Results 231 to 240 of about 208,910 (323)
Case series: Joubert syndrome and eosinophilic esophagitis
Abstract Joubert syndrome (JS) is a rare genetic disorder characterized by developmental abnormalities, particularly in the brainstem and cerebellar vermis, alongside multisystem manifestations such as kidney and liver anomalies, polydactyly, cleft lip or palate, and tongue defects.
Jonathon Schening +5 more
wiley +1 more source
Melatonin alleviates chronic intermittent hypoxia-induced gastric mucosal injury via attenuation of oxidative stress and JNK-mediated apoptotic signaling in rats. [PDF]
Ji HL +13 more
europepmc +1 more source
Abstract Cystic biliary atresia (CBA) is a rare variant of biliary atresia that closely resembles choledochal cyst (CC), complicating diagnosis and potentially delaying critical surgical intervention. We report two cases of CBA that were difficult to diagnose.
Hamza Hassan Khan +2 more
wiley +1 more source
The role of virus in nasal inflammation. [PDF]
Wang C, Zhang YM, Li M, Cheng KJ.
europepmc +1 more source
The Brief Case: Knee joint infection caused by <i>Neisseria mucosa</i>. [PDF]
Zheng C +11 more
europepmc +1 more source
Intestinal mucormycosis in a captive tiger. [PDF]
Cappelleri A +5 more
europepmc +1 more source
Prolonged persistence of tissue-resident memory cells in the upper airway following SARS-CoV-2 infection and vaccination. [PDF]
Cha H +7 more
europepmc +1 more source

