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Differential
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abdominal distention

abducens nerve paralysis

abortion, spontaneous

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acute disseminated encephalomyelitis

acute necrotizing encephalitis

addiction, heroin

Addison's disease

adrenal crisis, acute

adrenal medullary tissue

advances in neurology

adverse drug reaction

agenesis of aqueduct of Sylvius

agenesis of corpus callosum

aggression

Aicardi-Goutieres syndrome

Aicardi's syndrome

airway obstruction

alcohol

alcohol, neurologic complications with

Aldrich's syndrome

Alexanders disease

Alexanders disease, adult onset

algorithm

alopecia

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

alveolar hypoventilation

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, iatrogenic

amyotrophic lateral sclerosis

aneurysm, intracranial

aneurysm, intracranial, development of new

aneurysm, intracranial, developmental

aneurysm, intracranial, growth

aneurysm, intracranial, natural history

aneurysm, intracranial, treatment of

aneurysm, multiple intracranial

aneurysm, size

Angelman syndrome

angiography, cerebral

angiokeratoma

angiotensin-converting enzyme, inhibitors

antibiotics, neurologic complications with

anticoagulant, complications of

anticoagulant, reversal of

anticoagulant, treatment

anticonvulsants

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

apraxia of eye movements

aqueduct of Sylvius, stenosis

arteriovenous malformation

arteriovenous malformation, cerebral

arthralgia

arthritis

arthrogryposis multiplex

ataxia telangiectasia

atlanto-axial subluxation

atomic bomb

ATP1A3 gene

attention deficit disorder with hyperactivity

attention span

atypical

audiogram

auditory evoked brainstem potentials

auditory evoked potentials

autism

autoimmune disease

autoimmune epilepsy

autonomic dysfunction

B 12 deficiency

Babinski sign in new born

banana sign

Bannayan-Riley-Ruvalcaba syndrome

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

battered child syndrome

behavior modification

bitemporal visual field defect

blood dyscrasias, neurologic findings with

bone density, increased

bone marrow biopsy

bone marrow transplantation

bovine spongiform encephalopathy

brachial plexus neuropathy

brachial plexus neuropathy, familial

brain transplantation

Brown-Vialetto-Van Laere syndrome

burst suppression pattern, electroencephalogram

cabergoline

cachexia

cafe au lait spots

calcification, intracranial

calcification, intraventricular

calcification, periventricular

calcitonin

Canavan's disease

carbonic anhydrase II deficiency

carcinoembryonic antigen

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, metrizamide

cataracts

cataracts, congenital

cavernous sinus

cavernous sinus, metastasis to

cavum Vergae

celiac disease, adult

celiac disease, childhood

Central America

central hypoventilation, congenital

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebral cortex

cerebral cortical atrophy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, recurrent

cerebrovascular accident, severity

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, women

cerebrovascular accident, young adult

cerebrovascular disease, infant and childhood

Charcot-Marie-Tooth

chemotherapy, CNS treatment and complications with

cherry red spot

chilbran skin lesions

child abuse

children

cholelithiasis

chondrodysplasia punctata

chorea

choreoathetosis

chorionic gonadotropin

chorioretinitis

choroid plexus, tumor of

chromophobe adenoma

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cigarette smoking

cisterna magna, enlarged

cisternogram, radionuclide

citicoline

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

cocaine, intrauterine exposure

Cockayne's syndrome

codfish vertebrae

Coffin-Siris syndrome

cognition

cognitive delay

cold hands sign

collagen vascular disease

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myopathy

congenital myopathy, inflammatory

congestive heart failure

cornea, opacification in infancy-causes of

cornea, opacity of

corneal transplant

Cornelia de Lange syndrome

corpus callosum

corpus callosum, atrophy of

corpus callosum, thinning

cortical blindness

coumarin

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranial volume

craniopharyngioma

Craniosynostosis

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, high-pitched

cry, weak

cryopyrin-associated periodic syndrome

cryptorchidism

cultured skin fibroblasts

cyst, arachnoid, infant

cyst, arachnoid, location of

cyst, benign intracranial

cytochrome c oxidase, deficiency

cytokines

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

Dandy Walker malformation

deafness

deafness, congenital

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, childhood

dementia, rapidly progressive

dementia, transmissible

dentate nuclei

dentate nuclei, lesion of

depression

depression, psychotic

dermatitis

dermatitis herpetiformis

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

dexamethasone suppression test

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetic ketoacidosis

diagnostic criteria

diarrhea

diencephalic syndrome

diet

differential diagnosis

difficulty climbing stairs

disability, neurological

dislocated hip, congenital

disseminated intravascular coagulation(DIC)

