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Differential
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aceruloplasminemia
Addison's disease
adverse drug reaction
alcohol, neurologic complications with
alcoholism
aminoacidurias
amyloidosis
anemia
ankle edema
anticonvulsants
anticonvulsants, untoward effects of
Arnold Chiari malformation
ascites
ataxia
ataxia telangiectasia
ataxia, sensory
autism
B 12 deficiency
Babinski sign
basilar artery occlusion
blindness
blindness, nutritional
blood dyscrasias, neurologic findings with
brainstem, lesion of
burning feet
carcinoma
carcinoma of pancreas
CAT scan, abnormal
cataracts
ceftriaxone
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
ceruloplasmin, serum
checklists
child abuse
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
coma
complications
confusion
copper
copper deficiency
copper metabolism, abnormal
corpus callosum
corpus callosum, lesion of
Cushing's syndrome
deep gray nuclei
dementia
dental prostheses
denture cream
depression
diabetes mellitus
diabetic coma, diagnosis and treatment
diet
differential diagnosis
disability, neurological
disorientation
dissociated sensory loss
diuretic
drooling
dysarthria
dysdiadochokinesia
dystonia
eating disorder
edema, pedal
electrolyte imbalance
encephalitis
encephalitis, viral
encephalopathy
esophageal varices
Fabry's disease
facial expression abnormality
falling
familial
ferritin, elevated
ferritinemia
foot numbness
fracture, long bone
Friedreich's ataxia
gait disorder
gastrectomy, neurologic complications following
gastric partitioning
gene
gene mutation
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
glioma
Google
handwriting
head injury
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hyperadrenalism
hyperparathyroidism
hyperreflexia
hyperthyroidism
hypoalbuminemia
hypochloremia
hypoglycemia
hypokalemia
hyponatremia
hypoparathyroidism
hypotension, systemic
hypothyroidism
iatrogenic neurologic disorders
imbalance
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
infant, evaluation of
intellectual deficit
intellectual deterioration
internet
iron, brain
iron, serum, low
Jakob-Creutzfeldt disease
jaundice
Kayser-Fleischer ring
Leigh's disease
leukopenia
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
liver function enzymes
long bone lesion
lymphoma involving CNS
malabsorption
malabsorption syndrome
Marinesco-Sjogren syndrome
mental retardation
mental status, abnormal
metabolic disorder, primary
metachromatic leukodystrophy
mimics
misdiagnosis
molecular genetics
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, gradient-echo
MRI, negative
MRI, paramagnetic effect
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
multiple sclerosis
multiple sclerosis, cognitive presenttion
myelitis, longitudinal
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myopathy
nausea and vomiting
neoplasm, intracranial
neoplasm, primary of CNS
nerve conduction studies
neuritis, causes of
neuroendocrinology
neurologic complications of, burns
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic signs
NeurologicDx
neuropathology
neuropathy
neuropsychiatry
neutropenia
numbness, extremity
nutritional deficiency
obesity
optic atrophy
optic neuropathy
optic neuropathy, nutritional
osmotic demyelination syndrome
pain, abdominal
pancytopenia
paranoia
paresthesias
paresthesias, generalized
penicillamine
pernicious anemia
personality change
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
polyneuropathy
polyradiculoneuropathy
pons, lesion of
porphyria
posterior column disease
postural abnormality
pregnancy, neurologic complications in
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
psychiatric disorder
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, cause of
quadriplegia
remote effect of cancer on the nervous system
renal stones
retinopathy
retroperitoneal hemorrhage
review article
rib fracture
rigidity
risk factors
Romberg's sign
seizure
selective eating
sensory loss
skull bone, thickening
slit lamp examination
small-bowel bypass
sodium valproate
somatosensory evoked potentials
spinal cord, cervical
spinal cord, lesion of
spinocerebellar degeneration
splenomegaly
subdural hematoma
swayback
symmetric brain lesions
syphilis, neurologic complications with
systemic lupus erythematosus
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiazide diuretic
thrombocytopenia
treatment of neurologic disorder
tremor
trichopoliodystrophy
trientine dihydrochloride
unconsciousness
urinary incontinence
visual loss
visual loss, progressive
vitamin A deficiency
vitamin deficiency
vitamin supplementation
vitamin, multiple
Von Hippel Lindau
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
zinc
Showing articles 500 to 550 of 1340 << Previous Next >>

