Neudle.com: muscle rigidity

Neurology Specific Literature Search

Differential
(Click to cross reference)

abdominal tenderness

abducens nerve paralysis

abstinence syndrome

accomodation, abnormal

acquired immunodeficiency syndrome

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adult polyglucosan body disease

advances in neurology

adverse drug reaction

affect, inappropriate

akinesia of eyelid function

alcohol intolerance

alcohol, neurologic complications with

alien hand syndrome

alkylating agents

alpha and gamma motor system

alpha-synuclein

altered states of consciousness

alternating hemiplegia

alternating rapid movement

Alzheimer's disease

amaurosis fugax, unilateral vs.bilateral

aminoacidopathies

amphiphysin antibodies

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, differential diagnosis

ANA-negative systemic lupus erythematosus

anesthesia, general

aneurysm, anterior communicating

aneurysm, aortic arch

aneurysm, intracranial

angiitis, granulomatous of CNS

angiitis, isolated of CNS

angiography, cerebral, beaded vessels

angiography, cerebral

animal exposure

ankle, swelling of

anterior horn cell disease

anti Ri antibody

antiamphiphysin

antibiotics, neurologic complications with

anticholinergic drugs

anticholinergic drugs, side effects of

anticonvulsants

antispasticity drugs

antiviral agents

aortic arch stenosis

aortic arch study

aphasia, global

aphasia, progressive, primary

apnea, primary central

apraxia of eye movements

apraxia of eyelid opening

arm swing, reduced

arrhythmia, cardiac

arterial dissection, aorta

arteritis, temporal

arthrogryposis multiplex

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

auditory and vestibular pathways

autoimmune cerebellar ataxia

autoimmune disease

autonomic dysfunction

autonomic nervous system

axonal degeneration

baclofen withdrawal

bacterial endocarditis, neurologic manifestations of

bacterial infection

basal ganglia, calcification of

basal ganglia, degeneration

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

baylisascariasis

behavioral disorder

Bell's phenomenon

beta adrenergic agonist

bicaudate index

biologic markers

biopterin deficiency

blepharophimosis

blindness, sudden

blinking, reduced

blood brain barrier

blood dyscrasias, neurologic findings with

bone marrow biopsy

bone marrow infarction

bone marrow necrosis

bone marrow transplantation

Borrelia burgdorferi infection

botulinum toxin

brain biopsy, false negative

brain scan, abnormal

brainstem, atrophy

brainstem, dysfunction

brainstem, infarction of

brainstem, lesion of

brucellosis, nervous system involvement with

Brudzinski's sign

bulbar dysfunction

burning feet, differential diagnosis of

calcification, intracranial

calf hypertrophy

cancer, unknown origin

carbon monoxide poisoning

carcinoma of bladder

carcinoma of breast

carcinoma of lung

carcinoma of unknown origin

carpo-pedal spasm

CAT scan, abnormal

CAT scan, angiography

CAT scan, chest

CAT scan, dense artery sign

CAT scan, emission

CAT scan, emission, abnormal

catatonia, lethal

cauda equina, enhancement

cauda equina, lesion of

caudate nucleus, atrophy

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar degeneration

cerebellar edema

cerebellar lesion

cerebellum, disease of

cerebral cortical atrophy

cerebral embolism

cerebral embolism, mechanical extraction

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count, normal

cerebrospinal fluid, cytology

cerebrospinal fluid, cytology, false negative

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, eosinophilia of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, gold sol.curve of

