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advances in neurology
adverse drug reaction
alcohol
alcohol, neurologic complications with
algorithm
aminoacidurias
amyloidosis
amyotrophic lateral sclerosis
anemia
anemia, hemolytic
anterocollis
anticholinergic drugs
aphonia
artane
arthrogryposis multiplex
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
Babinski sign
basal ganglia
basal ganglia, lesion, bilateral
benign essential tremor
bent spine syndrome
biopterin deficiency
blepharospasm
botulinum toxin
bradykinesia
Brueghel's syndrome
camptocormia
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, muscle
catecholamine
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
chorea, causes of
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 14
cirrhosis
cirrhosis, causes of childhood
Clinical Pathologic Conference(C.P.C.)
clonazepam
cogwheel rigidty
complications
conversion reaction
creatine phosphokinase(CPK)elevated
dementia
depression
dermatomyositis
developmental retardation
diurnal variation
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysphagia
dysphonia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, painful
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
efficacy
electromyogram
encephalitis, brainstem
epidemiology of neurology
equinovarus
familial
gait disorder
gamma amino butyric acid
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
Gilles de la Tourette syndrome
globus pallidus
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
Hallervorden Spatz disease
handwriting
head nodding
head tilt
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatitis
hepatolenticular degeneration(Wilson's disease)
homovanillic acid
Huntington's chorea
hyperekplexia
hyperreflexia
iron, brain
Kayser-Fleischer ring
klippel feil syndrome
kyphosis
laminectomy
laminectomy, lumbar
laterocollis
L-dopa
leg spasms
leg spasms, painful
low back pain
migraine
migraine, children
misdiagnosis
molecular genetics
monoamines
mononeuropathy
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI, abnormal
MRI, eye of tiger sign
MRI, gradient-echo
MRI, paramagnetic effect
MRI, susceptibility weighted
multiple sclerosis
muscle biopsy
muscle diseases, characteristics of
muscle weakness
muscle weakness, proximal
muscle, metabolic disorders of
muscular dystrophy
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenic crisis
myopathy
myopathy, carcinomatous
myopathy, metabolic
myopathy, thyroid disease causing
myositis
myotonia dystrophica
nerve conduction studies
neuritis, causes of
neurodegeneration with brain iron accumulation
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathy
neuropathy, diabetic
neurotransmitter
norepinephrine
obsessive-compulsive disorder
old age, neurology of
pain
pancytopenia
PANK2 mutation
paraspinal muscle
paraspinal muscle weakness
Parkinson disease
Parkinson disease, juvenile
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
patient information and support
penicillamine
phenylketonuria
poliomyelitis
polymyositis
polyneuropathy
porphyria
postoperative neurologic complications
postural abnormality
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
radiculopathy
reflex sympathetic dystrophy
retrocollis
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
salivation, excessive
sarcoidosis
schizophrenia
scoliosis
seizure
seizure, stimulus sensitive
sensory tricks
sinemet
slit lamp examination
spastic dysphonia
speech disorder
speech disorder, non aphasic
splenomegaly
startle reaction
stiff man syndrome
stimulation, deep brain
stooped posture
tardive dyskinesia
tardive dystonia
tetrabenazine
tic
toe walking
tonic foot response
torticollis
torticollis, benign paroxysmal
torticollis, familial
torticollis, infants and children
torticollis, post traumatic
trauma
treatment of neurologic disorder
tremor
tremor, jaw
tremor, leg
tremor, post traumatic
tremor, postural
tremor, treatment of
tremor, voice
uric acid, low
vasospasm, cerebral
walking, difficulty with
weakness, progressive
Werdnig-Hoffman disease
wheelchair
workup
writers cramp
Showing articles 1250 to 1300 of 1744 << Previous Next >>

Magnetic Resonance Imaging in Isolated Noncompressive Spinal Cord Syndromes
Ann Neurol 22:714-723, Miller,D.H.,et al, 1987

The Aetiology of Mirror Writing:A New Hypothesis
JNNP 50:1572-1578, Tashiro,K.,et al, 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Neurofibromatosis
Editorial, Lancet 1:663-6641987., , 1987

Renal Cell Carcinoma in von Hippel-Lindau Syndrome
Am J Med 82:236-238, Malek,R.S.,et al, 1987

Adrenoleukodystrophy:Dietary Oleic Acid Lowers Hexacosanoate Levels
Ann Neurol 21:230-231, 232-2391987., Rizzo,W.B.,et al, 1987

A New Dietary Therapy for Adrenoleukodystrophy:Biochemical & Preliminary Clinical Results in 36 Patients
Ann Neurol 21:230-231, 240-2491987., Moser,A.B.,et al, 1987

Familial Occurrence of Spontaneous Dissection of the Internal Carotid Artery
Stroke 18:246-251, Mokri,B.,et al, 1987

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

Evidence That the Gene for Tuberous Sclerosis is on Chromosome 9
Lancet 1:659-661, Fryer,A.E.,et al, 1987

