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acid maltase deficiency

advances in neurology

adverse drug reaction

alpha-fetoprotein

Alzheimer's disease

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, epidemiology of

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

anterior horn cell disease

anterior tibial muscle weakness

apraxia of eye movements

areflexia

arthrogryposis multiplex

asymptomatic

ataxia

ataxia telangiectasia

ataxia, cerebellar

ataxia, truncal

benign congenital hypotonia

Brugada syndrome

bulbar palsy, progressive

calf hypertrophy

carcinoembryonic antigen

carcinoma

central core disease

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

chromosomal abnormality

chromosome 11

chromosome 5

chronic polyneuritis, children

Clinical Pathologic Conference(C.P.C.)

clinodactyly

coma

complications

congenital heart disease

congenital myopathy

congestive heart failure

constipation

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

Dejerine-Sottas syndrome

denervation of muscle

denervation potentials

dermatomyositis

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diaphragmatic paralysis

differential diagnosis

distal muscle atrophy

distal muscle weakness

electrocardiogram, abnormal

electromyogram

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

enzyme, muscle disease

epidemiology of neurology

eye movement, disorders of

facial weakness, bilateral

facioscapulohumeral syndrome

familial

fasciculation

Fazio-Londe's disease

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

growth retardation

Guillain Barre syndrome

gynecomastia

heavy metal intoxication

history of neurology

human T-lymphotropic virus type I(HTLV-I)

hypoxic encephalopathy

immunodeficiency

immunosuppression

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

infant, evaluation of

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

Isaacs syndrome

klippel feil syndrome

Kugelberg-Welander syndrome

leg weakness, bilateral

leg weakness, unilateral

leukemia

lid closure, weakness of

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, spinal cord

multiple system atrophy

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle diseases, characteristics of

muscle hypertrophy

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, differential diagnosis of

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, distal weakness

myasthenia gravis, limb-girdle

myasthenic crisis

myelopathy

myelopathy, chronic progressive

myopathy, carcinomatous

myopathy, centronuclear

myopathy, mitochondrial

myopathy, thyroid disease causing

myositis

myotonia congenita

myotonia dystrophica

nemaline rod myopathy

nerve conduction studies

neuritis, causes of

neurocutaneous disease

neuroendocrinology

neurofibrillary degeneration

neurologic disease, diagnoses of

neurologic evaluation

neuromyotonia

neuronal ceroid-lipofuscinosis

neuronal degeneration

neuropathology

neuropathy

neuropathy, diabetic

neuropathy, hereditary peripheral

newborn, evaluation of

nusinersen

ocular motility, disorders of

Onufrowicz nucleus

Oppenheim muscular dystrophy

paraparesis, familial spastic

Parkinson disease

pathology

patient information and support

peroneal muscle atrophy, causes of

phrenic nerve

placebo

poison, mercury

poison, neurologic problems with

pregnancy, neurologic complications in

primary lateral sclerosis

progeria

prognosis

progressive muscular dystrophy

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

radiation hypersensitivity

risk-benefit assessment

scoliosis, neurologic association with

screening

skin, lesions in neurologic disorders

SMN1 gene

spinal cord

spinal cord degeneration

spinal cord, lesion of

spinal cord, pathologic exam of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

spinocerebellar ataxia

stiff man syndrome

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

sudden death

survival motor neuron gene

telangiectases

term infant

tongue, fasciculations of

torticollis

treatment of neurologic disorder

tricresylphosphate

trinucleotide repeats

walking, difficulty with

weakness

weakness, generalized

weakness, infant

weakness, progressive

weaning from respirator, failure to

weight loss

Werdnig-Hoffman disease

West disease

wheelchair

whistle, inability to

winging of scapula

workup

X-linked bulbospinal neuronopathy

Showing articles 300 to 350 of 7279 << Previous Next >>

Lymphocytic Infiltrates in the Spinal Cord in Amyotrophic Lateral Sclerosis
Arch Neurol 50:30-36, Engelhardt,J.I.,et al, 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Competent Pts with Adv States of Perm Paralysis Have the Right to Forgo Life-Sustaining Therapy
Neurol 43:224-225, Bernat,J.L.,et al, 1993

Multiple Cerbral Hemorrhages in HTLV-I-Associated Myelopathy
Neurol 43:412-414, Smith,D.,et al, 1993

Conjugal Amyotrophic Lateral Sclerosis:Report of a Young Married Couple
Neurol 43:2378-2380, Cornblath,D.R.,et al, 1993

Brain Imaging in Late-Onset CM2 Gangliosidosis
Neurol 43:2055-2058, Streifler,J.Y.,et al, 1993

