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Differential
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Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
affect, inappropriate
akinetic mute
Alexanders disease
amniocentesis
asymptomatic
ataxia
attention deficit disorder with hyperactivity
auditory evoked brainstem potentials
Balint's syndrome
Bassen-Kornzweig syndrome
behavioral disorder
Binswanger disease
blindness
bone marrow transplantation
brain biopsy
brain scan, abnormal
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
cataracts
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
children
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
color vision
color vision, impaired
complications
conjunctival biopsy
corpus callosum, lesion of
cortical blindness
crying, pathologic
cultured skin fibroblasts
deafness
decerebrate posture
dementia
dementia, childhood
dementia, presenile
dementia, rapidly progressive
demyelinating disease
diet
DNA probes
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysmorphic
dysphagia
dysphasia
dyspraxia
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalopathy
enzyme, defect
epidemiology of neurology
erucic acid therapy
evoked potentials
familial
fatty acid, elevated plasma content
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gangliosidosis GM1
gangliosidosis, generalized
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
grasp reflex
Hallervorden Spatz disease
hearing loss
hearing problems in children
hepatomegaly
HMGcoA reductase inhibitors
hormone replacement
hyperpigmentation of skin
hyperreflexia
hypogonadism
hypotonia
impotence
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
intellectual deterioration
Kearns-Sayre syndrome
Kluver-Bucy syndrome
Krabbe's disease
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
lipid storage disorder of CNS
Lorenzo's oil
lovastatin
macular degeneration
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
misdiagnosis
mitochondrial disease
mortality
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, demyelinating disease
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
muscular dystrophy
myelodysplasia
myelomalacia
myopathy, mitochondrial
myopia
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
Niemann-Pick disease
night blindness
oleic acid therapy
ophthalmoplegia, plus syndrome
optic atrophy
optic nerve
optic neuropathy
paraparesis
paraparesis, familial spastic
paraparesis, spastic
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
peroxisomal disease
peroxisomes
personality change
pigmentary retinopathy
polyneuropathy
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
quadriparesis
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
seizure
seizure, neonatal
sensorineural hearing loss
skin, biopsy
skin, darkening of
somatosensory evoked potentials
spinal cord, lesion of
spinal cord, pathologic exam of
spinocerebellar degeneration
spongy degeneration of brain
steroid therapy, CNS treatment and complications with
symmetric brain lesions
tapetoretinal degeneration
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular atrophy
testicular biopsy
treatment of neurologic disorder
ultrasonography
urinary incontinence
Usher's syndrome
very long chain fatty acids
visual evoked response
visual field defect
visual loss
visual loss, slow
weight loss
white matter disease
white matter disease, unilateral
x-linked hydrocephalus
x-linked mental retardation
Showing articles 300 to 350 of 577 << Previous Next >>

Clinicopath Conf
Tuberculosis of Mediastinal Lymph Nodes, Case 3-1993, NEJM 328:195-202993., , 1993

Molecular Genetic Advances in Fragile X Syndrome
J Pediatr 122:169-185, Tarleton,J.C.&Saul,R.A., 1993

Tuberculosis Meningitis in the Southwest United States
Neurol 43:1775-1778, Davis,L.E.,et al, 1993

Comparison of Striatal 18F-dopa Uptake in Adult-Onset Dystonia-Parkinsonism, Parkinson's & Dopa-Responsive Dystonia
Neurol 43:1563-1568, Turjanski,N.,et al, 1993

Extradural Haematoma in a Child After an Apparently Mild Head Injury
BMJ 306:1665-1666, Nee,P.A.,et al, 1993

Risk of Sports Activities in Children with Down's Syndrome and Atlantoaxial Instability
Lancet 342:511-514, Cremers,M.J.G.,et al, 1993

Syncope After Eating
NEJM 328:1572, Schima,W.,et al, 1993

Communicating Hydrocephalus, Basilar Invagination, and Other Neurologic Features in Osteogenesis Imperfecta
Neurol 43:2603-2608, Charnas,L.R.&Marini,J.C., 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

