Neudle.com: Parkinson disease familial

Differential
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abducens nerve paralysis

acoustic nerve

acoustic neurinoma

acoustic neurinoma, bilateral

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholism

algorithm

alkylating agents

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

aluminum

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

amygdala

amyloid plaques

amyloidosis

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

anatomy of

anosmia

anticholinergic drugs

aphasia, progressive, primary

attention deficit disorder with hyperactivity

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

benign essential tremor, refractory

bent spine syndrome

beta adrenergic blocker

blood dyscrasias, neurologic findings with

brain transplantation

brainstem, neoplasms of

brainstem, vascular malformation of

caffeine

calcification, intracranial

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

CAT scan, muscle

catecholamine

cavernous hemangioma

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar hemangioma

cerebellar hemorrhage

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy

cerebral vasculature, calcification

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure low

cerebrovascular accident

cerebrovascular accident, recurrent

ceruloplasmin, serum

Charcot-Marie-Tooth

Chediak-Higashi syndrome

chemotherapy, CNS treatment and complications with

children

choline acetyltransferase

chorea

chorea, causes of

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate island sign

cirrhosis

Clinical Pathologic Conference(C.P.C.)

controversies in neurology

conversion reaction

copper metabolism, abnormal

corpus callosum, lesion of

corpus callosum, thinning

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst

cyst, peritumoral

cyst, epidermoid of CNS

cyst, neoplastic cerebellum

cyst, parenchymal

degenerative diseases of CNS

delay in diagnosis

delusion

dementia

dementia, age at onset

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

depression

developmental milestones

developmental milestones, loss of

developmental retardation

developmental venous anomalies

diabetes mellitus

diagnostic criteria

differential diagnosis

diplopia

disability, neurological

diurnal variation

dopa responsive dystonia

dopamine

dopamine agonist

dopaminergic dysfunction

drooling

drug induced neurologic disorders

Durett hemorrhages

dysarthria

dyskinesia

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, face

dystonia, focal

dystonia, painful

dystonia, prevalence of

dystonia, symptomatic

dystonia, treatment of

encephalopathy, progressive

enzyme, defect

ependymoma

epidemiology of neurology

eye movement, disorders of

Fabry's disease

facial nerve palsy

facial nerve palsy, bilateral

facial pain

Fahr disease

failed medical management

fine motor function, impaired

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontotemporal dementia, behavioral variant

gamma amino butyric acid

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

gests antagoniste

Gilles de la Tourette syndrome

glabellar sign

glioblastoma multiforme(astrocytoma Gr.III)

glioma

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

grimacing

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination

hallucination, visual

hemangioma, brainstem

hematuria, gross

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration, non-Wilsonian

hepatomegaly

hepatosplenomegaly

heralding manifestation

hydroxyindole acetic acid 5(5HIAA)

hyperactivity

hyperammonemic encephalopathy

hypotension, neurologic causes of

hypotension, systemic

hypotonia

iatrogenic neurologic disorders

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inborn errors of metabolism

incidental finding

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inflexibility, mental

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

intracerebral hemorrhage, lobar

intracerebral hemorrhage, recurrent

intracranial pressure, increased

intrathecal chemotherapy

iron, brain

iron, serum

isoniazid

Jakob-Creutzfeldt disease

jaundice

jaw pain

Kayser-Fleischer ring

kinesia paradoxica

Korsakoff's psychosis

L-dopa, drug interactions with and side effects of

leg spasms

leg spasms, painful

Leigh's disease

lenticular nucleus, lesion of, bilateral

lethargy

leucine-rich repeat kinase 2 gene

leukemia, neurologic findings assoc.with

leukocyte peroxidase

leukoencephalopathy

Lewy body

Lewy body disease, diffuse

life expectancy

lightheaded

lipid storage disorder of CNS

liver disease

liver function enzymes

liver transplantation

lobar atrophy

locus ceruleus, lesion of

low back pain

lymphoma, primary of CNS

malformation, vascular

malformation, vascular, cerebral

meningitis, carcinomatous

meningoencephalopathy

methotrexate

methylhydrazine derivatives

microangiopathy, brain

microcephaly

micrographia

microhemorrhage, intracerebral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

