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 1200 to 1250 of 2417 << Previous Next >>

X-Linked Pure Familial Spastic Paraparesis
Arch Neurol 52:665-669, Cambi,F.,et al, 1995

Rapid Antibody Test for Fragile X Syndrome
Lancet 345:1147-1148, Willemsen,R.,et al, 1995

Psychogenic Parkinsonism
Arch Neurol 52:802-810, Lang,A.E.,et al, 1995

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

Zinc-Induced Deterior in Wilson's Disease Aborted by Trtm with Penicillamine, Dimercaprol, & A Novel Zero Copper Diet
Arch Neurol 52:10-11, Walshe,J.M.,et al, 1995

Neuroleptic Drug Exposure and Treatment of Parkinsonism in the Elderly:A Case-Control Study
Am J Med 99:48-54, Avorn,J.,et al, 1995

Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Involuntary Movement Disorders Associated with Felbamate
Neurol 45:185-187, Kerrick,J.M.,et al, 1995

The Shaken Infant Syndrome
BMJ 310:344-345, Carty,H.&Ratcliffe,J., 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

Levorotatory Form of 5-Hydroxytryptophan in Friedreich's Ataxia
Arch Neurol 52:456-460, Trouillas,P.,et al, 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

MRI of the Brain in Wilson Disease:T2 Signal Loss Under Therapy
J Comput Assist Tomogr 19:635-638, Engelbrecht,V.,et al, 1995

Kayser-Fleischer Ring:Hepatolenticular Degeneration (Wilson's Disease)
Neurol 45:1261-1262, Finelli,P.F., 1995

Hereditary Leukoencephalopathy and Palmoplantar Keratoderma:A New Disorder with Increased Skin Collagen Content
Neurol 45:331-337, Lossos,A.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Effect on Parkinsonian Signs and Symptoms of Bilateral Subthalamic Nucleus Stimulation
Lancet 345:91-95, Limousin,P.,et al, 1995

Primary Orthostatic Tremor
BMJ 310:143-144, Britton,T.C.&Thompson,P.D., 1995

Tourette's Syndrome:A Model Neuropsychiatric Disorder
JAMA 273:498-501, Hyde,T.M.&Weinberger,D.R., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Lower Cognitive Performance in Normal Older Adult Male Twins Carrying the Apolipoprotein E-E4 Allele
Arch Neurol 51:1189-1192, Reed,T.,et al, 1994

Post-Traumatic Movement Disorders:Central and Peripheral Mechanisms
Neurol 44:2006-2014, Jankovic,J., 1994

Oral and Genital Tardive Pain Syndromes
Neurol 44:2115-2119, Ford,B.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Clinicopathologic Correlations of HIV-1-Associated Vacuolar Myelopathy:An Autopsy-Based Case-Control Study
Neurol 44:2159-2164, DalPan,G.J.,et al, 1994

Superoxide Dismutase and ALS
Lancet 344:1651-1652, Orrell,R.W.&deBelleroche,J.S., 1994

Monomelic Amyotrophy
Muscle & Nerve 17:1129-1134994., Donofrio,P.D., 1994

DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
JNNP 57:1260-1262, Silander,K.,et al, 1994

Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities
Neurol 44:2250-2252, Gouider,R.,et al, 1994

Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
Neurol 44:2253-2257, Chance,P.F.,et al, 1994

Benign Familial Nocturnal Alternating Hemiplegia of Childhood
Neurol 44:1812-1814, Andermann,E.,et al, 1994

Increased Risk of Parkinson's Disease in Parents and Siblings of Patients
Ann Neurol 36:659-661, Payami,H.,et al, 1994

Worsening of Neurologic Syndrome in Patients with Wilson's Disease with Initial Penicillamine Therapy
Arch Neurol 44:490-493, Brewer,G.J.,et al, 1994

Frequency and Pathogenesis of Hemodynamic Stroke
Stroke 25:2179-2182, Bladin,C.F.&Chambers,B.R., 1994

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

Periventricular Heterotopia and Epilepsy
Neurol 44:51-55, Huttenlocher,P.R.,et al, 1994

Clinical Assessment of Extrapyramidal Signs in Nursing Home Patients Given Antipsychotic Medication
Arch Int Med 154:1113-1117, Avorn,J.,et al, 1994

Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
Arch Neurol 51:757-766, Schwankhaus,J.D.,et al, 1994

Increased Risk of Alzheimer's Disease in Mothers of Adults with Down's Syndrome
Lancet 344:353-356, Schupf,N.,et al, 1994

Showing articles 1200 to 1250 of 2417 << Previous Next >>