Neudle.com: urine test for metabolic disorders

Differential
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abdominal distention

acoustic nerve

advances in neurology

aggression

agitation

alcohol intoxication

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

aminoacylase 1 deficiency

anticoagulant, treatment

attention deficit disorder with hyperactivity

autism

autonomic dysfunction

BAL

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basophilic stippling of red blood cells

bath salts, psychoactive

behavior, combative

behavioral disorder

behavioral disorder, acute

Benedict's solution test

bifid uvula

biotin

biotin deficiency

biotinidase deficiency

bismuth

body odor

bone marrow suppression

burn injury

calcification, intracranial

calcium oxalate crystals

Canavan's disease

cardiomegaly

cardiomyopathy

carnitine deficiency myopathy

cerebral cortical atrophy

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral venous thrombosis

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, glycine

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

cocaine

coenzyme Q10

coenzyme Q10 deficiency

congenital deformities

congenital myopathy

cornea, abnormal

cortical vein thrombosis

cranial nerve palsies

creatine phosphokinase(CPK)elevated

creatinine, elevated

cultured skin fibroblasts

demyelinating disease

dermatitis

designer drugs

developmental evaluation

developmental milestones, loss of

developmental retardation

diabetes insipidus

diarrhea

diet

dinitrophenylhydrazine(D.N.P.H.)reaction

diplegia, atonic

diplegia, spastic cerebral

disorientation

distal muscle weakness

drooling

drug abuse

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

dural sinus thrombosis

electrocardiogram, abnormal

electroconvulsive therapy

encephalopathy, acute

encephalopathy, metabolic

encephalopathy, neonatal

enzyme, defect

enzyme, muscle disease

eye movement, disorders of

Fabry's disease

facial nerve palsy, bilateral

fingernails, abnormal

gastrointestinal bleeding

gene

gene mutation

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

glycine

glycogen storage disease

grimacing

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, differential diagnosis of

Guthrie test

hallucination

hallucination, auditory

hearing problems in children

heavy metal intoxication

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

homocystinuria

hyperammonemic encephalopathy

inborn errors of metabolism

inclusion body myositis

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

internuclear ophthalmoplegia, bilateral

ischemic exercise test

isopropyl alcohol

jaw contractures

karyotyping

Kayser-Fleischer ring

ketoacidosis

ketonuria

klippel feil syndrome

lactic acidemia

lactic dehydrogenase(LDH)

language disorders in children

lead poisoning

leg weakness, bilateral

leukocyte enzyme abnormality

leukodystrophy

leukoencephalopathy

leukoencephalopathy, toxic

leukopenia

levamisole

level of consciousness, decreased

level of consciousness, decreased acute

lipid storage disorder of CNS

liver disease

liver function enzymes

liver transplantation

Lowe's syndrome

lysosomal storage disease

macrocephaly

malignant hyperpyrexia

maple syrup urine disease

marfanoid skeletal abnormalities

mental status, abnormal

mental status, abnormal, acute

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

methcathinone

midline defect in children

misdiagnosis

mitochondrial disease

molecular genetics

mortality

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, demyelinating disease

MRI, diffusion weighted

mucopolysaccharidoses

muscle atrophy, progressive

muscle atrophy, static

muscle biopsy

muscle cramp

muscle pain

muscle phosphofructokinase deficiency

muscle phosphorylase deficiency

muscle stiffness

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, Duchenne

myopathy, drug-induced

myopathy, metabolic

myopathy, mitochondrial

nerve conduction studies

neuritis, heavy metals causing

neurologic complications of, surgery

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neurologic testing

neuromuscular disease, electrodiagnosis of

neuropathy

neuropathy, peripheral

ophthalmoplegia, neonatal

opisthotonus

optic atrophy

ornithine transcarbamylase deficiency

osteoarthrosis

osteoporosis

pain, leg

palatopharyngeal incompetence

Parkinsonism syndrome

peripheral blood smear

peripheral blood smear, abnormal

personality change

phenylketonuria

phenylketonuria, adult onset

phosphorylase b kinase deficiency

pleocytosis of cerebrospinal fluid

pleural effusion

polyneuropathy

position sensation, abnormal

practice guidelines

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive neurologic disorder

proprioception, abnormal

proteinuria

proximal muscle atrophy

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

pyridoxine deficiency

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

sclerae, hyperpigmented

screaming

second wind phenomena

seizure

seizure, advice to parents and teachers regarding

seizure, children

seizure, neonatal

seizure, psychosocial aspects of

seizure, pyridoxine dependent

seizure, treatment of

self harm

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

skin, biopsy

skin, lesions in neurologic disorders

skin, pink

speech disorder, childhood

spina bifida

spondylolysis

spongy degeneration of brain

steroid therapy, CNS treatment and complications with

stimulant drugs

stool, guaiac positive

sweating, abnormality of

sympathomimetic drugs

toxins, nervous system

treatment of neurologic disorder

tremor

tremulousness

urea-cycle enzymopathies

urine test for metabolic disorders

urine test in toxic screen

weakness, generalized

weakness, progressive

weight loss

white matter disease

x-linked mental retardation

Showing articles 800 to 850 of 17368 << Previous Next >>

Reduction of Angiotensin-Converting Enzyme in Substantia Nigra in Early-Onset Schizophrenia
NEJM 300:502-503, Arregui,A.,et al, 1979

Cyclophosphamide Therapy of Severe Systemic Necrotizing Vasculitis
NEJM 301:235-238, Fauci,A.S.,et al, 1979

Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification
Neurol 29:1057-1061, Markesbery,Wm.R., 1979