cerebrospinal fluid, intraventricular

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, pressure increased

cerebrospinal fluid, pressure low

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, multiple

cerebrovascular accident, young adult

ceruloplasmin, serum

Charcot-Marie-Tooth

chasing the dragon

chelation therapy

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

chewing, impaired

choreoathetosis

choreoathetosis, paroxysmal

chromosomal abnormality

cirrhosis, infancy

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clostridium tetani

clubbing of fingers

cocaine, intrauterine exposure

coccidioidomycosis

cogwheel rigidty

cold hands sign

cold intolerance

cold temperature

collagen vascular disease

coma, causes of

coma, unknown etiology

complement deficiency

concentration, impaired

conduction block

confusional state, acute

Congo red stain

conjugate gaze, forced

conjunctival injection

contactin associated protein like 2 antibodies

contractures, joint

controversies in neurology

convergence, impaired

conversion reaction

corpus callosum, infarction of

cortical blindness

cortical infarction

cortical-basal ganglionic degeneration

cost effectiveness

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein

C-reactive protein, elevated

creatine phosphokinase(CPK)elevated

critical care unit

cry, high-pitched

crying, pathologic

cultured skin fibroblasts

cylindrical spiral

cytomegalic inclusion disease

cytomegalovirus infection

dantrolene sodium

decerebrate posture

decorticate posture

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed muscle relaxation

dementia, childhood

dementia, rapidly progressive

dementia, reversible

dementia, treatment of

dense basilar artery sign

dense middle cerebral artery sign

dentate nuclei, lesion of

dermatomyositis

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

differential diagnosis

disability, neurological

distal muscle atrophy

distal muscle weakness

doll's head maneuver

dopa responsive dystonia

dopamine agonist

dopamine antagonist

dropped head syndrome

drug abuse, inhalation

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

drug induced neurologic disorders in children

drug interactions

drug withdrawal

dural sinus thrombosis

dysdiadochokinesia

dysequilibrium syndrome

dysferlinopathy

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dysostosis multiplex

dystonia musculorum deformens

dystonia, children

dystonia, drug induced

dystonia, focal

dystonia, paroxysmal

dystonia, treatment of

echocardiogram, transesophageal

echocardiogram, transthoracic, false negative

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electroencephalogram, triphasic delta waves

electroencephalogram, video monitoring with

electron microscopy

embolism, paradoxical

embolism, septic

embolism, vertebral-basilar artery

emergencies, neurologic

empyema, epidural-spinal

empyema, subdural-spinal

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, eastern equine

encephalitis, Powassan

encephalitis, viral

encephalomyelitis

encephalomyelitis, autoimmune

encephalomyelitis, parainfectious

encephalopathy, acute

encephalopathy, delayed

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

endocarditis, acute bacterial

endocarditis, infectious

endovascular therapy

enterovirus infection of CNS

enzyme inhibition

epidemiology of neurology

epilepsia partialis continua

episodic disorders

erythema migrans

esophageal varices

evidence-based research

exercise intolerance

extrapyramidal movement disorder, progressive

eye closure, forced

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

facial nerve palsy

facial nerve palsy, bilateral

facial rigidity

fasciculation, benign

feeding disorder

fine motor function, impaired

fingerprint bodies

flaccid paralysis

flu-like illness

fourth ventricle, compression

fracture, long bone

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

Friedreich's ataxia, late onset

frontal behavioral spatial syndrome

frontal lobe, pathologic signs of

frontal lobe, space occupying lesion of

fundus, abnormality of

fungal infection, CNS

F-wave response

gag reflex, depressed

gait, festinating

gamma amino butyric acid

gammaglobulin therapy, intravenous

gangliosidosis GM1

gangliosidosis GM2

gastrocnemius muscle weakness

gastroenteritis

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamic acid decarboxylase, antibody