Spinal Cord Compression from Epidural Metastases
NEJM 327:614-619, Byrne,T.N., 1992

Unilateral Diaphragmatic Paralysis:An Electrophysiological Study
JNNP 55:316-318, Lagueny,A.,et al, 1992

Referred FAcial Pain from Lung Carcinoma
Neurol 42:1841-1842, Bongers,K.M.,et al, 1992

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

Delayed Diagnosis of Pediatric Cervical Spine Injury
Pediatrics 89:1185-1188, Orenstein,J.B.,et al, 1992

Clinicopath Conf
PEOMS Syndrome, Case 39-1992, NEJM 327:1014-1021992., , 1992

The Sit-up Test:An Alternative Clinical Test for Evaluating Pediatric Torticollis
Pediatrics 90:612-615, Caputo,A.R.,et al, 1992

Horseback Riding and Head Injuries
Committee on Sports Medicine and Fitness, Pediatrics 89:5121992., , 1992

Clinicopath Conf
Churg-Strauss Syndrome, Case 18-1992, NEJM 326:1204-1212992., , 1992

Clinicopath Conf
Cat-Scratch Disease, with Encephalopathy, Case 22-1992, NEJM 326:1480-148992., , 1992

Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
Multicenter Study Group, JAMA 267:2609-26151992., , 1992

Guillain-Barre Syndrome after Chlamydia Pneumoniae Infection
NEJM 326:576-577, Haidi,S.,et al, 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

Intraosseous Meningioma:CT and MR Appearance
J Comput Assist Tomogr 16:1000-1001, Lee,H.,et al, 1992

Soft Tissue Swelling and Acute Skull Fractures
J Pediatr 121:737-739, Kleinman,P.K.&Spevak,M.R., 1992

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
NEJM 325:1720-1738, Sutherland,G.R.,et al, 1991

Clinicopath Conf
Case 50-1991, Renal Cell Carcinoma & Inflammatory Polyneuropathy (? paraneoplastic) , NEJM 325:1723-, 735, 199, 1991

Pleuropulmonary Disease Associated with Dopamine Agonist Therapy
Ann Neurol 30:613-616, Bhatt,M.H.,et al, 1991

Mental Retardation in Turner Syndrome
J Pediatr 118:415-417, VanDyke,D.L.,et al, 1991

More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation
Lancet 338:1562-1563, , 1991

Dopa-responsive Dystonia:[18F]Dopa Positron Emission Tomography
Ann Neurol 30:24-30, Sawle,G.V.,et al, 1991

The Phenotype of the X-Linked Dystonia-Parkinsonism Syndrome, An Assessment of 42 Cases in the Philippines
Medicine 70:179-187, Lee,J.V.,et al, 1991

Golf Related Head Injuries in Children
BMJ 302:1505-1506, Smith,R.A.,et al, 1991

Pneumocystis Carinii Pneumonia in Patients with Primary Brain Tumors
Arch Neurol 48:406-409, Henson,J.W.,et al, 1991

Prevalence and Incidence of Becker Muscular Dystrophy
Lancet 337:1022-1024, Bushby,K.M.D.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

MR Imaging of the Brain in Patients with Diabetes Insipidus
AJR 157:123-132, , 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Neuroanatomy of Fragile X Syndrome:The Posterior Fossa
Ann Neurol 29:26-32, Reiss,A.L.,et al, 1991

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
Roberts. R. G. , et al, Lancet 336:1523-1526., , 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Clinicopath Conf
Malignant Angioendotheliomatosis, Am J Med 88:522-5281990., , 1990

Posttraumatic Cerebral Infarction Diagnosed by CT:Prevalence, Origin, and Outcome
AJR 154:1293-1298, Mirvis,S.E.,et al, 1990



Showing articles 300 to 350 of 577 << Previous Next >>