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2007, 1, ISBN 0443079412, x, 652 p., [8] p. of plates
This practical, clinical reference from the two leading movement disorder experts focuses on the problems of diagnosing and managing all movement disorders. It... 
diagnosis | physiopathology | Pathophysiology | therapy | Movement disorders
Book
2005, ISBN 0521825814, xxii, 642
Studies of human movement have proliferated in recent years, and there have been many studies of spinal pathways in humans, their role in movement, and their... 
Spinal cord | physiopathology | Spinal Cord Diseases | Motor ability | physiology | Motor Activity | Movement disorders | Diseases
Book
2015, ISBN 110706600X, ix, 197
"Medications that may produce movement disorders are widely used. The resulting disorders are often highly disconcerting for the patient and their relatives,... 
Neurotoxicity Syndromes | diagnosis | Treatment | Movement Disorders | therapy | etiology | Other branches of medicine | Movement disorders | Drugs
eBook
2009, ISBN 1405170417, xv, 216
Authored by members of the British Bobath Tutors Association, Bobath Concept: Theory and Clinical Practice in Neurological Rehabilitation is a practical... 
Bobath, Berta | methods | Bobath, Karel | Physical Therapy Modalities | Rehabilitation | Motor learning | Patients | Movement disorders | Central Nervous System Diseases
Book
2014, Cambridge medicine, ISBN 1107024617, xvii, 455
Movement disorders - ranging from parkinsonism to a variety of hyperkinetic disorders, such as tremors, dystonic, chorea and myoclonus - can be the presenting... 
Neurologic manifestations of general diseases | physiopathology | Neurologic Manifestations | Pathophysiology | Movement Disorders | etiology | Etiology | Movement disorders
Book
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 12/2018, Volume 41, Issue 6, pp. 1299 - 1301
Due to a typesetting error the wrong Table 2 was used. The correct Table 2 is shown here: 
Movement disorders
Journal Article
2010, Second edition, ISBN 9780750698528, xi, 279
Movement Disorders in Childhood, Second Edition, provides the most up-to-date information on the diseases and disorders that affect motor control, an important... 
Movement disorders in children | Clinical & internal medicine
eBook
Movement disorders, ISSN 0885-3185, 05/2017, Volume 32, Issue 5, pp. 1 - 1
Journal Article
Journal of Inherited Metabolic Disease, ISSN 0141-8955, 4/2008, Volume 31, Issue 2, pp. 230 - 239
Creatine deficiency syndromes, either due to AGAT, GAMT or SLC6A8 deficiencies, lead to a complete absence, or a very strong decrease, of creatine within the... 
Biochemistry, general | Human Genetics | Pediatrics | Internal Medicine | Medicine & Public Health | Metabolic Diseases | GUANIDINOACETATE METHYLTRANSFERASE DEFICIENCY | LINKED MENTAL-RETARDATION | ARGININE RESTRICTION | ENERGY HOMEOSTASIS | ENDOCRINOLOGY & METABOLISM | GENETICS & HEREDITY | IN-SITU HYBRIDIZATION | MAGNETIC-RESONANCE | CLINICAL CHARACTERISTICS | RAT-BRAIN | TRANSPORTER GENE SLC6A8 | INBORN ERROR | Glycine - analogs & derivatives | Glycine - metabolism | Prognosis | Guanidinoacetate N-Methyltransferase - genetics | Humans | Brain - enzymology | Amidinotransferases - genetics | Developmental Disabilities - genetics | Intellectual Disability - genetics | Membrane Transport Proteins - deficiency | Amino Acid Metabolism, Inborn Errors - genetics | Developmental Disabilities - enzymology | Membrane Transport Proteins - genetics | Movement Disorders - enzymology | Intellectual Disability - enzymology | Creatine - deficiency | Amidinotransferases - deficiency | Genetic Predisposition to Disease | Language Development Disorders - genetics | Speech Disorders - genetics | Language Development Disorders - enzymology | Phenotype | Animals | Guanidinoacetate N-Methyltransferase - deficiency | Movement Disorders - congenital | Speech Disorders - enzymology | Movement Disorders - genetics | Amino Acid Metabolism, Inborn Errors - enzymology | Creatine | Central nervous system
Journal Article