glycine receptor antibodies

glycogen storage disease

Gowers maneuver

gram positive rod

granular osmiphilic material

granuloma, pulmonary

granulomatous hypophysitis

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, etiology of

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

head circumference and brain development

head retraction reflex

headache, bifrontal

headache, elderly

headache, new onset

headache, persistent

headache, positional

headache, progressive

headache, recurrent

headache, severe

headache, sudden onset of

headache, vascular

headache, worst of life

health insurance

helminthic infection of CNS

hematoma, intracerebral

hematuria, microscopic

hemiparesis, transient

hemoglobin abnormality, neurologic complications of

hemophilus influenza

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

heralding manifestation

herniated disc, differential diagnosis of

hexosaminidase-A

human immunodeficiency virus type 1

Huntington's chorea

Huntington's chorea, akinetic-rigid form

Huntington's disease, children

hydrocephalus, normal pressure

hyperbilirubinemia

hyperexcitable peripheral nerve disorder

hyperintense vessel sign

hyperpigmentation of skin

hypertension, cerebrovascular disease with

hypertensive crisis

hyperthyroidism

hypertonia, congential

hypoalbuminemia

hypoglycorrhachia

hypometric saccades

hypomyelination

hyponatremia with cerebral disorders

hyponatremic encephalopathy

hypoparathyroidism

hypotonia, infants

iatrogenic neurologic disorders

ideomotor apraxia

ileus, paralytic

imbalance, postural

immediate recall

immune checkpoint inhibitors

immune-related adverse events

immunoelectrophoresis, serum

immunofluorescent"band"test

immunohistochemistry

immunology and the nervous system

immunomodulation

immunosuppression

immunosuppressive agents

inability to stand on tiptoes

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion body myositis

incontinence, fecal

infantile bilateral striatal necrosis

infection, recurrent

intellectual deficit

intellectual deterioration

internal capsule

interneurone disease

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, differential diagnosis of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, multiple

intracranial pressure, increased

intrathecal antispasticity drugs

iodine deficiency

Isaacs syndrome

ischemic exercise test

Jakob-Creutzfeldt disease

jaw contractures

jaw jerk, abnormal

Kayser-Fleischer ring

kinesia paradoxica

klippel feil syndrome

Korsakoff's psychosis

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

lactic dehydrogenase(LDH)

L-dopa, drug interactions with and side effects of

L-dopa, potentiators of

leg spasms, painful

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

leukemia, neurologic findings assoc.with

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, toxic

level of consciousness, decreased

Lewy body disease, diffuse

limbic encephalitis

lipid storage disorder of CNS

livedo reticularis

liver function enzymes

liver transplantation

locked-in syndrome

low back pain, chronic

low birth weight

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, cervical

lymphocytic choriomeningitis

lymphocytic meningoradiculitis

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malformation, vascular

malformation, vascular, cerebral

malignancy screen

malignant hyperpyrexia

marche a petits pas

McArdle's disease

meconium staining

mediastinum, mass of

medulla oblongata, lesion of

melanoma, malignant

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis, aseptic

meningitis, bacterial

meningitis, CSF findings in

meningitis, drug induced

meningitis, elderly

meningitis, eosinophilic

meningitis, fungal

meningitis, gram negative

meningitis, leukemic

meningitis, lupus

meningitis, meningococcal

meningitis, recurrent

meningitis, syphilitic

meningococcemia

meningoencephalitis

meningoencephalomyelitis

meningoencephalopathy

mental retardation

mental status, abnormal

metabolic acidosis

methylhydrazine derivatives

microhemorrhage, intracerebral

midbrain, atrophy

midbrain, infarction of

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

Mini Mental Status Examination

mitral valve lesion

mitral valve vegetation

molecular genetics

monoamine oxidase inhibitors

monoclonal antibodies

Morvan's fibrillary chorea

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, psychogenic

movement disorder, treatment of

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, eye of tiger sign

MRI, FLAIR, hyperintense vessels

MRI, gradient-echo

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, sulcal hyperintensity

MRI, susceptibility weighted

multinucleated giant cell

multiple sclerosis

multiple sclerosis, diet in

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple sclerosis, treatment of

multiple system atrophy

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle hypertrophy

muscle pain-fasciculation syndrome

muscle phosphorylase deficiency

muscle relaxant

muscle stiffness

muscle tenderness

muscle twitching

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

muscle, metabolic disorders of

muscular dystrophy

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, treatment of

myasthenic crisis

myasthenic syndrome

myasthenic syndrome, treatment of

mycoplasma pneumoniae

myoclonic jerks

myoclonus, action

myoclonus, epilepsy

myoclonus, sleep

myopathy, amyloid

myopathy, carcinomatous

myopathy, hypocalcemic

myopathy, necrotizing

myopathy, thyroid disease causing

myotonia congenita

myotonia dystrophica

myotonic crisis

nasal stuffiness

nausea and vomiting

neisseria meningitis

neonatal abstinence syndrome

neoplasm, metastatic to CNS

nerve conduction studies

nerve conduction studies, motor

nerve root enhancement

neuritis, causes of

neuroendocrinology

neuroleptic induced catatonia

neuroleptic malignant syndrome

neuroleptic, atypical

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromyotonia and axonal neuropathy

