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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 50 to 100 of 2468 << Previous Next >>

Occipital Condyle Syndrome
Neurol 103:e210067, Mirian,A.,et al, 2024

Reversible Cerebral Atrophy and Substantia Nigra Changes after Vitamin B12 Treatment in Infantile Tremor Syndrome
Neurol 103:e210076, Singh,R.,et al, 2024

Clinicopathologic Conference, Psychotic Disorder Due to a General Medical Condition (postictal psychosis)
NEJM 391:2036-2046, Case 37-2024, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Leptomeningitis with Communicating Hydrocephalus in an Immunocompromised Patient with Disseminated Sporotrichosis
Neurol 103:e209586, Taborda,M.H.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

MR Imaging Findings in Anti-Leucine-Rich Glioma Inactivated Protein 1 Encephalitis:A Systematic Review and Meta-Analysis
AJNR 45:977-986, Almeida,F.C.,et al, 2024

Ictal Whistling Associated with Dominant Parahippocampal Gyrus Cortical Dysplasia
Neurol 103:e209489, Hartnett,P.,et al, 2024

A 60-Year-Old Woman with Rapidly Progressive Muscle Weakness and Ophthalmoparesis
Neurol 103:e209708, Wannarong,T.,et al, 2024

Clinicopathologic Conference, Nutritional Optic Neuropathy Due to Multiple Nutritional Deficits, Including Vitamin A, Copper, and Zinc Deficiencies
NEJM 391:641-650, Gaier,E.D.,et al, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

Neurovascular Complications of Iatrogenic Fusarium solani Meningitis
NEJM 390:522-529, Strong, N.,et al, 2024

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

Clinicopathologic Conference, Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis
NEJM 390:843-851, Case 7-2024, 2024

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

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

Primary Diffuse Leptomeningeal Melanocytosis, A Diagnoatic Conundrum
Neurol 101:e576-3580, Selvarajan,J.M.P.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

Cognitive and Clinical Characteristics of Patients with Limbic-Predominant Age-Related TDP-43 Encephalopathy
Neurol 100:e2027-e2035, Pagnotti,R.M.B.,et al, 2023

Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
Neurol 100:1111-1116, Mankad,J.P. & Lavingia,J.R., 2023

Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

Trial of Globus Pallidus Focused Ultrasound Ablation in Parkinsons Disease
NEJM 388:683-693, 759, Krishna,V.,et al, 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

A 36-Year-Old Man With Asymmetric Muscle Weakness
Neurol 99"1057-1061, Harada,Y.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

A 31-Year-Old Man with Sequential Vision Loss
Neurol 98:163-169, Fortes, B.,et al, 2022

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Leber Hereditary Optic Neuropathy with Longitudinal Spinal Cord Lesion Mimicking Spinal Cord Infarction
Neurol 98:468-469, Zhao, B.,et al, 2022



Showing articles 50 to 100 of 2468 << Previous Next >>