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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 2
1999 1
2002 2
2003 1
2004 2
2005 1
2006 2
2007 3
2008 3
2011 1
2012 1
2013 1
2014 1
2015 1
2022 0
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19 results
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Page 1
Parkinson's disease with camptocormia.
Bloch F, Houeto JL, Tezenas du Montcel S, Bonneville F, Etchepare F, Welter ML, Rivaud-Pechoux S, Hahn-Barma V, Maisonobe T, Behar C, Lazennec JY, Kurys E, Arnulf I, Bonnet AM, Agid Y. Bloch F, et al. Among authors: hahn barma v. J Neurol Neurosurg Psychiatry. 2006 Nov;77(11):1223-8. doi: 10.1136/jnnp.2006.087908. Epub 2006 Jun 5. J Neurol Neurosurg Psychiatry. 2006. PMID: 16754693 Free PMC article.
[Semantic dementia: reflexions of a French working group for diagnostic criteria and constitution of a patient cohort].
Moreaud O, Belliard S, Snowden J, Auriacombe S, Basaglia-Pappas S, Bernard F, Bon L, Boutantin J, Boutoleau-Bretonnière C, Charnallet A, Coutant E, David D, Deramecourt V, Gaestel Y, Garnier S, Guichart E, Hahn-Barma V, Lebail B, Lebrun-Givois C, Lamy E, Le Carret N, Lemesle B, Memin A, Parienté J, Pasquier F, Renou P, Rouaud O, Sarazin M, Thomas-Antérion C, Vercelletto M, Virat-Brassaud ME. Moreaud O, et al. Among authors: hahn barma v. Rev Neurol (Paris). 2008 Apr;164(4):343-53. doi: 10.1016/j.neurol.2008.02.031. Epub 2008 Apr 3. Rev Neurol (Paris). 2008. PMID: 18439926 Review. French.
Homozygosity in Huntington's disease.
Dürr A, Hahn-Barma V, Brice A, Pêcheux C, Dodé C, Feingold J. Dürr A, et al. Among authors: hahn barma v. J Med Genet. 1999 Feb;36(2):172-3. J Med Genet. 1999. PMID: 10051023 Free PMC article. No abstract available.
Neuropsychological methods in mild cognitive impairment.
Hahn-Barma V, Chamayou C, Rogan C, Sarazin M, Dubois B. Hahn-Barma V, et al. Dialogues Clin Neurosci. 2004 Dec;6(4):396-9. doi: 10.31887/DCNS.2004.6.4/vhahnbarma. Dialogues Clin Neurosci. 2004. PMID: 22034137 Free PMC article. No abstract available.
Similar amyloid-β burden in posterior cortical atrophy and Alzheimer's disease.
de Souza LC, Corlier F, Habert MO, Uspenskaya O, Maroy R, Lamari F, Chupin M, Lehéricy S, Colliot O, Hahn-Barma V, Samri D, Dubois B, Bottlaender M, Sarazin M. de Souza LC, et al. Among authors: hahn barma v. Brain. 2011 Jul;134(Pt 7):2036-43. doi: 10.1093/brain/awr130. Brain. 2011. PMID: 21705422
Mental deficiency in three families with SPG4 spastic paraplegia.
Ribaï P, Depienne C, Fedirko E, Jothy AC, Viveweger C, Hahn-Barma V, Brice A, Durr A. Ribaï P, et al. Among authors: hahn barma v. Eur J Hum Genet. 2008 Jan;16(1):97-104. doi: 10.1038/sj.ejhg.5201922. Epub 2007 Oct 24. Eur J Hum Genet. 2008. PMID: 17957230
Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.
Le Ber I, Camuzat A, Hannequin D, Pasquier F, Guedj E, Rovelet-Lecrux A, Hahn-Barma V, van der Zee J, Clot F, Bakchine S, Puel M, Ghanim M, Lacomblez L, Mikol J, Deramecourt V, Lejeune P, de la Sayette V, Belliard S, Vercelletto M, Meyrignac C, Van Broeckhoven C, Lambert JC, Verpillat P, Campion D, Habert MO, Dubois B, Brice A; French research network on FTD/FTD-MND. Le Ber I, et al. Among authors: hahn barma v. Brain. 2008 Mar;131(Pt 3):732-46. doi: 10.1093/brain/awn012. Epub 2008 Feb 1. Brain. 2008. PMID: 18245784
19 results