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Differential
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acetaminophen
aciduria
adverse drug reaction
agitation
alcohol, neurologic complications with
alcoholism
altered states of consciousness
ammonia
anasarca
anatomy of
anorexia nervosa
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, enzyme inducing
anticonvulsants, untoward effects of
arteriovenous malformation
arteriovenous malformation, cerebral
ascites
aspartate aminotransferase
asterixis
asterixis, causes of
asterixis, unilateral
ataxia
ataxia, progressive
ataxic gait
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
behavioral disorder, acute
Behcet's syndrome
blood gases, arterial
carbamazepine
carbamazepine, toxicity
carbamyl phosphate synthetase-I deficiency
carbon monoxide poisoning
carcinoma
carcinoma of pancreas
CAT scan
CAT scan, abnormal
central pontine myelinolysis
cerebellar hemorrhage
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral infarction
cerebral palsy
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, amonia
cerebrospinal fluid, glutamine
cerebrospinal fluid, pressure increased
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, recurrent
chemotherapy, CNS treatment and complications with
children
chorea
cingulate gyrus
cirrhosis
Clinical Pathologic Conference(C.P.C.)
coma
coma, episodic
coma, sudden onset
coma, unknown etiology
complications
confusion
confusional state, acute
congestive heart failure
corpus callosum, thinning
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
developmental retardation
dialysis
differential diagnosis
disorientation
downward deviation of eyes
drowsiness
drug interactions
drug overdose
dysphagia
dyspnea
dyspraxia
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
emphysema
encephalitis
encephalitis, Japanese
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
enzyme, defect
enzyme, induction
episodic neurologic deficits
Fahr disease
failure to thrive
familial
fatigue
feeding disorder
fever
flavivirus
flumazenil
gait disorder
gait, spastic
gastric partitioning
gene mutation
genetic neurologic disorders
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamine
grasp reflex
grimacing
growth retardation
gyrus, abnormal
headache
hepatic encephalopathy
hepatic encephalopathy, acute
hepatic encephalopathy, treatment of
hepatic failure
hepatic failure, acute
hepatitis B virus
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hyperalimentation
hyperammonemic encephalopathy
hyperbilirubinemia
hypercapnia
hyperglycemia
hyperphosphatasia
hypoalbuminemia
hypoglycemia
hyponatremia
hypothermia
hypothermia, causes of
hypoxia
hypoxic encephalopathy
iatrogenic neurologic disorders
ileal conduit urinary diversion
imbalance
immunosuppressive agents
inattention
inborn errors of metabolism
infection
influenza A virus
insular cortex
internal capsule
intracranial pressure monitoring
intracranial pressure, increased
Jakob-Creutzfeldt disease
jaundice
lactate
lactic acidemia
lactic dehydrogenase(LDH)
laminar necrosis, cortical
leg swelling
Leigh's disease
lenticular nucleus, lesion of, bilateral
lethargy
leukoencephalopathy
level of consciousness, decreased
liver biopsy
liver disease
liver function enzymes
liver transplantation
lung transplantation
lymphoma
malformation, vascular
malformation, vascular, cerebral
memory, impairment of
mental retardation
mental status, abnormal
metabolic acidosis
metabolic disorder, primary
methylmalonic acidemia
methylmalonic aciduria
misdiagnosis
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, FLAIR
MRI, high signal intensity of basal ganglia
MRI, T1 weighted high signal foci
MRS
multiple myeloma
myelopathy
myelopathy, hepatic
myoclonus
nausea and vomiting
nerve conduction studies
neurofibromatosis 1
neuroleptic
neurologic complications
neurologic complications of, chronic pulmonary disease
neurologic complications of, systemic disease
neuropathy
neurotoxin
nutritional deficiency
old age, neurology of
opisthotonus
optic atrophy
organ transplantation
ornithine transcarbamylase deficiency
osmotic demyelination syndrome
papilledema
paraparesis, spastic
Parkinsonism syndrome
polycythemia, secondary
portal caval shunt
postpartum
postpartum coma
pregnancy, neurologic complications in
premature infant
premature infant, problems in
prisoner
prognosis
progressive neurologic disorder
propionic aciduria
prothrombin time, prolonged
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
pyramidal tract
rapidly progressing neurologic illness
recurrent
renal replacement therapy
renal transplantation
respiratory failure
reversible neurologic disorder
review article
Reye's syndrome
Reye's syndrome, adult
risk factors
screaming
seizure
seizure, neonatal
serum alanine aminotransferase
serum glutamic oxaloacetic transaminase
shunt procedure, ventricular
sodium valproate
sodium valproate, toxicity
somnolence
spasticity
speech, slowed
status epilepticus
status epilepticus, intractable
stuporous
suck reflex
suicide
symmetric brain lesions
tacrolimus
thalamus, lesion of
thalamus, lesion of-bilateral
toe walking
topiramate
treatment of neurologic disorder
tremor
tremulousness
uncal herniation
unconsciousness
urea
urea-cycle enzymopathies
ureterosigmoidostomy
urinary retention
urinary tract infection
urine test for metabolic disorders
viral infection
viral infection, CNS
visual acuity, decreased
walking, difficulty with
weight loss
white matter disease
white matter disease, subcortical
zinc
Showing articles 0 to 50 of 734 Next >>

