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aciduria
acoustic nerve, vestibular division of
acoustic neurinoma
acoustic neurinoma, bilateral
acquired immunodeficiency syndrome
adrenal mass
advances in neurology
adverse drug reaction
Alexanders disease
algorithm
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, familial, late onset
Alzheimer's disease, pathogenesis
amniocentesis
amyloidosis
aneurysm
aneurysm, intracranial
aneurysm, intracranial, familial
anterior horn cell disease
antiviral agents
apolipoprotein E
APP
APP gene
areflexia
arrhythmia, cardiac
astrocytoma
ataxia
ataxia, cerebellar
ataxia, hereditary
atrial myxoma
audiogram
auditory evoked brainstem potentials
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
autonomic dysfunction
baclofen
basal ganglia, lesion of
basal ganglia, lesion, bilateral
blindness
brainstem, dysfunction
brainstem, lesion of
cafe au lait spots
CAG repeats
carcinoma
cardiomyopathy
CAT scan, abdomen
CAT scan, abnormal
cataracts
caudate nucleus, lesion of, bilateral
cavernous hemangioma
CD4 counts
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebral embolism
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, young adult
children
chorea
chromosomal abnormality
chromosome 1
chromosome 14
chromosome 17
chromosome 21
chromosome 22
chromosome 4
chromosome 5
chromosome 6
chromosome 9
coagulopathy
congenital heart disease
congenital myopathy
constipation
contractures, joint
cranial nerve tumor
creatine phosphokinase(CPK)elevated
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dentatorubral-pallidoluysian atrophy
developmental retardation
diet
differential diagnosis
DNA probes
dopa responsive dystonia
drug induced neurologic disorders
dysarthria
dyskinesia
dystonia
dystonia, children
Ehlers-Danlos syndrome
electromyogram
encephalitis, autoimmune
encephalopathy
endoscopy
enzyme, defect
ependymoma
Fabry's disease
facial weakness, bilateral
familial
fasciculation
fibromuscular dysplasia
fragile-X syndrome
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glioma
GLUT1
GLUT1 deficiency syndrome
glutamate dehydrogenase deficiency
hamartoma
headache
hearing loss
hemoglobin abnormality, neurologic complications of
hereditary hemorrhagic telangiectasia(HHT)
high arched palate
highly active antiretroviral therapy
history of neurology
HLA
homocystinuria
human immunodeficiency virus type 1
huntingtin
Huntington's chorea
hydrocephalus
hydrocephalus, treatment of
hypertension
hypoglycorrhachia
hyporeflexia
hypotonia
hypotonia, infants
immune reconstitution inflammatory syndrome
inborn errors of metabolism
intellectual deficit
interferon
interferon beta 1-a
interferon beta 1-b
intracerebral hemorrhage
intracerebral hemorrhage, young adult
iris, abnormal
iron, brain
islet cell tumor
karyotyping
ketogenic diet
learning disability
learning disability, in children
Legius syndrome
lenticular nucleus, lesion of, bilateral
life expectancy
Lisch nodules
long bone lesion
lordosis
lumbar puncture
lymphoma
macrocephaly
macular degeneration
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
meningioma
meningioma, familial
meningioma, multiple
mental retardation
merlin
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
MRI
MRI, abnormal
MRI, muscle
MRI, paramagnetic effect
MRI, spine
multiple sclerosis
multiple sclerosis, clinical patterns
multiple sclerosis, diagnosis of
multiple sclerosis, pathogenesis
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, Duchenne
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenic syndrome
myoclonic jerks
myopathy
myotonia dystrophica
neck weakness
nemaline rod myopathy
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-familial occurrence
nerve growth factor
neurocutaneous disease
neurofibroma
neurofibromatosis 1
neurofibromatosis 2
neurofibromatosis 2, presymptomatic
neurofibromin
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuronal degeneration
neuropathology
neuropathy
neurotomy
next-generation sequencing
NF1 gene
nusinersen
nystagmus
ocular motility, disorders of
ophthalmoplegia
optic atrophy
optic glioma
palatal myoclonus
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal exertion-induced dyskinesia
patient information and support
pheochromocytoma
polycythemia, primary
practice guidelines
preclinical
precocious puberty
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
presenilin-1 gene
presenilin-2 gene
prognosis
progressive neurologic disorder
protein C deficiency
pruritus
pseudarthrosis
pseudoxanthoma elasticum
Purkinje cell
pyramidal tract dysfunction
recombinant DNA
repetitive nerve stimulation
respiratory failure
retinal degeneration
retinitis pigmentosa
review article
RFLPs
rigid spine syndrome
Riley-Day syndrome
root lesion, nerve
Rosenthal fiber encephalopathy
Rosenthal fibers
schwannoma
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, familial
seizure, neonatal
seizure, petit mal
sensory ganglia
sensory ganglia, abnormal
shunt procedure, ventricular
Shy-Drager syndrome
sickle cell disease
skin, lesions in neurologic disorders
skull x-ray, abnormal
skull x-ray, bony defect on
slit lamp examination
SMN1 gene
spasticity
speech disorder
spinal cord
spinal cord degeneration
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, extramedullary intradural
spinal cord, neoplasm, intramedullary
spinal cord, neoplasm, neurofibroma
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
SPRED1 mutation
steroid
striatal encephalitis
survival motor neuron gene
symmetric brain lesions
third ventricle
thrombocytopenia
tinnitus
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tuberous sclerosis
type 1 muscle fiber
ubiquilin 1
urinary catecholamines
ventriculostomy
ventriculostomy, endoscopic
Von Hippel Lindau
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
web sites
white freckles
Wood's light
workup
X-linked bulbospinal neuronopathy
Showing articles 1450 to 1500 of 2452 << Previous Next >>

