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Neurobiology of Disease, ISSN 0969-9961, 2009, Volume 37, Issue 2, pp. 370 - 383
Abstract Transgenic mice expressing the human superoxide dismutase 1 (SOD-1) mutant at position 93 (G93A) develop a phenotype resembling amyotrophic lateral... 
Neurology | Choline acetyl transferase | Amyotrophic lateral sclerosis | Lithium | Synaptic boutons | Transgenic G93A mouse | Brainstem motor neurons | ADULT RATS | CELLS IN-VITRO | NITRIC-OXIDE SYNTHASE | CU/ZN SUPEROXIDE-DISMUTASE | SPINAL-CORD | AMYOTROPHIC-LATERAL-SCLEROSIS | NEUROSCIENCES | DIFFERENTIAL VULNERABILITY | HYPOGLOSSAL NERVE ANASTOMOSIS | NEURON DEGENERATION | DISEASE PROGRESSION | Neuroprotective Agents - therapeutic use | Amyotrophic Lateral Sclerosis - physiopathology | Humans | Nerve Degeneration - physiopathology | Vagus Nerve - drug effects | Facial Nerve - drug effects | Male | Cytoprotection - physiology | Amyotrophic Lateral Sclerosis - drug therapy | Brain Stem - drug effects | Choline O-Acetyltransferase - metabolism | Motor Neurons - pathology | Vagus Nerve - pathology | Hypoglossal Nerve - drug effects | Lithium - therapeutic use | Neuroprotective Agents - pharmacology | Cranial Nerves - pathology | Brain Stem - pathology | Nerve Degeneration - prevention & control | Cytoprotection - drug effects | Trigeminal Nerve - physiopathology | Disease Models, Animal | Biomarkers - metabolism | Drug Administration Schedule | Lithium - pharmacology | Biomarkers - analysis | Axons - drug effects | Trigeminal Nerve - pathology | Mice, Transgenic | Treatment Outcome | Brain Mapping - methods | Vagus Nerve - physiopathology | Hypoglossal Nerve - pathology | Motor Neurons - metabolism | Cranial Nerves - drug effects | Amyotrophic Lateral Sclerosis - pathology | Trigeminal Nerve - drug effects | Animals | Axons - pathology | Choline O-Acetyltransferase - analysis | Cranial Nerves - physiopathology | Brain Stem - physiopathology | Mice | Facial Nerve - pathology | Hypoglossal Nerve - physiopathology | Facial Nerve - physiopathology | Nerve Degeneration - drug therapy | Superoxide dismutase | Superoxide | Neurons | Analysis | Choline | Index Medicus
Journal Article
Journal Article
Journal of Neurophysiology, ISSN 0022-3077, 03/2016, Volume 115, Issue 3, pp. 1372 - 1380
Power spectral analyses of electrical signals from respiratory nerves reveal prominent oscillations above the primary rate of breathing. Acute exposure to... 
Hypoxia | Motoneuron | Respiratory | Plasticity | Synaptic Potentials | Hypoglossal Nerve - physiology | Animals | Long-Term Potentiation | Hypoxia - physiopathology | Male | Mice | Hypoglossal Nerve - physiopathology | Index Medicus | motoneuron | hypoxia | plasticity | respiratory | Control of Movement
Journal Article
Muscle and Nerve, ISSN 0148-639X, 05/2010, Volume 41, Issue 5, pp. 679 - 684
Hereditary amyloidosis of the Finnish type (HAF, or familial amyloid polyneuropathy type IV) is an autosomal dominant disease that has been described most... 
