| French national protocol for the management of congenital ichthyosis. |
Severino-Freire, M ; Granier Tournier, C ; Chiaverini, C ; Audouze, A ; Morice-Picard, F ; Texier, H & al |
Ann Dermatol Venereol |
2024 |
|
| Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. |
Bessis, D ; Bursztejn, AC ; Morice-Picard, F ; Capri, Y ; Barbarot, S ; Aubert, H & al |
J Eur Acad Dermatol Venereol |
2024 |
|
| Oral health status in patients with inherited epidermolysis bullosa: a comparative multicenter study. |
Joseph, C ; Marty, M ; Dridi, SM ; Verhaeghe, V ; Bailleul-Forestier, I ; Chiaverini, C & al |
Quintessence Int |
2023 |
|
| Vascular endothelial growth factor, tissue factor, coagulation and fibrinolysis markers in slow-flow vascular malformations: a prospective study of treatment with sirolimus. |
Maruani, A ; Moineau, AG ; Boccara, O ; Mazereeuw-Hautier, J ; Leducq, S ; Bessis, D & al |
Br J Dermatol |
2023 |
|
| cLFM-Qol: A specific quality of life measurement tool for children from 11 to 15 years with low-flow malformations. |
Godeau, M ; Shourick, J ; Dreyfus, I ; Casassa, É ; Bergeron, A ; Severino-Freire, M & al |
J Eur Acad Dermatol Venereol |
2023 |
|
| Intramuscular capillary-type hemangioma: Diagnosis, treatment, and outcomes. A French multicentric retrospective study of 66 cases. |
Orly, J ; Bisdorff, A ; Fraissenon, A ; Joly, A ; Boulouis, G ; Guibaud, L & al |
Eur J Radiol |
2023 |
|
| Folliculitis decalvans and dystrophic epidermolysis bullosa: a significant association. |
Matard, B ; Bourrat, E ; Cavalié, M ; Chiaverini, C ; Reygagne, P |
Br J Dermatol |
2022 |
|
| Allogeneic stem cell transplantation as a curative therapeutic approach for VEXAS syndrome: a case report. |
Loschi, M ; Roux, C ; Sudaka, I ; Ferrero-Vacher, C ; Marceau-Renaut, A ; Duployez, N & al |
Bone Marrow Transplant |
2022 |
|
| Dermatoscopic and clinical features of congenital or congenital-type nail matrix nevi: A multicenter prospective cohort study by the International Dermoscopy Society. |
Pham, F ; Boespflug, A ; Duru, G ; Phan, A ; Poulalhon, N ; Weiler, L & al |
J Am Acad Dermatol |
2022 |
|
| Case Report, Practices Survey and Literature Review of an Under-Recognized Pediatric Vascular Disorder: The BASCULE Syndrome. |
Baurens, N ; Briand, C ; Giovannini-Chami, L ; De Guillebon De Resnes, JM ; Hubiche, T ; Chiaverini, C & al |
Front Pediatr |
2022 |
|
| Dermatologic manifestations in paediatric neurofibromatosis type 2: a cross sectional descriptive multicentric study. |
Legoupil, S ; Bessis, D ; Picard, F ; Mallet, S ; Mazereeuw, J ; Phan, A & al |
Orphanet J Rare Dis |
2022 |
|
| Quality of life of children with capillary malformations of the lower limbs: Evolution and associated factors. Data from the French national paediatric cohort, CONAPE. |
Robert, J ; Marchand, A ; Mazereeuw-Hautier, J ; Boccara, O ; Martin, L ; Chiaverini, C & al |
Ann Dermatol Venereol |
2022 |
|
| Perception of Oral Health-Related Quality of Life in Children with Epidermolysis Bullosa: A Quantitative and Qualitative Study. |
Marty, M ; Chiaverini, C ; Milon, C ; Costa-Mendes, L ; Kémoun, P ; Mazereeuw-Hautier, J & al |
JDR Clin Trans Res |
2022 |
|
| Safety and efficacy of low-dose PI3K inhibitor taselisib in adult patients with CLOVES and Klippel-Trenaunay syndrome (KTS): the TOTEM trial, a phase 1/2 multicenter, open-label, single-arm study. |
Luu, M ; Vabres, P ; Devilliers, H ; Loffroy, R ; Phan, A ; Martin, L & al |
Genet Med |
2021 |
|
| Central nervous system screening in capillary malformation-arteriovenous malformation syndrome: An observational study. |
Boccara, O ; Mazereeuw, J ; Martin, L ; Bessis, D ; Hubiche, T ; Chiaverini, C & al |