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dopamine agonist

doppler, transcranial

drooling

drug abuse

drug abuse, toxic screen In

drug induced neurologic disorders

drug withdrawal

dural graft, cadaveric

dural sinus thrombosis

electroencephalogram, abnormalities of

electroencephalogram, complications with

electroencephalogram, depth electrode

electroencephalogram, periodic complexes

electroencephalogram, sleep spindles

electromyogram

electron microscopy

electrophoretic pattern, CSF

ELISA

embolization, therapeutic, coils

embryogenesis

emergencies, neurologic

empty sella

encephalitis, brainstem

encephalitis, sequelae in

encephalitis, viral

encephalocele

encephalopathy

encephalopathy, metabolic

encephalopathy, progressive

enterovirus infection of CNS

enzyme treatment

enzyme, defect

enzyme, muscle disease

epidemiology of neurology

epidermal nevus syndrome

epileptic encephalopathy

episodic disorders

erectile dysfunction

ethics in neurology

ethylmalonic aciduria

ethylmalonic encephalopathy

eye movement, disorders of

eyebrows, abnormal

eyes, sunken

facial anomalies

facial appearance, abnormal

facial asymmetry

facial expression abnormality

facial weakness, bilateral

fetal alcohol syndrome

fibrin split products

fibrinolytic agents

fibroblast growth factor

fibromyalgia

fine motor function, impaired

finger tapping

fingernails, abnormal

fingernails, hypoplastic

fluorescene in situ hybridization

foam cells

follicle stimulating hormone

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glioblastoma multiforme(astrocytoma Gr.III)

glucose tolerance test, abnormal

GLUT1

GLUT1 deficiency syndrome

gluten ataxia

gluten sensitivity

gluten-free diet

glycogen debranching enzyme deficiency

glycogen storage disease

growth hormone antagonist

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

head circumference and brain development

head injury

head injury, hypothalamic and pituitary damage

head injury, pediatric

head lag

headache

headache, children

headache, drug induced

headache, severe

headache, thunderclap

headache, worst of life

hearing loss

hearing problems in children

heart block

heart murmur

heart valve, prosthetic

heart valve, repair

hemangioma

hemifacial spasm

hemihypertrophy, congenital

hemiparesis

hemoglobin abnormality, neurologic complications of

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemorrhage, intracranial, newborn