Corneal lattice dystrophy | Familial amyloid neuropathy | Gelsolin | Facial palsy | Hereditary amyloidosis | facial palsy | SUBSTITUTION | POLYNEUROPATHY | LIVER-TRANSPLANTATION | GELSOLIN AMYLOIDOSIS | gelsolin | familial amyloid neuropathy | corneal lattice dystrophy | FAF | NEUROSCIENCES | CLINICAL NEUROLOGY | GENE | MUTATION | hereditary amyloidosis | EXPERIENCE | Peripheral Nervous System Diseases - diagnosis | Genetic Testing | Cranial Nerve Diseases - genetics | Humans | Middle Aged | Facial Nerve Diseases - metabolism | Male | Peripheral Nervous System Diseases - physiopathology | Amyloid Neuropathies, Familial - physiopathology | Young Adult | Electrodiagnosis | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | DNA Mutational Analysis | Inheritance Patterns - genetics | Adult | Female | Peripheral Nerves - metabolism | Peripheral Nervous System Diseases - genetics | Cranial Nerve Diseases - physiopathology | Disability Evaluation | Amyloid Neuropathies, Familial - genetics | Cranial Nerves - metabolism | Genotype | Oculomotor Nerve Diseases - diagnosis | Corneal Dystrophies, Hereditary - diagnosis | Facial Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - metabolism | Hypoglossal Nerve Diseases - metabolism | Mutation - genetics | Oculomotor Nerve Diseases - physiopathology | Cranial Nerve Diseases - diagnosis | Peripheral Nerves - physiopathology | Neurologic Examination | Genetic Markers - genetics | Adolescent | Finland | Cranial Nerves - physiopathology | Aged | Gelsolin - genetics | Germany | Oculomotor Nerve Diseases - metabolism | Amyloid Neuropathies, Familial - diagnosis | Index Medicus
Journal Article
JOURNAL OF NEUROPHYSIOLOGY, ISSN 0022-3077, 11/2011, Volume 106, Issue 5, pp. 2450 - 2470
Journal Article
Thorax, ISSN 0040-6376, 07/2016, Volume 71, Issue 10, pp. 923 - 931
Journal Article
Neurological Sciences, ISSN 1590-1874, 12/2008, Volume 29, Issue 6, pp. 497 - 498
Journal Article
Muscle & Nerve, ISSN 0148-639X, 05/2016, Volume 53, Issue 5, pp. 762 - 769
IntroductionHereditary gelsolin amyloidosis (GA) is a rare condition caused by the gelsolin gene mutation. The diagnostic triad includes corneal lattice... 
cranial neuropathy | amyloidosis | gelsolin | bilateral facial paresis | facial paresis grading | Facial paresis grading | Amyloidosis | Gelsolin | Cranial neuropathy | Bilateral facial paresis | GSN GENE | NEUROSCIENCES | FINNISH TYPE FAF | POLYNEUROPATHY TYPE-IV | CLINICAL NEUROLOGY | LATTICE CORNEAL-DYSTROPHY | HEARING-LOSS | NEUROPATHY | FAMILIAL AMYLOIDOSIS | MERETOJAS SYNDROME | HEREDITARY AMYLOIDOSIS | MUTATION | Vestibulocochlear Nerve Diseases - physiopathology | Cutis Laxa - etiology | Humans | Middle Aged | Vestibulocochlear Nerve Diseases - etiology | Oculomotor Nerve Diseases - etiology | Male | Amyloid Neuropathies, Familial - physiopathology | Facial Nerve Diseases - etiology | Hypoglossal Nerve Diseases - physiopathology | Corneal Dystrophies, Hereditary - physiopathology | Facial Paralysis - physiopathology | Aged, 80 and over | Adult | Female | Electromyography | Amyloidosis - complications | Cranial Nerve Diseases - physiopathology | Hypoglossal Nerve Diseases - etiology | Trigeminal Nerve Diseases - physiopathology | Trigeminal Nerve Diseases - etiology | Amyloid Neuropathies, Familial - complications | Amyloidosis - physiopathology | Neural Conduction | Facial Nerve Diseases - physiopathology | Oculomotor Nerve Diseases - physiopathology | Facial Muscles - physiopathology | Cranial Nerve Diseases - etiology | Corneal Dystrophies, Hereditary - complications | Aged | Facial Paralysis - etiology | Development and progression | Paralysis, Facial | Gene mutations | Wood products | Workshops | Index Medicus
Journal Article