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Sensitive Skin in Children.

Misery L, Taïeb C, Brenaut E, Huet F, Abasq-Thomas C, Sayag M, Bodemer C.

Acta Derm Venereol. 2019 Nov 19. doi: 10.2340/00015555-3376. [Epub ahead of print] No abstract available.


Pathophysiology and management of sensitive skin: position paper from the special interest group on sensitive skin of the International Forum for the Study of Itch (IFSI).

Misery L, Weisshaar E, Brenaut E, Evers AWM, Huet F, Ständer S, Reich A, Berardesca E, Serra-Baldrich E, Wallengren J, Linder D, Fluhr JW, Szepietowski JC, Maibach H; Special Interest Group on sensitive skin of the International Forum for the Study of Itch (ISFI).

J Eur Acad Dermatol Venereol. 2019 Oct 28. doi: 10.1111/jdv.16000. [Epub ahead of print]


Pathology of Rotavirus-driven Multiple Organ Failure in a 16-month-old Boy.

Tarris G, Belliot G, Callier P, Huet F, Martin L, de Rougemont A.

Pediatr Infect Dis J. 2019 Dec;38(12):e326-e328. doi: 10.1097/INF.0000000000002472.


Pruritus in Autoimmune and Inflammatory Dermatoses.

Zeidler C, Pereira MP, Huet F, Misery L, Steinbrink K, Ständer S.

Front Immunol. 2019 Jun 21;10:1303. doi: 10.3389/fimmu.2019.01303. eCollection 2019. Review.


Sensitive skin is a neuropathic disorder.

Huet F, Misery L.

Exp Dermatol. 2019 Jun 26. doi: 10.1111/exd.13991. [Epub ahead of print]


Hearing impairment as an early sign of alpha-mannosidosis in children with a mild phenotype: Report of seven new cases.

Lehalle D, Colombo R, O'Grady M, Héron B, Houcinat N, Kuentz P, Moutton S, Sorlin A, Thevenon J, Delanne J, Gay S, Racine C, Garde A, Tran Mau-Them F, Philippe C, Vitobello A, Nambot S, Huet F, Duffourd Y, Feillet F, Thauvin-Robinet C, Marlin S, Faivre L.

Am J Med Genet A. 2019 Sep;179(9):1756-1763. doi: 10.1002/ajmg.a.61273. Epub 2019 Jun 26.


Is hypertriglyceridemia atherogenic?

Huet F, Roubille C, Roubille F.

Curr Opin Lipidol. 2019 Aug;30(4):291-299. doi: 10.1097/MOL.0000000000000622.


Carriage of a Single Strain of Nontoxigenic Corynebacterium diphtheriae bv. Belfanti (Corynebacterium belfantii) in Four Patients with Cystic Fibrosis.

Pivot D, Fanton A, Badell-Ocando E, Benouachkou M, Astruc K, Huet F, Amoureux L, Neuwirth C, Criscuolo A, Aho S, Toubiana J, Brisse S.

J Clin Microbiol. 2019 Apr 26;57(5). pii: e00042-19. doi: 10.1128/JCM.00042-19. Print 2019 May.


Which high-sensitivity troponin variable best characterizes infarct size and microvascular obstruction?

Schaaf M, Huet F, Akodad M, Gorce-Dupuy AM, Adda J, Macia JC, Delseny D, Leclercq F, Cristol JP, Marin G, Mewton N, Roubille F.

Arch Cardiovasc Dis. 2019 May;112(5):334-342. doi: 10.1016/j.acvd.2018.12.001. Epub 2019 Feb 15.


Current pharmaceutical developments in atopic dermatitis.

Misery L, Huet F, Gouin O, Ständer S, Deleuran M.

Curr Opin Pharmacol. 2019 Jun;46:7-13. doi: 10.1016/j.coph.2018.12.003. Epub 2019 Jan 2. Review.


Potential Uses of Sacubitril/Valsartan: Need for Data on Efficacy and Safety.