hemorrhagic diathesis

heralding manifestation

hereditary multiple exostoses

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

Hirschprung's disease

human immunodeficiency virus type 1

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, exvacuo

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hydrocephalus, treatment of

hydroxyglutaric aciduria

hyperactivity

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypopigmentation of skin

hypopituitarism

hypoplastic left heart syndrome

hyporeflexia

hypotelorism

hypothalamus

hypothalamus, damage to

hypothalamus, disturbance of

hypothalamus, lesion of

hypothalamus, neoplasm of

hypothermia

hypothermia, causes of

hypothyroidism

hypothyroidism, congenital

iatrogenic neurologic disorders

imbalance

immunodeficiency

immunofluorescent exam of CSF cells

in situ hybridization

inability to stand on tiptoes

inborn errors of metabolism

inclusion bodies, intranuclear

increased intracranial venous pressure

infant, evaluation of

infantile spasm

infection

infection, recurrent

infectious mononucleosis

intellectual deterioration

intelligence quotient

interferon

interferon alpha

interferon inducer

interpupillary distance

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, small

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, children

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kearns-Sayre syndrome

ketogenic diet

Klinefelter's syndrome

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

kyphosis

lactate

lactic acidemia

laminar necrosis, cortical

language disorders in children

learning disability, in children

Leber's hereditary optic neuropathy

leg numbness

leg weakness, bilateral

leukemia, prophylactic treatment of CNS

leukoencephalopathy, differential diagnosis

leukotrienes

level of consciousness, decreased

lipid storage disorder of CNS

liver function enzymes

lymphocytic choriomeningitis

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lysosomal storage disease

malabsorption syndrome

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, Vein of Galen

malnutrition and brain development

megalencephaly, idiopathic

melanomatosis, primary malignant

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, late neurologic sequelae in

meningitis, neurologic aspects and complications of

mental status, abnormal

MERRF syndrome

mestinon

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

methadone

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

micrencephaly

microcephaly

micrognathia

microhemorrhage, intracerebral

microsurgery, transsphenoidal

midline defect in children

migraine

migraine, seizures in

Miller-Dieker syndrome

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

MNGIE syndrome

molecular genetics

molybdenum cofactor deficiency

monoamines

monoamines, brain

monoclonal antibodies

monoclonal gammopathy

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, angiography

MRI, angiography, serial

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

mucopolysaccharidoses

mucopolysacchariduria

multiple sclerosis

multiple system atrophy

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, LAMA2

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

mycotic aneurysm

myelination of nervous system

myelitis

myelitis, transverse

myeloma, osteosclerotic

myoclonus, stimulus sensitive

myopathy

myopathy, distal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myxedema, neurologic manifestations of

neonatal abstinence syndrome

neonatal infection, viral

neoplasm, hormone producing

neoplasm, hormone producing, ectopic

neoplasm, intracranial

neoplasm, intracranial with metastasis extracranially

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, pituitary

neoplasm, pituitary, incidental

neoplasm, pituitary, surgical treatment

neoplasm, pituitary, treatment of

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-infants

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

nerve growth factor

nerve growth stimulating activity

nerve root enhancement

neural tube defect

neuroblastoma

neurocutaneous disease

neurologic complications of, surgery

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory, hereditary

neuroprotective agents

newborn, evaluation of

nutritional deficiency

ocular motility, disorders of

old age, neurology of

ophthalmoplegia, progressive external

opiate

opportunistic infection

optic atrophy

optic atrophy, bilateral

optic atrophy, infants

optic atrophy, unilateral

optic foramina

optic foramina, abnormal

optic nerve

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

oral ulcerations

organ transplantation

organoid nevus syndrome

organomegaly

orthostatic hypotension

orthostatic hypotension, idiopathic

osteogenesis imperfecta

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

pain

pain, leg

palatal myoclonus

Pallister-Hall syndrome

palpebral fissure, short

pancytopenia

papilledema

paraparesis

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

paresthesias

paresthesias, hands

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinson disease, dystonia with

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

parvovirus

PAS positive

patent ductus arteriosus

pathology

patient information and support

penis, pigmented macules

perceptual-motor dysfunction

pergolide

periventricular leukomalacia

philtrum, hypoplastic

phocomelia

photophobia

photosensitivity, skin

pigmentary retinopathy

pituitary, dysfunction

pituitary, enlargement

pituitary, hormones of

pituitary, hyppoplasia

pituitary, lesion of

pituitary, microadenoma

plasma cell dyscrasia

plasmacytoma

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

plethora

pneumoencephalogram(PEG)

POEMS syndrome

polydactyly

polyhydramnios

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polyneuropathy

polyps, gastrointestinal tract

pons, atrophy

port wine nevus

posterior fossa, mass of

posterior pituitary ectopia

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primitive neuroectodermal tumors

