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Journal of Cardiovascular Development and Disease
|
December 24, 2025
Virtual Reality to Enhance Understanding of Congenital Heart Disease
Shanti L Narasimhan, Ali H Mashadi, Syed Murfad Peer, et al.
Journal of Neurology
|
July 2, 2013
Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia
Kishore R Kumar, Nicholas F Blair, Himesha Vandebona, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 3, 2012
Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease
Meike Kasten, Lena Kertelge, Vera Tadic, et al.
Journal of the Peripheral Nervous System : JPNS
|
February 28, 2022
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy
Bianca R Grosz, Igor Stevanovski, Sara Negri, et al.
Neurogenetics
|
September 30, 2016
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing
Kishore R Kumar, G M Wali, Mahesh Kamate, et al.
Frontiers in Immunology
|
October 10, 2022
Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
Clarissa M Koch, Andrew D Prigge, Leah Setar, et al.
Cerebellum (London, England)
|
January 25, 2023
Two New Families and a Literature Review of ELOVL4-Associated Spinocerebellar Ataxia Type 34
Masahiro Nishide, Kathleen Le Marquand, Mark R Davis, et al.
Infection and Immunity
|
July 4, 2018
Terminal Deoxynucleotidyl Transferase Is Not Required for Antibody Response to Polysaccharide Vaccines against Streptococcus pneumoniae and Salmonella enterica Serovar Typhi
Vivek Belde, Matthew P Cravens, Dania Gulandijany, et al.
Human Mutation
|
November 24, 2019
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants
Franca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Human Mutation
|
August 7, 2018
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants
Franca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Page
of 27
Search research articles
Search
Showing results (191-200 of 267) with videos related to
Sort By:
Page
of 27
Journal of Cardiovascular Development and Disease
|
December 24, 2025
Virtual Reality to Enhance Understanding of Congenital Heart Disease
Shanti L Narasimhan, Ali H Mashadi, Syed Murfad Peer, et al.
Journal of Neurology
|
July 2, 2013
Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegia
Kishore R Kumar, Nicholas F Blair, Himesha Vandebona, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
May 3, 2012
Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease
Meike Kasten, Lena Kertelge, Vera Tadic, et al.
Journal of the Peripheral Nervous System : JPNS
|
February 28, 2022
Long read sequencing overcomes challenges in the diagnosis of SORD neuropathy
Bianca R Grosz, Igor Stevanovski, Sara Negri, et al.
Neurogenetics
|
September 30, 2016
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing
Kishore R Kumar, G M Wali, Mahesh Kamate, et al.
Frontiers in Immunology
|
October 10, 2022
Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
Clarissa M Koch, Andrew D Prigge, Leah Setar, et al.
Cerebellum (London, England)
|
January 25, 2023
Two New Families and a Literature Review of ELOVL4-Associated Spinocerebellar Ataxia Type 34
Masahiro Nishide, Kathleen Le Marquand, Mark R Davis, et al.
Infection and Immunity
|
July 4, 2018
Terminal Deoxynucleotidyl Transferase Is Not Required for Antibody Response to Polysaccharide Vaccines against Streptococcus pneumoniae and Salmonella enterica Serovar Typhi
Vivek Belde, Matthew P Cravens, Dania Gulandijany, et al.
Human Mutation
|
November 24, 2019
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants
Franca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Human Mutation
|
August 7, 2018
Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants
Franca Vulinovic, Victor Krajka, Torben J Hausrat, et al.
Page
of 27