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Differential
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abdominal distention
acquired immunodeficiency syndrome
acute disseminated encephalomyelitis
adverse drug reaction
affective disorders
agitation
alcohol
alcoholic polyneuropathy
alcoholism
algorithm
amblyopia
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
anemia, hemolytic
anemia, iron deficiency
anemia, megaloblastic
anesthesia, general
angiitis, granulomatous of CNS
angiitis, isolated of CNS
ankle edema
anorexia
anticonvulsants, untoward effects of
antiendomysial antibodies
areflexia
arsenic
arterial dissection, precipitating events
arthralgia
ascending paralysis
ascites
ataxia
ataxia, cerebellar
ataxia, sensory
ataxic gait
athetosis
auditory evoked brainstem potentials
autoantibodies
autoimmune disease
autonomic dysfunction
autonomic neuropathy
B 12 deficiency
B 12 deficiency, infants
B 12 metabolism, defective
B12
B12 binding protein, abnormal
Babinski sign
bacterial infection
basal ganglia, lesion of
Behcet's syndrome
blepharospasm
blindness
blood dyscrasias, neurologic findings with
bone pain
brain atrophy
brain biopsy
brain fog
breast feeding
bruit, cranial
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
carbon monoxide poisoning
carotid artery disease
carotid artery stenosis
CAT scan
CAT scan, dementia
CAT scan, emission, abnormal
celiac disease, adult
central nervous system, infection of
central pontine myelinolysis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral ischemia
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, prevention of
cerebrovascular disease, risk factors in
cervical spine
cervical spine injury
cervical spondylosis
chemotherapy, CNS treatment and complications with
children
chorea
chorea, causes of
choreoathetosis
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
cognition
colchicine
collagen vascular disease
coma
complications
concentration, impaired
confusion
congestive heart failure
controversies in neurology
copper deficiency
corpus callosum
corpus callosum, lesion of
cortical blindness
C-reactive protein, elevated
delusion
dementia
dementia, clinical diagnosis
dementia, diagnostic evaluation of
dementia, differential diagnosis of
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, treatment of
demyelinating disease
dental procedure, neurologic complications with
depression
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes mellitus
diarrhea
diet
differential diagnosis
dilantin
dilantin, toxicity
disability, neurological
dissociated sensory loss
distal muscle weakness
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
drug induced neurologic disorders
dyspnea
dyspraxia
dysthyroidism
dystonia
dystonia, focal
ecchymoses
electrical sensation
electroencephalogram
electrophoretic pattern, serum
emotional lability
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
epidemiology of neurology
ergotism
evidence-based research
evoked potentials
failure to thrive
falling
fatigue
fine motor function, impaired
folic acid
folic acid deficiency
foot drop
F-wave response
gabapentin
gait disorder
gastrectomy, neurologic complications following
gastric biopsy
gastric partitioning
gastric surgery
gastritis
gastrointestinal disease, neurologic complications
genetic neurologic disorders
genetic testing
girdle sensation
gliadin antibodies
gliomatosis cerebri
glossitis
glucose level, serum
glucose tolerance test, abnormal
gluten sensitivity
gluten-free diet
hallucination
hallucination, auditory
hand numbness
hand weakness
hearing loss
helicobacter pylori
hemichorea
hemorrhagic diathesis
hepatosplenomegaly
heralding manifestation
herniated disc, cervical
hip flexor weakness
Hispanics
histamine-2 receptor blockers
HLA
homocysteine, serum
homocystinuria
human immunodeficiency virus type 1
human immunodeficiency virus type 1, asymptomatic
hyperbilirubinemia
hyperesthesia
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertensive encephalopathy
hypocalcemia
hypogonadism
hypomagnesemia
hypopigmentation of skin
hypoproteinemia
hypoprothrombinemia
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
inattention
incontinence, fecal
incoordination
infant, evaluation of
infantile tremor syndrome
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intestinal biopsy
