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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.
JAMA Neurology|January 16, 2013
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementRita João Guerreiro, Ebba Lohmann, José Miguel Brás, et al.
Clinical Neurology and Neurosurgery|January 24, 2017
Clinical and genetic features of PKAN patients in a tertiary centre in TurkeyNihan Hande Akcakaya, Sibel Ugur Iseri, Birdal Bilir, 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.
Neurobiology of Aging|July 19, 2017
Mutations in TYROBP are not a common cause of dementia in a Turkish cohortLee Darwent, Susana Carmona, Ebba Lohmann, et al.
BMC Neurology|March 29, 2022
Genotype-Phenotype correlations of SCARB2 associated clinical presentation: a case report and in-depth literature reviewBurcu Atasu, Ayse Nur Ozdag Acarlı, Basar Bilgic, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 27, 2015
A new F-box protein 7 gene mutation causing typical Parkinson's diseaseEbba Lohmann, Anne-Sophie Coquel, Aurélie Honoré, et al.
Plos One|September 16, 2016
Mutation Frequency of the Major Frontotemporal Dementia Genes, MAPT, GRN and C9ORF72 in a Turkish Cohort of Dementia PatientsGamze Guven, Ebba Lohmann, Jose Bras, 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.
Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.
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