Results 101 to 110 of about 20,702 (273)
Pediatric Feeding Disorder: Consensus Definition and Conceptual Framework [PDF]
Pediatric feeding disorders (PFDs) lack a universally accepted definition. Feeding disorders require comprehensive assessment and treatment of 4 closely related, complementary domains (medical, psychosocial, and feeding skill-based systems and associated
Browne, Joe +14 more
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Long-term follow-up results of endoscopic treatment of gastroesophageal reflux disease with the MUSE TM endoscopic stapling device [PDF]
Background The initial 6-month data for MUSE™ (Medigus, Omer, Israel) endoscopic stapling device were reported (Zacherl et al. in Surg Endosc 29:220–229, 2015).
Bapaye, Amol +7 more
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ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun +2 more
wiley +1 more source
Current Status of Anti-Reflux Surgery as a Treatment for GERD
Anti-reflux surgery (ARS) is an efficient treatment option for gastroesophageal reflux disease (GERD). Despite growing evidence of the efficacy and safety of ARS, medications including proton pump inhibitors (PPIs) remain the most commonly administered ...
Jooyeon Lee +9 more
doaj +1 more source
The use of preoperative ventral botulinum toxin for giant hiatal hernia management.
Francisco Tustumi +8 more
doaj +1 more source
Population-based trend analysis of laparoscopic Nissen and Toupet fundoplications for gastroesophageal reflux disease [PDF]
Background: The Nissen and Toupet fundoplications are the most commonly used techniques for surgical treatment of gastroesophageal reflux disease. To date, no population-based trend analysis has been reported examining the choice of procedure and short ...
Guller, U., Rosella, L., Zingg, U.
core
ABSTRACT Thyroid hormone resistance (RTH) is a rare genetic disorder characterized by diminished responsiveness of target tissues to thyroid hormones, primarily due to mutations in the thyroid hormone receptor‐beta (TR‐β) gene. This condition could lead to an increased level of Thyroid stimulating hormone (TSH) and varying degrees of hypothyroid ...
Ahmad Al‐Bitar +3 more
wiley +1 more source
Dysphagia in children with esophageal atresia: current diagnostic options [PDF]
© 2017 Georg Thieme Verlag KGDysphagia or swallowing disorder is very common (range, 15–52%) in patients with esophageal atresia. Children present with a wide range of symptoms.
Allegaert, K +3 more
core +1 more source
Abstract Somatostatin is a naturally occurring polypeptide hormone that exerts its effect on the gastrointestinal tract by reducing exocrine and endocrine secretion, resulting in decreased motility, gastric emptying, splanchnic blood flow, fat absorption, lymphatic flow, and gallbladder contraction.
Bailey Dunn +4 more
wiley +1 more source
Comorbid Conditions in Idiopathic Pulmonary Fibrosis: Recognition and Management. [PDF]
Idiopathic pulmonary fibrosis (IPF), a fibrosing interstitial pneumonia of unknown etiology, primarily affects older adults and leads to a progressive decline in lung function and quality of life.
Collard, Harold R, Oldham, Justin M
core +2 more sources

