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Differential
(Click to cross reference)
agitation
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, inflammatory type
anemia
angina pectoris
angiography, neurologic complications with
angioneurotic edema
ankle edema
anticholinergic drugs
anticholinergic drugs, side effects of
anticoagulant, complications of
aphasia
aphasia, global
areflexia
arrhythmia, cardiac
arsenic
arthralgia
ascending paralysis
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
atherosclerosis, generalized
autism
autonomic dysfunction
bacterial infection
bacterial infection, CNS
BAL
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
behavioral disorder
bone marrow suppression
brain biopsy
BUN, elevated
Canavan's disease
cancer, cerebrovascular accident complicating patients with
carcinoma
carcinoma of lung
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
catatonia
catatonia, lethal
central nervous system, infection of
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, multiple
cherry red spot
chest pain
chest x-ray, abnormal
children
chromosomal abnormality
chromosome 6
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cocaine
coma
confusion
conjunctivitis
coronary artery bypass
cortical blindness
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
dementia
dementia, rapidly progressive
demyelinating disease
dermatitis
developmental milestones, loss of
developmental retardation
diarrhea
diet
disseminated intravascular coagulation(DIC)
distal muscle weakness
drug abuse
drug abuse, neurologic complications of
drug abuse, toxic screen In
drug induced neurologic disorders
drug withdrawal
dystonia
ecchymoses
edema, pedal
electrocardiogram, abnormal
electromyogram
embolism
embolism, atheromatous
embolism, cholesterol
embolism, retinal
emergencies, neurologic
encephalopathy
encephalopathy, acute
encephalopathy, neonatal
endocarditis
endocarditis, marantic
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
erythrocyte
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
failure to thrive
familial
fatigue
feeding disorder
femoral artery catheterization
fever
fibrin split products
filariasis
fingernails, abnormal
gait disorder
gangliosidosis GM1
gangliosidosis GM2
gangrene
gastroenteritis
gastrointestinal bleeding
gene
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
glycogen storage disease
gram negative rod
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hallucination
hand weakness
head lag
headache
headache, severe
heart murmur
heavy metal intoxication
helminthic infection of CNS
hematuria, gross
hematuria, microscopic
hemiplegia
hemoglobinuria
hepatitis
hepatosplenomegaly
hyperammonemic encephalopathy
hyperamylasemia
hyperbilirubinemia
hyperglycinemia
hyperkeratosis
hypertension
hyperthermia
hyponatremia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
inborn errors of metabolism
infection
intraaortic balloon pump
ischemic exercise test
lactic dehydrogenase(LDH)
Legionella pneumophilia
Legionnaires'disease
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, toxic
leukopenia
levamisole
lipid storage disorder of CNS
livedo reticularis
liver disease
liver function enzymes
Loa loa
loiasis
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
McArdle's disease
Mees lines
meningitis, aseptic
mental retardation
mental status, abnormal
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
microangiopathic hemolytic anemia
misdiagnosis
mitochondrial disease
mitral valve vegetation
molecular genetics
mortality
MRI
MRI, abnormal
MRI, demyelinating disease
MRI, diffusion weighted
MRI, false negative
multinucleated giant cell
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle weakness
myoclonic jerks
myoglobinuria
myopathy
nausea and vomiting
nerve conduction studies
neuritis, heavy metals causing
neuroleptic
neuroleptic malignant syndrome
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuropathy
neuropathy, peripheral
neuropathy, toxic
neurotransmitter
opisthotonus
optic atrophy
ornithine transcarbamylase deficiency
pain
pain, back
pain, flank
pancreatitis
pancytopenia
paraphasias
parasitic infection, CNS
paresthesias
paresthesias, feet
paresthesias, hands
PAS positive
pathology
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
personality change
petechiae
phenylketonuria
phosphorylase b kinase deficiency
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
polyneuropathy
position sensation, abnormal
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proprioception, abnormal
proteinuria
pruritus
psychomotor retardation
pulmonary infiltrates
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
renal failure
renal infarct
respiratory failure
review article
rhabdomyolysis
rigidity
risk factors
Sandhoff's disease
screaming
second wind phenomena
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
self-mutilation
semialdehyde dehydrogenase deficiency
serologic testing
serotonin syndrome
skin, biopsy
skin, lesions in neurologic disorders
spinal cord, infarction of
splenic infarcts
splinter hemorrhages
spongy degeneration of brain
stuporous
sweating
sweating, abnormality of
thrombocytopenia
treatment of neurologic disorder
tropical disease
urea-cycle enzymopathies
uremia
urinalysis, abnormal
urinary casts
urine test for metabolic disorders
urine test in toxic screen
urine, dark
urine, white blood cells in
vasculitides
weakness
weight loss
white matter disease
Showing articles 0 to 50 of 3460 Next >>