Chromosome 20 Ring:A Chromosomal Disorder Associated with a Particular Electroclinical Pattern
Epilepsia 39:942-951, Canevini,M.P.,et al, 1998

Chronic Traumatic Brain Injury in Professional Soccer Players
Neurol 51:791-796, Matser,J.T.,et al, 1998

Alcohol-Related Acute Axonal Polyneuropathy,A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol 55:1329-1334, Wohrle,J.C.,et al, 1998

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

Prothrombotic Disorders in Infants and Children with Cerebral Thromboembolism
Arch Neurol 55:1539-1543, deVeber,G.,et al, 1998

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Methylphenidate in Early Poststroke Recovery:A Double-Blind, Placebo-Controlled Study
Arch Phys Med Rehabil 79:1047-1050, Grade,C.,et al, 1998

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

Leukotriene C4-synthesis Deficiency:A New Inborn Error of Metabolism Linked to a Fatal Developmental Syndrome
Lancet 352:1514-1517,1487, Mayatepek,E.&Flock.B., 1998

Neuroimaging Findings in Late Infantile GM1 Gangliosidosis
AJNR 19:1628-1630, Chen,C-Y.,et al, 1998

Binocular Vertical Diplopia
Mayo Clin Proc 73:55-66, Brazis,P.W.&Lee,A.G., 1998

Gastorintestinal Manifestations of Scleroderma
Gastroenterol Clin 27:563-594, Rose,S.,et al, 1998

Antiepileptics and Blood Dyscrasias: A Cohort Study
Pharmacotherapy 18:1277-1283, Blackburn,S.C.F.,et al, 1998

Usefulness of CT and MR Imaging in the Diagnosis of Acute Wernickes Encephalopathy
AJR 171:1131-1137, Antunez, E.,et al, 1998

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Wernicke's Encephalopathy:An Excitotoxicity Hypothesis
Metabolic Brain Disease 12:183-192, McEntee,W.J., 1997

Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997

Coma From Long-Term Overingestion of Isoniazid
Arch Int Med 157:2518-2520, Salkind,A.R.&Hewitt,C.C., 1997

Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Association of Tuberous Sclerosis of Temporal Lobes with Autism and Atypical Autism
Lancet 349:392-395, Bolton,P.F.&Griffiths,P.D., 1997

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Evaluation of Neurologic Function in Gulf War Veterans:A Blinded Case-Control Study
JAMA 227:223-230, 2591997., Haley,R.W.,et al, 1997

Muscle-Eye-Brain Disease:A Neuropathological Study
Ann Neurol 41:173-180, Haltia,M.,et al, 1997

Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997

The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997

Clinical Course of a Cohort in the Cuban Epidemic Optic and Peripheral Neuropathy
Neurol 48:19-22, Mojon,D.S.,et al, 1997

Occupational Exposures to Metals as Risk Factors for Parkinson's Disease
Neurol 48:650-658, Gorell,J.M.,et al, 1997

CT and MR Findings of Neuroacanthocytosis
J Comput Assist Tomogr 21:221-222, Okamoto,K.,et al, 1997

Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997

Cognitive Function and Academic Performance in Neurofibromatosis 1:North
K. N. , et al, Neurol 48:1121-11277., , 1997

Long-Term Cognitive Impairment Associated with Caudate Stroke
Stroke 28:970-975, Bokura,H.&Robinson,R.G., 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

Serial Neuropsychological Assess & Magnetic Resonance Imagingf Analysis in Multiple Sclerosis
Arch Neurol 54:1018-1025, Hohol,M.J.,et al, 1997

Prevalence and Severity of Cognitive Impairment with and without Dementia in an Elderly Population
Lancet 349:1793-1796, Graham,J.E.,et al, 1997

A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997

Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997

Clinical Features of Perineuritis
Muscle & Nerve 20:1153-1157997., Sorenson,E.J.,et al, 1997

A Longitudinal Magnetic Resonance Imaging Study of Brain Changes in Adolescents with Anorexia Nervosa
Arch Pediatr Adolesc Med 151:793-797, Katzman,D.K.,et al, 1997

The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
Ann Neurol 42:360-364, Claes,S.,et al, 1997

Severe Hypoglycaemia and Cognitive Impairment in Diabetes
BMJ 313:767-768, Deary,I.J., 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
JAMA 276:1805-1810, 18431996., Schendel,D.E.,et al, 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Whipple Disease Confined to the Central Nervous System in Childhood
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 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



Showing articles 500 to 550 of 1340 << Previous Next >>