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1993, Handbücher zur Sprach- und Kommunikationswissenschaft, ISBN 9783110113242, Volume Bd. 8, xiv, 962
Book
Neurology, ISSN 0028-3878, 2010, Volume 74, Issue 1, pp. 42 - 49
Journal Article
Pediatric Research, ISSN 0031-3998, 03/2015, Volume 77, Issue 3, pp. 398 - 405
Primary care pediatricians and a variety of specialist physicians strive to define an accurate diagnosis for children presenting with impairment of expressive... 
GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY | AMIDINOTRANSFERASE AGAT DEFICIENCY | SLC6A8 DEFICIENCY | GAMT DEFICIENCY | LINKED MENTAL-RETARDATION | ARGININE RESTRICTION | PROTON NMR-SPECTROSCOPY | MAGNETIC-RESONANCE | PEDIATRICS | TRANSPORTER DEFICIENCY | INBORN ERROR | Developmental Disabilities - drug therapy | Humans | Movement Disorders - diagnosis | Amidinotransferases - genetics | Language Development Disorders - etiology | Male | Movement Disorders - epidemiology | Amino Acid Metabolism, Inborn Errors - epidemiology | Incidence | Speech Disorders - pathology | Developmental Disabilities - pathology | Amino Acid Metabolism, Inborn Errors - genetics | Language Development Disorders - epidemiology | Brain Diseases, Metabolic, Inborn - pathology | Amino Acid Metabolism, Inborn Errors - pathology | Brain Diseases, Metabolic, Inborn - genetics | Intellectual Disability - epidemiology | Creatine - genetics | Mental Retardation, X-Linked - pathology | Creatine - biosynthesis | Intellectual Disability - pathology | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Developmental Disabilities - epidemiology | Speech Disorders - epidemiology | Utah - epidemiology | Brain Diseases, Metabolic, Inborn - drug therapy | Movement Disorders - genetics | Amino Acid Metabolism, Inborn Errors - drug therapy | Mental Retardation, X-Linked - epidemiology | Language Development Disorders - drug therapy | Speech Disorders - drug therapy | Guanidinoacetate N-Methyltransferase - genetics | Infant | Developmental Disabilities - genetics | Brain Diseases, Metabolic, Inborn - epidemiology | Creatine - blood | Creatine - physiology | Mental Retardation, X-Linked - drug therapy | Brain Diseases, Metabolic, Inborn - diagnosis | Intellectual Disability - genetics | Amino Acid Metabolism, Inborn Errors - diagnosis | Mental Retardation, X-Linked - genetics | Language Development Disorders - diagnosis | Mental Retardation, X-Linked - diagnosis | Creatine - deficiency | Female | Developmental Disabilities - diagnosis | Speech Disorders - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Amidinotransferases - deficiency | Magnetic Resonance Spectroscopy - methods | Creatine - urine | Language Development Disorders - genetics | Movement Disorders - pathology | Language Development Disorders - pathology | Speech Disorders - genetics | Intellectual Disability - drug therapy | Guanidinoacetate N-Methyltransferase - deficiency | Intellectual Disability - diagnosis | Movement Disorders - congenital | Sex Factors | Movement Disorders - drug therapy
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 08/2015, Volume 57, Issue 8, pp. 706 - 717
Aim The neurobiological contributions of childhood language disorder are not well understood. Yet there is increasing evidence that language disorder is... 
SIGNAL | AUTISM | ABNORMALITIES | INHERITED SPEECH | PEDIATRICS | DYSFUNCTION | FUNCTIONAL MRI | BRAIN | CLINICAL NEUROLOGY | WORKING-MEMORY | IMPAIRMENT | CHILDREN | Brain - pathology | Language Disorders - physiopathology | Child | Brain - physiopathology | Humans | Language Disorders - pathology
Journal Article
Brain, ISSN 0006-8950, 2006, Volume 129, Issue 6, pp. 1385 - 1398
Journal Article
Brain and Language, ISSN 0093-934X, 03/2012, Volume 120, Issue 3, pp. 310 - 320
► Compared brain structure and function in SLI, unaffected siblings, and typical peers. ► More grey matter in SLI in the left inferior frontal cortex. ► Less... 
Developmental disorders | Functional magnetic resonance imaging | Lateralisation | Language specialisation | Voxel-based morphometry | ACTIVATION | MRI | INHERITED SPEECH | AUDIOLOGY & SPEECH-LANGUAGE PATHOLOGY | BLOOD-FLOW | NEUROSCIENCES | PSYCHOLOGY, EXPERIMENTAL | CHILDREN | LINGUISTICS | DYSPHASIA | AUDITORY-CORTEX | DISORDER | TASK-DIFFICULTY | FMRI | Suprasegmentals | Neurological Impairments | Developmental Disabilities | Language Processing | Correlation | Diagnostic Tests | Task Analysis | Naming | Control Groups | Expressive Language | Intonation | Brain Hemisphere Functions | Morphology (Languages) | Auditory Stimuli | Language Impairments | Siblings | Putamen - pathology | Humans | Caudate Nucleus - pathology | Male | Caudate Nucleus - physiopathology | Auditory Perceptual Disorders - pathology | Young Adult | Putamen - physiopathology | Auditory Cortex - physiopathology | Female | Functional Laterality - physiology | Language Development Disorders - physiopathology | Temporal Lobe - pathology | Child | Brain - physiopathology | Frontal Lobe - physiopathology | Language Development Disorders - pathology | Auditory Cortex - pathology | Speech Perception - physiology | Magnetic Resonance Imaging | Temporal Lobe - physiopathology | Language Tests | Adolescent | Brain - pathology | Auditory Perceptual Disorders - physiopathology | Frontal Lobe - pathology
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 2016, Volume 25, Issue 3, pp. 546 - 557
Journal Article
Journal Article