UofT Libraries is getting a new library services platform in January 2021.
Learn more about the change.
Search Articles
Movement disorders, ISSN 0885-3185, 05/2019, Volume 34, Issue 5, pp. 625 - 636
cerebral palsy | inborn errors of metabolism | spasticity | ataxia | dystonia | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Brain - diagnostic imaging | Monosaccharide Transport Proteins - deficiency | Lesch-Nyhan Syndrome - therapy | Spastic Paraplegia, Hereditary - diagnosis | Humans | Movement Disorders - diagnosis | Folic Acid Deficiency - therapy | Lesch-Nyhan Syndrome - genetics | Cerebral Palsy - diagnosis | Multiple Carboxylase Deficiency - genetics | Carbohydrate Metabolism, Inborn Errors - therapy | Brain Diseases, Metabolic, Inborn - genetics | Dyskinesias - genetics | Folic Acid Deficiency - genetics | Multiple Carboxylase Deficiency - physiopathology | Carbohydrate Metabolism, Inborn Errors - diagnosis | Monosaccharide Transport Proteins - genetics | Chorea - physiopathology | Creatine - genetics | Hyperargininemia - physiopathology | Dyskinesias - physiopathology | Dystonia - physiopathology | Pelizaeus-Merzbacher Disease - diagnosis | Plasma Membrane Neurotransmitter Transport Proteins - genetics | Carbohydrate Metabolism, Inborn Errors - physiopathology | Magnetic Resonance Imaging | Hyperargininemia - diagnosis | Movement Disorders - physiopathology | Dyskinesias - diagnosis | Hyperargininemia - genetics | Ataxia Telangiectasia - genetics | Lesch-Nyhan Syndrome - diagnosis | Brain Diseases, Metabolic, Inborn - therapy | Muscle Spasticity - physiopathology | Movement Disorders - genetics | Multiple Carboxylase Deficiency - diagnosis | Multiple Carboxylase Deficiency - therapy | GTP-Binding Protein alpha Subunits, Gi-Go - genetics | Spastic Paraplegia, Hereditary - genetics | Cerebral Palsy - physiopathology | Lesch-Nyhan Syndrome - physiopathology | Mental Retardation, X-Linked - physiopathology | Carbohydrate Metabolism, Inborn Errors - genetics | Brain Diseases, Metabolic, Inborn - diagnosis | Mental Retardation, X-Linked - genetics | Mental Retardation, X-Linked - diagnosis | Hyperargininemia - therapy | Creatine - deficiency | Thyroid Nuclear Factor 1 - genetics | Pelizaeus-Merzbacher Disease - therapy | Spastic Paraplegia, Hereditary - physiopathology | Mental Retardation, X-Linked - therapy | Ataxia Telangiectasia - diagnosis | Ataxia Telangiectasia - physiopathology | Plasma Membrane Neurotransmitter Transport Proteins - deficiency | Ataxia - physiopathology | Ataxia Telangiectasia - therapy | Diagnosis, Differential | Pelizaeus-Merzbacher Disease - genetics | Spastic Paraplegia, Hereditary - therapy | Brain Diseases, Metabolic, Inborn - physiopathology | Folic Acid Deficiency - physiopathology | Dyskinesias - therapy | Movement Disorders - therapy | Pelizaeus-Merzbacher Disease - physiopathology | Folic Acid Deficiency - diagnosis | Adenylyl Cyclases - genetics | Cerebral palsy | Development and progression | Medical genetics | Neuroimaging | Genetic counseling | Etiology | Chorea | Spasticity | Ataxia | Dystonia | Children | Paralysis | Neurodevelopmental disorders | Metabolic disorders | Index Medicus
Journal Article
Pain medicine (Malden, Mass.), ISSN 1526-2375, 11/2009, Volume 10, Issue 8, pp. 1389 - 1394
Epidural (Injection Space) | Steroids | Medicine, General & Internal | Anesthesiology | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Steroids - administration & dosage | Postoperative Complications - etiology | Humans | Postoperative Complications - prevention & control | Arteries - injuries | Fluoroscopy - methods | Male | Methylprednisolone - adverse effects | Iatrogenic Disease - prevention & control | Urinary Bladder, Neurogenic - chemically induced | Infarction - physiopathology | Embolism - physiopathology | Spinal Cord Injuries - pathology | Urinary Bladder, Neurogenic - physiopathology | Surgery, Computer-Assisted - adverse effects | Lumbar Vertebrae - surgery | Injections, Epidural - adverse effects | Low Back Pain - physiopathology | Radiculopathy - drug therapy | Paraplegia - physiopathology | Spinal Cord Injuries - chemically induced | Zygapophyseal Joint - physiopathology | Aged, 80 and over | Radiculopathy - physiopathology | Female | Paraplegia - chemically induced | Embolism - chemically induced | Infarction - chemically induced | Zygapophyseal Joint - drug effects | Infarction - pathology | Steroids - adverse effects | Steroids - chemistry | Postoperative Complications - physiopathology | Lumbar Vertebrae - diagnostic imaging | Embolism - pathology | Surgery, Computer-Assisted - methods | Arteries - pathology | Injections, Epidural - methods | Low Back Pain - drug therapy | Leg - innervation | Magnetic Resonance Imaging | Arteries - physiopathology | Aged | Lumbar Vertebrae - pathology | Spinal Cord Injuries - physiopathology | Leg - physiopathology | Methylprednisolone - administration & dosage | Complications and side effects | Care and treatment | Corticosteroids | Pain | Air pollution | Paralysis | Methylprednisolone | Air quality management | Index Medicus
Journal Article
Human molecular genetics, ISSN 0964-6906, 06/2016, Volume 25, Issue 12, pp. 2404 - 2416
Spastic Paraplegia, Hereditary - genetics | Retina - growth & development | Humans | Mandible - growth & development | Tooth - growth & development | Brain - growth & development | Mutation, Missense | Skeleton - physiopathology | Mitochondria - genetics | Mandible - physiopathology | Spastic Paraplegia, Hereditary - physiopathology | Disease Models, Animal | Optic Atrophy - genetics | Chorea - physiopathology | Brain - physiopathology | Retina - physiopathology | Skeleton - growth & development | Optic Atrophy - physiopathology | Head - growth & development | Head - physiopathology | Mitochondria - pathology | Metabolism, Inborn Errors - genetics | Proteins - genetics | Animals | Tooth - physiopathology | Mice | Bone Development - genetics | Chorea - genetics | Metabolism, Inborn Errors - physiopathology | Index Medicus
Journal Article
Human molecular genetics, ISSN 0964-6906, 06/2018, Volume 27, Issue 11, pp. 1892 - 1904
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Neurons - pathology | Humans | Paraplegia - genetics | Male | Tubulin - genetics | Cell Movement - genetics | Intellectual Disability - genetics | Paraplegia - physiopathology | Spindle Apparatus - genetics | Kinesin - genetics | Adult | Female | Neurons - metabolism | Child | Optic Atrophy - genetics | Spinocerebellar Ataxias - genetics | Cell Proliferation - genetics | Intellectual Disability - diagnostic imaging | Spinocerebellar Ataxias - diagnostic imaging | Optic Atrophy - physiopathology | Spinocerebellar Ataxias - physiopathology | Polyneuropathies - physiopathology | Spinocerebellar Degenerations - physiopathology | Microtubules - pathology | Spinocerebellar Degenerations - genetics | Sensorimotor Cortex - physiopathology | Intellectual Disability - physiopathology | Microtubules - genetics | Adolescent | Polyneuropathies - genetics | Protein Binding | Muscle Spasticity - physiopathology | Muscle Spasticity - diagnostic imaging | Sensorimotor Cortex - metabolism | Muscle Spasticity - genetics | Optic Atrophy - diagnostic imaging | Index Medicus
Journal Article
Journal of Applied Physiology, ISSN 8750-7587, 07/2007, Volume 103, Issue 1, pp. 140 - 147
Sternomastoid muscles | Respiratory muscles | Mechanical ventilation | Physiology | Sport Sciences | Life Sciences & Biomedicine | Science & Technology | Fundamental and applied biological sciences. Psychology | Biological and medical sciences | Pneumonia - physiopathology | Pneumonia - therapy | Intercostal Muscles - innervation | Humans | Middle Aged | Heart Failure - physiopathology | Male | Pulmonary Disease, Chronic Obstructive - physiopathology | Heart Failure - blood | Paraplegia - blood | Esophagus - physiopathology | Heart Failure - therapy | Time Factors | Paraplegia - physiopathology | Treatment Failure | Pulmonary Disease, Chronic Obstructive - blood | Aged, 80 and over | Adult | Pneumonia - blood | Electromyography | Diaphragm - innervation | Diaphragm - physiopathology | Stomach - physiopathology | Neck Muscles - physiopathology | Respiratory Center - physiopathology | Neck Muscles - innervation | Sepsis - physiopathology | Carbon Dioxide - blood | Pressure | Oxygen - blood | Inhalation | Pulmonary Disease, Chronic Obstructive - therapy | Paraplegia - therapy | Sepsis - therapy | Aged | Sepsis - blood | Exhalation | Respiratory Function Tests | Ventilator Weaning | Intercostal Muscles - physiopathology | Hydrogen-Ion Concentration | Throat | Muscular system | Respiratory system | Patients | Index Medicus
Journal Article
Nature medicine, ISSN 1078-8956, 11/2018, Volume 24, Issue 11, pp. 1677 - 1682
