PAPER Ridolfi E, Barone C, Scarpini E, Galimberti D
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PAPER Sullivan MD, Katon WJ, Lovato LC, Miller ME, Murray AM, Horowitz KR, Bryan RN, Gerstein HC, Marcovina S, Akpunonu BE, Johnson J, Yale JF, Williamson J, Launer LJ
Association of Depression With Accelerated Cognitive Decline Among Patients With Type 2 Diabetes in the ACCORD-MIND Trial.
JAMA Psychiatry. 2013 Aug 14; PubMed: 23945905PAPER Roy T, Lloyd CE
Epidemiology of depression and diabetes: a systematic review.
J Affect Disord. 2012 Oct;142 Suppl:S8-21. PubMed: 23062861PAPER Jessen F, Wiese B, Bickel H, Eiffländer-Gorfer S, Fuchs A, Kaduszkiewicz H, Köhler M, Luck T, Mösch E, Pentzek M, Riedel-Heller SG, Wagner M, Weyerer S, Maier W, van den Bussche H,
Prediction of dementia in primary care patients.
PLoS One. 2011;6(2):e16852. PubMed: 21364746PAPER Katon WJ, Lin EH, Williams LH, Ciechanowski P, Heckbert SR, Ludman E, Rutter C, Crane PK, Oliver M, Von Korff M
Comorbid depression is associated with an increased risk of dementia diagnosis in patients with diabetes: a prospective cohort study.
J Gen Intern Med. 2010 May;25(5):423-9. PubMed: 20108126PAPER Katon W, Lyles CR, Parker MM, Karter AJ, Huang ES, Whitmer RA
Association of depression with increased risk of dementia in patients with type 2 diabetes: the Diabetes and Aging Study.
Arch Gen Psychiatry. 2012 Apr;69(4):410-7. PubMed: 22147809PAPER , Buse JB, Bigger JT, Byington RP, Cooper LS, Cushman WC, Friedewald WT, Genuth S, Gerstein HC, Ginsberg HN, Goff DC, Grimm RH, Margolis KL, Probstfield JL, Simons-Morton DG, Sullivan MD
Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial: design and methods.
Am J Cardiol. 2007 Jun 18;99(12A):21i-33i. PubMed: 17599422PAPER Ameur A, Stewart JB, Freyer C, Hagström E, Ingman M, Larsson NG, Gyllensten U
Ultra-deep sequencing of mouse mitochondrial DNA: mutational patterns and their origins.
PLoS Genet. 2011 Mar;7(3):e1002028. PubMed: 21455489PAPER Tazen S, Figueroa K, Kwan JY, Goldman J, Hunt A, Sampson J, Gutmann L, Pulst SM, Mitsumoto H, Kuo SH
Amyotrophic Lateral Sclerosis and Spinocerebellar Ataxia Type 2 in a Family With Full CAG Repeat Expansions of ATXN2.
JAMA Neurol. 2013 Aug 19; PubMed: 23959108PAPER Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet AM, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A,
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
Neurology. 2007 Nov 20;69(21):1970-5. PubMed: 17568014PAPER Gwinn-Hardy K, Chen JY, Liu HC, Liu TY, Boss M, Seltzer W, Adam A, Singleton A, Koroshetz W, Waters C, Hardy J, Farrer M
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese.
Neurology. 2000 Sep 26;55(6):800-5. PubMed: 10993999PAPER Infante J, Berciano J, Volpini V, Corral J, Polo JM, Pascual J, Combarros O
Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating in motor neuron disease.
Mov Disord. 2004 Jul;19(7):848-52. PubMed: 15254952PAPER Furtado S, Payami H, Lockhart PJ, Hanson M, Nutt JG, Singleton AA, Singleton A, Bower J, Utti RJ, Bird TD, de la Fuente-Fernandez R, Tsuboi Y, Klimek ML, Suchowersky O, Hardy J, Calne DB, Wszolek ZK, Farrer M, Gwinn-Hardy K, Stoessl AJ
Profile of families with parkinsonism-predominant spinocerebellar ataxia type 2 (SCA2).
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ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling.
Neurobiol Aging. 2012 Aug;33(8):1847.e15-21. PubMed: 22425256PAPER Chen YZ, Bennett CL, Huynh HM, Blair IP, Puls I, Irobi J, Dierick I, Abel A, Kennerson ML, Rabin BA, Nicholson GA, Auer-Grumbach M, Wagner K, De Jonghe P, Griffin JW, Fischbeck KH, Timmerman V, Cornblath DR, Chance PF
DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4).
Am J Hum Genet. 2004 Jun;74(6):1128-35. PubMed: 15106121Current Filters
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