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European Journal of Human Genetics : EJHG
|
April 8, 2025
Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes
German Demidov, Steven Laurie, Annalaura Torella, et al.
Parkinsonism & Related Disorders
|
March 1, 2016
Abnormal interhemispheric inhibition in musician's dystonia - Trait or state?
Tobias Bäumer, Alexander Schmidt, Marcus Heldmann, et al.
NPJ Parkinson'S Disease
|
February 17, 2025
Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease
Clara Krüger, Shen-Yang Lim, Alissa Buhrmann, et al.
European Journal of Human Genetics : EJHG
|
June 5, 2024
Quality assurance for next-generation sequencing diagnostics of rare neurological diseases in the European Reference Network
Aleš Maver, Katja Lohmann, Fran Borovečki, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 27, 2023
The New p.F1700L LRRK2 Variant Causes Parkinson's Disease by Extensively Increasing Kinase Activity
Max Borsche, Neringa Pratuseviciute, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 22, 2026
Co- and Multi-Pathologies in Parkinson's Disease: An International Parkinson and Movement Disorder Society Scientific Issues Committee Review
Michele Matarazzo, Per Borghammer, Inas Elsayed, et al.
NPJ Parkinson'S Disease
|
January 10, 2026
Metabolomic breath landscape analysis unravels lipid biomarker candidates in patients with genetic and idiopathic Parkinson's disease
Madiha Malik, Norbert Brüggemann, Tatiana Usnich, et al.
International Journal of Molecular Sciences
|
September 9, 2022
Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated Neurodegeneration
Sokhna Haissatou Diaw, Christos Ganos, Simone Zittel, et al.
BMC Neurology
|
June 24, 2022
Blastic plasmacytoid dendritic cell neoplasm and cerebral toxoplasmosis: a case report
Anna Maria Florescu, Anne Louise Tølbøll Sørensen, Henrik Vedel Nielsen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 7, 2016
PLA2G6 mutations and Parkinsonism: Long-term follow-up of clinical features and neuropathology
Christine Klein, Tobias Löchte, Suzanne M Delamonte, et al.
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of 27
Search research articles
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Showing results (91-100 of 267) with videos related to
Sort By:
Page
of 27
European Journal of Human Genetics : EJHG
|
April 8, 2025
Correction: Structural variant calling and clinical interpretation in 6224 unsolved rare disease exomes
German Demidov, Steven Laurie, Annalaura Torella, et al.
Parkinsonism & Related Disorders
|
March 1, 2016
Abnormal interhemispheric inhibition in musician's dystonia - Trait or state?
Tobias Bäumer, Alexander Schmidt, Marcus Heldmann, et al.
NPJ Parkinson'S Disease
|
February 17, 2025
Updated MDSGene review on the clinical and genetic spectrum of LRRK2 variants in Parkinson´s disease
Clara Krüger, Shen-Yang Lim, Alissa Buhrmann, et al.
European Journal of Human Genetics : EJHG
|
June 5, 2024
Quality assurance for next-generation sequencing diagnostics of rare neurological diseases in the European Reference Network
Aleš Maver, Katja Lohmann, Fran Borovečki, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 27, 2023
The New p.F1700L LRRK2 Variant Causes Parkinson's Disease by Extensively Increasing Kinase Activity
Max Borsche, Neringa Pratuseviciute, Susen Schaake, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 22, 2026
Co- and Multi-Pathologies in Parkinson's Disease: An International Parkinson and Movement Disorder Society Scientific Issues Committee Review
Michele Matarazzo, Per Borghammer, Inas Elsayed, et al.
NPJ Parkinson'S Disease
|
January 10, 2026
Metabolomic breath landscape analysis unravels lipid biomarker candidates in patients with genetic and idiopathic Parkinson's disease
Madiha Malik, Norbert Brüggemann, Tatiana Usnich, et al.
International Journal of Molecular Sciences
|
September 9, 2022
Mutant WDR45 Leads to Altered Ferritinophagy and Ferroptosis in β-Propeller Protein-Associated Neurodegeneration
Sokhna Haissatou Diaw, Christos Ganos, Simone Zittel, et al.
BMC Neurology
|
June 24, 2022
Blastic plasmacytoid dendritic cell neoplasm and cerebral toxoplasmosis: a case report
Anna Maria Florescu, Anne Louise Tølbøll Sørensen, Henrik Vedel Nielsen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 7, 2016
PLA2G6 mutations and Parkinsonism: Long-term follow-up of clinical features and neuropathology
Christine Klein, Tobias Löchte, Suzanne M Delamonte, et al.
Page
of 27