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 700 to 750 of 1030 << Previous Next >>

Cranial Nerve Deficit:A Clue to the Diagnosis of Ethylene Glycol Poisoning
Am J Med 87:91-92, Palmer,B.F.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Brain Tumors in Children
J Pediatr 114:511-519, Kadota,R.P.,et al, 1989

Opsoclonus in Organophosphate Poisoning
Arch Neurol 46:704-705, Pullicino,P.&Aquilina,J., 1989

Environmental Factors and Parkinson's Disease:A Case-Control Study in China
Neurol 39:660-664, Tanner,C.M.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

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

Agenesis of the Corpus Callosum:A Marker for Inherited Metabolic Disease
Neurol 39:847-848, Kolodny,E.H., 1989

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Randomised Double Blind Controlled Trial of Cyclosporin in Multiple Sclerosis
JNNP 52:559-565, Rudge,P.,et al, 1989

Dorsal Radiculopathy Resulting from Podophyllin Toxicity
Neurol 39:607-608, Gorin,F.,et al, 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,et al, 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

MR Findings in Methotrexate-Induced CNS Abnormalities
AJR 153:1283-1288, Ebner,F.,et al, 1989

Chemotherapy for Malignant Gliomas? Committee on Health Care Issues
American Neurologic Association, Ann Neurol 25:88-891989., , 1989

Spasm of the Near Reflex Associated with Metabolic Encephalopathy
Neurol 39:150, Moster,M.L.&Hoenig,E.M., 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

The Reversible Dementias:Do They Reverse?
Ann Int Med 109:476-486, Clarfield,A.M., 1988

Cyclosporin Neurotoxicity in Cardiac Transplant Recipients
JNNP 51:1434-1437, Lane,R.J.M.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

Unusual Presentation of Cis-Platinum Neuropathy
Neurol 38:488-490, Mollman,J.E.,et al, 1988

Cerebrovascular Complications of L-Asparaginase Therapy
Neurol 38:127-133, Feinberg,W.M.&Swenson,M.R., 1988

Pelagic Paralysis
Lancet 1:161-164, Mills,A.R.&Passmore,R., 1988

Treatment of Epidural Cord Compressions from Hodgkin's Disease with Chemotherapy
Am J Med 84:555-558, Burch,P.A.&Grossman,S.A., 1988

Central Nervous System Metastases from Non-Hodgkin's Lymphoma:Treatment & Prophylaxis
Am J Med 84:425-435, Recht,L.,et al, 1988

Visual System Toxicity Following Intra-arterial Chemotherapy
Neurol 38:284-289, Kupersmith,M.J.,et al, 1988

Amaurotic Family Idiocy
Am J Dis Child 142:53-56, Abt,I.A., 1988

Treatment of Chiasmatic/Hypothalamic Gliomas of Childhood with Chemotherapy:An Update
Ann Neurol 23:79-85, Packer,R.J.,et al, 1988

Neonatal Neurologic and Electroencephalographic Effects of Intrauterine Cocaine Exposure
J Pediatr 113:354-358, Doberczak,T.M.,et al, 1988

Orofacial Dyskinesia in Stupor and Coma
Neurol 38:1331-1332, Noda,S.,et al, 1988

Dangers from Methylprednisolone Acetate Therapy by Intraspinal Injection
Arch Neurol 45:804-806, Nelson,D.A., 1988

MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission
Neurol 38:751-754, Montagne,P.,et al, 1988

Cognitive Impairment and Sensory Loss Associated with Chronic Low-Level Ethylene Oxide Exposure
Neurol 38:567-569, Crystal,H.A.,et al, 1988

Extrapyramidal and Other Neurologic Manifestations Associated with Carbon Disulfide Fumigant Exposure
Arch Neurol 45:537-540, Peters,H.A.,et al, 1988

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

Paraplegia and Quadriplegia after Intrathecal Chemotherapy
Arch Phys Med Rehabil 69:1054-1056, Werner,R.A., 1988

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Neurologic Complications of Bone marrow Transplantation
In Neurol Complic of Transplants, Neurologic Clinics, 6:377-378988., Davis,D.G.&Patchell,R.A., 1988

Inborn Errors of Metabolism in Children Referred with Reye's Syndrome, A Changing Pattern
JAMA 260:3167-3170, 3178-31801988., Rowe,P.C.,et al, 1988

Successful Chemotherapy for Recurrent Malignant Oligodendroglioma
Ann Neurol 23:360-364, Cairncross,J.G.&Macdonald,D.R., 1988

Treatment Response in Malignant Optic Glioma of Adulthood
Neurol 38:1071-1074, Albers,G.W.,et al, 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

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

Unusual Neurotoxicity Associated with Amiodarone Therapy
Arch Int Med 147:881-884, Palakurthy,P.R.,et al, 1987

Showing articles 700 to 750 of 1030 << Previous Next >>