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acquired immunodeficiency syndrome
activated protein C resistance
activities of daily living
activities of daily living scale
addiction, heroin
adrenoleukodystrophy
alcohol
Alexanders disease
algorithm
Alzheimer's disease
amphotericin B
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
ANA
anomic aphasia
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
aphasia
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
apolipoprotein E
apraxia
arthritis
ascites
aspiration
aspirin
ataxia
ataxia, cerebellar
ataxia, progressive
athetosis
attention span
behavioral disorder
Behcet's syndrome
blepharospasm
blindness
blood dyscrasias, neurologic findings with
bone marrow biopsy
bone marrow transplantation
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
bruxism
bulimia
calculations
callosal angle
carbenoxolone
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
carphology
CAT scan
CAT scan, abnormal
CAT scan, delta sign, empty
CAT scan, dementia
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, venography
cataplexy
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebral infarction
cerebral ischemia
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid, drainage of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, cost of
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease, risk factors in
cerebrovascular disease, treatment of
cherry red spot
chewing movements
children
chloroquine
cholestasis
cholesterol
cholesterol, HDL
chorea
choreoathetosis
chromosome 18
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
clofibrate
coagulopathy
cognition
cognition, slowed
complications
comprehension, impaired
compulsivity
confusion
conjunctival biopsy
controversies in neurology
cornea, abnormal
cornea, opacity of
cortical dysplasia, focal
cortical-basal ganglionic degeneration
cost effectiveness
craniectomy, decompressive
cultured skin fibroblasts
D-dimer
decision aids
decision analysis
degenerative diseases of CNS
dementia
dementia, childhood
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, reversible
depression
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
dipyridamole
disseminated intravascular coagulation(DIC)
diuretic
drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dysmorphic
dysphagia
dystonia
ecchymoses
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electron microscopy
embolism, platelet
emotional lability
encephalopathy
endovascular therapy
enolase
enzyme treatment
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
evidence-based research
executive dysfunction
eye movement, disorders of
facial appearance, abnormal
Factor V Leiden
falling
false negative
familial
fever
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
fluency
foam cells
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gadolinium
gait disorder
gait, magnetic
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glabellar sign
glycogen storage disease
grasp reflex
head injury
head injury, pediatric
headache
headache, persistent
headache, severe
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatic failure
hepatitis
hepatomegaly
hepatosplenomegaly
herpes simplex encephalitis
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hypercholesterolemia
hypertension
hypokalemia
hypotonia
hypoxic encephalopathy
imbalance
immunosuppression
immunosuppressive agents
impulsivity
in situ hybridization
inappropriate behavior
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
infantile hemiplegia
infection, recurrent
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
interobserver agreement
intracranial hypertension, benign
intracranial pressure, increased
intrathecal medication
ipecac
irritability
Jakob-Creutzfeldt disease
jaundice
jaw jerk, abnormal
Jewish
Kluver-Bucy syndrome
Krabbe's disease
language disorder in adults
learning disability, in children
leukemia
leukemia, neurologic findings assoc.with
level of consciousness, decreased
Lewy body disease, diffuse
lipid lowering agent
lipid storage disorder of CNS
lipids
liquorice
liver disease
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
lupus anticoagulant
lysosomal storage disease
masked facies
memory
memory, defect of recent
memory, impairment of
memory, recent
meningitis
metachromatic leukodystrophy
microaneurysm, retinal
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
mimics
misdiagnosis
Montreal cognitive assessment
mood change
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, false negative
MRI, negative
MRI, serial
MRI, venography
mucopolysaccharidoses
muscle pain
muscle swelling
muscle tenderness
muscle weakness
muscle weakness, causes of
mutism
myeloproliferative disorder
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, drug-induced
myopathy, hypokalemic
myopathy, proximal
myopathy, steroid induced
nausea and vomiting
neuroaxonal dystrophy
neurofibrillary degeneration
neuroleptic
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
Niemann-Pick disease
nonsteroidal anti-inflammatory drug
nystagmus
obsessive-compulsive disorder
ophthalmoplegia
ophthalmoplegia, plus syndrome
optokinetic nystagmus, abnormal
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
palmomental response
paraparesis
paraphasias
paraplegia, in flexion
Parkinsonism syndrome
paroxysmal nocturnal hemoglobinuria
pathologic reflex
perhexiline maleate
perseveration
personality change
Pick bodies
picking at skin
Pick's disease
pitfalls
plasminogen deficiency
platelet inhibiting drugs
pneumonia
polycythemia, primary
polymerase chain reaction
practice guidelines
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prethrombotic state
primary thrombocythemia
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
protein C deficiency
protein S deficiency
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pulmonary embolism
quadriplegia
rectal biopsy
Red flags
release phenomena
repetition, impaired
reversible neurologic disorder
review article
rhabdomyolysis
risk factors
roaming behavior
rooting reflex
S-100 protein
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
sickle cell disease
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
steroid therapy, CNS treatment and complications with
straight sinus
suck reflex
sulfinpyrazone
superior sagittal sinus thrombosis
systemic illness
systemic lupus erythematosus
tachycardia
tangential
tau protein
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporal lobectomy
thrombocytopenia
thrombophlebitis
tissue plasminogen activator, intravenous
transient ischemic attack
transient ischemic attack, treatment of
treatment of neurologic disorder
triglycerides
upgaze, paralysis of
urinary incontinence
ventricular enlargement
vincristine neurotoxicity
walking, difficulty with
wheelchair
white matter disease
word-finding difficulty
workup
Showing articles 0 to 50 of 67 Next >>

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

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

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

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Protein S Deficiency in HIV Associated Ischaemic Stroke:An Epiphenomenon of HIV Infection
JNNP 76:1455-1456,1331, Mochan,A.,et al, 2005

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

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

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

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

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

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

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

Serum S-100 and Neuron-Specific Enolase for Prediction of Regaining Consciousness After Global Cerebral Ischemia
Stroke 29:2363-2366, Martens,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Risk of Cerebral Sinus Thrombosis in Oral Contraceptive Users Who Are Carriers of Hered Prothrombotic Cond
BMJ 316:589-592, deBruijn,S.F.T.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

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

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,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

Cerebral Venous Thrombosis in Adults:A Study of 40 Cases From Saudi Arabia
Stroke 26:1193-1195, Daif,A.,et al, 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

Prothrombotic States in Young People with Idiopathic Stroke:Prospective Study
Stroke 25:287-290, Baringarrementeria,F., 1994

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

Ischemic Stroke Due to Deficiency of Coagulation Inhibitors, Report of 10 Young Adults
Stroke 24:19-25, Martinez,H.R.,et al, 1993

Free Protein S Deficiency in Acute Ischemic Stroke, A Case-Control Study
Stroke 24:224-227, Mayer,S.A.,et al, 1993

An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
Stroke 24:603-605, Rich,C.,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

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

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

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

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

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

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

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990



Showing articles 0 to 50 of 67 Next >>