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Annals of Neurology
|
October 29, 2005
Common variants of LRRK2 are not associated with sporadic Parkinson's disease
Saskia Biskup, Jakob C Mueller, Manu Sharma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 3, 2017
A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation
Katharina Vill, Wolfgang Müller-Felber, Bader Alhaddad, et al.
Human Mutation
|
January 12, 2007
Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD)
Sheila A Fisher, Andrea Rivera, Lars G Fritsche, et al.
Acta Neuropathologica
|
May 5, 2011
Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death
Matthias Elstner, Christopher M Morris, Katharina Heim, et al.
Thrombosis and Haemostasis
|
December 19, 2014
Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome
Philipp von Hundelshausen, Konrad Oexle, Kiril Bidzhekov, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 27, 2017
Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism
Caroline Biagosch, Raga Deepthi Ediga, Svenja-Viola Hensler, et al.
Stem Cell Research
|
August 17, 2019
Generation of a human induced pluripotent stem cell line (HMGUi002-A) from a healthy male individual
Xianming Wang, Andrzej R Malinowski, Julia Beckenbauer, et al.
Annals of Clinical and Translational Neurology
|
October 1, 2019
Phenotypic variability of GABRA1-related epilepsy in monozygotic twins
Martin Krenn, Margot Ernst, Matthias Tomschik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 8, 2006
Clinical picture, evolution and peculiar molecular findings in a very large pedigree with Wolfram syndrome
Fortunato Lombardo, Pietro Chiurazzi, Konstanze Hörtnagel, et al.
Plos One
|
May 7, 2015
Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels
Antònia Flaquer, Susanne Rospleszcz, Eva Reischl, et al.
Page
of 54
Search research articles
Search
Showing results (61-70 of 536) with videos related to
Sort By:
Page
of 54
Annals of Neurology
|
October 29, 2005
Common variants of LRRK2 are not associated with sporadic Parkinson's disease
Saskia Biskup, Jakob C Mueller, Manu Sharma, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
February 3, 2017
A homozygous splice variant in AP4S1 mimicking neurodegeneration with brain iron accumulation
Katharina Vill, Wolfgang Müller-Felber, Bader Alhaddad, et al.
Human Mutation
|
January 12, 2007
Case-control genetic association study of fibulin-6 (FBLN6 or HMCN1) variants in age-related macular degeneration (AMD)
Sheila A Fisher, Andrea Rivera, Lars G Fritsche, et al.
Acta Neuropathologica
|
May 5, 2011
Expression analysis of dopaminergic neurons in Parkinson's disease and aging links transcriptional dysregulation of energy metabolism to cell death
Matthias Elstner, Christopher M Morris, Katharina Heim, et al.
Thrombosis and Haemostasis
|
December 19, 2014
Recurrent spontaneous coronary dissections in a patient with a de novo fibrillin-1 mutation without Marfan syndrome
Philipp von Hundelshausen, Konrad Oexle, Kiril Bidzhekov, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
May 27, 2017
Elevated glutaric acid levels in Dhtkd1-/Gcdh- double knockout mice challenge our current understanding of lysine metabolism
Caroline Biagosch, Raga Deepthi Ediga, Svenja-Viola Hensler, et al.
Stem Cell Research
|
August 17, 2019
Generation of a human induced pluripotent stem cell line (HMGUi002-A) from a healthy male individual
Xianming Wang, Andrzej R Malinowski, Julia Beckenbauer, et al.
Annals of Clinical and Translational Neurology
|
October 1, 2019
Phenotypic variability of GABRA1-related epilepsy in monozygotic twins
Martin Krenn, Margot Ernst, Matthias Tomschik, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
February 8, 2006
Clinical picture, evolution and peculiar molecular findings in a very large pedigree with Wolfram syndrome
Fortunato Lombardo, Pietro Chiurazzi, Konstanze Hörtnagel, et al.
Plos One
|
May 7, 2015
Mitochondrial GWA Analysis of Lipid Profile Identifies Genetic Variants to Be Associated with HDL Cholesterol and Triglyceride Levels
Antònia Flaquer, Susanne Rospleszcz, Eva Reischl, et al.
Page
of 54