Results 71 to 80 of about 3,502,714 (164)

Genetic and phenotypic characterization of Ethiopian durum wheat: A comprehensive review of trait diversity and breeding potential

Agrosystems, Geosciences &Environment, Volume 9, Issue 3, September 2026.
Abstract Ethiopian durum wheat (Triticum turgidum ssp. durum) is a globally significant crop recognized for its rich genetic diversity, stress adaptation, and high grain quality. This review consolidates over 20 years of research on the phenotypic and genotypic characterization of Ethiopian durum wheat landraces, focusing on trait discovery, genome ...
Agegnehu Mekonnen Tessema, Fikru Mekonnen Abebe, Yosef Gebrehawaryat Kidane, Daniel Hailegiorgis   +3 more
wiley   +1 more source

Protein losing enteropathy: comprehensive review of the mechanistic association with clinical and subclinical disease states

, 2017
David G Levitt,1,* Michael D Levitt,2,* 1Department of Integrative Biology and Physiology, University of Minnesota, 2Research Service, Veterans Affairs Medical Center, Minneapolis, MN, USA *These authors contributed equally to this work Abstract: Protein
Levitt MD, Levitt DG
core  

Giardia infection: Protein-losing enteropathy in an adult with immunodeficiency

, 2015
The case of a 52-year-old woman with a past history of thymoma resection who presented with chronic diarrhea and generalized edema is the focal point of this article.
Santos, TN, Lorena, SL, Pereira-Filho, Rogerio Antunes, Cabral, VLR, Furtado, Alexandre Khodr, Nagasako, Cristiane Kibune, Lorena, Sonia Leticia, Pereira, RA, Furtado, AK, Nagasako, CK, Mansour, Eli, Mansour, E, Cabral, Virginia Lucia Ribeiro, Santos, Thiago Nunes   +13 more
core   +1 more source

Management of Refractory and Difficult‐To‐Treat Inflammatory Bowel Disease: An Expert Opinion Review

JCC Plus, Volume 1, Issue 5, September 2026.
This expert opinion offers a practical framework for refractory and difficult‐to‐treat IBD: confirm inflammation objectively, distinguish pharmacologic from structural and functional disease, and then escalate. Across ten clinical questions, the evidence is often limited to case series, and the resulting statements are identified as expert opinion ...
Filiz Akyuz, Oguz Kagan Bakkaloglu, Nalan Gulsen Unal, Ismail Hakki Kalkan, Mehmet Arhan, Ibrahim Hatemi, Taylan Kav, Murat Toruner, Hale Akpinar, Ahmet Tezel, Aykut Ferhat Celik   +10 more
wiley   +1 more source

Modern approaches to the diagnosis and treatment of protein-losing enteropathy in children

Zdorovʹe Rebenka
Recently, pediatricians have been paying increasing attention to diseases accompanied by the syndrome of protein-losing enteropathy, as this condition is challenging to diagnose and treat, especially in younger children, and significantly affects a child’
O.H. Shadrin, L.F. Slepova, O.P. Hladyshko, V.M. Fisun, T.M. Archakova, M.V. Bondarenko   +5 more
doaj   +1 more source

Results From a Phase 2, Open‐Label Study Evaluating the Safety, Tolerability, and Effect on Ataxia of GLM101 in Three Adult Patients With PMM2‐CDG

Journal of Inherited Metabolic Disease, Volume 49, Issue 5, September 2026.
ABSTRACT Phosphomannomutase 2 congenital disorder of glycosylation (PMM2‐CDG) is a rare, autosomal recessive disease caused by PMM2 deficiency, which impairs conversion of mannose‐6‐phosphate into mannose‐1‐phosphate (M1P) and disrupts N‐linked glycosylation.
Mercedes Serrano, Florencia Epifani, Rose Marino, Peter McWilliams   +3 more
wiley   +1 more source

Protein-losing enteropathy associated with systemic lupus erythematosus: response to cyclophosphamide

, 2015
Protein-losing enteropathy is a rare manifestation of systemic lupus erythematosus (SLE) leading to hypoalbuminemia and anasarca. We report the case of a woman with SLE who presented chronic hypoalbuminemia diagnosed as protein-losing enteropathy ...
de Castro, GRW, Appenzeller, S, Bertolo, MB, Costallat, LTL   +3 more
core   +1 more source

CD55 Deficiency, Early-Onset Protein-Losing Enteropathy, and Thrombosis

, 2017
BACKGROUND Studies of monogenic gastrointestinal diseases have revealed molecular pathways critical to gut homeostasis and enabled the development of targeted therapies.
Ozen, Ahmet and Comrie, William A. and Ardy, Rico C. and Conde, Cecilia Dominguez and Dalgic, Buket and Beser, Omer F. and Morawski, Aaron R. and Karakoc-Aydiner, Elif and Tutar, Engin and Baris, Safa and Ozcay, Figen and Serwas, Nina K. and Zhang, Yu and Matthews, Helen F. and Pittaluga, Stefania and Folio, Les R. and Aksu, Aysel Unlusoy and McElwee, Joshua J. and Krolo, Ana and Kiykim, Ayca and Baris, Zeren and Gulsan, Meltem and Ogulur, Ismail and Snapper, Scott B. and Houwen, Roderick H. J. and Leavis, Helen L. and Ertem, Deniz and Kain, Renate and Sari, Sinan and Erkan, Tulay and Su, Helen C. and Boztug, Kaan and Lenardo, Michael J.
core   +3 more sources

Non‐Invasive Assessment of Endothelial Dysfunction and Arterial Stiffness in Fontan Circulation

European Journal of Clinical Investigation, Volume 56, Issue 9, September 2026.
The Fontan procedure is the definitive treatment for complex congenital heart disease, creating a circulation without a subpulmonary ventricle. This altered hemodynamic state negatively affects endothelial function, contributing to progressive organ dysfunction and long‐term morbidity.
Amalia Baroutidou, Eleni Pagkopoulou, Vasileios Kamperidis, Antonios Ziakas, Theodoros Dimitroulas, George Giannakoulas   +5 more
wiley   +1 more source

A Rare Complication of Giardiasis in Children: Protein-losing Enteropathy

, 2018
Protein-losing enteropathy may develop as a complication of a wide spectrum of diseases. Three cases of giardiasis that presented with acute onset of hypoalbuminemia were documented, and resolution of protein loss after treatment was also confirmed. Thus,

core   +1 more source