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Differential
(Click to cross reference)
abdominal distention
adrenoleukodystrophy
alopecia
alternating rapid movement
Alzheimer's disease
Alzheimer's disease, familial
amenorrhea
anemia
anomic aphasia
anorexia
antibiotics
aphasia
apraxia
areflexia
arteriopathy
arthralgia
arthritis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia, infarction
behavioral disorder
Bing-Neel syndrome
blindness
bradyphrenia
brain biopsy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
central nervous system, infection of
cephalosporins
cerebellar atrophy, primary
cerebellar lesion
cerebellar plaques, amyloid
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
children
chorioretinitis
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
coma
confusion
creatine phosphokinase(CPK)elevated
cry, abnormal
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diarrhea
diplopia
disorientation
dizziness
downward gaze, paralysis of
dysarthria
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
electron microscopy
electrophoretic pattern, serum
electroretinograph
encephalopathy
encephalopathy, progressive
endocarditis, marantic
enzyme, defect
epistaxis
exercise
exercise intolerance
eye movement, disorders of
facial movement disorder
false negative
familial
fatigue
feeding disorder
fever
fingerprint bodies
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gangliosidosis GM2
gangliosidosis GM2-AB variant
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
globoid cells
glossitis
glucose tolerance test, abnormal
glycogen storage disease
gram positive rod
granular osmiphilic material
granulomatous disease
growth retardation
Guillain Barre syndrome
hallucination
hallucination, visual
hands, fisted
head lag
hemiparesis
hemiplegia
hemorrhagic diathesis
hepatomegaly
hepatosplenomegaly
hippocampus
hippocampus, hyperintense
hydrocephalus
hydrocephalus, normal pressure
hyperphagia
hyperpigmentation of skin
hypertonia
hyperviscosity
hypoalbuminemia
hypothalamus, damage to
hypothalamus, disturbance of
immunofluorescence
immunosuppressive agents
impotence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
infection
insomnia
intellectual deficit
intellectual deterioration
intestinal biopsy
intracerebral hemorrhage
irritability
ischemic exercise test
Jakob-Creutzfeldt disease
Krabbe's disease
kuru
kuru plaques
Lafora body
Lafora's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
limbic encephalitis
lymph node biopsy
lymphadenopathy
macroglobulinemia
malabsorption
malabsorption syndrome
malaise
McArdle's disease
meconium staining
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
mental status, abnormal
migraine
misdiagnosis
mitral valve vegetation
molecular genetics
mononeuritis multiplex
mononeuropathy
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, spinal cord
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle pain
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle weakness
mycobacterium avium-intracellulare
myelopathy
myoclonus
myoclonus, epilepsy
myoglobinuria
narcolepsy
negative
nerve biopsy
nerve conduction studies
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, sensory
night sweats
Notch3 gene
nystagmus
nystagmus, vertical
ocular motility, disorders of
oculomasticatory myorhythmia
ophthalmoplegia
ophthalmoplegia, total
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve, enlarged
pain
pain, abdominal
papilledema
paresthesias
Parkinson disease
PAS positive
PAS positive material in the brain
pericarditis
personality change
phosphorylase b kinase deficiency
pleocytosis of cerebrospinal fluid
pleural effusion
pleurisy
pneumonia
polydipsia
polymerase chain reaction
polyneuropathy
polyps, gastrointestinal tract
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract
Red flags
renal failure
retinal hemorrhages
retinopathy
review article
sea-blue histiocytes
second wind phenomena
sedimentation rate, elevated
seizure
seizure, children
seizure, intractable
seizure, teenager
senile plaques
skin, biopsy
skin, darkening of
sleep pathology and physiology
slow virus infection of CNS
small vessel disease
somnolence
spasticity
sphingolipodoses
spinal cord, lesion of
splenomegaly
spongy degeneration of brain
startle myoclonus
startle reaction
steatorrhea
storage disease of CNS
stuttering
subarachnoid hemorrhage
symmetric brain lesions
systemic illness
tapetoretinal degeneration
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular biopsy
thalamus, lesion of-bilateral
tinnitus
treatment of neurologic disorder
tremor
tremor, intention
trimethoprim-sulfamethoxazole
upgaze
upgaze, paralysis of
urinary 17 hydroxycorticosteroids
urinary 17 ketosteroids
urinary incontinence
urine, dark
uveitis
vasculopathy
vertical gaze
viral infection, CNS
vision, blurred
visual acuity, decreased
visual loss
visual loss, slow
vitreous opacities
vitritis
Waldenstrom's macroglobulinemia
walking, difficulty with
weakness
weakness, progressive
weight loss
wheelchair
Whipple's disease
white matter disease
Showing articles 0 to 50 of 371 Next >>

