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Differential
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activities of daily living
activities of daily living scale
adrenoleukodystrophy
Alexanders disease
algorithm
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
ANA
anomic aphasia
aphasia
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
apraxia
arthritis
ascites
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ataxia, progressive
athetosis
attention span
behavioral disorder
blepharospasm
blindness
bone marrow biopsy
bone marrow transplantation
brain atrophy
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brain biopsy, indication
bruxism
bulimia
calculations
callosal angle
carphology
CAT scan
CAT scan, abnormal
CAT scan, dementia
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CAT scan, emission, abnormal
cataplexy
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebrospinal fluid, drainage of
cherry red spot
chewing movements
children
cholestasis
cholesterol, HDL
chorea
choreoathetosis
chromosome 18
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
cognition
cognition, slowed
comprehension, impaired
compulsivity
confusion
conjunctival biopsy
controversies in neurology
cornea, abnormal
cornea, opacity of
cortical dysplasia, focal
cortical-basal ganglionic degeneration
cultured skin fibroblasts
decision aids
decision analysis
degenerative diseases of CNS
dementia
dementia, childhood
dementia, diagnostic evaluation of
dementia, differential diagnosis of
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dementia, frontal lobe type
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depression
developmental milestones, loss of
developmental retardation
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dysarthria
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ecchymoses
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electron microscopy
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enzyme treatment
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falling
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fever
fluency
foam cells
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frontal lobe, behavior with disease of
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frontotemporal dementia, behavioral variant
gait disorder
gait, magnetic
gangliosidosis GM1
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gangliosidosis, generalized
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
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genetic neurologic disorders
genetic testing
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hydrocephalus, normal pressure
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in situ hybridization
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inclusion bodies, intracytopasmic
incoordination
infection, recurrent
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
intrathecal medication
irritability
Jakob-Creutzfeldt disease
jaundice
jaw jerk, abnormal
Jewish
Kluver-Bucy syndrome
Krabbe's disease
language disorder in adults
learning disability, in children
Lewy body disease, diffuse
lipid storage disorder of CNS
liver disease
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
lysosomal storage disease
masked facies
memory
memory, defect of recent
memory, impairment of
memory, recent
metachromatic leukodystrophy
microaneurysm, retinal
mimics
misdiagnosis
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, serial
mucopolysaccharidoses
mutism
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neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
Niemann-Pick disease
nystagmus
obsessive-compulsive disorder
ophthalmoplegia
ophthalmoplegia, plus syndrome
optokinetic nystagmus, abnormal
palmomental response
paraparesis
paraphasias
paraplegia, in flexion
Parkinsonism syndrome
pathologic reflex
perseveration
personality change
Pick bodies
picking at skin
Pick's disease
pneumonia
polymerase chain reaction
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prognosis
progressive multifocal leucoencephalopathy
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progressive supranuclear palsy
psychiatric disorder
psychiatric problems in neurologic disorders
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psychosis
quadriplegia
rectal biopsy
Red flags
release phenomena
repetition, impaired
reversible neurologic disorder
review article
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roaming behavior
rooting reflex
safety
schizophrenia
seizure
seizure, intractable
seizure, intractable, treatment of
seizure, laughing as manifestation
seizure, surgical treatment of
seizure, treatment of
semantic dementia
sexual behavior, disorder of
short stature
shunt procedure, lumboperitoneal
shunt procedure, ventricular
single photon emission computed tomography
skin, biopsy
sleep pathology and physiology
snout reflex
somnolence
spasticity
speech disorder
speech, loss of
sphingomyelin
splenomegaly
spongy degeneration of brain
stem cell transplantation
stereotyped behavior
steroid therapy, CNS treatment and complications with
suck reflex
systemic illness
systemic lupus erythematosus
tachycardia
tangential
tau protein
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporal lobectomy
thrombocytopenia
treatment of neurologic disorder
upgaze, paralysis of
urinary incontinence
ventricular enlargement
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
workup
Showing articles 0 to 41 of 41

Clinicopathologic Conference, Normal Pressure Hydrocephalus
NEJM 384:1350-1358, Case 10-2021, 2021

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Inherited Metabolic Diseases of the Nervous System, Infantile Niemann-Pick Disease
Adams & Victors Principles of Neurology, Chp 37, pg 958, Ropper, A.H.,et al, 2014

Frontotemporal Dementia
BMJ 347:f4827, Warren, J.D.,et al, 2013

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Clinicopath Conf., Pick's Disease, Case 11-2000
NEJM 342:1110-1117, , 2000

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

A Case of Sporadic Pick Disease With Onset at 27 Years
Arch Neurol 56:1289-1291, Jacob,J.,et al, 1999

What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
Neurol 49:62-69, Litvan,I.,et al, 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Clinicopath Conf
Focal Cortical Dysplasia, Case 7-1996, NEJM 334:586-592996., , 1996

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

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

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

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

The Pathology and Nosology of Primary Progressive Aphasia
Neurol 44:2065-2072, Kertesz,A.,et al, 1994

Pick's Disease Versus Alzheimer's Disease:A Comparison of Clinical Characteristics
Neurol 43:289-292, Mendez,M.F.,et al, 1993

Niemann-Pick Disease Type C:Diagnosis and Outcome in Children, with Particular Reference to Liver disease
J Pediatr 123:242-247, Kelly,D.A.,et al, 1993

Neimann-Pick Disease Type C in a Middle-Aged Woman
Neurol 43:1435-1436, Lanska,D.J.&Lanska,M.J., 1993

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

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

The Diagnosis of Childhood Neurodegenerative Disorders Presenting as Dementia in Adults
Neurol 41:794-798, Coker,S.B., 1991

Pick's Disease:A Case Clinically Resembling Amyotrophic Lateral Sclerosis
Neurol 41:1831-1833, Sam,M.,et al, 1991

Adult Sphingomyelinase Deficiency:Report of 2 Patients who Initially Presented with Psychiatric Disorders
Neurol 40:132-136, Dubois,G.,et al, 1990

The Spectrum of Imaging and Neuropsychological Findings in Pick's Disease
Neurol 39:362-368, Knopman,D.S.,et al, 1989

Positron Emission Tomography & Histopathology in Pick's Disease
Neurol 37:439-445, Kamo,H.,et al, 1987

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

The Human Kluver-Bucy Syndrome
Neurol 33:1141-1145, Lilly,R.,et al, 1983

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

An Ultramicroscopic Study of Skin & Conjunctival Biopsies in Chronic Neuro. Disorders of Childhood
Ann Neurol 9:163-173, Arsenio-Nunes,M.L.,et al, 1981

Kluver-Bucy Syndrome in Pick disease:Clinical & patho-logic Correlations
Neurol 31:1415-1422, Cummings,J.L.,et al, 1981

Clinical Neuropathological Conference
(Ed) , Dis Ner Sys 34:124, 1973, Pick's Disease., Aronson,S.&Aronson,B., 1973

Niemann-Pick Disease
Correspondence NEJM 289:590, Dacremont,G.,et al, 1973

Progressive Paresis of Vertical Gaze in Lipid Storage Disease
Neurol 21:896, Grover,W., 1971



Showing articles 0 to 41 of 41