Neudle.com: familial tremor

Neurology Specific Literature Search

Differential
(Click to cross reference)

adrenergic blocker

advances in neurology

adverse drug reaction

airway obstruction

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alpha adrenergic blocker

alternating rapid movement

Alzheimer's disease

amyotrophic lateral sclerosis, differential diagnosis

amyotrophic lateral sclerosis, misdiagnosis

anemia, hemolytic

ankle reflex, absent

ankle, swelling of

anticholinergic drugs

anticonvulsants

anticonvulsants, untoward effects of

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, sensory

ataxia, truncal

ataxic-dystonia syndromes

athetosis, causes of

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

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

biologic markers

blinking, reduced

botulinum toxin

botulinum toxin, complications of

brainstem, lesion of

Brueghel's syndrome

calcification, intracranial

calcium antagonist

carbon monoxide poisoning

carbonic anhydrase inhibitor

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

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 venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

ceruloplasmin, serum

Charcot-Marie-Tooth

chorea, causes of

choreoathetosis

chromosomal abnormality

cingulate island sign

cirrhosis, causes of childhood

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

coat-hanger pain

cogwheel rigidty

complicated migraine

copper metabolism, abnormal

corpus callosum, lesion of

corpus callosum, thinning

cyst, parenchymal

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

delayed dentition

dementia, childhood

dementia, familial

developmental milestones

developmental milestones, loss of

developmental retardation

dexterity, impaired

differential diagnosis

disability, neurological

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

drug induced neurologic disorders

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, laryngeal

dystonia, post traumatic

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

electroencephalogram, abnormalities of

electron microscopy

electronystagmography

emotional lability

encephalitis, Japanese

encephalitis, viral

epidemiology of neurology

erectile dysfunction

esophageal varices

evoked potentials

exome sequencing

eye movement, disorders of

facial appearance, abnormal

facial expression abnormality

failed medical management

familial hemiplegic migraine

fatal familial insomnia

fine motor function, impaired

finger nose finger test

fingerprint bodies

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

fragile-X syndrome, carrier

Friedreich's ataxia

frontal lobe, pathologic signs of

gait, festinating

gamma amino butyric acid

gamma knife therapy

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

glucose tolerance test, abnormal

granular osmiphilic material

Hallervorden Spatz disease

heavy metal intoxication

heel-knee-shin test

hemochromatosis

hemochromatosis, primary

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatolenticular degeneration(Wilson's disease), screening for

hepatosplenomegaly

heralding manifestation

homovanillic acid

Huntington's chorea

hyperthyroidism

hypoalbuminemia

hypometric saccades

hypomyelination

hypotension, neurologic causes of

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

inborn errors of metabolism

inclusion bodies

inclusion bodies, eosinophilic cytoplasmic

inclusion bodies, intranuclear

inclusion bodies, ubiquitin

intellectual deficit

intellectual deterioration

intelligence quotient

intrinsic hand muscles, wasting of

Jakob-Creutzfeldt disease

joint hypermobility

Kayser-Fleischer ring

kinesia paradoxica

kyphoscoliosis, neurologic causes of

lactic acidemia

laminectomy, lumbar

L-dopa, drug interactions with and side effects of

leg weakness, bilateral

Leigh's disease

lenticular nucleus, lesion of, bilateral

leukoencephalopathy

leukoencephalopathy, differential diagnosis

Lewy body disease, diffuse

liver function enzymes

liver transplantation

locus ceruleus, lesion of

marche a petits pas

memory, impairment of

mental retardation

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

midbrain, atrophy

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, hemiplegic

mitochondrial disease

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, treatment of

MRI, diffusion weighted

multiple sclerosis

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle stiffness

myoclonic jerks

myoclonus, epilepsy

myoclonus, essential

nerve conduction studies

neuroendocrinology

neurofibromatosis 1

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neuropathy, sensory

neurotransmitter

nigrostriatal pathway

nutritional deficiency

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

orthostatic hypotension

osmotic demyelination syndrome

ovarian insufficiency

palatal myoclonus

paraparesis, spastic

Parkinson disease

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 material in the brain

patient information and support

Pelizaeus Merzbacher

personality change

phenylketonuria

poison, neurologic problems with

pons, lesion of

positional head-hanging test

postoperative neurologic complications

postural abnormality

practice guidelines

pregnancy, neurologic complications in

progressive neurologic disorder

progressive supranuclear palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychosocial aspects