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Kuru
Adams & Victors Principles of Neurology, Chp 33, pg 773, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

The Patient Has the Diagnosis
Lancet 378:1436, Jubany,L.I.,et al, 2010

Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
NEJM 360:1656-1665, Case 12-2009, 2009

Whipples Disease
NEJM 356:55-66, Fenollar,F.,et al, 2007

Neurologic Presentation of Whipple Disease
Medicine 81:443-457, Gerard,A.,et al, 2002

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

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

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

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

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Sweat Gland Duct Cells in Lafora Disease:Diagnosis by Skin Biopsy
Neurol 31:1564-1568, Carpenter,S.,et al, 1981

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Amyloid Neuropathy & Tremor in Waldenstrom's Macroglobulinemia
Arch Neurol 37:240-242, Bajada,S.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Cerebral Whipple's Disease With Negative Jejunal Histology
NEJM 300:907-921, Feurle,G.E.,et al, 1979

Clinical & Extraneural Histologic Diagnosis of Neuronal Ceroidlipofuscinosis
Neurol 28:1008-1012, Miley,C.E.III.,et al, 1978

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

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

Polyneuropathy in Waldenstrom's Macroglobulinemia
Arch Neurol 35:423, Julien,J.,et al, 1978

A Syndrome of Progressive Muscle Spasm, Alopecia, & Diarrhea
Neurol 28:458, Satoyoshi,E., 1978

Meningitis in Whipple's Disease
BMJ 2:14-15, Thompson,D.G.,et al, 1978

Lymph-Node Bacilliform Bodies Resembling Those of Whipple's Disease in a Pt Without Intestinal Involvement, Mansbach
Ann Int Med 89:64-66, II,C.M.,et al, 1978

CT Scanning & Diagnosis of Adrenoleukodystrophy
Neurol 27:884, Greenberg,H.S.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Whipple's Disease of the Central Nervous System
Acta Neuropath 36:31, Silbert,S.W.,et al, 1976

Neurologic Complications After Treatment for Whipple's Disease:A Report of Four Patients
Medicine 55:467, Knox,D.L.,et al, 1976

Isolation & Characterization of an Aetiological Agent in Whipple's Disease
BMJ 3:568, Clancy,R.L.,et al, 1975

Whipple's Disease:A Review of 19 Pnts from one Hospital & a Review of the Literature since 1950
Medicine 49:175, Maizel,H.,et al, 1970

Cerebral Complications of Whipple's Disease
Brain 88:137, Smith,W.T.,et al, 1965

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

Risk of False Acetylcholine Receptor Autoantibody Positivity by Radioimmunoprecipitation Assay in Clinical Practice
Neurol 104:e213498, Zara,P.,et al, 2025

Clinicopathologic Conference, Brain Abscess Due to Infection with Listeria Monocytogeneses
NEJM 391:1529-1538, Case 33-2024, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

IgG4-Related Orbital Inflammation
https://EyeWiki.org, Oct, Chelnis,J. & Gervasio,K.A., 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

Sweet Syndrome
Stat Pearls www.ncbi.nlm.gov, Sept, Goyal,V.P. & Holmes,H, 2022

Stroke Mimics in the Acute Setting: Role of Multimodal CT Protocol
AJNR 43:216-222, Prodi, E.,et al, 2022

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022

Diagnosis and Subtyping of Listeria Ventriculitis in an Immunocompetent Host
Neurol 99:123-126, Zhao, C.W.,et al, 2022

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,et al, 2022

Clinicopathological Conference, Chronic Candida Albicans Meningitis
NEJM 387:641-650, Case 25-2022, 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022



Showing articles 0 to 50 of 371 Next >>