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Collezione AOU Città della Salute di Torino

  

Items : 45

Expanding the phenotypic spectrum of PROS: reclassifying isolated lateralised overgrowth. in Journal of medical genetics / J Med Genet. 2025 Mar 20;62(4):276-280. doi: 10.1136/jmg-2024-110364.
2025
AOU Città della Salute di Torino

Gazzin A; Reynolds G; Massuras S; Luca M; Coppo P; Carli D; Piglionica M; Martino S; Bagnulo R; Ferrero GB; Resta N; Mussa A;

Matching clinical and genetic data in pediatric patients at risk of developing cystic kidney disease. in Pediatric nephrology (Berlin, Germany) / Pediatr Nephrol. 2025 Mar;40(3):743-753. doi: 10.1007/s00467-024-06548-6. Epub 2024 Oct 10.
2025
AOU Città della Salute di Torino

Lonardi P; Amoroso A; Carli D; Arruga F; Migliorero M; Saglia C; Romeo CM; Luca M; Pieretti S; Camilla R; Mattozzi F; Martins VH; Del Prever GMB; Faini AC; Mioli F; Vaisitti T; Bracciamà V; Deaglio S; Peruzzi L;

Molecular and Clinical Features of Adrenocortical Tumors in Beckwith-Wiedemann Spectrum. in Cancers / Cancers (Basel). 2024 Nov 26;16(23):3967. doi: 10.3390/cancers16233967.
2024
AOU Città della Salute di Torino

Carli D; Rondot F; Luca M; Campello A; Vallero SG; Tirtei E; Gazzin A; Cardaropoli S; Montanari F; Graziano C; Quarello P; Saadat A; Sparago A; Ferrero GB; Fagioli F; Mussa A;

Functional evaluation of a novel nonsense variant of the calcium-sensing receptor gene leading to hypocalcemia. in European journal of endocrinology / Eur J Endocrinol. 2024 Mar 30;190(4):296-306. doi: 10.1093/ejendo/lvae035.
2024
AOU Città della Salute di Torino

Saglia C; Arruga F; Scolari C; Kalantari S; Albanese S; Bracciamà V; Corso Faini A; Brach Del Prever G; Luca M; Romeo C; Mioli F; Migliorero M; Tessaris D; Carli D; Amoroso A; Vaisitti T; De Sanctis L; Deaglio S;

The spectrum of heart defects in the TRAF7-related multiple congenital anomalies-intellectual disability syndrome. in Proceedings of the National Academy of Sciences of the United States of America / Proc Natl Acad Sci U S A. 2024 Mar 19;121(12):e2317601121. doi: 10.1073/pnas.2317601121. Epub 2024 M
2024
AOU Città della Salute di Torino

Pisan E; De Luca C; Brancati F; Sanchez Russo R; Li D; Bhoj E; Wenger T; Marwaha A; Johnson N; Beneteau C; Brischoux-Boucher E; Houge G; Paulsen J; Hammer TB; Ek J; Schweitzer D; Russell BE; Dutra-Clarke M; Nelson S; Douine ED; Corona RI; Dudding T; Thomson H; Low K; Belnap N; Iascone M; Priolo M; Carli D; Mussa A; et alii...

Identification of DNA methylation episignature for the intellectual developmental disorder, autosomal dominant 21 syndrome, caused by variants in the CTCF gene. in Genetics in medicine : official journal of the American College of Medical Genetics / Genet Med. 2024 Mar;26(3):101041. doi: 10.1016/j.gim.2023.101041. Epub 2023 Dec 3.
2024
AOU Città della Salute di Torino

Alders MM; Merla G; Brusco A; Trajkova S; Mussa A; Shukarova-Angelovska E; Carli D; Asaftei SD; Piccione M; Vissers L; Salzano E; Tedder ML; Gerkes EH; Zonneveld-Huijssoon E; Brooks A; Kerkhof J; McConkey H; Levy MA; Haghshenas S; Relator R; Karimi K; Mol MO; Bouman A; Sadikovic B;

