| | Title | Authors / Editors | Date |
|
unige:156579 |
Cancer predisposition syndromes as a risk factor for early second primary neoplasms after childhood cancer - A national cohort study |
Waespe, Nicolas; Belle, Fabiën; Redmond, Shelagh; Schindera, Christina; ... Kuehni, Claudia E |
2021 |
|
unige:156600 |
Deciphering the natural history of SCA7 in children |
Bah, M G; Rodriguez, D; Cazeneuve, C; Mochel, F; ... Mignot, C |
2020 |
|
unige:145886 |
Usefulness of genetic testing in sudden cardiac arrest survivors with or without previous clinical evidence of heart disease |
Asatryan, Babken; Schaller, André; Seiler, Jens; Servatius, Helge; ... Medeiros-Domingo, Argelia |
2019 |
|
unige:146004 |
The spectrum of intermediate SCN8A-related epilepsy |
Johannesen, Katrine M; Gardella, Elena; Encinas, Alejandra C; Lehesjoki, Anna-Elina; ... Møller, Rikke S |
2019 |
|
unige:143481 |
A rare cause of a cholestatic jaundice in a north african teenager |
Schreiner, Philipp; Stieger, Bruno; Mclin, Valérie Anne; Rougemont-Pidoux, Anne-Laure; ... Müllhaupt, Beat |
2019 |
|
unige:137980 |
Tests préimplantatoires de l’embryon en médecine de reproduction |
Benard, Julie Gabrielle Anne; Targa Barrera, Célia; Murisier, Fabien; Giacobino, Ariane; Streuli, Isabelle |
2019 |
|
unige:115121 |
Mutational epidemiology of congenital fibrinogen disorders |
Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite |
2018 |
|
unige:138158 |
A genomic screen for angiosuppressor genes in the tumor endothelium identifies a multifaceted angiostatic role for bromodomain containing 7 (BRD7) |
van Beijnum, Judy R; Nowak-Sliwinska, Patrycja; van Berkel, Maaike; Wong, Tse J; Griffioen, Arjan W |
2017 |
|
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: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:45205 |
Identification of VPS35 mutations replicated in French families with Parkinson disease |
Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A |
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: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:21243 |
Marked hemiatrophy in carriers of Duchenne muscular dystrophy |
Rajakulendran, Sanjeev; Kuntzer, Thierry; Dunand, Murielle; Yau, Shu C.; ... Hanna, Michael G. |
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 |
Genetic testing
add all
remove all