J Am Acad Dermatol |
2021 |
|
| Oral status in patients with inherited epidermolysis bullosa: A multicentric observational study. |
Chiaverini, C ; Marty, M ; Dridi, SM ; Campana, SC ; Canceill, T ; Bailleul-Forestier, I & al |
J Am Acad Dermatol |
2021 |
|
| Sirolimus (Rapamycin) for Slow-Flow Malformations in Children: The Observational-Phase Randomized Clinical PERFORMUS Trial. |
Maruani, A ; Tavernier, E ; Boccara, O ; Mazereeuw-Hautier, J ; Leducq, S ; Bessis, D & al |
JAMA Dermatol |
2021 |
|
| Annular lipoatrophy of the ankle: Four new pediatric cases and a review of the literature. |
Touhouche, TA ; Tournier, E ; Lamant, L ; Hardy, J ; Taieb, A ; Labreze, C & al |
Pediatr Dermatol |
2021 |
|
| Health care transition for patients with vascular malformations: a French multicenter cross-sectional study. |
Vermersch, C ; Boccara, O ; Chiaverini, C ; Mazereeuw-Hautier, J ; Sigg, N ; Mallet, S & al |
Orphanet J Rare Dis |
2021 |
|
| Gastrostomy for infants with severe epidermolysis bullosa simplex in neonatal intensive care. |
Marro, M ; De Smet, S ; Caldari, D ; Lambe, C ; Leclerc-Mercier, S ; Chiaverini, C |
Orphanet J Rare Dis |
2021 |
|
| Clinical and neuroimaging findings in 33 patients with MCAP syndrome: A survey to evaluate relevant endpoints for future clinical trials. |
Garde, A ; Guibaud, L ; Goldenberg, A ; Petit, F ; Dard, R ; Roume, J & al |
Clin Genet |
2021 |
|
| Genotypic and phenotypic analysis of 34 cases of inherited junctional epidermolysis bullosa caused by COL17A1 mutations. |
Hérissé, AL ; Charlesworth, A ; Bellon, N ; Leclerc-Mercier, S ; Bourrat, E ; Hadj-Rabia, S & al |
Br J Dermatol |
2021 |
|
| Neurofibromatosis 1 French national guidelines based on an extensive literature review since 1966. |
Bergqvist, C ; Servy, A ; Valeyrie-Allanore, L ; Ferkal, S ; Combemale, P ; Wolkenstein, P |
Orphanet J Rare Dis |
2020 |
|
| Laser treatment of epidermal nevi: A multicenter retrospective study with long-term follow-up. |
Alkhalifah, A ; Fransen, F ; Le Duff, F ; Lacour, JP ; Wolkerstorfer, A ; Passeron, T |
J Am Acad Dermatol |
2020 |
|
| A systematic review of outcome reporting in laser treatments for dermatological diseases. |
Fransen, F ; Tio, DCKS ; Prinsen, CAC ; Haedersdal, M ; Hedelund, L ; Laubach, HJ & al |
J Eur Acad Dermatol Venereol |
2020 |
|
| Reverse Phenotyping in Patients with Skin Capillary Malformations and Mosaic GNAQ or GNA11 Mutations Defines a Clinical Spectrum with Genotype-Phenotype Correlation. |
Jordan, M ; Carmignac, V ; Sorlin, A ; Kuentz, P ; Albuisson, J ; Borradori, L & al |
J Invest Dermatol |
2020 |
|
| Incontinentia pigmenti in boys: Causes and consequences. |
Chambelland, A ; Aubert, H ; Bourrat, E ; Morice-Picard, F ; Puzenat, E ; Lacour, JP & al |
Ann Dermatol Venereol |
2020 |
|
| Cutaneous lipomas and macrocephaly as early signs of PTEN hamartoma tumor syndrome. |
Martin, H ; Bessis, D ; Bourrat, E ; Mazereeuw-Hautier, J ; Morice-Picard, F ; Balguerie, X & al |
Pediatr Dermatol |
2020 |
|
| Topical ropivacaine for analgesia of aplasia cutis congenita in newborns with hereditary epidermolysis bullosa. |
Chambelland, A ; Devos, C ; Casagrande, F ; Chiaverini, C |
Orphanet J Rare Dis |
2020 |
|
| Topical sirolimus 0.1% for treating cutaneous microcystic lymphatic malformations in children and adults (TOPICAL): protocol for a multicenter phase 2, within-person, randomized, double-blind, vehicle-controlled clinical trial. |
Leducq, S ; Caille, A ; Barbarot, S ; Bénéton, N ; Bessis, D ; Boccara, O & al |
Trials |
2019 |
|
| Naevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal naevus) and mosaic FGFR3 and FGFR2 mutations. |
Bessis, D ; Petit, A ; Battistella, M ; Bourrat, E ; Girard, C ; Pallure, V & al |