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

Tourette Syndrome
Editorial, Lancet 1:3081987., , 1987

Caffeine & Tremor
Neurol 37:169-172, Koller,W.,et al, 1987

Dementia of the Alzheimer Type:Clinical & Family Study of 22 Twin Pairs
Neurol 37:359-363, Nee,L.E.,et al, 1987

Genetic Linkage in Neurologic Diseases
Editorial, NEJM 316:1018-10201987., Martin,J.B., 1987

Myelopathies & Retroviral Infections
Ann Neurol 21:113-115, Johnson,R.T.&McArthur,J.C., 1987

Tropical Spastic Paraparesis:HTLV-I Antibodies in Patients from the Seychelles
NEJM 316:51, Roman,G.C.,et al, 1987

Endemic Tropical Spastic Paraparesis Associated with HTLV-I:A Clinical & Seroepidem Study of 25 Cases
Ann Neurol 21:123-130, Vernant,J.C.,et al, 1987

Chronic Progressive Myelopathy Associated with Elevated Antibodies to HTLV-I & Adult T-Cell Leukemialike Cells
Ann Neurol 21:117-121, Osame,M.,et al, 1987

Antibody to Human T-Lymphotropic Virus Type I In West-Indian-Born UK Residents with Spastic Paraparesis
Lancet 1:415-416, Newton,M.,et al, 1987

Disorders of the Autonomic Nervous System:Part 1. Pathophysiology & Clinical Features
Ann Neurol 21:419-430, McLeod,J.G.&Tuck,R.R., 1987

Familial Cavernous Malformations of the Central Nervous System & Retina
Ann Neurol 21:578-583, Dobyns,W.B.,et al, 1987

Von Hippel-Lindau Disease in an Adolescent
Pediatrics 79:632-637, Seitz,M.L.,et al, 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Adult Polycystic Kidney Disease & Intracranial Aneurysms
BMJ 295:526, Saifuddin,A.&Dathan,J.R.E., 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Analysis of Risk Factors for Stroke in a Cohort of Men Born in 1913
NEJM 317:521-526, Welin,L.,et al, 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

The Combined Use of Positron Emission Tomography & DNA Polymorphisms for Preclinical Detection of Huntington's Disease
Neurol 37:1441-1447, Hayden,M.R.,et al, 1987

Essential Tremor:A Review
Neurol 37:1194-1197, Findley,L.J.&Koller,W.C., 1987

A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
Neurol 37:1542-1544, Goetz,C.G.,et al, 1987

Risk Factors for Alzheimer's Disease:A Case-Control Study
Neurol 37:1630-1633, Shalat,S.T.,et al, 1987

Multiple Sclerosis & Systemic Lupus Erythematosus, Occurrence in Two Generations of the Same Family
Arch Int Med 147:1317-1320, Sloan,J.B.,et al, 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Adult-Onset Spinocerebellar Syndrome with Idiopathic Vitamin E Deficiency
Ann Neurol 22:84-87, Yokota,T.,et al, 1987

Human T-Lymphotropic Virus Type I Antibodies in The Serum of Pts with Tropical Spastic Paraparesis in the Seychelles
Arch Neurol 44:605-607, Roman,G.C.,et al, 1987

Tropical Spastic Paraparesis in the Seychelles Islands:A Clinical & Case-Control Neuroepidemiologic Study
Neurol 37:1323-1328, Roman,G.C.,et al, 1987

Cerebral Ventricular Dilation in Congenital Myotonic Dystrophy
J Pediatr 111:372-376, Regev,R.,et al, 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Central Core Disease, Clinical Features in 13 Patients
Medicine 66:389-396, Shuaid,A.,et al, 1987

Familial Recurrent Bell's Palsy with Ocular Motor Palsies
Neurol 37:1369-1371, Aldrich,M.S.,et al, 1987

Hereditary Motor & Sensory Neuropathy, X-Linked:A Half Century Follow-Up
Neurol 37:1460-1465, Rozear,M.P.,et al, 1987

Prenatal Diagnosis & Detection of Carriers with DNA Probes in Duchenne's Muscular Dystrophy
NEJM 316:985-993, 1018-10201987., Darras,B.T.,et al, 1987

Ocular Complications of Tangier Disease
Am J Med 83:991-994, Pressley,T.A.,et al, 1987

Symptomatic Atlantoaxial Dislocation in Down's Syndrome
Ann Neurol 21:606-609, Chaudhry,V.,et al, 1987

MR Imaging in a Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 11:1057-1058, Tanfani,G.,et al, 1987

Cervicomedullary Compression in Young Patients with Achondroplasia:Value of Neurologic & Respiratory Eval
J Pediatr 110:522-530, Reid,C.S.,et al, 1987

The Autosomal Dominant Form of"Pure"Familial Spastic Paraplegia:Clinical Findings & Linkage Analysis of a Pedigree
Neurol 37:910-915, Boustany,R.M.N.,et al, 1987

MR Imaging of Pelizaeus-Merzbacher Disease
J Comput Assist Tomogr 11:591-593, Penner,M.W.,et al, 1987

Magnetic Resonance Imaging in Pelizaeus-Merzbacher Disease
Neuroradiology 29:403-405, Journel,H.,et al, 1987



Showing articles 1250 to 1300 of 1744 << Previous Next >>