Huet F, Akodad M, Kalmanovitch E, Adda J, Agullo A, Batistella P, Roubille C, Roubille F.

Am J Cardiovasc Drugs. 2019 Feb;19(1):1-10. doi: 10.1007/s40256-018-0306-z. Review.


[A (too) successful renal denervation].

Huet F, Vernhet H, Roubille F.

Ann Cardiol Angeiol (Paris). 2019 Feb;68(1):61-63. doi: 10.1016/j.ancard.2018.08.030. Epub 2018 Oct 2. French.


Characteristics of Pruritus in Relation to Self-assessed Severity of Atopic Dermatitis.

Huet F, Faffa MS, Poizeau F, Merhand S, Misery L, Brenaut E.

Acta Derm Venereol. 2019 Mar 1;99(3):279-283. doi: 10.2340/00015555-3053.


Is hypertriglyceridemia atherogenic?

Roubille F, Sultan A, Huet F, Leclercq F, Macia JC, Gervasoni R, Delseny D, Akodad M, Roubille C.

Presse Med. 2018 Sep;47(9):757-763. doi: 10.1016/j.lpm.2018.08.009. Epub 2018 Sep 24. Review.


Exploring collagen remodeling and regulation as prognosis biomarkers in stable heart failure.

Dupuy AM, Kuster N, Curinier C, Huet F, Plawecki M, Solecki K, Roubille F, Cristol JP.

Clin Chim Acta. 2019 Mar;490:167-171. doi: 10.1016/j.cca.2018.08.042. Epub 2018 Sep 1.


The impact of atopic dermatitis on sexual health.

Misery L, Seneschal J, Reguiai Z, Merhand S, Héas S, Huet F, Taieb C, Ezzedine K.

J Eur Acad Dermatol Venereol. 2019 Feb;33(2):428-432. doi: 10.1111/jdv.15223. Epub 2018 Sep 23.


An hs-TNT Second Peak Associated with High CRP at Day 2 Appears as Potential Biomarkers of Micro-Vascular Occlusion on Magnetic Resonance Imaging after Reperfused ST-Segment Elevation Myocardial Infarction.

Huet F, Akodad M, Kuster N, Kovacsik H, Leclercq F, Dupuy AM, Gervasoni R, Khoury G, Macia JC, Cristol JP, Roubille F.

Cardiology. 2018;140(4):227-236. doi: 10.1159/000490881. Epub 2018 Aug 23.


Sensitive skin can be small fibre neuropathy: results from a case-control quantitative sensory testing study.

Huet F, Dion A, Batardière A, Nedelec AS, Le Caër F, Bourgeois P, Brenaut E, Misery L.

Br J Dermatol. 2018 Nov;179(5):1157-1162. doi: 10.1111/bjd.17082. Epub 2018 Sep 16.


Association between two painful and poorly understood conditions: Irritable bowel and sensitive skin syndromes.

Misery L, Duboc H, Coffin B, Brenaut E, Huet F, Taieb C.

Eur J Pain. 2019 Jan;23(1):160-166. doi: 10.1002/ejp.1296. Epub 2018 Sep 4.


Real-life study of anti-itching effects of a cream containing menthoxypropanediol, a TRPM8 agonist, in atopic dermatitis patients.

Misery L, Santerre A, Batardière A, Hornez N, Nedelec AS, Le Caër F, Bourgeois P, Huet F, Neufang G.

J Eur Acad Dermatol Venereol. 2019 Feb;33(2):e67-e69. doi: 10.1111/jdv.15199. Epub 2018 Aug 20. No abstract available.


Development and validation of a new tool to assess the Burden of Sensitive Skin (BoSS).

Misery L, Jourdan E, Abadie S, Ezzedine K, Brenaut E, Huet F, Sayag M, Taieb C.

J Eur Acad Dermatol Venereol. 2018 Dec;32(12):2217-2223. doi: 10.1111/jdv.15186. Epub 2018 Aug 16.


