Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal contractions
abdominal distention
acanthocytosis
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome-related complex
acute disseminated encephalomyelitis
Addison's disease
advances in neurology
adverse drug reaction
agitation
algorithm
alopecia
Alzheimer's disease
amenorrhea
amnesia
amyloid angiopathy, cerebral
ANA
anemia
anemia, iron deficiency
anemia, megaloblastic
aneurysm, intracranial
angiitis, granulomatous of CNS
angiitis, isolated of CNS
anorexia
anti IgLON5
antibiotics
antibiotics, neurologic complications with
anticonvulsants
anticonvulsants, untoward effects of
antiendomysial antibodies
aphasia
aphonia
aqueduct of Sylvius, stenosis
aqueductal stenosis
arachnoiditis
areflexia
arteritides
arthralgia
arthritis
aspartate aminotransferase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, sensory
ataxia, truncal
ataxic gait
atrial myxoma
autoantibodies
autoimmune disease
axonopathy, distal
B 12 deficiency
bacterial endocarditis, neurologic manifestations of
bacterial infection
bacterial infection, CNS
basal ganglia, calcification of
basilar impression
Bassen-Kornzweig syndrome
Behcet's syndrome
Bergmann's gliosis
bilateral periventricular nodular heterotopia
bladder dysfunction
blind spot, enlarged
blindness
bloating
bone density
bone marrow biopsy
bone pain
bone scanning
bradyphrenia
brain biopsy
brain fog
brainstem, infarction of
brainstem, lesion of
Brueghel's syndrome
burning feet
burning paresthesia
calcification, gyral
calcification, intracranial
carbon monoxide poisoning
carcinoma
carcinoma of lung
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, ring sign
cataracts
cecum perforation
ceftriaxone
celiac disease, adult
celiac disease, childhood
celiac disease, epilepsy and cerebral calcification
central nervous system, infection of
central pontine myelinolysis
cephalosporins
cerebellar ataxia, hereditary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebellum
cerebellum, disease of
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral embolism
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, recurrent
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
children
chorioretinitis
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonazepam
clubbing of fingers
cognition
colchicine
cold intolerance
colectomy
collagen vascular disease
collagenous sprue
complications
compression fracture
confusion
constipation
copper
copper deficiency
coprolalia
corpus callosum
cortical blindness
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
cystic fibrosis, neurologic complications with
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, presenile
dementia, treatment of
demyelinating disease
dental prostheses
denture cream
depression
dermatitis
dermatitis herpetiformis
developmental retardation
diabetes mellitus
diarrhea
diet
differential diagnosis
dilantin
dilantin, factors influencing metabolism of
dilantin, serum level
diplopia
disorientation
dissociated sensory loss
dizziness
D-lactate acidosis
downward gaze, paralysis of
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysphagia
dysthyroidism
dystonia
dystonia, focal
ecchymoses
edema, pedal
electroencephalogram
electroencephalogram, abnormalities of
electron microscopy
electroretinograph
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
endocarditis
endocarditis, marantic
eye movement, disorders of
facial movement disorder
failure to thrive
falling
false negative
false positive VDRL
fatigue
fever
floppy infant
folic acid deficiency
fracture, long bone
gadolinium
gait disorder
gait, waddling
ganglionitis
gastrectomy, neurologic complications following
gastric partitioning
gastric surgery
gastritis
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gaze palsy, vertical
genetic neurologic disorders
gliadin antibodies
gliomatosis cerebri
glossitis
glucose tolerance test, abnormal
glutamic acid decarboxylase, antibody
gluten ataxia
gluten sensitivity
gluten-free diet
gram positive rod
granulomatous disease
growth retardation
hallucination, visual
headache
headache, episodic
hearing loss
helicobacter pylori
hemiballismus
hemichorea
hemiparesis
hemiplegia
hemorrhagic diathesis
hepatitis
hepatomegaly
heralding manifestation
heterotopia
hippocampus
hippocampus, hyperintense
histamine-2 receptor blockers
HLA
homocysteine, serum
human immunodeficiency virus type 1
hydrocephalus
hypergammaglobulinemia
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypersomnia
hypertensive encephalopathy
hyperthyroidism
hypoalbuminemia
hypocalcemia
hypocholesterolemia
hypoglycorrhachia
hypogonadism
hypokalemia
hypomagnesemia
hypometric saccades
hypoparathyroidism
hypoparathyroidism, idiopathic
hypoproteinemia
hypoprothrombinemia
hyporeflexia
hypothalamus, damage to
hypothalamus, disturbance of
hypothalamus, lesion of
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
imbalance
immune reconstitution inflammatory syndrome
immunosuppressive agents
immunotherapy
impotence
incontinence, fecal
infection
insomnia
intellectual deficit
intestinal biopsy
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial pressure, increased
iron, serum, low
jaundice
lactic acidemia
