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Differential
(Click to cross reference)
abducens nerve paralysis
abducens nerve paralysis, bilateral
Addison's disease
adverse drug reaction
amenorrhea
ammonia
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
cerebral cortex
chiasmal syndromes
children
Chvostek sign
cingulate gyrus
cisternogram, metrizamide
Clinical Pathologic Conference(C.P.C.)
clivus
coma
coma, sudden onset
complicated migraine
confusion
craniopharyngioma
Cushing's syndrome
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diplopia
diplopia, monocular
dopamine agonist
empty sella syndrome
encephalopathy
encephalopathy, acute
ethambutol
exome sequencing
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
HHH syndrome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperadrenalism
hyperammonemic encephalopathy
hypercalcemia
hyperinsulinism
hyperkalemia
hyperparathyroidism
hyperthyroidism
hypokalemic periodic paralysis
hypoparathyroidism
hypopituitarism
hypothalamus
hypothalamus, disturbance of
hypothalamus, neoplasm of
hypothyroidism
iatrogenic neurologic disorders
impotence
infection
insular cortex
insular cortex, lesion
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
MRI, diffusion weighted
multiple sclerosis
muscle weakness
muscle weakness, causes of
myasthenia gravis
myoclonus
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
ornithine transcarbamylase deficiency
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
temporal lobe, lesion
temporal lobe, lesion, bilateral
tetany
third nerve palsy
thyrotoxicosis
treatment of neurologic disorder
Trousseau's sign
tuberculoma
urea-cycle enzymopathies
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 4300 to 4350 of 4627 << Previous Next >>

Trichlorethylene
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 36, North-Holland Publ Co, 457, Feldman,R.G., 1979

Familial Lumbar Spinal Stenosis with Acute Disc Herniation, Case Reports of Four Brothers
J Neurosurg 51:234-236, Varughese,G.,et al, 1979

Sarcoidosis & Its Ophthalmic Manifestations
Am J Ophthmol 86:648-655, Obenauf,C.D.,et al, 1978

Reversible Mental Symptoms in Temporal Arteritis
J Nerv Ment Dis 166:446-447, Cochran,J.W.,et al, 1978

Computerised Tomography in Severe Methanol Intoxication
BMJ 2:929-930, Aquilonius,S-M.,et al, 1978

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Muscle Fiber-Type Disproportion
Arch Neurol 35:823-826, Eisler,T.,et al, 1978

Venous Angioma of the Optic Chiasm
Ann Neurol 4:470-471, Fermaglich,J.,et al, 1978

Hereditary Paroxysmal Ataxia:Response to Acetazolamide
Neurol 28:1259-1264, Griggs,R.C.,et al, 1978

Clinical Pathological Conference, Reticulum Cell Sarcoma of Brain
NEJM 299:1349-1359, Case Record 49-1978,Mass.Gen.Hosp., 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Autosomal Dominant Neurological Disorders
Ann Neurol 4:548-552, Brady,R.O.,et al, 1978

Toluene Optic Neuropathy
Ann Neurol 4:390, Keane,J.R., 1978

Adult-onset GM2 Gangliosidosis
Neurol 28:1117-1123, O'Neill,B.,et al, 1978

Abnormal Iris Vasculature in Myotonic Dystrophy
Arch Neurol 35:224, Stern,L.Z.,et al, 1978

Nemaline (Rod) Myopathy:The Need for Histochemical Evaluation of Affected Families
Ann Neurol 4:37, Bender,A.N.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,et al, 1978

Monozygotic Twins With Presumed Metachromatic Leukodystrophy
Arch Neurol 35:689-691, Hashimoto,T.,et al, 1978

Malignant Optic Gliomas in Adults
Arch Neurol 35:731-735, Harper,C.G.,et al, 1978

Optic Neuropathies
NEJM 299:533-536, Lessell,S., 1978

Cerebrovascular Disease in Infants & Children:A Study of Incidence, Clinical Features, & Survival
Neurol 28:763-768, Schoenberg,B.S.,et al, 1978

Mirror Movements after Childhood Hemiparesis
Neurol 28:1152-1158, Woods,B.T.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

Prolonged Partial Complex Status Epilepticus:EEG & Behavioral Observations
Neurol 28:863-869, Engel,J.Jr.,et al, 1978

Familial Chorea & Myoclonus Epilepsy
Neurol 28:913-919, Takahata,N.,et al, 1978

Total Blindness after Trivial Frontal Head Trauma:Bilateral Indirect Optic Nerve Injury
Neurol 28:1066-1068, Venable,H.P.,et al, 1978

Memory Impairment in Korsakoff's Psychosis:A Correlation with Brain Noradrenergic Activity
Science 202:905-907, McEntee,W.J.,et al, 1978

Acquired Stuttering
Neurol 28:1159-1165, Helm,N.A.,et al, 1978

Familial Incidence of Ruptured Intracranial Aneurysms
Arch Neurol 35:675-677, Acosta-Rua,G.J., 1978

Clinical & Anatomic Findings in a Case of Auditory Agnosia
Arch Neurol 35:712-719, Oppenheimer,D.R.,et al, 1978

Epidemiologic Assessment of Chronic Atrial Fibrillation & Risk of Stroke:The Framingham Study
Neurol 28:973-977, Wolf,P.A.,et al, 1978

Ataxia Telangiectasia
Arch Neurol 35:553-554, Teplitz,R.L., 1978

Tics & Tourette's:A Continuum of Symptoms
Ann Neurol 4:145-148, Golden,G.S., 1978

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Adult Onset of the Dandy-Walker Syndrome
Arch Neurol 35:672-674, Lipton,H.L.,et al, 1978

Hypertensive Encephalopathy:A Clinicopathologic Study of 20 Cases
Neurol 28:928-939, Chester,E.M.,et al, 1978

Obstructive Sleep Apnea in Family Members
NEJM 299:969-973, Strohl,K.P.,et al, 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features
Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978

Ocular Involvement in Whipple's Disease
Arch Ophthalmol 96:1431-1436, Font,R.L.,et al, 1978

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Systemic Membrane Defect in the Proximal Muscular Dystrophies
NEJM 299:841-846, Pickard,N.A.,et al, 1978

Aphasia & Related Disturbances
Textbook of Med, Ed. R. W. Wilkins, Little Brown & Co. , Boston, p. 867, Benson,F.D., 1978

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

Clinical pathological conference
Von Hippel-Lindau disease, Case Record 1-1978, NEJM 298:95978., , 1978

Glycine Encephalopathy
NEJM 298:687, Ch'ien,L.T., 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Familial Hypopituitarism with Large Sella Turcica
NEJM 298:698, Parks,J.S.,et al, 1978



Showing articles 4300 to 4350 of 4627 << Previous Next >>