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 100 to 150 of 2832 << Previous Next >>

Monozygotic Twins with Parkinson's Disease
Ann Neurol 19:402-405, Koller,W.,et al, 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

Association Between Essential Tremor & Parkinson's Disease
Ann Neurol 17:329-333, Gereghty,J.J.,et al, 1985

Involvement of Upper-Airway Muscles in Extrapyramidal Disorders
NEJM 311:438-442, Vincken,W.G.,et al, 1984

Familial Occurrence of Amyotrophic Lateral Sclerosis, Parkinsonism, & Dementia
Ann Neurol 16:642-648, Schmitt,H.P.,et al, 1984

Chediak-Higashi Syndrome
Arch Neurol 41:1001-1002, Pettit,R.E.,et al, 1984

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Taste & Smell in Disease (First of Two Parts)
NEJM 308:1275-1279, Schiffman,S.S., 1983

Parkinson's Disease in 65 Pairs of Twins & in a Set of Quadruplets
Neurol 33:815-824, Ward,C.D.,et al, 1983

Twin Study of Parkinson Disease
Neurol 31:77-80, Duvoisin,R.C.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Neurological Disease In Ex-Far-East Prisoners Of War
Lancet 2:135-137, Gibberd,F.B.,et al, 1980

Diagnosis & Treatment, Physiologic & Pathologic Tremors
Ann Int Med 93:460-465, Jankovic,J.,et al, 1980

Familial Fatal Parkinsonism with Alveolar Hypoventilation & Mental Depression
Ann Neurol 6:523-531, Purdy,A.,et al, 1979

Azorean Disease of the Nervous System
NEJM 296:1505, Romanul,F.C.A.,et al, 1977

Familial Idiopathic Cerebral Calcifications
et al. , JNNP 40:280977., Boller,F., 1977

Juvenile Parkinsonism Treated with Levodopa
Arch Neurol 34:244, Sachdev,K.K.,et al, 1977

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Dysautonomia, Its Significance in Neurologic Disease (Specialty Conference)
Calif Med 117:28, Wichser,J.,et al, 1972

Clinical Diagnosis of the Dyskinesias
Med Clin of North Am 56:1321, Duvoisin,R., 1972

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025

Long-Term Consumption of Ultraprocessed Foods and Prodromal Features of Parkinson Disease
Neurol 104:e213562, Wang,P.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Safety and Efficacy of Staged, Bilateral Focused Ultrasound Thalamotomy in Essential Tremor, An Open-Label Clinical Trial
JAMA Neurol 81:939-946, Kaplitt,M.G.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

SGLT2 Inhibitor Use and Risk of Dementia and Parkinson Disease Among Patients With Type 2 Diabetes
Neurol 103:e209805, Kim,H.K.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Rabbit Syndrome
Neurol102:e209275, Huynh,T.U., & Beckley, E.H., 2024

Association of Coffee Consumption and Prediagnostic Caffeine Metabolites with Incident Parkinson Disease in a Population-Based Cohort
Neurol 102:e209201, Zhao,Y.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Showing articles 100 to 150 of 2832 << Previous Next >>