 9 June 2017

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

scientific article

Papular, profuse, and precocious keratosis pilaris.

scientific article published on 6 December 2011

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

scientific article published in February 2016

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

scientific article published on 12 November 2008

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

scientific article published on 11 November 2019

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

scientific article published on 01 August 2019

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

scientific article published on 7 November 2017

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

scientific article published on 2 February 2016

Spectrum of Clinical Responses to Therapies in Infantile Bullous Pemphigoid

scientific article published on 14 January 2016

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

scientific article published on 3 November 2009

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

scientific article

Therapeutic patient education in atopic dermatitis: worldwide experiences.

scientific article

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

scientific article published on 28 August 2017

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

scientific article published on 01 December 2020

Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa

scientific article published on 01 December 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.

scientific article

List of works by Christine Chiaverini

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.