Neudle.com: metabolic acidosis

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Differential
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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

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

diabetic ketoacidosis

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

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

feeding disorder

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

hypercoagulable state

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

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

maple syrup urine disease

marche a petits pas

memory, impairment of

meningitis, aseptic

mental retardation

mental status, abnormal

mental status, abnormal, acute

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

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

Parkinsonism syndrome

paroxysmal neurologic deficits

partial thromboplastin time, prolonged

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

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

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 500 to 550 of 1030 << Previous Next >>

Transient Encephalopathy after Paclitaxel (Taxol) Infusion
Neurol 46:1596-1599, Perry,J.R.&Warner,E., 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Transient Ara-C Leukoencephalopathy:MR Findings
J Comput Assist Tomogr 20:161-169, Patel,A.G.&Rao,R., 1996

A Reversible Posterior Leukoencephalopathy Syndrome
NEJM 334:494-500, Hinchey,J.,et al, 1996

Neurotoxicity Related to the Use of Topical Tretinoin (Retin-A)
Ann Int Med 124:227-228, Bernstein,A.L.&Leventhal-Rochon,J.L., 1996

Childhood Leukemia:Central Nervous System Abnormalities During and After Treatment
AJNR 17:295-310, Chen,C-Y.,et al, 1996

Peripheral Neuropathy Secondary to Docetaxel (Taxotere)
Neurol 46:108-111, 21996., New,P.Z.,et al, 1996

Peripheral Neurotoxicity Induced by Docetaxel
Neurol 46:104-108, 21996., Hilkens,P.H.E.,et al, 1996

Neuroimaging Findings in Patients on Immunosuppressive Therapy:Experience with Tacrolimus Toxicity
AJR 166:683-688, Appignani,B.A.,et al, 1996

Chemotherapy without Radiation Therapy as Initial Treatment for Primary CNS Lymphoma in Older Patients
Neurol 46:435-439, Freilich,R.J.,et al, 1996

Ecstasy and Neurodegeneration
BMJ 312:1493, Green,A.R.&Goodwin,G.M., 1996

Manganese Toxicity in Children Receiving Long-Term Parental Nutrition
Lancet 347:1218-1221, Fell,J.M.E.,et al, 1996

The"Gulf War Syndrome"-Is There Evidence of Dysfunction in the Nervous System
JNNP 60:449-451, Jamal,G.A.,et al, 1996

The Residual Cognitive Effects of Heavy Marijiana Use in College Students
Pope. H. G. & Yurgelun-Todd, D. , JAMA 275:521-527, , 1996

Cortical Hyperintensity on Proton Density-Weighted Images:An MR Sign of Cyclosporine-Related Encephalopathy
AJNR 17:337-344, Jansen,O.,et al, 1996

Clinical and Pathological Features in Hydrocarbon-Induced Parkinsonism
Ann Neurol 40:922-925, Pezzoli,G.,et al, 1996

Regional Subacute Cranial Neuropathies Following Internal Carotid Cisplatin Infusion
Neurol 47:1088-1090, Alderson,L.M.,et al, 1996

Atrophy of Bilateral Extraocular Muscles
J Neuro-Ophthalmol 16:286-288, Okamoto,K.,et al, 1996

Immunosuppression-Induced Leukoencephalopathy from Tacrolimus (FK506)
Ann Neurol 40:575-580, Small,S.L.,et al, 1996

Myasthenic Symptoms in Patients with Mitochondrial Myopathies
Muscle & Nerve 18:1338-1340, LeForestier,N.,et al, 1995

Neuromuscular Effects of Papuan Taipan Snake Venom
Ann Neurol 38:916-920, Connolly,S.,et al, 1995

Reversible MRI Abnormalities Following Seizures
Neurol 45:104-108, Yaffe,K.,et al, 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Multifocal Inflammatory Leukoencephalopathy Associated with Levamisole Therapy
Neurol 45:374-376, Kimmel,D.W.,et al, 1995

Aminophylline for Methotrexate-Induced Neurotoxicity
Lancet 345:544-547, Bernini,J.C.,et al, 1995

The Ciguatera Poisoning Syndrome from Farm-Raised Salmon
Ann Int Med 122:113-114, DiNubile,M.J.&Hokama,Y., 1995

Neurotox of Antimicrob & Antimalarial Agents
In Intox of Nervous System, Part II, Handbk Clin Neurol, Elsevier Science 21 (65) :471., Moorhouse,D.F.,et al, 1995

Acute Isoniazide Neurotoxicity in an Urban Hospital
Pediatrics 94:700-704, Shah,B.R.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Assoc of Myasthenia Gravis with Extrathymic Hodgkin's Lymphoma:Resol of Myasth Sympt Following Antineopl Therapy
Neurol 45:1019, Abrey,L.E.&Askanas,V., 1995

Neuropsychological Effects of Long-Term Exposure to Organophosphates in Sheep Dip
Lancet 345:1135-1139, Stephens,R.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Sarin Poisoning in Matsumoto, Japan
Lancet 346:290-293, Morita,H.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Combined System Disease after Nitrous Oxide Anesthesia:A Case Report
Neurol 45:1224-1225, McMorrow,A.M.,et al, 1995

'Anesthesia Paresthetica':Nitrous Oxide-Induced Cobalamin Deficiency
Neurol 45:1608-1610, 14351995., Kinsella,L.J.&Green,R., 1995

Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
J Pediatr 127:193-199, Majnemer,A.&Shevell,M.I., 1995

Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995

Conditions That Mimic Stroke in the Emergency Department
Arch Neurol 52:1119-1122, Libman,R.B.,et al, 1995

Diphtheritic Neuropathy
Muscle & Nerve 18:1460-1463995., Greange,A.,et al, 1995

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

Epidemic Optic Neuropathy in Cuba-Clinical Characterization and Risk FActors
NEJM 333:1176-1182, Bern,C.,et al, 1995

'Complicated Migraine-like Episodes'in Children Following Cranial Irridiation and Chemotherapy
Neurol 45:1837-1840, Shuper,A.,et al, 1995

Neurological Sequelae of Cyanide Intoxication-The Patterns of Clinical MRI & Pet Findings
Ann Neurol 38:825-828, Rosenow,F.,et al, 1995

MR Findings in Methanol Intoxication
AJNR 16:1783-1786, Gaul,H.P.,et al, 1995

Neurotoxicity in Liver Transplant Recipients with Cyclosporine Immunosuppression
Neurol 45:1962-1964, Wijdicks,E.F.M.,et al, 1995

Delayed Dystonia with Striatal CT Lucencies Induced by a Mycotoxin (3-Nitropropionic Acid)
Neurol 45:2178-2183, He,F.,et al, 1995

Anticholinergic Poisoning Associated with Herbal Tea
Arch Int Med 155:2245-2248, Hsu,C.K.,et al, 1995

Current Management of Primary Central Nervous Lymphoma
Oncology 9:63-78, DeAngelis,L.M., 1995

Showing articles 500 to 550 of 1030 << Previous Next >>