Neudle.com: acidosis metabolic

Differential
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abdominal distention

acetazolamide

aciduria

acyl CoA dehydrogenase deficiency

addiction, heroin

adverse drug reaction

aggression

agitation

alcohol intoxication

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

alcoholism

alkalosis, respiratory

antibiotics, neurologic complications with

autonomic dysfunction

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

bat bite

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

biotin deficiency, juvenile form

biotinidase deficiency

buried bumper syndrome

cachexia

calcification, intracranial

carbonic anhydrase II deficiency

carnitine deficiency myopathy

CAT scan

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, false negative

cataracts

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebral cortex

cerebral cortical atrophy

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

children

chorea

chromosome 19

chronic progressive external ophthalmoplegia

Clinical Pathologic Conference(C.P.C.)

coagulopathy

cocaine

coenzyme Q10

coenzyme Q10 deficiency

coma

coma, sudden onset

compartment syndrome

compartment syndrome, abdominal

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

degenerative diseases of CNS

delay in diagnosis

delirium

dementia

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

diplopia

disability, neurological

disorientation

disseminated intravascular coagulation(DIC)

disulfiram

dizziness

D-lactate acidosis

downward deviation of eyes

drug abuse

drug abuse, toxic screen In

drug induced neurologic disorders

electrocardiogram, abnormal

electroencephalogram, abnormalities of

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

endocarditis

endocarditis, marantic

enzyme, defect

episodic neurologic deficits

ethylene glycol

exercise

exercise intolerance

exercise-induced neurologic dysfunction

exome sequencing

eye movement, disorders of

gastrointestinal bleeding

gastrostomy, percutaneous endoscopic

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus, hemorrhage

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

growth retardation

gyrus, abnormal

hallucination

hallucination, auditory

hemianopia, transient

hemiparesis

hemiparesis, transient

hemiplegia

hemorrhagic diathesis

hemorrhagic shock encephalopathy syndrome

hepatic failure

hepatomegaly

heralding manifestation

herniated disc, differential diagnosis of

herpes simplex encephalitis

hirsutism

Hispanics

histochemistry of muscle

hydrophobia

hyperammonemic encephalopathy

hypercapnia

hypercoagulable state

iatrogenic neurologic disorders

inborn errors of metabolism

intellectual deterioration

internal capsule

intracranial pressure, increased

intravenous drug abuse

Kearns-Sayre syndrome

laminar necrosis, cortical

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

level of consciousness, decreased

level of consciousness, decreased acute

lipid storage myopathy

liver function enzymes

Lowe's syndrome

lysosomal storage disease

malabsorption

malignant hyperpyrexia

maple syrup urine disease

marche a petits pas

MELAS syndrome

memory, impairment of

meningeal enhancement

meningitis

meningitis, aseptic

mental retardation

mental status, abnormal

mental status, abnormal, acute

mesial temporal lobe

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metformin

methcathinone

methylmalonic acidemia

methylmalonic aciduria

microangiopathic hemolytic anemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, FLAIR

MRI, gyral enhancement

MRI, gyral swelling

MRI, serial

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRS

mucormycosis

multiple organ failure

multiple sclerosis, differential diagnosis of

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myopathy, mitochondrial

myopathy, proximal

myotonia

myotonia congenita

myotonia, treatment of

neonatal epileptic encephalopathy

nephrotic syndrome

neuroendocrinology

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular blockade

neuronal ceroid-lipofuscinosis

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neurotoxic

neurotoxicity, acute

neurotoxin

next-generation sequencing

normal

nutritional deficiency

nystagmus

nystagmus, rotary

obesity

occipital lobe, infarction

occipital lobe, infarction, bilateral

occipital lobe, lesion of

ophthalmoplegia

ophthalmoplegia, progressive external

optic atrophy

optic foramina

optic foramina, abnormal

ornithine transcarbamylase deficiency

paramyotonia congenita

paranoia

paraplegia

paresthesias

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

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyridoxine

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis

rabies prophylaxis

rabies, nervous system involvement with

ragged-red fibers

rapidly progressing neurologic illness

renal tubular acidosis

respiratory tract infection

retina, abnormal

retinitis pigmentosa

reversible neurologic disorder

salicylate intoxication

seizure, drug-induced

seizure, intractable

seizure, intractable, treatment of

seizure, neonatal

seizure, treatment of

self harm

sensorineural hearing loss

shock, hypovolemic

short stature

skin, biopsy

skin, lesions in neurologic disorders

skin, pink

skull x-ray, abnormal

spinal cord, infarction of

splenomegaly

spontaneous remission

status epilepticus

stimulant drugs

stool, guaiac positive

striatonigral degeneration

striatonigral degeneration, infantile

symmetric brain lesions

sympathomimetic drugs

systemic illness

tachycardia

tachypnea

temporal lobe, lesion

temporal lobe, lesion, bilateral

tetany

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

thiamine deficiency

thrombocytopenia

thrombotic microangiopathy

toxins, nervous system

transient neurologic deficit

treatment of neurologic disorder

urea-cycle enzymopathies

uremia

uremic encephalopathy

urinalysis, abnormal

urine sediment

urine test for metabolic disorders

urine test in toxic screen

vision, failure of in childhood

visual acuity, decreased

visual loss

visual loss, progressive

visual loss, slow

vitamin deficiency

walking, difficulty with

weakness

weakness, fluctuating

weakness, generalized

weakness, proximal

weight loss

Wernicke's encephalopathy

white matter disease

white matter disease, subcortical

whole genome sequencing

workup

x-linked mental retardation

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Arch Int Med 150:1751-1753, Brent,J.,et al, 1990

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
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Hemorrhagic Shock and Encephalopathy:Clinical, Pathologic, and Biochemical Features
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Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Perinatal Brain Damage:Predictive Value of Metabolic Acidosis & The Apgar Score
BMJ 297:24-27, Ruth,V.J.&Raivio,K.O., 1988

Acute Extrapyramidal Syndrome in Methylmalonic Acidemia:"Metabolic Stroke"Involving the Globus Pallidus
J Pediatr 113:1022-1027, Heidenreich,R.,et al, 1988

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Bilateral Lucency of the Globus Pallidus Complicating Methylmalonic Acidemia
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D-Lactate Encephalopathy
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Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
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Acute Cocaine Poisoning
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Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
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Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
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Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
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Effects of Acetazolamide on Myotonia
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Increased Prevalence of Nitrous Oxide-Induced Subacute Combined Degeneration of the Spinal Cord: Clinical and Imaging Findings
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A 67-Year-Old Man with Exercise Intolerance nd Progressive Weakness
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Bilateral Posterior Limb Internal Capsule T2 Hyperintensity and Severe Cerebellar Atrophy in 2 Lifelong Friends
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Infantile Epileptic Spasms Syndrome (West Syndrome)
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Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
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Chronic Neuropsychiatric Sequelae Associated with Kambo Intoxication
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A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
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A Rare Neurotoxicity Syndrome Following Opioid Intoxication
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Neuroimaging Features of Biotinidase Deficiency
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Neonatal Seizures
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Extracranial Etiology of Acute Onset Ataxia and Weakness
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Association Between Occupational Exposure to Formaldehyde and Cognitive Impairment
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Showing articles 50 to 100 of 1046 << Previous Next >>