DNA methylation analysis in patients with neurodevelopmental disorders improves variant interpretation and reveals complexity. in HGG advances / HGG Adv. 2024 Jul 18;5(3):100309. doi: 10.1016/j.xhgg.2024.100309. Epub 2024 May 15.
2024
AOU San Luigi di Orbassano
AOU Città della Salute di Torino

Mussa A; Banka S; Jenkinson S; Metcalfe K; Campbell CM; Sukarova-Angelovska E; Pasini B; Petlichkovski A; McConkey H; Rooney K; Rzasa J; Dimartino P; Pippucci T; Giorgio E; Rinninella A; Pullano V; Cardaropoli S; Carestiato S; Mandrile G; Palermo F; Marinoni R; Carli D; Di Gregorio E; Ferrero E; Giovenino C; Pavinato L; Rossi Sebastiano M; Trajkova S; Kerkhof J; 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...

Relevance of next generation sequencing (NGS) data re-analysis in the diagnosis of monogenic diseases leading to organ failure. in BMC medical genomics / BMC Med Genomics. 2023 Nov 27;16(1):303. doi: 10.1186/s12920-023-01747-w.
2023
ASL Città di Torino
AOU Città della Salute di Torino

Amoroso A; Carli D; Alberti C; Roccatello D; Fenoglio R; Mussa A; Calvo PL; Peruzzi L; Scolari C; Romeo CM; Luca M; Kalantari S; Brach Del Prever GM; Faini AC; Mioli F; Trotta L; Bracciamà V; Saglia C; Deaglio S; Vaisitti T;

Epidemiology of the disorders of the Pik3ca-related overgrowth spectrum (Pros). in European journal of human genetics : EJHG / Eur J Hum Genet. 2023 Nov;31(11):1333-1336. doi: 10.1038/s41431-023-01414-9. Epub 2023 Jun 26.
2023
AOU Città della Salute di Torino

Ranieri C; Resta N; Turchiano A; Bagnulo R; Piglionica M; La Selva R; Coppo P; Luca M; Gazzin A; Carli D; Cardaropoli S; Reynolds G; Mussa A;

Skewed X-chromosome inactivation in unsolved neurodevelopmental disease cases can guide re-evaluation For X-linked genes. in European journal of human genetics : EJHG / Eur J Hum Genet. 2023 Nov;31(11):1228-1236. doi: 10.1038/s41431-023-01324-w. Epub 2023 Mar 6.
2023
AOU San Luigi di Orbassano
AOU Città della Salute di Torino

Ferrero GB; Delledonne M; Rossato M; Tartaglia M; Pippucci T; De Rubeis S; Buxbaum JD; Pasini B; Mandrile G; Bruselles A; Froukh T; Dimartino P; Mussa A; Palermo F; Carli D; Battaglia A; Bertoli L; Fadda A; Rinninella A; Salmin P; Carestiato S; Sukarova-Angelovska E; Ferrero E; Brusco A; Pullano V; Cardaropoli S; Pavinato L; Trajkova S; Giovenino C; et alii...

Jansen-de Vries syndrome: Expansion of the PPM1D clinical and phenotypic spectrum in 34 families. in American journal of medical genetics. Part A / Am J Med Genet A. 2023 Jul;191(7):1900-1910. doi: 10.1002/ajmg.a.63226. Epub 2023 May 14.
2023
AOU Città della Salute di Torino

Wojcik MH; Srivastava S; Agrawal PB; Balci TB; Callewaert B; Calvo PL; Carli D; Caudle M; Colaiacovo S; Cross L; Demetriou K; Drazba K; Dutra-Clarke M; Edwards M; Genetti CA; Grange DK; Hickey SE; Isidor B; Küry S; Lachman HM; Lavillaureix A; Lyons MJ; Marcelis C; Marco EJ; Martinez-Agosto JA; Nowak C; Pizzol A; Planes M; Prijoles EJ; et alii...

