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Differential
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abdominal distention

abdominal muscle paralysis

abdominal protrusion

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

adverse drug reaction

alcohol, heart involvement with

alcohol, neurologic complications with

alpha glucosidase

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, bulbar

amyotrophic lateral sclerosis, atypical

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, misdiagnosis

amyotrophic lateral sclerosis, prognosis

anterior horn cell disease

anti signal recognition particle antibody

arrhythmia, cardiac

arthrogryposis multiplex

aspartate aminotransferase

ataxia, sensory

atrioventricular block

autoimmune disease

azidodeoxythymidine

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, children

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

burning paresthesia

calcification, intracranial

calf hypertrophy

cardiovascular disease

carpal tunnel syndrome

CAT scan, abnormal

CAT scan, false negative

central core disease

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebral cortical atrophy

cerebral embolism

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

Charcot-Marie-Tooth

chewing, impaired

chromosomal abnormality

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cold temperature

conduction block

congenital heart disease

congestive heart failure

contractures, joint

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

delay in diagnosis

dementia, frontotemporal

dermatomyositis

developmental milestones

developmental retardation

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic amyotrophy

differential diagnosis

difficulty climbing stairs

dislocated hip, congenital

distal muscle atrophy

distal muscle weakness

drug induced neurologic disorders

dysferlinopathy

dystrophic calcification

electrocardiogram, abnormal

electromyogram, decremental response

electron microscopy

Emery-Dreifuss muscular dystrophy

encephalomyelitis

encephalomyelitis, parainfectious

encephalopathy, progressive

entrapment neuropathy

enzyme treatment

enzyme, muscle disease

epidemiology of neurology

extraocular muscle lesion

facial weakness

facial weakness, bilateral

fatigable chewing

finger flexor weakness

finger weakness

flu-like illness

gammaglobulin therapy, intravenous

gastrocnemius muscle weakness

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

glycogen debranching enzyme deficiency

glycogen storage disease

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

headache, severe

headache, worst of life

heart block, complete

heralding manifestation

hip flexor weakness

histochemistry of muscle

human immunodeficiency virus type 1

hyperparathyroidism

hyperthyroidism

hypotonia, infants

immediate recall

immunosuppressive agents

inability to stand on tiptoes

inclusion bodies

inclusion bodies, eosinophilic intranuclear

inclusion body myositis

intestinal pseudoobstruction

intrinsic hand muscles, wasting of

klippel feil syndrome

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lactic acidemia

leg weakness, bilateral

leg weakness, unilateral

level of consciousness, decreased

lid closure, weakness of

life expectancy

lumbosacral plexopathy

lumbosacral plexus

lumbosacral plexus, neuritis

lymphadenopathy

lymphadenopathy, cervical

lysosomal storage disease

lysosomes, abnoral

malignant hyperpyrexia

McArdle's disease

medulla oblongata, lesion of

meningeal enhancement

meningoencephalomyelitis

mental retardation

mental status, abnormal

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve prolapse

molecular genetics

monoclonal gammopathy

monoclonal gammopathy of uncertain significance

mononeuritis multiplex

motor neuron disease

motor neuron disease, spontaneous recovery

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle phosphorylase deficiency

muscle stiffness

muscle strength, testing

muscle tenderness

muscle wasting, diffuse

muscle weakness

muscle weakness, insidious onset of

muscle weakness, proximal

muscle, metabolic disorders of

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, differential diagnosis of

muscular dystrophy, distal, Miyoshi

muscular dystrophy, Duchenne

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

myasthenia gravis

