Results 71 to 80 of about 1,188,382 (179)
Case report: Guillain-Barre syndrome with pneumococcus – A new association in pediatrics
Guillain-Barre Syndrome, an acute flaccid paralysis known to be caused by recent Gastro-intestinal infections mainly campylobacter, and Respiratory infections mainly mycoplasma pneumoniae and influenza.
Hassan El Khatib +4 more
doaj +1 more source
ABSTRACT Background Chikungunya virus (CHIKV) is an arbovirus that causes an acute febrile illness with intense muscle and joint pain, with the possibility of progressing to a chronic or neurological stage. We conducted a systematic review and meta‐analysis with the aim of evaluating the accuracy of real‐time reverse transcriptase polymerase chain ...
Róger J. Costa +8 more
wiley +1 more source
Governance of Long‐Term Scientific Infrastructure: Public Value Does Not Protect Itself
Abstract Long‐term scientific infrastructure, including physical archives, monitoring networks, and place‐based research facilities, is frequently described as important but is rarely protected by enforceable governance. When administrative reorganization or budget pressure threatens such infrastructure, the scientific community typically responds with
A. Veltri
wiley +1 more source
Characteristics of Guillain-Barré syndrome cases.
Characteristics of Guillain-Barré syndrome cases.
Ditte Mølgaard-Nielsen (505602) +27 more
core +1 more source
ABSTRACT Background and Aims Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) is an immune‐mediated neuropathy that may cause persistent disability despite immunoglobulin treatment. Ion channel dysfunction has been demonstrated in CIDP, but no therapies specifically target this mechanism.
Peter Nørregaard Hansen +5 more
wiley +1 more source
Guillain-Barré syndrome: clinical variants and their pathogenesis.
Numerous clinical subtypes of Guillain-Barré syndrome have been described over the century since the original description of the syndrome.
Winer, John, J.B. Winer
core +1 more source
Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency
ABSTRACT Primary pyruvate dehydrogenase complex deficiency (PDCD) comprises a group of monogenic disorders caused by pathogenic variants in genes encoding subunits of, or regulatory components affecting, the pyruvate dehydrogenase complex. The clinical phenotype spans a broad continuum, ranging from early onset congenital lactic acidosis to infantile ...
Nandaki Keshavan +23 more
wiley +1 more source

