Neudle.com: familial parkinsonism

Differential
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acoustic neurinoma, bilateral

advances in neurology

adverse drug reaction

alcohol, neurologic complications with

alcoholism

algorithm

alternating hemiplegia

alternating hemiplegia of childhood

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

anticipation

anxiety

aphasia

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

bent spine syndrome

beta adrenergic blocker

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 atrophy, secondary

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 palsy

cerebral vasculature, calcification

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, recurrent

ceruloplasmin, serum

Chediak-Higashi syndrome

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

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst

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

diabetes mellitus

diagnostic criteria

differential diagnosis

disability, neurological

disinhibition-dementia-parkinsonism-amyotrophic complex

diurnal variation

dopa responsive dystonia

dopamine

dopamine agonist

dopaminergic dysfunction

drooling

drug induced neurologic disorders

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, treatment of

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, progressive

enzyme, defect

epidemiology of neurology

eye movement, disorders of

Fragile-X associated tremor/ataxia-syndrome

fragile-X syndrome

Friedreich's ataxia

frontotemporal dementia, behavioral variant

gait disorder

gait, festinating

galactorrhea

gamma amino butyric acid

gamma knife therapy

gangliosidosis GM1

gaze palsy

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

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

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)

hyperammonemic encephalopathy

hypotension, neurologic causes of

hypotension, systemic

hypotonia

iatrogenic neurologic disorders

imbalance

imbalance, postural

impulsivity

inborn errors of metabolism

inclusion bodies

inclusion bodies, intracytopasmic

inclusion bodies, intranuclear

inflexibility, mental

intellectual deficit

intellectual deterioration

intracerebral hemorrhage

iron, brain

Jakob-Creutzfeldt disease

jaundice

Kayser-Fleischer ring

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

leukocyte peroxidase

leukoencephalopathy

Lewy body

Lewy body disease, diffuse

life expectancy

lipid storage disorder of CNS

liver disease

liver function enzymes

liver transplantation

lobar atrophy

locus ceruleus, lesion of

low back pain

malformation, vascular

malformation, vascular, cerebral

meningitis, carcinomatous

microangiopathy, brain

microcephaly

micrographia

microhemorrhage, intracerebral

mitochondrial disease

mitochondrial disease, pathogenesis

mitochondrial encephalomyopathy

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, hyperkinetic

movement disorder, treatment of

MRI

MRI pattern

MRI, abnormal

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

MRS

multiple sclerosis

multiple system atrophy

neurodegeneration with brain iron accumulation

neuroendocrinology

neurologic complications of, surgery

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neurotransmitter

next-generation sequencing

Niemann-Pick disease

nigrostriatal pathway

obsessive-compulsive disorder

old age, neurology of

Ondine's curse

opened mouth

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optokinetic nystagmus, abnormal

orthostatic hypotension

orthostatic hypotension, idiopathic

pain

pain, increased response

palilalia

pallido-ponto-nigral degeneration

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

pigmentary retinopathy

poison, neurologic problems with

POLG1 gene

polymerase chain reaction

pons, atrophy

pontocerebellar atrophy

portal caval shunt

postural abnormality

precipitating factors

preclinical

primary familial brain calcification

prisoners of war, neurologic complications in

PRKN gene

prognosis

progressive infantile poliodystrophy

progressive neurologic disorder

progressive subcortical gliosis

progressive supranuclear palsy

prolactin, elevated

propranolol

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

ptosis

pulmonary function tests

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

radiation therapy, stereotactic

raphe nuclei

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

recurrent

Red flags

release phenomena

respirations in CNS disease

respiratory failure

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 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

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

valsalva maneuver

varicella zoster virus

varicella zoster virus, encephalitis

walking, difficulty with

war

weakness, progressive

white matter disease, subcortical

whole genome sequencing

wide based gait

word-finding difficulty

workup

writers cramp

X-linked dystonia-parkinsonism syndrome

Showing articles 1300 to 1350 of 2866 << Previous Next >>

Frequency of Dementia in Parkinson Disease
Arch Neurol 42:428-431, Aarsland,D.,et al, 1996

Case-Control Study of Idiopathic Parkinson's Disease and Dietary Vitamin E Intake
Neurol 46:1270-1274, Morens,D.M.,et al, 1996

Multicenter, Placebo-Controlled Trial of Cabergoline Taken Once Daily in the Treatment of Parkinson's Disease
Neurol 46:1062-1065, Hutton,J.T.,et al, 1996

Survival & Prolif of Nonneural Tissu, with Obstr of Cereb Ventric, In Parkinson Pt Trt with Fetal Allografts
Neurol 46:1219-1225, Folkerth,R.D.&Durso,R., 1996

