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Differential
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advances in neurology
Alzheimer's disease
amyloid angiopathy, cerebral
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, childhood
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, juvenile
amyotrophic lateral sclerosis, Parkinson-dementia-complex
amyotrophic lateral sclerosis, post-encephalitic
anterior horn cell disease
arm weakness
asthma
asthma, poliomyelitis-like syndrome with
atlanto axial dislocation, congenital
biologic markers
bulbar palsy
bulbar palsy, progressive
cavernous sinus, syndrome
children
chromosomal abnormality
degenerative diseases of CNS
dementia
dementia, frontotemporal
differential diagnosis
distal muscle atrophy
distal muscle weakness
dysphagia
dyspnea
electromyogram
encephalocele
epidemiology of neurology
exercise
familial
fasciculation
fibrillations
flaccid paralysis
Friedreich's ataxia
gene
genetic linkage
genetic neurologic disorders
hemangioma
hoarseness
Huntington's chorea
hyperreflexia
infantile tremor syndrome
intrinsic hand muscles, wasting of
Jakob-Creutzfeldt disease
juvenile distal and segmental muscular atrophy
Kugelberg-Welander syndrome
leg atrophy
leg weakness, unilateral
Lewy body disease, diffuse
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
misdiagnosis
molecular genetics
monomelic amyotrophy
monoparesis
motor neuron disease
motor neuron disease, juvenile form
MRI
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MRI, disappearing lesion on
MRI, functional
MRI, spinal cord
multiple sclerosis
multiple system atrophy
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle twitching
muscle wasting, diffuse
muscle weakness
muscular dystrophy
muscular dystrophy, Duchenne
myelomalacia
myotonia dystrophica
nasal speech
neck weakness
nerve conduction studies
neurofibromatosis 1
neurofibromatosis 2
neurologic disease, diagnoses of
ophthalmoplegia
ophthalmoplegia, painful
paraparesis, spastic
Parkinson disease
periodic paralysis
periodic paralysis, thyrotoxic
pes cavus
poliomyelitis-like illness
prognosis
rash
recombinant DNA
review article
RFLPs
spasticity
spina bifida
spinal cord, cervical
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
subacute myelo-opticoneuropathy(S.M.O.N.)complex
subarachnoid hemorrhage
Tolosa Hunt syndrome
tongue, atrophy
tongue, fasciculations of
tongue, weakness
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
viral infection, CNS
weight loss
West Nile fever
Showing articles 400 to 450 of 3229 << Previous Next >>

Reduced Basal Ganglia Volume Associated with the Gene for Huntington's Disease in Asymptomatic at-Risk Persons
Neurol 44:823-828, Aylward,E.H.,et al, 1994

Further Reg Var of Acute Polyneuro:Bifacial or 6th Nerve Paresis, Lumbar Polyrad & Ataxia/Phary Cervical-Brachial Wkness
Arch Neurol 51:671-675, Ropper,A.H., 1994

Extent of Pontine Pyramidal Tract Wallerian Degeneration and Outcome after Supratentorial Hemorrhagic Stroke
Stroke 25:1207-1210, Fukui,K.,et al, 1994

The Ocular Manifestations of Multiple Sclerosis, 2, Abnormalities of Eye Movements
JNNP 55:863-868, Barnes,D.&McDonald,W.I., 1992

Prognostic Significance of Conjugate Eye Deviation in Stroke Patients
Stroke 22:200-202, Tijssen,C.C.,et al, 1991

The Sensitivity of Transcranial Cortical Magnetic Stimulation in Detecting Pyramidal Tract Lesions in Clin Definite MS
Neurol 41:566-569, Mayr,N.,et al, 1991

Neurologic Aspects of Cobalamin Deficiency
Medicine 70:229-245, Healton,E.B.,et al, 1991

Visual Loss in Tuberous Sclerosis
Neurol 41:1915-1917, Dotan,S.A.,et al, 1991

Primary Lateral Sclerosis in a Child
Neurol 39:1530-1532, Grunnet,M.L.,et al, 1989

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Periodic Lateralized Epileptiform Discharges in a Patient with Definite Multiple Sclerosis
Clin Electroenceph 18:38-40, Awerbuch,G.I.&Verma,N.P., 1987

Magnetic Resonance Imaging in Clinically Isolated Lesions of the Brain Stem
JNNP 49:737-743, Ormerod,I.E.C.,et al, 1986

