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Differential
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abducens nerve paralysis
agitation
Alexanders disease
Alexanders disease, adult onset
alternating hemiplegia
alternating hemiplegia of childhood
amaurosis fugax
aminoacidopathies
anemia
aneurysm
anorexia
antibiotics
anxiety
aphasia
arteritides
arthralgia
astrogliopathy
ataxia
ataxic gait
atrial fibrillation
autoimmune disease
autonomic dysfunction
bat bite
behavioral disorder
Borrelia miyamotoi infection
brainstem, infarction of
brainstem, lesion of
bulbar palsy
cachexia
carotid artery disease
carotid artery occlusion, neck
carotid artery stenosis
carpal tunnel syndrome
cataracts
cauda equina, enhancement
central nervous system, infection of
cerebral hypoperfusion
cerebral infarction
cerebral venous thrombosis
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
chemotherapy, CNS treatment and complications with
children
chills
chorea
choreoathetosis
choreoathetosis, paroxysmal
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
coma
complications
confusion
congestive heart failure
conjunctival injection
conversion reaction
cranial nerve enhancement
deafness
deafness, unilateral
delirium
dementia
developmental retardation
diabetes insipidus
diarrhea
diplopia
disorientation
drowsiness
dysarthria
dyskinesia, buccal lingual facial
dystonia
dystonia, psychogenic
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
emotional lability
encephalitis
encephalitis, focal
encephalitis, viral
encephalopathy
encephalopathy, acute
endarterectomy, carotid
episodic neurologic deficits
epistaxis
exercise intolerance
eye movement, disorders of
eye movement, painful
eye, pain in
face, numbness of
facial movement disorder
facial nerve palsy
facial weakness
facial weakness, bilateral
failure to thrive
familial
fatigue
fever
flaccid paralysis
floaters
fundus, abnormality of
gait disorder
gene
gene mutation
genetic neurologic disorders
GFAP gene
Graves ophthalmopathy
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hallucination
hallucination, visual
headache
heat intolerance
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hemiplegia
hepatomegaly
hyperreflexia
hypertension
hyperthermia
hyperthyroidism
hypoglycorrhachia
hypokalemia
hypokalemic paralysis
iatrogenic neurologic disorders
immunosuppression
inborn errors of metabolism
infection
insomnia
intellectual deficit
intracerebral hemorrhage
lactic acidemia
L-dopa
L-dopa, controlled release
leg weakness, bilateral
lethargy
leukemia
leukocytosis
leukodystrophy
level of consciousness, decreased
lysosomal storage disease
macrocephaly
mastoiditis
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, neutrophilic
meningitis, treatment of
meningoencephalitis
mental status, abnormal
metabolic disorder, primary
methotrexate
mimics
misdiagnosis
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, paroxysmal
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, negative
MRI, sulcal hyperintensity
muscle biopsy
muscle pain
muscle weakness
myasthenia gravis
myeloradiculopathy
myoclonic jerks
myoclonus
myopathy
nasal septum, perforation of
nausea and vomiting
neck stiffness
neck weakness
negative
nerve root enhancement
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic symptoms
neurologic symptoms, unexplained
neurologic testing
neuropathy
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxic
neurotoxicity, acute
neutropenia
New England
night sweats
ophthalmoplegia
opsoclonus
otitis, neurologic complications with
pain
pain, abdominal
pain, leg
pain, testicular
palatal myoclonus
papilledema
paraparesis
Parkinsonism syndrome
paroxysmal neurologic deficits
periarteritis nodosa
periodic limb movements
periodic movements during sleep
periodic paralysis
periodic paralysis, thyrotoxic
peroxisomal disease
personality change
personality disorder
phonophobia
PLEDs
PLEDs, bilateral independent
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
pulmonary infiltrates
quadriparesis, progressive
quadriplegia
rabies, nervous system involvement with
rash
restless leg syndrome
retinal artery occlusion
retinopathy
retro-orbital pain
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
risk factors
scotoma
sedimentation rate, elevated
seizure
serologic testing
serologic testing of cerebrospinal fluid
shaking
sinemet
sinusitis
skin, biopsy
skin, lesions in neurologic disorders
sleep
somnolence
sonophobia
spirochete infection
stare
staring spells
steroid therapy, CNS treatment and complications with
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subacute sclerosing panencephalitis, adult onset
tachycardia
temporal lobe, lesion
temporalis muscle wasting
testicular biopsy
third nerve palsy
thyroid function tests
thyroid gland, enlarged
thyrotoxicosis
tinnitus
toxic encephalopathy
transient ischemic attack
transient ischemic attack, limb shaking
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, psychogenic
trigeminal neuropathy
trigeminal neuropathy, sensory
unconsciousness
unconsciousness, transient
urea-cycle enzymopathies
uremia
vertigo
viral infection, CNS
vision, blurred
vision, blurred, monocular
visual field defect
visual loss
weakness
weakness, episodic
weakness, generalized
weakness, progressive
weight loss
word-finding difficulty
Showing articles 1950 to 2000 of 3598 << Previous Next >>

Neurologic Complications Following Chiropractic Manipulation:A Survey of California Neurologists
Neurol 45:1213-1215, Lee,K.P.,et al, 1995

Postoperative Neurologic Complications after Open Heart Surgery on Young Infants
Arch Pediatr Adolesc Med 149:764-768, Miller,G.,et al, 1995

Exacerbation of Idiopathic Parkinson's Disease by Naproxen
BMJ 311:422, Shaunak,S.,et al, 1995

