Neudle.com: nerve growth stimulating activity

Differential
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abducens nerve paralysis

abortion, spontaneous

acetazolamide

acoustic nerve

acoustic neurinoma

acoustic neurinoma, bilateral

acquired immunodeficiency syndrome

acrochordon

acromegaly

acute disseminated encephalomyelitis

acute necrotizing encephalitis

adrenal medullary tissue

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

Aicardi's syndrome

Alexanders disease

Alexanders disease, adult onset

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Alzheimer's disease

amenorrhea

aminoacidopathies

amyotrophic lateral sclerosis

anticoagulant, complications of

anticoagulant, treatment

apraxia of eye movements

aqueduct of Sylvius, stenosis

arbovirus

areflexia

arthralgia

arthrogryposis multiplex

ataxia telangiectasia

atlanto-axial subluxation

ATP1A3 gene

audiogram

auditory evoked brainstem potentials

auditory evoked potentials

autoimmune epilepsy

autonomic dysfunction

B 12 deficiency

basal ganglia, calcification of

basilar impression

behavioral disorder

bevacizumab

bitemporal visual field defect

bone density, increased

bone marrow biopsy

bone marrow transplantation

bovine spongiform encephalopathy

bradycardia

brain biopsy

brain scan

brain transplantation

Brown-Vialetto-Van Laere syndrome

bulbar palsy

burst suppression pattern, electroencephalogram

cabergoline

cachexia

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

cataracts

cataracts, congenital

cavernous sinus

cavernous sinus, metastasis to

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar degeneration

cerebellar hypoplasia

cerebral cortical atrophy

cerebral palsy

cerebral venous thrombosis

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, xanthochromia of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chromosomal abnormality

chromosome 11

chromosome 3

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

cocaine

cocaine, intrauterine exposure

Cockayne's syndrome

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

Cornelia de Lange syndrome

cortical blindness

coumarin

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

cry, weak

cryopyrin-associated periodic syndrome

cryptorchidism

cultured skin fibroblasts

cytochrome c oxidase, deficiency

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

deafness

deafness, congenital

degenerative diseases of CNS

dementia

dementia, rapidly progressive

dementia, transmissible

depression

depression, psychotic

dermatitis

developmental disability

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diagnostic criteria

diarrhea

differential diagnosis

diplopia

dissociated sensory loss

dopamine agonist

drooling

drug abuse

drug induced neurologic disorders

dural sinus thrombosis

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

electron microscopy

emergencies, neurologic

empty sella

encephalitis, brainstem

encephalopathy

encephalopathy, progressive

epidemiology of neurology

eye movement, disorders of

eyes, sunken

facial anomalies

facial appearance, abnormal

facial asymmetry

facial nerve palsy

facial weakness

facial weakness, bilateral

gastrointestinal motility

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

glioblastoma multiforme(astrocytoma Gr.III)

glucose tolerance test, abnormal

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

headache, drug induced

headache, severe

headache, thunderclap

headache, worst of life

hearing loss

hearing problems in children

heart block

hemifacial spasm

hemiparesis

hemorrhage, intracranial, newborn

hemorrhagic diathesis

heparin

hepatomegaly

hepatosplenomegaly

heralding manifestation

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis 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

human immunodeficiency virus type 1

Hunter's syndrome

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, non-communicating(obstructive)

