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Thomas Meitinger

Showing results (31-40 of 536) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2007
Anticholinergic-responsive gait freezing in a patient with pantothenate kinase-associated neurodegenerationChul Hyoung Lyoo, Holger Prokisch, Thomas Meitinger, et al.
Brain : a Journal of Neurology|June 1, 2014
Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable diseaseTobias B Haack, Dirk Klee, Tim M Strom, et al.
Plos One|August 26, 2014
Mitochondrial genetic variants identified to be associated with BMI in adultsAntònia Flaquer, Clemens Baumbach, Jennifer Kriebel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2019
Fatal metabolic decompensation in carbonic anhydrase VA deficiency despite early treatment and control of hyperammonemiaFabian Baertling, Matias Wagner, Theresa Brunet, et al.
Stroke|February 26, 2005
ALOX5AP gene and the PDE4D gene in a central European population of stroke patientsElin Lõhmussaar, Andreas Gschwendtner, Jakob C Mueller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2005
Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndromeJuliane Winkelmann, Peter Lichtner, Benno Pütz, et al.
Annals of Clinical and Translational Neurology|December 1, 2020
A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathyMelanie Brugger, Fiona Becker-Dettling, Theresa Brunet, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 25, 2016
The many faces of paediatric mitochondrial disease on neuroimagingFabian Baertling, Dirk Klee, Tobias B Haack, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22Astrid Golla, Annette Jansson, Juliane Ramser, et al.
BMC Psychiatry|October 18, 2005
Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatoniaGerald Stöber, Bernd Kohlmann, Markus Iekiera, et al.
Pageof 54

Showing results (31-40 of 536) with videos related to

Sort By:
Pageof 54
Movement Disorders : Official Journal of the Movement Disorder Society|November 14, 2007
Anticholinergic-responsive gait freezing in a patient with pantothenate kinase-associated neurodegenerationChul Hyoung Lyoo, Holger Prokisch, Thomas Meitinger, et al.
Brain : a Journal of Neurology|June 1, 2014
Infantile Leigh-like syndrome caused by SLC19A3 mutations is a treatable diseaseTobias B Haack, Dirk Klee, Tim M Strom, et al.
Plos One|August 26, 2014
Mitochondrial genetic variants identified to be associated with BMI in adultsAntònia Flaquer, Clemens Baumbach, Jennifer Kriebel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 24, 2019
Fatal metabolic decompensation in carbonic anhydrase VA deficiency despite early treatment and control of hyperammonemiaFabian Baertling, Matias Wagner, Theresa Brunet, et al.
Stroke|February 26, 2005
ALOX5AP gene and the PDE4D gene in a central European population of stroke patientsElin Lõhmussaar, Andreas Gschwendtner, Jakob C Mueller, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 27, 2005
Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndromeJuliane Winkelmann, Peter Lichtner, Benno Pütz, et al.
Annals of Clinical and Translational Neurology|December 1, 2020
A homozygous truncating variant in CCDC186 in an individual with epileptic encephalopathyMelanie Brugger, Fiona Becker-Dettling, Theresa Brunet, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|July 25, 2016
The many faces of paediatric mitochondrial disease on neuroimagingFabian Baertling, Dirk Klee, Tobias B Haack, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
Chronic recurrent multifocal osteomyelitis (CRMO): evidence for a susceptibility gene located on chromosome 18q21.3-18q22Astrid Golla, Annette Jansson, Juliane Ramser, et al.
BMC Psychiatry|October 18, 2005
Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatoniaGerald Stöber, Bernd Kohlmann, Markus Iekiera, et al.
Pageof 54