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abdominal distention

acyl CoA dehydrogenase deficiency

addiction, heroin

adverse drug reaction

alcohol intoxication

alcoholic withdrawal states, DT's, convulsions, etc.

alkalosis, respiratory

aminoacidopathies

anesthesia, general

anorexia nervosa

antibiotics, neurologic complications with

arrhythmia, cardiac

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

autonomic dysfunction

B 12 deficiency

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

biotin deficiency

biotin deficiency, juvenile form

biotinidase deficiency

blindness, sudden

buried bumper syndrome

calcification, intracranial

carbonic anhydrase II deficiency

carnitine deficiency

carnitine deficiency myopathy

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, false negative

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebral cortex

cerebral cortical atrophy

cerebral infarction

cerebral palsy, risk factors

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, nonvascular territory

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coenzyme Q10 deficiency

coma, sudden onset

compartment syndrome

compartment syndrome, abdominal

compression fracture

conjunctival biopsy

cornea, abnormal

cortical blindness

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

dementia, rapidly progressive

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes dialysis basal ganglia syndrome

diabetes mellitus

diabetes mellitus, neurologic manifestations of

differential diagnosis

disability, neurological

disseminated intravascular coagulation(DIC)

D-lactate acidosis

downward deviation of eyes

drug abuse, toxic screen In

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electron microscopy

emotional lability

encephalitis, viral

encephalomyopathy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis, marantic

episodic neurologic deficits

ethylene glycol

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

eye movement, disorders of

facial asymmetry

facial weakness

failure to thrive

fingerprint bodies

fracture, pathologic

gastrointestinal bleeding

gastrostomy, percutaneous endoscopic

genetic counselling

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

growth retardation

hallucination, auditory

headache, severe

hemianopia, transient

hemiparesis, transient

hemorrhagic diathesis

hemorrhagic shock encephalopathy syndrome

hepatic failure

heralding manifestation

herniated disc, differential diagnosis of

herpes simplex encephalitis

histochemistry of muscle

hyperammonemic encephalopathy

hyperbilirubinemia

hypercoagulable state

hyperhomocysteinemia

hypersegmented polys

hypoxia, newborn

iatrogenic neurologic disorders

ileus, paralytic

immunofluorescence

inborn errors of metabolism

inclusion bodies

intellectual deficit

intellectual deterioration

internal capsule

intracranial pressure, increased

intravenous drug abuse

isopropyl alcohol

Kearns-Sayre syndrome

keratoconjunctivitis

lactic acidemia

lactic dehydrogenase(LDH)

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lentiform fork sign

level of consciousness, decreased

level of consciousness, decreased acute

lipid storage myopathy

liver function enzymes

Lowe's syndrome

lysosomal storage disease

malignant hyperpyrexia

marche a petits pas

memory, impairment of

meningitis, aseptic

mental retardation

mental status, abnormal

mental status, abnormal, acute

metabolic acidosis

metabolic disorder, primary

methylmalonic acid, serum

methylmalonic acidemia

methylmalonic aciduria

microangiopathic hemolytic anemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, susceptibility weighted

multiple organ failure

multiple sclerosis, differential diagnosis of

muscle relaxant

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myoclonus, epilepsy

myopathy, mitochondrial

myopathy, proximal

myotonia congenita

myotonia, treatment of

nausea and vomiting

neonatal epileptic encephalopathy

nephrotic syndrome

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular blockade

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

neuropathy, peripheral

neurotoxicity, acute

nutritional deficiency

nystagmus, rotary

occipital lobe, infarction

occipital lobe, infarction, bilateral

ophthalmoplegia

ophthalmoplegia, progressive external

optic foramina, abnormal

ornithine transcarbamylase deficiency

pain, abdominal

paramyotonia congenita

paresthesias, hands

Parkinsonism syndrome

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

pernicious anemia

peroxisomal disease

personality change

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pons, lesion of

posterior cerebral artery territory infarction

precipitating factors

prevention of neurologic disorders

progressive neurologic disorder

propionic aciduria

psychiatric problems in neurologic disorders

psychomotor retardation

psychotic behavior

pulmonary edema

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

rabies prophylaxis

rabies, nervous system involvement with

ragged-red fibers

rapidly progressing neurologic illness

renal failure, acute

renal tubular acidosis

respiratory tract infection

retina, abnormal

retinitis pigmentosa

reversible neurologic disorder

salicylate intoxication

seizure, children

seizure, drug-induced

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, treatment of

sensorineural hearing loss

shock, hypovolemic

skin, lesions in neurologic disorders

skull x-ray, abnormal

small-bowel bypass

speech, loss of

speech, pressured

spinal cord, infarction of

spontaneous remission

status epilepticus

stimulant drugs

stool, guaiac positive

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

symmetric brain lesions

sympathomimetic drugs

systemic illness

temporal lobe, lesion

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine deficiency

thrombocytopenia

thrombotic microangiopathy

toxic encephalopathy

toxins, nervous system

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

Trousseau's syndrome

uncal herniation

upgaze, paralysis of

urea-cycle enzymopathies

uremic encephalopathy

urinalysis, abnormal

urine test for metabolic disorders

urine test in toxic screen

violent behavior

viral infection

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual loss, progressive

visual loss, slow

vitamin deficiency

walking, difficulty with

weakness, fluctuating

weakness, generalized

weakness, proximal

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

x-linked mental retardation

Showing articles 100 to 135 of 135 << Previous

A Systematic Approach to the Diagnosis of Suspected Central Nervous System Lymphoma
JAMA Neurol 70:311-319, Scott, B.J.,et al, 2013

