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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
apraxia
areflexia
arrhythmia, cardiac
arthralgia
arylsulfatase A
arylsulfatase B
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
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
brain atrophy
brain biopsy
brainstem
brainstem, atrophy
brainstem, lesion of
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
CAG repeats
calcification, intracranial
Canavan's disease
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
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
children
choking
chorea
choreoathetosis
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
coma
complications
cone-rod dystrophy
confusion
conjunctival biopsy
conjunctivitis
consanguinity
contractures, joint
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
dwarfism
dysarthria
dyschromatopsia
dysmetria
dysmorphic
dysphagia
dyspraxia
dystonia
ear, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
emergencies, ocular
empty sella
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
enophthalmous
enzyme, defect
episodic disorders
equinovarus
evoked potentials
exercise intolerance
exome sequencing
eye injury
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial nerve palsy
failure to thrive
falling
false negative
familial
fatigue
feeding disorder
fever
fever, recurrent
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
funduscopic exam
gait disorder
galactocerebrosidase
gangliosidosis GM2
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
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
handwriting
head circumference
head lag
headache
hearing loss
hearing loss, bilateral
hearing problems in children
heart block
heel-knee-shin test
hemiparesis
hepatomegaly
hexosaminidase-A
hirsutism
HLA
hydrocephalus
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
hypogonadism
hypotonia
hypotonia, infants
imbalance
immunofluorescence
inborn errors of metabolism
inclusion bodies
infantile bilateral striatal necrosis
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracranial hypertension, benign
intracranial pressure, increased
intrauterine
iritis
iron, brain
irritability
Jewish
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
lysosomes, abnoral
macrocephaly
macular degeneration
marche a petits pas
Marcus Gunn pupil
MELAS syndrome
memory, impairment of
meningioma
meningitis, aseptic
meningitis, carcinomatous
meningitis, chronic
mental retardation
MERRF syndrome
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methylmalonic aciduria
microcephaly
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
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
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
negative
nerve biopsy
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
rash
recurrent
red eye
red free light
red free light, fundus exam with
refractive errors
Refsum's disease
renal failure
respiratory failure
retina, abnormal
retinal degeneration
retinal detachment
retinal ischemia
retinal lesion
retinal nerve fiber layer
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinitis pigmentosa
retinoblastoma
retinopathy
retropulsion
review article
RFLPs
rigidity
Romberg's sign
Schilder's disease
sclerosteosis
scoliosis
scotoma
scotoma, central
screening
sea-blue histiocytes
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
strokelike episodes
substantia nigra
sudden death
sural nerve
symmetric brain lesions
syndactyly
systemic illness
tapetoretinal degeneration
Tay-Sachs disease
thalamus, lesion of
titubation
tongue, enlarged
tonic spasms
trauma
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
war
weakness
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
Wolfram syndrome
x-linked hydrocephalus
Showing articles 750 to 800 of 4512 << Previous Next >>

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Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
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Teaching NeuroImage: The House Soign in Behavioral Varianht Frontotemporal Dementia
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A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
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Progressive Headache and Diplopia in an 89-Year-Old Man
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Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
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A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
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RNF213 Polymorphisms in Intracranial Artery Dissection
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A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
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Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
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Clinical Reasoning: A 39-Year-Old Returning traveler with Acute Encephalopathy and Strokes
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Clinicopathologic Conference, Cryptococcal Meningoencephalitis
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Ictal Whistling Associated with Dominant Parahippocampal Gyrus Cortical Dysplasia
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MR Imaging Findings in Anti-Leucine-Rich Glioma Inactivated Protein 1 Encephalitis:A Systematic Review and Meta-Analysis
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Giant Cell Arteritis With Optic Perineuritis
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Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and Children
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Congenital and Acquired Chiari Syndrome
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Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
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Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
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Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
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Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
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Clinical Features, Diagnosis and Management of Klinefelter Syndrome
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MR Restricted Diffusion in Anterior Ischemic Optic Neuropathy in Giant Cell Arteritis
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Vascular Malformations of the Central Nervous System
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Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
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Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
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Neurovascular Complications of Iatrogenic Fusarium solani Meningitis
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Ischemic Retinopathy from Prolonged Orbital Compression
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Multiple "Rings" in the Brain
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Primary Brain Tumours in Adults
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Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
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Trial of Botulinum Toxin for Isolated or Essential Head Tremor
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A 22-Year-Old Man with Multifocal Brain and Osseous Lesions
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Showing articles 750 to 800 of 4512 << Previous Next >>