intracerebral hemorrhage
inverted V sign
iron, serum, low
irritability
jaundice
laboratory values, normal
lactic dehydrogenase(LDH)
leg numbness
leg weakness, bilateral
leukoencephalopathy
leukoencephalopathy, differential diagnosis
Lhermitte's sign
limb shaking
limbic encephalitis
liver function enzymes
long bone lesion
low back pain
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malabsorption
malabsorption syndrome
memory, defect of recent
memory, impairment of
mental status, abnormal
metabolic disorder, primary
metformin
methylmalonic acid, serum
methylmalonic acidemia
methylmalonic aciduria
midbrain, lesion of
migraine
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
monoclonal gammopathy
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, high signal foci on
MRI, serial
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle weakness
myelitis, longitudinal
myeloma, osteosclerotic
myeloneuropathy
myelopathy
myelopathy, tract-specific
myelopathy, vacuolar
myoclonus
myopathy
nanging
neck trauma
neoplasm, primary of CNS
nerve conduction studies
neuritis
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, burden
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, etiologies of
neuropathy, hereditary peripheral
neuropathy, iatrogenic
neuropathy, medication induced
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neuropathy, toxic
neuropathy, work up for
neuropsychiatry
neurotoxic
neurotoxin
newborn, evaluation of
night sweats
nitrous oxide
normal
numbness, ascending
numbness, extremity
numbness, generalized
nutritional deficiency
nystagmus
obesity
old age, neurology of
optic atrophy
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, nutritional
organomegaly
orthostatic hypotension
pain
pain, abdominal
pain, back
pain, leg
pain, neuropathic
pancytopenia
papilledema
paranoia
paraparesis
paraparesis, spastic
paraplegia
paresthesias
paresthesias, feet
paresthesias, generalized
paresthesias, hands
Parkinson disease
pellagra
peripheral blood smear
peripheral blood smear, abnormal
pernicious anemia
personality change
phenothiazine, dyskinesia associated with
phenylketonuria
plasma R binder deficiency
plasmacytoma
POEMS syndrome
polyneuropathy
polyradiculoneuropathy
position sensation, abnormal
posterior column disease
posterior leukoencephalopathy syndrome
posterior tibial nerve
posterior tibial nerve compression
practice guidelines
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
proton pump inhibitors
pseudoathetosis
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychosis, acute
psychotic behavior
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyridoxine deficiency
quadriparesis
radiation therapy, CNS treatment and complications with
Red flags
regional enteritis
remote effect of cancer on the nervous system
retinal hemorrhages
reversible neurologic disorder
review article
risk factors
Romberg's sign
sarcoidosis
sarcoidosis, CNS
sclerosis, bone
scotoma
scotoma, central
screening
seizure
sensory level
sensory loss
sensory loss, cutaneous
sensory loss, glove-stocking
shaking
sickle cell disease
skin, biopsy
skin, darkening of
skin, discoloration
skin, lesions in neurologic disorders
somatosensory evoked potentials
spasticity
speech, pressured
spinal cord
spinal cord, cervical
spinal cord, lesion of
splenomegaly
sprue
steatorrhea
substantia nigra
swayback
symmetric brain lesions
syncope
systemic illness
tachycardia
tangential
tarsal tunnel syndrome
tetany
thiamine
thiamine deficiency
thrombocytosis
thyroid function tests
thyroiditis
thyrotoxicosis
tongue, smooth
tongue, swelling
transcobalamin II, abnormal
transcobalamin II, hereditary absence of
transglutaminase antibodies
treatment of neurologic disorder
tremor
tremor, leg
tremor, orthostatic
ulcerative colitis
urinary incontinence
urine, dark
vascular endothelial growth factor
vasculitides
vasculopathy
vegetarianism
Venereal Disease Research Laboratory test
vertigo
vibratory sensation, abnormal
visual evoked response
visual loss
visual loss, slow
vitamin D deficiency
vitamin deficiency
vitamin supplementation
vitamin therapy
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
Wernicke's encephalopathy
Whipple's disease
white hair
white matter disease
wide based gait
word-finding difficulty
workup
writing
Showing articles 450 to 500 of 803 << Previous Next >>

