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Differential
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acridine orange-RNA fluorescence
adult polyglucosan body disease
algorithm
aneurysm
aneurysm, intracranial
aneurysm, intracranial, treatment of
angiography, spinal
ankylosing spondylitis
aqueduct of Sylvius, stenosis
aqueductal stenosis
astrocytoma
ataxia
ataxia, cerebellar
autonomic dysfunction
axonal degeneration
Babinski sign
bladder dysfunction
brainstem, atrophy
Brugada syndrome
bulbar palsy
CAT scan
CAT scan, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
CAT scan, spine
cataracts
cerebellar atrophy, primary
cerebellum, neoplasms of
cerebral cortical atrophy
cervical spine
Charcot-Marie-Tooth
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
complications
corpus callosum, thinning
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
dementia
diabetes insipidus
diabetes mellitus
differential diagnosis
diffuse idiopathic skeletal hyperostosis
dysarthria
dystonia
ears of the Lynx MR sign
electrocardiogram, abnormal
enzyme, muscle disease
epidemiology of neurology
exome sequencing
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
familial
fistula, arterio-venous, dural
F-wave response
gait disorder
gait, spastic
gene mutation
genetic neurologic disorders
genetic testing
glucose tolerance test, abnormal
glycogen storage disease
gynecomastia
head injury
headache
headache, severe
headache, sudden onset of
hearing loss
histochemistry
histochemistry of muscle
H-reflex testing
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperinsulinism
hyperreflexia
hypertension
hyposmia
hypotension, systemic
imbalance
inclusion bodies
intellectual deterioration
intracerebral hemorrhage
intracranial pressure, increased
intrinsic hand muscles, wasting of
Japan
Jewish
Kugelberg-Welander syndrome
laminectomy, cervical
laminectomy, lumbar
laughing
laughing, pathologic
leg weakness, bilateral
leukoencephalopathy
life expectancy
liver disease
malformation, vascular
malformation, vascular, dural
memory, defect of recent
memory, impairment of
mental retardation
monoparesis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
multiple system atrophy
muscle biopsy
muscle cramp
muscle weakness
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, neurogenic hypothesis of
myasthenia gravis
myelogram
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myeloradiculopathy
myocardial injury
myocytolysis
myopathy
myopathy, mitochondrial
myopathy, neurogenic hypothesis of
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve root hypertrophy
neurogenic atrophy
neurogenic bladder
neurogenic stunned myocardium
neurogenic vs.myopathic atrophy
neurologic disease, diagnoses of
neuropathy
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, peripheral
neuropathy, sensory
next-generation sequencing
nystagmus
Onufrowicz nucleus
optic atrophy
pain
pain, back
pain, central
pain, foot
pain, leg
paraparesis
paraparesis, familial spastic
paraparesis, spastic
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymyositis
polyneuropathy, familial
posterior longitudinal ligament, ossification of
prognosis
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
pulmonary edema
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
retinopathy
review article
risk factors
seizure
sensorineural hearing loss
sensory loss
Shy-Drager syndrome
spastic ataxia
spastic paraplegia, type 11
spastic paraplegia, type 7
spasticity
spinal cord, compression of
spinal cord, enlargement
spinal cord, infarction of
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal cord, vascular malformation of
spinal muscular atrophy
spinal stenosis
spinal stenosis, cervical canal
spinal stenosis, familial
spondylosis
stiff legs
subarachnoid hemorrhage
sudden death
syncope
treatment of neurologic disorder
trinucleotide repeats
unconsciousness
urinary incontinence
urinary urgency
vasospasm
vasospasm, cerebral
walking, difficulty with
weakness
weakness, progressive
wheelchair
white matter disease
Wolfram syndrome
X-linked bulbospinal neuronopathy
x-ray, spine
Showing articles 750 to 800 of 2489 << Previous Next >>

A Longitudinal Study of Brain Volume Changes in Normal Aging Using Serial Registered Magnetic Resonance Imaging
Arch Neurol 60:989-994, Scahill,R.I.,et al, 2003

Polymyositis Masquerading as Motor Neuron Disease
Arch Neurol 60:1001-1003, Ryan,A.,et al, 2003

Taenia solium Cysticercosis
Lancet 362:547-556, Garcia,H.H.,et al, 2003

Language Function and Dysfunction in Corticobasal Degeneration
Neurol 61:493-499, Graham,N.L.,et al, 2003

MR Imaging Findings in African Trypansomiasis
AJNR 24:1383-1385, Gill,D.S.,et al, 2003

Occurrence of Amyotrophic Lateral Sclerosis Among Gulf War Veterans
Neurol 61:742-749, Horner,R.D.,et al, 2003

Excess Incidence of ALS in Young Gulf War Veterans
Neurol 61:750-756, Haleyl,R.W., 2003

Multiple Sclerosis Presenting as Lower Motor Neuron Wasting and Weakness of the Distal Upper Extremity
Neurol 61:1303-1304, Chong,P.S.T.,et al, 2003

Posterior Ischemic Optic Neuropathy After Hemodialysis
Ophthalmol 110:1216-1218, Buono,L.M.,et al, 2003