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, diabetic

neuropathy, motor

neuropathy, motor, multifocal

neuropathy, multifocal

neuropathy, painful

neuropathy, peripheral

neuropathy, peripheral, treatment

next-generation sequencing

nitrogen mustard

NMDA antagonists

nonsteroidal anti-inflammatory drug

nutritional deficiency

nystagmus, rotary

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

oculocephalic reflex

oculogyric crisis

old age, neurology of

ophthalmoplegia

ophthalmoplegia, total

ophthalmoplegic migraine

opportunistic infection

opsoclonus-myoclonus syndrome

optic chiasm, enlarged

optic nerve, enlarged

optic neuritis, bilateral

optic neuropathy

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

orthostatic hypotension

osteoarthritis, lumbar spine

overlap syndrome

pain, abdominal

palatal myoclonus

paralysis, acute

paralysis, acute areflexic

parameningeal infection

paramyotonia congenita

paraneoplastic brainstem encephalitis

paraplegia, acute

paraspinal muscle

paresthesias, feet

paresthesias, hands

Parkinson disease

Parkinson disease, asymmetric onset

Parkinson disease, axial symptoms

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, etiology of

Parkinson disease, freezing phenomena in

Parkinson disease, hemiparesis in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, nonmotor problems of

Parkinson disease, on-off phenomena in

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinson disease, unilateral

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

Parkinsonism, freezing phenomena in

paroxysmal dystonic choreoathetosis

paroxysmal neurologic deficits

paroxysmal neurologic disorder

PAS positive material in the brain

patent foramen ovale

pathologic reflex

patient information and support

pediatric neurology

penguin silhouette sign

Penumbra System

percussion induced muscle contraction

periarteritis nodosa

pericardial friction rub

periodic paralysis, thyrotoxic

peroxisomal disease

personality change

phencyclidine poisoning

phenothiazine, dyskinesia associated with

phosphorylase b kinase deficiency

physical therapy

pigmentary retinopathy

pituitary stalk

pituitary stalk, enlarged

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

pleural effusion

pneumoencephalogram(PEG)

poliomyelitis-like illness

polymerase chain reaction

polymyalgia rheumatica

polyneuropathy, chronic inflammatory demyelinating

polyneuropathy, uremic

pons, infarction of

postoperative neurologic complications

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

progressive encephalomyelitis with rigidity syndrome

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

proprioception, abnormal

proximal muscle atrophy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychomotor retardation