Water content of limestones submitted to realistic wet deposition: a CIME2 chamber simulation.

Chabas A, Sizun JP, Gentaz L, Uring P, Phan A, Coman A, Alfaro SC, Saheb M, Pangui E, Zapf P, Huet F.

Environ Sci Pollut Res Int. 2018 Aug;25(24):23973-23985. doi: 10.1007/s11356-018-2433-0. Epub 2018 Jun 8.


Clinical Characteristics of Pruritus in Systemic Sclerosis Vary According to the Autoimmune Subtype.

Gourier G, Théréné C, Mazeas M, Abasq-Thomas C, Brenaut E, Huet F, Sonbol H, Campillo E, Lemerle J, Pasquier E, Le Moigne E, Saraux A, Devauchelle-Pensec V, Misery L, Renaudineau Y.

Acta Derm Venereol. 2018 Aug 29;98(8):735-741. doi: 10.2340/00015555-2980.


Letter to the editor concerning "comparative prognostic value of postprocedural creatine kinase myocardial band and high-sensitivity troponin T in patients with non-ST-segment elevation myocardial infarction undergoing percutaneous coronary intervention".

Akodad M, Huet F, Dupuy AM, Lotierzo M, Cristol JP, Roubille F.

Catheter Cardiovasc Interv. 2018 Sep 1;92(3):633-634. doi: 10.1002/ccd.27618. Epub 2018 May 4. No abstract available.


Patient Burden is Associated with Alterations in Quality of Life in Adult Patients with Atopic Dermatitis: Results from the ECLA Study.

Misery L, Seneschal J, Reguiai Z, Merhand S, Héas S, Huet F, Taïeb C, Ezzedine K.

Acta Derm Venereol. 2018 Jul 11;98(7):713-714. doi: 10.2340/00015555-2940. No abstract available.


Unexpected diagnosis of a SHH nonsense variant causing a variable phenotype ranging from familial coloboma and Intellectual disability to isolated microcephaly.

Bruel AL, Thevenon J, Huet F, Jean-Marcais N, Odent S, Dubourg C, Lehalle D, Tran Mau-Them F, Philippe C, Moutton S, Houcinat N, Gay S, Guibaud L, Duffourd Y, Rivière JB, Faivre L, Thauvin-Robinet C.

Clin Genet. 2018 Jul;94(1):182-184. doi: 10.1111/cge.13211. Epub 2018 Mar 2. No abstract available.


Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility.

Esteve C, Francescatto L, Tan PL, Bourchany A, De Leusse C, Marinier E, Blanchard A, Bourgeois P, Brochier-Armanet C, Bruel AL, Delarue A, Duffourd Y, Ecochard-Dugelay E, Hery G, Huet F, Gauchez P, Gonzales E, Guettier-Bouttier C, Komuta M, Lacoste C, Maudinas R, Mazodier K, Rimet Y, Rivière JB, Roquelaure B, Sigaudy S, Stephenne X, Thauvin-Robinet C, Thevenon J, Sarles J, Levy N, Badens C, Goulet O, Hugot JP, Katsanis N, Faivre L, Fabre A.

Am J Hum Genet. 2018 Mar 1;102(3):364-374. doi: 10.1016/j.ajhg.2018.01.009. Epub 2018 Feb 8.


Sensitive skin in France: a study on prevalence, relationship with age and skin type and impact on quality of life.

Misery L, Jourdan E, Huet F, Brenaut E, Cadars B, Virassamynaïk S, Sayag M, Taieb C.

J Eur Acad Dermatol Venereol. 2018 May;32(5):791-795. doi: 10.1111/jdv.14837. Epub 2018 Mar 23.


Reconstructed human epidermis for in vitro studies on atopic dermatitis: A review.

Huet F, Severino-Freire M, Chéret J, Gouin O, Praneuf J, Pierre O, Misery L, Le Gall-Ianotto C.

