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CAPPUCCIO G
Collezione AOU Città della Salute di Torino

Items : 6

Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration. in Nature communications / Nat Commun. 2025 Mar 12;16(1):2479. doi: 10.1038/s41467-025-56628-w.

2025
AOU Città della Salute di Torino

Groeneweg S; van Geest FS; Martín M; Dias M; Frazer J; Medina-Gomez C; Sterenborg RBTM; Wang H; Dolcetta-Capuzzo A; de Rooij LJ; Teumer A; Abaci A; van den Akker ELT; Ambegaonkar GP; Armour CM; Bacos I; Bakhtiani P; Barca D; Bauer AJ; van den Berg SAA; van den Berge A; Bertini E; van Beynum IM; Brunetti-Pierri N; Brunner D; Cappa M; Cappuccio G; Castellotti B; Castiglioni C; et alii...

Blepharophimosis with intellectual disability and Helsmoortel-Van Der Aa Syndrome share episignature and phenotype. in American journal of medical genetics. Part C, Seminars in medical genetics / Am J Med Genet C Semin Med Genet. 2024 Dec;196(4):e32089. doi: 10.1002/ajmg.c.32089. Epub 2024 Jun 1

2024
AOU Città della Salute di Torino

Sousa SB; Kini U; Oliveira D; Zollino M; Metcalfe K; Yamamoto T; Bourgois A; Perrin L; Vincent-Devulder A; Weber S; Faivre L; Vitobello A; Ciaccio C; D'Arrigo S; Hennekam RCM; Henneman P; Alders M; Skinner C; Tedder ML; McConkey H; Kerkhof J; Relator R; Levy MA; Brusco A; Carli D; Reilly J; Trajkova S; Sarli C; van der Laan L; et alii...

Genotypes and phenotypes heterogeneity in PIK3CA-related overgrowth spectrum and overlapping conditions: 150 novel patients and systematic review of 1007 patients with PIK3CA pathogenetic variants. in Journal of medical genetics / J Med Genet. 2023 Feb;60(2):163-173. doi: 10.1136/jmedgenet-2021-108093. Epub 2022 Mar 7.

2023
AOU Città della Salute di Torino

Di Giacomo MC; Cereda A; Capurso M; Piscopo C; Accadia M; Morando C; Della Monica M; Memo L; Novelli C; Garavelli L; Cappuccio G; Onesimo R; Zampino G; Selicorni A; Forleo C; Bukvic N; Susca FC; De Luisi A; Piglionica M; Loconte DC; Turchiano A; Maitz S; Melis D; Bartuli A; Ferrero GB; Bagnulo R; Buonuomo PS; Pantaleo A; Ranieri C; et alii...

Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study. in The Journal of clinical endocrinology and metabolism / J Clin Endocrinol Metab. 2022 Feb 17;107(3):e1136-e1147. doi: 10.1210/clinem/dgab750.

2022
AOU Città della Salute di Torino

van Geest FS; Groeneweg S; van den Akker ELT; Bacos I; Barca D; van den Berg SAA; Bertini E; Brunner D; Brunetti-Pierri N; Cappa M; Cappuccio G; Chatterjee K; Chesover AD; Christian P; Coutant R; Craiu D; Crock P; Dewey C; Dica A; Dimitri P; Dubey R; Enderli A; Fairchild J; Gallichan J; Garibaldi LR; George B; Hackenberg A; Heinrich B; Huynh T; et alii...

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy. in American journal of human genetics / Am J Hum Genet. 2021 May 6;108(5):857-873. doi: 10.1016/j.ajhg.2021.04.001.

2021
AOU Città della Salute di Torino

Voisin N; Schnur RE; Douzgou S; Hiatt SM; Rustad CF; Brown NJ; Earl DL; Keren B; Levchenko O; Geuer S; Verheyen S; Johnson D; Zarate YA; Han?árová M; Amor DJ; Bebin EM; Blatterer J; Brusco A; Cappuccio G; Charrow J; Chatron N; Cooper GM; Courtin T; Dadali E; Delafontaine J; Del Giudice E; Doco M; Douglas G; Eisenkölbl A; et alii...

Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study. in The lancet. Diabetes & endocrinology / Lancet Diabetes Endocrinol. 2020 Jul;8(7):594-605. doi: 10.1016/S2213-8587(20)30153-4.

2020
AOU Città della Salute di Torino

Groeneweg S; van Geest FS; Abac? A; Alcantud A; Ambegaonkar GP; Armour CM; Bakhtiani P; Barca D; Bertini ES; van Beynum IM; Brunetti-Pierri N; Bugiani M; Cappa M; Cappuccio G; Castellotti B; Castiglioni C; Chatterjee K; de Coo IFM; Coutant R; Craiu D; Crock P; DeGoede C; Demir K; Dica A; Dimitri P; Dolcetta-Capuzzo A; Dremmen MHG; Dubey R; Enderli A; et alii...