Diffuse Lewy Body Disease:Clinical Features in Nine Cases without Coexistent Alzheimer's Disease
JNNP 60:531-538, Hely,M.A.,et al, 1996

Double-Blind Comparison of Cabergoline & Bromocriptine in Parkinson's Disease Pts with Motor Fluctuations
Neurol 47:785-788, Inzelberg,R.,et al, 1996

Gamma Knife Pallidotomy in Advanced Parkinson's Disease
Ann Neurol 39:535-538, Friedman,J.H.,et al, 1996

Diet and Parkinson's Diseae I:A Possible Role for the Past Intake of Specific Foods and Food Groups
Neurol 47:636-643, Hellenbrand,W.,et al, 1996

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

Mapping of Hereditary Neuralgic Amyotrophy (Familial Brachial Plexus Neuropathy) to Distal Chromosome 17q
Neurol 46:1128-1132, Pellegrino,J.E.,et al, 1996

Phenotypic Heterogen in Hered Neurop with Liability to Press Palsies Assoc with Chromosome 17p11. 2-12 Delet
Neurol 46:1133-1137, Pareyson,D.,et al, 1996

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

Intelligence and the X Chromosome
Lancet 347:1814-1815, Turner,G., 1996

MR Findings in Tay-Sachs Disease
J Comput Assist Tomogr 20:551-555, Mugikura,S.,et al, 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Reversible Parkinsonism and Cognitive Impairment with Chronic Valproate Use
Neurol 47:626-635, Armon,C.,et al, 1996

Familial Temporal Lobe Epilepsy:A Common Disorder Identified in Twins
Ann Neurol 40:227-235, Berkovic,S.F.,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

Chronic Myelopathy Associated with Human Herpesvirus-6
Neurol 45:2015-2017, Mackenzie,I.R.A.,et al, 1995

Inclusion Body Myositis and Myopathies
Ann Neurol 38:705-713, Griggs,R.C.,et al, 1995

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340995., Forestier,N.L.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Familial Acephalgic Migraine
Neurol 45:2293-2294, Ziegler,D.K., 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,et al, 1995

Exacerbation of Idiopathic Parkinson's Disease by Naproxen
BMJ 311:422, Shaunak,S.,et al, 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

Encephalopathy with Parkinsonian Features in Children Following Bone Marrow Transplantations and High-Dose Amphotericin B
Ann Neurol 37:810-814, Mott,S.H.,et al, 1995

Familial Autoimmune Myasthenia Gravis:Report of Four Families
JNNP 58:729-731, Evoli,A.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

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

The Effect of Deprenyl and Levodopa on the Progression of Parkinson's Disease
Ann Neurol 38:771-777, Olanow,C.W.,et al, 1995

Complementary Positron Emission Tomographic Studies of the Striatal Dopaminergic System in Parkinson's Disease
Arch Neurol 52:1183-1190, Antonini,A.,et al, 1995

MRI In Patients with Suspected Vascular Parkinsonism
Neurol 45:2183-2188, Jijlmans,J.C.M.,et al, 1995

Early Differential Diagnosis of Parkinson's Disease with F-flurodeoxyglucose and Positron Emission Tomography
Neurol 45:1995-2004, Eidelberg,D.,et al, 1995

Effect of GPi Pallidotomy on Motor Function in Parkinson's Disease
Lancet 346:1383-1387, Lozano,A.M.,et al, 1995

Clinical and[18F]dopa PET Findings in Early Parkinson's Disease
JNNP 59:597-600, Morrish,P.K.,et al, 1995

Generalized Mitochondrial Dysfunction in Parkinson's Disease Detected by Magnetic Resonance Spectroscopy of Muscle
Neurol 45:2097-2099, Penn,A.M.W.,et al, 1995

Decreased SPECT[123I]B-CIT Striatal Uptake Correlates with Symptom Severity in Parkinson's Disease
Ann Neurol 38:589-598, Seibyl,J.P.,et al, 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

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

Non-Progressive Familial Idiopathic Intracranial Calcification:A Family Report
JNNP 59:432-434, Callender,J.S., 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

Comparison of Therapeutic Effects & Mortality Data of Levodopa & Levodopa with Selegiline in Pts with Early, Mild Parkinson's
BMJ 311:1602-1607, 15831995., Lee,A.J.,et al, 1995

Comparative Study of Selegiline Plus L-Dopa-Carbidopa VS L-Dopa-Carbidopa Alone in Trtm of Parkinson's Disease
Ann Neurol 37:95-98, Brannan,T.&Yahr,M.D., 1995

Showing articles 1300 to 1350 of 2866 << Previous Next >>