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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 1400 to 1450 of 2452 << Previous Next >>

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

Brief Report:Deletion of the Dystrophin Muscle-Promoter Region Associated with X-Linked Dilated Cardiomyopathy
NEJM 329:921-925, 9601993., Muntoni,F.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Epstein-Barr Virus DNA in Cerebrospinal Fluid from Patients with AIDS-Related Primary Lymphoma of the Central Nervous System
Lancet 342:398-401, Cinque,P.,et al, 1993

Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
Pediatrics 91:988-989, Moorman,C.M.&Elston,J.S., 1993

Atypical Leber's Hereditary Optic Neuropathy with Molecular Confiramtion
Arch Neurol 50:470-473, Weiner,N.C.,et al, 1993

Leber's Hereditary Optic Neuropathy, New Genetic Considerations
Arch Neurol 50:540-548, Newman,N.J., 1993

Identical Twins with Similar Onset of Parkinson's Disease:A Case Report
Neurol 43:1159-1161, Pahwa,R.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Seizure Characteristics in Chromosome 20 Benign Familial Neonatal Convulsions
Neurol 43:1355-1360, Ronen,G.M.,et al, 1993

Toxoplasmic Encephalitis in Patients with the Acquired Immunodeficiency Syndrome
NEJM 329:995-1000, Luft,B.J.,et al, 1993

Choroid Plexus Infection in Cerebral Toxoplasmosis in AIDS Patients
Neurol 43:2035-2040, Falangola,M.F.&Petito,C.K., 1993

Randomized Trial of Dapsone & Aerosol Pentamidine for Prophylaxis of Pneumocystis Carinii Pneumonia & Toxoplasmic Enceph
Am J Med 95:573-583, Torres,R.A.,et al, 1993

Neurosurgical Management of the Acquired Immunodeficiency Syndrome
West J Med 158:249-253, Andrews,B.T.&Kenefick,T.P., 1993

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

MR Imaging of the Brain in Patients with AIDS:Value of Routine Use of IV Gadopentetate Dimeglumine
AJR 160:153-157, Jensen,M.C.&Brant-Zawadzki,M., 1993

Movement Disorders with Cerebral Toxoplasmosis and AIDS
Movement Disorders 8:107-112, Nath,A.,et al, 1993

Neurologic Prognosis of Cytomegalovirus Polyradiculomyelopathy in AIDS
Neurol 43:493-499, Cohen,B.A.,et al, 1993

Peripheral Nervous System Involvement in Large Cohort of HIV-Infected Individuals
Arch Neurol 50:167-171, Barohn,R.J.,et al, 1993

Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993

Subcortical Dementia
BMJ 307:1-2, Dunne,F.J., 1993

Interferon Beta-1b is Effective in Relapsing-Remitting MS
Clinical Results of a Placebo-Controlled Trial, IFNB MS Study Grp, Neurol 43:655-661, 64193., , 1993

Interferon Beta-1b is Effective in Relapsing Remitting MS, MRI Analysis Results of Placebo-Control Trial
Neurol 43:662-667, 6411993., Paty,D.W.,et al, 1993

Tourette's Syndrome in Monozygotic Twins:Relationship of Tic Severity to Neuropsychological Function
Arch Neurol 50:725-728, Randolph,C.,et al, 1993

Late-Onset Friedreich's Ataxia, Molecular Genetics, Clinical Neurophysiology, and Magnetic Resonance Imaging
Arch Neurol 50:803-806, Klockgether,T.,et al, 1993

The Photic Sneeze Reflex:Literature Review and Discussion
Neurol 43:868-871, Whitman,B.W.&Packer,R.J., 1993

The DNA Laboratory and Neurolgoical Practice
JNNP 56:229-233, Harding,A., 1993

Nature and Incidence of Peripheral Nerve Syndromes in HIV Infection
JNNP 56:372-381, Fuller,G.N.,et al, 1993

Cytomegalovirus Ventriculoencephalitis in AIDS, A Syndrome with Distinct Clin & Path FEatures
Medicine 72:67-77, Kalayjian,R.C.,et al, 1993

Unsuspected Varicalla-Zoster Virus Encephalitis in a Child with Acquired Immunodeficiency Syndrome
J Pediatr 123:418-422, Silliman,C.C.,et al, 1993

Asymptomatic and Neurologically Symptomatic HIV-Seropositive Subjects:Results of Long-Term MR Imaging and Clinical Follow-up
AJR 188:727-733, Post,M.J.D.,et al, 1993

Therapy for Human Immunodeficiency Virus Infection
NEJM 328:1686-1695, Hirsch,M.S.&D'Aquila,R., 1993

Ziduvudine Treatment of the AIDS Dementia Complex:Results of a Placebo-Controlled Trial
Ann Neurol 33:343-349, Sidtis,J.J.,et al, 1993

Diffuse Microgliosis Associated with Cerebral Atrophy in the Acquired Immunodeficiency Syndrome
Ann Neurol 34:65-70, Gelman,B.B., 1993

What Cuases Brain Atrophy in Human Immunodeficiency Virus Infection?
Ann Neurol 34:128-129, Petito,C.K., 1993

Human Immunodeficiency Virus Type 1 Infection and Myopathy:Clinical Relevance of Zidovudine Therapy
Ann Neurol 34:206-211, Grau,J.M.,et al, 1993

Myopathies Assoc with HIV and Zidovudine:Can Their Effects be Distinguished?
Neurol 43:971-976, Simpson,D.M.,et al, 1993

Optic Neuritis and HIV-1 Infection
JNNP 56:705-707, Sweeney,B.J.,et al, 1993

Vitamin B12 Deficiency and Nervous System Disease in HIV Infection
Arch Neurol 50:807-811, Robertson,K.R.,et al, 1993

White Matter Lesions and Cerebral Atrophy on MR Images in Patients with and without AIDS Dementia Complex
AJR 161:177-181, Broderick,D.F.,et al, 1993

The Prevalence of CT Abnor of the Cerebrum in 100 Consecutive Children Symptomatic with the HIV
Ann Neurol 34:198-205, DeCarli,C.,et al, 1993

Opportunistic Cerebral Vasculopathy & Stroke in Patients with Acquired Immunodeficiency Syndrome
Arch Neurol 50:430-432, Kieburtz,K.D.,et al, 1993

Relationship of CD4 Counts to Neurophysiological Function to HIV-1-Infected Homosexual Men
Arch Neurol 50:517-521, Boccellari,A.A.,et al, 1993

False Positive Tests for HIV in a Woman with Lupus and Renal Failure
NEJM 328:1281-1282, Jindal,R.,et al, 1993

Human Immunodeficiency Virus-Related Headache
Neurol 43:1098-1100, Brew,B.J.&Miller,J., 1993

Progressive Multifocal Leukoencephalopathy in 47 HIV-Sero (+) Pts:Neuroimaging, Clin, Path Correl
Radiolgoy 187:233-240, Whiteman,M.L.H.,et al, 1993

Human Immunodeficiency Virus Type 1 Infection of the Nervous System:Pathogenetic Mechanisms
Ann Neurol 33:429-436, Epstein,L.G.&Gendelman,H.E., 1993

CNS Lymphomatoid Granulomatosis in AIDS:CT and MR Appearances
AJR 161:381-383, George,J.C.,et al, 1993

Cryptococcal Meningitis after Unusual Exposures to Birds
NEJM 328:1354-1355, Fessel,W.J., 1993



Showing articles 1400 to 1450 of 2452 << Previous Next >>