Neudle.com: familial parkinsonism

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acoustic neurinoma, bilateral

advances in neurology

adverse drug reaction

airway obstruction

alcohol, neurologic complications with

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

Alzheimer's disease

Alzheimer's disease, familial

amyloid plaques

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

anticholinergic drugs

aphasia, progressive, primary

ataxia, cerebellar

ataxia, hereditary

ataxia, progressive

ataxia, truncal

athetosis, causes of

attention deficit disorder with hyperactivity

autonomic dysfunction

autonomic dysfunction, acute

autonomic nervous system

autonomic neuropathy

bacterial infection

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

bent spine syndrome

beta adrenergic blocker

biologic markers

biopterin deficiency

blinking, reduced

botulinum toxin

calcification, intracranial

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, isodense lesion with acute hemorrhage

CAT scan, muscle

cavernous hemangioma

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral infarction, subcortical

cerebral ischemia

cerebral vasculature, calcification

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, recurrent

ceruloplasmin, serum

Chediak-Higashi syndrome

chorea, causes of

choreoathetosis

chromosomal abnormality

chronic progressive external ophthalmoplegia

cingulate island sign

Clinical Pathologic Conference(C.P.C.)

coat-hanger pain

cogwheel rigidty

compression fracture

contractures, joint

controversies in neurology

conversion reaction

copper metabolism, abnormal

corpus callosum, lesion of

corpus callosum, thinning

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, parenchymal

degenerative diseases of CNS

delay in diagnosis

dementia, age at onset

dementia, familial

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes mellitus

diagnostic criteria

differential diagnosis

disability, neurological

disinhibition-dementia-parkinsonism-amyotrophic complex

diurnal variation

dopa responsive dystonia

dopamine agonist

dopaminergic dysfunction

drug induced neurologic disorders

dyskinesia, causes of

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, cervical

dystonia, children

dystonia, classification

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, painful

dystonia, treatment of

emotional lability

encephalitis, brainstem

encephalitis, viral

encephalopathy, progressive

epidemiology of neurology

erectile dysfunction

exercise intolerance

eye movement, disorders of

Fabry's disease

facial nerve palsy

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontotemporal dementia, behavioral variant

gait, festinating

gamma amino butyric acid

gamma knife therapy

gangliosidosis GM1

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

gests antagoniste

Gilles de la Tourette syndrome

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glutamate dehydrogenase deficiency

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hallucination, visual

hemangioma, brainstem

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration, non-Wilsonian

hepatosplenomegaly

heralding manifestation

homovanillic acid

Horner's syndrome

Huntington's chorea

hydroxyindole acetic acid 5(5HIAA)