A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission
Arch Neurol 36:553-556, Barron,S.A.,et al, 1979

Peripheral Neuropathy in Arsenic Smelter Workers
Neurol 29:939-944, Feldman,R.G.,et al, 1979

Ethylene Oxide Neurotoxicity:Report of Four Cases & Review of the Literature
Neurol 29:978-983, Gross,J.A.,et al, 1979

Pseudotumor Cerebri & Insecticide Intoxication
Neurol 29:1222-1227, Sanborn,G.E.,et al, 1979

Trichlorethylene
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 457, Feldman,R.G., 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Carnitine Deficiency Acute Postpartum Crisis
Ann Neurol 4:558-561, Angelini,C.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Progressive Dialysis Encephalopathy
Ann Neurol 4:199-204, Lederman,R.J.,et al, 1978

Toluene Optic Neuropathy
Ann Neurol 4:390, Keane,J.R., 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Leukoencephalopathy in Oculocraniosomatic Neuromuscular Disease With Ragged-Red Fibers
Arch Neurol 35:643-647, Bertorini,T.,et al, 1978

Malignant Optic Gliomas in Adults
Arch Neurol 35:731-735, Harper,C.G.,et al, 1978

Myoglobinuria & Renal Failure after Status Epilepticus
Neurol 28:200, Singhal,P.C.,et al, 1978

The Cherry-red Spot-Myoclonus Syndrome
Ann Neurol 3:234, Rapin,I.,et al, 1978

Perhexiline Neuropathy:A Clinicopathological Study
Ann Neurol 3:259, Said,G., 1978

Effects of Acetazolamide on Myotonia
Ann Neurol 3:531, Griggs,R.C.,et al, 1978

Abnor CT Scans of Brain in Asympt. Chil with Acute Lymph. Leuk. after Prophy. Treat of CNS with Radia & Intrathe Chemo
NEJM 298:815, Peylan-Ramu,N.,et al, 1978

A Synd of Methylmal Acid, Homocystinuria, Megaloblas. Anemia & Neurol Abnor. in a Vit B-12-def Breast-fed Infant of veget
NEJM 299:317, Higginbottom,M.C., 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Prolonged Encephalopathy with Arsenic Poisoning
Neurol 28:853-855, Freeman,J.W.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Subarachnoid Hemorrhage Complicating Acute Poststreptococcal Glomerulonephritis
Arch Neurol 35:473, DeBeukelaer,M.M.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Possible Biochemical Basis of Memory Disorder in Alzheimer Disease
Ann Neurol 3:471, Smith,C.M.,et al, 1978

Intrathecal Methotrexate Causing Paraplegia in a Middle-Aged Woman
Acta Haemat 60:59-60, Weiss,S.,et al, 1978

Neuromuscular Diseases that Affect the Eye
International Ophthal Clx 18:103, Black,J., 1978

Primary Reticulum Cell Sarcoma of the Brain in Wiskott-Aldrich Syndrome
Arch Neurol 34:633, Model,L.M., 1977

Neuropathology of Sanfilippo Syndrome
Ann Neurol 2:161, Ghatak,N.R.,et al, 1977

CNS Lesions in Cystinuria
Arch Neurol 34:638, Blackburn,C.R.B.,et al, 1977

"Disappearing"Spinal Cord Compression:Oncolytic Effect of Glucocorticoids on Epidural Metastases
Ann Neurol 2:409, Posner,J.B.,et al, 1977

Recurrent Laryngeal Nerve Paralysis in Patients Receiving Vincristine & Vinblastine
BMJ 1:1251, Whittaker,J.A., 1977

Chronic Hexosaminidase A & B Deficiency
et al. , Ann Neurol 2:156977., Goldie,W.D., 1977

Methyl Bromide Intoxication:Neurologic Features, Including Simulation of Reye Syndrome
Neurol 27:959, Shield,L.K.,et al, 1977

Purine Phosphoribosyltransferase in Gilles de la Tourette Syndrome
NEJM 296:210, VanWoert,M.H.,et al, 1977

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency
Ann Neurol 1:276, Karpati,G.,et al, 1977

Leukoencephalopathy in Childhood Leukemia
et al. , Neurol 27:609977., Devivo,D.C., 1977

Abnormality of a Thiamine-Requiring Enzyme in Patients with Wernicke-Korsakoff Syndrome
NEJM 297:1367, Blass,J.P.,et al, 1977

Brain Stem Toxoplasmosis Complicating Hodgkin's Disease
Arch Neurol 34:636, Slavick,H.E.,et al, 1977

Dapsone Motor Neuropathy--An Axonal Disease
Neurol 26:514, Gutmann,L.,et al, 1976

Low Activities of the Pyruvate & Oxoglutarate Dehydrogenase Complexes in Five Patients with Friedreich's Ataxia
NEJM 295:62, Blass,J.P.,et al, 1976

Septicemia & Meningitis in Children Splenectomized for Hodgkin's Disease
NEJM 295:798, Chilcote,R.R.,et al, 1976

Treatment of Hydrazine-Induced Coma with Pyridoxine
NEJM 294:938, Kirklin,J.K.,et al, 1976

Neurologic Disorders in Renal Failure (1st of Two Parts)
NEJM 294:143, Raskin,N.H.,et al, 1976

Remote Cerebral Infarction as a Presenting Manifestation of Brain Tumor
Milit Med 141:548, Finelli,P.F., 1976

Organic Mental Changes With Fluorouracil Therapy
JAMA 235:248-249, Greenwald,E.S., 1976

Showing articles 800 to 850 of 17368 << Previous Next >>