Hahn V - Search Results

1

Expanding the Spectrum of Genes Involved in Huntington Disease Using a Combined Clinical and Genetic Approach.

Mariani LL, Tesson C, Charles P, Cazeneuve C, Hahn V, Youssov K, Freeman L, Grabli D, Roze E, Noël S, Peuvion JN, Bachoud-Levi AC, Brice A, Stevanin G, Durr A. Mariani LL, et al. Among authors: hahn v. JAMA Neurol. 2016 Sep 1;73(9):1105-14. doi: 10.1001/jamaneurol.2016.2215. JAMA Neurol. 2016. PMID: 27400454

2

Diagnosis of "sporadic" Huntington's disease.

Dürr A, Dodé C, Hahn V, Pêcheux C, Pillon B, Feingold J, Kaplan JC, Agid Y, Brice A. Dürr A, et al. Among authors: hahn v. J Neurol Sci. 1995 Mar;129(1):51-5. doi: 10.1016/0022-510x(94)00250-r. J Neurol Sci. 1995. PMID: 7751845

3

[Asymptomatic "child" of the parent affected by Huntington disease].

Dürr A, Gargiulo M, Prouvost B, Lahlou K, Lagroua I, Hahn V, Feingoud J. Dürr A, et al. Among authors: hahn v. Encephale. 2000 Apr;26 Spec No 3:34-5. Encephale. 2000. PMID: 10858930 French. No abstract available.

4

Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease.

Jacquemont ML, Campion D, Hahn V, Tallaksen C, Frebourg T, Brice A, Durr A. Jacquemont ML, et al. Among authors: hahn v. J Med Genet. 2002 Feb;39(2):E2. doi: 10.1136/jmg.39.2.e2. J Med Genet. 2002. PMID: 11836371 Free PMC article. No abstract available.

5

Mutation in the catalytic domain of protein kinase C gamma and extension of the phenotype associated with spinocerebellar ataxia type 14.

Stevanin G, Hahn V, Lohmann E, Bouslam N, Gouttard M, Soumphonphakdy C, Welter ML, Ollagnon-Roman E, Lemainque A, Ruberg M, Brice A, Durr A. Stevanin G, et al. Among authors: hahn v. Arch Neurol. 2004 Aug;61(8):1242-8. doi: 10.1001/archneur.61.8.1242. Arch Neurol. 2004. PMID: 15313841

6

Personality and Neuropsychological Profiles in Friedreich Ataxia.

Sayah S, Rotgé JY, Francisque H, Gargiulo M, Czernecki V, Justo D, Lahlou-Laforet K, Hahn V, Pandolfo M, Pelissolo A, Fossati P, Durr A. Sayah S, et al. Among authors: hahn v. Cerebellum. 2018 Apr;17(2):204-212. doi: 10.1007/s12311-017-0890-5. Cerebellum. 2018. PMID: 29086357

7

Huntington's Disease with Small CAG Repeat Expansions.

Heinzmann A, Sayah S, Lejeune FX, Hahn V, Teichmann M, Monin ML, Marchionni E, Gérard F, Charles P, Pariente J, Durr A. Heinzmann A, et al. Among authors: hahn v. Mov Disord. 2023 Jul;38(7):1294-1306. doi: 10.1002/mds.29427. Epub 2023 Jun 8. Mov Disord. 2023. PMID: 37288993

8

Lateral Temporal Lobe: An Early Imaging Marker of the Presymptomatic GRN Disease?

Caroppo P, Habert MO, Durrleman S, Funkiewiez A, Perlbarg V, Hahn V, Bertin H, Gaubert M, Routier A, Hannequin D, Deramecourt V, Pasquier F, Rivaud-Pechoux S, Vercelletto M, Edouart G, Valabregue R, Lejeune P, Didic M, Corvol JC, Benali H, Lehericy S, Dubois B, Colliot O, Brice A, Le Ber I; Predict-PGRN study group. Caroppo P, et al. Among authors: hahn v. J Alzheimers Dis. 2015;47(3):751-9. doi: 10.3233/JAD-150270. J Alzheimers Dis. 2015. PMID: 26401709 Free PMC article.

9

Executive and social-cognitive determinants of environmental dependency syndrome in behavioral frontotemporal dementia.

Flanagan EC, Lagarde J, Hahn V, Guichart-Gomez E, Sarazin M, Hornberger M, Bertoux M. Flanagan EC, et al. Among authors: hahn v. Neuropsychology. 2018 May;32(4):377-384. doi: 10.1037/neu0000433. Neuropsychology. 2018. PMID: 29809029

10

Characterization of the initial complaint and care pathways prior to diagnosis in very young sporadic Alzheimer's disease.

Olivieri P, Hamelin L, Lagarde J, Hahn V, Guichart-Gomez E, Roué-Jagot C, Sarazin M. Olivieri P, et al. Among authors: hahn v. Alzheimers Res Ther. 2021 Apr 29;13(1):90. doi: 10.1186/s13195-021-00829-0. Alzheimers Res Ther. 2021. PMID: 33926533 Free PMC article.

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