Neudle.com: familial tremor

Differential
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acetazolamide

adrenergic blocker

advances in neurology

adverse drug reaction

agoraphobia

airway obstruction

alcohol

alcohol, neurologic complications with

alcoholism

Alexanders disease

Alexanders disease, adult onset

algorithm

alpha adrenergic blocker

alprazolam

alternating rapid movement

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

ataxia telangiectasia

ataxic-dystonia syndromes

athetosis

athetosis, causes of

attention deficit disorder with hyperactivity

atypical

auditory evoked brainstem potentials

autism

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

Behcet's syndrome

benign essential tremor

benign essential tremor, refractory

beta adrenergic blocker

botulinum toxin, complications of

calcification, intracranial

calcium antagonist

camptocormia

carbon monoxide poisoning

carbonic anhydrase inhibitor

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

cataracts

catecholamine

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral blood flow

cerebral cortical atrophy

cerebral infarction

cerebral ischemia

cerebral palsy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

chromosomal abnormality

chromosome 14

chromosome 3

cingulate island sign

cirrhosis

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

copper metabolism, abnormal

corpus callosum, lesion of

corpus callosum, thinning

degenerative diseases of CNS

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

diarrhea

diet

differential diagnosis

dilantin

disability, neurological

distal muscle atrophy

distal muscle weakness

dizziness

dopa responsive dystonia

dopamine

dopamine agonist

drooling

drug induced neurologic disorders

dysarthria

dysdiadochokinesia

dyskinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, laryngeal

dystonia, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

DYT1 mutation

edema, pedal

efficacy

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

emotional lability

encephalitis

encephalitis, Japanese

encephalitis, viral

epidemiology of neurology

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

Fahr disease

failed medical management

falling

familial

familial hemiplegic migraine

fasciculation

fatal familial insomnia

fatigue

fine motor function, impaired

finger nose finger test

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, pathologic signs of

gabapentin

gait disorder

gait, festinating

gamma amino butyric acid

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

globus pallidus

globus pallidus, lesion of

glucose tolerance test, abnormal

granular osmiphilic material

grimacing

gynecomastia

Hallervorden Spatz disease

heavy metal intoxication

heel-knee-shin test

hemochromatosis

hemochromatosis, primary

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatitis

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatomegaly

hepatosplenomegaly

heralding manifestation

hypotension, neurologic causes of

hypotonia

hypoxic encephalopathy

iatrogenic neurologic disorders

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deterioration

intelligence quotient

intrinsic hand muscles, wasting of

iron, brain

Jakob-Creutzfeldt disease

jaundice

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

kyphoscoliosis, neurologic causes of

L-dopa, drug interactions with and side effects of

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

leukopenia

Lewy body

Lewy body disease, diffuse

lightheaded

liver disease

liver function enzymes

liver transplantation

locus ceruleus, lesion of

marche a petits pas

masked facies

memory, impairment of

mental retardation

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

metoprolol

micrographia

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI

MRI, abnormal

MRI, diffusion weighted

MRI, negative

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

nerve conduction studies

neuroendocrinology

neurofibromatosis 1

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuronopathy

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuropathy, sensory

neurotoxin

neurotransmitter

nigrostriatal pathway

nimodipine

norepinephrine

nutritional deficiency

nystagmus

nystagmus, pendular

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

old age, neurology of

opened mouth

optic atrophy

orthostatic hypotension

osmotic demyelination syndrome

ovarian insufficiency

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

past pointing

patient information and support

poison, neurologic problems with

POLR3B

pons, lesion of

positional head-hanging test

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

prion disease

prognosis

progressive neurologic disorder

progressive supranuclear palsy

propranolol

pruritus

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis

psychosocial aspects

pulmonary function tests

Purkinje cell

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quality of life

radiation therapy, stereotactic

radiculopathy

raphe nuclei

reading disorder, acquired

reflex sympathetic dystrophy

renal stones

respirations in CNS disease

saccadic eye movements, abnormal

safety

salivation, excessive

seizure, differential diagnosis of

seizure, psychomotor-temporal lobe

single photon emission computed tomography

skin, biopsy

skin, darkening of

sleep pathology and physiology

slit lamp examination

smell

Smell Identification Test

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

speech, slowed

speech, soft

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 12

spinocerebellar ataxia type 28

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

spinopontine atrophy, dominant

splenium of corpus callosum

stimulation, deep brain

stimulation, thalamic

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

stridor

striopallidodentate calcifications, familial idiopathic

stuttering

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

sural nerve

symmetric brain lesions

teeth, number of in infants

testicular enlargement

tetrabenazine

thalamotomy

thalamotuberal artery

thalamus

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

tongue, fasciculations of

tonic foot response

topiramate

torticollis

torticollis, post traumatic

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, post traumatic

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

trientine dihydrochloride

trinucleotide repeats

twins

ultrasonography

ultrasonography, head

ultrasonography, high-intensity focused

vertigo, migraine causing

vestibulopathy

vibratory sensation, abnormal

visual evoked response

vitamin deficiency

vitamin E

vitamin E deficiency

voice, abnormality of

walking frame

walking, difficulty with

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

zinc

Showing articles 1350 to 1400 of 2417 << Previous Next >>

Use of Twin Cohorts for Research in Alzheimer's Disease
Neurol 43:261-267, Breitner,J.C.S.,et al, 1993

