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Endocrine
|
September 18, 2021
Pre- versus post-operative untargeted plasma nuclear magnetic resonance spectroscopy metabolomics of pheochromocytoma and paraganglioma
Nikolaos G Bliziotis, Leo A J Kluijtmans, Sebastian Soto, et al.
Acta Neuropathologica
|
December 17, 2021
DTYMK is essential for genome integrity and neuronal survival
Jo M Vanoevelen, Jörgen Bierau, Janine C Grashorn, et al.
Human Molecular Genetics
|
March 27, 2009
Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival
Vishwanathan Hucthagowder, Eva Morava, Uwe Kornak, et al.
Circulation Research
|
January 19, 2018
Mutations in <i>CYB561</i> Causing a Novel Orthostatic Hypotension Syndrome
Maarten P van den Berg, Rowida Almomani, Italo Biaggioni, et al.
JAMA Network Open
|
July 25, 2019
Association of a Multifaceted Intervention With Ordering of Unnecessary Laboratory Tests Among Caregivers in Internal Medicine Departments
Renuka S Bindraban, Marlou van Beneden, Mark H H Kramer, et al.
Journal of Translational Autoimmunity
|
August 4, 2020
Frequencies and clinical associations of myositis-related antibodies in The Netherlands: A one-year survey of all Dutch patients
Anouk C M Platteel, Brigitte A Wevers, Johan Lim, et al.
Journal of Neuroimmunology
|
October 14, 2022
Enrichment of serum IgG4 in MuSK myasthenia gravis patients
Dana L E Vergoossen, Annabel M Ruiter, Kevin R Keene, et al.
Journal of Inherited Metabolic Disease
|
September 11, 2022
Novel cerebrospinal fluid biomarkers of glucose transporter type 1 deficiency syndrome: Implications beyond the brain's energy deficit
Tessa M A Peters, Jona Merx, Pieter C Kooijman, et al.
Circulation
|
May 24, 2019
N-Glycosylation Defects in Humans Lower Low-Density Lipoprotein Cholesterol Through Increased Low-Density Lipoprotein Receptor Expression
Marjolein A W van den Boogert, Lars E Larsen, Lubna Ali, et al.
Cell
|
July 20, 2010
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder
Vincent Cantagrel, Dirk J Lefeber, Bobby G Ng, et al.
Page
of 49
Search research articles
Search
Showing results (441-450 of 483) with videos related to
Sort By:
Page
of 49
Endocrine
|
September 18, 2021
Pre- versus post-operative untargeted plasma nuclear magnetic resonance spectroscopy metabolomics of pheochromocytoma and paraganglioma
Nikolaos G Bliziotis, Leo A J Kluijtmans, Sebastian Soto, et al.
Acta Neuropathologica
|
December 17, 2021
DTYMK is essential for genome integrity and neuronal survival
Jo M Vanoevelen, Jörgen Bierau, Janine C Grashorn, et al.
Human Molecular Genetics
|
March 27, 2009
Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival
Vishwanathan Hucthagowder, Eva Morava, Uwe Kornak, et al.
Circulation Research
|
January 19, 2018
Mutations in <i>CYB561</i> Causing a Novel Orthostatic Hypotension Syndrome
Maarten P van den Berg, Rowida Almomani, Italo Biaggioni, et al.
JAMA Network Open
|
July 25, 2019
Association of a Multifaceted Intervention With Ordering of Unnecessary Laboratory Tests Among Caregivers in Internal Medicine Departments
Renuka S Bindraban, Marlou van Beneden, Mark H H Kramer, et al.
Journal of Translational Autoimmunity
|
August 4, 2020
Frequencies and clinical associations of myositis-related antibodies in The Netherlands: A one-year survey of all Dutch patients
Anouk C M Platteel, Brigitte A Wevers, Johan Lim, et al.
Journal of Neuroimmunology
|
October 14, 2022
Enrichment of serum IgG4 in MuSK myasthenia gravis patients
Dana L E Vergoossen, Annabel M Ruiter, Kevin R Keene, et al.
Journal of Inherited Metabolic Disease
|
September 11, 2022
Novel cerebrospinal fluid biomarkers of glucose transporter type 1 deficiency syndrome: Implications beyond the brain's energy deficit
Tessa M A Peters, Jona Merx, Pieter C Kooijman, et al.
Circulation
|
May 24, 2019
N-Glycosylation Defects in Humans Lower Low-Density Lipoprotein Cholesterol Through Increased Low-Density Lipoprotein Receptor Expression
Marjolein A W van den Boogert, Lars E Larsen, Lubna Ali, et al.
Cell
|
July 20, 2010
SRD5A3 is required for converting polyprenol to dolichol and is mutated in a congenital glycosylation disorder
Vincent Cantagrel, Dirk J Lefeber, Bobby G Ng, et al.
Page
of 49