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APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases.
PLoS Med. 2017 Mar 28;14(3):e1002270. doi: 10.1371/journal.pmed.1002270. eCollection 2017 Mar.
PLoS Med. 2017.
PMID: 28350801
Free PMC article.
Assessment of Mendelian and risk-factor genes in Alzheimer disease: A prospective nationwide clinical utility study and recommendations for genetic screening.
Nicolas G, Zaréa A, Lacour M, Quenez O, Rousseau S, Richard AC, Bonnevalle A, Schramm C, Olaso R, Sandron F, Boland A, Deleuze JF, Andriuta D, Anthony P, Auriacombe S, Balageas AC, Ballan G, Barbay M, Béjot Y, Belliard S, Benaiteau M, Bennys K, Bombois S, Boutoleau-Bretonnière C, Branger P, Carlier J, Cartz-Piver L, Cassagnaud P, Ceccaldi MP, Chauviré V, Chen Y, Cogez J, Cognat E, Contegal-Callier F, Corneille L, Couratier P, Cretin B, Crinquette C, Dauriat B, Dautricourt S, de la Sayette V, de Liège A, Deffond D, Demurger F, Deramecourt V, Derollez C, Dionet E, Doco Fenzy M, Dumurgier J, Dutray A, Etcharry-Bouyx F, Formaglio M, Gabelle A, Gainche-Salmon A, Godefroy O, Graber M, Gregoire C, Grimaldi S, Gueniat J, Gueriot C, Guillet-Pichon V, Haffen S, Hanta CR, Hardy C, Hautecloque G, Heitz C, Hourregue C, Jonveaux T, Jurici S, Koric L, Krolak-Salmon P, Lagarde J, Lanoiselée HM, Laurens B, Le Ber I, Le Guyader G, Leblanc A, Lebouvier T, Levy R, Lippi A, Mackowiak MA, Magnin E, Marelli C, Martinaud O, Maureille A, Migliaccio R, Milongo-Rigal E, Mohr S, Mollion H, Morin A, Nivelle J, Noiray C, Olivieri P, Paquet C, Pariente J, Pasquier F, Perron A, Philippi N, Planche V, Pouc…
See abstract for full author list ➔
Nicolas G, et al. Among authors: lanoiselee hm.
Genet Med. 2024 May;26(5):101082. doi: 10.1016/j.gim.2024.101082. Epub 2024 Jan 24.
Genet Med. 2024.
PMID: 38281098
Free article.
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Familial autoimmunity in neurological patients with GAD65 antibodies: an interview-based study.
Muñiz-Castrillo S, Vogrig A, Montagnac C, Joubert B, Benaiteau M, Casez O, Chaumont H, Hopes L, Lanoiselée HM, Navarro V, Thomas B, Ursu R, Gonçalves D, Fabien N, Ducray F, Julier C, Honnorat J.
Muñiz-Castrillo S, et al. Among authors: lanoiselee hm.
J Neurol. 2021 Jul;268(7):2515-2522. doi: 10.1007/s00415-021-10424-w. Epub 2021 Feb 5.
J Neurol. 2021.
PMID: 33544221
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Immunopathogenesis and proposed clinical score for identifying Kelch-like protein-11 encephalitis.
Vogrig A, Péricart S, Pinto AL, Rogemond V, Muñiz-Castrillo S, Picard G, Selton M, Mittelbronn M, Lanoiselée HM, Michenet P, Benaiteau M, Pariente J, Zéphir H, Giordana C, Montaut S, Salhi H, Bachoumas P, Montcuquet A, Letovanec I, Uro-Coste E, Honnorat J.
Vogrig A, et al. Among authors: lanoiselee hm.
Brain Commun. 2021 Aug 26;3(3):fcab185. doi: 10.1093/braincomms/fcab185. eCollection 2021.
Brain Commun. 2021.
PMID: 34557666
Free PMC article.
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Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes.
Schramm C, Charbonnier C, Zaréa A, Lacour M, Wallon D; CNRMAJ collaborators; Boland A, Deleuze JF, Olaso R; ADES consortium; Alarcon F, Campion D, Nuel G, Nicolas G.
Schramm C, et al.
Genome Med. 2022 Jun 28;14(1):69. doi: 10.1186/s13073-022-01070-6.
Genome Med. 2022.
PMID: 35761418
Free PMC article.
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Are c.436G>A mutations less severe forms of Lafora disease? A case report.
Lanoiselée HM, Genton P, Lesca G, Brault F, De Toffol B.
Lanoiselée HM, et al.
Epilepsy Behav Case Rep. 2014 Jan 19;2:19-21. doi: 10.1016/j.ebcr.2013.11.003. eCollection 2014.
Epilepsy Behav Case Rep. 2014.
PMID: 25667860
Free PMC article.
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