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000

Ischemic Core and Penumbra in Human Stroke
Stroke 30:93-99, Kaufmann,A.M.,et al, 1999

Long-Term Evaluation of Bilateral Fetal Nigral Transplantation in Parkinson Disease
Arch Neurol 56:179-187, Hauser,R.A.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Globus Pallidus Deep Brain Stimulation for Generalized Dystonia:Clinical and PET Investigation
Neurol 53:871-874, Kumar,R.,et al, 1999

Nuclear Medicine in Neurology and Psychiatry
Lancet 354:1107-1111, Costa,D.C.,et al, 1999

Diagnosis and Treatment of Wilson's Disease
Semin Neurol 19:261-270, Brewer,G.J.,et al, 1999

Cerebral Injury After Cardiac Surgery,Identification of a Group of Extraordinary Risk
Stroke 30:514-522, Wolman,R.L.,et al, 1999

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

The Human Genome Project,Application in the Diagnosis and Treatment of Neurologic Diseases
Arch Neurol 55:1287-1290, Evans,G.A., 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

PET with 18 Fluorodeoxyglucose and Hexamethylpropylene Amine Oxime SPECT in Late Whiplash Syndrome
Neurol 51:345-350, 3361998., Bicik,I.,et al, 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

Cerebral Manifestation of Wilson's Disease Successfully Treated with Liver Transplantation
Neurol 51:863-865, Bax,R.T.,et al, 1998

Limbic Encephalitis:Comparison of FDG PET and MR Imaging Findings
AJR 170:1659-1660, Provenzale,J.M.,et al, 1998

Hypothalamic Activation in Cluster Headache Attacks
Lancet 352:275-278, 2531998., May,A.,et al, 1998

Permanent Cortical Damage Detected by Flumazenil Positron Emission Tomography in Acute Stroke
Stroke 29:454-461, Heiss,W.,et al, 1998

Imaging the Brain, Part 1 & 2
NEJM 338:812-820, 889-8961998., Gilman,S., 1998

Wobbly Handwriting
Lancet 351:336, Rosario,M.A.F.,et al, 1998

Parkinson's Disease
NEJM 339:1044-1053,1130-1143, Lang,A.E.&Lozano,A.M., 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Characterizing the Target of Acute Stroke Therapy
Stroke 28:866-872, Fisher,M., 1997

Atypical MRI Features of Wilson's Disease:High Signal in Globus Pallidus on T1-Weighted Images
Neuroradiology 39:171-174, Mochizuki,H.,et al, 1997

Sympathetic Cardioneuropathy in Dysautonomias
NEJM 336:696-702, 7211997., Goldstein,D.S.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Measurement of Acetylcholinesterase by PET in the Brains of Healthy Controls & Pts with Alzheimer's Disease
Lancet 349:1805-1809, Iyo,M.,et al, 1997

Genetic Testing of Children at Risk for Huntington's Disease
Neurol 49:1048-1053, Nance,M.A.,et al, 1997

Genetic Testing for Alzheimer Disease, Practical and Ethical Issues
Arch Neurol 54:1226-1229, Roses,A.D., 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
JAMA 277:832-836, Post,S.G.,et al, 1997

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Acute Phenytoin Toxicity Followed by Seizure Breakthrough From a Ticlopidine-Phenytoin Interaction
Arch Neurol 53:1191-1192, Privitera,M.&Welty,T.E., 1996

Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
J Pediatr 128:770-775, Levy,H.L.,et al, 1996

Preclinical Evidence of Alzheimer's Disease in Persons Homozygous for the e4Allele for Apolipoprotein E
NEJM 334:752-758, 7911996., Reiman,E.M.,et al, 1996

Ticlopidine Impairs Phenytoin Clearance:A Case Report
Neurol 46:1172-1173, Riva,R.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Treatment of Wilson Disease with Ammonium Tetrathiomolybdate
Arch Neurol 53:1017-1025, Brewer,G.J.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Neuroimaging Findings in Patients with AIDS
Clin Inf Dis 22:906-919, Walot,I.,et al, 1996

Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease
Ann Neurol 39:132-136, Furtado,S.,et al, 1996

Wilson Disease:Findings at MR Imaging and CT of the Brain with Clinical Correlation
Radiology 198:531-536, van Wassenaer-van Hall,H.N.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
Neurol 46:527-531, Brandt,J.,et al, 1996

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

Spontaneous Neurological Recovery After Stroke and the Fate of the Ischemic Penumbra
Ann Neurol 40:216-226, Furlan,M.,et al, 1996

Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
Arch Neurol 53:493-497, Zappacosta,B.,et al, 1996

Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996



Showing articles 450 to 500 of 803 << Previous Next >>