Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
adoption
advances in neurology
adverse drug reaction
affective disorders
algorithm
Alzheimer's disease
Alzheimer's disease, familial
amyotrophic lateral sclerosis
anxiety
apraxia
asymptomatic
ataxia, hereditary
autoimmune disease
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
CAG repeats
carcinoma
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
caudate nucleus
caudate nucleus, atrophy
caudate nucleus, lesion of
central nervous system, infection of
cerebral cortical atrophy
cerebral glucose metabolism
cerebrospinal fluid, gamma amino butyric acid
children
chorea
chorea, causes of
chorea, senile
choreoathetosis
chromosomal abnormality
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition
congenital birth defects
controversies in neurology
degenerative diseases of CNS
dementia
dentatorubral-pallidoluysian atrophy
depression
differential diagnosis
DNA probes
dying
dysarthria
dysphasia
dystonia
employment
ethics in neurology
eye movement, disorders of
familial
fragile-X syndrome
Friedreich's ataxia
gait disorder
gamma amino butyric acid
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
grimacing
health insurance
huntingtin
Huntington's chorea
Huntington's chorea, differential diagnosis
Huntington's chorea, genetic counselling
Huntington's chorea, late onset
Huntington's chorea, membrane abnormality
Huntington's chorea, misdiagnosis of
Huntington's chorea, presymptomatic detection of
Huntington's chorea, sporadic form
Huntington's disease, children
hyperreflexia
hypotonia
imbalance
intellectual deficit
intellectual deterioration
internet
L-dopa
lymphocyte capping, diminished
manic-depressive
medical-legal aspects of neurology
memory, impairment of
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
mortality
motor neuron disease
motor signs
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, functional
MRI, volumetry
MRS
muscular dystrophy
muscular dystrophy, Duchenne
myopathy
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
neurofibromatosis 1
neurofibromatosis 2
neurologic disease
neurologic disease, diagnoses of
neurologic history
neuronal migration disorder
neuropathology
neuropathology, brain
neuropathy, amyloid
neurotransmitter
NMDA receptors
old age, neurology of
Parkinson disease
peptides, brain
personality change
polymerase chain reaction
polymerase chain reaction, false negative
polymerase chain reaction, false positive
practice guidelines
preclinical
prevention of neurologic disorders
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychomotor retardation
psychosis
quality of life
reaction time
recombinant DNA
review article
RFLPs
rigidity
risk factors
saccadic eye movements
saccadic eye movements, abnormal
screening
seizure
somatostatin
spasticity
speech disorder
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar degeneration
striatum, lesion of
substance P
suicide
Tay-Sachs disease
treatment of neurologic disorder
trinucleotide repeats
viral infection, CNS
visuospatial disturbance
weight loss
X-linked bulbospinal neuronopathy
Showing articles 800 to 850 of 2007 << Previous Next >>

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

CSF Evaluation in Primary CNS Lymphoma Patients by PCR of the CDR III IgH Genes
Neurol 58:390-396,339, Gleissner,B.,et al, 2002

Recombinant Interferon-a-induced Chorea and Frontal Subcortical Dementia
Neurol 58:328-330, Moulignier,A.,et al, 2002

Cervical Disc Prolapse with Cord Compression Presenting with Choreoathetosis and Dystonia
Neurol 58:661-662, Tan,E.K.,et al, 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
J Pediatr 140:242-246, Wolf,B.,et al, 2002

Diffusion-Weighted and Gradient Echo Magnetic Resonance Findings of Hemichorea-Hemiballismus Associated with Diabetic Hyperglycemia
Arch Neurol 59:448-452, Chu,K.,et al, 2002

Diagnosis of X-Linked Myotubular Myopathy by Detection of Myotubularin
Ann Neurol 50:42-46, Laporte,J.,et al, 2001

Subclinical Dopaminergic Dysfunction in Asymptomatic Parkinson's Disease Patients' Relatives with a Decreased Sense of Smell
Ann Neurol 50:34-41, Berendse,H.W.,et al, 2001

The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
NEJM 345:17-24,57, Ducros,A.,et al, 2001

