Neudle.com: "optic atrophy infants"

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abducens nerve paralysis

abducens nerve paralysis, bilateral

abducens nerve paralysis, children

abortion, spontaneous

aciduria

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

agenesis of corpus callosum

anticoagulant, complications of

anticoagulant, treatment

antiphospholipid antibodies

antiviral agents

apnea

aqueduct of Sylvius, obstruction

aqueduct of Sylvius, stenosis

arachnoiditis

areflexia

Argyll Robertson pupil

arthralgia

arthrogryposis multiplex

auditory evoked brainstem potentials

basal ganglia, lesion of

basal ganglia, lesion, bilateral

battered child syndrome

behavioral disorder

bitemporal visual field defect

blindness

bone biopsy

bone density

bone density, increased

bone marrow transplantation

brainstem, glioma in children

brainstem, neoplasms of

bruit

bruit, cranial

calcification, intracranial

Canavan's disease

CAT scan

CAT scan, abnormal

CAT scan, disappearing lesion on

CAT scan, false negative

CAT scan, serial

CAT scan, venography

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebral cortical atrophy

cerebral edema

cerebral folate deficiency syndrome

cerebral palsy

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, infancy and childhood

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

cisterna magna

Clinical Pathologic Conference(C.P.C.)

congenital infection, CNS

congenital infection, viral

congenital malformation

congestive heart failure

conjunctival biopsy

conjunctivitis

contractures, joint

controversies in neurology

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

cortical blindness

cortical blindness, transient

coumarin

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniectomy, decompressive

craniopharyngioma

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cyanosis

cyst, cortical parenchyma

cyst, ventricular

cysticercosis

cysticercosis, cerebral

cysticercosis, intraventricular

cysticercosis, subarachnoid

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

dementia

dementia, childhood

demyelinating disease

developmental disability

developmental milestones, loss of

developmental retardation

diabetes insipidus

differential diagnosis

diplopia

disability, neurological

dural sinus thrombosis

electroencephalogram, abnormalities of

electromyogram

electron microscopy

emergencies, neurologic

encephalopathy, metabolic

encephalopathy, neonatal

epidemiology of neurology

episodic disorders

episodic neurologic deficits

erythema migrans

evidence-based research

evoked potentials

exercise intolerance

eye injury

eye movement, disorders of

eye, pain in

facial weakness

facial weakness, bilateral

fibrinolytic agents, intra-venous local infusion

fine motor function, impaired

fingerprint bodies

floppy infant

flow study, carotid artery

folic acid

folic acid deficiency

fontanel, bulging

fourth ventricle, cyst

fourth ventricle, neoplasm of

frontal bossing

frontal lobe, pathologic signs of

fundus, abnormality of

gaze palsy, supranuclear

gene

gene mutation

genetic counselling

genetic diagnosis, prenatal

genetic neurologic disorders

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

head bobbing

head circumference

head injury

head injury, pediatric

hearing loss, bilateral

hearing problems in children

helminthic infection of CNS

hemianopia

hemianopia, homonymous

hemiparesis

hemorrhage, intracranial, newborn

Horner's syndrome, childhood

hydrocephalus

hydrocephalus, communicating

hydrocephalus, complications with

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, non-communicating(obstructive)

hydrocephalus, transient

hydrocephalus, treatment of

hypothalamus, lesion of

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracranial hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

learning disability, in children

Leber's hereditary optic neuropathy

lethargy

leukemia

leukemia, neurologic findings assoc.with

leukocytosis

leukodystrophy

level of consciousness, decreased

life expectancy

liver function enzymes

lumbar puncture, complications of

Lyme disease

Lyme disease, children

lymphoma

lymphoma involving CNS

lysosomal storage disease

lysosomes, abnoral

macrocephaly

macular degeneration

malformation, CNS, congenital

malformation, Vein of Galen

malignant optic glioma of adulthood

marche a petits pas

Marcus Gunn pupil

MELAS syndrome

memory, impairment of

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, bacterial-negative CSF culture

