Neudle.com: dystonia truncal

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adverse drug reaction

akinesia of eyelid function

alexia without agraphia

alien hand syndrome

alpha-fetoprotein

Alzheimer's disease

anticholinergic drugs

anticholinesterase

aphasia, progressive, primary

apraxia of eye movements

apraxia of eyelid opening

arm swing, reduced

arylsulfatase A

ataxia telangiectasia

ataxia, cerebellar

ataxia, hereditary

ataxia, paroxysmal

ataxia, progressive

ataxia, truncal

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

bent spine syndrome

biologic markers

biopterin deficiency

biotin deficiency

biotin deficiency, juvenile form

biotin-responsive basal ganglia disease

botulinum toxin

brainstem, dysfunction

brainstem, lesion of

bulbar dysfunction

calcification, intracranial

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, false negative

CAT scan, muscle

caudate nucleus, atrophy

central hypoventilation

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar pontine angle

cerebellar pontine angle tumor

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral palsy, associated problems with

cerebral peduncle

cerebrovascular accident

ceruloplasmin, serum

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cogwheel rigidty

cold intolerance

conjugate gaze, forced

conversion reaction

cortical-basal ganglionic degeneration

cranial nerve palsies

creatine phosphokinase(CPK)elevated

crying, pathologic

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dexterity, impaired

diabetes mellitus

diagnostic criteria

differential diagnosis

diurnal variation

dopa responsive dystonia

down-beat nystagmus

drug induced neurologic disorders

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dyskinesia, buccal lingual facial

dyskinesia, facial

dystonia musculorum deformens

dystonia, cervical

dystonia, classification

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, painful

dystonia, post traumatic

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

emotional lability

encephalitis, autoimmune

episodic disorders

episodic neurologic deficits

esophageal varices

ethics in neurology

exercise-induced neurologic dysfunction

extrapyramidal movement disorder, progressive

eye movement, disorders of

facial expression abnormality

fine motor function, impaired

fourth ventricle, enlargement of

fourth ventricle, neoplasm of

frontal behavioral spatial syndrome

gangliosidosis GM1

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

globus pallidus, stimulation

growth retardation

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

health insurance

hemianopia, homonymous

hemifacial spasm

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

heralding manifestation

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's disease, children

hypoalbuminemia

hypometric saccades

iatrogenic neurologic disorders

ideomotor apraxia

imbalance, postural

immunodeficiency

immunosuppression

incontinence, fecal

intellectual deficit

intellectual deterioration

intracranial pressure, increased

Jakob-Creutzfeldt disease

jaw jerk, abnormal

Kayser-Fleischer ring

laughing, pathologic

leg spasms, painful

leg weakness, bilateral

lenticular nucleus, lesion of, bilateral

liver function enzymes

lysosomal storage disease

manganese intoxication

memory, defect of recent

memory, impairment of

mental retardation

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

midbrain, atrophy

midbrain, infarction of

molecular genetics

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, psychogenic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, eye of tiger sign

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, mouse ears

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle hypertrophy

muscle spasm, face

muscle weakness

muscular dystrophy

myasthenia gravis

myelopathy, chronic progressive

myoclonic jerks

myopathy, metabolic

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neurocutaneous disease

neuroendocrinology

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, tempo

neurologic evaluation

neurologic examination

neurologic signs

neurologic symptoms

neuroophthalmology

numb clumsy hands syndrome

nystagmus, vertical

obsessive-compulsive disorder

ocular motility, disorders of

ocular myopathy

ocular myopathy, differential diagnosis

old age, neurology of

ophthalmoplegia

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, axial symptoms

Parkinson disease, differential diagnosis of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism syndrome

penguin silhouette sign

personality change

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polycythemia, secondary

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

postural abnormality

precipitating factors

pregnancy, neurologic complications in

primary episodic ataxia

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pure sensory stroke

pyramidal tract

pyramidal tract dysfunction

radiation hypersensitivity

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

release phenomena

respirations in CNS disease

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

rigidity, axial

saccadic eye movements, abnormal

salivation, excessive

sea-blue histiocytes

sensorineural hearing loss

sensory loss, cortical

sequencing difficulty

shoulder, elevation

single photon emission computed tomography

skin, lesions in neurologic disorders

sleep apnea, obstructive

sleep pathology and physiology

slit lamp examination

speech disorder

speech disorder, childhood

spinal cord, lesion of

spinal muscular atrophy

stem cell transplantation

stimulation, deep brain

stimulation, deep brain, bilateral

stooped posture

striatum, lesion of

striatum, lesion of, bilateral

substantia nigra

swallow evaluation

symmetric brain lesions

tardive dystonia

tetrahydrobiopterin

thalamus, infarction of

thrombocytopenia

tonic foot response

treatment of neurologic disorder

treatment, empirical

tremor, intention

tremor, postural

tricyclic antidepressant

trientine dihydrochloride

trinucleotide repeats

upgaze, paralysis of

urinary incontinence

urinary sulfatidase excretion

vision, blurred

visual evoked response

visual field defect

visual symptoms

vocal cord paralysis

walking, difficulty with

weakness, progressive

Whipple's disease

white matter disease

wide based gait

Showing articles 650 to 700 of 1183 << Previous Next >>

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Blepharospasm:Report of a Workshop
Neurol 46:1213-1218, Hallett,M.&Daroff,R.B., 1996

Falls and Urinary Incontinence in a 66-Year Old Woman
Lancet 347:1738, Yusuf,S.W.,et al, 1996