A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
JAMA Neurol 70:120-124, Konikkara, J.,et al, 2013

Clinicopathologic Conference, Adult T-cell Leukemia-lymphoma Associated with HTLV-1
NEJM 367:552-563, Case 24-2012, 2012

Dilemmas in the Diagnosis of Acute Community-Acquired Bacterial Meningitis
Lancet 380:1684-1692,1623, Brouwer, M.,et al, 2012

Clinicalpathologic Conference, Vitamin B12 Deficiency due to Pernicious Anemia
NEJM 366:1626-1633, Case 13-2012, 2012

Random skin biopsy and bone marrow biopsy for diagnosis of intravascular large B cell lymphoma
Ann Hematol 90:417-421, Matsue, K.,et al, 2011

Diagnosis of intravascular lymphoma: usefulness of random skin biopsies
Brain Neurol 63:451-458, Nakano, N.M., 2011

Neurological disturbances caused by intravascular lymphomatosis
Brain Nerve 63:443-449, Mizutani, T., 2011

Epidemic Profile of Shiga-Toxin-Producing Escherichia coli O104:H4 Outbreak in Germany
NEJM 365:1771-1780, Frank, C.,et al, 2011

Spinal Cord Sarcoidosis: Clinical and Laboratory Profile and Outcome of 31 Patients in a Case-Control Study
Medicine 89:133-140, Cohen-Aubart,F.,et al, 2010

Intravascular Lymphoma Masquerading as Multiembolic Stroke Developing After Coronary Artery By-Pass Surgery
The Neurologist 15:98-101, Sumer,M.,et al, 2009

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

Intravascular Lymphoma: The Oncologists "Great Imitator"
The Oncologist 11:496-502, Zuckerman, D.,et al, 2006

Clinicopath Conf., MELAS Syndrome
NEJM 353:2271-2280, Case 36-2005, 2005

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Pituitary Lymphoma Presenting as Fever of Unknown Origin
J Clin Endocrinol Metab 86:1470-1476, Landman, R.E.,et al, 2001

Intravascular Malignant Lymphomatosis with Neurologic Presentation: Factors Facilitating Antemortem Diagnosis
South Med J 91:672-676, Devlin,T.,et al, 1998

Neurologic manifestations of intravascular lymphomatosis
Acta Neurol Scand 91:494-499, Chapin, J.E.,et al, 1995

Bacterial Meningitis in Children:Pathophysiology and Treatment
Neurol 42:739-748, Ashwal,S.,et al, 1992

Clinicopath Conf
Thrombotic Thrombocytopenic Purpura, Case 30-1991, NEJM 325:265-273991., , 1991

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

Cerebrospinal Fluid Lactate Dehydrogenase Levels in Early Stroke and Transient Ischemic Attacks
Stroke 21:854-857, Lampl,Y.,et al, 1990

Clinicopath Conf
Malignant Angioendotheliomatosis, Am J Med 88:522-5281990., , 1990

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Hypoparathyroidism
Cecil Textbook of Medicine 18th Ed, W B Saunders Co, Phila, p149688., Arnaud,C.D., 1988

Clinicopath Conf
Malignant Lymphoma, Intravascular, Large-Cell, Immunoblastic type (Malignant Angioendotheliomatosis), , Case86,NEJM 315:874-885,1986., 1986

Pathophysiological & Prognostic Significance of Cerebrospinal Fluid Lactate in Cerebral Malaria
Lancet 1:776-778, White,N.J.,et al, 1985

CSF Lactate in Diseases of the CNS
Arch Int Med 143:85-87, Jordan,G.W.,et al, 1983

Community-Acquired Purulent Meningitis of Unknown Etiology
Arch Neurol 38:749-753, Geiseler,P.J.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Hypoparathyroidism & Elevated Muscle Enzymes
Neurol 30:192-195, Shane,E.,et al, 1980

Serum LDH-5 in Carriers of Duchenne Muscular Dystrophy
Neurol 29:239-241, Burt,D.,et al, 1979

Adult Toxoplasmosis Presenting as Polymyositis & Cerebellar Ataxia
Ann Int Med 82:367, Greenlee,J.,et al, 1975

The Use of Serum Lactate Dehydrogenase Isoenzymens in the Diagnosis of Muscle Disease
Neurol 19:26, Hooshmard,H.,et al, 1969

Contributions of Serum Enzymes to the Diagnosis of Myocardial Injury
Med Concepts of CVD 36:49, , 1967

Contributions of Serum Enzymes & Isozymes to the Diagnosis of Myocardial Injury
Med Concept of CVD 36:43, Cohen,L., 1967

Showing articles 100 to 135 of 135 << Previous