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Zeynep Tufekcioglu

Showing results (11-20 of 15) with videos related to

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Journal of Alzheimer'S Disease : JAD|November 27, 2018
Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal DementiaGamze Guven, Başar Bilgic, Zeynep Tufekcioglu, et al.
Magma (New York, N.Y.)|July 22, 2022
Identification of metabolic correlates of mild cognitive impairment in Parkinson's disease using magnetic resonance spectroscopic imaging and machine learningSevim Cengiz, Dilek Betul Arslan, Ani Kicik, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 8, 2020
The cerebral blood flow deficits in Parkinson's disease with mild cognitive impairment using arterial spin labeling MRIDilek Betul Arslan, Hakan Gurvit, Ozan Genc, et al.
Parkinsonism & Related Disorders|August 22, 2019
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish familyDemy J S Kuipers, Zeynep Tufekcioglu, Başar Bilgiç, et al.
Parkinsonism & Related Disorders|March 29, 2017
The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPANSimone Olgiati, Okan Doğu, Zeynep Tufekcioglu, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Journal of Alzheimer'S Disease : JAD|November 27, 2018
Peripheral GRN mRNA and Serum Progranulin Levels as a Potential Indicator for Both the Presence of Splice Site Mutations and Individuals at Risk for Frontotemporal DementiaGamze Guven, Başar Bilgic, Zeynep Tufekcioglu, et al.
Magma (New York, N.Y.)|July 22, 2022
Identification of metabolic correlates of mild cognitive impairment in Parkinson's disease using magnetic resonance spectroscopic imaging and machine learningSevim Cengiz, Dilek Betul Arslan, Ani Kicik, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 8, 2020
The cerebral blood flow deficits in Parkinson's disease with mild cognitive impairment using arterial spin labeling MRIDilek Betul Arslan, Hakan Gurvit, Ozan Genc, et al.
Parkinsonism & Related Disorders|August 22, 2019
Late-onset phenotype associated with a homozygous GJC2 missense mutation in a Turkish familyDemy J S Kuipers, Zeynep Tufekcioglu, Başar Bilgiç, et al.
Parkinsonism & Related Disorders|March 29, 2017
The p.Thr11Met mutation in c19orf12 is frequent among adult Turkish patients with MPANSimone Olgiati, Okan Doğu, Zeynep Tufekcioglu, et al.
Pageof 2