monoamine oxidase inhibitors

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI pattern

MRI, abnormal

MRI, contrast enhanced

MRI, eye of tiger sign

MRI, functional

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, incidental finding

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

multiple sclerosis

multiple system atrophy

neoplasm, intracranial

neoplasm, intracranial-incidence and epidemiology of

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-treatment of

neoplasm, primary intracerebral

neoplasm, primary intracerebral, reoperation

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-familial occurrence

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-surgical treatment of

neoplasm, primary of CNS-treatment of

neurodegeneration with brain iron accumulation

neuroendocrinology

neurofibrillary degeneration

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic symptoms

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neurotoxin

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

obsessive-compulsive disorder

old age, neurology of

ophthalmoplegia, progressive external

opiate

optic atrophy

optokinetic nystagmus, abnormal

orthostatic hypotension

orthostatic hypotension, idiopathic

pain

pain, head

pain, increased response

paraspinal muscle weakness

paratrigeminal syndrome

paresthesias

Parkinson disease

Parkinson disease, arteriosclerotic

Parkinson disease, atypical

Parkinson disease, benign tremulous

Parkinson disease, classification

Parkinson disease, dementia with

Parkinson disease, diagnosis

Parkinson disease, differential diagnosis of

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, early symptoms

Parkinson disease, etiology of

Parkinson disease, familial

Parkinson disease, freezing phenomena in

Parkinson disease, heterogeneity of

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, misdiagnosis

Parkinson disease, pathogenesis of

Parkinson disease, presymptomatic detection

Parkinson disease, rapid onset

Parkinson disease, rapid progression

Parkinson disease, subtypes

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinson disease, young onset

Parkinsonism multiple-system atrophy

Parkinsonism plus syndrome

Parkinsonism syndrome

Parkinsonism-dementia complex

paroxysmal hemiplegia

paroxysmal neurologic deficits

patient information and support

pigmentary retinopathy

pituitary, adenoma

pleocytosis of cerebrospinal fluid

poison, neurologic problems with

POLG1 gene

polymerase chain reaction

pons, atrophy

pontocerebellar atrophy

portal caval shunt

postural abnormality

pramipexole

precipitating factors

preclinical

pregnancy, neurologic complications in

primary familial brain calcification

prisoners of war, neurologic complications in

PRKN gene

procarbazine

prognosis

progressive infantile poliodystrophy

progressive neurologic disorder

progressive supranuclear palsy

prolactin, elevated

propranolol

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary function tests

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

quality of life

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

raphe nuclei

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

recurrent

Red flags

release phenomena

respirations in CNS disease

respiratory failure

restless leg syndrome

retinal hemangioma

retinopathy

reversible neurologic disorder

sensorineural hearing loss

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

small vessel disease

small vessel disease, cerebral

smell

Smell Identification Test

speech disorder, childhood

speech, loss of

speech, soft

spinal cord, lesion of

spinal cord, neoplasm

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

stimulation, deep brain

stimulation, thalamic

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

stridor

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subarachnoid hemorrhage

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

thalamotuberal artery

thalamus

thalamus, focused ultrasound ablation

thalamus, lesion of-bilateral

transient neurologic deficit

trauma

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, voice

tremor, wing beating

trinucleotide repeats

tripping

twins

tyrosine hydroxylase deficiency

ultrasonography

ultrasonography, head

undiagnosed

valsalva maneuver

varicella zoster virus

varicella zoster virus, encephalitis

vasculopathy

vasospasm, cerebral

vinblastine

vincristine neurotoxicity

walking, difficulty with

war

weakness, progressive

white matter disease, subcortical

word-finding difficulty

workup

wrist drop

writers cramp

X-linked dystonia-parkinsonism syndrome

Showing articles 50 to 100 of 3032 << Previous Next >>

Neuropsychological and Quality of Life Outcomes 12 Months After Unilateral Thalamic Stimulation for Essential Tremor
JNNP 74:305-311, Fields,J.A.,et al, 2003

Alzheimer's Disease and Parkinson's Disease
NEJM 348:1356-1364, Nussbaum,R.L. &Ellis,C.E., 2003

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Therapies for Movement Disorders
Arch Neurol 59:699-702, Goetz,C.G &Hinson,V.K., 2002

