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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
myelogram
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myeloradiculopathy
myocardial injury
myocytolysis
myopathy
myopathy, mitochondrial
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 0 to 50 of 2390 Next >>

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

SPG7 Mutations Explain a Significant Proportion of French Canadian Spastic Ataxia Cases
Eur J Hum Genet 24:1016-1021, Choquet,K.,et al, 2016

Brugada Syndrome in Spinal and Bulbar Muscular Atrophy
Neurol 82:1813-1821, Araki, A.,et al, 2014

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Diagnosis and Treatment of Ossification of the Posterior Longitudinal Ligament of the Spine:8 Cases and Lit Review
Am J Med 92:296-306, Trojan,D.A.,et al, 1992

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Facioscapulohumeral Dystrophy, In Skeletal Muscle Pathology
Churchhill Livingstone, NY, p285, 30392., Mastaglia,F.L.&Walton,J., 1992

Venous Infarction of the Spinal Cord Resulting from Dural Arteriovenous Fistula:MR Imaging Findings
Larsson, E-M, AJNR 12:739-743991., , 1991

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Bladder Dysfunction in Progressive Autonomic Failure
BMJ 293:223-224, Kirby,R.S.&Bannister,R., 1986

Acridine Orange-Nucleic Acid Fluorescence
Arch Neurol 37:641-644, Perl,D.P.,et al, 1980

Peripheral Neuropathy in Myotonic Dystrophy
Arch Neurol 35:741-745, Olson,N.D.,et al, 1978

Neurogenic Muscular Atrophy Simulating Facioscapulohumeral Muscular Dystrophy
J Neurol Sci 9:389, Furukawa,T.,et al, 1969

Increased Intracanial Pressure & Pulmonary Edema, Pt. I
J Neurosurg 28:112, Ducker,T.B., 1968

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Automated Detection of Normal Pressure Hydrocephalus Using CT Imaging for Calculating the Ventricle-to-Subarachnoid Volume Ratio
AJNR 46:141-146, Knittel,J.J.,et al, 2025

Automated Idiopathic Normal Pressure Hydrocephalus Diagnosis via Artificial Intelligence-Based 3D T1 MRI Volumetric Analysis
AJNR 46:33-40, Lee,J.,et al, 2025

Bilaterally Symmetrical Globus Pallidus Infarction
Ann Neurol 97:254-255, Chen,L.,et al, 2025

Black Turbinate Sign as an Early Clue of Rhino-Orbital-Cerebral Mucormycosis
Neurol 104:e210202, Xie,J.S.,et al, 2025

Epidural Steroids for Cervical and Lumbar Radicular Pain and Spinal Stenosis Systematic Review Summary
Neurol 104:e213361, Armon,C.,et al, 2025

Teaching NeuroImage: The House Soign in Behavioral Varianht Frontotemporal Dementia
Neurol 104:e213519, Ioannidis,S.,et al, 2025

A 62-Year-Old Man with Symmetric Saddle Hypoesthesia and Sphincter Dysfunction
Neurol 104:e213712, Crausaz,L.,et al, 2025

A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
Neurol 104:e213713, Rawat,R.,et al, 2025

Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
Cureus doi:10.7759/CUREUS.32182, Sweedan,Y.G.,et al, 2025

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

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

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

Itching Frequency and Neuroanatomic Correlated in Frontotemporal Lobar Degeneration
JAMA Neurol 81:977-984, Hadad,R.,et al, 2024

A 61-Year-Old Man With Progressive Right Leg Numbness and Weakness
Neurol 103:e209900, Jones,F.J.S.,et al, 2024

Clinical Features, Diagnosis and Management of Klinefelter Syndrome
www.UptoDaate.com, Matsumoto,A.M. & Anawals,B.D., 2024

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

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



Showing articles 0 to 50 of 2390 Next >>