Neudle.com: urine test for metabolic disorders

Differential
(Click to cross reference)

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 850 to 900 of 17368 << Previous Next >>

Case Records of the MassGeneral Hospital, Case 41-1975, Acute Intermittent Porphyria
NEJM 293:817, Woods,B., 1975

Germinoma of third Ventricle (Case Record of MGH)
NEJM 293:653, Locke,S.,et al, 1975

Acquired Toxoplasmosis
Arch Neurol 32:335, Townsend,J.,et al, 1975

Methotrexate Dist. in CSF after IV, Ventricular & Lumbar Inject
NEJM 293:161, Shapiro,W.R.,et al, 1975

Case Record, PVAH, (Case A-77-75) Toxoplasmosis
December 10, Finelli,P.F.,et al, 1975

Neurotoxicity of Commonly Used Antineoplastic Agents
NEJM 291:75, 1271974., Weiss,H.,et al, 1974

Narcotic Abuse:Neurologic Complications in Pedi & Adolescent Pts
JAMA 66:426, French,J.H.,et al, 1974

Clinical Pathological Conference-The Man Without a History-CA of Lung with Marantic Endocarditis & Cerebral Emboli
JAMA 227:1052, Locke,S.,et al, 1974

Clinical Advances in the Evaluation of Deep Coma
MCV Quart 10:152, Suter,C., 1974

Hepatic Encephalopathy:Current Status
Gastroenter 66:121:1974., Schenker,S.,et al, 1974

Infiltration of the Leptomeninges by Systemic Cancer:a Clinical & Pathologic Study
Arch Neurol 30:122, Olson,M.E.,et al, 1974

Vincristine Neurotoxicity
Ann Int Med 80:733-737, Rosenthal,S.,et al, 1974

Neurologic Manifest. of Infective Endocarditis:A Review
Stroke 4:958, Greenlee,J.E.,et al, 1973

Epidemiology of Motor-Neuron Diseases
NEJM 288:1047, Bobwick,A.R.,et al, 1973

Central Nervous System Infections in Patients with Cancer
Medicine 52:563, Chernik,N.L.,et al, 1973

Leigh's Syndrome:The Adult Form of Subacute Necrotizing Encephalomyelopathy with Predilection for the Brainstem
Neurol 23:1030, Sipe,J.C., 1973

The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica
p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973

Corneal Opacification in Infancy
MCV Quart 8:230, Ching,F., 1972

Case Records of MGH-NEJM 286:1047
1972 Progressive Multifocal Leukoencephalopathy., , 1972

Case Records of MGH-NEJM 286:309
1972 Pseudomonas Meningitis with Cavernous Sinus, Carotid Artery & Sphenoid Sinus Involvement., , 1972

Case Record of MGH-NEJM Atheromatous Emboli to Brain
Kidney, 286:11461972., , 1972

Neurological Complications of Systemic Cancer
Med Clin North Am 55:625, Posner,J., 1971

Infectious Complications of Neoplastic Disease
Med Clin North Am 55:729, Armstrong,D.,et al, 1971

Aphasia Current Conceps
NEJM 284:654, Geschwind,N., 1971

Encephalomyelopathy of Leigh
Editorial BMJ 238, 1971, May., , 1971

Neurology of the Leukemias & Lymphomas-Editorial
BMJ 442, 1971 Nov., , 1971

Clinical Spectrum of Ocular Bobbing
JNNP 33:771, Susac,J.O.,et al, 1970

Neurologic Disorders Seen In the Uremic Patient
Arch Int Med 126:781, Tyler,H.R., 1970

Neurologic Disorders in Renal Failure
Am J Med 44:734, Tyler,H.R., 1968

Neurological Dysfunction Associated with Nonketonic Hyperglycemic
Arch Neurol 19:525, Maccario,M., 1968

Subacute Necrotizing Encephalopathy in Late Adolescence
Arch Neurol 18:478, Hardman,J.M.,et al, 1968

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968

Ocular Complications of Vincristine Therapy
Arch Ophthalmol 78:709, Albert,D.M.,et al, 1967

Diseases of Muscles-Clinical Manifestations & Differential Diagnosis
The New Physic 263, 1967, Oct., Boshes,L., 1967

Inherited Aminoacidopathies Demonstrating Vitamin Dependency
NEJM 281:145, Rosenberg,L., 1965

Angiokeratoma Corporis Diffusum
Quart J Med 31:177, 1962 April., Wise,D.,et al, 1962

Neurologic Manifestations of Chronic Carbon Monoxide Poisoning
NEJM 261:1217-1220, Gilbert,G.J.,et al, 1959

Carbon Monoxide Asphyxia, A Common Clinical Entity
Canad M A J 78:182-185, Katz,M., 1958

Seizure Disorder
Lead Poisoning, Case Study-Rocom Laboratories., , 1850

Minamata:A Living Death
Text by D. Johnson Maryknol Missions, , 1850

Targeting Orexin Receptors to Treat Narcolepsy
NEJM 392:1968-1971, Saper,C.B., 2025

Progress Toward Mitigating Disability Progression in Multiple Sclerosis
NEJM 392:1966-1968, Calabresi,P.A., 2025

A 62-Year-Old Man with Symmetric Saddle Hypoesthesia and Sphincter Dysfunction
Neurol 104:e213712, Crausaz,L.,et al, 2025

General AI May Revolutionize Neurology 0 Or It Might be Bad
JAMA Neurol doi 10.1001/JAMANEUROL.2025.0905, Westover,M.B. & Westover,A.M., 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

Use and Eligibility for Glucose-Like Peptide-1 Receptor Agonist Treatment for Primary Preveention of Stroke
Neurol 104:e213739, Wilson,L.M. & Anderson,T.S., 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Upadacitinib - An Up-and-Comer for Treatment of Giant-Cell Arteritis
NEJM 392:2062-2064, Koster,M.J. & Warrington,K.J., 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

Showing articles 850 to 900 of 17368 << Previous Next >>