J Dermatol Sci. 2018 Mar;89(3):213-218. doi: 10.1016/j.jdermsci.2017.11.015. Epub 2017 Dec 1. Review.


Area at risk can be assessed by iodine-123-meta-iodobenzylguanidine single-photon emission computed tomography after myocardial infarction: a prospective study.

Hedon C, Huet F, Ben Bouallegue F, Vernhet H, Macia JC, Cung TT, Leclercq F, Cade S, Cransac F, Lattuca B, Vandenberghe D, Bourdon A, Benkiran M, Vauchot F, Gervasoni R, D'estanque E, Mariano-Goulart D, Roubille F.

Nucl Med Commun. 2018 Feb;39(2):118-124. doi: 10.1097/MNM.0000000000000782.


Progressive nodular histiocytosis improved by methotrexate.

Huet F, Brenaut E, Costa S, Lemasson G, Sonbol H, Misery L.

Eur J Dermatol. 2017 Dec 1;27(6):661-663. doi: 10.1684/ejd.2017.3115. No abstract available.


Reducing diagnostic turnaround times of exome sequencing for families requiring timely diagnoses.

Bourchany A, Thauvin-Robinet C, Lehalle D, Bruel AL, Masurel-Paulet A, Jean N, Nambot S, Willems M, Lambert L, El Chehadeh-Djebbar S, Schaefer E, Jaquette A, St-Onge J, Poe C, Jouan T, Chevarin M, Callier P, Mosca-Boidron AL, Laurent N, Lefebvre M, Huet F, Houcinat N, Moutton S, Philippe C, Tran-Mau-Them F, Vitobello A, Kuentz P, Duffourd Y, Rivière JB, Thevenon J, Faivre L.

Eur J Med Genet. 2017 Nov;60(11):595-604. doi: 10.1016/j.ejmg.2017.08.011. Epub 2017 Aug 12.


Toward the Standardization of Mycological Examination of Sputum Samples in Cystic Fibrosis: Results from a French Multicenter Prospective Study.

Coron N, Pihet M, Fréalle E, Lemeille Y, Pinel C, Pelloux H, Gargala G, Favennec L, Accoceberry I, Durand-Joly I, Dalle F, Huet F, Fanton A, Boldron A, Loeuille GA, Domblides P, Coltey B, Pin I, Llerena C, Troussier F, Person C, Marguet C, Wizla N, Thumerelle C, Turck D, Bui S, Fayon M, Duhamel A, Prévotat A, Wallaert B, Leroy S, Bouchara JP, Delhaes L.

Mycopathologia. 2018 Feb;183(1):101-117. doi: 10.1007/s11046-017-0173-1. Epub 2017 Jul 26.


[DRESS syndrome and agranulocytosis, a rare combination].

Lavenant P, Roue JM, Huet F, Abasq C, Misery L, Rioualen S.

Arch Pediatr. 2017 Aug;24(8):752-756. doi: 10.1016/j.arcped.2017.05.010. Epub 2017 Jun 29. French.


Interest of colchicine in the treatment of acute myocardial infarct responsible for heart failure in a mouse model.

Akodad M, Fauconnier J, Sicard P, Huet F, Blandel F, Bourret A, de Santa Barbara P, Aguilhon S, LeGall M, Hugon G, Lacampagne A, Roubille F.

Int J Cardiol. 2017 Aug 1;240:347-353. doi: 10.1016/j.ijcard.2017.03.126. Epub 2017 Apr 1.


Randomised controlled trial demonstrates that fermented infant formula with short-chain galacto-oligosaccharides and long-chain fructo-oligosaccharides reduces the incidence of infantile colic.

Vandenplas Y, Ludwig T, Bouritius H, Alliet P, Forde D, Peeters S, Huet F, Hourihane J.

Acta Paediatr. 2017 Jul;106(7):1150-1158. doi: 10.1111/apa.13844. Epub 2017 Apr 19.


[Epidemiology of strokes in pediatry].