Amyotrophic Lateral Sclerosis:T2 Shortening in Motor Cortex at MR Imaging
Radiology 189:843-846, Oba,H.,et al, 1993

Evidence for a Dopaminergic Deficit in Sporadic Amyoptrophic Lateral Sclerosis on Positron Emission Scanning
Lancet 324:1016-1018, Takahashi,H.,et al, 1993

Differential Diagnosis of Guillain-Barre Synd, In Guillain-Barre Synd
Thieme Med Publ, Ch 3, p 42993., Parry,G.J., 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Human T Lymphotropic Virus Type I-Assoc Myelopathy, A Rpt of 10 Pts Born in US
Arch Neurol 49:1113-1118, Sheremata,W.A.,et al, 1992

Chronic Myelopathy Associated with Human T-Lymphotropic Virus Type I (HTLV-I)
Ann Int Med 117:933-946, Gessain,A.&Gout,O., 1992

Clinicopath Conf
Motor Neuron Disease, Progressive-Muscular-Atrophy Type, Case 43-1992, NEJM 327:1298-130592., , 1992

MRI and SPECT in Amyotrophic Lateral Sclerosis, Demonstr of Upper Motor Neurone Invol by Neuroimaging
Neuroradiology 34:389-393, Udaka,F.,et al, 1992

Serum Antibodies to L-Type Calcium Channels in Patients with Amyotrophic Lateral Sclerosis
NEJM 327:1721-1728, 17521992., Smith,R.G.,et al, 1992

Presence of HTLV-I Proviral DNA in Central Nervous System of Patients with HTLV-I-Associated Myelopathy
Ann Neurol 31:39-45, Kira,J.,et al, 1992

GM-1 Ganglioside for Spinal-Cord Injury
NEJM 326:493, Schonhofer,P.S., 1992

Motor Neurone Disease
BMJ 304:459-460, Norris,F.H., 1992

Motor Neurone Disease:A Hospice Perspective
BMJ 304:471-473, O'Brien,T.,et al, 1992

Chronic Neurodegenerative Disease Associated with HTLV-II Infection
Lancet 339:645-646, Hjelle,B.,et al, 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Surgical Treatment of Cervical Spondylotic Myelopathy:Time for a Controlled Trial
Neurol 42:5-13, Rowland,L.P., 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Amyotrophic Lateral Sclerosis and Lymphoma:Bone Marroe Examination and Other Diagnostic Tests
Neurol 42:1101-1102, Rowland,L.P.,et al, 1992

Anti-Hu-Associated Pareneoplastic Encephalomyelitis/Sensory Neuronopathy
Medicine 71:59-72, Dalmau,J.,et al, 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Decreased Glutamate Transport by the Brain and Spinal Cord in Amyotrophic Lateral Sclerosis
NEJM 326:1464-1468, 14931992., Rothstein,J.D.,et al, 1992

Brain Imaging in Human Immunodeficiency Virus Infection
Semin Neurol 12:57-69, Ketonen,L.&Tuite,M.J., 1992

Myelopathy Associated with Human T Cell Lymphotropic Virus Type 1 in a White European Native to England
BMJ 305:453, Ali,A.&Rudge,P., 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Progressive Motor Neuron Disease Associated with Electrical Injury
Muscle & Nerve 14:977-980991., Sirdofsky,M.D.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Olfactory Impairment in Motor Neuron Disease:A Pilot Study
JNNP 54:927-928, Elian,M., 1991

Subacute, Reversible Motor Neuron Disease
Neurol 41:1541-1544, Tucker,T.,et al, 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

HTLV-I-Associated Myelopathy:Clinicopathologic Correlation with Localization of Provirus to Spinal Cord
Neurol 41:1990-1992, Bhigjee,A.I.,et al, 1991

Lymphoma, Motor Neuron Diseases, and Amyotrophic Lateral Sclerosis
Ann Neurol 29:78-86, Younger,D.S.,et al, 1991

The Role of HTLV in HIV-1 Neurologic Disease
Neurol 41:197-202, Berger,J.R.,et al, 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Poliomyelitis-Like paralysis During Recovery from Acute Bronchial Asthma:Possible Etiology and Risk Fators
Pediatrics 88:276-279, Shahar,E.M.,et al, 1991

HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis in the United States
Neurol 41:1355-1357, Janssen,R.S.,et al, 1991

Acute Paralytic Poliomyelitis Presenting as Guillain-Barre Syndrome
J Infection 22:129-133, Yohannan,M.D.,et al, 1991

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

Showing articles 300 to 350 of 7279 << Previous Next >>