Childhood Chronic Inflammatory Demyelinating Neuropathies:Clinical Course and Long-term Follow-up
Neurol 47:98-102, Nevo,Y.,et al, 1996

Clinicopath Conf
Tangier Disease, Case 16-1996, NEJM 334:1389-1394996., , 1996

Hereditary Spastic Paraplegia:Advances in Genetic Research
Neurol 46:1507-1514, Fink,J.K.,et al, 1996

Clinical Correlates of White Matter Findings on Cranial Magnetic Resonance Imaging of 3301 Elderly People
Stroke 27:1274-1282, 12691996., Longstreth,W.T.,et al, 1996

Treatment of Advanced Parkinson's Disease by Posterior GPi Pallidotomy:1-Year Results of a Pilot Study
Ann Neurol 40:355-366, 3411996., Baron,M.S.,et al, 1996

Gait Disorders in Older Adults
J Am Geriatr Soc 44:434-452, Alexander,N.B., 1996

Movement Disorders Associated with the Serotonin Selective Reuptake Inhibitors
J Clin Psychiatry 57:449-454, Leo,R.J., 1996

Mycoplasma Pneumoniae Infection Associated with an Acute Brainstem Syndrome
Acta Neurol Scand 93:203-206, OBrien, P.M.,et al, 1996

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
JNNP 59:406-412, Factor,S.A.,et al, 1995

Esophageal Carcinoma Metastatic to the Brain:Clin Value & Cost-Effect of Enhanced Head CT Before Esophagectomy
AJNR 16:1915-1921, Gabrielsen,T.O.,et al, 1995

Investigations of Disorders of Balance
JNNP 59:568-578, Rudge,P.&Bronstein,A.M., 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

Delayed Dystonia with Striatal CT Lucencies Induced by a Mycotoxin (3-Nitropropionic Acid)
Neurol 45:2178-2183, He,F.,et al, 1995

Clinicopath Conf
Granulomatous Angiitis of CNS, Case 33-1995, NEJM 333:1135-1143995., , 1995

Paroxysmal Dyskinesias:Clinical Features and Classification
Ann Neurol 38:571-579, Demirkiran,M.&Jankovic,J., 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Pain and Remote Weakness in Limbs Injected with Botulinum Toxin A for Writer's Cramp
Lancet 346:154-156, Sheean,G.L.,et al, 1995

Midcervical Central Cord Syndrome:Numb & Clumsy Hands Due to Midline Cervical Disc Protrusion at C3-4 Intervert Level
JNNP 58:607-613, Nakajima,M.&Hirayama,K., 1995

Low Back Pain
BMJ 310:929-932, Jenner,J.R.&Barry,M., 1995

Genetic Homogeneity Between Childhood-Onset and Adult-Onset Autosomal Recessive Spinal Muscular Atrophy
Lancet 346:741-742, Brahe,C.,et al, 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995

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

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

Clinical and Topographical Range of Callosal Infarction:A Clinical and Radiological Correlation Study
JNNP 59:238-242, Giroud,M.&Duman,R., 1995

Medial Medullary Syndrome:Report of 18 New Patients and a Review of the Literature
Stroke 26:1548-1552, Kim,J.S.,et al, 1995

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

Diphenhydramine is Effective in the Treatment of Idiopathic Dystonia
Arch Neurol 52:405-407, Truong,D.D.,et al, 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

Neuroblastoma-Associated Opsoclonus-Myoclonus Treated with IVIgG
J Pediatr 127:328-329, Petruzzi,M.J.&deAlarcon,P.A., 1995

Paraneoplastic Cerebellar Degeneeration with Anti-Yo Antibody in a Man
Neurol 45:1226-1227, Felician,O.,et al, 1995

Erdheim-Chester Disease and Slowly Progressive Cerebellar Dysfunction
JNNP 58:238-240, Fukazawa,T.,et al, 1995

Treatable Gait Disorder & Polyneuropathy Assoc with High Titer Serum IgM Binding to Atg that Copurify with MAG
Muscle & Nerve 17:1293-1300994., Pestronk,A.,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

Clinicopath Conf
Mycoplasma Pneumoniae Infection, Case 42-1994, NEJM 331:1437-1444994., , 1994

Neurologic Evaluation of the Optimally Healthy Oldest Old
Arch Neurol 51:1205-1211, Kaye,J.A.,et al, 1994

Pseudochoreoatheotosis:Movement Associated with Loss of Proprioception
Arch Neurol 51:1103-1109, Sharp,F.R.,et al, 1994

Clinicopath Conf
Primary Malignant Lymphoma of CNS, Diffuse, Large-Cell]B-Cell Type, Case 36-1994, NEJM 331:861-8684., , 1994

Neurologic Manifestations of HIV Infection
Ann Int Med 121:769-785, Simpson,D.M.&Tagliati,M., 1994

Control of Posture in Patients with Neurologically Asymptomatic HIV Infect & Pts with Beginning HIV-1-Related Encephal
Arch Neurol 51:1232-1235, Arendt,G.,et al, 1994

Levodopa Failure in Chronic Manganism
Neurol 44:1600-1602, 15831994., Lu,C-S.,et al, 1994

Brief Report:Relief of Spinal Cord Compression from Vertebral Hemangioma by Intralesional Injection of Absolute Ethanol
NEJM 331:508-511, Heiss,J.D.,et al, 1994

Showing articles 650 to 700 of 1183 << Previous Next >>