Fits and Strokes
Lancet 358:120, Sharma,P.,et al, 2001

Coma in a Young Anorexic Woman
Lancet 357:1944, Blans,M.J.,et al, 2001

Response to Cancer Therapy in a Patient with a Paraneoplastic Choreiform Disorder
Neurol 57:719-722, Croteau,D.,et al, 2001

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
Stroke 32:877-882, Maher,C.O.,et al, 2001

Cocaine-Induced Persistent Dyskinesias
Neurol 56:964-965, Weiner,W.J.,et al, 2001

Advances in the Genetics of Cerebrovascular Disease and Stroke
Neurol 56:997-1008, Hademenos,G.J.,et al, 2001

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

Impact of the Human Genome Projects and Identification of a Stroke Gene
Stroke 32:1239-1241, Alberts,M.J., 2001

Ballistic-Choreic Movements as the Presenting Feature of Renal Cancer
Arch Neurol 58:1133-1135, Kujawa,K.A.,et al, 2001

Is Patent Foramen Ovale a Family Trait?
Stroke 32:1563-1566, Arquizan,C.,et al, 2001

Clinical and Genetic Aspects of Distal Myopathies
Muscle Nerve 24:1440-1450, Saperstein,D.S.,et al, 2001

Complete Genomic Screen in Parkinson Disease
JAMA 286:2239-2244, Scott,W.K.,et al, 2001

Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
Ann Neurol 50:665-668, Prass,K.,et al, 2001

Oculopharyngeal Muscular Dystrophy in Hispanic New Mexicans
JAMA 286:2437-2440, Becher,M.W.,et al, 2001

Prospective Follow-up of 33 Asymptomatic Patients with Familial Cerebral Cavernous Malformations
Neurol 57:1825-1828, Labauge,P.,et al, 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Chorea and Antiphospholipid Antibodies: Treatment with Methotrexate
Neurol 56:137-138, Paus,S.,et al, 2001

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Morvans Syndrome: Peripheral and Central Nervous System and Cardiac Involvement With Antibodies to Voltage-Gated Potassium Channels
Brain 124:2417-2426, Liguori,R., et al, 2001

Morvans Syndrome Associated With Voltage-Gated K+ Channel Antibodies
Neurol 54:771-772, Barber,P.A., et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Long-term Effect of Bone-marrow Transplantation for Childhood-onset Cerebral X-linked Adrenoleukodystrophy
Lancet 356:713-718, Shapiro,E. et al, 2000

Practice Parameter: Screening and Diagnosis of Autism
Neurol 55:468-479, Filipek,P.A. et al, 2000

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
Stroke 31:2742-2750, Bederson,J.B.,et al, 2000

Hemidystonia and Hemichoreoathetosis as an Initial Manifestation of Moyamoya Disease
Arch Neurol 57:1510-1512, Lyoo,C.H.,et al, 2000

Chorea Resulting From Paraneoplastic Striatal Encephalitis
JNNP 69:512-515, Tani,T.,et al, 2000

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
Neurol 55:1661-1667, Iglesias,S.,et al, 2000

A Locus for Paroxysmal Kinesigenic Dyskinesia Maps to Human Chromosome 16
Neurol 54:125-130, Bennett,L.B.,et al, 2000

Very Late-Onset Friedreich Ataxia Despite Large GAA Triplet Repeat Expansions
Arch Neurol 57:246-251, Bidichandani,S.I.,et al, 2000

The Brain Code in Health and Disease
Arch Neurol 57:50-51, Rosenberg,R.N., 2000

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

Congenital Muscular Dystrophy with Rigid Spine Syndrome:A Clinical, Pathological, Radiological, and Genetic Study
Ann Neurol 47:152-161, 143, Flanigan,K.M.,et al, 2000

GCG Genetic Expansions in Italian Patients with Oculopharyngeal Muscular Dystrophy
Neurol 54:608-614, Mirabella,M.,et al, 2000

Hereditary Recurrent Focal Neuropathies, Clinical and Molecular Features
Neurol 54:546-551, Stogbauer,F.,et al, 2000



Showing articles 800 to 850 of 2007 << Previous Next >>