A Case of Contralateral Left Main Bronchial-Esophageal Fistula Following Right Lower Lobectomy with Systematic Mediastinal Lymph Node Dissection. [PDF]
Tanigawa T +5 more
europepmc +1 more source
We demonstrate the direct‐laser patterning of a gold thin film on polymethyl methacrylate to fabricate a temperature sensor for dentures. The temperature sensor‐embedded smart dentures are evaluated in an oral environment, enabling in‐situ monitoring for elderly healthcare.
Han Ku Nam +7 more
wiley +1 more source
Thoracoscopic-guided paraesophageal abscess drainage in foreign body-induced esophageal perforation: a case report. [PDF]
Lin MC, Chen YY.
europepmc +1 more source
Gastrointestinal Manifestations in Rubinstein‐Taybi Syndrome
ABSTRACT Rubinstein–Taybi syndrome is a rare genetic condition associated with a wide range of physical, cognitive, and developmental impairments, yet its gastrointestinal manifestations remain poorly characterized. Case reports and small series suggest a high prevalence of gastroesophageal reflux, constipation, dysphagia, and nutritional compromise ...
Mohamad Abi Nassif +3 more
wiley +1 more source
Cervical esophagocolic anastomosis leakage caused by a tension pneumothorax after an esophagocoloplasty for caustic esophageal stricture in a child: a case report. [PDF]
Zabeirou A +7 more
europepmc +1 more source
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken +4 more
wiley +1 more source
CLINICAL EFFECTIVENESS OF ENDOSCOPIC SUBMUCOSAL DISSECTION IN THE MANAGEMENT OF SUPERFICIAL ESOPHAGEAL NEOPLASMS ASSOCIATED WITH BARRETT'S ESOPHAGUS. [PDF]
Vianna DE Oliveira RM +3 more
europepmc +1 more source
In-to-out body path loss for wireless radio frequency capsule endoscopy in a human body [PDF]
Joseph, Wout +4 more
core +2 more sources
Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet +10 more
wiley +1 more source
Downhill Esophageal Variceal Rupture Caused by Superior Vena Cava Syndrome in NUT Carcinoma: A Case Report. [PDF]
Okuno K +4 more
europepmc +1 more source