A Case of Acute Encephalopathy and Rigidity in a 30-Year-Old Man
Neurol 93:759-763, Hurtubise, B. & MacLellan, A., 2019

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

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

Utility of Urinalysis in Discriminating Cardioembolic Stroke Mechanism
Arch Neurol 64:667-670, Viehman,J.A.,et al, 2007

Neurological Findings in Aminoacylase 1 Deficiency
Neurol 68:2151-2153, Sass,J.O.,et al, 2007

Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria
Eur J Radiol Extra 54: 5-9, Teksam,M.,et al., 2005

Clinical Spectrum of Succinic Semialdehyde Dehydrogenase Deficiency
Neurol 60:1413-1417, Pearl,P.L.,et al, 2003

Clinicopath Conf, Infection with Loa loa
NEJM 346:115-122, Case 1-2002, 2002

Legionella Infection
emedicine.com, Mobeen,R., 2002

Clinicopath Conf,Cerebral Amyloid Angiogpathy and Giant-Cell Inflammatory Reaction to Beta 4-Amyloid and Vasculitis, Case 10-2000
NEJM 342:957-965, , 2000

Acute, Drug-Induced, Life-Threatening Neurological Syndromes
The Neurologist 4:196-210, Richard,I.H., 1998

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Clinicopath Conf
CA of Lung, DIC, Marantic Endocarditis, Multiple CVA's, Case 36-1991, NEJM 325:714-726., , 1991

Progressive Neuropathy & Recurrent Myoglobinuria in a Child with Long-chain 3-Hydroxyacylcoenzyme A Dehydrogenase Defic
J Pediatr 118:744-746, Dionisi,C.,et al, 1991

Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,et al, 1989

Screening for Inherited Metabolic Diseases in Adults with Neurological Disease
Lancet 1:1101, Wierzbicki,A.S.,et al, 1988

Cholesterol Crystal Embolization:A Review of 221 Cases in the English Literature
Angiology 38:769-784, Fine,M.J.,et al, 1987

Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
P. D. , et al, Muscle & Nerve 10:114-120, , 1987

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Possible Pathophysiology of Neurologic Abnormalities assoc. with Nonketotic hyperglycinemia
NEJM 294:1295, Ramson,B.R., 1976

Specificity of the Urine Inhibitor Test for Leigh's Disease
Neurol 24:885, Pincus,J.H.,et al, 1974

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Clinicopatholigical Conference, Plasmodium Falciparum Malaria
NEJM 309:549-556, Case 4-2024, 2024

A 54-Year-Old Woman with Progressive Headache and Neurologic Decline
Neurol 102:e209190, Cheng,Y. & Zachariah,J., 2024

Clinicopathologic Conference, Legionella Infection Complicated by Rhabdomyolysis
NEJM 391:1039-1048, Case 29-2024, 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

Clinicopathologic Conference, Infective Endocarditis Due to Haemophilus Parainfluenza
NEJM 391:2148-2157, Case 38-2024, 2024

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Posterior Reversible Encephalopathy Syndrome
NEJM 388:2171-2178, Geocadin,R.G., 2023

Sweet Syndrome
Stat Pearls www.ncbi.nlm.gov, Sept, Goyal,V.P. & Holmes,H, 2022

Spontaneous Escherichia Coli Meningitis and Brain Abscess in an Immunocompetent Adult
Cureus doi.10.7759/CUREUS.208728, Jeter,K.et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

Lenvatinib Therapy for Advanced Thyroid Cancer: Real-Life Data on Safety, Efficacy, and Some Rare Side Effects
JENDSO 6:1-7, Hamidi, S.,et al, 2022

A Case of Acute Akinetic Mutism and Encephalopathy
Neurol 99:761-766, Jain, V.,et al, 2022

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Clinicopathologic Conference, Lead Poisoning
NEJM 385:2378-2388, Case 38-2021, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Clinicopathologic Conference, Acute human immunodeficiency virus type 1
NEJM 385:641-648, Case 24-2021, 2021

Clinical Presentation, Diagnosis, and Treatment of Atrioesophageal Fistula Resulting From Atrial Fibrillation Ablation
J Cardiovasc Electrophysiol 32:2441-2450, Della Rocca,D.G.,et al, 2021

Bilateral Middle Cerebellar Peduncle Lesions:Neuroimaging Features and Differential Diagnoses
Brain Behav 10:e01778, Jiang,J.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

Clinicopathologic Conference, Borrelia Miyamotoi Infection
NEJM 383:1578-1586, Case 32-2020, 2020

Central Nervous System Involvement in Erdheim-Chester Disease
Neurol 95:e2746-e2754, Aubart,F.C.,et al, 2020

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019



Showing articles 0 to 50 of 3460 Next >>