Search research articles
Contact Us
Filters
Showing results (431-440 of 585) with videos related to
Page
of 59
Sort By:
Current Biology : CB
|
March 26, 2013
A revised timescale for human evolution based on ancient mitochondrial genomes
Qiaomei Fu, Alissa Mittnik, Philip L F Johnson, et al.
American Journal of Medical Genetics. Part A
|
November 9, 2020
Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature
Mimi Tin-Yan Seto, Aida M Bertoli-Avella, Ka Wang Cheung, et al.
Neuroimage
|
July 28, 2009
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, et al.
Brain : a Journal of Neurology
|
December 27, 2013
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
Martial Mallaret, Matthis Synofzik, Jaeho Lee, et al.
Parkinsonism & Related Disorders
|
December 24, 2022
Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variants
Tatiana Usnich, Maria Olmedillas, Nathalie Schell, et al.
The Journal of Allergy and Clinical Immunology
|
October 30, 2016
Evolution and predictive value of IgE responses toward a comprehensive panel of house dust mite allergens during the first 2 decades of life
Daniela Posa, Serena Perna, Yvonne Resch, et al.
Annals of Neurology
|
February 10, 2016
Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients
Rebecca Schüle, Sarah Wiethoff, Peter Martus, et al.
Journal of Clinical Medicine
|
October 26, 2024
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 Participants
Sabine Rösner, Luba M Pardo, Aida M Bertoli-Avella, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 14, 2020
The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings
Volha Skrahina, Hanaa Gaber, Eva-Juliane Vollstedt, et al.
Parkinsonism & Related Disorders
|
February 5, 2019
Role of ANO3 mutations in dystonia: A large-scale mutational screening study
Luisa Olschewski, Silvia Jesús, Han-Joon Kim, et al.
Page
of 59
Search research articles
Search
Showing results (431-440 of 585) with videos related to
Sort By:
Page
of 59
Current Biology : CB
|
March 26, 2013
A revised timescale for human evolution based on ancient mitochondrial genomes
Qiaomei Fu, Alissa Mittnik, Philip L F Johnson, et al.
American Journal of Medical Genetics. Part A
|
November 9, 2020
Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature
Mimi Tin-Yan Seto, Aida M Bertoli-Avella, Ka Wang Cheung, et al.
Neuroimage
|
July 28, 2009
Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, et al.
Brain : a Journal of Neurology
|
December 27, 2013
The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation
Martial Mallaret, Matthis Synofzik, Jaeho Lee, et al.
Parkinsonism & Related Disorders
|
December 24, 2022
Frequency of non-motor symptoms in Parkinson's disease patients carrying the E326K and T369M GBA risk variants
Tatiana Usnich, Maria Olmedillas, Nathalie Schell, et al.
The Journal of Allergy and Clinical Immunology
|
October 30, 2016
Evolution and predictive value of IgE responses toward a comprehensive panel of house dust mite allergens during the first 2 decades of life
Daniela Posa, Serena Perna, Yvonne Resch, et al.
Annals of Neurology
|
February 10, 2016
Hereditary spastic paraplegia: Clinicogenetic lessons from 608 patients
Rebecca Schüle, Sarah Wiethoff, Peter Martus, et al.
Journal of Clinical Medicine
|
October 26, 2024
Hereditary Transthyretin-Related Amyloidosis Ongoing Observational Study: A Baseline Report of the First 3167 Participants
Sabine Rösner, Luba M Pardo, Aida M Bertoli-Avella, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 14, 2020
The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings
Volha Skrahina, Hanaa Gaber, Eva-Juliane Vollstedt, et al.
Parkinsonism & Related Disorders
|
February 5, 2019
Role of ANO3 mutations in dystonia: A large-scale mutational screening study
Luisa Olschewski, Silvia Jesús, Han-Joon Kim, et al.
Page
of 59