Clinicopathologic Conference, Noncirrhotic hyperammonemia after Roux-en-Y Gastric Bypass
NEJM 389:1221-1230, Case 30-2023, 2023

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Chemotherapy-Associated Hyperammonemic Encephalopathy
Neurol 94:e874-e877, Briard, J.N.,et al, 2020

Pathophysiology and Management of Hyperammonemia in Organ Transplant Patients
Am J Kidney Dis PMID:31040091, Seethapathy, H. & Fenves, A.Z., 2019

Idiopathic Hyperammonemia after Solid Organ Transplantation: Primarily a Lung Problem? A Single-Center Experience and Systematic Review
ClinTransplant 31:e12957, Krutsinger, D.,et al, 2017

Clinicopathologic Conference, Fulminant Liver Failure Associated with Hepatitis B Virus Infection
NEJM 375:163-171, Case 21-2016, 2016

A Young Man with Recurrent Coma and Refractory Status Epilepticus
JAMA Neurol 73:1243-1244, Sheikh, Z.,et al, 2016

A 27-Year Old Man with Rapidly Progressive Coma
Neurol 85:e74-e78, Wong,J.M.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Hepatic Stupor and Coma (Hepatic, or Portal-Systemic Encephalopathy)
Adams & Victors Principles of Neurology Chp 40, pg 1142, Ropper, A.H.,et al, 2014

Risk Factors of Hyperammonemia in Patients with Epilepsy Under Valproic Acid Therapy
Medicine 93:e66, Tseng, Y.L.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Inherited Hypeammonemia
Adams & Victors Principles of Neurology, Chp 37, pg 952, Ropper, A.H.,et al, 2014

Diffusion-Weighted Imaging in Acute Hyperammonemic Encephalopathy
Neurohosp 3:125-130, Rosario, M.,et al, 2013

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Hyperammonemic Encephalopathy
Neurol 78:600-601, Capizzano,A.A.,et al, 2012

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Acute Hepatic Encephalopathy: Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Findings, and Correlation With Plasma Ammonia Level and Clinical Outcome
AJNR 31:1471-1479, McKinney,A.M.,et al, 2010

Acute Hyperammonemic Encephalopathy in Adults: Imaging Findings
AJNR 32:413-418, U-King-Im,J.M.,et al, 2010

MRI Findings Associated With Acute Liver Failure
Neurol 72:2130-2131, Fridman,V.,et al, 2009

Mysteriod Episodic Coma
Lancet 371:2222, Ferenczi,E.,et al., 2008

MR Imaging Findings in Hepatic Encephalopathy
AJNR 29:1612-1621, Rovira,A.,et al, 2008

