Export 46 results:
Autore Titolo Tipo [ Anno(Desc)]
Filtri: First Letter Of Title è H  [Clear All Filters]
2010
Bua J, Marchetti F, Faleschini E, Ventura A, Bussani R. Hepatic glycogenosis in an adolescent with diabetes. J Pediatr 2010;157(6):1042.
Carréra MCampos, Moura P, Crovella S, de Souza PRoberto El, de Alencar LCláudio A, Sarinho E. High polymorphism of the MBL2 gene in patients with atopic dermatitis. Ann Allergy Asthma Immunol 2010;105(1):39-42.
Padovan L, Segat L, Pontillo A, Antcheva N, Tossi A, Crovella S. Histatins in non-human primates: gene variations and functional effects. Protein Pept Lett 2010;17(7):909-18.
Segat L, Catamo E, Fabris A, Morgutti M, D'Agaro P, Campello C, Crovella S. HLA-G*0105N allele is associated with augmented risk for HIV infection in white female patients. AIDS 2010;24(12):1961-4.
Davanzo R, Giurici N, Demarini S. Hot water and preparation of infant formula: how hot does it have to be to be safe?. J Pediatr Gastroenterol Nutr 2010;50(3):352-3.
de Mendonça VGuimarães, Guimarães MJosé Beze, Filho JLuiz de Li, de Mendonça CGuimarães, Martins DBruneska G, Crovella S, de Alencar LCláudio A. [Human papillomavirus cervical infection: viral genotyping and risk factors for high-grade squamous intraepithelial lesion and cervix cancer]. Rev Bras Ginecol Obstet 2010;32(10):476-85.
2011
Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, d'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P. Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. J Med Genet 2011;48(6):369-74.
Tanaka N, Izawa K, Saito MK, Sakuma M, Oshima K, Ohara O, Nishikomori R, Morimoto T, Kambe N, Goldbach-Mansky R, Aksentijevich I, Basile Gde Saint, Neven B, van Gijn M, Frenkel J, Aróstegui JI, Yagüe J, Merino R, Ibañez M, Pontillo A, Takada H, Imagawa T, Kawai T, Yasumi T, Nakahata T, Heike T. High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. Arthritis Rheum 2011;63(11):3625-32.
Comar M, Bonifacio D, Zanconati F, Di Napoli M, Isidoro E, Martini F, Torelli L, Tognon M. High prevalence of BK polyomavirus sequences in human papillomavirus-16-positive precancerous cervical lesions. J Med Virol 2011;83(10):1770-6.
Bortot B, Athanasakis E, Brun F, Rizzotti D, Mestroni L, Sinagra G, Severini GMaria. High-throughput genotyping robot-assisted method for mutation detection in patients with hypertrophic cardiomyopathy. Diagn Mol Pathol 2011;20(3):175-9.
Fabris A, Segat L, Catamo E, Morgutti M, Vendramin A, Crovella S. HLA-G 14 bp deletion/insertion polymorphism in celiac disease. Am J Gastroenterol 2011;106(1):139-44.
Abu-Amero KK, Faletra F, Gasparini P, Parentin F, Pensiero S, Alorainy IA, Hellani AM, Catalano D, Bosley TM. Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations. Ophthalmic Genet 2011;32(4):212-6.

Amministrazione Trasparente