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hydrocephalus, treatment of

hyperbilirubinemia

hyperhidrosis

hyperhomocysteinemia

hyperpigmentation of skin

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypopigmentation of skin

hypopituitarism

hyporeflexia

hypothyroidism

hypothyroidism, congenital

hypotonia

hypotonia, infants

iatrogenic neurologic disorders

imbalance

immunodeficiency

immunofluorescent exam of CSF cells

immunosuppression

impotence

impulsivity

inclusion bodies, intranuclear

infantile spasm

infection

infection, recurrent

infectious mononucleosis

insect repellent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon

interferon alpha

interferon inducer

intestinal pseudoobstruction

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

iodine deficiency

iododeoxyuridine

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, variant

jaundice

joint hypermobility

Kearns-Sayre syndrome

Klinefelter's syndrome

kyphoscoliosis, neurologic causes of

lactate

lactic acidemia

laminar necrosis, cortical

lanreotide

Leber's hereditary optic neuropathy

level of consciousness, decreased

liver function enzymes

lysosomal storage disease

macrocephaly

macular degeneration

malformation, CNS, congenital

MELAS syndrome

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningoencephalitis

menses

mental retardation

mental status, abnormal

MERRF syndrome

metabolic acidosis

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

microcephaly

micropthalmia

microsurgery

microsurgery, transsphenoidal

migraine

migraine, seizures in

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

monoclonal gammopathy

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, disappearing lesion on

mucopolysaccharidoses

multiple sclerosis

multiple system atrophy

mumps virus

muscle biopsy

muscle weakness

muscle weakness, proximal

mutism

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis

myelitis, transverse

myeloma, osteosclerotic

myopathy, mitochondrial

myxedema, neurologic manifestations of

nausea and vomiting

neck, webbed

negative

neonatal infection, viral

neoplasm, intracranial with metastasis extracranially

neoplasm, pituitary

neoplasm, pituitary, treatment of

neoplasm, primary intracerebral

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-incidence of

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

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurofibromatosis 2

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, focal

neuropathology, brain

neuropathy

neuropathy, diabetic

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, peripheral, treatment

neuropathy, sensory, hereditary

neuroprotective agents

ocular motility, disorders of

ophthalmoplegia

ophthalmoplegia, progressive external

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

organomegaly

orthostatic hypotension, idiopathic

osteogenesis imperfecta

Paget's disease, psychosis in

Paget's disease, spinal cord problem in

parasitic infection, CNS

paresthesias

Parkinson disease

Parkinson disease, dystonia with

Parkinson disease, surgical treatment of

Parkinson disease, treatment of

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pathology

patient information and support

pectus carinatum

pectus excavatum

pediatric neurology

periventricular leukomalacia

personality change

petechiae

pheochromocytoma

photosensitivity, skin

pigmentary retinopathy

pituitary, enlargement

pituitary, hormones of

pituitary, microadenoma

plasma cell dyscrasia

plasmacytoma

PLEDs

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

POEMS syndrome

polyhydramnios

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

polyneuropathy

polyps, gastrointestinal tract

pons, atrophy

precipitating factors

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

progressive neurologic disorder

prolactin, elevated

protein 14-3-3, cerebrospinal fluid

proteinuria

proton beam therapy

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pulmonary stenosis

pupil, abnormality in neurologic disorders

quadriparesis

radiation hypersensitivity

radiation necrosis

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

radiculopathy

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

renal failure

renal tubular acidosis

respiratory failure

retinal artery occlusion

riboflavin transporter deficiency

scoliosis, neurologic association with

seizure

seizure, children

seizure, focal

seizure, injury following

seizure, neonatal

seizure, psychomotor-temporal lobe

sella turcica, enlargement of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

septo-optic dysplasia

serologic testing

serum alanine aminotransferase

sexually transmitted disease

short neck

short stature

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

Shy-Drager syndrome

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray

skull x-ray, abnormal

skull x-ray, bony defect on

sleep apnea

small for dates infant, problems in

somatomedin-C

somatostatin analogue

spasticity

spinal cord, compression of

spinal muscular atrophy

splenomegaly

spongy degeneration of brain

status epilepticus

stem cell transplantation

stent, venous sinus

steroid therapy, CNS treatment and complications with

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

subdural hematoma

subdural hematoma, neonates and infants

subgaleal fluid collection

subtemporal decompression

superior orbital fissure syndrome

superior sagittal sinus thrombosis

suprasellar lesion

sweating, abnormality of

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

talk

telangiectases

temporal lobe, lesion

testosterone, serum, low

toxoplasmosis, congenital

transplacental virus infections

travel, foreign

treatment of neurologic disorder

trigeminal neuralgia

ultrasonography, head

upgaze, paralysis of

urine test for metabolic disorders

vaccinia

valvulopathy

varicella zoster virus

variola

vascular endothelial growth factor

vectors of infection

vein of Galen

ventriculostomy

ventriculostomy, endoscopic

vertebral-basilar insufficiency

viral infection

viral infection, CNS

viral infection, transmission

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

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

Mitochondrial Myopathies
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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

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome
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Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Clinicopathological Conference
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Clin. Path. Conference
Osteopetrosis, Malignant Juvenile Form, Case Record 37-1982, NEJM 307:735-74382., , 1982

Cockayne Syndrome
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Septo-optic Dysplasia in an Infant of a Diabetic Mother
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Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
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Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
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Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

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Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
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Neurological Complications of Infantile Osteopetrosis
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School Failure & Deafness After"Silent"Congenital Cytomegalovirus Infection
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Increased Nerve-growth Stimulating Activity in Disseminated Neurofibromatosis
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