Implications of an Underlying Beckwith-Wiedemann Syndrome for Wilms Tumor Treatment Strategies. in Cancers / Cancers (Basel). 2023 Feb 17;15(4):1292. doi: 10.3390/cancers15041292.
2023
AOU Città della Salute di Torino

Quarello P; Carli D; Biasoni D; Gerocarni Nappo S; Morosi C; Cotti R; Garelli E; Zucchetti G; Spadea M; Tirtei E; Spreafico F; Fagioli F;

CAPRIN1 haploinsufficiency causes a neurodevelopmental disorder with language impairment, ADHD and ASD. in Brain : a journal of neurology / Brain. 2023 Feb 13;146(2):534-548. doi: 10.1093/brain/awac278.
2023
AOU Città della Salute di Torino

Pavinato L; Delle Vedove A; Carli D; Ferrero M; Carestiato S; Howe JL; Agolini E; Coviello DA; van de Laar I; Au PYB; Di Gregorio E; Fabbiani A; Croci S; Mencarelli MA; Bruno LP; Renieri A; Veltra D; Sofocleous C; Faivre L; Mazel B; Safraou H; Denommé-Pichon AS; van Slegtenhorst MA; Giesbertz N; van Jaarsveld RH; Childers A; Rogers RC; Novelli A; De Rubeis S; et alii...

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...

Mulibrey nanism and immunological complications: a comprehensive case report and literature review. in Frontiers in immunology / Front Immunol. 2023 Dec 5;14:1303251. doi: 10.3389/fimmu.2023.1303251. eCollection 2023.
2023
AOU Città della Salute di Torino

Licciardi F; Montin D; Rosenzweig SD; Delmonte OM; Ferroni F; Carli D; Quarello P; Biasin E; Stoddard J; Niemela J; Bosticardo M; Pala F; Gazzin A; Notarangelo LD;

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. in Nature genetics / Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18.
2022
AOU Città della Salute di Torino

Fu JM; Satterstrom FK; Peng M; Brand H; Collins RL; Dong S; Wamsley B; Klei L; Wang L; Hao SP; Stevens CR; Cusick C; Babadi M; Banks E; Collins B; Dodge S; Gabriel SB; Gauthier L; Lee SK; Liang L; Ljungdahl A; Mahjani B; Sloofman L; Smirnov AN; Barbosa M; Betancur C; Brusco A; Chung BHY; Cook EH; et alii...

Clinical and molecular characterization of patients affected by Beckwith-Wiedemann spectrum conceived through assisted reproduction techniques. in Clinical genetics / Clin Genet. 2022 Oct;102(4):314-323. doi: 10.1111/cge.14193. Epub 2022 Jul 21.
2022
AOU Città della Salute di Torino

Bartuli A; Cardaropoli S; Tannorella P; Pignata L; Sparago A; Cerrato F; Macchiaiolo M; Tarani L; Sirchia F; Sara O; Uliana V; Spina J; Falco M; Prada E; Melis D; Leoni C; Milani D; Cocchi G; Operti M; Russo S; Carli D; Riccio A; Ferrero GB; Mussa A;

Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: Another piece added to the puzzle of mosaic RASopathies. in Genes, chromosomes & cancer / Genes Chromosomes Cancer. 2022 Nov;61(11):689-695. doi: 10.1002/gcc.23086. Epub 2022 Jul 16.
2022
AOU Città della Salute di Torino

Santoro F; Bertin D; Stella A; Vallero SG; Garganese A; Iacoviello M; Ranieri C; Bagnulo R; Pantaleo A; Coppo P; Cardaropoli S; Turchiano A; Mussa A; Carli D; Ferrero GB; Resta N;

Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I. in Genes, chromosomes & cancer / Genes Chromosomes Cancer. 2022 Jan;61(1):10-21. doi: 10.1002/gcc.22997. Epub 2021 Sep 3.
2022
AOU Città della Salute di Torino

Carli D; Grosso E; Soli F; Madeo S; Rocchetti LM; Bigoni S; Graziano C; Sangiorgi L; Ponti G; Garavelli L; Boschi E; Caleffi E; Martorana D; Uliana V; Riva M; Goldoni M; Pisani F; Percesepe A;

Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in Caucasians. in International journal of environmental research and public health / Int J Environ Res Public Health. 2022 Feb 20;19(4):2448. doi: 10.3390/ijerph19042448.
2022
AOU Città della Salute di Torino

Defabianis P; Mussa A; Ninivaggi R; Carli D; Romano F;

Functional analysis of TLK2 variants and their proximal interactomes implicates impaired kinase activity and chromatin maintenance defects in their pathogenesis. in Journal of medical genetics / J Med Genet. 2022 Feb;59(2):170-179. doi: 10.1136/jmedgenet-2020-107281. Epub 2020 Dec 15.
2022
AOU Città della Salute di Torino

Ferrero GB; Buxbaum JD; Dimartino P; De Rubeis S; Colson C; Ranguin K; Giuffrè M; Antona V; Radio FC; Giorgio E; Carli D; Prota V; Pippucci T; Bruselles A; Ciolfi A; Arauz-Garofalo G; Vilaseca M; Gay M; Andreoli C; Sanchiz-Calvo M; Pavinato L; Villamor-Payà M; Tartaglia M; Martinelli S; Stracker TH; Brusco A;

Overexpression of INSM1, NOTCH1, NEUROD1, and YAP1 genes is associated with adverse clinical outcome in pediatric neuroblastoma. in Virchows Archiv : an international journal of pathology / Virchows Arch. 2022 Dec;481(6):925-933. doi: 10.1007/s00428-022-03406-4. Epub 2022 Sep 19.
2022
AOU Città della Salute di Torino

Volante M; Fagioli F; Carli D; Bianchi M; Orlando G; Tampieri C; Bertero L; Osella-Abate S; Napoli F; Metovic J; Papotti M;

Successful treatment with MEK-inhibitor in a patient with NRAS-related cutaneous skeletal hypophosphatemia syndrome. in Genes, chromosomes & cancer / Genes Chromosomes Cancer. 2022 Dec;61(12):740-746. doi: 10.1002/gcc.23092. Epub 2022 Sep 19.
2022
AOU Città della Salute di Torino

Medico E; Brusco A; Ramenghi U; Palumbo M; Pullano V; Lepri FR; Cesario C; La Selva R; Coppo P; Tessaris D; Cardaropoli S; Carli D; De Sanctis L; Ferrero GB; Mussa A;

Mosaic RASopathies: A review of disorders caused by somatic pathogenic variants in the genes of the RAS/MAPK pathway. in American journal of medical genetics. Part C, Seminars in medical genetics / Am J Med Genet C Semin Med Genet. 2022 Dec;190(4):520-529. doi: 10.1002/ajmg.c.32021. Epub 2022 Dec
2022
AOU Città della Salute di Torino

Carli D; Resta N; Ferrero GB; Ruggieri M; Mussa A;

Wilms tumour occurring in a patient with osteopathia striata with cranial sclerosis: A still unsolved biological question. in Pediatric blood & cancer / Pediatr Blood Cancer. 2021 Sep;68(9):e29132. doi: 10.1002/pbc.29132. Epub 2021 May 24.
2021
AOU Città della Salute di Torino

Spadea M; Mussa A; Brusco A; Ferrero GB; Sirchia F; Giorgio E; Carli D; Perotti D; Quarello P; Ciceri S; Spreafico F; Fagioli F;

Correspondence on "Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities," by Carmignac et al. in Genetics in medicine : official journal of the American College of Medical Genetics / Genet Med. 2021 Nov;23(11):2223-2224. doi: 10.1038/s41436-021-01256-0. Epub 2021 Jul 7.
2021
AOU Città della Salute di Torino

Mussa A; Carli D; Rossi K; Lepore Signorile M; Piglionica M; Ranieri C; Simone C; Lugli L; Grossi V; Resta N; Calabrese O;

Kaposiform hemangioendothelioma further broadens the phenotype of PIK3CA-related overgrowth spectrum. in Clinical genetics / Clin Genet. 2021 Nov;100(5):624-627. doi: 10.1111/cge.14047. Epub 2021 Aug 23.
2021
AOU Città della Salute di Torino

