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Amino Acids, ISSN 0939-4451, 9/2015, Volume 47, Issue 9, pp. 1853 - 1863
Journal Article
Amino Acids, ISSN 0939-4451, 9/2015, Volume 47, Issue 9, pp. 1865 - 1874
Journal Article
Amino Acids, ISSN 0939-4451, 9/2015, Volume 47, Issue 9, pp. 1893 - 1908
Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of nitric oxide (NO) synthesis, whereas l-arginine (Arg) and l-homoarginine (hArg) serve as... 
Biochemistry, general | N G -Methyltransferases | Homoarginine | Neurobiology | ADMA | Life Sciences | Analytical Chemistry | Life Sciences, general | Arginine | Biochemical Engineering | Proteomics | Knockout mouse | SAM | Methyltransferases | RAT-LIVER | LIVER AMIDINOTRANSFERASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | HEART-FAILURE | SYMMETRIC DIMETHYLARGININE | CREATINE | SUBSTRATE-SPECIFICITY | PLASMA | GLYCINE AMIDINOTRANSFERASE | NITRIC-OXIDE | N-G-Methyltransferases | CARDIOVASCULAR RISK | Developmental Disabilities - blood | Developmental Disabilities - drug therapy | Language Development Disorders - blood | Language Development Disorders - drug therapy | Speech Disorders - drug therapy | Guanidinoacetate N-Methyltransferase - genetics | Humans | Middle Aged | Amidinotransferases - genetics | Male | Developmental Disabilities - genetics | Coronary Artery Disease - blood | Arginine - analogs & derivatives | Arginine - administration & dosage | Intellectual Disability - genetics | Intellectual Disability - blood | Amino Acid Metabolism, Inborn Errors - genetics | Peripheral Arterial Disease - genetics | Amidinotransferases - blood | Peripheral Arterial Disease - blood | Adult | Female | Child | Guanidinoacetate N-Methyltransferase - blood | Speech Disorders - blood | Amidinotransferases - deficiency | Language Development Disorders - genetics | Peripheral Arterial Disease - drug therapy | Speech Disorders - genetics | Coronary Artery Disease - drug therapy | Guanidinoacetate N-Methyltransferase - metabolism | Movement Disorders - blood | Amidinotransferases - metabolism | Amino Acid Metabolism, Inborn Errors - blood | Mice, Knockout | Intellectual Disability - drug therapy | Animals | Homoarginine - biosynthesis | Arginine - biosynthesis | Guanidinoacetate N-Methyltransferase - deficiency | Movement Disorders - congenital | Adolescent | Coronary Artery Disease - genetics | Mice | Movement Disorders - genetics | Amino Acid Metabolism, Inborn Errors - drug therapy | Movement Disorders - drug therapy | Analysis | Nitric oxide | Transferases | Resveratrol | Physiological aspects | Biosynthesis | Chemical properties | Methylation | Index Medicus | Human | Proteins | Synthesis | Asymmetry | Coronary artery disease | Patients | Ingestion
Journal Article
Journal Article
Neuropediatrics, ISSN 0174-304X, 06/2018, Volume 49, Issue 3, pp. 185 - 192
Abstract This study investigated the effect of hippotherapy on gross motor function (Gross Motor Function Measure [GMFM]-66, GMFM dimension E and D) and... 
Original Article | cerebral palsy | quality of life | gross motor function | physiotherapy | hippotherapy | CONTROLLED-TRIAL | GAIT | CLINICAL NEUROLOGY | BALANCE | THERAPY | SYMMETRY | ABILITY | PEDIATRICS | HEALTH | PROGRAM
Journal Article
Neuropediatrics, 06/2018, Volume 49, Issue 3, p. 185
This study investigated the effect of hippotherapy on gross motor function (Gross Motor Function Measure [GMFM]-66, GMFM dimension E and D) and quality of life... 
Journal Article
Neuropediatrics, 12/2014, Volume 45, Issue 6, p. 346
Leigh syndrome (MIM 25600), also known as infantile subacute necrotizing encephalomyelopathy, is a neurodegenerative disorder with characteristic bilateral... 
Membrane Proteins - genetics | Pedigree | Humans | Brain - pathology | Female | Leigh Disease - mortality | Mitochondrial Proteins - genetics | Mutation | Leigh Disease - genetics | Child | Leigh Disease - pathology | Siblings
Journal Article
Translational Neuroscience, ISSN 2081-3856, 6/2011, Volume 2, Issue 2, pp. 138 - 141
Congenital muscular dystrophy (MDC) is a group of rare hereditary myopathies with an early onset of progressive muscle weakness and dystrophic changes as... 
White matter lesions | Neurology | Neurosciences | Medicine & Public Health | Congenital muscular dystrophy | MRI | Neurobiology | Central nervous system | Neurosurgery | Grey matter lesions | POPULATION | WHITE-MATTER | INVOLVEMENT | DISORDERS | LEVEL | NEUROSCIENCES | BRAIN ABNORMALITIES | MUTATION | EPILEPSY | MR SPECTROSCOPY | MEROSIN DEFICIENCY
Journal Article
3/2013, Volume 28, Issue 3, 11
Book Review
Neuropediatrics, ISSN 0174-304X, 2014, Volume 45, Issue 6, pp. 346 - 353
Leigh syndrome (MIM 25600), also known as infantile subacute necrotizing encephalomyelopathy, is a neurodegenerative disorder with characteristic bilateral... 
Original Article | Leigh syndrome | hydrocephalus | brain malformation | long survival | SURF1 | SURF1 GENE | CLINICAL NEUROLOGY | CYTOCHROME-C-OXIDASE | COX DEFICIENCY | DISEASE | PEDIATRICS | MUTATIONS | EXPRESSION
Journal Article
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