progressive neurologic disorder

prolactin

prolactin, elevated

prolactinoma

protein 14-3-3, cerebrospinal fluid

proteinuria

proton beam therapy

pruritus

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

pulmonary infiltrates

pulmonary stenosis

pupil, abnormality in neurologic disorders

pupil, ectopic-congenital

pyramidal tract dysfunction

quadriparesis

quadriplegia

radiation hypersensitivity

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiation, ionizing

radiation, ionizing, intrauterine

radiculopathy

radioimmunoassay

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

reading problem, causes of

recombinant DNA

recurrent

red eye

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

research

respirations in CNS disease

respirator

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

retinal artery occlusion

riboflavin transporter deficiency

Schwartz-Jampel syndrome

sclerae, blue

sclerosis, bone

scoliosis

scoliosis, neurologic association with

seizure, drug resistance

seizure, focal

seizure, injury following

seizure, psychomotor-temporal lobe

seizure, withdrawal

sella turcica, enlargement of

sella turcica, hypoplasia of

sella turcica, tomography of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

sensory loss

septo-optic dysplasia

serologic testing

serum alanine aminotransferase

serum tumor markers

sexual intercourse

sexually transmitted disease

short neck

short stature

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

shunt procedure, ventriculo-peritoneal

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray

skull x-ray, abnormal

skull x-ray, bony defect on

sleep

sleep apnea

sleep apnea, central

sleep pathology and physiology

small for dates infant, problems in

small vessel disease

smiling

somatomedin-C

somatosensory evoked potentials

somatostatin analogue

speech disorder, childhood

speech, delayed development of

spina bifida

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

splenomegaly

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

stem cell transplantation

stent, venous sinus

steppage gait

stereotyped behavior

steroid therapy, CNS treatment and complications with

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subdural effusion

subdural hematoma

subdural hematoma, neonates and infants

subgaleal fluid collection

subtemporal decompression

suck, poor

sudden infant death syndrome

sulfite oxidase deficiency

superior orbital fissure syndrome

superior sagittal sinus thrombosis

suprasellar lesion

sweating, abnormality of

symmetric brain lesions

syphilis, diagnosis and treatment

syphilis, neurologic complications with

temporal lobe, lesion

testosterone, serum, low

tetracycline

third ventricle, mass of

thrombocytopenia

thrombocytosis

thyroid function tests

tissue plasminogen activator, intravenous

toe walking

tongue, enlarged

tongue, protrusion of

TORCH infections

toxoplasmosis, CNS

toxoplasmosis, congenital

transient neurologic deficit

transilumination of skull

transplacental virus infections

travel, foreign

treatment of neurologic disorder

trinucleotide repeats

trisomes

trisomy 9p

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

upgaze, paralysis of

urea-cycle enzymopathies

uric acid, low

urinary 17 hydroxycorticosteroids

urinary 17 ketosteroids

urinary incontinence

urine test for metabolic disorders

urine test in toxic screen

vaccinia

valvulopathy

Van der Knaap disease

varicella zoster virus

variola

vascular endothelial growth factor

ventriculogram, metrizamide

ventriculostomy

ventriculostomy, endoscopic

vertebral anomalies

vertebral-basilar insufficiency

vibratory sensation, abnormal

viral infection

viral infection, CNS

viral infection, transmission

Virchow-Robin spaces, dilated

viseromegaly

vision, blurred

visual acuity, decreased

visual evoked response

walking, difficulty with

weakness

weakness, generalized

weakness, progressive

white matter disease, periventricular

white matter disease, subcortical

x-linked mental retardation

x-ray, cervical spine

yawning movements

Zika virus infection

Showing articles 150 to 200 of 289 << Previous Next >>

Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections
Neuroradiology 33:239-242, Sugita,K.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
JAMA 264:605-609, 6221990., Yamazaki,J.N.&Schull,W.J., 1990

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Acromegaly
NEJM 322:966-977, Melmed,S., 1990

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Acromegaly in an Infant
Pediatrics 83:998-1002, Blumberg,D.L.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Reversible Suprasellar Pituitary Mass Secondary to Hypothyroidism
JAMA 262:3175, 31771989., Atchison,J.A.,et al, 1989

Pediatric Acquired Immunodefieiency Syndrome
Am J Dis Child 142:29-35, Belman,A.L.,et al, 1988

Human Growth Hormone Therapy & Creutzfeldt-Jakob Disease:A Drama in Three Acts
Pediatrics 81:85-92, Brown,P., 1988