Resta N; Ferrero GB; Fagioli F; Cardaropoli S; Ranieri C; Santoro F; La Selva R; Francia di Celle P; Coppo P; Manicone R; Kalantari S; Carli D; Mussa A;

Bowel loop sign in a newborn. in Archives of disease in childhood. Fetal and neonatal edition / Arch Dis Child Fetal Neonatal Ed. 2021 May;106(3):1-2. doi: 10.1136/archdischild-2020-318939. Epub 2
2021
AOU Città della Salute di Torino

Suteu L; Carli D; Cortese MG; Schleef J; Guanà R; Garofalo S; Ferrero GB; Gennari F;

A new case of Smith-Kingsmore syndrome with somatic MTOR pathogenic variant expands the phenotypic spectrum to lateralized overgrowth. in Clinical genetics / Clin Genet. 2021 May;99(5):719-723. doi: 10.1111/cge.13931. Epub 2021 Feb 8.
2021
AOU Città della Salute di Torino

Resta N; Iacoviello M; Ranieri C; Cardaropoli S; Zinali F; La Selva R; Coppo P; Fusillo A; Ferrero GB; Carli D; Mussa A;

Evolution over Time of Leg Length Discrepancy in Patients with Syndromic and Isolated Lateralized Overgrowth. in The Journal of pediatrics / J Pediatr. 2021 Jul;234:123-127. doi: 10.1016/j.jpeds.2021.01.020. Epub 2021 Jan 16.
2021
AOU Città della Salute di Torino

Mussa A; Ferrero GB; Andreacchio A; Resta N; Marcucci L; Cardaropoli S; Cravino M; Spolaore S; Zinali F; Paonessa M; Carli D; De Pellegrin M; Franceschi L;

Clinical spectrum and follow-up in six individuals with Lamb-Shaffer syndrome (SOX5). in American journal of medical genetics. Part A / Am J Med Genet A. 2021 Feb;185(2):608-613. doi: 10.1002/ajmg.a.62001. Epub 2020 Dec 9.
2021
AOU Città della Salute di Torino

Romano C; Ferrero GB; Galesi O; Giorgio E; Magini P; Carli D; Greco D; Innella G; Brusco A; Graziano C;

Lateralized and Segmental Overgrowth in Children. in Cancers / Cancers (Basel). 2021 Dec 7;13(24):6166. doi: 10.3390/cancers13246166.
2021
AOU Città della Salute di Torino

Mussa A; Carli D; Cardaropoli S; Ferrero GB; Resta N;

2021
AOU Città della Salute di Torino

Mussa A; Carli D; Giorgio E; Villar AM; Cardaropoli S; Carbonara C; Campagnoli MF; Galletto P; Palumbo M; Olivieri S; Isella C; Andelfinger G; Tartaglia M; Botta G; Brusco A; Medico E; Ferrero GB;

New Insights into Potocki-Shaffer Syndrome: Report of Two Novel Cases and Literature Review. in Brain sciences / Brain Sci. 2020 Oct 28;10(11):788. doi: 10.3390/brainsci10110788.
2020
AOU Città della Salute di Torino

Trajkova S; Di Gregorio E; Ferrero GB; Carli D; Pavinato L; Delplancq G; Kuentz P; Brusco A;

Esophageal duplication cyst in newborn. in Pediatrics and neonatology / Pediatr Neonatol. 2020 Feb;61(1):121-122. doi: 10.1016/j.pedneo.2019.08.007. Epub 2019 Sep 5.
2020
AOU Città della Salute di Torino

Ferrero GB; Carli D; Cortese MG; Suteu L; Guanà R; Schleef J; Garofalo S; Gennari F;

Chronic subdural hematoma: A previously unreported life-threatening complication in adult with Sotos syndrome. in American journal of medical genetics. Part A / Am J Med Genet A. 2020 Dec;182(12):3052-3055. doi: 10.1002/ajmg.a.61900. Epub 2020 Oct 14.
2020
AOU Città della Salute di Torino

Ferrero GB; Mussa A; Bongioanni MR; Bergui M; Gazzin A; Carli D;

