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 850 to 900 of 1030 << Previous Next >>

Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982

Neurotoxic Effects of Cisplatin Therapy
Arch Neurol 39:719-720, Walsh,T.J.,et al, 1982

Immediate & Delayed Neurotoxicity After Mechlorethamine Preparation for Bone Marrow Transplantation
Ann Int Med 97:182-189, Sullivan,K.M.,et al, 1982

Neurotoxicity of the Pyrimidine Synthesis Inhibitor N-Phosphonoacetyl-L-Aspartate
Ann Neurol 12:175-183, Wiley,R.G.,et al, 1982

Malignant Glioma, Results of Combined Modality Therapy
JAMA 248:62-65, Cooper,J.S.,et al, 1982

Treatment of Neuroectodermal Brain Tumors
Ann Neurol 12:231-237, Shapiro,W.R., 1982

Ocular Bobbing in Metabolic Encephalopathy:Clinical, Pathologic, & Electrophysiologic Study
Neurol 32:1029-1031, Drake,M.E.,et al, 1982

Misonidazole Neuropathy:A Clinical, Electrophysiological, & Histological Study
Ann Neurol 12:10-17, Melgaard,B.,et al, 1982

Vincristine-induced Laryngeal Nerve Paralysis
Neurol 32:1285-1288, Delaney,P., 1982

Leukoencephalopathy After Inhaling"Heroin"Pyrolysate
Lancet 2:1233-1237, Wolters,E.C.,et al, 1982

Stroke Due to Treatment with L-Asparginase in an Adult
NEJM 307:1643, Lederman,G.S., 1982

Neurologic Manifestations of Podophyllin Toxicity
Neurol 32:308-311, Filley,C.M.,et al, 1982

Acute Polyneuropathy After Poisoning By A New Organophosphate Insecticide
NEJM 306:155-157, Senanayake,N.,et al, 1982

Sources of Error in the Diagnosis of Guillain-Barre Syndrome
Muscle & Nerve 5:111-117, Feit,H.,et al, 1982

Conjugate Deviation of Gaze in Hepatic Encephalopathy
JNNP 45:1168, Sandyk, R.et al, 1982

Effects of Prophyl. Treat. of CNS on Intellect. Funct. of Children with Acute lymph. Leuk
Am J Med 71:47-52, Moss,H.A., 1981

Disulfiram Neuropathy
Neurol 31:730-735, Mokri,B.,et al, 1981

Polyneuropathy After Massive Exposure to Parathion
Neurol 31:603-605, deJager,A.E.J.,et al, 1981

Brainstem Auditory Evoked Response in the Diagnosis of Pediatric Neurologic Diseases
Neurol 31:832-840, Hecox,K.E.,et al, 1981

Biochemical Evidence Of Dysfunction Of Brain Neurotransmitters In The Lesch-Nyhan Syndrome
NEJM 305:1106-1111, Lloyd,K.G.,et al, 1981

Fatal Vidarabine Toxicity in a Patient With Normal Renal Function
JAMA 246:1703-1705, VanEtta,L.,et al, 1981

Myoclonic Seizures Following Chlorambucil Overdose
Jr. , Ann Neurol 9:191-194981., Byrne,T.N., 1981

Toxic Substances & the Nervous System:The Role of Clinical Observation
JNNP 44:1-8, LeQuesne,P.M., 1981

Acute Thallium Poisoning, Toxicological & Morphological Studies of the Nervous System
Ann Neurol 10:38-44, Davis,L.E.,et al, 1981

Focal Encephalopathy Following Methotrexate Therapy
Arch Neurol 38:450-452, Packer,R.J.,et al, 1981

Dural Sinus Thrombosis in Children With Acute Lympho-blastic Leukemia
JAMA 246:2837-2839, Steinherz,P.G.,et al, 1981

Methyl Bromide Poisoning Seen Initially as Psychosis
Arch Neurol 38:529-530, Zatuchni,J.,et al, 1981

Changes in the Basal Ganglia Following Cyanide Poisoning
J Comput Assist Tomogr 5:755-756, Finelli,P.F., 1981

Neurological Complications of Ethylene Glycol Intoxication
Arch Neurol 38:724-726, Berger,J.R.,et al, 1981

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Ciguatera Fish Poisoning in Miami
JAMA 244:254-258, Lawrence,D.N.,et al, 1980

Prediction of BCNU Pulmonary Toxicity In Patients With Malignant Gliomas, An Assessment of Risk Factors
NEJM 303:183-188, Aronin,P.A.,et al, 1980

The McConnell Missile Accident, Clinical Spectrum of Nitrogen Dioxide Exposure
JAMA 244:1221-1223, Yockey,C.C.,et al, 1980

Clin. Path. Conference
BCNU Pneumonitis, (Cerebellar Astrocytoma, Treated with BCNU) . Case Record 41-1980, NEJM 303:927-93, , 1980, 1980

Long-term Neurological Implications of Somnolence Syndrome in Children with Acute Lymphocyte Leukemia
Ann Neurol 8:273-277, Ch'ien,L.T.,et al, 1980

Amelioration Of Neurologic Abnormalities After"Enzyme Replacement"In Adenosine Deaminase Deficiency
NEJM 303:377-380, Hirschhorn,R.,et al, 1980

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Successful Treatment of Inorganic Mercury Neurotoxicity with N-acetyl-penicillamine Despite an Adverse Reaction
Neurol 30:1000-1001, Markowitz,L.,et al, 1980

Dysconjugate Gaze in Hepatic Coma
Ann Neurol 8:328-329, Caplan,L.R.,et al, 1980

Fatal Myeloencephalopathy Caused by Intrathecal Vincristine
Neurol 30:867-871, Slyter,H.,et al, 1980

Clin. Path. Conference
Type B Botulism, Unclassified Form, Case Record 48-1980, NEJM 303:1347-135580., , 1980

It's Always the Big Ones That Should Get Away
Editorial, JAMA 244:272-2731980., , 1980

Acute Ataxia Associated with Ciguatera-type (Grouper) Tropical Fish Poisoning, Letter
Ann Neurol 7:491, Jones,H.R.Jr., 1980

Methanol Poisoning:A Clinical & Pathological Study
Ann Neurol 8:161-167, McLean,D.R.,et al, 1980

The Neurotoxicity of the Rat Poison Vacor, A Clinical Study of l2 Cases
NEJM 302:73-77, LeWitt,P.A., 1980

Neurological Dysfunction of the Bladder in Workers Exposed to Dimethylaminopropronitrile
JAMA 243:741-745, Kreiss,K.,et al, 1980

Neuropathy & Mitochondrial Myopathy
Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980

Detection of Phenylketonuria in Autistic & Psychotic Children
JAMA 243:126-128, Lowe,T.L.,et al, 1980

Fetal Methylmercury Poisoning:Clinical & Toxicological Data on 29 Cases
Ann Neurol 7:348-353, Marsh,D.O.,et al, 1980

Clinical Significance of Periodic EEG Patterns
Arch Neurol 37:15-20, Kuroiwa,Y.,et al, 1980

Showing articles 850 to 900 of 1030 << Previous Next >>