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alcohol intolerance
alternating rapid movement
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
autonomic dysfunction
Babinski sign
bradykinesia
CAG repeats
cardiomyopathy
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar vermis
choking
chromosomal abnormality
chromosome 6
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Collier's sign
consanguinity
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
diabetes mellitus
diplopia
distal muscle atrophy
dysarthria
dysmorphic
dysphagia
dystonia
familial
fasciculation
fatigue
finger nose finger test
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gaze palsy
gaze palsy, supranuclear
gene
genetic counselling
genetic neurologic disorders
genetic testing
glutamate dehydrogenase deficiency
handwriting
hearing loss
heel-knee-shin test
hyperreflexia
hypertonia
imbalance
incoordination
leg weakness, bilateral
life expectancy
memory, impairment of
mental retardation
misdiagnosis
molecular genetics
mortality
MRI, abnormal
MRI, spinal cord
multiple system atrophy
myelomalacia
myoclonus
neurologic disease, diagnoses of
neuropathology
neuropathy
nystagmus
nystagmus, vertical
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
Parkinson disease
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pes cavus
position sensation
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
pyramidal tract
pyramidal tract dysfunction
review article
scoliosis
sensory loss
spastic ataxia
spasticity
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinocerebellar tract
tremor
tremor, cerebellar
trinucleotide repeats
upgaze, paralysis of
vibratory sensation
vibratory sensation, abnormal
visual acuity, decreased
vitamin deficiency
vitamin E
vitamin E deficiency
walking, difficulty with
wheelchair
wide based gait
workup
Showing articles 50 to 100 of 683 << Previous Next >>

COVID-19: A Global Threat to the Nervous System
Ann Neurol 88:1-11, Koralnik, I.J. & Tyler, K.L., 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Paraneoplastic Encephalomyelitis with Glutamic Acid Decarboxylase Antibodies Presenting as Longitudinal Pyramidal Tract Hyperintensity
JAMA Neurol 77:899-900, Miralles, C.,et al, 2020

Scoping Review of Prevalence of Neurologic Comorbidities in Patients Hospitalized for COVID-19
Neurol 95:77-84, Herman, C.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Childhood Multisystem Inflammatory Syndrome
NEJM 383:393-395, Levin, M., 2020

Arthralgia as an Initial Presentation of COVID-19
Rheumatol Int doi:10.1007/s00296-020-04561-0, Joob, B. & Wiwanitkit, V., 2020

Atypical Deep Cerebral Vein Thrombosis with Hemorrhagic Venous Infarction in a Patient Positive for COVID-19
AJNR 41:1377-1379, Chougar, L.,et al, 2020

Cerebral Venous Thrombosis Associated with COVID-19
AJNR 41:1370-1376, Cavalcanti, D.D.,et al, 2020

Clinicopathologic Conference, Cerebrovascular Accident Probably Related to SARS-CoV2 Infection
NEJM 383:764-773, Case 26-2020, 2020

Steroid-Responsive Encephalitis in Coronavirus Disease 2019
Ann Neurol 88:423-427, Pilotto, A.,et al, 2020

Leukoencephalopathy Associated with Severe COVID-19
AJNR 41:1641-1645, Lang, M.,et al, 2020

Spinal Xanthomatosis
Neurol 95:e1615-e1616, Valencia-Sanchez, C.,et al, 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

Leg Weakness and Stiffness at the Emergency Room
Neurol 92:e622-e625, af Edholm, K.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Progressive Proximal Weakness in a 56-year-old Man with Bone Pain
Neurol 93:939-944, Torabi,T.,et al, 2019

Relapsing-Remitting Severe Bickerstaffs Brainstem Encephalitis
BMJ 394:684, Tyrakowska, Z.,et al, 2019

Diagnostic Tools for Immune Causes of Encephalitis
Clin Microbiol Infect 25:431-436, Lascano, A.M.,et al, 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Hemorrhagic Encephalitis Associated with H3N2 Influenza A Viral Pneumonia
Neurol 90:336-337, AbdelRazek, M.A.,et al, 2018

Headache and Altered Mental Status
Neurol 90:e1267-e1270, Spera, K.M.,et al, 2018

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

A 22-year-old postpartum woman with new-onset seizures and headache
Neurol 90:1631-1635, McGehrin, K.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

Clinicopathologic Conference, Digitalis Toxicity
NEJM 378:1931-1938, Case 15-2018, 2018

A 23-year-old woman with fever and vertical diplopia
Neurol 90:e2006-e2010, Lin, D.J.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia: An MRI Study of 16 French Cases
AJNR 39:1657-1661, Codjia, P.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Lymphocytic Choriomeningitis Virus (LCMV) Infection
www.Medscape.com Sept, McDonald, P.J.,et al, 2017

Gradually Progressive Spastic Ataxia in a Young Man Steadily Unsteady
JAMA Neurol 74:238-241, Dubey, D.,et al, 2017

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

A Middle-aged man with Progressive Ophthalmoparesis, Ataxia, and Spastic Paraparesis
JAMA Neurol 74:733-736, Kung, N.H.,et al, 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Idiopathic Thoracic Spontaneous Spinal Epidural Hematoma
Case Reports Surg doi:10.1155/2016/5430708, Aycan, A.,et al, 2016

Extensive Vasogenic Edema in Bickerstaff Brainstem Encephalitis
Neurol 86:e38-e39, Nerrant, E.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

Finger Clonus
Neurol 86:e118-e119, Moccia,M.,et al, 2016

A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
Neurol 86:e173-e176, Elkhider, H.,et al, 2016

Majority of 30-Day Readmissions after Intracerebral Hemorrhage are Related to Infections
Stroke 47:1768-1771, Lord, A.S.,et al, 2016



Showing articles 50 to 100 of 683 << Previous Next >>