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Differential
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acromegaly
acromicria
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
alopecia
amenorrhea
amniocentesis
anemia
Angelman syndrome
angiography, cerebral
ankle edema
anosmia
anti Ma
anti Ta
areflexia
arrhythmia, cardiac
arthritis
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoantibodies
autoimmune disease
azospermia
B 12 deficiency
basal ganglia, calcification of
behavior, combative
behavioral disorder
bone marrow transplantation
brain biopsy
brain scan, abnormal
bromocriptine
cabergoline
cachexia
cafe au lait spots
calcification, intracranial
carcinoma
carcinoma of lung
cardiomyopathy
caries
carotid artery occlusion, intracranial
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
celiac disease, childhood
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
chiasmal syndromes
children
chromophobe adenoma
chromosomal abnormality
chromosome 15
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Cockayne's syndrome
coenzyme Q10
coenzyme Q10 deficiency
collateral circulation
complications
contractures, joint
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
cryptorchidism
cultured skin fibroblasts
Cushing's syndrome
degenerative diseases of CNS
dementia
dementia, childhood
demyelinating disease
dermatitis herpetiformis
developmental retardation
diabetes insipidus
diarrhea
diet
dopamine agonist
drooling
dysarthria
dysmetria
dysmorphic
dysphagia
dysphasia
eating disorder
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalitis
encephalitis, brainstem
epidemiology of neurology
erectile dysfunction
evoked potentials
exome sequencing
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
failure to thrive
familial
fatty acid, elevated plasma content
feeding disorder
fingers, abnormal
fluorescein angiography
foot drop
F-wave response
gadolinium
gait disorder
galactorrhea
gastrointestinal disease, neurologic complications
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
genital hypoplasia
gluten ataxia
gluten sensitivity
gluten-free diet
gonadotropin-releasing hormone
gray hair
groin pain
growth hormone
growth hormone deficiency
growth retardation
gynecomastia
hair, loss
hand flapping
headache
hearing loss
hepatitis
hepatosplenomegaly
herniated disc
herniated disc, thoracic
hirsutism
HLA
hormone replacement
hormone therapy
hyperphagia
hyperpigmentation of skin
hypodontia
hypogonadism
hypogonadism, hypogonadotropic
hypomyelination
hypopigmentation of skin
hypopituitarism
hyposmia
hypothalamus
hypothalamus, damage to
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunosuppression
impotence
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
infertility
intellectual deficit
iris, abnormal
Kallmann's syndrome
Klinefelter's syndrome
learning disability
leukodystrophy
leukodystrophy, 4H
leukoencephalopathy
libido
libido, decreased
limbic encephalitis
liver disease
long bone lesion
Lorenzo's oil
low back pain
magnetic stimulation, brain
malabsorption
memory, impairment of
menses, irregular
mental retardation
misdiagnosis
molecular genetics
monoclonal gammopathy
monoparesis
mortality
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, spinal cord
multiple sclerosis, differential diagnosis of
muscle biopsy
muscular dystrophy
myeloma, osteosclerotic
myelopathy
myopia
myotonia
myotonia dystrophica
neck weakness
neoplasm, pituitary
neoplasm, pituitary, incidental
neoplasm, pituitary, treatment of
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronal migration disorder
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
next-generation sequencing
nystagmus
obesity
octreotide
ocular myopathy
oculopharyngeal muscular dystrophy
olfactory bulb
oligomenorrhea
oligospermia
ophthalmoplegia
optic atrophy
optic neuropathy
oral ulcerations
organomegaly
osteoporosis
ovarian dysgenesis
P300
pain
pain, abdominal
pain, back
pain, leg
papilledema
paraparesis
paraparesis, spastic
paraplegia
penis, small
perimetry
peroxisomal disease
Perrault syndrome
photosensitivity, skin
pigmentary retinopathy
pituitary
pituitary stalk
pituitary stalk, lesion of
pituitary, adenoma
pituitary, dysfunction
pituitary, hormones of
pituitary, lesion of
pituitary, microadenoma
plasmacytoma
plethora
POEMS syndrome
polyneuropathy
practice guidelines
Prader-Labhart-Willi syndrome
prenatal diagnosis by amniocentesis
progeria
prognosis
progressive neurologic disorder
prolactin
prolactin, elevated
prolactinoma
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
ptosis, familial
puberty
puberty, delayed
pulmonary infiltrates
radiation therapy, CNS treatment and complications with
rash
remote effect of cancer on the nervous system
retinopathy
review article
sarcoidosis
sarcoidosis, CNS
sclerosis, bone
seizure
sella turcica, enlargement of
sensorineural hearing loss
serologic testing
serum tumor markers
short stature
sinuses, diseases of
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull x-ray, abnormal
smell
somatosensory evoked potentials
somatostatin analogue
spinal cord, compression of
splenomegaly
steroid therapy, CNS treatment and complications with
stooped posture
strabismus
suck, poor
suprasellar lesion
synkinesis
systemic illness
teeth, abnormal
temper tantrums
temporal lobe, lesion
temporal lobe, lesion, bilateral
temporalis muscle wasting
testicular atrophy
testicular biopsy
testicular germinoma
testicular teratoma
testosterone
testosterone, serum
testosterone, serum, low
third ventricle, wall
thrombocytosis
tongue, protrusion of
treatment of neurologic disorder
tremor
tremulousness
ubiquitination
urinary gonadotropin
vascular endothelial growth factor
visual acuity, decreased
visual evoked response
visual field defect
visual fields
visual loss
vitiligo
weakness, generalized
weight loss
Werner's syndrome
white matter disease
wide based gait
workup
X-linked bulbospinal neuronopathy
Showing articles 1600 to 1650 of 2365 << Previous Next >>