meningitis, basilar

meningitis, children

meningitis, chronic

meningitis, CSF cell count-normal

meningitis, cysticercosis

meningitis, eosinophilic

meningitis, factors influencing mortality in

meningitis, late neurologic sequelae in

meningitis, neurologic aspects and complications of

meningitis, pneumococcal

meningitis, spinal fluid smear and culture-negative

meningitis, TB

meningitis, treatment of

meningoencephalitis

mental retardation

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic aciduria

midbrain, neoplasm of

migraine, seizures in

misdiagnosis

mitochondrial disease

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, high signal foci on

neonatal infection, viral

neoplasm, intracranial

neoplasm, intracranial-presenting as head injury

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-children

neoplasm, pituitary

neoplasm, posterior fossa

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-intraventricular

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve biopsy

nerve conduction studies

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neuroendocrinology

neurofibromatosis 1

neurolipidosis IV

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic examination, focal

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathy

neuropathy, peripheral

nystagmus

nystagmus, see-saw

obesity

occipital lobe, lesion of

ophthalmoplegia

ophthalmoplegia, painful

optic atrophy

optic atrophy, bilateral

optic atrophy, infants

optic canal

optic canal, enlargement of

optic chiasm, enlarged

optic chiasm, lesion of

optic disc edema

optic glioma

optic nerve

optic nerve, compression of

optic nerve, enlarged

optic nerve, hypoplasia of

optic nerve, neoplasm of

optic neuritis

optic neuritis, bilateral

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

pars planitis

pediatric neurology

periventricular leukomalacia

petechiae

pitfalls

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pons, atrophy

pontine glioma

practice guidelines

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prethrombotic state

prevention of neurologic disorders

prognosis

progressive neurologic disorder

proptosis, unilateral

protein C deficiency

protein S deficiency

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pupil

pupil, abnormality in neurologic disorders

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

quadriparesis

quadriplegia

quality of life

radiation therapy, CNS treatment and complications with

sedimentation rate, elevated

sella turcica, enlargement of

sensorineural hearing loss

serologic testing

serum alanine aminotransferase

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, biopsy

skull x-ray

skull x-ray, abnormal

slit ventricle syndrome

small for dates infant, problems in

spasticity

spinal cord

spinal cord, lesion of

spinal cord, neoplasm

spinal cord, pathologic exam of

spirochete infection

splenomegaly

spongy degeneration of brain

startle reaction

stem cell transplantation

steroid therapy, CNS treatment and complications with

stillbirth

strabismus

subdural hematoma

subdural hematoma, neonates and infants

subgaleal fluid collection

superior sagittal sinus thrombosis

suprasellar lesion

sural nerve

symmetric brain lesions

tissue plasminogen activator, intravenous

titubation

Tolosa Hunt syndrome

trauma

treatment of neurologic disorder

tremor

trigeminal nerve

trigeminal nerve, abnormality of

trochlear nerve palsy

ultrasonography, head

umbilical-cord blood transplantation

urea-cycle enzymopathies

urine test for metabolic disorders

uveitis

vein of Galen

ventricle, slit-like, CAT scan

ventricular enlargement

ventriculostomy

ventriculostomy, endoscopic

vertigo

vision, blurred

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

walking, difficulty with

weight gain

white matter disease

white matter disease, subcortical

wide based gait

workup

x-linked hydrocephalus

Showing articles 0 to 50 of 4321 Next >>

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Hydrocephalus in Children
Lancet 387:788-799, Kahle, K.T.,et al, 2016

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

Intracranial Neoplasms and Paraneoplastic Disorders, Ependymoma
Adams & Victors Principles of Neurology, Chp 31, pg 655, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Tay Sachs Disease
Adams & Victors Principles of Neurology, Chp 37, pg 957, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuroaxonal Dystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 972, Ropper, A.H.,et al, 2014

A Young Man with Progressive Subcortical Lesions and Optic Nerve Atrophy
Neurol 79:e63, Komatsuzaki, S.,et al, 2012

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Contemporary management and recent advances in paediatric hydrocephalus
BMJ 343:d4191, Kandasamy, J.,et al, 2011

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Clinicopath Conf., Prolactinoma
NEJM 347:1604-1611, Case 35-2002, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Optic Neuropathy in Children With Lyme Disease
Pediatrics 108:477-481, Rothermel,H.,et al, 2001

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Acute Obstructive Hydrocephalus complicating Bacterial Meningitis in Childhood
BMJ 316:1887-1889, Mactier,H.,et al, 1998

Pitfalls in the Diagnosis of Ventricular Shunt Dysfunction:Radiology Reports and Ventricular Size
Pediatrics 101:1031-1036, Iskandar,B.J.,et al, 1998

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Neuro-Ophthalmic Manifestations of Lyme Disease
J Neuro-Ophthalmol 17:108-121, Balcer,L.J.,et al, 1997

Postoperative Cerebral Edema Occurring in Children with Slit Ventricles
Pediatrics 99:625-630, Eldredge,E.,et al, 1997

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Focal Tectal Tumors:Management and Prognosis
Neurol 44:953-956, Squires,L.A.,et al, 1994

Gliomas of the Anterior Visual Pathway
Surv Ophthalmol 38:427-452, Dutton, J., 1994

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

Craniopharyngyoma in Children
In Brain Tumors in Children, W B Saunders Co, Phila, Neurologic Clinics 9:453-46591., Sanford,R.A.&Muhbauer,S., 1991

Tuberculous Meningitis in Children:Treatment with Isoniazid and Rifampicin for Twelve Months
J Pediatr 114:875-879, Visudhiphan,P.&Chiemchanya,S., 1989

Vein of Galen Malformation: Diagnosis and Management
Neurosurgery 20:747-758, Johnston,I.H.,et al, 1987

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Clinicopathological Conference Metachromatic Leukodystrophy (juvenile type)
Case 7-1984, NEJM 310:445-4551984., , 1984

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

Ocular Defects in Children with Cerebral Palsy
BMJ 281:487-488, Black,P.D., 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Guillain-Barre Syndrome with Hydrocephalus in Early Infancy
Arch Neurol 34:567, Gilmartin,R.C.,et al, 1977

Neurological Complications of Infantile Osteopetrosis
Ann Neurol 2:378, Lehman,R.A.W.,et al, 1977

Acquired Sixth-Nerve Paresis in Children
Arch Ophthal 83:574-579, Robertson,D.M.,et al, 1970

Optic Atrophy in Childhood
Pediatrics 34:670, 1964 (Nov) ., Schwartz,J.F.,et al, 1964

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
www.UptoDate.com, Sept, Flanagan,E.P. & Tillema,J-M, 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Showing articles 0 to 50 of 4321 Next >>