Neudle.com: nystagmus hereditary

Differential
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abducens nerve paralysis

acetazolamide

adenosine deaminase deficiency

adverse drug reaction

Africa

agenesis of corpus callosum

albinism

alcohol

alcohol, neurologic complications with

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

anemia

anosmia

anterior spinal artery

aphasia

apnea

apnea, primary central

apraxia of eye movements

areflexia

Arnold Chiari malformation

ataxia telangiectasia

atlanto-axial subluxation

ATP1A3 gene

autonomic dysfunction

autosomal rcessive spastic ataxia of Charlevoix-Saguenay

Babinski sign

bacterial infection

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign essential tremor

brainstem, dysfunction

brainstem, hypoplasia

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

Brown-Vialetto-Van Laere syndrome

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar peduncle

cerebellar vermis

cerebellum, disease of

cerebellum, neoplasms of

cerebral edema

cerebrospinal fluid

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, young adult

channelopathy

Chediak-Higashi syndrome

chromosomal abnormality

chromosome 11

chromosome 19

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

congenital malformation

congenital ocular motor apraxia

consanguinity

contractures, joint

conus medullaris, lesion of

corneal dystrophy

cough

cranial nerve palsies

cranial nerves

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

cultured skin fibroblasts

cyanide poison

deafness

deafness, bilateral progressive vs.unilateral acute

deafness, unilateral

degenerative diseases of CNS

dementia

dementia, familial

dementia, frontotemporal

dementia, presenile

demyelinating disease

developmental abnormality of brain

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, chemical

diabetes mellitus, neurologic manifestations of

diabetes mellitus, ocular complications in

diabetic cranialneuropathies

diagnostic criteria

differential diagnosis

diplopia

disconnection syndrome

down-beat nystagmus

down-beat nystagmus, primary position of gaze

electroencephalogram, abnormalities of

electromyogram

electronystagmography

electroretinograph

encephalopathy

enzyme, defect

epidemiology of neurology

episodic disorders

episodic neurologic deficits

evoked potentials

exercise

eye movement, disorders of

Fabry's disease

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

failure to thrive

falling

familial

familial hemiplegic migraine

familial periodic ataxia

fasciculation

feeding disorder

fever

finger nose finger test

fourth ventricle, enlargement of

Friedreich's ataxia

frontotemporal dementia, behavioral variant

fundus, abnormality of

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

granulomatosis with polyangiitis

granulomatous disease

hemophagocytic lymphohistiocytosis, cerebromeningeal

inborn errors of metabolism

inclusion bodies, intracytopasmic

incoordination

infantile bilateral striatal necrosis

infection, recurrent

intellectual deficit

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intracranial pressure, increased

iritis

irritability

Jakob-Creutzfeldt disease

kyphoscoliosis, neurologic causes of

kyphosis

lactic acidemia

Leber's congenital amaurosis

leukoencephalopathy, differential diagnosis

leukopenia

light-near dissociation, causes of

lipid storage disorder of CNS

livedo reticularis

lymphadenopathy

lymphoma involving CNS

lymphomatoid granulomatosis

macrocephaly

malformation, CNS, congenital

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

memory, impairment of

meningismus

meningitis, carcinomatous

microcephaly

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine

migraine, hemiplegic

misdiagnosis

mitochondrial disease

molecular genetics

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, spinal cord

multiple sclerosis, differential diagnosis of

multiple system atrophy

myasthenia gravis

myasthenia gravis, familial incidence of

myasthenia gravis, nystagmus in

myasthenia gravis, ocular

myasthenia gravis, sensory loss with

neoplasm, primary of CNS

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuromyotonia

neuronopathy

neuronopathy, sensory

neuroophthalmology

neuropathology

neuropathy

neuropathy, demyelinating

neuropathy, peripheral

neurotoxin

neutropenia

next-generation sequencing

Niemann-Pick disease

nystagmus

nystagmus, dissociated

nystagmus, gaze-evoked

nystagmus, gaze-paretic

nystagmus, hereditary

nystagmus, monocular

nystagmus, pendular

nystagmus, periodic

nystagmus, primary position of gaze

nystagmus, rotary

nystagmus, upbeating-in primary position of gaze

nystagmus, vertical

ocular motility, disorders of

ophthalmic artery occlusion

optical coherence tomography

optokinetic nystagmus, abnormal

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pleocytosis of cerebrospinal fluid

POLG1 gene

pons, hypoplasia

precipitating factors

pregnancy, neurologic complications in

pretectal syndrome

primary episodic ataxia

prion disease

prognosis

progressive neurologic disorder

pseudointernuclear ophthalmoplegia

psychiatric problems in neurologic disorders

psychological testing, neurologic problems

psychomotor retardation

psychosis

ptosis

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, light reflex, abnormal

Purkinje cell

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyramidal tract, uncrossed

pyruvate metabolism, abnormality of

quadriparesis

quadriplegia

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

recurrent

release phenomena

renal tubular acidosis

rheumatoid arthritis, neurologic complications of

riboflavin transporter deficiency

rigidity

Romberg's sign

scoliosis

scoliosis, neurologic association with

seizure

seizure, children

sensorineural hearing loss

sensory loss

sensory loss, leg

skin, lesions in neurologic disorders

spinal cord, ischemic lesion of

spinal cord, neoplasm

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar degeneration

spinopontine atrophy, dominant

splenomegaly

spongy degeneration of brain

status epilepticus

steroid therapy, CNS treatment and complications with

stress, emotional

striatonigral degeneration

striatonigral degeneration, infantile

striatum, lesion of

striatum, lesion of, bilateral

subcortical U fibers

syphilis, neurologic complications with

thalamus, lesion of-bilateral

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

vertigo, treatment of

vestibular areflexia

vestibulopathy

vision, failure of in childhood

visual acuity, decreased

visual evoked response

Von Hippel Lindau

walking, difficulty with

walking, difficulty with in dark

weakness

weakness, generalized

weakness, progressive

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Familial Meningioma
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Convergence Nystagmus Associated with Arnold-Chiari Malformation
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A Large Kindred with Autosomal Dominant Parkinson's Disease
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Treatment of Late Infantile Metachromatic Leukodystrophy by Bone Marrow Transplantation
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Abnormalities of Horizontal Gaze, Clinical, Oculographic and Magnetic Resonance Imaging Findings, II Gaze Palsy and INO
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Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
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Electroencephalography Laboratory Diagnosis of Prolonged QT Interval
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Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
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Progress in Tuberous Sclerosis
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Neuropsychological Changes in Olivopontocerebellar Atrophy
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MRI in Familial Multiple Sclerosis
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A Comparison of Sporadic and Familial Multiple Sclerosis
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Excessive Muscular Fatigue in Patients with Spastic Paraparesis
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Combined Resting-Postural Tremor of Lower Limbs:Another Essential Trem, or Variant
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Prion Dementia Without Characteristic Pathology
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Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews
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Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
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Transvrse Myelitis and Spastic Paraparesis in a Patient with HIV Infection
NEJM 322:1322, Dodson,D., 1990

Familial Spastic Paraparesis Syndrome Associated with HTLV-I Infection
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Nicotine and Tobacco-Induced Nystagmus
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Recurrent Meningitis in a Patient with Congenital Deficiency of the C9 Component of Complement
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Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
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Showing articles 1350 to 1400 of 2207 << Previous Next >>