Terfenadine-Induced Tremor
Ann Neurol 33:226, Soto,J.,et al, 1993

Sleep Paralysis
Lancet 341:406-407, Dahlitz,M.&Parkes,J.D., 1993

Movement Disorders with Cerebral Toxoplasmosis and AIDS
Movement Disorders 8:107-112, Nath,A.,et al, 1993

Stimulus-Specific pathological Laughter:A Case Report with Discrete Unilateral Localization
Neurol 43:229-230, Doorenbos,D.I.,et al, 1993

Real and Imagined Clinicopathological Limits of"Prior Dementia"
Lancet 341:127-129, Brown,P.,et al, 1993

Infectious Prions or Cytotoxic Metabolites?
Lancet 341:159-161, Pablos-Mendez,A.,et al, 1993

Erythromelalgia:Association with Hereditary Sensory Neuropathy and Response to Amitriptyline
Neurol 43:621-622, Herskovitz,S.,et al, 1993

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Intramedullary Spinal Sarcoidosis:Clinical and Magnetic Resonance Imaging Characteristics
Neurol 43:333-337, Junger,s.S.,et al, 1993

Acyclovir-Induced Neurotoxicity:Concentration-Side Effect Relationship in Acyclovir Overdose
Am J Med 94:212-215, Haefeli,W.E.,et al, 1993

Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Familial Aggregation of Stroke
Stroke 24:1366-1371, Kiely,D.K.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Genetic Susceptibility in Familial Multiple Sclerosis not Linked to the Myelin Basic Protein Gene
Lancet 341:1179-1181, Rose,J.,et al, 1993

Tardive Stereotype and Other Movement Disorders in Tardive Dyskinesias
Neurol 43:937-941, Stacy,M.,et al, 1993

The Prevalence of Metoclopramide-Induced Tardive Dyskinesia and Acute Extrapyramidal Movement Disorders
Arch Int Med 153:1469-1475, Ganzini,L.,et al, 1993

Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
Arch Neurol 50:725-728, Randolph,C.,et al, 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

Thalamic Stimulation & Prox Tremor, A Specific Target in Nucleus Ventrointermedius Thalamik
Arch Neurol 50:498-500, Nguyen,J-P.&Degos,J-D., 1993

Progression After Chronic Manganese Exposure
Neurol 43:1479-1483, Huang,C.C.,et al, 1993

Conjugal Alzheimer's Disease:Is There an Increased Risk in Offspring?
Ann Neurol 34:396-399, Bird,T.D.,et al, 1993

The Photic Sneeze Reflex:Literature Review and Discussion
Neurol 43:868-871, Whitman,B.W.&Packer,R.J., 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Migraine Madness:Recurrent Psychosis after Migraine
JNNP 56:416-418, Fuller,G.N.,et al, 1993

Spastic Ataxia Associated with Human T-Cell Lymphotropic Virus Type II Infection
Ann Neurol 33:411-414, Harrington,W.J.,et al, 1993

Isolation of HTLV-II from Pt with Chronic, Prog Neurol Dis Clin Indistinguish from HAM/Tropical Spastic Paraparesis
Ann Neurol 33:392-396, Jacobson,S.,et al, 1993

Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993

Movement Disorders in Astrocytomas of the Basal Ganglia and the Thalamus
JNNP 55:1162-1167, Krauss,J.K.,et al, 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

Parkinson's Disease in Twins Studied with 18 F-Dopa and Positron Emission tomography
Neurol 42:1894-1900, Burn,D.J.,et al, 1992

Unilateral Transpl of Human Fetal Mesencephalic Tissue Into the Caudate Nucleus of Pts with Parkinson's
NEJM 327:1541-1548, Spencer,D.D.,et al, 1992

Survival of Implanted Fetal Dopamine Cells & Neuro Improvement 12 to 46 Months after Transpl for Parkinson's
NEJM 327:1549-1555, 15891992., Freed,C.R.,et al, 1992

Bilateral Fetal Mesencephalic Grafting in Two Patients with Parkinsonism Induced by MPTP
NEJM 327:1556-1563, 15891992., Widner,H.,et al, 1992

The Use of Fetal Tissue in Research on Parkinson's Disease
NEJM 327:1591-1592, Kassirer,J.P.&Angell,M., 1992

Botulinum Toxin, Useful in Adult Onset Focal Dystonias
BMJ 305:1169-1170, Lees,A.J., 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Brief Report:Autosomal Dominant Familial Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia
NEJM 327:1069-1074, Bilous,R.W.,et al, 1992

Familial Rectal Pain:A Type of Reflex Epilepsy?
Ann Neurol 32:824-826, Schubert,R.&Cracco,J.B., 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

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

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Familial Multiple Sclerosis:MRI Findings in Clinically Affected and Unaffected Siblings
JNNP 55:883-886, Teinari,P.J.,et al, 1992

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

Tardive Dyskinesia Presenting as Severe Dysphagia
JNNP 55:1203-1204, Gregory,R.P.,et al, 1992

Showing articles 1350 to 1400 of 2417 << Previous Next >>