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Differential
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abdominal distention

acid maltase deficiency

acid maltase deficiency, adult

acromegaly

acute intermittant porphyria

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholic polyneuropathy

aneurysm, thoracic aortic

anterior horn cell disease

anticonvulsants

antineurofascin antibodies

aortic wall, thickened

aortitis

areflexia

arrhythmia, cardiac

arterial dissection, aorta

arterial dissection, wall thickness

autonomic dysfunction

brachial neuritis, acute

cardiovascular disease

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, emission, abnormal

CAT scan, metrizamide

CAT scan, muscle

CAT scan, myelogram with

cataracts

cauda equina

cauda equina, enhancement

cauda equina, lesion of

cavernous sinus

cavernous sinus, lesion of

central nervous system, infection of

cerebellar lesion

cerebral ischemia

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular disease, cardiovascular disease with

cerebrovascular disease, risk factors in

chromosomal abnormality

chromosome 17

claudication, intermittent of cauda equina

Clinical Pathologic Conference(C.P.C.)

CLOVES syndrome

complications

confusion

congenital malformation

congenital myopathy

congestive heart failure

contactin associated protein like 1 antibodies

contractures, joint

coronary artery disease

corticotropin level

corticotropin-releasing factor

cortisol, elevated

cranial nerve enlargement

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cysticercosis, cerebral

cysticercosis, disseminated

cysticercosis, intraventricular

cysticercosis, miliary

deafness

deep gray nuclei

Dejerine-Sottas syndrome

delay in diagnosis

denervation of muscle

dentate nuclei

dentate nuclei, lesion of

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

diamond on quadriceps

diaphragmatic paralysis

differential diagnosis

difficulty climbing stairs

dilantin

diplopia

distal muscle atrophy

distal muscle weakness

dysthyroid ocularmyopathy

dystonia

dystonia, post traumatic

dystrophin

dystrophin associated proteins

echocardiogram

echocardiogram, LVH

edema, periorbital

electrocardiogram, abnormal

electrocardiogram, LVH

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

encephalopathy

encephalopathy, progressive

entrapment neuropathy

enzyme, defect

eosinophilic fasciitis

epidermal nevus syndrome

exercise

exophthalmus

extraocular muscle enlargement

facial hair, excessive

facial pain

facial pain, atypical

facial weakness

facial weakness, bilateral

failed medical management

fine motor function, impaired

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

gammaglobulin therapy, intravenous

gammaglobulin therapy, intravenous, refractory

genetic diagnosis, prenatal

genetic neurologic disorders

Graves ophthalmopathy

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

hemiatrophy, congenital

hemidiaphragm, paralysis of

hemihypertrophy, congenital

hemihypertrophy, facial

hemimegalencephaly

hemiparesis

hepatomegaly

hereditary myopathy with early respiratory failure

hypopigmentation of skin

intrinsic hand muscles, wasting of

irritability

Isaacs syndrome

Kobberling-Dunnigan syndrome

Krabbe's disease

Kugelberg-Welander syndrome

kyphoscoliosis, neurologic causes of

lacrimal gland enlargement

laminectomy, cervical

laminectomy, lumbar

learning disability

learning disability, in children

left ventricular dilatation

leg atrophy

leg numbness

leg swelling

leg weakness, unilateral

leukemia

leukocyte enzyme abnormality

liver function enzymes

lordosis

lumbosacral plexopathy

lymphoma

lymphopenia

macrocephaly

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malignant hyperpyrexia

masseter muscle hypertrophy

mental status, abnormal

monoclonal gammopathy

mononeuritis multiplex

mononeuropathy

mononeuropathy chronic inflammatory demyelinating

MRI, contrast enhanced

MRI, cranial nerves

MRI, hypointense signal foci on

MRI, lumbosacral plexus

MRI, muscle

MRI, optic nerve

MRI, orbit

MRI, peripheral nerve

MRI, spinal cord

MRI, spine

MRI, vessel wall

MRI, vessel wall enhancement

MRS

mucormycosis

multimodal neuroimaging

multiple myeloma

muscle atrophy, focal

muscle atrophy, progressive

muscle biopsy

muscle cramp

muscle hypertrophy

muscle hypertrophy, congenital

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Becker, carrier

muscular dystrophy, cardiovascular changes with

muscular dystrophy, central nervous system abnormality

muscular dystrophy, classification

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, dystrophin normal

muscular dystrophy, facioscapulohumeral

muscular dystrophy, female occurrence of

muscular dystrophy, limb-girdle

muscular dystrophy, pattern of muscle involvement

myelogram

myelopathy

myeloradiculopathy

myocardial infarction

neoplasm, hormone producing, ectopic

neoplasm, metastatic to muscle

neoplasm, metastatic to orbit

neoplasm, peripheral nerve

nephrotic syndrome

nerve biopsy

nerve conduction studies

nerve enlargement

nerve hypertrophy

nerve injury

nerve root enhancement

nerve root hypertrophy

neuritis

neuritis, causes of

neuritis, heavy metals causing

neurocutaneous disease

neurologic disease, diagnoses of

neurologic examination

neuropathy, autoimmune

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, hypertrophic

neuropathy, medication induced