The Topography of Metabolic Deficits in Posterior Cortical Atrophy (the Visual Variant of Alzheimers Disease) with FDG-PET
JNNP 74:1521-1529, Nestor,P.J.,et al, 2003

Two Unusual Cases of Visual Loss Following Severe Non-Surgical Blood Loss
Eye 16:185-189, Michaelides,M.,et al, 2002

Vein of Galen Aneurysmal Malformation: Diagnosis and Treatment of 13 Children With Extended Clinical Follow-Up
AJNR 23:1717-1724, Jones,B.V.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

T2-weighted MRI Differentiates Multiple System Atrophy from Parkinson's Disease
Neurol 59;1265-1267, Kraft,E.,et al, 2002

Poliomyelitis Due to West Nile Virus
NEJM 347:1280-1281, Glass,J.D.,et al, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Delayed Neuropathy and Myelopathy After Organophosphate Intoxication
NEJM 347:1119-1121, Chuang,C.,et al, 2002

Late Onset Postpartum Eclampsia: A Rare and Difficult Diagnosis
J Neurol 249:1287-1291, Dziewas,R.,et al, 2002

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

Clinicopath Conf., Prolactinoma
NEJM 347:1604-1611, Case 35-2002, 2002

Cerebellar Oedema and Sideroblastic Anaemia
Lancet 360:2046, Rojas-Marcos,I.,et al, 2002

A Longitudinal Study of Abnormalities on MRI and Disability From Multiple Sclerosis
NEJM 346:158-164,199, Brex,P.A.,et al, 2002

Thrombolysis in Stroke Beyond Three Hours: Targeting Patients With Diffusion and Perfusion MRI
Ann Neurol 51:11-13,28, Warach,S., 2002

Diffusion-weighted MRI Differentiates the Parkinson Variant of Multiple System Atrophy from PD
Neurol 58:575-580, Schocke,M.F.H.,et al, 2002

Diagnostic Criteria Used in Studies of Reflex Sympathetic Dystrophy
Neurol 58:522-526, van de Beek,W.-J.T.,et al, 2002

Ipsilateral Thalamic MRI Abnormality in an Epilepsy Patient
Neurol 58:641-644, Nagasaka,T.,et al, 2002

Serial MRI Findings in a Case of Primary Lateral Sclerosis
Neurol 58:647-649, Smith,C.D., 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Euthanasia and Physician-Assisted Suicide Among Patients with Amyotrophic Lateral Sclerosis in the Netherlands
NEJM 346:1638-1644, Veldink,J.H.,et al, 2002

Isolated Hand Palsy Due to Cortical Infarction: Localization of the Motor Hand Area
Neurol 58:1412-1414, Takahashi,N.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Spontaneous Intracranial Hypotension Causing Reversible Frontotemporal Dementia
Neurol 58:1285-1287, Hong,M.,et al, 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Results of Radiotherapy for Drooling in Amyotrophic Lateral Sclerosis
Neurol 58:1308, Stalpers,L.J.A. &Moser,E.C., 2002

Evolving Treatment Strategies for Epilepsy
JAMA 287:2917-2920, Diaz-Arrastia,R.,et al, 2002

Mimic Syndromes in Sporadic Cases of Progressive Spinal Muscular Atrophy
Neurol 58:1593-1596, Visser,J.,et al, 2002

Utility of Clinical Criteria in Differentiating Frontotemporal Lobar Degeneration (FTLD) From AD
Neurol 58:1608-1615, Rosen,H.J.,et al, 2002

Practice Paramenter: Neuroimaging of the Neonate
Neurol 58:1726-1738, Ment,L.R.,et al, 2002

Application of the New McDonald Criteria to Patients with Clinically Isolated Syndromes Suggestive of Mulitple Sclerosis
Ann Neurol 52:47-53, Dalton,C.M.,et al, 2002

Cranial MR Findings in Chronic Toluene Abuse by Inhalation
AJNR 23:1173-1179,1072, Aydin, K.,et al, 2002

Predictors of Hemorrhagic Transformation After Intravenous Recombinant Tissue Plasminogen Activator
Stroke 33:2047-2052, Selim,M.,et al, 2002

The Final Month of Life in Patients with ALS
Neurol 59:428-431, Ganzini,L.,et al, 2002

Clinical Features and ATTCT Repeat Expansion in Spinocerebellar Ataxia Type 10
Arch Neurol 59:1285-1290, Grewal,R.P.,et al, 2002

Progressive Ventricular Enlargement in Patients with Clinically Isolated Syndromes is Associated with the Early Development of Multiple Sclerosis
JNNP 73:141-147, Dalton,C.M.,et al, 2002

Radiotherapy-induced Cerebral Abnormalities in Patients with Low-grade Glioma
Neurol 59:121-123,8, Postma,T.J.,et al, 2002

Early Symptom Progression Rate is Related to ALS Outcome
Neurol 59:99-103, Chio,A.,et al, 2002

Lesions of the Corpus Callosum: MR Imaging and Differential Considerations in Adults and Children
AJR 179:251-257, Bourekas,E.C.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002



Showing articles 750 to 800 of 2489 << Previous Next >>