myasthenia gravis, differential diagnosis

myasthenia gravis, limb-girdle

myasthenia gravis, misdiagnosis of

myasthenic crisis

mycoplasma pneumoniae

myopathy, alcoholic

myopathy, amyloid

myopathy, autoimmune

myopathy, carcinomatous

myopathy, drug-induced

myopathy, hereditary

myopathy, inclusion body

myopathy, inclusion body with Paget's disease

myopathy, mitochondrial

myopathy, necrotizing

myopathy, proximal

myopathy, quadriceps

myopathy, steroid induced

myopathy, thyroid disease causing

myopathy, vacuolar

myositis, focal

myotonia dystrophica

myotonic discharges

nausea and vomiting

nemaline rod myopathy

nemaline rod myopathy, adult onset

nerve conduction studies

neuritis, causes of

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuroophthalmology

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, motor, multifocal

neuropathy, painful

neuropathy, peripheral

next-generation sequencing

nystagmus, rotary

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

pacemaker, cardiac-transvenous

Paget's disease

pain, abdominal

paraproteinemia

paraspinal muscle

paraspinal muscle weakness

parathyroid adenoma

plasma cell dyscrasia

pleocytosis of cerebrospinal fluid

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic inflammatory demyelinating, variant form

polyneuropathy, chronic inflammatory demyelinating-pure motor syn

polyneuropathy, chronic inflammatory demyelinating-sens atax var

polyneuropathy, chronic inflammatory demyelinating-variant forms

polyradiculoneuropathy

Pompe's disease of glycogen storage

positive sharp waves

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

progressive neurologic disorder

progressive spinal muscular atrophy

proximal muscle atrophy

pseudohypertrophy

quadriceps atrophy

quadriceps weakness

radionuclide imaging, heart

ragged-red fibers

rapidly progressing neurologic illness

repetitive nerve stimulation

respiratory failure

respiratory tract infection

retina, abnormal

rheumatoid arthritis

sclerosis, bone

scoliosis, neurologic association with

sensorineural hearing loss

sensory symptoms

serologic testing

shoulder, subluxation

spinal cord, lesion of

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, classification

spinal muscular atrophy, intermediate form

standing difficulty

steroid therapy, CNS treatment and complications with

stiff man syndrome

strokelike episodes

survival motor neuron gene

systemic illness

tandem gait, ataxic

temporalis muscle wasting

tongue, enlarged

tongue, fasciculations of

tongue, weakness

toxins, nervous system

transverse smile

treatment of neurologic disorder

trinucleotide repeats

upgaze, paralysis of

upward deviation of eyes

walking, difficulty with

weakness, fatiguable

weakness, generalized

weakness, progressive

weakness, proximal

weakness, rapidly progressive

weaning from respirator, failure to

Werdnig-Hoffman disease

white matter disease

winging of scapula

X-linked bulbospinal neuronopathy

X-linked myopathy

x-linked myopathy with excessive autophagy

Showing articles 700 to 750 of 4234 << Previous Next >>

Reversible Ipecac Myopathy
Arch Neurol 42:188-190, Mateer,J.E.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Amyotrophic Lateral Sclerosis:A Double-Blind Crossover Trial of Thyrotropin-Releasing Hormone
JNNP 47:1332-1334, Imoto,K.,et al, 1984

Nystagmus in Motor Neuron Disease:Clinicopathological Study of Two Cases
Ann Neurol 16:71-77, Kushner,M.J.,et al, 1984

Inhibition of Terminal Axonal Sprouting by Serum From Patients with Amyotrophic Lateral Sclerosis
NEJM 311:933-939, Gurney,M.E.,et al, 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

Myasthenia Gravis & Myasthenic Syndromes
Ann Neurol 16:519-534, Engel,A.G., 1984

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

Monomelic Amyotrophy
Arch Neurol 41:388-394, Gourie-Devi,M.,et al, 1984

Benign Focal Amyotrophy
Arch Neurol 41:678-679, Riggs,J.E.,et al, 1984

Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT
Neurol 34:1456-1460, Yamamoto,T.,et al, 1984

Clinicopathological Conference
Maroteaux-Lamy Syndrome, Case 44-1983, NEJM 309:1109-1117983., , 1983

Endocrine Myopathies
BMJ 287:705-708, Kendall-Taylor,P.,et al, 1983

Conjugal Amyotrophic Lateral Sclerosis
Ann Neurol 14:699, Paolino,E.,et al, 1983

Neurodegenerative Disease of Infancy & Childhood
Ann Neurol 13:351-364, Dyken,P.,et al, 1983