Br J Dermatol |
2019 |
|
| Orofacial management for epidermolysis bullosa during wisdom tooth removal surgery: A technical note. |
Delebarre, H ; Chiaverini, C ; Vandersteen, C ; Savoldelli, C |
J Stomatol Oral Maxillofac Surg |
2019 |
|
| Laser treatment of hyperpigmented lesions: position statement of the European Society of Laser in Dermatology. |
Passeron, T ; Genedy, R ; Salah, L ; Fusade, T ; Kositratna, G ; Laubach, HJ & al |
J Eur Acad Dermatol Venereol |
2019 |
|
| Clinical Profile of Methotrexate-resistant Juvenile Localised Scleroderma. |
Hardy, J ; Boralevi, F ; Mallet, S ; Cabrera, N ; Belot, A ; Phan, A & al |
Acta Derm Venereol |
2019 |
|
| Acquired linear hyperpigmentation of the lips - a new entity? |
Almutairi, A ; Claeys, A ; Bahadoran, P ; Brun, P ; Guardoli, D ; Freychet, F & al |
J Eur Acad Dermatol Venereol |
2019 |
|
| Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment. |
Castela, E ; Tulic, MK ; Rozières, A ; Bourrat, E ; Nicolas, JF ; Kanitakis, J & al |
Br J Dermatol |
2019 |
|
| 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 & al |
Br J Dermatol |
2019 |
|
| Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation. |
Bessis, D ; Miquel, J ; Bourrat, E ; Chiaverini, C ; Morice-Picard, F ; Abadie, C & al |
Br J Dermatol |
2019 |
|
| Treatment of Severe Hailey-Hailey Disease With Apremilast. |
Kieffer, J ; Le Duff, F ; Montaudié, H ; Chiaverini, C ; Lacour, JP ; Passeron, T |
JAMA Dermatol |
2018 |
|
| Dermoscopy of eccrine angiomatous hamartoma: The spitzoid pattern. |
Kelati, A ; Chiaverini, C ; Giacchero, D ; Ilie, M ; Lacour, JP ; Bahadoran, P |
JAAD Case Rep |
2018 |
|
| [Ichthyosis prematurity syndrome: Two new cases]. |
Severino-Freire, M ; Bing Lecointe, AC ; Bourrat, E ; Pichery, M ; Jonca, N ; Chiaverini, C & al |
Ann Dermatol Venereol |
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. |
Maruani, A ; Boccara, O ; Bessis, D ; Guibaud, L ; Vabres, P ; Mazereeuw-Hautier, J & al |
Trials |
2018 |
|
| Propranolol pharmacokinetics in infants treated for Infantile Hemangiomas requiring systemic therapy: Modeling and dosing regimen recommendations. |
Del Frari, L ; Léauté-Labrèze, C ; Guibaud, L ; Barbarot, S ; Lacour, JP ; Chaumont, C & al |
Pharmacol Res Perspect |
2018 |
|
| Burnlike scars: A sign suggestive of KLHL24-related epidermolysis bullosa simplex. |
Alkhalifah, A ; Chiaverini, C ; Charlesworth, A ; Has, C ; Lacour, JP |
Pediatr Dermatol |
2018 |
|
| Alitretinoin reduces erythema in inherited ichthyosis. |
Onnis, G ; Chiaverini, C ; Hickman, G ; Dreyfus, I ; Fischer, J ; Bourrat, E & al |
Orphanet J Rare Dis |
2018 |
|
| [Clinical and evolutionary characteristics of a child with aquagenic keratoderma: A retrospective study of 12 patients]. |
Denos, C ; Dreyfus, I ; Chiaverini, C ; Labreze, C ; Abasq, C ; Phan, A & al |
Ann Dermatol Venereol |
2018 |
|
| Search for RASA1 Variants in Capillary Malformations of the Legs in 113 Children: Results from the French National Paediatric Cohort CONAPE. |
Maruani, A ; Durieux-Verde, M ; Mazereeuw-Hautier, J ; Boccara, O ; Martin, L ; Chiaverini, C & al |
Acta Derm Venereol |
2018 |
|
| Clinical and haemodynamic risk factors associated with discrepancies in lower limb length with capillary malformations: data from the national paediatric French cohort CONAPE. |
Samimi, M ; Durieux-Verde, M ; Caille, A ; Mazereeuw-Hautier, J ; Boccara, O ; Martin, L & al |
Br J Dermatol |
2018 |
|
| Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex. |
Brun, J ; Chiaverini, C ; Devos, C ; Leclerc-Mercier, S ; Mazereeuw, J ; Bourrat, E & al |
Orphanet J Rare Dis |
2017 |
|
| PLACK syndrome resulting from a new homozygous insertion mutation in CAST. |
