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Movement Disorders : Official Journal of the Movement Disorder Society
|
May 19, 2022
Reply to: "Comment on: Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood"
Jeannette Hübener-Schmid, Kirsten Kuhlbrodt, Julien Peladan, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
August 12, 2018
Circulating cell-free DNA: A potential biomarker to differentiate inflammation and infection during radiochemotherapy
Kerstin Zwirner, Franz J Hilke, German Demidov, et al.
Acta Neuropathologica Communications
|
December 29, 2018
Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?
Stefanie Beck-Wödl, Klaus Harzer, Marc Sturm, et al.
Clinical and Translational Radiation Oncology
|
December 13, 2024
Tumor sequencing before and after neoadjuvant chemoradiotherapy in locally advanced rectal cancer: Genetic tumor characterization and clinical outcome
Kerstin Clasen, Nadja Ballin, Leon Schütz, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
July 21, 2020
Dynamics of cell-free tumour DNA correlate with treatment response of head and neck cancer patients receiving radiochemotherapy
Franz J Hilke, Francesc Muyas, Jakob Admard, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
September 15, 2021
[Twin research in Germany]
Paul Enck, Miriam Goebel-Stengel, Olaf Rieß, et al.
Plos One
|
March 22, 2013
Reconstructing Roma history from genome-wide data
Priya Moorjani, Nick Patterson, Po-Ru Loh, et al.
Molecular Genetics & Genomic Medicine
|
February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome
Dennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.
BMC Medical Education
|
July 15, 2020
The impact of an audience response system on a summative assessment, a controlled field study
Thorsten Schmidt, Anastasia Gazou, Angelika Rieß, et al.
Parkinsonism & Related Disorders
|
December 8, 2018
The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature
Andreas Traschütz, Judith van Gaalen, Mayke Oosterloo, et al.
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Search research articles
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Showing results (1-10 of 25) with videos related to
Sort By:
Page
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Movement Disorders : Official Journal of the Movement Disorder Society
|
May 19, 2022
Reply to: "Comment on: Polyglutamine-Expanded Ataxin-3: A Target Engagement Marker for Spinocerebellar Ataxia Type 3 in Peripheral Blood"
Jeannette Hübener-Schmid, Kirsten Kuhlbrodt, Julien Peladan, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
August 12, 2018
Circulating cell-free DNA: A potential biomarker to differentiate inflammation and infection during radiochemotherapy
Kerstin Zwirner, Franz J Hilke, German Demidov, et al.
Acta Neuropathologica Communications
|
December 29, 2018
Homozygous TBC1 domain-containing kinase (TBCK) mutation causes a novel lysosomal storage disease - a new type of neuronal ceroid lipofuscinosis (CLN15)?
Stefanie Beck-Wödl, Klaus Harzer, Marc Sturm, et al.
Clinical and Translational Radiation Oncology
|
December 13, 2024
Tumor sequencing before and after neoadjuvant chemoradiotherapy in locally advanced rectal cancer: Genetic tumor characterization and clinical outcome
Kerstin Clasen, Nadja Ballin, Leon Schütz, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
July 21, 2020
Dynamics of cell-free tumour DNA correlate with treatment response of head and neck cancer patients receiving radiochemotherapy
Franz J Hilke, Francesc Muyas, Jakob Admard, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz
|
September 15, 2021
[Twin research in Germany]
Paul Enck, Miriam Goebel-Stengel, Olaf Rieß, et al.
Plos One
|
March 22, 2013
Reconstructing Roma history from genome-wide data
Priya Moorjani, Nick Patterson, Po-Ru Loh, et al.
Molecular Genetics & Genomic Medicine
|
February 10, 2023
Genome sequencing identifies complex structural MLH1 variant in unsolved Lynch syndrome
Dennis Witt, Ulrike Faust, Gertrud Strobl-Wildemann, et al.
BMC Medical Education
|
July 15, 2020
The impact of an audience response system on a summative assessment, a controlled field study
Thorsten Schmidt, Anastasia Gazou, Angelika Rieß, et al.
Parkinsonism & Related Disorders
|
December 8, 2018
The movement disorder spectrum of SCA21 (ATX-TMEM240): 3 novel families and systematic review of the literature
Andreas Traschütz, Judith van Gaalen, Mayke Oosterloo, et al.
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of 3