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 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

word-finding difficulty

workup

writers cramp

X-linked dystonia-parkinsonism syndrome

Showing articles 650 to 700 of 2832 << Previous Next >>

A Randomized Trial of Deep-Brain Stimulation for Parkinsons Disease
NEJM 355:896-908, Deuschl,G.,et al, 2006

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

Nonsteroidal Anti-Inflammatory Drugs and the Incidence of Parkinson Disease
Neurol 66:1097-1099, Hernan,M.A.,et al, 2006

Practice Parameter: Evaluation and Treatment of Depression, Psychosis, and Dementia in Parkinson Disease (An Evidence-Based Review)
Neurol 66:996-1002, Miyasaki,J.M.,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

Practice Parameter: Diagnosis and Prognosis of New Onset Parkinson Disease (An Evidence-Based Review)
Neurol 66:968-975, Suchowersky,O.,et al, 2006

The Parkinsons Complex: Parkinsonism Is Just the Tip of the Iceberg
Ann Neurol 59:591-596, Langston,J.W., 2006

Practice Parameter: Neuroprotective Strategies and Alternative Therapies for Parkinson Disease (An Evidence-Based Review)
Neurol 66:976-982, Suchowersky,O.,et al, 2006

Safety of Rasagiline in Elderly Patients with Parkinson Disease
Neurol 66:1427-1429, Goetz,C.G.,et al, 2006

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

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

Diffusion-Weighted Magnetic Resonance Imaging in the Syndrome of Acute Bilateral Basal Ganglia Lesions in Diabetic Uremia
Mov Disord 21:1267-1270, Kim, T.,et al, 2006

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

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

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

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

A Randomized Placebo-Controlled Trial of Rasagiline in Levodopa-Treated Patients with Parkinson Disease and Motor Fluctuations
Arch Neurol 62:241-248, The PRESTO Study, 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

Rasagiline as an Adjunct to Levodopa in Patients With Parkinsons Disease and Motor Fluctuations (LARGO, Lasting Effect in Adjunct Therapy With Rasagiline Given Once Daily, Study)
Lancet 365:947-954, 914, Rascol,O., et al, 2005

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

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Quantatative Assessment of Driving Performance in Parkinson's Disease
JNNP 76:176-180, 159, Wood, J.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

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

Donepezil for Dementia in Parkinsons Disease: A Randomised, Double Blind, Placebo Controlled, Crossover Study
JNNP 76:934-939,903, Ravina,B.,et al, 2005

Short-Term Paroxetine Treatment Does Not Alter the Motor Response to Levodopa in PD
Neurol 64:1797-1798, Chung,K.A.,et al, 2005

[99mTc]TRODAT-1 SPECT Imaging Correlates with Odor Identification in Early Parkinson Disease
Neurol 64:1716-1720, Siderowf,A.,et al, 2005

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

Searching for a Relationship Between Manganese and Welding and Parkinsons Disease
Neurol 64:2021-2028, 2001, Jankovic,J., 2005

Practice Parameter:Therapies for Essential Tremor
Neurol 64:2008-2020, Zesiewicz,T.A.,et al, 2005

Neurologic Manifestations in Welders with Pallidal MRI T1 Hyperintensity
Neurol 64:2033-2039,2001, Josephs,K.A.,et al, 2005

New and Reliable MRI Diagnosis for Progressive Supranuclear Palsy
Neurol 64:2050-2055, Oba,H.,et al, 2005

Pleuropulmonary Fibrosis After Long-term Treatment With the Dopamine Agonist Pergolide for Parkinson Disease
Arch Neurol 62:1290-1295, Tintner,R.,et al, 2005

Sudden Uncontrollable Somnolence and Medication Use in Parkinson Disease
Arch Neurol 62:1242-1248, Avorn,J.,et al, 2005

Camptocormia
Neurol 65:355-359, Azher,S.N. &Jankovic,J., 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

Diagnosis and Initial Management of Parkinsons Disease
NEJM 353:1021-1027, Nutt,J.G.&Wooten,G.F., 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

Neurologic Spectrum of Chronic Liver Failure and Basal Ganglia T1 Hyperintensity on Magnetic Resonance Imaging, Probably Manganese Neurotoxicity
Arch Neurol 62:1385-1390, Klos,K.J.,et al, 2005

Showing articles 650 to 700 of 2832 << Previous Next >>