Brain MR Imaging in Acute Hyperammonemic Encephalopathy Arising from Late-Onset Ornithine Transcarbamylase Deficiency
AJNR 24:390-393, Takanashi,J-i.,et al, 2003

Acute Confusional State Following Liver Transplantation for Alcoholic Liver Disease
Neurol 59:601-605, Buis,C.I.,et al, 2002

Urinary Tract Infection and Coma
Lancet 360:996, De Jonghe,B.,et al, 2002

Hyperammonemic Encephalopathy in Multiple Myeloma
NEJM 346:1674-1675, Kwan,L.,et al, 2002

Coma in a Young Anorexic Woman
Lancet 357:1944, Blans,M.J.,et al, 2001

Acute Hepatic Encephalopathy with Diffuse Cortical Lesions
Neuroradiology 43:551-554, Arnold, S.M.,et al, 2001

Valproate-Induced Hyperammonemic Encephalopathy in the Presence of Topiramate
Neurol 54:230-232, Hamer,H.M.,et al, 2000

Clumsiness, Confusion, Coma, and Valproate
Lancet 353:1408, Ellaway,C.J.,et al, 1999

Hepatic Encephalopathy and Ascites
Lancet 350:1309-1315, Jalan,R.&Hayes,P.C., 1997

Treatment of Hepatic Encephalopathy
NEJM 337:473-479, Riordan,S.M.,et al, 1997

Valproic Acid-Induced Hyperammonemic Encephalopathy:MR Appearance
AJNR 15:1779-1781, Baganz,M.D.&Dross,P.E., 1994

Inborn Errors of Urea Synthesis
Ann Neurol 35:133-141, Batshaw,M.L., 1994

Postpartum Coma and Death Due to Carbamoyl-Phosphate Synthetase I Deficiency
Ann Int Med 120:216-217, Wong,L-J.C.,et al, 1994

Ornithine Transcarbamylase Deficiency Presenting with Strokelike Episodes
J Pediatrics 122:423-425, Christodoulou,J.,et al, 1993

Arginase Deficiency Presenting as Cerebral Palsy
Pediatrics 91:995-996, Scheuerle,A.E.,et al, 1993

MRI Pallidal Hyperintensity & Brain Atrophy in Cirrhotic Pts:2 Different MRI Patterns of Clin Deterior?
Neurol 43:2570-2573, Kulisevsky,J.,et al, 1993

Clinicopath Conf
Hepatic Encephalopathy in a 40-Year-Old Woman, Am J Med 90:374-3801991., , 1991

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus
NEJM 322:1652-1669, Arn,P.H.,et al, 1990

Hyperammonemic Encephalopathy in Urinary Diversion with Urea-Splitting Urinary Tract Infection
Arch Int Med 150:2389-2392, Kaveggia,F.F.,et al, 1990

Episodic Confusion and Tremor Associated with Extrahepatic Portacaval Shunting in Cirrhotic Liver Disease
Neurol 39:403-405, Russell,D.M.,et al, 1989

Reye's Syndrome in Adults, Diagnostic Considerations
Arch Int Med 147:61-64, Meythaler,J.M.&Varma,R.R., 1987

Hepatic Encephalopathy
NEJM 313:865-873, Fraser,C.L.&Arieff,A.I., 1985

Hyperammonemic Encephalopathy Due to Essential Amino Acid Hyperalimentation
Arch Int Med 144:2278-2279, Grazer,R.E.,et al, 1984

Hyperammonemic Encephalopathy Related to Ureterosigmoidostomy
Arch Neurol 41:1211-1212, Edwards,R.H., 1984

Neurologic Outcome in Children with Inborn Errors of Urea Synthesis
NEJM 310:1500-1505, Msall,M.,et al, 1984

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

Detection of Urea Cycle Enzymopathies in Childhood
Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984

Clinical Features of Carbamyl Phosphate Synthetase-I Deficiency in an Adult
Ann Neurol 16:90-93, Call,G.,et al, 1984



Showing articles 0 to 50 of 734 Next >>