hyperammonemic encephalopathy

hypometric saccades

hypoparathyroidism

hypotension, neurologic causes of

hypotension, systemic

iatrogenic neurologic disorders

imbalance, postural

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inflexibility, mental

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

Jakob-Creutzfeldt disease

Kayser-Fleischer ring

kinesia paradoxica

lactic acidemia

lacunar infarction

L-dopa, drug interactions with and side effects of

leg spasms, painful

Leigh's disease

lenticular nucleus, lesion of, bilateral

leucine-rich repeat kinase 2 gene

leukocyte peroxidase

leukoencephalopathy

Lewy body disease, diffuse

life expectancy

lipid storage disorder of CNS

liver function enzymes

liver transplantation

locus ceruleus, lesion of

malformation, vascular

malformation, vascular, cerebral

marche a petits pas

melanoma, malignant

meningitis, carcinomatous

microangiopathy, brain

microhemorrhage, intracerebral

migraine with aura

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, eye of tiger sign

MRI, functional

MRI, gradient-echo

MRI, high signal intensity of basal ganglia

MRI, paramagnetic effect

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple system atrophy

muscle weakness

muscular dystrophy

myasthenia gravis

myelopathy, hepatic

myoclonus, epilepsy

myopathy, metabolic

neurodegeneration with brain iron accumulation

neuroendocrinology

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuropathology, brain

neuropathy, peripheral

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

nystagmus, monocular

nystagmus, rotary

nystagmus, vertical

obsessive-compulsive disorder

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

optokinetic nystagmus, abnormal

orthostatic hypotension

orthostatic hypotension, idiopathic

pain, increased response

pallido-ponto-nigral degeneration

paraparesis, spastic

paraspinal muscle

paraspinal muscle weakness

paratrigeminal syndrome

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

personality change

phenylketonuria

pigmentary retinopathy

poison, neurologic problems with

polymerase chain reaction

pontocerebellar atrophy

portal caval shunt

postural abnormality

precipitating factors

primary familial brain calcification

prisoners of war, neurologic complications in

progressive infantile poliodystrophy

progressive neurologic disorder

progressive subcortical gliosis

progressive supranuclear palsy

prolactin, elevated

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

radiation therapy, stereotactic

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

release phenomena

respirations in CNS disease

respiratory failure

reversible neurologic disorder

Riley-Day syndrome

seizure, children

sensorineural hearing loss

shoulder, pain in

Shy-Drager syndrome

single photon emission computed tomography

skin, lesions in neurologic disorders

small vessel disease

small vessel disease, cerebral

Smell Identification Test

SNCA duplication

spastic dysphonia

speech disorder

speech disorder, childhood

speech, loss of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar degeneration

status epilepticus

stereotyped behavior

stimulation, deep brain

stimulation, thalamic

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

strokelike episodes

subarachnoid hemorrhage

substantia nigra

subthalamic nucleus

subthalamic nucleus deep brain stimulation

tardive dyskinesia

tardive dystonia

tetrahydrobiopterin

thalamus, lesion of-bilateral

thrombocytopenia

tonic foot response

transient neurologic deficit

treatment of neurologic disorder

tremor, cerebellar

tremor, classification

tremor, differential diagnosis of

tremor, intention

tremor, physiologic

tremor, postural

tremor, resting

tremor, surgical treatment of

tremor, thalamic stimulation for suppression of

tremor, treatment of

tremor, wing beating

trinucleotide repeats

tyrosine hydroxylase deficiency

valsalva maneuver

varicella zoster virus

varicella zoster virus, encephalitis

vasospasm, cerebral

viral infection, CNS

walking, difficulty with

weakness, progressive

white matter disease

white matter disease, subcortical

word-finding difficulty

X-linked dystonia-parkinsonism syndrome

Showing articles 700 to 750 of 2832 << Previous Next >>

Pathological Gambling Caused by Drugs Used to Treat Parkinson Disease
Arch Neurol 62:1377-1381, Dodd,M.L.,et al, 2005

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

Neuropathology of Dementia in Parkinsons Disease: A Prospective, Community-Based Study
Ann Neurol 58:773-776,663, Aarsland,D.,et al, 2005

Cabergoline-Related Severe Restrictive Mitral Regurgitation
NEJM 353:1974-1975, Rosen,C.J., 2005

Occupation and Parkinsonism in Three Movement Disorders Clinics
Neurol 65:1430-1435, Goldman,S.M.,et al, 2005

Excessive Daytime Sleepiness and Subsequent Development of Parkinson Disease
Neurol 65:1442-1446, Abbott,R.D.,et al, 2005

Levodopa Addiction in Idiopathic Parkinson Disease
Neurol 65:1508, Borek,L.L &Friedman,J.H., 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

Modafinil for Daytime Somnolence in Parkinsons Disease: Double Blind, Placebo Controlled Parallel Trial
JNNP 76:1636-1639, Ondo,W.G.,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

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

The role of radiotracer imaging in Parkinson disease
Neurol 64:208-215, Ravina, B., et al, 2005

Amorphine-induced eosinophilic panniculitis and hypereosinophilia in Parkinson disease
Neurol 64:392-393, Pot, C., et al, 2005

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

Levodopa and the Progression of Parkinson's Disease
NEJM 351:2498-2508, The Parkinson Study Group, 2004

Rivastigmine for Dementia Associated with Parkinson's Disease
NEJM 351:2509-2518,2547, Emre,M.,et al, 2004

Correlation Between Antemortem Magnetic Resonance Imaging Findings and Pathologically Confirmed Corticobasal Degeneration
Arch Neurol 61:1881-1884, Josephs,K.A.,et al, 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Monoamine Oxide Type B Inhibitors in Early Parkinson's Disease:Meta-Analysis of 17 Randomised Trials Involving 3525 Patients
BMJ 329:593-596, Ives,N.J.,et al, 2004

Frequency of Orthostatic Hypotension in a Community Based Cohort of Patients with Parkinson's Disease
JNNP 75:1470-1471, Allcock,L.M.,et al, 2004

Autonomic Failure as the Initial Presentation of Parkinson Disease and Dementia with Lewy Bodies
Neurol 63:1093-1095, Kaufmann,H.,et al, 2004

Glabellar and Palmomental Reflexes in Parkinsonian Disorders
Neurol 63:1096-1098, Brodsky,H.,et al, 2004

Post-Stroke Movement Disorders; Report of 56 Patients
JNNP 75:1568-1574, Alarcon,F.,et al, 2004

The Occurence of Guillain-Barre Syndrome Within Families
Neurol 63:1747-1750, Geleijns,K.,et al, 2004

Natural History of Nonketotic Hyperglycinemia in 65 Patients
Neurol 63:1847-1853, Hoover-Fong,J.E.,et al, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Neuroprotection in Parkinson Disease, Mysteries, Myths, and Misconceptions
JAMA 291:358-364, Schapira,A.H.V.&Olanow,C.W., 2004

Ophthalmologic Features of Parkinson's Disease
Neurol 62:177-180, Biousse,V.,et al, 2004

Effect of Levodopa Treatment for Parkinsonism in Welders
Neurol 62:730-733, Koller,W.C.,et al, 2004

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Neurobrucellosis:Clinical and Neuroimaging Correlation
AJNR 25:395-401, Al-Sous,M.W.,et al, 2004

Reversible Parkinsonism with Normal B-CIT-SPECT in Patients Exposed to Sodium Valproate
Neurol 62:1435-1437, Easterford,K.,et al, 2004

Developmental Dyslexia
Lancet 363:1451-60, Demonet,J-F.,et al, 2004

Treatment of Parkinson's Disease with Pergolide and Relation to Restrictive Valvular Heart Disease
Lancet 363:1179-1183, Van Camp,G.,et al, 2004

Parkinson's Disease
Lancet 363:1783-1793, Samii,A.,et al, 2004

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

Basal Ganglia Hyperperfusion in a Patient with Systemic Lupus Erythematosus-Related Parkinsonism
Neurol 63:395-396, Lee,P.H.,et al, 2004

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Stalevo for Parkinson's Disease
The Medical Letter 46:39, , 2004

Hereditary Spastic Paraplegia
Arch Neurol 61:849-855,830, Orlacchio,A.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Idiopathic Hyposmia As a Preclinical Sign of Parkinson's Disease
Ann Neurol 56:173-181,169, Ponsen,M.M.,et al, 2004

Surgical and Hardware Complications of Subthalamic Stimulation
Neurol 63:612-616, Lyons,K.E.,et al, 2004

Neurological Sequelae in Twins Born After Assisted Conception: Controlled National Cohort Study
BMJ 329:311-314, Pinborg,A.,et al, 2004

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

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

A Double-blind Placebo-controlled Trial of Botulinum Toxin B for Sialorrhea in Parkinson's Disease
Neurol 62:37-40, Ondo,W.G.,et al, 2004

Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004

Transmissible Spongiform Encephalopathies
Lancet 363:51-61, Collins,S.J.,et al, 2004

Showing articles 700 to 750 of 2832 << Previous Next >>