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	Title	Authors / Editors	Date
unige:94830	Genetic Counseling and Testing for Alzheimer's Disease and Frontotemporal Lobar Degeneration: An Italian Consensus Protocol	Bocchetta, Martina; Mega, Anna; Bernardi, Livia; Di Maria, Emilio; ... Bruni, Amalia C	2016
unige:45205	Identification of VPS35 mutations replicated in French families with Parkinson disease	Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A	2012
unige:32314	Identification of a novel F11 missense mutation (Ile463Ser) in a family with congenital factor XI deficiency	Tirefort, Yordanka; Uhr, Mario R; Neerman Arbez, Marguerite; De Moerloose, Philippe	2012
unige:31843	Les tests génétiques peuvent-ils être utiles pour la prévention cardiovasculaire ?	Bochud, Murielle; Fellmann, Florence; Guessous, Idris	2012
unige:32728	A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family	Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite	2011
unige:23474	Early Event-Related Cortical Activity Originating in the Frontal Eye Fields and Inferior Parietal Lobe Predicts the Occurrence of Correct and Error Saccades	Ptak, Radek; Camen, Christian; Morand, Stéphanie; Schnider, Armin	2011
unige:21243	Marked hemiatrophy in carriers of Duchenne muscular dystrophy	Rajakulendran, Sanjeev; Kuntzer, Thierry; Dunand, Murielle; Yau, Shu C.; ... Hanna, Michael G.	2010
unige:11651	Telomere length is not predictive of dementia or MCI conversion in the oldest old	Zekry Berger, Dina Selma; Herrmann, François; Irminger-Finger, Irmgard; Ortolan, Laura; ... Krause, Karl-Heinz	2010
unige:114066	The CST3 B haplotype is associated with frontotemporal lobar degeneration	Benussi, L; Ghidoni, R; Galimberti, D; Boccardi, Marina; ... Binetti, G	2010
unige:19536	Inferior vena cava agenesis: Association with bilateral lower-limb deep vein thrombosis in young males	Guanella, Raphaël; Glauser, Frédéric; Bounameaux, Henri; Mazzolai, Lucia	2009
unige:45179	Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms	Ibáñez, Pablo; Lesage, Suzanne; Janin, Sabine; Lohmann, Ebba; ... Brice, Alexis	2009
unige:19928	A multidisciplinary study of patients with early-onset PD with and without parkin mutations	Lohmann, E.; Thobois, S.; Lesage, S.; Broussolle, E.; ... Brice, A.	2009
unige:19175	Are parkin patients particularly suited for deep-brain stimulation?	Lohmann, Ebba; Welter, Marie-Laure; Fraix, Valerie; Krack, Paul; ... Brice, Alexis	2008
unige:114072	Effect of the XbaI polymorphism of estrogen receptor alpha on postmenopausal gray matter	Boccardi, Marina; Scassellati, Catia; Ghidoni, Roberta; Testa, Cristina; ... Frisoni, Giovanni	2008
unige:8702	MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother	Dayer, Alexandre; Bottani, Armand; Bouchardy, Isabelle; Fluss, Joel Victor; ... Morris, Michael Andréw	2007
unige:33304	Do allelic variants of the connexin37 1019 gene polymorphism differentially predict for coronary artery disease and myocardial infarction?	Wong Christen, Cindy Wai Yin; Christen, Thomas; Pfenniger, Anna; James, Richard William; Kwak, Brenda	2007
unige:9174	L'apport de la génétique moléculaire en cardiologie clinique : l'exemple de la cardiomyopathie hypertrophique	Fokstuen, Siv; Blouin, Jean-Louis; Lyle, Robert; Lerch, René; ... Sigwart, Ulrich	2005
unige:92718	Primary care physicians' knowledge and attitudes towards genetic testing for breast-ovarian cancer predisposition	Escher, Monica; Sappino, Pascal	2000
unige:72956	Le cancer colo-rectal héréditaire sans polyadénomatose associée	Pocard, M; Soravia, Claudio	1999
unige:9205	Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene	Hutter, P.; Antonarakis, Stylianos; Delozier-Blanchet, C. D.; Morris, Michael Andréw	1994

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