Alkhalifah, A ; Chiaverini, C ; Del Giudice, P ; Supsrisunjai, C ; Hsu, CK ; Liu, L & al |
J Dermatol Sci |
2017 |
|
| Treatment of Elastosis Perforans Serpiginosa Using a Fractional Carbon Dioxide Laser. |
Kelati, A ; Lagrange, S ; Le Duff, F ; Lacour, JP ; Passeron, T |
JAMA Dermatol |
2017 |
|
| Germline Loss-of-Function Mutations in EPHB4 Cause a Second Form of Capillary Malformation-Arteriovenous Malformation (CM-AVM2) Deregulating RAS-MAPK Signaling. |
Amyere, M ; Revencu, N ; Helaers, R ; Pairet, E ; Baselga, E ; Cordisco, M & al |
Circulation |
2017 |
|
| Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing. |
Kuentz, P ; St-Onge, J ; Duffourd, Y ; Courcet, JB ; Carmignac, V ; Jouan, T & al |
Genet Med |
2017 |
|
| [Hereditary epidermolysis bullosa: French national guidelines (PNDS) for diagnosis and treatment]. |
Chiaverini, C ; Bourrat, E ; Mazereeuw-Hautier, J ; Hadj-Rabia, S ; Bodemer, C ; Lacour, JP |
Ann Dermatol Venereol |
2017 |
|
| Successful treatment of angiokeratoma circumscriptum naeviforme with long pulse alexandrite laser. |
Lorgeou, A ; Chiaverini, C ; Le Duff, F ; Lacour, JP ; Passeron, T |
J Eur Acad Dermatol Venereol |
2017 |
|
| Exacerbation of Hailey-Hailey disease by topiramate. |
Alkhalifah, A ; Montaudié, H ; Lacour, JP ; Lantéri-Minet, M ; Passeron, T |
J Eur Acad Dermatol Venereol |
2017 |
|
| Prognosis and response to laser treatment of early-onset hypertrophic port-wine stains (PWS). |
Passeron, T ; Salhi, A ; Mazer, JM ; Lavogiez, C ; Mazereeuw-Hautier, J ; Galliot, C & al |
J Am Acad Dermatol |
2016 |
|
| Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa. |
Chiaverini, C ; Passeron, T ; Lacour, JP |
J Am Acad Dermatol |
2016 |
|
| Inherited epidermolysis bullosa and squamous cell carcinoma: a systematic review of 117 cases. |
Montaudié, H ; Chiaverini, C ; Sbidian, E ; Charlesworth, A ; Lacour, JP |
Orphanet J Rare Dis |
2016 |
|
| Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial. |
Chiaverini, C ; Roger, C ; Fontas, E ; Bourrat, E ; Bourdon-Lanoy, E ; Labrèze, C & al |
Orphanet J Rare Dis |
2016 |
|
| Evaluation of learning disabilities in segmental neurofibromatosis. |
Marmottant-Debled, E ; Chiaverini, C ; Fossoud, C ; Passeron, T ; Barbarot, S ; Lacour, JP |
Br J Dermatol |
2016 |
|
| Skin Patterns Associated with Upper Airway Infantile Haemangiomas: A Retrospective Multicentre Study. |
Uthurriague, C ; Boccara, O ; Catteau, B ; Fayoux, P ; Léauté-Labrèze, C ; Chiaverini, C & al |
Acta Derm Venereol |
2016 |
|
| Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis. |
Thomas, AC ; Zeng, Z ; Rivière, JB ; O''''Shaughnessy, R ; Al-Olabi, L ; St-Onge, J & al |
J Invest Dermatol |
2016 |
|
| Treatment of resistant port-wine stains with bosentan and pulsed dye laser: a pilot prospective study. |
Taquin, H ; Lacour, JP ; Le Duff, F ; Chiaverini, C ; Passeron, T |
J Eur Acad Dermatol Venereol |
2016 |
|
| A prospective study of risk for Sturge-Weber syndrome in children with upper facial port-wine stain. |
Dutkiewicz, AS ; Ezzedine, K ; Mazereeuw-Hautier, J ; Lacour, JP ; Barbarot, S ; Vabres, P & al |
J Am Acad Dermatol |
2015 |
|
| [Item 111 - UE 4 Hemangiomas and skin vascular malformations]. |
|
Ann Dermatol Venereol |
2015 |
|
| [Recessive epidermolysis bullosa due to composite heterozygote mutations in the COL7A1 gene]. |
Abdou, A ; Daoui, L ; Charlesworth, A ; Chiaverini, C ; Algros, MP ; Puzenat, E & al |
Ann Dermatol Venereol |
2015 |
|
| Oral erythromycin therapy in epidermolysis bullosa simplex generalized severe. |
Chiaverini, C ; Fontas, E ; Vabres, P ; Bessis, D ; Mazereeuw, J ; Charlesworth, A & al |
Br J Dermatol |
2015 |
|