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 750 to 800 of 17620 << Previous Next >>

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis
NEJM 310:1630-1634, Brushlow,S.W.,et al, 1984

CT Abnormalities & Altered Methotrexate Clearance in Children with CNS Leukemia
Neurol 34:229-233, Duffner,P.K.,et al, 1984

Cerebellar Hemorrhage Complication Methylmalonic & Propionic Acidemia
Arch Neurol 41:1293-1296, Dave,P.,et al, 1984

Seizures in Childhood Lymphoblastic Leukaemia Patients
Lancet 2:1422-1424, Ochs,J.J.,et al, 1984

Diagnosis & Treatment of Lumbosacral Plexopathies in Patients with Cancer
Arch Neurol 41:1282-1285, Pettigrew,L.C.,et al, 1984

Detection of Urea Cycle Enzymopathies in Childhood
Arch Neurol 41:758-760, Trauner,D.A.,et al, 1984

Long-Lasting Neurological Sequelae After Lithium Intoxication
Acta Psychiatr Scand 70:594-602, Schou,M., 1984

Intraventricular Methotrexate Therapy of Leptomeningeal Metastasis from Breast Carcinoma
Neurol 33:1565-1572, OngerboerdeVisser,B.W.,et al, 1983

Clinical Epidemology of Toxic-Oil Syndrome
NEJM 309:1408-1414, Kilbourne,E.M.,et al, 1983

Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

Acute Cocaine Poisoning
Am J Med 75:1061-1064, Jonsson,S.,et al, 1983

Lafora Disease:Liver Histopathology in Presymptomatic Children
Ann Neurol 14:86-89, Baumann,R.J.,et al, 1983

Ethylene Oxide Polyneuropathy
Neurol 33:377-380, Kuzuhara,S.,et al, 1983

Ethylene Oxide-Induced Polyneuropathy
Arch Neurol 40:419-421, Finelli,P.F.,et al, 1983

Adult Inorganic Lead Intoxication:Presentation of 31 New Cases & a Review of Recent Advances in the Literature
Medicine 62:221-247, Cullen,M.R.,et al, 1983

Hyperammonemic Encephalopathy During Hemodialysis
Ann Int Med 99:190-191, Canzanello,V.J.,et al, 1983

Sensory Neuropathy from Pyridoxine Abuse
NEJM 309:445-448, Schaumburg,H.,et al, 1983

Neurotoxicity of Radiological Contrast Agents
Ann Neurol 13:469-484, Junck,L.,et al, 1983

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

Subdural Tension Pneumocephalus Following Surgery
J Comput Assist Tomogr 6:903-906, Monajati,A.,et al, 1982

Evoked Potentials in Neurological Diagnosis
BMJ 285:1678-1679, Mastaglia,F.L.,et al, 1982

Central Nervous System Infection in the Chronically Immunosuppressed
Medicine 61:166-188, Hooper,D.C.,et al, 1982

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

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

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

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

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

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

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

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

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

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

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

Phencyclidine:The New American Street Drug
Editorial, BMJ 281:1511-15121980., , 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

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

A Diagnostic Index of Active Demyelination:Myelin Basic Protein in Cerebrospinal Fluid
Ann Neurol 8:25-31, Cohen,S.R.,et al, 1980

Use of Adrenal Biopsy in Diagnosing Adreno-leukomyeloneuropathy
Arch Neurol 37:634-636, Weiss,G.M.,et al, 1980

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,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

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

Showing articles 750 to 800 of 17620 << Previous Next >>