Anticerebellar Antibodies in Neurologically Normal Patients with Ovarian Neoplasm
Neurol 39:1605-1609, Brashear,H.R.,et al, 1989

Variables Predicting Surgical Outcome in Symptomatic Hydrocephalus in the Elderly
Neurol 39:1601-1604, Graff-Radford,R.N.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

MR Imaging of Neurocysticercosis
AJR 153:857-866, Teitelbaum,G.P.,et al, 1989

A Radiologic Study of Dynamic Processes in Lacunar Dementia
Stroke 20:1488-1493, Tanaka,Y.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Narcolepsy Associated with Lesions of the Diencephalon
Neurol 39:1505-1508, Aldrich,M.S.&Naylor,M.W., 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

The Cerebellum in Sagittal Plane-Anatomic-MR Correlation:1. The Vermis
AJR 153:829-835, Courchesne,E.,et al, 1989

A New Sign of Neurofibromatosis on Magnetic Resonance Imaging of Children
Arch Neurol 46:1222-1224, Goldstein,S.M.,et al, 1989

Interhemispheric Transfer in Patients with Incomplete Section of the Corpus Callosum, Verification with MRI
Arch Neurol 46:437-443, Risse,G.L.,et al, 1989

Outcome After Posthemorrhagic Ventriculomegaly in Comparison with Mild Hemorrhage Without Ventriculomegaly
J Pediatr 114:109-114, Shankaran,S.,et al, 1989

Magnetic Resonance Imaging in Pathologically Proven Hallervorden-Spatz Disease
Neurol 39:440-442, Schaffert,D.A.,et al, 1989

The Natural History of Prenatally Diagnosed Cerebral Ventriculomegaly
JAMA 261:1785-1788, Drugan,A.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

The Spectrum of Imaging and Neuropsychological Findings in Pick's Disease
Neurol 39:362-368, Knopman,D.S.,et al, 1989

The Significance of MRI Abnormalities in Children with Neurofibromatosis
Neurol 39:373-378, Duffner,P.K.,et al, 1989

The Effects of Alcoholism on Skeletal and Cardiac Muscle
NEJM 320:409-415, 458-4601989., Urbano-Marquez,A.,et al, 1989

Sneddon Syndrome:CT, Arteriography, and MR Imaging
J Comput Assist Tomogr 13:119-122, Blom,R.J., 1989

Motoneuron Disease:A Disorder Secondary to Solvent Exposure?
Lancet 1:73-76, 82-831989., Hawkes,C.H.,et al, 1989

Phenobarbital Rheumatism in Patients with Brain Tumor
Ann Neurol 25:92-94, Taylor,L.P.&Posner,J.B., 1989

Multiple Sclerosis-Like Illness Occurring with Human Immunodeficiency Virus Infection
Neurol 39:324-329, Berger,J.R.,et al, 1989

Neurological Disease Associated with Antiphospholipid Antibodies
Ann Neurol 25:221-227, Briley,D.P.,et al, 1989

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Cerebellar Degeneration in Neuroleptic Malignant Synd:Neuropath & Review of Lit Concerning Heat-Related Nervous Syst Injury
JNNP 52:387-391, Lee,S.,et al, 1989

Cerebellar Atrophy Following Acute Intoxication with Phenytoin
Neurol 39:432-433, Masur,H.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Cerebrovascular Disease & Antiphospholipis Antibodies in SLE, Lupus-Like Dis, & Primary Antiphospholipid Synd
Am J Med 86:391-399, Asherson,R.A.,et al, 1989

MR Imaging in Progressive Suupranuclear Palsy and Shy-Drager Syndrome
J Comput Assist Tomogr 13:555-560, Savoiardo,M.,et al, 1989

Frontal Lobe Syndrome in a Patient with Bilateral Globus Pallidus Lesions
Arch Neurol 46:1024-1027, Strub,R.L., 1989

Magnetic Resonance Imaging of Spinal Cord Lesions in Multiple Sclerosis
JNNP 52:459-466, Honig,L.S.&Sheremata,W.A., 1989

Quantitation of Cerebral Atrophy in Preclinical and End-Stage Alzheimer's Disease
Ann Neurol 25:450-459, delaMonte,S.M., 1989

Intermittent Obstructive Hydrocephalus in the Arnold-Chiari Malformation
Ann Neurol 26:401-404, Vrabee,T.R.,et al, 1989

Radiation-Induced Dementia in Patients Cured of Brain Metastases
Neurol 39:789-796, DeAngelis,L.M.,et al, 1989

The Alien Hand Syndrome, Clinical and Postmortem Findings
Arch Neurol 46:456-459, Banks,G.,et al, 1989

Occluded Fourth Ventricle After Multiple Shunt Revisions for Hydrocephalus
Pediatrics 83:981-985, Coker,S.B.&Anderson,C.L., 1989

Management Problems in Acute Hydrocephalus after Subarachnoid Hemorrhage
Stroke 20:747-753, Hasan,D.,et al, 1989

Acute Hydrocephalus After Subarachnoid Hemorrhage
Stroke 20:715-717, Heros,R.C., 1989

Factors Assoc with Hydrocephalus after Subarachnoid Hemorrhage
Arch Neurol 46:744-752, Graff-Redford,N.R.,et al, 1989

Tuberculous Meningitis in Children:Treatment with Isoniazid and Rifampicin for Twelve Months
J Pediatr 114:875-879, Visudhiphan,P.&Chiemchanya,S., 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989



Showing articles 1600 to 1650 of 2365 << Previous Next >>