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Differential
(Click to cross reference)
abducens nerve paralysis
abducens nerve paralysis, bilateral
Addison's disease
adverse drug reaction
amenorrhea
aneurysm
aneurysm, intracranial
aphasia
aqueduct of Sylvius, stenosis
aqueductal stenosis
arcuate scotoma, differential diagnosis of
ataxia, cerebellar
bitemporal visual field defect
bromocriptine
calcification, intracranial
carcinoembryonic antigen
carcinoma of rectum
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, base of skull
CAT scan, false negative
CAT scan, metrizamide
CAT scan, skull bone changes
cavernous hemangioma
chiasmal syndromes
children
Chvostek sign
cisternogram, metrizamide
Clinical Pathologic Conference(C.P.C.)
clivus
coma
complicated migraine
craniopharyngioma
Cushing's syndrome
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diplopia
diplopia, monocular
dopamine agonist
empty sella syndrome
ethambutol
exophthalmus
familial
fasciculation
fever
fundus, abnormality of
funduscopic exam
galactorrhea
genetic neurologic disorders
growth retardation
hallucination, auditory
Hand-Schuller-Christian disease
head injury
headache
headache, severe
headache, sudden onset of
hemiachromatopsia, homonymous
hemianopia
hemianopia, homonymous
hemianopia, monocular
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperadrenalism
hypercalcemia
hyperinsulinism
hyperkalemia
hyperparathyroidism
hyperthyroidism
hypokalemic periodic paralysis
hypoparathyroidism
hypopituitarism
hypothalamus
hypothalamus, disturbance of
hypothalamus, neoplasm of
hypothyroidism
iatrogenic neurologic disorders
impotence
infection
intracranial pressure, increased
intrinsic hand muscles, wasting of
islet cell tumor
Leber's hereditary optic neuropathy
level of consciousness, decreased
libido
libido, decreased
malformation, vascular
malformation, vascular, cryptic
memory, impairment of
meningismus
meningitis
meningitis, iatrogenic
meningitis, TB
migraine
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
multiple sclerosis
muscle weakness
muscle weakness, causes of
myasthenia gravis
myoedema
myopathy
myxedema coma
myxedema, neurologic manifestations of
nausea and vomiting
neoplasm, metastatic to CNS
neoplasm, pituitary
neoplasm, pituitary, incidental
neoplasm, pituitary, treatment of
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-incidence of
neoplasm, primary of CNS-metastasizing to subarachnoid space
neoplasm, primary of CNS-treatment of
neuroendocrinology
neurologic disease, diagnoses of
nose blowing
nystagmus
nystagmus, see-saw
obesity
ophthalmoplegia
ophthalmoplegia, total
optic atrophy
optic chiasm
optic chiasm, hemorrhage in
optic chiasm, herniation
optic chiasm, lesion of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
optic tract
optic tract, lesion of
pain, periorbital
papilledema
paranoia
parathyroid adenoma
pheochromocytoma
photophobia
pinealoma
pituitary, adenoma
pituitary, apoplexy
pituitary, enlargement
pituitary, lesion of
pituitary, metastasis to
pituitary, microadenoma
polyuria
postoperative neurologic complications
primary aldosteronism
prolactinoma
psychosis
quadrantanopsia, homonymous
review article
Riddoch phenomenon
scotoma
scotoma, central
scotoma, paracentral-homonymous
seizure
sella turcica, enlargement of
short stature
skull bone, erosion
spinal cord, metastasis to
suprasellar lesion
tetany
third nerve palsy
thyrotoxicosis
treatment of neurologic disorder
Trousseau's sign
tuberculoma
urinary frequency
vertigo
vision, blurred
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual field defect, altitudinal
visual field defect, monocular
visual loss
visual loss, sudden
weight gain
weight loss
Showing articles 450 to 500 of 4544 << Previous Next >>

Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
Arch Neurol 49:170-173, Malik,S.,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

Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
Brain 115:979-989, Harding,A.E.,et al, 1992

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992

A Clinical Study of Noonan Syndrome
Arch Dis Child 67:178-183, Sharland, M.,et al, 1992

Thyroid-Associated Eye Disease:Clinical Management
Lancet 338:29-32, Fells,P., 1991

