GENOTYPING ANALYSES OF TUBERCULOSIS CASES IN U.S.- AND FOREIGN-BORN MASSACHUSETTS RESIDENTS


A Rare Cause of Neonatal Hypotonia: First Case of Autosomal Recessive Fast-Channel Congenital Myasthenic Syndrome Type 1B in Albania

Hypotonia is a concern, with high morbidity and poor outcomes in 10% of neonatal care cases.Neonatal hypotonia presents a diagnostic Cover Ups challenge for neonatologists, as it may be a sign of a central nervous disorder (hypoxic-ischemic insult, intracranial hemorrhage, cerebral palsy), inborn errors of metabolism, a primary neuromuscular disord

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Hyaluronic acid-curcumin nanoparticles for preventing the progression of experimental autoimmune uveitis through the Keap1/Nrf2/HO-1 signaling pathway

Abstract Globally, uveitis is a collection of intraocular inflammatory disorders that affect mainly the uvea, resulting in irreversible blindness and a heavy socioeconomic burden.Excessive autoimmune inflammation and oxidative stress are major drivers that contribute to the initiation and progression of uveitis.Nevertheless, current therapeutic met

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