Neudle.com: "hyperphenylalaninemia"

Differential
(Click to cross reference)

acute disseminated encephalomyelitis

Addison's disease

amyloid angiopathy, cerebral

anemia

anemia, megaloblastic

anesthesia, general

angiitis, granulomatous of CNS

angiitis, isolated of CNS

attention deficit disorder with hyperactivity

Benedict's solution test

calcification, intracranial

carbon monoxide poisoning

carcinoma of pancreas

catecholamine

central nervous system, infection of

central pontine myelinolysis

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral ischemia

cerebral palsy

cerebral palsy, associated problems with

cerebral palsy, pure ataxic

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

chemotherapy, CNS treatment and complications with

congenital deformities

corpus callosum

corpus callosum, hypoplastic

cortical blindness

Cushing's syndrome

dementia

demyelinating disease

depression

developmental retardation

diet

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

diplegia, atonic

diplegia, spastic cerebral

disability, neurological

dystonia musculorum deformens

eczema

electroconvulsive therapy

electroencephalogram

electroencephalogram, abnormalities of

encephalitis

encephalitis, human immunodeficiency virus type 1

gamma amino butyric acid

genetic neurologic disorders

Gilles de la Tourette syndrome

gliomatosis cerebri

Guthrie test

hearing loss

hearing problems in children

hepatic encephalopathy

hepatic encephalopathy, treatment of

hepatolenticular degeneration(Wilson's disease)

homocystinuria

homovanillic acid

human immunodeficiency virus type 1

hypertensive encephalopathy

hyperthyroidism

hypoglycemia

hypoparathyroidism

hypopigmentation of skin

hypothyroidism

hypotonia

hypotonia, infants

inborn errors of metabolism

inborn errors of metabolism, screening

incoordination

intellectual deficit

intellectual deficit, treatable causes of

intellectual deterioration

intelligence quotient

karyotyping

klippel feil syndrome

language disorders in children

L-dopa

leg weakness, bilateral

leukodystrophy

leukoencephalopathy

leukoencephalopathy, differential diagnosis

limbic encephalitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

maple syrup urine disease

mental retardation

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

midline defect in children

migraine

mitochondrial disease

MRI, demyelinating disease

MRI, diffusion weighted

MRI, FLAIR

MRI, high signal foci on

MRI, negative

MRS

multiple sclerosis

multiple sclerosis, cognitive presenttion

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

neoplasm, intracranial

neoplasm, primary of CNS

palatopharyngeal incompetence

phenylketonuria, adult onset

phenylketonuria, maternal

phenylketonuria, variant form of

pheochromocytoma

porphyria

posterior leukoencephalopathy syndrome

pregnancy, neurologic complications in

prognosis

progressive multifocal leucoencephalopathy

progressive neurologic disorder

psychiatric manifestations of brain tumors

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

radiation therapy, CNS treatment and complications with

seizure, advice to parents and teachers regarding

seizure, psychosocial aspects of

seizure, treatment of

self harm

self-mutilation

skin, lesions in neurologic disorders

speech disorder, childhood

spina bifida

stuttering

subcortical U fibers

symmetric brain lesions

syphilis, neurologic complications with

systemic lupus erythematosus

tardive dyskinesia

torticollis

trauma

treatment of neurologic disorder

tremor

urine test for metabolic disorders

Showing articles 0 to 26 of 26

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Inherited Metabolic Diseases of the Nervous System, The Phenylketonuria
Adams & Victors Principles of Neurology, Chp 37, pg 968, Ropper, A.H.,et al, 2014

Overview of Phenylketonuria
UptoDate (May), Bodamer,O.A., 2008

Phenylketonuria
eMedicine (December), Arnold,G.L., 2007

Diffusion-Weighted Imaging and Proton MR Spectroscopy of White Matter Abnormalities in a Case of Phenylketonuria
Eur J Radiol Extra 54: 5-9, Teksam,M.,et al., 2005

Phenylketonuria Presenting in Adulthood as Progressive Spastic Paraparesis With Dementia
JNNP 71:795-797, Kasim,S.,et al, 2001

Diffusion-Weighted Imaging of White Matter Abnormalities in Patients with Phenylketonuria
AJNR 22:1583-1586, Phillips,M.D.,et al, 2001

Spastic Paraparesis after Anaesthesia
Lancet 353:554, Lee,P.,et al, 1999

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
J Pediatr 128:770-775, Levy,H.L.,et al, 1996

Phenylketonuria:Findings at MR Imaging & Localized in Vivo H-1 MR Spectroscopy of Brain in Pts with Early Treatment
Radiology 201:413-420, Pietz,J.,et al, 1996

Magnetic Resonance Imaging in Phenylketonuria:Reversal of Cerebral White Matter Change
J Pediatr 127:251-255, Cleary,M.A.,et al, 1995

Magnetic Resonance Imaging of the Brain in Phenylketonuria
Lancet 344:87-90, Cleary,M.A.,et al, 1994

Intellectual Development in 12-Year Old Children Treated for Phenylketonuria
Am J Dis Child 145:35-39, Azen,C.G.,et al, 1991

Cranial MR in Phenylketonuria
J Comput Assist Tomogr 14:458-460, Shaw,D.W.W.,et al, 1990

Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990

EEG in Phenylketonuria, Attempt to Establish Clinical Importance of EEG Changes
Arch Neurol 38:122-126, Gross,P.T.,et al, 1981

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

Hyperphenylalaninemia Due To A Deficiency of Biopterin
NEJM 299:673-679, Stanley,S.K.,et al, 1978

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Newborn Metabolic Screening:Past & Prospect
NEJM 293:824, Levy,H., 1975

Unrecognized Adult Phenylketonuria
NEJM 289:395, 1973, 289:1040, 1973, 290:1084., Perry,T.,et al, 1974

Organic Disease Presenting as a Psychiatric Syndrome
Postgrad Med 54:78, , 1973

Pediatric Neurology
Psych Annals 2:1, , 1972

New Kind of PKU
Pediatrics Consultant Sept 1971, pp 68-70., Johnson,C., 1971

Three Pediatric Problems That Worry Parents
Consultant, MayJun, p. 1270., Bakwin,H.,et al, 1970

Showing articles 0 to 26 of 26