Syncope:1991
Am J Med 90:1-5, Linzer,M., 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
NEJM 323:1488-1489, Johns,D.R., 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

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

Current Management of Amaurosis Fugax
The Amaurosis Fugax Study Group, Stroke 21:201-2081990., , 1990

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

Neurofibromatosis Type 1 (Recklinghausen's Disease) , Neurologic and Cognitive Assessment
Am J Dis Child 143:833-837, Eldridge,R.,et al, 1989

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

Subacute Combined Degeneration of the Spinal Cord
In Rowland's, Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 691, Mancall,E.L., 1989

The Rational Management of Idiopathic Intracranial Hypertension
Arch Neurol 46:1049-1051, Corbett,J.J.&Thompson,H.S., 1989

Surgical Treatment of Progressive Visual Loss in Traumatic Optic Neuropathy, Report of Two Cases
J Neurosurg 70:799-801, Guy,J.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Noninvasive Eval of Extracranial Carotid Arteries in Patients with Cerebrovascular Events & Atrial Fib
Arch Int Med 148:1785-1788, Weinberger,J.,et al, 1988

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

Computed Tomography and Magnetic Resonance Imaging in the Diagnosis of Inflammatory Disease of the Optic Nerve
Surv Ophthalmol 31:352-355, McCrary,J.A.,et al, 1987

Clinicopath. Conference
Malignant Lymphoma (B-Cell Type) , Brain (Right-Frontal-Lobe White Matter) , Case 22-1986, NEJM 314:, 498-150, 1986

The Posterior Cerebral Artery Syndrome
Can J Neurol Sci 13:232-239, Fisher,C.M., 1986

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Somatization Disorder, One of Medicine's Blind Spots
JAMA 254:3075-3079, Quill,T.E., 1985

Leber's Congenital Amaurosis
Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984

Small Bowel Resection with Vitamin E Deficiency & Progressive Spinocerebellar Syndrome
Neurol 34:1046-1052, Bertoni,J.M.,et al, 1984

Cerebro-ocular Dysgenesis (Walker-Warberg Syndrome) :Neuropathologic & Etiologic Analysis
Neurol 34:1531-1541, Williams,R.S.,et al, 1984

Clinicopathological Conference
Case 2-1984, Fabry's Disease, NEJM 310:106-114984., , 1984

Gerstmann-Straussler-Scheinker Disease with Coincidental Familial Onset
Ann Neurol 14:670-678, Hudson,A.J.,et al, 1983

Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983

Detection Of Adrenoleucodystrophy Carriers By Means Of Evoked Potentials
Lancet 2:852-853, Moloney,J.B.,et al, 1982

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

Occipital Lobe Infarctions:Perimetry & Computed Tomography
Neurol 31:1098-1106, Spector,R.H.,et al, 1981

Optic Neuritis in Familial MS
Neurol 31:1138-1142, Ebers,G.C.,et al, 1981

Confrontation Visual Field Techniques in the Detection of Anterior Visual Pathway Lesions
Ann Neurol 10:28-34, Trobe,J.D.,et al, 1981

Relative Afferent Pupillary Defects in Optic Neuritis
Am J Ophthalmol 92:685-690, Cox, T.A.,et al, 1981

Osteopetrosis, Renal Tubular Acidosis & Basal Ganglia Calcification in Three Sisters
Am J Med 69:64-74, Whythe,M.P.,et al, 1980

Leber's Optic Neuropathy
Editorial, BMJ 280:1097-10981980., , 1980

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

Nervous System Toxicity of Chemo Agents
Young, DF, in Vinken PJ, Bruyn GW, Handbook of Clin Neurol, North-Holland Publ Co, Amster, Vol 39, 1, 80, p 104, 1980

Adult Type Neuronal Storage Disease with Neuraminidase Deficiency
Ann Neurol 6:232-244, Miyatake,T.,et al, 1979

Reversal of an Afferent Pupillary Defect with Cold Water Drinking
Ann Neurol 6:456, Czarnecki,J.S., 1979

Marfan Syndrome
NEJM 300:772-777, Pyeritz,R.E.,et al, 1979



Showing articles 450 to 500 of 4544 << Previous Next >>