lactic dehydrogenase(LDH)
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
limbic encephalitis
liver disease
liver function enzymes
Lyme disease
lymph node biopsy
lymphadenopathy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malabsorption
malabsorption syndrome
malaise
mammillary bodies
mast cell
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, bacterial
meningitis, carcinomatous
meningitis, diagnosis
meningitis, lymphomatous
meningoencephalitis
mental status, abnormal
mestinon
metabolic acidosis
metformin
methylmalonic acid, serum
midbrain, lesion of
migraine
migraine, treatment of
mimics
misdiagnosis
mitochondrial disease
mitral valve vegetation
molecular genetics
mononeuropathy multiplex
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, FLAIR
MRI, negative
MRI, serial
MRI, spinal cord
MRI, volumetry
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, anticholinesterase malabsorption in
myasthenia gravis, anticholinesterase serum levels in
mycobacterium avium-intracellulare
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonic ataxia
myoclonic jerks
myoclonus
myoclonus, abdominal
myoclonus, cortical
myoclonus, epilepsy
myoclonus, segmental
myoclonus, stimulus sensitive
myoclonus-ataxia syndrome
myopathy
myorhythmia
myositis
narcolepsy
nausea and vomiting
neoplasm, metastatic to CNS
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, false negative
neuritis, causes of
neuroendocrinology
neurologic complications of, systemic disease
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, motor
neuropathy, multifocal
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
night blindness
night sweats
nutritional deficiency
nystagmus
nystagmus, pendular
nystagmus, vertical
ocular motility, disorders of
oculomasticatory myorhythmia
ophthalmoplegia
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
optic chiasm
optic chiasm, lesion of
optic neuritis
oral ulcerations
osteomalacia
osteoporosis
pain
pain, abdominal
pain, neuropathic
pain, total body
palatal myoclonus
papilledema
paresthesias
paresthesias, generalized
Parkinsonism syndrome
partial thromboplastin time, prolonged
PAS positive
PAS positive material in the brain
pericarditis
pernicious anemia
personality change
petechiae
phenylketonuria
plasmapheresis
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
pneumonia
polydipsia
polymerase chain reaction
polymerase chain reaction, false negative
polymyositis
polyneuropathy
polyps, gastrointestinal tract
posterior column disease
posterior inferior cerebellar artery syndrome
posterior leukoencephalopathy syndrome
practice guidelines
pregnancy, neurologic complications in
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
prothrombin time, prolonged
proton pump inhibitors
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychotic behavior
ptosis
puberty
puberty, delayed
Purkinje cell
pyridoxine deficiency
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
Ramsay Hunt syndrome
Raynaud's phenomenon
refractory sprue
regional enteritis
remote effect of cancer on the nervous system
reticulum antibodies
reticulum cell sarcoma
retinal hemorrhages
retinitis pigmentosa
retinopathy
retrobulbar neuritis
review article
rheumatoid arthritis factor(R.A.factor)
rickets
risk factors
salivation, excessive
sarcoidosis
sarcoidosis, CNS
scleroderma
scleroderma, neurologic involvement with
scotoma
scotoma, paracentral-homonymous
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, focal
seizure, intractable
seizure, medication failure
seizure, pregnancy
sensory loss
serologic testing
seronegative
serum alanine aminotransferase
short stature
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
skin, darkening of
skin, hematoma
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
slurred speech
small-bowel bypass
small-bowel resection
sodium valproate
somatosensory evoked potentials
somnolence
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, biopsy
spinal cord, enlargement
spinal cord, injury of
spinal cord, lesion of
spinocerebellar degeneration
splenomegaly
sprue
status epilepticus
steatorrhea
steroid therapy, CNS treatment and complications with
stool, loose
swayback
symmetric brain lesions
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic mastocytosis
tandem gait, ataxic
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
tetany
thrombosis, cerebral
thyroiditis
tinnitus
tonic spasms
toxoplasmosis, CNS
transglutaminase antibodies
treatment of neurologic disorder
tremor
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trimethoprim-sulfamethoxazole
ulcerative colitis
upgaze
upgaze, paralysis of
uremia
urinary 17 hydroxycorticosteroids
urinary 17 ketosteroids
urinary incontinence
uveitis
vascular headache, food causing
vasculitides
vasculopathy
Venereal Disease Research Laboratory test
vertical gaze
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
vitamin A
vitamin A deficiency
vitamin D
vitamin D deficiency
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitamin K deficiency
vitreous hemorrhage
vitreous opacities
vitritis
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
workup
zinc
Showing articles 50 to 100 of 150 << Previous Next >>