Biochemistry & Molecular Biology | Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Cell Biology | Research & Experimental Medicine | Motor Activity - physiology | Electric Stimulation | Transcutaneous Electric Nerve Stimulation | Humans | Male | Paralysis - rehabilitation | Paraplegia - physiopathology | Muscle, Skeletal - physiopathology | Paralysis - physiopathology | Adult | Spinal Cord Injuries - rehabilitation | Electromyography | Paraplegia - rehabilitation | Spinal Cord Injuries - physiopathology | Nerve Net - physiopathology | Paraplegia | Care and treatment | Patient outcomes | Lumbosacral region | Neural stimulation | Health aspects | Methods | Spinal cord injuries | Brain | Networks | Spinal cord | Stability | Motor activity | Spinal cord injury | Neuromodulation | Hip | Weight | Electrical stimuli | Support systems | Training | Sensorimotor system | Rehabilitation | Paralysis | Extremities | Index Medicus
Journal Article
American journal of physiology. Heart and circulatory physiology, ISSN 0363-6135, 02/2020, Volume 318, Issue 2, pp. H223 - H237
Cardiac & Cardiovascular Systems | Physiology | Peripheral Vascular Disease | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Blood Pressure | Mesenteric Arteries - physiopathology | Bradycardia - physiopathology | Rats | Male | Sympathetic Nervous System - physiopathology | Tachycardia - etiology | Rats, Sprague-Dawley | Tachycardia - physiopathology | Receptors, Purinergic - metabolism | Synaptic Transmission | Animals | Norepinephrine - metabolism | Quadriplegia - physiopathology | Excitatory Postsynaptic Potentials | Paraplegia - physiopathology | Adenosine Triphosphate - metabolism | Bradycardia - etiology | Mesenteric Arteries - innervation | Spinal Cord Injuries - physiopathology | Frequency dependence | Spinal cord | Spinal cord injury | Arteries | Paraplegia | Rodents | Nerves | Amperometry | Frequency response | Blood pressure | Reflexes | Spleen | Cardiac ventricles | Neurotransmitter release | Kidneys | Complications | Paraplegics | Quality of life | Electrical measurement | Tachycardia | Bradycardia | Neurotransmitters | Nitric oxide | Norepinephrine | Spinal cord injuries | ATP | Neurotransmission | Index Medicus
Journal Article
American journal of medical genetics. Part A, ISSN 1552-4825, 2016, Volume 170A, Issue 7, pp. 1820 - 1825
Trichorhinophalangeal syndrome type 1 | concomitant mutations | exome sequencing | ARSACS | syndrome | Fitzsimmons syndrome | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Spastic Paraplegia, Hereditary - genetics | Dysarthria - physiopathology | Hair Diseases - genetics | Nose - abnormalities | Brachydactyly - physiopathology | Dysarthria - diagnosis | Spastic Paraplegia, Hereditary - diagnosis | Humans | Male | Fingers - physiopathology | Spinocerebellar Ataxias - congenital | Heat-Shock Proteins - genetics | Spinocerebellar Ataxias - diagnosis | Hair Diseases - physiopathology | Female | Fingers - abnormalities | Nuclear Proteins - genetics | Child | Spastic Paraplegia, Hereditary - physiopathology | Langer-Giedion Syndrome - physiopathology | Spinocerebellar Ataxias - genetics | Nose - physiopathology | Langer-Giedion Syndrome - genetics | Repressor Proteins - genetics | Spinocerebellar Ataxias - physiopathology | Receptors, Cytoplasmic and Nuclear - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Exome - genetics | Brachydactyly - genetics | Brachydactyly - diagnosis | Muscle Spasticity - diagnosis | High-Throughput Nucleotide Sequencing | Muscle Spasticity - physiopathology | Muscle Spasticity - genetics | Dysarthria - genetics | Autism | Boycotts | Twins | Analysis | Genomics | Index Medicus
Journal Article
Frontiers in neuroscience, ISSN 1662-4548, 02/2020, Volume 14, pp. 74 - 74
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Cytochrome | Membranes | Cognitive ability | Homeostasis | Cytotoxicity | Lipids | Identification | Neurotoxicity | Mitochondria | Enzymatic activity | Sterols | Neurodegeneration | Ataxia | Lipid metabolism | Motor neurons | Enzymes | Phenotypes | Neurodegenerative diseases | Neurons | Spasticity | Metabolism | Cholesterol | Hereditary spastic paraplegia | Axons | Acids | Mutation | Endoplasmic reticulum | Bile | Life Sciences | Neurons and Cognition | Neurobiology | myelin | cholesterol | metabolism | phospholipids | fatty acids | sphingolipids
Journal Article