Export 1075 results:
Autore [ Titolo(Asc)] Tipo Anno
Filtri: First Letter Of Last Name è G  [Clear All Filters]
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
V
Pascazio L, Bembich S, Nardone IB, Vecchiet C, Guarino G, Clarici A. Validation of the Italian translation of the affective neuroscience personality scales. Psychol Rep 2015;116(1):97-115.
U
Lenarduzzi S, Vozzi D, Morgan A, Rubinato E, D'Eustacchio A, Osland TM, Rossi C, Graziano C, Castorina P, Ambrosetti U, Morgutti M, Girotto G. Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis. Hear Res 2015;320:18-23.
Lenarduzzi S, Vozzi D, Morgan A, Rubinato E, D'Eustacchio A, Osland TM, Rossi C, Graziano C, Castorina P, Ambrosetti U, Morgutti M, Girotto G. Usher syndrome: an effective sequencing approach to establish a genetic and clinical diagnosis. Hear Res 2015;320:18-23.
Floridia M, Ravizza M, Guaraldi G, Pinnetti C, Martinelli P, Tamburrini E. Use of specific antiretroviral regimens among HIV-infected women in Italy at time of conception: 2001-2011. AIDS Patient Care STDS 2012;26(8):439-43.
Crocco S, Martelossi S, Giurici N, Villanacci V, Ventura A. Upper gastrointestinal involvement in paediatric onset Crohn's disease: prevalence and clinical implications. J Crohns Colitis 2012;6(1):51-5.
Robino A, Mezzavilla M, Pirastu N, La Bianca M, Gasparini P, Carlino D, Tepper BJ. Understanding the role of personality and alexithymia in food preferences and PROP taste perception. Physiol Behav 2016;157:72-8.
Frassanito L, Zanfini BA, Pitoni S, Germini P, Del Vicario M, Draisci G. Ultrasound-guided genitofemoral nerve block for inguinal hernia repair in the male adult: a randomized controlled pilot study. Minerva Anestesiol 2018;84(2):189-195.
T
Bianco AMonica, Faletra F, Vozzi D, Girardelli M, Knowles A, Tommasini A, Zauli G, Marcuzzi A. Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Mol Med Rep 2015;12(4):6128-32.
Athanasakis E, Fabretto A, Faletra F, Mocenigo M, Morgan A, Gasparini P. Two Novel COH1 Mutations in an Italian Patient with Cohen Syndrome. Mol Syndromol 2012;3(1):30-33.
Pastore S, Gortani G, Maschio M, Di Leo G, Ventura A. Two lumens, one diagnosis. J Pediatr 2011;159(3):511.
Fabretto A, Kutsche K, Harmsen M-B, Demarini S, Gasparini P, Fertz MCristina, Zenker M. Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I. Eur J Med Genet 2010;53(5):322-4.
da Silva RCelerino, Coelho AVictor Cam, Arraes LClaudio, Brandão LAndré Cav, Crovella S, Guimarães RLima. TRIM5 gene polymorphisms in HIV-1-infected patients and healthy controls from Northeastern Brazil. Immunol Res 2016;

Amministrazione Trasparente