Béjot Y, Delpont B, Blanc C, Darmency V, Huet F, Giroud M.

Soins Pediatr Pueric. 2017 Mar - Apr;38(295):12-13. doi: 10.1016/j.spp.2017.01.002. French.


Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome.

Quartier A, Poquet H, Gilbert-Dussardier B, Rossi M, Casteleyn AS, Portes VD, Feger C, Nourisson E, Kuentz P, Redin C, Thevenon J, Mosca-Boidron AL, Callier P, Muller J, Lesca G, Huet F, Geoffroy V, El Chehadeh S, Jung M, Trojak B, Le Gras S, Lehalle D, Jost B, Maury S, Masurel A, Edery P, Thauvin-Robinet C, Gérard B, Mandel JL, Faivre L, Piton A.

Eur J Hum Genet. 2017 Apr;25(4):423-431. doi: 10.1038/ejhg.2016.204. Epub 2017 Feb 8.


Anti-inflammatory drugs as promising cardiovascular treatments.

Huet F, Akodad M, Fauconnier J, Lacampagne A, Roubille F.

Expert Rev Cardiovasc Ther. 2017 Feb;15(2):109-125. doi: 10.1080/14779072.2017.1273771. Epub 2016 Dec 28. Review.


Image Gallery: Erythroderma revealing a nonbullous bullous pemphigoid.

Huet F, Karam A, Lemasson G, Jouen F, Sonbol H, Misery L, Abasq-Thomas C.

Br J Dermatol. 2016 Nov;175(5):e136-e137. doi: 10.1111/bjd.14982. No abstract available.


Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability.

Gauthier-Vasserot A, Thauvin-Robinet C, Bruel AL, Duffourd Y, St-Onge J, Jouan T, Rivière JB, Heron D, Donadieu J, Bellanné-Chantelot C, Briandet C, Huet F, Kuentz P, Lehalle D, Duplomb-Jego L, Gautier E, Maystadt I, Pinson L, Amram D, El Chehadeh S, Melki J, Julia S, Faivre L, Thevenon J.

Am J Med Genet A. 2017 Jan;173(1):62-71. doi: 10.1002/ajmg.a.37969. Epub 2016 Sep 12.


Partly Fermented Infant Formulae With Specific Oligosaccharides Support Adequate Infant Growth and Are Well-Tolerated.

Huet F, Abrahamse-Berkeveld M, Tims S, Simeoni U, Beley G, Savagner C, Vandenplas Y, Hourihane JO.

J Pediatr Gastroenterol Nutr. 2016 Oct;63(4):e43-53. doi: 10.1097/MPG.0000000000001360.


Multi-Marker Strategy in Heart Failure: Combination of ST2 and CRP Predicts Poor Outcome.

Dupuy AM, Curinier C, Kuster N, Huet F, Leclercq F, Davy JM, Cristol JP, Roubille F.

PLoS One. 2016 Jun 16;11(6):e0157159. doi: 10.1371/journal.pone.0157159. eCollection 2016.


Clinical severity and molecular characteristics of circulating and emerging rotaviruses in young children attending hospital emergency departments in France.

de Rougemont A, Kaplon J, Fremy C, Legrand-Guillien MC, Minoui-Tran A, Payan C, Vabret A, Mendes-Martins L, Chouchane M, Maudinas R, Huet F, Dubos F, Hober D, Lazrek M, Bouquignaud C, Decoster A, Alain S, Languepin J, Gillet Y, Lina B, Mekki Y, Morfin-Sherpa F, Guigon A, Guinard J, Foulongne V, Rodiere M, Avettand-Fenoel V, Bonacorsi S, Garbarg-Chenon A, Gendrel D, Lebon P, Lorrot M, Mariani P, Meritet JF, Schnuriger A, Agius G, Beby-Defaux A, Oriot D, Colimon R, Lagathu G, Mory O, Pillet S, Pozzetto B, Stephan JL, Aho S, Pothier P; French National Rotavirus Network.