psychosis, acute

psychotic behavior

ptosis, bilateral

pulmonary opacity

pupil, dilated, bilateral

pure motor stroke

pyramidal tract

pyramidal tract dysfunction

quadriplegia, transient

quality of life

rapidly progressing neurologic illness

release phenomena

remote effect of cancer on the nervous system

renal transplantation

reserpine and reserpine like drugs

respiratory failure

respiratory tract infection

restless leg syndrome

reticulum cell sarcoma

retinitis pigmentosa

reversible neurologic disorder

rigidity, axial

rippling muscle disease

risus sardonicus

root lesion, nerve

saccadic eye movements, abnormal

salivation, excessive

Schmidt syndrome

Schwartz-Jampel syndrome

scoliosis, neurologic association with

sea-blue histiocytes

second wind phenomena

sedimentation rate

sedimentation rate, elevated

seizure, differential diagnosis of

seizure, duration

seizure, nonepileptic

seizure, withdrawal

selective serotonin reuptake inhibitors

self-mutilation

sensory loss, cortical

sensory symptoms

sequencing difficulty

serologic testing

serologic testing of cerebrospinal fluid

serotonin agonist

serotonin syndrome

shoulder, pain in

sickle cell disease

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

sodium channel dysfunction

spasticity, treatment of

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, compression of

spinal cord, compression, epidural abscess causing

spinal cord, lesion of

spine, tenderness

spirochete infection

splenic infarcts

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

stem cell transplantation

stereotaxic surgery

steroid therapy, CNS treatment and complications with

stiff limb syndrome

stiff man syndrome

stimulation, deep brain

stimulation, sensory

stooped posture

storage disease of CNS

stress, emotional

striatum, lesion of

strychnine poisoning

subdural hematoma

substantia nigra

sweating, abnormality of

symmetric brain lesions

synucleinopathy

syphilis, neurologic complications with

systemic illness

systemic inflammatory response syndrome

systemic lupus erythematosus

systemic lupus erythematosus, neurologic complications with

tandem gait, ataxic

Tay-Sachs disease

temporal artery, biopsy

temporal artery, tender

temporal lobe, lesion

temporal lobe, lesion, bilateral

tetanus antitoxin

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tick-borne encephalitis

tone, muscle, increased

tongue, enlarged

tongue, fasciculations of

tonic foot response

toxoplasmosis, acquired

toxoplasmosis, CNS

treatment of neurologic disorder

tremor, intention

tremor, resting

tricyclic antidepressant

trientine dihydrochloride

trifluoperazine

trinucleotide repeats

Trousseau's sign

tyrosine hydroxylase deficiency

ultrasonography

unconsciousness

upgaze, paralysis of

upward deviation of eyes

uremic encephalopathy

uremic twitching

urinary incontinence

urinary retention

urine test for metabolic disorders

urine test in toxic screen

varicella zoster virus

vertebral infarction

vertigo, cervical

vertigo, treatment of

very long chain fatty acids

vibratory sensation, abnormal

vincristine neurotoxicity

viral infection

viral infection, CNS

vision, blurred

visual evoked response

visual impairment

visual symptoms

vitamin B3, deficiency

vitamin deficiency

vitamin, multiple

vocal cord paralysis

voice, abnormality of

walking, difficulty with

weakness, acute

weakness, episodic

weakness, generalized

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

white matter disease

whole body imaging

wide based gait

Wolfram syndrome

yawning movements

zoster sine herpete

Showing articles 1400 to 1450 of 2896 << Previous Next >>

Dose-Ranging Study of Riluzole in Amyotrophic Lateral Sclerosis
Lancet 347:1425-1431, Lacomblez,L.,et al, 1996

Skin Involvement in Amyotrophic Lateral Sclerosis
lancet 347:1226-1227, Kolde,G.,et al, 1996

Acute Meningitis with a Negative Gram's Stain:Clinical and Management Outcomes in 171 Episodes
Am J Med 100:78-84, Elmore,J.G.,et al, 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Delayed-Onset Progressive Movement Disorders after Static Brain Lesions
Neurol 46:68-74, Scott,B.L.,et al, 1996

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Exacerbation of Myasthenia Gravis Associated with Cocaine Use
Neurol 46:271-272, Daras,M.,et al, 1996

Acute Rectus Muscle Palsy in Children as a Result of Orbital Myositis
J Pediatr 128:230-233, Pollard,F.,et al, 1996

HIV Encephalitis Presenting with Severe Generalized Chorea
Neurol 46:1163-1165, Gallo,B.V.,et al, 1996

Intravenous Immunoglobulin Treatment of Neurological Disease
JNNP 60:359-361, Otten,A.,et al, 1996

A Woman with a Relapsing Psychosis Who Got Better with Prednisone
Lancet 347:1288, Cohen,L.,et al, 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

Pure Motor Hand Weakness
Semin Neurol 16:75-81, Lewis,R.A., 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Sustained Myoglobinuria:The Presenting Manifestation of Dermatomyositis
Neurol 47:119-123, Rose,M.R.,et al, 1996

Multiple Mitochondrial DNA Deletions in Sporadic Inclusion Body Myositis:A Study of 56 Patients
Ann Neurol 39:789-795, Santorelli,F.M.,et al, 1996