neuropathy, onion bulb

neuropathy, peripheral

night blindness

night sweats

node of Ranvier

nodopathy, autoimmune

optic chiasm, enlarged

optic nerve

optic nerve sheath enhancement

optic nerve, compression of

optic nerve, enlarged

optic nerve, lesion of

optic neuropathy

optic neuropathy, bilateral

orbit, cellulitis of

orbit, inflammation in

orbit, pseudotumor of

paresthesias, lower extremity

PAS positive material in the brain

pathology

percussion induced muscle contraction

perineuritis

perineuritis, optic

peripheral nerve, lesion of

plasma cell dyscrasia

polyneuropathy

polyneuropathy, chronic idiopathic

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, chronic relapsing

polyneuropathy, familial

post polio syndrome

postural abnormality

prenatal diagnosis by amniocentesis

prognosis

progressive neurologic disorder

proptosis

proximal muscle atrophy

rhabdomyosarcoma of orbit

rigidity

rippling muscle disease

sensorineural hearing loss

skin, lesions in neurologic disorders

somnolence

spasticity

speech disorder, childhood

speech, delayed development of

spinal accessory nerve

spinal cord, compression of

spinal cord, neoplasm

spinal muscular atrophy

spinal muscular atrophy, adult onset

spinal muscular atrophy, intermediate form

spinal stenosis

spinal stenosis, familial

startle reaction

steppage gait

steroid

steroid therapy, CNS treatment and complications with

subarachnoid hemorrhage

subcutaneous nodules

sudden death

superior ophthalmic vein

survival motor neuron gene

symmetric brain lesions

syncope

syringomyelia

systemic illness

telangiectases, retinal

temporal artery

temporalis muscle enhancement

temporalis muscle hypertrophy

temporalis muscle swelling

thalamus, lesion of-bilateral

transient ischemic attack

trauma

treatment of neurologic disorder

tremor

trigeminal nerve

trigeminal nerve, abnormality of

trigeminal nerve, hypertrophy

trigeminal nerve, lesion of

trigeminal neuralgia

tripping

ultrasonography, nerve

urinary frequency

urine, dark

vasculitis, large vessel

vertebral artery wall thickness

vision, blurred

visual acuity, decreased

visual fields, constricted

visual loss

vital capacity

weakness

weakness, generalized

weakness, progressive

Showing articles 2050 to 2100 of 3218 << Previous Next >>

Hemifacial Spasm in Rochester & Olmsten County, Minnesota, 1960-21984
Arch Neurol 47:1233-1234, Auger,R.G.&Whisnant,J.P., 1990

Clinical & PET Studies in the'Extrapyramidal Syndrome'of Dementia of the Alzheimer Type
Arch Neurol 47:1318-1323, Tyrrell,P.J.,et al, 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

OKT3 Encephalopathy
Ann Neurol 28:837-838, Coleman,A.E.&Norman,D.J., 1990

Clinicopath Conf
Primary CNS Lymphoma with AIDS, Am J Med 88:169-1761990., , 1990

Benign Plexus Neuropathy in Children
J Pediatr 116:276-278, Zeharia,A.,et al, 1990

Distal Ulnar Neuropathy as a Cause of Finger Tremor:A Case Report
Neurol 40:153-154, Streib,E.W., 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Myopathy and Rhabdomyolysis Associated with Lovastatin-Gemfibrozil Combination Therapy
JAMA 264:71-75, Pierce,L.R.,et al, 1990

Peripheral Neuropathy in the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Neurol 40 1035-1040, Smith,B.E.&Dyck,P.J., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

Autosomal Dominant Cramping Disease
Arch Neurol 47:810-812, Ricker,K.&Moxley,R.T., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Poliomyelitis Outbreak in Isreal in 1988:A Report with two Commentaries
Lancet 335:1192-1198, Slater,P.E.,et al, 1990

Genetic Linkage of Hereditary Motor & SensoryNeuro Type I (Charcot-Marie-Tooth Disease) to Chrom 1 & 17
Neurol 40:1450-1453, Defesche,J.C.,et al, 1990

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

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990

Acute Intermittent Porphyria
JAMA 264:1290-1293, 1315-13161990., Sack,G.H., 1990

Relapse of Infant Botulism
Ann Neurol 28:187-189, Glauser,T.A.,et al, 1990

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

Progressive Myopathy in Hyperkalemic Periodic Paralysis
Arch Neurol 47:1013-1017, Bradkey,W.G.,et al, 1990

Suramin-Induced Polyneuropathy
Neurol 40:954-960, LaRocca,R.V.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

HIV-Related Neuromuscular Syndrome Simulating Motor Neuron Disease
Neurol 40:544-546, Verma,R.K.,et al, 1990

Acute Relapsing Guillain-Barre Syndrome after Long Asymptomatic Intervals
Arch Neurol 47:82-84, Wijdicks,E.F.&Ropper,A.H., 1990

Benefit of Intravenously Administered Immune Serum Globulin in Patients with Guillain-Barre Syndrome
J Pediatr 116:141-144, Shahar,E.,et al, 1990

Lyme Polyradiculoneuropathy Presenting as Increasing Abdominal Girth
Neurol 40:373-375, Daffner,K.R.,et al, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Muscle Cramps
Arch Int Med 150:511-518, McGee,S.R., 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Bismuth Absorption and Myoclonic Encephalopathy During Bismuth Subsalicylate Therapy
Ann Int Med 112:140-141, Mendelowitz,P.C.,et al, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Neurologic Crises in Hereditary Tyrosinemia
NEJM 322:432-437, Mitchell,G.,et al, 1990

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Association of the Eosinophilia-Myalgia Syndrome with the Ingestion of Tryptophan
NEJM 322:869-873, 9261990., Hertzman,P.A.,et al, 1990

Showing articles 2050 to 2100 of 3218 << Previous Next >>