Clin Microbiol Infect. 2016 Aug;22(8):737.e9-737.e15. doi: 10.1016/j.cmi.2016.05.025. Epub 2016 Jun 7.


A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome.

Masurel-Paulet A, Piton A, Chancenotte S, Redin C, Thauvin-Robinet C, Henrenger Y, Minot D, Creppy A, Ruffier-Bourdet M, Thevenon J, Kuentz P, Lehalle D, Curie A, Blanchard G, Ghosn E, Bonnet M, Archimbaud-Devilliers M, Huet F, Perret O, Philip N, Mandel JL, Faivre L.

Am J Med Genet A. 2016 Aug;170(8):2103-10. doi: 10.1002/ajmg.a.37765. Epub 2016 Jun 3.


Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis.

Bruel AL, Masurel-Paulet A, Rivière JB, Duffourd Y, Lehalle D, Bensignor C, Huet F, Borgnon J, Roucher F, Kuentz P, Deleuze JF, Thauvin-Robinet C, Faivre L, Thevenon J.

Clin Genet. 2017 Feb;91(2):333-338. doi: 10.1111/cge.12794. Epub 2016 Jun 5.


Expanding the Phenotype Associated with NAA10-Related N-Terminal Acetylation Deficiency.

Saunier C, Støve SI, Popp B, Gérard B, Blenski M, AhMew N, de Bie C, Goldenberg P, Isidor B, Keren B, Leheup B, Lampert L, Mignot C, Tezcan K, Mancini GM, Nava C, Wasserstein M, Bruel AL, Thevenon J, Masurel A, Duffourd Y, Kuentz P, Huet F, Rivière JB, van Slegtenhorst M, Faivre L, Piton A, Reis A, Arnesen T, Thauvin-Robinet C, Zweier C.

Hum Mutat. 2016 Aug;37(8):755-64. doi: 10.1002/humu.23001. Epub 2016 May 4.


Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole-exome sequencing as a first-line diagnostic test.

Thevenon J, Duffourd Y, Masurel-Paulet A, Lefebvre M, Feillet F, El Chehadeh-Djebbar S, St-Onge J, Steinmetz A, Huet F, Chouchane M, Darmency-Stamboul V, Callier P, Thauvin-Robinet C, Faivre L, Rivière JB.

Clin Genet. 2016 Jun;89(6):700-7. doi: 10.1111/cge.12732. Epub 2016 Apr 26.


Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management.

Avila M, Dyment DA, Sagen JV, St-Onge J, Moog U, Chung BHY, Mo S, Mansour S, Albanese A, Garcia S, Martin DO, Lopez AA, Claudi T, König R, White SM, Sawyer SL, Bernstein JA, Slattery L, Jobling RK, Yoon G, Curry CJ, Merrer ML, Luyer BL, Héron D, Mathieu-Dramard M, Bitoun P, Odent S, Amiel J, Kuentz P, Thevenon J, Laville M, Reznik Y, Fagour C, Nunes ML, Delesalle D, Manouvrier S, Lascols O, Huet F, Binquet C, Faivre L, Rivière JB, Vigouroux C, Njølstad PR, Innes AM, Thauvin-Robinet C.

Clin Genet. 2016 Apr;89(4):501-506. doi: 10.1111/cge.12688. Epub 2015 Nov 27.


Heterozygous deletion of the LRFN2 gene is associated with working memory deficits.

Thevenon J, Souchay C, Seabold GK, Dygai-Cochet I, Callier P, Gay S, Corbin L, Duplomb L, Thauvin-Robinet C, Masurel-Paulet A, El Chehadeh S, Avila M, Minot D, Guedj E, Chancenotte S, Bonnet M, Lehalle D, Wang YX, Kuentz P, Huet F, Mosca-Boidron AL, Marle N, Petralia RS, Faivre L.

Eur J Hum Genet. 2016 Jun;24(6):911-8. doi: 10.1038/ejhg.2015.221. Epub 2015 Oct 21.

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