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PAPER Koran ME, Hohman TJ, Thornton-Wells TA
Genetic interactions found between calcium channel genes modulate amyloid load measured by positron emission tomography.
Hum Genet. 2013 Sep 12; PubMed: 24026422PAPER Audo I, Bujakowska K, Orhan E, El Shamieh S, Sennlaub F, Guillonneau X, Antonio A, Michiels C, Lancelot ME, Letexier M, Saraiva JP, Nguyen H, Luu TD, Léveillard T, Poch O, Dollfus H, Paques M, Goureau O, Mohand-Saïd S, Bhattacharya SS, Sahel JA, Zeitz C
The familial dementia gene revisited: a missense mutation revealed by whole exome sequencing identifies ITM2B as a candidate gene underlying a novel autosomal dominant retinal dystrophy in a large family.
Hum Mol Genet. 2013 Sep 22; PubMed: 24026677PAPER Nakaaki S, Sato J, Torii K, Kawaguchi T, Kawaguchi A, Narumoto J, Mimura M
Neuroanatomical abnormalities before the onset of various types of delusions in a patient with Alzheimer disease.
J Neuropsychiatry Clin Neurosci. 2013 Summer;25(3):E65-6. PubMed: 24026751PAPER Leyton CE, Hodges JR
Towards a clearer definition of logopenic progressive aphasia.
Curr Neurol Neurosci Rep. 2013 Nov;13(11):396. PubMed: 24027007PAPER van Blitterswijk M, Baker MC, Dejesus-Hernandez M, Ghidoni R, Benussi L, Finger E, Hsiung GY, Kelley BJ, Murray ME, Rutherford NJ, Brown PE, Ravenscroft T, Mullen B, Ash PE, Bieniek KF, Hatanpaa KJ, Karydas A, Wood EM, Coppola G, Bigio EH, Lippa C, Strong MJ, Beach TG, Knopman DS, Huey ED, Mesulam M, Bird T, White CL, Kertesz A, Geschwind DH, Van Deerlin VM, Petersen RC, Binetti G, Miller BL, Petrucelli L, Wszolek ZK, Boylan KB, Graff-Radford NR, Mackenzie IR, Boeve BF, Dickson DW, Rademakers R
C9ORF72 repeat expansions in cases with previously identified pathogenic mutations.
Neurology. 2013 Oct 8;81(15):1332-41. PubMed: 24027057PAPER Absalon S, Kochanek DM, Raghavan V, Krichevsky AM
MiR-26b, Upregulated in Alzheimer's Disease, Activates Cell Cycle Entry, Tau-Phosphorylation, and Apoptosis in Postmitotic Neurons.
J Neurosci. 2013 Sep 11;33(37):14645-59. PubMed: 24027266PAPER Kolisnyk B, Al-Onaizi MA, Hirata PH, Guzman MS, Nikolova S, Barbash S, Soreq H, Bartha R, Prado MA, Prado VF
Forebrain deletion of the vesicular acetylcholine transporter results in deficits in executive function, metabolic, and RNA splicing abnormalities in the prefrontal cortex.
J Neurosci. 2013 Sep 11;33(37):14908-20. PubMed: 24027290PAPER Piccardo P, King D, Telling G, Manson JC, Barron RM
Dissociation of prion protein amyloid seeding from transmission of a spongiform encephalopathy.
J Virol. 2013 Nov;87(22):12349-56. PubMed: 24027305PAPER Chesser AS, Pritchard SM, Johnson GV
Tau Clearance Mechanisms and Their Possible Role in the Pathogenesis of Alzheimer Disease.
Front Neurol. 2013;4:122. PubMed: 24027553PAPER Chaudhuri KR, Odin P, Antonini A, Martinez-Martin P
Parkinson's disease: the non-motor issues.
Parkinsonism Relat Disord. 2011 Dec;17(10):717-23. PubMed: 21741874PAPER Berg D, Seppi K, Behnke S, Liepelt I, Schweitzer K, Stockner H, Wollenweber F, Gaenslen A, Mahlknecht P, Spiegel J, Godau J, Huber H, Srulijes K, Kiechl S, Bentele M, Gasperi A, Schubert T, Hiry T, Probst M, Schneider V, Klenk J, Sawires M, Willeit J, Maetzler W, Fassbender K, Gasser T, Poewe W
Enlarged substantia nigra hyperechogenicity and risk for Parkinson disease: a 37-month 3-center study of 1847 older persons.
Arch Neurol. 2011 Jul;68(7):932-7. PubMed: 21747034PAPER Mollenhauer B, Trautmann E, Sixel-Döring F, Wicke T, Ebentheuer J, Schaumburg M, Lang E, Focke NK, Kumar KR, Lohmann K, Klein C, Schlossmacher MG, Kohnen R, Friede T, Trenkwalder C,
Nonmotor and diagnostic findings in subjects with de novo Parkinson disease of the DeNoPa cohort.
Neurology. 2013 Sep 4; PubMed: 23997153PAPER Del Tredici K, Braak H
Lewy pathology and neurodegeneration in premotor Parkinson's disease.
Mov Disord. 2012 Apr 15;27(5):597-607. PubMed: 22508278PAPER Hughes AJ, Daniel SE, Blankson S, Lees AJ
A clinicopathologic study of 100 cases of Parkinson's disease.
Arch Neurol. 1993 Feb;50(2):140-8. PubMed: 8431132Current Filters
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