Is Chronic Respiratory Failure in Neuromuscular Diseases Worth Treating
JNNP 61:1-3, Shneerson,J.M., 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Clinical Heterogeneity of Adhalin Deficiency
Ann Neurol 39:196-202, Morandi,L.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Another Kind of Knapsack Palsy
Neurol 46:585-586, Pringle,C.E.,et al, 1996

Autonomic Ganglionitis with Severe Hypertension, Migraine, and Episodic but Fatal Hypotension
Neurol 47:817-821, Lee,H.C.,et al, 1996

Infarction of Superior Cerebellar Artery Presenting as Cerebellar Symptoms
Stroke 27:1679-1681, Terao,S.,et al, 1996

Risk of Stroke During Long-Term Anticoagulant Therapy in Patients After Myocardial Infarction
Ann Neurol 39:301-307, 2811996., Azar,A.J.,et al, 1996

Palliative Care in Neurology
Neurol 46:870-872, 5981996., Bernat,J.L.,et al, 1996

Restless Legs Syndrome and Leg Cramps in Fibromyalgia Syndrome:A Controlled Study
BMJ 312:1339, Yunus,M.B.&Aldag,J.C., 1996

Campylobacter Jejuni Infection and Anti-GM1 Antibodies in Guillain-Barre Syndrome
Ann Neurol 40:181-187, Jacobs,B.C.,et al, 1996

Needle Electromyography in the Thoracic Paraspinal Muscles of Motor Neuron Disease
No to Shinkei-Brain & Nerve 48:637-642996., Kyuno,K.,et al, 1996

Pediatric Ulnar Mononeuropathy:Report of 21 Electromyography-Documented Cases & Review of Literature
J Child Neurol 11:116-120, Felice,K.J.&Jones,H.R., 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Neuralgic Amyothrophy Misdiagnosed as Diaphragmatic Rupture
Muscle & Nerve 19:1181-1182996., Beydoun,S.R.&Rodriquez,R., 1996

Acute Myopathy of Intensive Care:Clinical, Electromyographic, and Pathological Aspects
Ann Neurol 40:645-654, Lacomis,D.,et al, 1996

Congenital Muscular Dystrophy with Primary Laminin a2 (Merosin) Deficiency Presenting as Inflammatory Myopathy
Ann Neurol 40:782-791, Pegoraro,E.,et al, 1996

Erroneous Diagnosis Corrected After 28 Years
Arch Neurol 53:1194-1196, Gordon,P.H.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Motor Neuron Disease, Lymphoproliferative Disease, and Bone Marrow Biopsy
Muscle & Nerve 19:1334-1337996., Louis,E.D.,et al, 1996

Immunoassays Fail to Detect Antibodies Against Neuronal Calcium Channels in Amyotrophic Lateral Sclerosis Serum
Ann Neurol 40:695-700, 6911996., Arsac,C.,et al, 1996

Lambert-Eaton Myasthenic Syndrome Presenting with Severe Respiratory Failure
Muscle & Nerve 19:1328-1333996., Nicolle,M.W.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

The Electrophysiological Study of Diff Dx Between ALS & Cervical Spondylotic Myelopathy
EMG & Clin Neurophysiology 35:231-238995., Kang,D.X.&Fan,D.S., 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Lambert-Eaton Myasthenic Syndrome:Clinical Diagnosis,Immune-Mediated Mechanisms,and Update on Therapies
Ann Neurol 37:S63-S73, Sanders,D.B., 1995

Assessment:Neurological Evaluation of Male Sexual Dysfunction
Report of the Therapeutics & Tech Assess Subcommittee of the AAN, Neurol 45:2287-229295., , 1995

Oral Sumatriptan-Associated Transmural Myocardial Infarction
Neurol 45:2274-2276, O'Connor,P.&Gladstone,P., 1995

Clinicopath Conf
Progressive Muscular Atrophy, Case 36-1995, NEJM 333:1406-1412995., , 1995

Showing articles 1400 to 1450 of 2896 << Previous Next >>