CNS Cryptococcosis in AIDS:Spectrum of MR Findings
J Comput Assist Tomogr 17:438-441, Andreula,C.F.,et al, 1993

Catastrophic Visual Loss Due to Cryptococcus Neoformans Meningitis
Medicine 72:207-224, Rex,J.H.,et al, 1993

Gadolinium-Enhanced MRI in a Patient with AIDS and the Ramsay-Hunt Syndrome
Neuroradiology 35:269, Li,J.,et al, 1993

Myoblast Transfer in Duchenne Muscular Dystrophy
Ann Neurol 34:8-18, Karpati,G.,et al, 1993

Tibial Muscular Dystrophy
Arch Neurol 50:604-608, Udd,B.,et al, 1993

Progressive Multifocal Leucoencephalopathy
Brit J Hosp Med 50:187-192, Sweeney,B.J.,et al, 1993

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome
Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993

Progr Myoclonus Epilepsy of Unverricht-Lundborg Type:Clin & Molecular Genetic Study from US 4 Affected Sibs
Neurol 43:2284-2286, Lehesjoki,A.E.,et al, 1993

Progressive Multifocal Leukoencephalopathy:Contrast Enhancement on CT Scans and MR Images
AJR 161:1049-1051, Wheeler,A.L.,et al, 1993

Cryptococcal Meningitis and AIDS
Clin Inf Dis 17:837-842, Powderly,W.G., 1993

Management of Cerebral Infection
JNNP 56:1243-1258, Anderson,M., 1993

Cranial Neuropathy Heralding Otherwise Occult AIDS-Related Large Cell Lymphoma
J Clin Neuro-Ophthalmol 13:113-118, Berger,J.R.,et al, 1993

Primary Central Nervous System Lymphomas-An Update
J Cancer Res Clin Oncol 119:7-27, Jellinger,K.A.&Paulus,W., 1992

Extrapyramidal side Effects of Antiemetics Presenting as Psychiatric Illness
Gen Hosp Psychiatry 14:192-195, Rodgers,C., 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