Subclinical Dopaminergic Dysfunction in Asymptomatic Parkinson's Disease Patients' Relatives with a Decreased Sense of Smell
Ann Neurol 50:34-41, Berendse,H.W.,et al, 2001

Complete Genomic Screen in Parkinson Disease
JAMA 286:2239-2244, Scott,W.K.,et al, 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Essential Tremor
NEJM 345:887-891, Louis,E.D., 2001

Thalamic Deep Brain Stimulation
Arch Neurol 58:218-222, Ondo,W.,et al, 2001

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

Functional Outcomes After Gamma Knife Thalamotomy for Essential Tremor and MS-Related Tremor
Neurol 55:443-446, Niranjan,A. et al, 2000

Deep Brain Stimulation of Subthalamic Area for Severe Proximal Tremor
Neurol 55:114-116, Kitagawa,M. et al, 2000

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

A Comparison of Continuous Thalamic Stimulation and Thalamotomy for Suppression of Severe Tremor
NEJM 342:461-468,505, Schuurman,P.R.,et al, 2000

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Bilateral Thalamic Stimulation for the Treatment of Essential Tremor
Neurol 53:1447-1450, Pahwa,R.,et al, 1999

Neuropsychological and Quality of Life Outcome after Thalamic Stimulation for Essential Tremor
Neurol 53:1774-1780, Troster,A.I.,et al, 1999

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

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Stereotactic Radiosurgical Pallidotomy and Thalamotomy with the Gamma Knife:MR Imaging Findings with Clinical Correlation-Preliminary Experience
Radiology 212:143-150, Friedman,D.P.,et al, 1999

Multicentre European Study of Thalamic Stimulation in Paarkinsonisn and Essential Tremor
JNNP 66:289-296, Limousin,P.,et al, 1999

Unilateral Thalamic Deep Brain Stimulation for Refractory Essential Tremor and Parkinson's Disease Tremor
Neurol 51:1063-1069, Ondo,W.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Hereditary Form of Parkinsonism-Dementia
Ann Neurol 43:768-781, Muenter,M.D.,et al, 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Reduction in Voice Tremor Under Thalamic Stimulation
Neurol 50:796-798, Carpenter,M.A.,et al, 1998

High-Frequency Unilateral Thalamic Stimulation in the Treatment of Essential and Parkinsonian Tremor
Ann Neurol 42:292-299, Koller,W.,et al, 1997

Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

A Gene for Parkinson Disease
Arch Neurol 54:1156-1157, Chase,T.N., 1997

Olfactory Dysfunction in Familial Parkinsonism
Neurol 49:1262-1267, Markopoulou,K.,et al, 1997

Familial Idiopathic Brain Calcification with Autosomal Dominant Inheritance
Neurol 48:645-649, Kobari,M.,et al, 1997

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

A Gene for Parkinson's Disease
BMJ 313:1278, Hawkes,C., 1996

Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996

Restless Legs Syndrome:Clinicoetiologic Correlates
Neurol 47:1435-1441, Ondo,W.&Jankovic,J., 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Deep Brain Stimulation for Essential Tremor
Neurol 46:1150-1153, Hubble,J.P.,et al, 1996

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle
Ann Neurol 38:355-356, Duvoisin,R.C.&Golbe,L.I., 1995

A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation
Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995

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

The Relationship of Essential Tremor to Other Movement Disorders:Report on 678 Patients
Ann Neurol 35, 717-7231994., Koller,W.C.,et al, 1994

Autosomal Dominant Parkinsoniam with Benign Course and Typical Lewy-Body Pathology
Neurol 43:2222-2227, Golbe,L.I.,et al, 1993

Identical Twins with Similar Onset of Parkinson's Disease:A Case Report
Neurol 43:1159-1161, Pahwa,R.,et al, 1993

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Effect of Stereotactic Thalamic Lesion on Essential Tremor
Lancet 340:206-207, Lakie,M.,et al, 1992

Olfactory Function in Essential Tremor
Neurol 42:1631-1632, Busenbark,K.L.,et al, 1992

Parkinson's Disease in Twins
Neurol 42:1453-1461, Vieregge,P.,et al, 1992

Showing articles 50 to 100 of 3032 << Previous Next >>