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Addison's disease
adrenomyeloneuropathy
advances in neurology
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agitation
algorithm
alternative medicine
Alzheimer's disease
Alzheimer's disease, behavioral symptoms
Alzheimer's disease, treatment of
amyotrophic lateral sclerosis
Angelman syndrome
anticholinesterase
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aphasia
apolipoprotein E
Asperger's syndrome
aspiration
ataxia
ataxia, cerebellar
ataxia, sensory
attention span
auditory evoked brainstem potentials
autism
autism, screening for
behavior
behavior, combative
behavioral disorder
bladder dysfunction
body odor
bone marrow transplantation
brain atrophy
C0ORF72
CAG repeats
calcification, intracranial
caregiver
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataplexy
caudate nucleus, atrophy
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral glucose metabolism
cerebral infarction, subcortical
cerebrospinal fluid
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, prognosis in
cerebrovascular accident, recurrent
cerebrovascular accident, rehabilitation of
children
chorea
chromosomal abnormality
chromosome 19
chromosome 7
Clinical Pathologic Conference(C.P.C.)
clonus
cobalamin C deficiency
cognition
compulsivity
corpus callosum, lesion of
cultured skin fibroblasts
cystinosis
degenerative diseases of CNS
delirium
delusion
dementia
dementia, familial
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demyelinating disease
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developmental evaluation
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eczema
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electroencephalogram, abnormalities of
electromyogram
emotional lability
employment
enzyme, defect
epidemiology of neurology
epsilon sarcoglycan gene
ethics in neurology
evoked potentials
Fabry's disease
falling
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family function
fasciculation
fetal alcohol syndrome
flow study, carotid artery
foam cells
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal lobe, atrophy
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gait disorder
gait, spastic
galactocerebrosidase
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
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genetic testing
giant axonal neuropathy
Gilles de la Tourette syndrome
gout
grasp reflex
grief reaction
hallucination
health insurance
hemiplegia
hepatic failure
hepatosplenomegaly
hoarding
homocystinuria
Huntington's chorea
Huntington's chorea, genetic counselling
Huntington's disease, children
hyperactivity
hyperhomocysteinemia
hyperreflexia
hypomyelination
hypotonia
imbalance
impulsivity
inappropriate behavior
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
incoordination
intellectual deficit
intellectual deterioration
intelligence quotient
internet
intracerebral hemorrhage
intrauterine
irritability
jaundice
karyotyping
Krabbe's disease
lacunar infarction
language delay
laughing, pathologic
learning disability
learning disability, in children
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
lobar atrophy
lysosomal storage disease
lysosomes, abnoral
magnetoencephalography
mania
memantine
memory
memory, evaluation of
memory, impairment of
mental retardation
mental retardation, family psychological problems in
methylmalonic acidemia
microangiopathy, brain
microhemorrhage, intracerebral
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine with aura
misdiagnosis
mongolism
mortality
motor neuron disease
mousy odor
movement disorder
MRI
MRI, abnormal
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, functional
MRI, spinal cord
multiple system atrophy
myelomalacia
myelopathy
myoclonic dystonia
myoclonus
myoclonus, action
nerve conduction studies
neurofibrillary degeneration
neuroleptic
neuroleptic, atypical
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
next-generation sequencing
Niemann-Pick disease
Notch3 gene
nystagmus
olanzapine
old age, neurology of
optic ataxia
optic atrophy
paraparesis, spastic
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, nonmotor problems of
Parkinsonism syndrome
Pelizaeus Merzbacher
personality change
pes cavus
phenylketonuria
Pick's disease
Prader-Labhart-Willi syndrome
prognosis
progressive neurologic disorder
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosocial aspects
pulmonary embolism
pyramidal
pyramidal tract dysfunction
quality of life
quetiapine
release phenomena
renal failure
repetitive questioning
review article
rigidity
risk factors
risperidone
rummaging
sarpropterin
screening
seizure
selective serotonin reuptake inhibitors
senile plaques
sensory loss
shadowing
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
small vessel disease
small vessel disease, cerebral
snout reflex
socialisation
somatosensory evoked potentials
spastic dysphonia
spasticity
speech disorder
splenomegaly
stem cell transplantation
stereotyped behavior
stereotyped behavior, drug induced
stimulant drugs
subarachnoid hemorrhage
subcortical U fibers
suck reflex
suicide
temporal lobe, atrophy
thrombophlebitis
tic
tongue, fasciculations of
treatment of neurologic disorder
treatment, non-pharmacologic
tremor
trinucleotide repeats
twins
umbilical-cord blood transplantation
vasculopathy
venous thrombosis, non-cerebral
vibratory sensation, abnormal
violent behavior
visual loss
wandering
weight loss
white matter disease
white matter disease, subcortical
workup
x-linked mental retardation
Showing articles 0 to 50 of 6255 Next >>

