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Journal of Medical Genetics
|
April 20, 2016
A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype
Charlotte L Alston, Caoimhe Howard, Monika Oláhová, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
July 12, 2015
Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis
Sudarshini Ramanathan, Kristina Prelog, Elizabeth H Barnes, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
June 7, 2018
A Phase II Study of Pembrolizumab in EGFR-Mutant, PD-L1+, Tyrosine Kinase Inhibitor Naïve Patients With Advanced NSCLC
A Lisberg, A Cummings, J W Goldman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 15, 2013
Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure
Gerald Pfeffer, Rita Barresi, Ian J Wilson, et al.
Brain : a Journal of Neurology
|
December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease
Rina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
The Lancet. Neurology
|
April 17, 2007
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release
Mar Matarín, W Mark Brown, Sonja Scholz, et al.
Scientific Reports
|
September 11, 2023
Fibulin-3 is necessary to prevent cardiac rupture following myocardial infarction
Lucy A Murtha, Sean A Hardy, Nishani S Mabotuwana, et al.
CNS Drugs
|
January 10, 2025
Repurposing Licensed Drugs with Activity Against Epstein-Barr Virus for Treatment of Multiple Sclerosis: A Systematic Approach
Vivien Li, Fiona C McKay, David C Tscharke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 8, 2021
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism
Francesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, et al.
European Journal of Neurology
|
March 9, 2022
Diagnosis, differential diagnosis and misdiagnosis of Susac syndrome
James D Triplett, Jessica Qiu, Billy O'Brien, et al.
Page
of 91
Search research articles
Search
Showing results (841-850 of 902) with videos related to
Sort By:
Page
of 91
Journal of Medical Genetics
|
April 20, 2016
A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype
Charlotte L Alston, Caoimhe Howard, Monika Oláhová, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)
|
July 12, 2015
Radiological differentiation of optic neuritis with myelin oligodendrocyte glycoprotein antibodies, aquaporin-4 antibodies, and multiple sclerosis
Sudarshini Ramanathan, Kristina Prelog, Elizabeth H Barnes, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
June 7, 2018
A Phase II Study of Pembrolizumab in EGFR-Mutant, PD-L1+, Tyrosine Kinase Inhibitor Naïve Patients With Advanced NSCLC
A Lisberg, A Cummings, J W Goldman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 15, 2013
Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure
Gerald Pfeffer, Rita Barresi, Ian J Wilson, et al.
Brain : a Journal of Neurology
|
December 10, 2003
The expression of DJ-1 (PARK7) in normal human CNS and idiopathic Parkinson's disease
Rina Bandopadhyay, Ann E Kingsbury, Mark R Cookson, et al.
The Lancet. Neurology
|
April 17, 2007
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release
Mar Matarín, W Mark Brown, Sonja Scholz, et al.
Scientific Reports
|
September 11, 2023
Fibulin-3 is necessary to prevent cardiac rupture following myocardial infarction
Lucy A Murtha, Sean A Hardy, Nishani S Mabotuwana, et al.
CNS Drugs
|
January 10, 2025
Repurposing Licensed Drugs with Activity Against Epstein-Barr Virus for Treatment of Multiple Sclerosis: A Systematic Approach
Vivien Li, Fiona C McKay, David C Tscharke, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
October 8, 2021
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism
Francesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, et al.
European Journal of Neurology
|
March 9, 2022
Diagnosis, differential diagnosis and misdiagnosis of Susac syndrome
James D Triplett, Jessica Qiu, Billy O'Brien, et al.
Page
of 91