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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 2700 to 2750 of 4627 << Previous Next >>

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Digitalis-Induced Visual Disturbances with Therapeutic Serum Digitalis Concentrations
Ann Int Med 123:676-680, Butler,V.P.,et al, 1995

Optic Neuropathy, Headache, & Diplopia with MRI Suggestive of Cerebral Arteritis in Relapsing Polychondritis
J Neuro-Ophthalmol 15:171-175, Massry,G.G.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Familial Acephalgic Migraine
Neurol 45:2293-2294, Ziegler,D.K., 1995

Accuracy of Transesophageal Echocardiography for Ident Left Atrial Thrombi:Prospective, Intraop Study
Ann Int Med 123:817-822, 8821995., Manning,W.J.,et al, 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Clinicopath Conf
Acute Disseminated Encephalomyelitis, (postviral encephalomyelitis) Case 37-1995, NEJM 333:1485-1493, 199, 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,et al, 1995

Cost-Effectiveness of Warfarin and Aspirin for Prophylaxis of Stroke in Patients with Nonvalvular Atrial Fibrillation
JAMA 274:1839-1845, Gage,B.F.,et al, 1995

Spinocerebellar Ataxias and Ataxins
NEJM 333:1351-1353, Rosenberg,R.N., 1995

Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
Stroke 26:1935-1940, Schievink,W.I.&Mokri,B., 1995

Prognosis for Survival After an Initial Stroke
Stroke 26:2011-2015, Lai,S.M.,et al, 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

Clinicopath Conf
Intravascular Lymphomatosis, Case 31-1995, NEJM 333:992-999995., , 1995

Pain in Anterior Ischemic Optic Neuropathy
J Neuro-Ophthalmol 15:9-10, Swartz,N.G.,et al, 1995

Persistent Positive Visual Phenomena in Migraine
Neurol 45:664-668, Liu,G.T.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Familial Autoimmune Myasthenia Gravis:Report of Four Families
JNNP 58:729-731, Evoli,A.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Bilateral Simultaneous Optic Neuropathy in Adults:Clinical, Imaging, Serological, and Genetic Studies
JNNP 58:70-74, Morrissey,S.P.,et al, 1995

Optic Nerve Decompr Surg for Nonarter Anterior Ischemic Optic Neuropathy (NAION) Not Effective & May Be Harmful
JAMA 273:625-632, 6661995., Kelman,S.,et al, 1995

Optic Neuritis:A Population-Based Study in Olmsted County, Minnesota
Neurol 45:244-250, Rodriquez,M.,et al, 1995

Clinicopath Conf
Neurolymphomatosis, Case 8-1995, NEJM 332:730-737995., , 1995

Autosomal Dominant, Familial Spastic Paraplegia, Type I:Clinical and Genetic Analysis of a Large North American Family
Neurol 45:325-331, Fink,J.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Functional Magnetic Resonance Imaging of the Brain
Ann Int Med 122:296-303, LeBihan,D.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Familial Occurrence of Cluster Headache
JNNP 58:341-343, Russell,M.B.,et al, 1995

On Politics and Health:An Epidemic of Neurologic Disease in Cuba
Ann Int Med 122:530-533, Roman,G.C., 1995

Investigation of Peripheral Neuropathy
JNNP 58:274-283, McLeod,J.G., 1995

Proximal Myotonic Myopathy, Clin Features of Disorder Similar to Myotonic Dystrophy
Arch Neurol 52:25-31, Ricker,K.,et al, 1995

Determining Brain Death in Adults
Neurol 45:1003-1011, Wijdicks,E.F.M., 1995

A Comparison of Surgical & Medical Therapy for Atrial Septal Defect in Adults
NEJM 333:469-473, 5131995., Konstantinides,S.,et al, 1995

Diffuse Leptomeningeal Gliomatosis with Osteoblastic Metastases and No Evidence of Intraaxial Lesions
AJNR 16:1018-1020, Pingi,A.,et al, 1995

Visual System Abnormalities in Adrenomyeloneuropathy
Ann Neurol 37:550-552, Kaplan,P.W.,et al, 1995

Clinicopath Conf
Qunidine-Induced Thrombocytopenia, Cerebral Hemorrhage, Case 15-1995, NEJM 332:1363-137095., , 1995

Neurosurgical Management of Cerebellar Haematoma and Infarct
JNNP 59:287-292, Mathew,P.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Newly Diagnosed Atrial Fibrillation and Acute Stroke, The Framingham Study
Stroke 26:1527-1530, Lin,H.J.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Kindreds of Dominantly Inherited Parkinson's Disease:Keys to the Riddle
Ann Neurol 38:355-356, Duvoisin,R.C.&Golbe,L.I., 1995

A Greek-American Kindred with Autosomal Dominant, Levodopa-Responsive Parkinsonism and Anticipation
Ann Neurol 38:373-378, 3551995., Markopoulou,K.,et al, 1995



Showing articles 2700 to 2750 of 4627 << Previous Next >>