Myopathy & Hypersensitivity to Phenytoin
Neurol 33:790-791, Harney,J.,et al, 1983

Amyotrophic Lateral Sclerosis & Pet Exposure
NEJM 309:244-245, Schenkman,M.,et al, 1983

Proximal Myopathy Due to Discrete Carcinomatous Metastases in Muscle
JNNP 46:358-360, Doshi,R.,et al, 1983

Oligoclonal IgG Bands in Cerebrospinal Fluid in Various Neurological Diseases
Ann Neurol 13:434-439, Chu,A.B.,et al, 1983

Quadriceps Myopathy:A Varient of the Limb-Girdle Dystrophy Syndrome
JNNP 46:355-357, Swash,M.,et al, 1983

Myositis of Chronic Graft Versus Host Disease
Neurol 33:1222-1224, Reyes,M.G.,et al, 1983

Acute Respiratory Failure in Motor Neuron Disease
Arch Neurol 40:30-32, Hill,R.,et al, 1983

Effect on Weakness & Spasticity in Amyotrophic Lateral Sclerosis of Thyrotropin-Releasing Hormone
Lancet 2:73-75, Engel,W.K.,et al, 1983

Syndromes of Amytrophic Lateral Sclerosis & Dementia:Relation to Transmissible Creutzfeldt-Jakob Disease
Ann Neurol 14:17-26, Salazar,A.M.,et al, 1983

Nonfamilial Amyotrophy with Dementia, etc
Advances in Neurology, Human Motor Neuron Diseases, Ed. Rowland, Raven Press, NY 1982 vol 36, p 173., Tyler,H.R., 1982

Clin. Path. Conference
Osteopetrosis, Malignant Juvenile Form, Case Record 37-1982, NEJM 307:735-74382., , 1982

Enigmatic Dyspnoea:An Unusual Presentation of Motor-Neuron Disease
Lancet 1:933-935, Nightingale,S.,et al, 1982

Long-Term Management of Respiratory Failure in Amyotrophic Lateral Sclerosis
Ann Neurol 12:18-23, Sivak,E.,et al, 1982

Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982

Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982

Amyotrophic Lateral Sclerosis & Paraproteinemia
Neurol 32:896-898, Krieger,C.,et al, 1982

Myopathy Due to Mercaptopropionyl Glycine
BMJ 285:939, Hales,D.S.M.,et al, 1982

Classic Amyotrophic Lateral Sclerosis With Dementia
Arch Neurol 39:681-683, Wilkstrom,J.,et al, 1982

Inclusion Body Myositis
Arch Neurol 39:760-764, Danon,M.J.,et al, 1982

Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982

Cardiomyopathy Associated with the Syndrome of Amyotrophic Chorea & Acanthocytosis
Ann Int Med 96:616-617, Faillace,R.T.,et al, 1982

Neurological Aspect of Hyponatraemia
Postgrad Med J 58:737-740, Daggett,P.,et al, 1982

A Prospective Study of Lacunar Infarction Using Computerized Tomography
Neurol 32:49-56, Donnan,G.A.,et al, 1982

Preservation of the Phrenic Motorneurons in Werdnig-Hoffman Disease
Ann Neurol 9:506-510, Kuzuhara,S.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

Myopathy Induced by Rifampicin
BMJ 283:105-106, Jenkins,P.,et al, 1981

Motor Neuron Disease:Decremental Responses to Repetitive Nerve Stimulation
Neurol 31:202-204, Bernstein,L.P.,et al, 1981

Vitamin E Deficiency in Werdnig-Hoffmann Disease
Ann Neurol 10:266-268, Shapira,Y.,et al, 1981

Circulating Immune Complexes in Neurologic Disease
Neurol 31:1402-1407, Noronha,A.B.C.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Arthrogryposis Multiplex Congenita
Editorial, BMJ 283:2-31981., , 1981

Pattern Reversal Visual Evoked Potentials
Arch Neurol 38:739-741, Bird,T.D.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Showing articles 700 to 750 of 4234 << Previous Next >>