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

Bilateral Pontine Gaze Palsy
Arch Neurol 42:93-94, Joseph,R.,et al, 1985

Demyelinating Disease Presenting As Wallenberg's Syndrome
Stroke 12:877-878, Smith,D.B.,et al, 1981

Epidermoid Tumors Involving the Fourth Ventricle
Neurosurgery 9:9-13, Rosario,M.,et al, 1981

Levels of y-Aminobutyric Acid in Cerebrospinal Fluid in Various Neurologic Disorders
Arch Neurol 37:352-355, Manyam,N.V.B.,et al, 1980

Clinical Correlations of Periodic Lateralized Epileptiform Discharges
Clin Electroenceph 8:191-202, Porecha,H.P.&Reilly,E.L., 1977

Bilateral Sixth Nerve Palsy
Arch Neurol 33:681, Keane,J.R., 1976

Isolated Facial Numbness
Ann Int Med 80:49, Horowitz,S., 1974

Case Records of MGH-NEJM 289:366
1973 Tuberculoma of Cerebral hemisphere & Brain Stem., , 1973

M. S. :A Review
BMJ 2:292, McAlpine,D., 1973

Clinical Pathological Conference, Scleroderma, Spastic Paraparesis & Chronic Myelogenous Leukemia
Prov. VAH, Dec. 12, 77., Finelli,P.F., 1850

Vertebrobasilart Dolichoectasia Presenting with Multiple Cranial Nerve Involvement
Neurol 104:213541, Freiherr von Seckendorff,A.,et al, 2025

Long-Term Effects of Antidarsagene Autotemcel for Metachromatic Leukodystrophy
NEJM 392:1609-1620, Fumagalli,F.,et al, 2025

Progress Toward Mitigating Disability Progression in Multiple Sclerosis
NEJM 392:1966-1968, Calabresi,P.A., 2025

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

Juvenile-Onset Dopa-Responsive Dystonia-Until It Isnt
Neurol 104:e213436, Paredes,N.C.,et al, 2025

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

Decompressive Carniectomy Plus Best Medical Treatment Versus Best Medical Treatment Alone for Spontaneous Severe Deep Supratentorial Intracerebral Haemorrhage:A Randomised Controlled Clinical Trial
Lancet 403:2395-2404, Beck,J.,et al, 2024

A 32-Year-Old Man with Painless Bilateral Shoulder Girdle Weakness and Atrophy
Neurol 103:e209915, Gutti,N.B.,et al, 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

Diagnostic MRI Score to Differentiate Susac Syndrome from Primary Angiitis of the Central Nervous System and Multiple Sclerosis
Ann Neurol 96:846-854, Marrodan,M.,et al, 2024

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

Slowly Expanding Lesions Differentiate Pediatric Multiple Sclerosis from Myelin Oligodendrocyte Glycoprotein Antibody Disease
Ann Neurol 96:1086-1091, Fadda,G.,et al, 2024

Adverse Events Associated with Disease-Modifying Drugs for Multiple Sclerosis
Neurol 102:e208006, Ng, HS.,et al, 2024

Inhibition of CD40L with Frexalimab in Multiple Sclerosis
NEJM 390:589-600, 662, Vermersch,P.,et al, 2024

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

Diagnosis and Management of Cerebral Venous Thrombosis:A Scientific Statement From the American Heart Association
Stroke 55:e77-e90, Saposnik,G.,et al, 2024

The Optic Nerve Should Graduate to Be the Fifth Lesion Site for the Diagnosis of Multiple Sclerosis
Neurol 102:e207919, Galetta,S. & Brownlee, W., 2024

Tuberous Sclerosis Complex:Clinical Features
www.UptoDate.com, Dec, Randle,S., et al, 2023

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Neurologic Manifestations of Long COVID Differ Based on Acute COVID-19 Severity
Ann Neurol 94:146-159, Giraldo,G.S.P.,et al, 2023

Association of Very Early treatment Initiation with the Risk of Long-Term Disability in Patients with a First Demyelinating Event
Neurol 101:e1280-e1292, 549, Cobo-Calvo,A.,et al, 2023

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

Management of Possible Multiple Sclerosis
NEJM 388:2195-2190, , 2023

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

A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
Neurol 101:e94-e98, AlSabah,A.,et al, 2023



Showing articles 400 to 450 of 3229 << Previous Next >>