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abdominal protrusion
abulia
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
agnosia
agnosia, visual
agraphia
akinetic mute
alexia
Alzheimer's disease
Alzheimer's disease, diagnosis of
Alzheimer's disease, visual variant
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anomic aphasia
antiviral agents
aphasia
aphasia, progressive, non-fluent
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
apraxia
apraxia, constructional
arthralgia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
attention span
automobile accidents
axonal spheroid
azidodeoxythymidine
B 12 deficiency
B12
behavioral disorder
binge eating
biologic markers
bone biopsy
bone pain
bone scanning
bradyphrenia
brain atrophy
brain biopsy
bruxism
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CD4 counts
central nervous system, infection of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar tonsils
cerebellum, disease of
cerebral cortical atrophy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, pressure low
cerebrovascular accident
cerebrovascular disease
Charles Bonnet's syndrome
children
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cognition
compulsivity
concentration, impaired
confusion
controversies in neurology
corpus callosum
corpus callosum, atrophy of
corpus callosum, lesion of
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
crying, pathologic
cryptococcal meningitis
cytomegalovirus infection
degenerative diseases of CNS
delirium
delusion
dementia
dementia, age at onset
dementia, clinical diagnosis
dementia, diagnostic classification
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, subcortical
dementia, treatment of
demyelinating disease
depression
diagnostic criteria
differential diagnosis
difficulty climbing stairs
disinhibition-dementia-parkinsonism-amyotrophic complex
drug withdrawal
dysarthria
dysmetria
dyspraxia
eating disorder
electroencephalogram, abnormalities of
electromyogram
emotional lability
encephalitis
encephalitis, human immunodeficiency virus type 1
encephalopathy
encephalopathy, metabolic
epidemiology of neurology
executive dysfunction
facial nerve palsy
falling
familial
fatigue
fever
fibrillations
finger nose finger test
flail arm syndrome
fluency
foot drop
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, lesion of
frontal lobe, pathologic signs of
frontotemporal brain sagging syndrome
frontotemporal dementia, behavioral variant
gait disorder
gait, apraxic
gait, waddling
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
genu of corpus callosum
glabellar sign
grasp reflex
Guillain Barre syndrome
hallucination
hallucination, visual
hallucination, visual, benign
headache
headache, chronic
hemianopia, homonymous
herpes simplex virus
herpes virus infection
herpes zoster
highly active antiretroviral therapy
hip flexor weakness
hippocampus
HIV CSF viral escape syndrome
human immunodeficiency virus type 1
Huntington's chorea
hypergraphia
hyperreflexia
hypersomnia
imbalance
imbalance, postural
impulsivity
inappropriate behavior
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
inclusion bodies, ubiquitin
inflexibility, mental
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
interpeduncular cistern, compressed
intracerebral hemorrhage
irritability
Jakob-Creutzfeldt disease
jaw jerk, abnormal
judgement, impaired
Kluver-Bucy syndrome
language disorder in adults
laughing, pathologic
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
Lewy body disease, diffuse
life expectancy
lobar atrophy
logopenia
loss of sympathy
lymphoma
lymphoma involving CNS
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, chronic
mental status, abnormal
mesial temporal sclerosis
midbrain, swollen
migraine
mimics
misdiagnosis
mononeuropathy
mononeuropathy multiplex
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, functional
MRI, serial
MRS
multinucleated giant cell
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
mutism
myelopathy
myelopathy, vacuolar
myopathy
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
neoplasm, primary intracerebral
neoplasm, primary of CNS
neuroaxonal leukodystrophy
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
nutritional deficiency
nystagmus
obsessive-compulsive disorder
ophthalmoplegia
ophthalmoplegia, total
opportunistic infection
opportunistic infection, CNS
Paget's disease
pain, increased response
pallido-ponto-nigral degeneration
palmomental response
paranoia
paraparesis
paraphasias
Parkinson disease
Parkinson disease, atypical
Parkinsonism syndrome
pathologic reflex
peduncular hallucinosis
perseveration
personality change
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
pons, flattened
posterior cortical atrophy
posterior leukoencephalopathy syndrome
prepontine cistern, effaced
primary intracranial hypotension
primary lateral sclerosis
prognosis
progranulin
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive subcortical gliosis
progressive supranuclear palsy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pyramidal tract dysfunction
radiculitis
rapidly progressing neurologic illness
Red flags
release phenomena
respiratory failure
respiratory tract infection
retrovirus
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
rigidity, axial
risk factors
rooting reflex
sagging of the brain
sclerosis, bone
seizure
semantic dementia
simultanagnosia
single photon emission computed tomography
single photon emission computed tomography, false negative
sleep pathology and physiology
snout reflex
speech disorder
splenium of corpus callosum
splenium of corpus callosum, displaced
stereotyped behavior
synucleinopathy
syphilis, diagnosis and treatment
systemic illness
tangential
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
tongue, atrophy
tonsillar herniation of cerebellum
toxoplasmosis, acquired
toxoplasmosis, CNS
trauma
treatment of neurologic disorder
tremor
ubiquitin
urinary incontinence
vegetarianism
viral infection
viral infection, CNS
viral load
visual field defect
visuospatial disturbance
vitamin deficiency
walking, difficulty with
wandering
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
Wingspan study
withdrawal, social
word-finding difficulty
writing
Showing articles 0 to 50 of 4261 Next >>

