نتائج البحث - "Meike Kasten"

1

Task matters - challenging the motor system allows distinguishing unaffected Parkin mutation carriers from mutation-free controls

المؤلفون: Martin Gögele, Maria Paulina Castelo-Rueda, Max Borsche, Irene Pichler, Christine Klein, Meike Kasten, Cleo Kritzinger, Clemens Egger, Norbert Brüggemann, Peter P. Pramstaller, Deborah Mascalzoni, Jannik Prasuhn, Andrew A. Hicks, Lynn Langlott

المصدر: Parkinsonism & Related Disorders. 86:101-104

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1070b6914d47367d587f793d0b6bd62Test
https://doi.org/10.1016/j.parkreldis.2021.03.028Test

2

Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease

المساهمون: Liu, Ganqiang [0000-0002-1921-9542], Dong, Xianjun [0000-0002-8052-9320], Maple-Grødem, Jodi [0000-0001-7142-0078], Elbaz, Alexis [0000-0001-9724-5490], Hung, Albert Y [0000-0003-3658-571X], Kõks, Sulev [0000-0001-6087-6643], Alves, Guido [0000-0003-0630-2870], Heutink, Peter [0000-0001-5218-1737], Scherzer, Clemens R [0000-0002-0567-9193], Apollo - University of Cambridge Repository

المصدر: Nature Genetics, 53(6), 787-793. NATURE RESEARCH
Nature genetics
Nature genetics 53(6), 787-793 (2021). doi:10.1038/s41588-021-00847-6

مصطلحات موضوعية: Oncology, Multifactorial Inheritance, Parkinson's disease, Apolipoprotein E4, Genome-wide association study, Disease, genetics [Cognition Disorders], genetics [Glucosylceramidase], Cognition, 0302 clinical medicine, genetics [Parkinson Disease], Risk Factors, Longitudinal Studies, GBA protein, human, genetics [Multifactorial Inheritance], genetics [Apolipoprotein E4], 0303 health sciences, education.field_of_study, Hazard ratio, Parkinson Disease, genetics [Synapses], Disease Progression, Glucosylceramidase, physiopathology [Parkinson Disease], medicine.medical_specialty, Population, genetics [Mutation], Biology, Article, 03 medical and health sciences, ddc:570, Internal medicine, Genetics, medicine, Humans, Dementia, Genetic Predisposition to Disease, education, Survival analysis, Proportional Hazards Models, 030304 developmental biology, Proportional hazards model, medicine.disease, Survival Analysis, pathology [Parkinson Disease], Genetic Loci, Mutation, Synapses, Cognition Disorders, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bf0b0d7828506bc8c9a0d7770570677Test
https://hdl.handle.net/1887/3249471Test

3

Applicability of optical coherence tomography angiography (OCTA) imaging in Parkinson’s disease

المؤلفون: Meike Kasten, Jost Lennart Lauermann, Pauline Plöttner, Norbert Brüggemann, Jan A M Sochurek, Jannik Prasuhn, Florian Alten, Mahdy Ranjbar

المصدر: Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-7 (2021)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cc01769831bc8b86f2c009816661fe2Test
http://europepmc.org/articles/PMC7943590Test

4

Discordance in monozygotic Parkinson's disease twins – continuum or dichotomy?

المؤلفون: Alexander Balck, Max Borsche, Meike Kasten, Norbert Brüggemann, Christine Klein, Philip Seibler, Katja Lohmann

المصدر: Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Vol 6, Iss 6, Pp 1102-1105 (2019)

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Pediatrics, medicine.medical_specialty, Parkinson's disease, Dizygotic twin, Concordance, Neurosciences. Biological psychiatry. Neuropsychiatry, Disease, Brief Communication, Imaging modalities, 03 medical and health sciences, 0302 clinical medicine, medicine, Diseases in Twins, Humans, RC346-429, Aged, Discordant Twin, business.industry, General Neuroscience, Parkinson Disease, Twins, Monozygotic, Middle Aged, medicine.disease, Substantia Nigra, 030104 developmental biology, Female, Neurology. Diseases of the nervous system, Neurology (clinical), business, Disease manifestation, Brief Communications, 030217 neurology & neurosurgery, RC321-571

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee08c1eb68687b5c6d9fb9c8ff11e95Test
http://europepmc.org/articles/PMC6562023Test

5

Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review

المؤلفون: Christine Klein, Meike Kasten, Connie Marras, Sonja Petkovic, Susen Schaake, Florentine M.J. Zeldenrust, Shahad Almuammar, Christina M. Lill, Anne Grünewald, Harutyun Madoev, Joanne Trinh, Inke R. König, Jana Huang, Katja Lohmann

المصدر: Movement Disorders. 33:1857-1870

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::497d887210b29fe0c9e9ee4c944c4e31Test
https://doi.org/10.1002/mds.27527Test

6

The Use of Vitamin K2 in Patients With Parkinson's Disease and Mitochondrial Dysfunction (PD-K2): A Theranostic Pilot Study in a Placebo-Controlled Parallel Group Design

المؤلفون: Jannik Prasuhn, Meike Kasten, Melissa Vos, Inke R. König, Sebastian M. Schmid, Britta Wilms, Christine Klein, Norbert Brüggemann

المصدر: Frontiers in Neurology
Frontiers in Neurology, Vol 11 (2021)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b626f90ef0b8ccc883425eb102e572b5Test
https://doi.org/10.3389/fneur.2020.592104Test

7

The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings

المساهمون: Ertan, Fatoş Sibel (ORCID 0000-0003-1339-243X & YÖK ID 112829), Skrahina, Volha, Gaber, Hanaa, Vollstedt, Eva-Juliane, Foerster, Toni M., Usnich, Tatiana, Curado, Filipa, Brueggemann, Norbert, Paul, Jefri, Bogdanovic, Xenia, Zulbahar, Selen, Olmedillas, Maria, Skobalj, Snezana, Ameziane, Najim, Bauer, Peter, Csoti, Ilona, Koleva-Alazeh, Natalia, Grittner, Ulrike, Westenberger, Ana, Kasten, Meike, Beetz, Christian, Klein, Christine, Rolfs, Arndt, ROPAD Study Group, School of Medicine

المصدر: Movement Disorders

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Movement disorders, Parkinson's disease, Disease, Regular Issue Articles, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Epidemiology, medicine, Humans, observational clinical study, business.industry, Brief Report, Neurosciences and neurology, Parkinson Disease, LRRK2, medicine.disease, Ashkenazi jews, Clinical trial, Observational Studies as Topic, 030104 developmental biology, Neurology, Cohort, Mutation, Observational clinical study, Genetic factors, GBA, genetic factors, Glucosylceramidase, Observational study, Brief Reports, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery