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Lambert-eaton Myasthenic Syndrome
Lambert-Eaton myasthenic syndrome
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Neurological disorders
(10)
Progressive sclerosing poliodystrophy
Luschka-Magendie foramina atresia
Hereditary sensory and autonomic neuropathies
Olfaction disorders
Zaspopathy
Zaspopathy
Neuromyotonia
Thomsen disease
Central core disease
Paramyotonia congenita
Accessory nerve disorder
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Rare diseases
Leukodystrophy, globoid cell
Multiple sulfatase deficiency
Florid cutaneous papillomatosis
Malignant hyperthermia
Zaspopathy
Diseases and disorders
(53)
Neuromuscular junction disease
Myasthenia gravis
Paraneoplastic cerebellar degeneration
Limbic encephalitis
Glossopharyngeal nerve diseases
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Postpoliomyelitis syndrome
Fukuyama type muscular dystrophy
Type i complex regional pain syndrome
Myopathies, structural, congenital
Becker's muscular dystrophy
Purpura, schoenlein-henoch
Paraneoplastic encephalomyelitis
Enterocolitis, pseudomembranous
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Lancereaux- -Mathieu-Weil Spirochetosis
Bethlem myopathy
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Encephalitis, arbovirus
Morvan disease
Intervertebral disk displacement
Phytanic acid storage disease
Rosenthal syndrome
Small cell lung cancer
Metatropic dwarfism
Hyperimmun- oglobulinemia E syndrome
Uveomening- oencephalitic syndrome
Centronuclear myopathy
Galactosemias
Brachial plexus neuropathies
Opsoclonus
Optic neuropathy, ischemic
Marinesco sjogren syndrome
Lgmd
Temporal arteritis
Small cell carcinoma
Levine-Critchley syndrome
Inflammatory myopathy
Leukemia, hairy cell
Dermatomyositis
Demyelination
Progressive sclerosing poliodystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Olfaction disorders
Zaspopathy
Central core disease
Multiple sulfatase deficiency
Malignant hyperthermia
Paramyotonia congenita
more...
Autoimmune diseases
Myoclonic Encephalopathy of infants
Autoimmune disorder
Myasthenia gravis
Purpura, schoenlein-henoch
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Dermatomyositis
Neurology
(17)
Adrenoleuk- odystrophy
Ramsay Hunt syndrome type I
Acquired epileptiform aphasia
Neuronopathy
Polymyositis
Polymyositis
Transverse myelitis
Muscle weakness
Electromyography
Myasthenia gravis
Paraneoplastic cerebellar degeneration
Limbic encephalitis
Myoclonic Encephalopathy of infants
Opsoclonus
Lgmd
Temporal arteritis
Levine-Critchley syndrome
Demyelination
more...
Neurophysiology
Myoneural junction
Presynaptic
Electromyography
Muscular disorders
(23)
Thyrotoxic Myopathy
Arthrogryposis
Central core disease
Centronuclear myopathy
Chronic progressive external ophthalmoplegia
Chronic progressive external ophthalmoplegia
Congenital myopathy
Diastasis recti
Inclusion body myositis
Laminopathy
Macrophagic myofasciitis
Metabolic myopathy
Mitochondrial myopathy
Muscular dystrophy
Myokmia
Myopathies, structural, congenital
Nemaline myopathy
Orofacial myological disorders
Pelvic Floor Muscle Disorder
Polymyositis
Torticollis
Writer's cramp
X-linked myotubular myopathy
Zenker's degeneration
more...
Muscular dystrophy organizations
Muscular Dystrophy Association
Myotonic Dystrophy Foundation
Muscular Dystrophy Campaign
Muscular Dystrophy Canada
Muscular Dystrophy Family Foundation
NeuroMuscular Centre
Symptoms
(9)
Blurry
Choking
Difficulty chewing
Difficulty talking
Paralysis
Paralysis
Swallowing difficulty
Weakness
Necrolytic migratory erythema
Muscle weakness
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Causes, incidence, and risk factors
Antibodies
Carcinoma
Muscle contraction
Myasthenia gravis
Signs and tests
Edrophonium
EMG
Muscle atrophy
Nerve conduction study
Caption
Mitochondrion
Nicotinic acetylcholine receptor
Sarcolemma
Synaptic vesicle
See also
(20)
Lems
Ocular myasthenia
Paraneoplastic syndromes
3,4-diaminopyridine
Hirayama syndrome
Hirayama syndrome
Dystrophin
Paraneoplastic syndromes, nervous system
Loken Senior syndrome
Plasmapheresis
Ann. Neurol.
CACNB2
Guanidine hydrochloride
Immune system
Muscle
Acetylcholine
Mycosis fungoides
Mullerian duct
Isoflurane
Autosomal dominant
Autosomal recessive
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