Neudle.com: COVID 19

Differential
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abducens nerve paralysis

abducens nerve paralysis, bilateral

acute disseminated encephalomyelitis

acute respiratory distress syndrome

advances in neurology

adverse drug reaction

antiphospholipid antibodies

artificial intelligence

asymptomatic

atypical

autonomic dysfunction

Babinski sign

basal ganglia, hemorrhage

basal ganglia, hemorrhage, bilateral

basal ganglia, lesion of

basal ganglia, lesion, bilateral

cauda equina, enhancement

cerebral infarction, hemorrhagic

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, cell count, normal

cerebrovascular accident

cerebrovascular accident, multiple

cerebrovascular accident, prevention of

cerebrovascular accident, prognosis in

cerebrovascular accident, secondary prevention

cerebrovascular accident, severity

cerebrovascular accident, three territory involvement

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, young adult

cerebrovascular disease

children

chills

Clinical Pathologic Conference(C.P.C.)

computers, medicine and

computers, neurologic diagnosis and

confusion

confusional state, acute

contagion

controversies in neurology

conversion reaction

coronary artery disease

cranial nerve enhancement

cranial nerve injury

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

dementia, rapidly progressive

depression

diplopia

disability rating scale, neurological

disability, neurological

electroencephalogram, abnormalities of

electromyogram

electronic health records

encephalitis

encephalitis, acute

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, parainfectious

endovascular therapy

EPIC electronic medical record

epidemiology of neurology

Guillain Barre syndrome

Guillain Barre syndrome, pharyngeal-cervical-brachial variant

Guillain Barre syndrome, variant forms of

heralding manifestation

hospital length of stay

hypercoagulable state

hyperreflexia

hypogeusia

hypoglossal nerve paralysis

hypoglycorrhachia

hyposmia

hypoxia

hypoxic encephalopathy

hypoxic-ischemic leukoencephalopathy

iatrogenic neurologic disorders

immunization, neurologic complications with

information technology

intellectual deficit

interferonopathy

intracerebral hemorrhage

intracerebral hemorrhage, bilateral

intracranial hypertension, benign

medical student education

memory, defect of recent

memory, impairment of

meningeal enhancement

meningitis

meningitis, aseptic

mental status, abnormal

microhemorrhage, intracerebral

middle cerebral artery, occlusion of

mortality

MRI, abnormal

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, high signal foci on

MRI, intravascular enhancement

MRI, linear enhancement

MRI, punctate pattern

MRI, spinal cord

MRI, spinal cord, increased intramedullary cord signal

MRI, T1 weighted high signal foci

multisystem inflammatory syndrome in children

myelitis, longitudinal

myelitis, transverse

myelopathy, ascending

nerve conduction studies

nerve injury

nerve root enhancement

neurocutaneous disease

neurocutaneous melanosis

neurohospitalist

neurologic complications

neurologic consultation

neurologic disease

neurologic disease, diagnoses of

neurologic education

neurologic evaluation

neurologic examination

neurologic examination, focal

neuropathology, brain

optic nerve, enhancement

personal protective equipment

pleocytosis of cerebrospinal fluid

pneumonia

polymerase chain reaction

posterior column disease

posterior leukoencephalopathy syndrome

psychiatric problems in neurologic disorders

psychosis

psychosis, acute

pulmonary embolism

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction, unilateral

quality of life

rapidly progressing neurologic illness

severe acute respiratory syndrome

skin, lesions in neurologic disorders

steroid responsive encephalitis

steroid therapy, CNS treatment and complications with

stroke disability scale

stroke protocol

superior ophthalmic vein

symmetric brain lesions

thrombolysis, mechanical

tissue plasminogen activator, intravenous

tongue deviation

transient neurologic deficit

treatment of neurologic disorder

troponin T

tumor necrosis factor

vaccination, neurologic complications with

vaccine

vagal neuropathy

vagus nerve, lesion of

walking, difficulty with

weakness

weaning from respirator, failure to

workup

Showing articles 50 to 87 of 87 << Previous

Miller Fisher Syndrome and Polyneuritis Cranialis in COVID-19
Neurol 95:e601-e605, Gutierrez-Ortiz, C.,et al, 2020

Generalized Myoclonus in COVID-19
Neurol 95:e767-e772, Rabano-Suarez, P.,et al, 2020

Magnetic Resonance Imaging Alteration of the Brain in a Patient with Coronavirus Disease 2019 (COVID-19) and Anosmia
JAMA Neurol 77:1028-1029, Politi, L.S.,et al, 2020

The Coronavirus Disease 2019 Crisis as Catalyst for Telemedicine for Chronic Neurological Disorders
JAMA Neurol 77:927-928, Bloem, B.R.,et al, 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

Tapia Syndrome at the Time of the COVID-19 Pandemic
Neurol 95:312-313, Decavel, P.,et al, 2020

Facial Nerve Palsy in COVID-19 Infection
Neurol 95:364-367, Goh, Y.,et al, 2020

Characteristics and Outcomes in Patients with COVID-19 and Acute Ischemic Stroke
Stroke 51:e254-e258, Ntaios, G.,et al, 2020

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

Neuropalliative Care Essentials for the COVID-19 Crisis
Neurol 95:394-398, Kluger, B.N.,et al, 2020

Adoption of Resident Teleneurology Training in the Wake of COVID-19
Neurol 95:404-407, Zha, A.M.,et al, 2020

Bilateral Globus Pallidus Lesions in a Patients with COVID-19
Neurol 95:454-457, Kulick-Soper, C.V.,et al, 2020

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

COVID-19-Related Encephalopathy Responsive to High-Dose Glucocorticoids
Neurol 95:543-546, Pugin, D.,et al, 2020

Bilateral Basal Ganglia Hemorrhage in a Patient with Confirmed COVID-19
AJNR 41:1797-1799, Daci, R.,et al, 2020

Clinical and Neuroimaging Correlation in Patients with COVID-19
AJNR 41:1791-1796, Yoon, B.C., 2020

A case of COVID-19-associated pharyngeal-cervical-brachial variant of Guillain-Barre syndrome
Neurol 95:978-983, Liberatore, G.,et al, 2020

Guillain-Barre Syndrome Associated with SARS-CoV-2
NEJM 382:2574-2576, Tuscano, G.,et al, 2020

Covd-19-Associated Myopathy Caused by Type 1 Interferonopathy
NEJM 383:2389-2390, Manzano, A.C.,et al, 2020

COVID-19-Associated PRES-like Encephalopathy with Perivascular Gadolinium Enhancement
AJNR 41:2206-2208, Conte, G.,et al, 2020

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
UpToDate (www.uptodate.com) Aug 21, Dichgans,M.,et al., 2007

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004

Clinical Spectrum of Episodic Ataxia Type 2
Neurol 62:17-22, Jen,J.,et al, 2004

Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Familial episodic Ataxia:Clinical Heterogeneity in Four Families Linked to Chromosome 19p
Ann Neurol 41:8-16, 41997., Baloh,R.W.,et al, 1997

Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
Neurol 48:1200-1203, Malandrini,A.,et al, 1997

Chromosome 19 Single-Locus & Multilocus Haplotype Assoc with MS, Evid of New Suscept Locus in Caucasian & Chinese Pts
JAMA 278:1256-1262, 12821997., Barcellos,L.F.,et al, 1997

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

A Gene for Hereditary Paroxysmal Cerebellar Ataxia Maps to Chromosome 19p
Ann Neurol 37:289-293, 2851995., Vahedi,K.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Showing articles 50 to 87 of 87 << Previous