pulmonary function tests

pursuit eye movements, abnormal

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quality of life

radiation therapy, stereotactic

reading disorder, acquired

reflex sympathetic dystrophy

respirations in CNS disease

respiratory failure

retinitis pigmentosa

Riley-Day syndrome

Rosenthal fibers

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

seizure, children

seizure, differential diagnosis of

seizure, psychomotor-temporal lobe

shoulder, pain in

single photon emission computed tomography

skin, darkening of

sleep pathology and physiology

slit lamp examination

Smell Identification Test

SNCA duplication

spastic dysphonia

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

speech, loss of

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

status epilepticus

stereotaxic surgery

stimulation, deep brain

stimulation, thalamic

storage disease of CNS

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

symmetric brain lesions

tandem gait, ataxic

tardive dyskinesia

tardive dystonia

teeth, abnormal

teeth, number of in infants

testicular enlargement

thalamotuberal artery

thalamus, focused ultrasound ablation

thalamus, infarction of

thalamus, lesion of

thalamus, lesion of-bilateral

thrombocytopenia

tongue, fasciculations of

tonic foot response

torticollis, post traumatic

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, orthostatic

tremor, physiologic

tremor, post traumatic

tremor, postural

tremor, psychogenic

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

tremor, writing

trientine dihydrochloride

trinucleotide repeats

ultrasonography

ultrasonography, head

ultrasonography, high-intensity focused

vasospasm, cerebral

vertigo, migraine causing

vibratory sensation, abnormal

visual evoked response

vitamin deficiency

vitamin E deficiency

voice, abnormality of

walking, difficulty with

white matter disease

wide based gait

X-linked bulbospinal neuronopathy

x-linked intellectual deficit

x-linked mental retardation

Showing articles 650 to 700 of 2417 << Previous Next >>

What is the Risk of Developing Parkinsonism Following Neuroleptic Use?
Neurol 66:941-943, Noyes,K.,et al, 2006

Practice Parameter: Treatment of Parkinson Disease with Motor Fluctuations and Dyskinesia (An Evidence-Based Review)
Neurol 66:983-995, Pahwa,R.,et al, 2006

Multiple Sclerosis in Twins From Continental Italy and Sardinia: A Nationwide Study
Ann Neurol 59:27-34, Ristori,G.,et al, 2006

Panic and Fear Induced by Deep Brain Stimulation
JNNP 77:410-412, Shapira,HN.A.,et al, 2006

Familial Dopa-Responsive Cervical Dystonia
Neurol 66:599-601, Schneider,S.A.,et al, 2006

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Young-Onset Dementia, A Practical Approach to Diagnosis
The Neurologist 12:2-13, Ridha,B. &Josephs,K.A., 2006

Varicella Zoster Virus Cerebellitis in a 66-Year-Old Patient Without Herpes Zoster
Lancet 367:182, Ratzka,P.,et al, 2006

Suicide After Deep Brain Stimulation of the Internal Globus Pallidus for Dystonia
Neurol 66:142-143, Foncke,E.M.J.,et al, 2006

Cetirizine-Induced Dystonic Movements
Neurol 66:143-144, Rajput,A. &Baerg,K., 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

The Clinical Spectrum of Neuralgic Amyotrophy in 246 cases
Brain 129:438-450, Alfen, N.V. & Baziel, G.M., 2006

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Etiological and Therapeutical Observations in a Case of Belly Dancers Dyskinesia
Movement Disorders 20:251-253, Linazasoro,G., et al, 2005

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

Cluster Headache:Pathogenesis,Diagnosis, and Management
Lancet 366:843-855, May,A., 2005

NT-3 Promotes Nerve Regeneration and Sensory Improvement in CMT1A Mouse Models and in Patients
Neurol 65:681-689, 662, Sahenk,Z.,et al, 2005

Science and Ethics of Sham Surgery, A Survey of Parkinson Disease Clinical Researchers
Arch Neurol 62:1357-1360,1343, Kim,S.Y.H.,et al, 2005

Quality of Life in Patients with Charcot-Marie-Tooth Disease
Neurol 65:922-924, Vinci,P.,et al, 2005

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Central Nervous System Involvement in Hereditary Neuropathy With Liability to Pressure Palsies
Arch Neurol 62:1911-1914, Sanahuja,J.,et al, 2005

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005

Bi-Hemispheric Anterior Cerebral Artery with Drop Attacks and Limb Shaking TIAs
Neurol 65:174, Gerstner,E.,et al, 2005

Vagal Nerve Stimulation Effect on Cerebellar Tremor in Multiple Sclerosis
Neurol 65:499, Marrosu,F.,et al, 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Pallidal vs Subthalamic Nucleus Deep Brain Stimulation in Parkinson Disease
Arch Neurol 62:554-560,533, Anderson,V.C.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

Autonomic Peripheral Neuropathy
Lancet 365:1259-1270, Freeman,R., 2005

The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
Neurol 64:1502-1507, Klunemann,H.H.,et al, 2005

Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
Ann Neurol 57:738-741,613, Castelnau,P.,et al, 2005

Brain Magnetic Resonance Imaging Findings in Patients with Mitochondrial Cytopathies
Arch Neurol 62:737-742, Barragan-Campos,H.M.,et al, 2005

Proton MR Spectroscopy in Wilson Disease: Analysis of 36 Cases
AJNR 26:1066-1071, Lucato,L.T.,et al, 2005

Tourettes Syndrome and Deep Brain Stimulation
JNNP 76:992-995, Houeto,J.L.,et al, 2005

Bilateral Deep-Brain Stimulation of the Globus Pallidus in Primary Generalized Dystonia
NEJM 352:5 459-467, 498, Vidailhet, M., et al, 2005

Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Genetic Factors in Alzheimer's Disease
NEJM 352: 862-863, 884, Bird, T., 2005

Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
NEJM 352:686-691, de Jong,M.D., et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

The Serotonin Syndrome
NEMJ 352:1112-20, Boyer, E.W. & Shannon, M., 2005

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

Showing articles 650 to 700 of 2417 << Previous Next >>