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

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

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Assessment and Management of Behavioral and Psychological Symptoms of Dementia
BMJ 350:h369, Kales, H.C.,et al, 2015

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004

Ten Most Commonly Asked Questions About the Psychiatric Aspects of Parkinson's Disease
The Neurologist 9:50-56, Reich,S.G. & Marsh,L., 2003

Learning Disability
Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996

Lower Cognitive Performance in Normal Older Adult Male Twins Carrying the Apolipoprotein E-E4 Allele
Arch Neurol 51:1189-1192, Reed,T.,et al, 1994

Memory Evaluation in Alzheimer's Disease, Caregivers'Appraisals and Objective Testing
Arch Neurol 50:92-97, Koss,E.,et al, 1993

Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
Arch Neurol 50:725-728, Randolph,C.,et al, 1993

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,et al, 1992

Clinicopath Conf
Pick's Diseae, Case 6-1992, NEJM 326:397-405992., , 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

Giant Axonal Neuropathy:Progressive Clinical and Radiologic CNS Involvement
Neurol 42:2220-2221, Richen,P.&Tandan,R., 1992

Social and Family Integration of Hemiplegic Elderly Patients 1 Year After Stroke
Stroke 21:1019-1022, Santus,G.,et al, 1990

Neurologic Complications in Long-Standing Nephropathic Cystinosis
Arch Neurol 46:543-548, Fink,J.K.,et al, 1989

Dementia in Down's Syndrome:Cerebral Glucose Utilization, Neuropsychological Assessment, and Neuropathology
Neurol 38:938-942, Schapiro,M.B.,et al, 1988

Psychological Management of the Retarded Child & Its Family
Psych Ann 3:Jul, Freeman,R., 1973

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

Clinicopathologic Conference, Psychotic Disorder Due to a General Medical Condition (postictal psychosis)
NEJM 391:2036-2046, Case 37-2024, 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

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

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Cannabis-Related Disorders and Toxic Effects
NEJM 389: 2267-2275, Gorelick,D.A., 2023

Toward Gerineuropalliative Care for Patients with Dementia
NEJM 389:775-778, Harrison,K.L.,et al, 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

Neuroimaging Biomarkers in a Patient with Probable Psychiatric-Onset Prodromal Dementia with Lewy Bodies
Neurol 99:654-657, Urso, D.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

Clinicopathologic Conference, Cotards Syndrome, Catatonia, Depression and Coronavirus Disease 2019
NEJM 387:1795-1802, , 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Association Between Occupational Exposure to Formaldehyde and Cognitive Impairment
Neurol 98:e633-e640, Letellier, N.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

A 72-Year-Old Woman with Rapidly Progressive Bilateral Hearing Loss
Neurol 98:632-637, Alsalem, A.,et al, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A Triad of Tremor, Ataxia, and Cognitive Impairment
Neurol 96:e1802-e1803, Au, L.W.C.,et al, 2021

National Institute of Neurological Disorders and Stroke Consensus Diagnostic Criteria for Traumatic Encephalopathy Syndrome
Neurol 96:848-863, Katz, D.I.,et al, 2021

Clinicopathologic Conference, Delayed Postthypoxic Leukoencephalopathy
NEJM 384:2438-2445, Case 19-2021, 2021

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020



Showing articles 0 to 50 of 6255 Next >>