Reflex Sympathetic Dystrophy in Children
BMJ 310:1648-1649, Lloyd-Thomas,A.R.&Lauder,G., 1995

The Prevention of Neurogenetic Disease
Arch Neurol 52:356-362, 3451995., Rosenberg,R.N.&Iannaccone,S.T., 1995

The Management of Thrombosis in the Antiphospholipid-Antibody Syndrome
NEJM 332:993-997, 10251995., Khamashta,M.A.,et al, 1995

Alien Hand Syndrome:Interhemispheric Motor Disconnection Due to a Lesion in the Midbody of the Corpus Callosum
Neurol 45:802-808, Geschwind,D.H.,et al, 1995

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

Cephalosporin-Induced Recurrent Aseptic Meningitis
Ann Neurol 37:815-817, Creel,G.B.&Hurtt,M., 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Clinical Relevance and Frequency of Transient Stenoses of the Middle and Anterior Cerebral Arteries in Bacterial Meningitis
Stroke 26:1399-1403, Muller,M.,et al, 1995

Myelitis Due to Coxsackievirus B Infection
Neurol 45:1626-1627, Jadoul,C.,et al, 1995

Myositis:Immunologic Contributions to Understanding Cause, Pathogenesis, and Therapy
Ann Int Med 122:715-724, Plotz,P.H.,et al, 1995

Proximal Myotonic Myopathy Syndrome in the Absence of Trinucleotide Repeat Expansions
Muscle & Nerve 18:782-783995., Stoll,G.,et al, 1995

Primary Adhalin Deficiency as a Cause of Muscular Dystrophy in Patients with Normal Dystrophin
Ann Neurol 38:367-372, 3531995., Ljunggren,A.,et al, 1995

Inclusion Body Myositis Presenting with Isolated Erector Spinae Paresis
Neurol 45:993-994, Hund,E.,et al, 1995

Amyloidosis Causing A Progressive Myopathy
Muscle & Nerve 18:1016-1018995., Nadkarni,N.,et al, 1995

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

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

Anterior Communicating Artery Aneurysm Paraparesis Syndrome:Clinical Manifestations and Pathologic Correlates
Neurol 45:45-50, Greene,K.A.,et al, 1995

The Risk of Stroke in Pts with First-Ever Retinal vs Hemispheric TIAs & High-Grade Carotid Stenosis
Arch Neurol 52:246-249, Streifler,J.Y.,et al, 1995

Sneddon's Syndrome is a Thrombotic Vasculopathy:Neuropathologic and Neuroradiologic Evidence
Neurol 45:557-560, Geschwind,D.H.,et al, 1995

Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 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

Critical Illness Neuromuscular Disease in Children Manifested as Ventilatory Dependence
J Pediatr 126:259-261, Sheth,R.D.,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

Lesion Localization in Periodic Lateralized Epileptiform Discharges:Gray or White Matter
Epilepsia, 36:58-621995., Raroque,H.G.&Purdy,P., 1995

Serotonin Syndrome
Neurol 45:219-223, Bodner,R.A.,et al, 1995

Involuntary Movement Disorders Associated with Felbamate
Neurol 45:185-187, Kerrick,J.M.,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

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

Improvement of Paraneoplastic Opsoclonus-Myoclonus After Protein A Column Therapy
NEJM 332:192, Nitschke,M.,et al, 1995

Renal Cell Carcinomatous Meningitis:Pathologic and Immunohistochemical Features
Neurol 45:189-191, Crino,P.B.,et al, 1995

Parkinsonism-Recognition and Differential Diagnosis
BMJ 310:447-452, Quinn,N., 1995

Classic Neurogenic Thoracic Outlet Syndrome in a Competitive Swimmer:A True Scalenus Anticus Syndrome
Muscle & Nerve 18:229-233995., Katirji,B.&Hardy,R.W., 1995

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Diagnosis of Whipple's Disease
NEJM 332:390-392, Dobbins,W.O., 1995

Postvaricella Basal Ganglia Infarction in Children
AJNR 16:449-452, Silverstein,F.S.&Brunberg,J.A., 1995

Incontinence in the Nursing Home
Ann Int Med 122:438-449, Ouslander,J.G.&Schnelle,J.F., 1995

Late-Onset Mitochondrial Myopathy
Ann Neurol 37:16-23, 31995., Johnston,W.,et al, 1995

Psychogenic Movement Disorders:Frequency, Clinical Profile and Characteristics
JNNP 59:406-412, Factor,S.A.,et al, 1995

Symptomatic Spinal Epidural Lipomatosis in a Patient with Cushings Disease
Neurol 45:2281-2283, Sivakumar,K.,et al, 1995

A 50-Year-Old Woman with Disabling Spinal Stenosis
JAMA 274:1949-1954, Garfin,S.R., 1995

Diphtheritic Neuropathy
Muscle & Nerve 18:1460-1463995., Greange,A.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Neurologic Complications of Lumbar Epidural Anesthesia and Analgesia
Neurol 45:1795-1801, Yuen,E.C.,et al, 1995

Lumbosacral Plexopathy Due to Benign Uterine Leiomyoma
Neurol 45:1943-1944, Felice,K.J.&Donaldson,J.O., 1995

Campylobacter Jejuni Infection and Guillain-Barre Syndrome
NEJM 333:1374-1379, 14151995., Rees,J.H.,et al, 1995

Eye Movement Abnormalities in Systemic Lupus Erythematosus
Arch Neurol 52:1145-1149, Keane,J.R., 1995



Showing articles 1950 to 2000 of 3598 << Previous Next >>