Neudle.com: optic atrophy hereditary

Differential
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abiotrophy

aciduria

adolescent medicine

adrenoleukodystrophy

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

alcohol intolerance

alopecia

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

ammonia

anosmia

apnea

apnea, primary central

auditory evoked brainstem potentials

Babinski sign

basal ganglia

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Bassen-Kornzweig syndrome

battered child syndrome

behavioral disorder

Behr's optic atrophy

biotin deficiency

biotinidase deficiency

bitemporal visual field defect

blindness

blindness, sudden

bone density

bone density, increased

bone marrow transplantation

bulbar palsy, childhood

bulbar palsy, progressive

cachexia

CAG repeats

calcification, intracranial

CAT scan, false negative

cataracts

cerebellar ataxia, children

cerebellar atrophy, primary

cerebral cortical atrophy

cerebral edema, vasogenic

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, protein of

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

Charcot-Marie-Tooth

cherry red spot

cherry red spot-myoclonus syndrome

chromosomal abnormality

chromosome 19

chronic progressive external ophthalmoplegia

cisternogram, radionuclide

Clinical Pathologic Conference(C.P.C.)

clonus

clubbing of fingers

clubfoot as related to neurologic disease

Cockayne's syndrome

coenzyme Q10 deficiency

color vision

color vision, impaired

controversies in neurology

cornea, opacity of

corpus callosum

corpus callosum, hypoplastic

cortical blindness

cortical blindness, transient

cranial neuropathy, multiple

craniopharyngioma

cry, weak

crying

cryopyrin-associated periodic syndrome

cryptorchidism

cultured skin fibroblasts

deafness

deep gray nuclei

degenerative diseases of CNS

dementia

dementia, childhood

dementia, thalamic

demyelinating disease

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

diagnostic criteria

diplegia, brachial

diplopia

dissociated sensory loss

DNA probes

drug induced neurologic disorders

electroencephalogram, abnormalities of

electromyogram

electron microscopy

electronystagmography

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, progressive

eye movement, disorders of

eyes, sunken

facial appearance, abnormal

finger nose finger test

fingerprint bodies

flaccid paralysis

flow study, carotid artery

fluorescein angiography

Friedreich's ataxia

frontal bossing

frontal lobe, pathologic signs of

fundus, abnormality of

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic testing

globoid cells

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

growth retardation

Hallervorden Spatz disease

hearing loss, bilateral

hearing problems in children

hydrocephalus, complications with

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hydrocephalus, treatment of

hydrocephalus, viral induced

hyperreflexia

hypertrophic intracranial pachymeningitis

inborn errors of metabolism

inclusion bodies

infantile bilateral striatal necrosis

intellectual deficit

intellectual deterioration

intestinal pseudoobstruction

intracranial hypertension, benign

intracranial pressure, increased

Kearns-Sayre syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

Laurence-Moon-Bardet-Biedl syndrome

Leber's hereditary optic neuropathy

Leigh's disease

Leigh's disease, adult variety

lenticular nucleus, lesion of, bilateral

leukocyte enzyme abnormality

leukocytosis

leukodystrophy

light-near dissociation, causes of

lysosomal storage disease

memory, impairment of

meningioma

meningitis, aseptic

meningitis, carcinomatous

metabolic disorder, primary

metachromatic leukodystrophy

metachromatic leukodystrophy, juvenile

methylmalonic aciduria

microcephaly

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, optic nerve

MRI, serial

MRI, spinal cord

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, differential diagnosis of

muscle atrophy, progressive

muscle biopsy

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelitis, longitudinal

myopathy, mitochondrial

nerve conduction studies

neuroaxonal dystrophy

neuroendocrinology

neurolipidosis IV

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination

neurologic signs

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, ataxia, retinitis pigmentosa

neuropathy, hereditary peripheral

neuropathy, peripheral

night blindness

normal

nutritional deficiency

nystagmus

nystagmus, monocular

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

obesity

occipital lobe, lesion of

ophthalmoplegia

ophthalmoplegia, progressive external

opisthotonus

optic atrophy

optic atrophy, bilateral

optic atrophy, hereditary

optic chiasm

optic chiasm, enlarged

optic chiasm, lesion of

optic disc cup

optic disc edema

optic foramina

optic foramina, abnormal

optic glioma

optic nerve

optic nerve, compression of

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic nerve, neoplasm of

optic neuritis

optic neuritis, bilateral

optic neuritis, treatment of

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, hereditary

optic neuropathy, ischemic

optic neuropathy, nutritional

optic neuropathy, toxic

optic tract, lesion of

optical coherence tomography

osteopetrosis

owl's eye sign of spinal cord

palatal myoclonus

pancytopenia

papilledema

paraparesis, familial spastic

paraparesis, spastic

paraplegia

Parkinson disease

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive material in the brain

peroxisomal disease

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

polyneuropathy, familial

precipitating factors

pregnancy, neurologic complications in

prenatal diagnosis by amniocentesis

pretectal syndrome

prisoners of war, neurologic complications in

prognathism

prognosis

progressive neurologic disorder

propionic aciduria

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

ptosis

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

Purkinje cell

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadriparesis

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

red free light, fundus exam with

retinal nerve fiber layer

retinal vasculitis

retinal vasculopathy

retinal vasculopathy with cerebral leukodystrophy

sedimentation rate, elevated

seizure

seizure, children

seizure, neonatal

sensorineural hearing loss

sensory loss

short stature

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, biopsy

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

spastic diplegia

spasticity

speech disorder

speech disorder, childhood

speech, loss of

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, pathologic exam of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

spongy degeneration of brain

startle myoclonus

startle reaction

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stooped posture

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

symmetric brain lesions

syndactyly

systemic illness

tapetoretinal degeneration

treatment of neurologic disorder

tremor

tremor, intention

trigeminal nerve, lesion of

trigeminal neuropathy

trinucleotide repeats

umbilical-cord blood transplantation

upgaze, paralysis of

urea-cycle enzymopathies

urinary incontinence

urine test for metabolic disorders

Usher's syndrome

uveitis

ventricular enlargement

ventriculostomy, endoscopic

vestibular function, tests of

viral infection, CNS

vision loss, sequential

vision, blurred

vision, failure of in childhood

visual acuity

visual acuity, decreased

visual acuity, decreased, monocular

visual evoked response

visual field defect

visual fields, constricted

visual impairment

visual loss

visual loss, progressive

visual loss, slow

visual loss, sudden

vitamin deficiency

walking, difficulty with

white matter disease, subcortical

wide based gait

Wolfram syndrome

x-linked hydrocephalus

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Myostatin Mutation Associated with Gross Muscle Hypertrophy in a Child
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Doxycycline and Intracranial Hypertension
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Clinical Spectrum of Episodic Ataxia Type 2
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The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
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Imaging Cerebral Atrophy:Normal Ageing to Alzheimer's Disease
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Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
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Susac Syndrome:Report of Four Cases and Review of the Literature
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Comparison of Different MRI Brain Atrophy Rate Measures with Clinical Disease Progression in AD
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Brainstem Involvement in Hypertensive Encephalopathy
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