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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 3900 to 3950 of 4627 << Previous Next >>

Clinicopathological Conference
Angiitis of Central Nervous System, Case 35-1985, NEJM 313:566-575985., , 1985

Hypomelanosis of Ito:Association with a Chromosomal Abnormality
Neurol 35:607-610, Miller,C.A.,et al, 1985

Cortical Blindness Complicating Wegener's Granulomatosis
BMJ 290:675, Payton,C.D.,et al, 1985

Sarcoidosis & Its Neurological Manifestations
Arch Neurol 42:909-917, Stern,B.J.,et al, 1985

Unilateral Blindness Caused by Infection with The Lyme Disease Spirochete, Borrelia Burgdorferi
Ann Int Med 103:382-384, Steere,A.C.,et al, 1985

Inflammatory Myopathies
Ann Neurol 17:215-227, 317-3231985., Mastaglia,F.L.,et al, 1985

MR Imaging in Fahr Disease
J Comput Assist Tomogr 9:790-792, Scotti,G.,et al, 1985

Adult GM1-Gangliosidosis:Clinical Patterns & Rectal Biopsy
Neurol 35:875-880, Nakano,T.,et al, 1985

Clinical Findings in Four Children with Biotinidase Deficiency Detected Through a Statewide Neonatal Screening Program
NEJM 313:16-19, 43-441985., Wolf,B.,et al, 1985

Clin. Path. Conference
Limbic Encephalitis (Paraneoplastic Encephalomyelitis) , Transitional-Cell CA of Urinary Bladder, Ca, e Re 30-1985,NEJM 313:249-257,1985., 1985

The Risk of Cerebrovascular & Cardiovascular Disease in Patients with Anterior Ischemia Optic Neuropathy
Arch Ophthalmol 103:1136-1142, Guyer,D.R.,et al, 1985

Optic Neuritis & Multiple Sclerosis
Arch Neurol 42:702-704, Ebers,G.C., 1985

Optic Neuritis or Multiple Sclerosis
Arch Neurol 42:704-710, Kurtzke,J.F., 1985

Lightning Streaks of Moore:A Cause of Recurrent Stereotypic Visual Disturbance
Neurol 35:1078-1081, Zaret,B.S., 1985

Hallervorden-Spatz Disease:Cysteine Accumulation & Cysteine Dioxygenase Deficiency in the Globus Palladus
Ann Neurol 18:482-489, Perry,T.L.,et al, 1985

Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification
NEJM 313:139-181, Sly,W.S.,et al, 1985

Complications of Intravenous Digital Subtraction Angiography
Arch Neurol 42:969-972, Ball,J.B.,et al, 1985

Congenital Heart Defects in Live-Born Children of Epileptic Parents
Arch Neurol 42:374-376, Friis,M.L.,et al, 1985

The Value of Visual Evoked Potential as a Screening Test in Neurofibromatosis
Arch Neurol 42:1072-1074, Jabbari,B.,et al, 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985

Dysthyroid Orbitopathy
Neurol 35:1628-1634, Dresner,S.C.&Kennerdell,J.S., 1985

Late-Onset Hallervorden-Spatz Disease Presenting as Familial Parkinsonism
Neurol 35:227-234, Jankovic,J.,et al, 1985

Neurological Findings in Patients with the Fragile-X Syndrome
JNNP 48:150-153, Finelli,P.F.,et al, 1985

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Metachromatic Leukodystrophy Manifesting as a Schizophrenic Disorder:Computed Tomographic Correlation
Ann Neurol 18:94-95, Finelli,P.F., 1985

Amaurosis Fugax as the Presenting Manifestation of Dural Arteriovenous Malformation
Stroke 16:891-893, Bogousslavsky,J.,et al, 1985

Arrhythmogenic Seizures:Diagnosis by Simultaneous EEG/ECG Recording
Neurol 35:1503-1506, Gilchrist,J.M., 1985

Cardiovascular Regulation & Lesions of the Central Nervous System
Ann Neurol 18:1-12, Talman,W.T., 1985

A Microangiopathic Syndrome of Encephalopathy, Hearing Loss & Retinal Arteriolar Occlusions
Neurol 35:1113-1121, Monteiro,M.L.R.,et al, 1985

Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Arch Neurol 42:1008-1010, Katz,D.A.,et al, 1985

Amnestic Syndrome & Vertical Gaze Palsy:Early Detection of Bilateral Thalamic Infarction by CT & NMR
Stroke 16:823-827, Swanson,R.A.&Schmidley,J.W., 1985

Risk Factors & Concomitants of Internal Carotid Artery Occlusion or Stenosis, A Study of 159 Cases
Arch Neurol 42:864-867, Bogousslavsky,J.,et al, 1985

Autosomal Recessive Distal Muscular Dystrophy:A Comparative Study with Distal Myopathy with Rimmed Vacuole Formation
Ann Neurol 17:51-59, Nonaka,I.,et al, 1985

Migrainous Ischemic Optic Neuropathy
Neurol 35:112-114, Katz,B.,et al, 1985

Permanent Visual Loss after Shunt Malfunction
Neurol 35:25-29, Arroyo,H.A.,et al, 1985

Familial Infantile Myasthenia Gravis
Arch Neurol 42:143-144, Gieron,M.A.,et al, 1985

Transient Ipsilateral Paresthesias (TIPs) with Transient Monocular Blindness
Arch Neurol 42:295, Ropper,A., 1985

Neurocardiology:An Interdisciplinary Area for the 80's
Arch Neurol 42:178-184, Natelson,B.H., 1985

Cerebral Haemorrhagic Infarction in Young Patients with Hereditary Protein C Deficiency
BMJ 290:350-352, Wintzen,A.R.,et al, 1985

Sino-Orbital Aspergillosis Associated with Total Ophthalmoplegia
Laryngoscope 95:190-192, Yumoto,E.,et al, 1985

Moyamoya and Other Causes of Stroke in Patients with Down Syndrome
pediatr Neurol 1:174-179, Pearson,E.,et al, 1985

GM1 Gangliosidosis:Clinical and Laboratory Findings in Eight Families
Hum Genet 70:347-354, Giugliani,R.,et al, 1985

Conjugal Multiple Sclerosis
In Handbook of Clinical Neurol, Elsivier Publ, Amsterdam 47:291985., Myrianthopoulos,N.C., 1985

Neurologic Complications of Systemic Cancer
In Neurologic Clinics 3:729-750, Patchell,R.A.&Posner,J.B., 1985

Takayasu Arteritis, A Study of 32 North American Patients
Medicine 64:89-99, Hall,S.,et al, 1985

Genetic Testing in Huntington's Disease
Ann Neurol 16:511-513, Koller,W.C.,et al, 1984

Machado-Joseph-Azorean Disease
Arch Neurol 41:921-925, Fowler,H.L., 1984

Familial Multisystem Atrophy with Possible Thalamic Dementia
Neurol 34:1213-1217, Katz,D.A.,et al, 1984

Hereditary Adult-Onset Leukodystrophy Simulating Chronic Progressive Multiple Sclerosis
NEJM 311:948-953, Eldridge,R.,et al, 1984

MR Imaging of Familial Basilar Impression
J Comput Assist Tomogr 8:953-956, Bewermeyer,H.,et al, 1984



Showing articles 3900 to 3950 of 4627 << Previous Next >>