Helicobacter pylori -- Is It a Novel Causative Agent in Vitamin B12 Deficiency?
Arch Int Med 160:1349-1353,1229, Kaptan,K.,et al, 2000

An Uncommon Cause of Recurrent Strokes
Stroke 31:2002-2003, Naegeli,B. et al, 2000

A Woman Who Left Her Wheelchair
Lancet 353:806, Mingrone,G.,et al, 1999

Cerebellar Ataxia Associated with Subclinical Celiac Disease Responding to Gluten-Free Diet
Neurol 53:1606-1608, Pellecchia,M.T.,et al, 1999

Polymerase Chain Reaction in the Diagnosis and Management of Central Nervous System Infections
Arch Neurol 56:1215-1219, DeBiasi,R.L.&Tyler,K.L., 1999

Insomnia for 5 Years
Lancet 354:1966, Lieb,K.,et al, 1999

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

Cervical Myelopathy Caused by Whipple's Disease
Neurol 50:1505-1506, Clarke,C.E.,et al, 1998

Diagnostic Utility of the Polymerase Chain Reaction in 2 Cases of Suspected Whipple Disease
Arch Int Med 158:801-803, Tasken,K.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Gastorintestinal Manifestations of Scleroderma
Gastroenterol Clin 27:563-594, Rose,S.,et al, 1998

Chronic Progressive Leukoencephalopathy in Adult Celiac Disease
Neurol 50:820-822, Beyenburg,S.,et al, 1998

Cerebral Involvement in Celiac Disease:A Serial MRI Study in a Patient with Brainstem & Cerebellar Symptoms
Neurol 49:1447-1450, Ghezzi,A.,et al, 1997

CSF Antigliadin Antibodies and the Ramsay Hunt Syndrome
Neurol 49:1131-1133, Chinnery,P.F.,et al, 1997

Whipple Disease
Medicine 76:170-184, Durand,D.V.,et al, 1997

Polymerase Chain Reaction-Based Detection of Tropheryma Whippelii in Central Nervous System Whipple's Disease
Ann Neurol 42:120-124, Lynch,T.,et al, 1997

Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996

A Man with Weight Loss, Ataxia, and Confusion for 3 Months
Lancet 347:448, Beversdorf,D.,et al, 1996

Does Cryptic Gluten Sensitivity Play a Part in Neurological Illness?
Lancet 347:369-370, Hadjivassiliou,M.,et al, 1996

Mastocytosis-Induced Nyctalopia
J Neuro-Ophthalmol 16:115-119, Lesser,R.L.,et al, 1996

Subcortical Heterotopia:A Distinct Clinicoradiologic Entity
AJNR 17:1315-1322, Barkovich,A.J., 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Whipple Disease Confined to the Central Nervous System in Childhood
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996

