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Brain : a Journal of Neurology
|
June 9, 2006
Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)
K Lasek, R Lencer, C Gaser, et al.
Plos One
|
June 28, 2007
A full-genomic sequence-verified protein-coding gene collection for Francisella tularensis
Tal Murthy, Andreas Rolfs, Yanhui Hu, et al.
Journal of the American Society of Nephrology : JASN
|
October 6, 2020
Biallelic Pathogenic <i>GFRA1</i> Variants Cause Autosomal Recessive Bilateral Renal Agenesis
Veronica Arora, Suliman Khan, Ayman W El-Hattab, et al.
Journal of Human Genetics
|
March 1, 2019
Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD
Shewata Pandita, Vijaya Ramachandran, Prahlad Balakrishnan, et al.
European Journal of Neurology
|
July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease population
K R Kumar, A Ramirez, A Göbel, et al.
Neuro-Degenerative Diseases
|
June 25, 2020
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters
Shen-Yang Lim, Jia Lun Lim, Azlina Ahmad-Annuar, et al.
Scientific Reports
|
March 15, 2024
Identifying delay in glymphatic clearance of labeled protons post-acute head trauma utilizing 3D ASL MRI (arterial spin labeling): a pilot study
Charles R Joseph, Jubin Kang Lim, Bryce N Grohol, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 14, 2018
Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population
Peter Bauer, Krishna Kumar Kandaswamy, Maximilian E R Weiss, et al.
Advances in Laboratory Medicine
|
June 28, 2024
Clinical, biochemical, and molecular profiles of three Sri Lankan neonates with pyruvate carboxylase deficiency
Eresha Jasinge, Mihika Fernando, Neluwa-Liyanage Ruwan Indika, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
August 13, 2025
Central Serous Chorioretinopathy occurs in High Frequency in Myelin Oligodendrocyte Glycoprotein Antibody Disease, Seropositive and Seronegative Neuromyelitis Optica Spectrum Disorders compared to Multiple Sclerosis and Healthy Controls
Bianca Knaack, Janine Rolfs, Hanna G Zimmermann, et al.
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Search research articles
Search
Showing results (511-520 of 632) with videos related to
Sort By:
Page
of 64
Brain : a Journal of Neurology
|
June 9, 2006
Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)
K Lasek, R Lencer, C Gaser, et al.
Plos One
|
June 28, 2007
A full-genomic sequence-verified protein-coding gene collection for Francisella tularensis
Tal Murthy, Andreas Rolfs, Yanhui Hu, et al.
Journal of the American Society of Nephrology : JASN
|
October 6, 2020
Biallelic Pathogenic <i>GFRA1</i> Variants Cause Autosomal Recessive Bilateral Renal Agenesis
Veronica Arora, Suliman Khan, Ayman W El-Hattab, et al.
Journal of Human Genetics
|
March 1, 2019
Identification of PKD1 and PKD2 gene variants in a cohort of 125 Asian Indian patients of ADPKD
Shewata Pandita, Vijaya Ramachandran, Prahlad Balakrishnan, et al.
European Journal of Neurology
|
July 21, 2012
Glucocerebrosidase mutations in a Serbian Parkinson's disease population
K R Kumar, A Ramirez, A Göbel, et al.
Neuro-Degenerative Diseases
|
June 25, 2020
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters
Shen-Yang Lim, Jia Lun Lim, Azlina Ahmad-Annuar, et al.
Scientific Reports
|
March 15, 2024
Identifying delay in glymphatic clearance of labeled protons post-acute head trauma utilizing 3D ASL MRI (arterial spin labeling): a pilot study
Charles R Joseph, Jubin Kang Lim, Bryce N Grohol, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 14, 2018
Development of an evidence-based algorithm that optimizes sensitivity and specificity in ES-based diagnostics of a clinically heterogeneous patient population
Peter Bauer, Krishna Kumar Kandaswamy, Maximilian E R Weiss, et al.
Advances in Laboratory Medicine
|
June 28, 2024
Clinical, biochemical, and molecular profiles of three Sri Lankan neonates with pyruvate carboxylase deficiency
Eresha Jasinge, Mihika Fernando, Neluwa-Liyanage Ruwan Indika, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
August 13, 2025
Central Serous Chorioretinopathy occurs in High Frequency in Myelin Oligodendrocyte Glycoprotein Antibody Disease, Seropositive and Seronegative Neuromyelitis Optica Spectrum Disorders compared to Multiple Sclerosis and Healthy Controls
Bianca Knaack, Janine Rolfs, Hanna G Zimmermann, et al.
Page
of 64