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 850 to 900 of 2417 << Previous Next >>

Surgery for Parkinson Disease
Arch Neurol 57:1118-1125, Lang,A.E., 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

The Brain Code in Health and Disease
Arch Neurol 57:50-51, Rosenberg,R.N., 2000

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

St Louis Encephalitis,A Review of 11 Cases in a 1995 Dallas, Tex, Epidemic
Arch Neurol 57:114-118, Wasay,M.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

Effects of Bilateral Posteroventral Pallidotomy on Gait of Subjects with Parkinson Disease
Arch Neurol 57:198-204, Siegel,K.L.&Metman,L.V., 2000

Hereditary Recurrent Focal Neuropathies, Clinical and Molecular Features
Neurol 54:546-551, Stogbauer,F.,et al, 2000

Risk of Subarachnoid Haemorrhage in First Degree Relatives of Patients with Subarachnoid Haemorrhage: Follow Up Study Based on National Registries in Denmark
BMJ 320:141-145, Gaist,D.,et al, 2000

Effect of Liver Transplantation on Neurological Manifestations in Wilson Disease
ArchNeurol 57:384-386, Stracciari,A.,et al, 2000

Desmin Myopathy, a Skeletal Myopathy with Cardiomyopathy Caused by Mutations in the Desmin Gene
NEJM 342:770-780, Dalakas,M.C.,et al, 2000

Shaky-Leg Syndrome and Vitamin B12 Deficiency
NEJM 342:981, Benito-Leon,J.&Porta-Etessam,J., 2000

Cardiac Dysfunction in Neuromuscular Diseases
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Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
AJNR 21:1016-1020, Matsubara,S.,et al, 2000

Long-Term Follow-Up of Unilateral Pallidotomy in Advanced Parkinson's Disease
NEJM 342:1708-1714, Fine,J.,et al, 2000

Association Between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
NEJM 342:1560-1567, Lucking,C.B.,et al, 2000

Myoclonus Secondary to Albuterol (Salbutamol) instillation
Neurol 54:2022-2023, Micheli,F.,et al, 2000

National Institutes of Health Consensus Conference: Tuberous Sclerosis Complex
Arch Neurol 57:662-665, Hyman,M.H.&Whittemore,V.H., 2000

Axial Parkinsonian Symptoms Can Be Improved: The Role of Levodopa and Bilateral Subthalamic Stimulation
JNNP 68:595-600, Bejjani,B.P.,et al, 2000

A Five-Year Study of the Incidence of Dyskinesia in Patients With Early Parkinson's Disease who were Treated with Ropinirole or Levodopa
NEJM 342:1484-1491, Rascol,O.,et al, 2000

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Hereditary Spastic Paraparesis: A Review of New Developments
JNNP 69:150-160, McDermott,C.J. et al, 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000

Hypertrophic Olivary Degeneration: Metaanalysis of the Temporal Evolution of MR Findings
AJNR 21:1073-1077, Goyal, M.,et al, 2000

Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
Clin Inf Dis 30:336-341, Lamas, C.C. & Eykyn, S.J., 2000

MR Angiography as a Screening Tool for Intracranial Aneurysms:Feasibility, Test Characteristics, and Interobserver Agreement
AJR 173:1469-1475, Raaymakers,T.W.M.,et al, 1999

A Locus for Febrile Seizures (FEB3) Maps to Chromosome 2q23-24
Ann Neurol 46:671-678, Peiffer,A.,et al, 1999

Genetic Localization of the Familial Adult Myoclonic Epilepsy (FAME) Gene to Chromosome 8q24
Neurol 53:1180-1183, Plaster,N.M.,et al, 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Distal Myopathies:Clinical and Molecular Diagnosis and Classification
JNNP 67:703-709, Mastaglia,F.J.&Laing,N.G., 1999

Evaluation of Surgery for Parkinson's Disease, A Report of the Therapeutics and Technology Assessment Subcommittee of the AAN
Neurol 53:1910-1921, Hallett,M.,et al, 1999

Effectiveness of Anticholinergics and Neuroleptic Dose Reduction on Neuroleptic-Induced Pleurothotonus (the Pisa Syndrome)
J Clin Psychopharmacol 19:277-280, Suzuki,T.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,et al, 1999

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Clinical Correlates of Vascular Parkinsonism
Arch Neurol 56:98-102, Winikates,J.&Jancovic,J., 1999

Long-Term Evaluation of Bilateral Fetal Nigral Transplantation in Parkinson Disease
Arch Neurol 56:179-187, Hauser,R.A.,et al, 1999

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Treatment of Attention-Deficit-Hyperactivity Disorder
NEJM 340:780-788, Elia,J.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

What Level of Care for the Neurofibromatoses?
Lancet 353:1114-1116, Huson,S.M., 1999

Familial Subarachnoid Hemorrhage, Outcome Study
Stroke 30:1099-1102, Ronkainen,A.,et al, 1999

Parkinsonism after Taking Ecstasy
NEJM 340:1443, Mintzer,S.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

Cerebral Injury After Cardiac Surgery,Identification of a Group of Extraordinary Risk
Stroke 30:514-522, Wolman,R.L.,et al, 1999

Paroxysmal Dyskinesias in Patients with HIV Infection
Neurol 52:109-114, Mirsattari,S.M.,et al, 1999

Showing articles 850 to 900 of 2417 << Previous Next >>