Results 71 to 80 of about 329,395 (176)

Exocrine pancreatic insufficiency in cholelithiasis [PDF]

, 2005
Zur Untersuchung der Prävalenz einer exokrinen Pankreasfunktionsstörung bei Gallensteinträgern wurden 91 Gallensteinpatienten und 94 Kontrollpatienten ohne Gallensteinerkrankung miteinander verglichen.
Bretz, Lars Dieter
core   +1 more source

Laparoscopic Modified One Anastomosis Gastric Bypass for Severe Obesity After Pancreaticoduodenectomy: A Safe Approach to the Hostile Abdomen, a First Case Report

The Kaohsiung Journal of Medical Sciences, EarlyView.
Chih‐Kun Huang, Ming‐Che Hsin, Long‐Bin Jeng, Ting‐Wei Chang   +3 more
wiley   +1 more source

Neuropsychological and Educational Outcomes in Shwachman–Diamond Syndrome—A Report From the North American Shwachman–Diamond Syndrome Registry

Pediatric Blood &Cancer, Volume 73, Issue 11, November 2026.
ABSTRACT Background Shwachman–Diamond syndrome (SDS) is a rare autosomal recessive ribosomopathy characterized by bone marrow failure and multisystem involvement, with emerging evidence of associated neurocognitive impairment. Methods We conducted a retrospective study of 240 individuals with biallelic Shwachman–Bodian–Diamond syndrome (SBDS) mutations
Jane Koo, Melissa Gerstle, Leah Cheng, Richard Cooper, Katherine Coyne, Claire Dusa, Naomi E. Joffe, Diana Schwarz, Sarah Steltz, Akiko Shimamura, Kasiani C. Myers, Thea Quinton   +11 more
wiley   +1 more source

Prevalence of exocrine pancreatic insufficiency at 12 months after acute pancreatitis: a prospective, multicentre, longitudinal cohort studyResearch in context

EClinicalMedicine
Summary: Background: Exocrine Pancreatic insufficiency (EPI) occurs following acute pancreatitis (AP) at variably reported rates and with unclear recovery timeline. The aim of this study was to establish the prevalence and predictors of EPI at 12 months
Anna Evans Phillips, Joseph Bejjani, Stacey Culp, Jennifer Chennat, Peter J. Lee, Jorge D. Machicado, Vikesh K. Singh, Elham Afghani, Mitchell L. Ramsey, Pedram Paragomi, Kimberly Stello, Melica Nikahd, Phil A. Hart, Georgios I. Papachristou   +13 more
doaj   +1 more source

Dorsal Pancreatic Agenesis Associated With New‐Onset Diabetes Mellitus and Acute Pancreatitis in an 18‐Year‐Old Man: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT Dorsal pancreatic agenesis (DPA) is a rare congenital disorder resulting from failure of development of the dorsal pancreatic bud. Complete DPA implies absence of the pancreatic neck, body, and tail and can be associated with both diabetes mellitus and pancreatitis. The patient was an 18‐year‐old man admitted with a history of epigastric pain,
Mugheesa Rab, Muhammad Hassaan Javaid, Rabia Narmeen Numani, Fozia Khanam, Muddassir Khalid, Fred Segawa   +5 more
wiley   +1 more source

Celiac disease with exocrine pancreatic insufficiency and dilated cardiomyopathy in pediatric patient: A rare case report

Gastroenterology & Endoscopy
Introduction: There are several clinical manifestations of celiac disease, an autoimmune enteropathy caused by gluten intake, including extra-intestinal and gastrointestinal symptoms.
Sabir Shah, Farhan Shahzad, Muhammad Hashim, Noor-e Saba, Rasheed Ul Haq, Irfan Ul Haq   +5 more
doaj   +1 more source

Current Status of Pancreatic Exocrine Insufficiency Diagnosis and Pancreatic Enzyme Replacement Therapy Implementation in Patients With Chronic Pancreatitis

JGH Open, Volume 10, Issue 10, October 2026.
ABSTRACT Aims The prevalence of chronic pancreatitis (CP) is increasing in Japan. This study aimed to elucidate the current status of pancreatic exocrine insufficiency (PEI) diagnosis and the prescription of pancreatic enzyme replacement therapy (PERT) in Japanese patients with CP.
Noriharu Itoh, Yuko Hasebe, Toru Yada, Kazutaka Nozawa   +3 more
wiley   +1 more source

Hypertriglyceridemia: Causes, Consequences, Diagnosis, and Management

MedComm, Volume 7, Issue 10, October 2026.
Hypertriglyceridemia (HTG) arises from the interplay between genetic susceptibility and secondary or precipitating factors, leading to dysregulated triglyceride‐rich lipoprotein (TRL) metabolism. Increased TRL production and impaired clearance promote distinct risk phenotypes: accumulation of apolipoprotein B(apoB)‐containing TRL remnants contributes ...
Shanshan Qi, Weiwei Chen, Kunhao Chen, Song Yang, Sibo Wang, Tongtian Ni, Dan Xu, Enqiang Mao, Erzhen Chen, Ying Chen   +9 more
wiley   +1 more source

Exocrine Pancreatic Insufficiency Manifesting Before Insulin Dependence in Adult‐Onset Type 1 Diabetes

Clinical Case Reports
Exocrine pancreatic insufficiency may precede insulin dependence in adult‐onset type 1 diabetes. Unexplained steatorrhea or weight loss in people with diabetes warrants further investigations including imaging of abdomen/pancreas, exocrine pancreatic ...
Panagiotis Pavlou, Shrawan Pandit, Janaka Karalliedde   +2 more
doaj   +1 more source

Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetesResearch in context

EBioMedicine
Summary: Background: Biallelic loss-of-function ZNF808 variants were recently identified as a cause of pancreatic agenesis characterised by insulin-treated permanent neonatal diabetes (PNDM), low birthweight and exocrine pancreatic insufficiency ...
James Russ-Silsby, Kevin Colclough, Matthew B. Johnson, Matthew N. Wakeling, Nick D.L. Owens, Shenali A. Amaratunga, Sarah E. Flanagan, Kashyap A. Patel, Andrew T. Hattersley, Elisa De Franco, Mohamed Abdullah, Hessa Alkandari, Zehra Aycan, Semra Çetinkaya, Nancy Elbarbary, Radha Ghildiyal, Susana Gonzalez, Shaun Gorman, Samar Hassan, Savita Khadse, Jan Lebl, Jaida Manzoor, Nikhil Shah, Tara Hussein Tayeb, Alaa Al Assi, Arya Anil, Diego Balboa, Urvashi Chitnavis, Juliette Davis, Doga Eskier, Michael Imbeault, Santiago Morell, Sachin Muralidharan, Timo Otonkoski, Jonna Saarimäki-Vire   +34 more
doaj   +1 more source