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Differential
(Click to cross reference)
advances in neurology
algorithm
amniocentesis
anatomy of
Angelman syndrome
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
attention deficit disorder with hyperactivity
autism
autonomic dysfunction
Babinski sign
behavioral disorder
brain atrophy
CAG repeats
CAT scan
CAT scan, abnormal
cerebellar atrophy, primary
cerebellar degeneration
cerebellar hypoplasia
cerebellar lesion
cerebellar vermis
cerebellum
cerebral cortical atrophy
cerebrospinal fluid, enzymes in
children
chromosomal abnormality
cognition
controversies in neurology
corpus callosum
corpus callosum, lesion of
corpus callosum, thinning
cost effectiveness
counselling
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
developmental evaluation
developmental retardation
DNA probes
dysarthria
dysmetria
dysmorphic
ear, abnormal
electroencephalogram
erectile dysfunction
face, elongated
facial appearance, abnormal
falling
familial
fetal alcohol syndrome
folic acid
fourth ventricle, enlargement of
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
gait disorder
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
hippocampus
huntingtin
Huntington's chorea
hyperactivity
imbalance
impulsivity
inborn errors of metabolism
inclusion bodies
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
intellectual deficit
intellectual deterioration
intelligence quotient
joint hypermobility
karyotyping
learning disability
learning disability, in children
memory, impairment of
mental retardation
mental retardation, familial
metabolic disorder, primary
metabolic disorder, primary-screening tests
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
molecular genetics
mongolism
mortality
movement disorder
MRI
MRI, abnormal
MRI, volumetry
multiple system atrophy
muscle weakness, proximal
muscular dystrophy
myopathy
myotonia dystrophica
neonatal screening, genetic neurologic disorders
neoplasm, primary intracranial
neoplasm, primary of CNS
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic testing
neuronal migration disorder
neuropathy
old age, neurology of
Parkinsonism syndrome
polymerase chain reaction
practice guidelines
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
psychiatric disorder
psychological testing
psychological testing, children
Rett's syndrome
review article
rigidity
screening
seizure
seizure, familial
serologic testing
simian crease
Southern immunoblot test
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenium of corpus callosum
stimulant drugs
tandem gait, ataxic
temporal lobe
temporal lobe, anatomy and physiology
term infant
testicular enlargement
treatment of neurologic disorder
tremor
tremor, intention
tremor, writing
trinucleotide repeats
vitamin, multiple
walking, difficulty with
white matter disease
writing
X-linked bulbospinal neuronopathy
x-linked mental retardation
Showing articles 300 to 350 of 583 << Previous Next >>

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

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

MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
AJR 158:413-416, Snyder,R.D.,et al, 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

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

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

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

MR Imaging of Adrenoleukodystrophy
Neuroradiology 33:25-29, Uchiyama,M.,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

Cranial Lymphangiomatosis Causing CSF Otorrhea and Recurrent Meningitis:CT Features
J Comput Assist Tomogr 14:121-123, Nazarian,G.K.,et al, 1990

Hyperostosis Cranialis Interna
NEJM 322:450-463, Manni,J.J.,et al, 1990

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
Acute Renal Failure, Anemia, & Seizures in a 67-year-old Man, Am J Med 88:60-68., , 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

The Clinical Spectrum of the Eosinophilia-Myalgia Syndrome Associated with L-Tryptophan Ingestion
Ann Int Med 113:124-134, Martin,R.W.,et al, 1990

L-Tryptophan-Associated Eosinophilic Perimyositis, Neuritis, and Fasciitis
Medicine 69:187-199, Kaufman,L.D.,et al, 1990

The Trauma of the Spine and Spinal Cord-II
BMJ 301:110-113, Swain,A.,et al, 1990

Head Injuries-I
BMJ 300:1515-1518, Bullock,R.&Teasdale,G., 1990

Dopa-Responsive Dystonia:The Spectrum of Clinical Manifestations in a Large North American Family
Neurol 40:66-69, Nygaard,T.G.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Acute Paraneoplastic Sensory Ganglionitis, NEJM 322:531-5431990., , 1990

Late Complication of Undetected Odontoid Fracture in Children
BMJ 300:319-320, Alp,M.S.&Crockard,H.A., 1990

Risks of Acute Traumatic Intracranial Haematoma in Children and Adults
BMJ 300:363-367, Teasdale,G.M.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Linkage of DNA Markers at Xq28 to Adrenoleukodystrophy & Adrenomyeloneuropathy Present in the Same Family
Arch Neurol 47:665-669, Willems,P.J.,et al, 1990

Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow Transplant
NEJM 322:1860-1866, Aubourg,P.,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

Pulmonary Arteriovenous Malformation Presenting with Brain Abscess
Am J Dis Child 144:1045-1047, Dove,A.M.,et al, 1990



Showing articles 300 to 350 of 583 << Previous Next >>