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

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

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

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

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

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinicopathologic Conference, Posterior Cortical Atrophy with Frontotemporal Lobe Dementia with Gene Mutation
JAMA Neurol 74:114-118, , 2017

Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
AJNR 37:774-781, Winton-Brown, T.T.,et al, 2016

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

Non-Alzheimers Dementia 1 Frontotemporal Dementia
Lancet 386:1672-1682, Bang, Jee.,et al, 2015

Degenerative Diseases of the Nervous System, Behavioral Variant FTLD
Adams & Victors Principles of Neurology, Chp 39, pg 1074, Ropper, A.H.,et al, 2014

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

Frontotemporal brain sagging syndrome
Neurol 76:1377-1382, Wicklund, M.R.,et al, 2011

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Rapidly Progressive Neurodegenerative Dementias
Arch Neurol 66:201-207, Josephs,K.A.,et al, 2009

Binge Eating is Associated With Right Orbitofrontal-Insular-Striatal Atrophy in Frontotemporal Dementia
Neurol 69:1424-1433, Woolley,J.D.,et al, 2007

A 34-Year-Old Man With Progressive Behavioral and Language Disturbance
Neurol 68:68-74, Miller,B.L.,et al, 2007

Frontotemporal Lobar Degeneration with Motor Neuron Disease
Arch Neurol 63:489-490, Clark,C.M. &Forman,M.S., 2006

CT and MR Imaging of Neuroaxonal Leukodystrophy Presenting as Early-Onset Frontal Dementia
AJNR 27:1037-1039, Mascalchi,M.,et al, 2006

Frontotemporal Dementia: Clinicopathological Correlations
Ann Neurol 59:952-962, Forman,M.S.,et al, 2006

Frontotemporal Lobar Degeneration
Arch Neurol 62:925-930, Johnson,J.K.,et al, 2005

Different Patterns of Magnetic Resonance Imaging Atrophy for Frontotemporal Lobar Degeneration Syndromes
Arch Neurol 62:1106-1110, Short,R.A.,et al, 2005

Most Cases of Dementia with Hippocampal Sclerosis May Represent Frontotemporal Dementia
Neurol 63:538-542, Hatanpaa,K.J.,et al, 2004

Spontaneous Intracranial Hypotension Causing Reversible Frontotemporal Dementia
Neurol 58:1285-1287, Hong,M.,et al, 2002

Utility of Clinical Criteria in Differentiating Frontotemporal Lobar Degeneration (FTLD) From AD
Neurol 58:1608-1615, Rosen,H.J.,et al, 2002

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

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

A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
JNNP 64:306-313, Talbot,P.R.,et al, 1998

Familial Aggregation in Frontotemporal Dementia
Neurol 50:1541-1545, Stevens,M.,et al, 1998

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

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Frontotemporal Dementia is on the MAP
Ann Neurol 41:139-140, Wilhelmsen,K.C., 1997

Alteration of White Matter MR Signal Intensity in Frontotemporal Dementia
AJNR 18:367-378, Kitagaki,H.,et al, 1997

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

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Frontotemporal Dementia and Early Alzheimer Disease:Differentiation with Frontal Lobe H-1 MR Spectroscopy
Radiology 203:829-836, Ernst,T.,et al, 1997

Midline Cerebral Morphometry Distinguishes Frontotemporal Dementia and Alzheimer's Disease
Neurol 48:978-985, Kaufer,D.I.,et al, 1997

Increased Writing Activity in Neurological Conditions:A Review and Clinical Study
JNNP 61:510-514, vanVugt,P.,et al, 1996

Frontal Lobe Degeneration:Clinical, Neuropsychologicaland SPECT Characteristics
Neurol 41:1374-1382, Miller,B.L.,et al, 1991

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

The Acquired Immunodeficiency Syndrome (AIDS) Dementia Complex
Ann Int Med 111:400-410, Ho,D.D.,et al, 1989

Neurologic Manifestations of AIDS
Medicine 66:407-437, McArthur,J.C., 1987



Showing articles 0 to 50 of 4261 Next >>