NBAS pathogenic variants: Defining the associated clinical and facial phenotype and genotype-phenotype correlations. in Human mutation / Hum Mutat. 2019 Jun;40(6):721-728. doi: 10.1002/humu.23734. Epub 2019 Mar 18.
2019
AOU Città della Salute di Torino

Carli D; Giorgio E; Pantaleoni F; Bruselles A; Barresi S; Riberi E; Licciardi F; Gazzin A; Baldassarre G; Pizzi S; Niceta M; Radio FC; Molinatto C; Montin D; Calvo PL; Ciolfi A; Fleischer N; Ferrero GB; Brusco A; Tartaglia M;

2019
AOU Città della Salute di Torino

Mussa A; Ciuffreda VP; Sauro P; Pagliardini V; Pagliardini S; Carli D; Kalish JM; Fagioli F; Pavanello E; Ferrero GB;

Defining an optimal time window to screen for hepatoblastoma in children with Beckwith-Wiedemann syndrome. in Pediatric blood & cancer / Pediatr Blood Cancer. 2019 Jan;66(1):e27492. doi: 10.1002/pbc.27492. Epub 2018 Sep 30.
2019
AOU Città della Salute di Torino

Ferrero GB; Carli D; Duffy KA; Mussa A; Kalish JM; Mussa A; Duffy KA; Carli D; Ferrero GB; Kalish JM;

Transcription alterations of KCNQ1 associated with imprinted methylation defects in the Beckwith-Wiedemann locus. in Genetics in medicine : official journal of the American College of Medical Genetics / Genet Med. 2019 Aug;21(8):1808-1820. doi: 10.1038/s41436-018-0416-7. Epub 2019 Jan 12.
2019
AOU Città della Salute di Torino

Williams CA; Ferrero GB; Bliek J; Acurzio B; Gabbarini F; Gazzin A; Mussa A; Angelini C; Carli D; Franzese M; Pignata L; Alders M; Frints SGM; Maas SM; Hill-Harfe K; Freschi A; Sparago A; Valente FM; Riccio A; Cerrato F;

Assisted reproduction techniques and prenatal diagnosis of Beckwith-Wiedemann spectrum presenting with omphalocele. in Journal of assisted reproduction and genetics / J Assist Reprod Genet. 2018 Oct;35(10):1925-1926. doi: 10.1007/s10815-018-1288-0. Epub 2018 Aug 8.
2018
AOU Città della Salute di Torino

Mussa A; Carli D; Cardaropoli S; Molinatto C; Ferrero GB; Mussa A; Carli D; Cardaropoli S; Molinatto C; Ferrero GB;

2017
AOU Città della Salute di Torino

Bonatti F; Adorni A; Matichecchia A; Mozzoni P; Uliana V; Pisani F; Garavelli L; Graziano C; Gnoli M; Carli D; Bigoni S; Boschi E; Martorana D; Percesepe A;

2017
AO Cuneo
AOU San Luigi di Orbassano
AOU Città della Salute di Torino

De Rubeis S; Pasini B; Grosso E; Buxbaum JD; Cirillo Silengo M; Provero P; De Marchi M; Restagno G; Pelle A; Giachino DF; Savin E; Gandione M; Brussino A; Ferrero M; Mancini C; Giorgio E; Cavalieri S; Talarico F; Pappi P; Zacchetti G; Zonta A; Ungari S; Sirchia F; Sorasio L; Naretto VG; Maffè A; Arduino C; Mandrile G; Keller R; et alii...

Assisted Reproductive Techniques and Risk of Beckwith-Wiedemann Syndrome. in Pediatrics / Pediatrics. 2017 Jul;140(1):e20164311. doi: 10.1542/peds.2016-4311. Epub 2017 Jun 20.
2017
AOU Città della Salute di Torino

Mussa A; Molinatto C; Cerrato F; Palumbo O; Carella M; Baldassarre G; Carli D; Peris C; Riccio A; Ferrero GB; Mussa A; Molinatto C; Cerrato F; Palumbo O; Carella M; Baldassarre G; Carli D; Peris C; Riccio A; Ferrero GB;