MR of Cerebral Whipple Disease
AJNR 16:1328-1329, Schnider,P.,et al, 1995

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

Brief Report:Diagnosis of Whipple's Disease by Molecular Analysis of Peripheral Blood
NEJM 331:1343-1346, Lowsky,R.,et al, 1994

Short-term Night Blindness Associated with Colon Resection and Hypovitaminosis A
Arch Ophthalmol 112:162-163, Sloan,D.B.,et al, 1994

Gadolinium-enhanced MRI in Cerebral Whipple's Disease
neuroradiology 35:581-583, Erdem,E.,et al, 1993

Coeliac Disease, Epilepsy, and Cerebral Calcifications
Lancet 340:439-443, Gobbi,G.,et al, 1992

Identification of the Uncultured Bacillus of Whipple's Disease
NEJM 327:293-301, 3461992., Relman,D.A.,et al, 1992

Bone Marrow Involvement by Whipple Bacillus
J Infect Dis 163:1169-1170, Jarolim,D.R.,et al, 1991

Abnormal Vitamin B12 Metabolism in Human Immunodeficiency Virus Infection
Arch Neurol 48:312-314, Kieburtz,K.D.,et al, 1991

Celiac Disease, Brain Atrophy, and Dementia
Neurol 41:372-375, Collin,P.,et al, 1991

Whipple's Disease Confined to the CNS Presenting with Multiple Intracerebral Mass Lesions
JNNP 54:989-992, Wroe,S.J.,et al, 1991

Oculo-Facial-Skeletal Myorhythmia in Whipple Disease:Treatment with Ceftriazone
Ann Int Med 112:467-469, Adler,C.H.&Galetta,S.L., 1990

MR Imaging of CNS Relapse of Whipple Disease
J Comput Assist Tomogr 14:815-817, Davion,T.,et al, 1990

Neuropsychiatric Disorders Caused by Cobalamin Deficiency in the Absence of Anemia or Macrocytosis
NEJM 318:1720-1728, 1752-17541988., Lindenbaum,J.,et al, 1988

Adult Coeliac Disease and Brainstem Encephalitis
JNNP 51:456-457, Brucke,T.,et al, 1988

Distal Axonopathy Associated with Chronic Gluten Enteropathy:A Treatable Disorder
Neurol 38:642-645, Kaplan,J.G.,et al, 1988

Hypoparathyroidism
Cecil Textbook of Medicine 18th Ed, W B Saunders Co, Phila, p149688., Arnaud,C.D., 1988

PAS Negative Granulomatous Lymphadenopathy in Whipple's Disease, Localization of Whipple Bacillus by EM
Am J Med 83:165-170, Wilcox,G.M.,et al, 1987

Movement Disorders & AIDS
Neurol 37:37-41, Nath,A.,et al, 1987

Whipple; s Disease Confined to the Central Nervous System
Ann Neurol 21:104-108, Adams,M.,et al, 1987

Oculomasticatory Myorhythmia:A Unique Movement Disorder Occurring in Whipple's Disease
Ann Neurol 20:677-683, Schwartz,M.A.,et al, 1986

Whipple's Disease of the Central Nervous System in Aids
NEJM 315:1029-1030, Jankovic,J., 1986

Isolated Vasculitis of the Central Nervous System in a Patient with Celiac Disease
Am J Med 81:1092-1094, Rush,P.J.,et al, 1986

Segmental Myoclonus Clinical and Pharmacologic Study
Arch Neurol 43:1025-1031, Jankovic,J.&Pardo,R., 1986

Blind Loop Syndrome, Vitamin E Malabsorption, & Spinocerebellar Degeneration
Neurol 35:338-342, Brin,M.F.,et al, 1985

Celiac Disease & Spinocerebellar Degeneration with Normal Vitamin E Status
Neurol 35:1199-1201, Ward,M.E.,et al, 1985

Improved Neurologic Function After Long-Term Correction of Vitamin E Deficiency in Children with Chronic Cholestasis
NEJM 313:1580-1586, Sokol,R.J.,et al, 1985



Showing articles 50 to 100 of 150 << Previous Next >>