Tuberculous Meningitis with Acellular Cerebrospinal Fluid in AIDS Patients
AIDS 6:1165-1167, Laguna,F.,et al, 1992

HIV Encephalopathy and Dementia
Psychiatr Clin North Am 15:455-466, Pajeau,A.K.&Roman,G.C., 1992

HIV-1 Infection and IV Drug Use:Longitudinal Neuropsych Eval of Asymptomatic Subjects
Neurol 42:1924-1930, Selnes,O.A.,et al, 1992

Cognitive Assessment of Human Immunodeficiency Virus-Exposed Children
Am J Dis Child 146:1479-1483, Levenson,R.L.,et al, 1992

Cerebral Artery Aneurysms in Children Infected with Human Immunodeficiency Virus
J Pediatr 121:927-930, Husson,R.N.,et al, 1992

Sensory Testing in Human Immunodeficiency Virus Type 1-Infected Men
Arch Neurol 49:1281-1284, Gulevich,S.J.,et al, 1992

Toxoplasmosis of the Central Nervous System in the Acquired Immunodeficiency Syndrome
NEJM 327:1643-1648, Porter,S.B.&Sande,M.A., 1992

Hydrocephalus & Prominence of the Choroid Plexus:An Unusual CT Present, of Cerebral Toxoplasmosis in AIDS
Can Assoc Radiol J 43:55-59, Bourgouin,P.M.,et al, 1992

Brain Biopsy for Intracranial Mass Lesions in AIDS
Lancet 340:1135, , 1992

The Role of Stereotactic Biopsy in the Management of HIV-Related Focal Brain lesions
Neurosurgery 30:825-829, Chappell,E.T.,et al, 1992

Emergence of Optic Pathway Gliomas in Children with Neurofibromatosis-1 After Normal Neuroimaging
J Pediatr 121:584-587, Listernick,R.,et al, 1992

Diagnostic Outcome in Children with Mutliple Cafe au Lait Spots
Pediatrics 90:924-927, Korf,B.R., 1992

Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Familial Multiple Sclerosis:MRI Findings in Clinically Affected and Unaffected Siblings
JNNP 55:883-886, Teinari,P.J.,et al, 1992

Genetic Susceptibility to Multiple Sclerosis Linked to Myelin Basic Protein Gene
Lancet 340:987-991, Tienari,P.J.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Intrafamilial Heterogeneity in Hereditary Motor Neuron Disease
Neurol 42:1488-1492, Applebaum,J.S.,et al, 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

De-Novo Mutation in Hereditary Motor and Sensory Neuropathy Type I
Lancet 339:1081-1082, Hoogendijk,J.E.,et al, 1992

Werdnig-Hoffman Disease & Chronic Distal Spinal Muscular Atrophy with Apparent Autosomal Dom Inherit
Ann Neurol 32:404-407, Boylan,K.B.&Cornblath,D.R., 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Parkinson's Disease in Twins
Neurol 42:1453-1461, Vieregge,P.,et al, 1992

Morphometry, Histopathology, and Tomography of Cerebral Atrophy in the Acquired Immunodeficiency Syndrome
F. C. , Ann Neurol 32:31-40-1992., Gelman,B.B.&Guinto,Jr, 1992

Familial Inclusion Body Myositis:Evidence for Autosomal Dominant Inheritance
Neurol 42:897-902, Nevile,H.E.,et al, 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Spinal Cord Toxoplasma Lesion in AIDS:MR Findings
J Comput Assist Tomogr 16:817-819, Poon,T.P.,et al, 1992

A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig
Neurol 42:2251-2257, Mikati,M.A.,et al, 1992

Giant Axonal Neuropathy:Progressive Clinical and Radiologic CNS Involvement
Neurol 42:2220-2221, Richen,P.&Tandan,R., 1992



Showing articles 1450 to 1500 of 2452 << Previous Next >>