Difference Between Herpes Simplex Virus Type I & Type 2 Neonatal Encephalitis in Neurological Outcome
Lancet 1:1-4, Corey,L.,et al, 1988

Neonatal Brain Tumors:CT & MR Findings
J Comput Assist Tomogr 12:10-20, Radkowski,M.A.,et al, 1988

Neurofibromatosis 2 (Bilateral Acoustic Neuro-fibromatosis)
NEJM 318:684-688, Martuza,R.L.&Eldridge,R., 1988

The Decline and Fall of Creutzfeldt-Jakob Disease Associated with Human Growth Hormone Therapy
Neurol 38:1135-1137, Brown,P., 1988

Creutzfeldt-Jakob Disease Following Pituitary-Derived Human Growth Hormone Therapy:A New American Case
Neurol 38:1131-1133, Marzewski,D.J.,et al, 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Radiological Case of the Month:3rd Ventricle Arachnoid Cyst
Am J Dis Child 142:1081-1082, Wells,R.G.,et al, 1988

Myopathy and Cystine Storage in Muscles in a Patient with Nephropathic Cystinosis
NEJM 392:1461-1464, Gahl,W.A.,et al, 1988

Isolated Growth Hormone Deficiency after Cerebral Edema Complicating Diabetic Ketoacidosis
NEJM 316:857-859, Keller,R.J.&Wolfsdorf,J.I., 1987

Does Growth Hormone Cause Relapse of Brain Tumors
Lancet 1:711-713, Clayton,P.E.,et al, 1987

Pituitary Growth Hormone from Human Cadavers:Neurologic Disease in Ten Recipients
Neurol 37:1211-1213, Rappaport,E.B.&Graham,D.J., 1987

Iatrogenic Creutzfeldt-Jakob Disease
Neurol 37:1520-1522, Rappaport,E.B., 1987

Computed Tomographic Findings of Brain & Skull in Myotonic Dystrophy
JNNP 50:435-438, Avrahami,E.,et al, 1987

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

Transplantation in Parkinson's Disease:Two Cases of Adrenal Medullary Grafts to the Putamen
Ann Neurol 22:457-468, Lindvall,O.,et al, 1987

The Dandy-Walker Syndrome
In Handbk of Clin Neurology, Elsevier Publ, Amsterdam, 50:32387., Epstein,M.H.&Johanson,C.E., 1987

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Ultrasound Screening for Spina Bifida:Cranial & Cerebellar Signs
Lancet 2:72-74, Nicolaides,K.H.,et al, 1986

Cavum Vergae, Association with Neurologic Abnormality & Diagnosis by Magnetic Resonance Imaging
Arch Neurol 43:821-823, Miller,M.E.,et al, 1986

Neurologic Correlates of Osteogenesis Imperfecta
Arch Neurol 43:150-152, Tsipouras,P.,et al, 1986

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Neurologic Manifestations of the Organoid Nevus Syndrome
Arch Neurol 42:236-240, Clancy,R.R.,et al, 1985

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Human Growth Hormone & Creutzfeldt-Jakob Disease
Ann Int Med 103:288-289, Raiti,S., 1985

Creutzfeldt-Jakob Disease in a Young Adult with Idiopathic Hypopituitarism, Relation to Growth Hormone
NEJM 313:731-733, Koch,T.K.,et al, 1985

Clinical & Path Features & Lab Confirmation of Creutzfeldt-Jakob Disease with Pituitary Derived Human Growth Hormone
NEJM 313:734-738, Gibbs,C.J.,et al, 1985

Potential Epidemic of Creutzfeldt-Jakob Disease from Human Growth Hormone Therapy
NEJM 313:728-731, Brown,P.,et al, 1985

Increased Head Circumference in Patients with Duchenne Muscular Dystrophy
Ann Neurol 17:620-621, Schmidt,B.,et al, 1985

Mitochondrial Myopathies
Ann Neurol 17:521-538, DiMauro,S.,et al, 1985

Coffin-Siris Syndrome, Neuropathologic Findings
Arch Neurol 42:350-353, DeBassio,W.A.,et al, 1985

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

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

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