Results 61 to 70 of about 1,665,682 (212)

Proso Millet (Panicum miliaceum): Nutritional Composition, Functional Attributes, and Health Implications

Future Postharvest and Food, EarlyView.
A nutrient‐dense grain, proso millet is well‐known for its high protein content and vital amino acids. It is high in fiber, vitamins, and minerals and has many health advantages, including promoting heart health, enhancing digestion, and helping with weight management.
Sangeeta Yadav, Pratiksha Singh, Mazia Ahmed, Pinki Saini   +3 more
wiley   +1 more source

A Multicenter Observational Study Comparing Survival of Pugs and Dogs of Other Breeds With Protein‐Losing Enteropathy

Journal of Veterinary Internal Medicine
Background Protein‐losing enteropathy (PLE) in dogs often carries a guarded prognosis, and it is unclear if survival differs among breeds. Hypothesis/Objectives Survival of pugs with PLE is shorter than that of other breeds of dogs with PLE.
Harry Swales, Daniel J. Batchelor, Tereza Bodnárová, Andrew Kent, Susan Campbell, Adam G. Gow, Margaux Kuijlaars, Peter‐John M. Noble, Anna Threlfall, Paolo Silvestrini, Jennifer Stallwood, Harry Warwick, Alexander J. German   +12 more
doaj   +1 more source

Effects of the discharge plan on the caregiving load of people with chronic disease: Quasi-experimental study

, 2023
Hospitalization due to non-transmissible chronic disease (NTCD) affects people and health institutions negatively. Healthcare systems need integral strategies to minimize this impact.
Sánchez Herrera B., Guevara Lozano, Maryory, Pulido Barragán S.P., Carvajal Carrascal G., Fuentes Ramírez A.   +4 more
core   +1 more source

Long‐term clinical trajectory of microvillus inclusion disease associated with STXBP2‐related familial hemophagocytic lymphohistiocytosis type 5: A case report

Journal of Parenteral and Enteral Nutrition, EarlyView.
Abstract Familial hemophagocytic lymphohistiocytosis type 5 is caused by biallelic pathogenic variants in STXBP2, which encodes syntaxin‐binding protein, a key regulator of vesicle trafficking. In addition to immune dysregulation, patients with familial hemophagocytic lymphohistiocytosis type 5 may present with severe, persistent diarrhea associated ...
Hiroyuki Tanaka, Mariko Sekiguchi, Yuko Kajiho, Tetsuo Ushiku, Jun Fujishiro, Motohiro Kato   +5 more
wiley   +1 more source

A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter. [PDF]

PLoS Genetics, 2015
Previously, we proposed a rare autosomal recessive inherited enteropathy characterized by persistent blood and protein loss from the small intestine as chronic nonspecific multiple ulcers of the small intestine (CNSU).
Junji Umeno, Tadakazu Hisamatsu, Motohiro Esaki, Atsushi Hirano, Naoya Kubokura, Kouichi Asano, Shuji Kochi, Shunichi Yanai, Yuta Fuyuno, Katsuyoshi Shimamura, Naoki Hosoe, Haruhiko Ogata, Takashi Watanabe, Kunihiko Aoyagi, Hidehisa Ooi, Kenji Watanabe, Shigeyoshi Yasukawa, Fumihito Hirai, Toshiyuki Matsui, Mitsuo Iida, Tsuneyoshi Yao, Toshifumi Hibi, Kenjiro Kosaki, Takanori Kanai, Takanari Kitazono, Takayuki Matsumoto   +25 more
doaj   +1 more source

The safe and effective use of tofacitinib and ustekinumab combination therapy in infantile onset inflammatory bowel disease

JPGN Reports, EarlyView.
Abstract Infantile‐onset inflammatory bowel disease (IOIBD) is a rare and severe subset of very‐early‐onset IBD, often associated with immune dysregulation and poor response to conventional therapies. Data regarding the use of Janus kinase inhibitors (JAKI) in this population is limited.
Smridhi Mahajan, Christian Wysocki, Bhaskar Gurram   +2 more
wiley   +1 more source

Atypical Rapid Onset of Olmesartan-Induced Enteropathy with Recurrence After Rechallenging

Diseases
Background: Olmesartan-induced enteropathy is a rare complication of a widely used angiotensin II receptor blocker. Patients usually present with chronic diarrhea and weight loss. Histologically, villous atrophy and intraepithelial lymphocyte infiltrates
Lila Bekkai, Aymen Ibn Majah, Laurine Verset, Lucas Jacobs, Charline Danneel, Okyay Elkilic, Frédéric Collart, Joëlle Nortier, Maxime Taghavi   +8 more
doaj   +1 more source

Peripheral and intestinal T lymphocyte subsets in dogs with chronic inflammatory enteropathy [PDF]

Abbreviations: BCS, body condition score; BSA, bovine serum albumin; CBC, complete blood count; CCECAI, clinical canine chronic enteropathy activity index; CD, clusters of differentiation;CIBDAI, clinical IBD activity index; CIE, chronic inflammatory ...
García-Sancho, Mercedes, García-Sancho Téllez, Mercedes Guadalupe, Mercedes García‐Sancho, Díaz-Regañón Fernández, David Rafael, David Díaz‐Regañón, Villaescusa, Alejandra, Lydia Calleja‐Bueno, Rodríguez Franco, Fernando, Calleja Bueno, Lydia, Fernando Rodríguez‐Franco, Agulla Pérez, Beatriz, Villaescusa Fernández, Alejandra, Olmeda, Patricia, Calleja-Bueno, Lydia, Alejandra Villaescusa, Agulla, Beatriz, Patricia Olmeda, Sainz Rodríguez, Ángel, Ángel Sainz, Beatriz Agulla, Díaz-Regañón, David   +20 more
core   +1 more source

Endoscopic findings in patients with Shwachman–Diamond syndrome: A report from the North American Shwachman–Diamond syndrome registry

JPGN Reports, EarlyView.
Abstract Objectives Shwachman–Diamond syndrome (SDS) is an inherited bone marrow failure disorder, and its endoscopic phenotype is poorly defined. We sought to characterize endoscopic findings in patients with genetically confirmed SDS. Methods Retrospective registry study of 45 patients with biallelic Shwachman–Bodian–Diamond syndrome mutations and ...
Elizabeth Korn, Jane Koo, Diana Schwarz, Meghan Haney, Juan Putra, Jaeson Kim, Leah Cheng, Sarah Steltz, Lois Schwarz, Sara Loveless, Richard Cooper, Claire Dusa, Kasiani C. Myers, Akiko Shimamura, Andrew Wehrman, Amit S. Grover   +15 more
wiley   +1 more source

Reversal of surgical biliary diversion with ileal bile acid transport inhibitors: A new chapter in progressive familiar intrahepatic cholestasis type 1 management?

JPGN Reports, EarlyView.
Abstract Progressive Familial Intrahepatic Cholestasis type 1 (PFIC1) is a multisystem disorder. Although liver transplant (LT) resolves the hepatic disease, post‐LT complications may occur, including severe enteropathy and graft steatosis caused by impaired bile acids handling by the native intestine.
Teresa Botelho, Giulia Jannone, Roberto Tambucci, Catherine de Magnee, Isabelle Scheers, Etienne Sokal, Xavier Stephenne   +6 more
wiley   +1 more source