Results 51 to 60 of about 47,738 (314)

Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study

Hepatology, EarlyView., 2022
Natural history of liver disease in a large international cohort of children with Alagille syndrome: Results from the GALA study. Abstract Background and Aims Alagille syndrome (ALGS) is a multisystem disorder, characterized by cholestasis. Existing outcome data are largely derived from tertiary centers, and real‐world data are lacking.
Shannon M. Vandriel, Li‐Ting Li, Huiyu She, Jian‐She Wang, Melissa A. Gilbert, Irena Jankowska, Piotr Czubkowski, Dorota Gliwicz‐Miedzińska, Emmanuel M. Gonzales, Emmanuel Jacquemin, Jérôme Bouligand, Nancy B. Spinner, Kathleen M. Loomes, David A. Piccoli, Lorenzo D'Antiga, Emanuele Nicastro, Étienne Sokal, Tanguy Demaret, Noelle H. Ebel, Jeffrey A. Feinstein, Rima Fawaz, Silvia Nastasio, Florence Lacaille, Dominique Debray, Henrik Arnell, Björn Fischler, Susan Siew, Michael Stormon, Saul J. Karpen, Rene Romero, Kyung Mo Kim, Woo Yim Baek, Winita Hardikar, Sahana Shankar, Amin J. Roberts, Helen M. Evans, M. Kyle Jensen, Marianne Kavan, Shikha S. Sundaram, Alexander Chaidez, Palaniswamy Karthikeyan, Maria Camila Sanchez, Maria Lorena Cavalieri, Henkjan J. Verkade, Way Seah Lee, James E. Squires, Christina Hajinicolaou, Chatmanee Lertudomphonwanit, Ryan T. Fischer, Catherine Larson‐Nath, Yael Mozer‐Glassberg, Cigdem Arikan, Henry C. Lin, Jesus Quintero Bernabeu, Seema Alam, Deirdre A. Kelly, Elisa Carvalho, Cristina Targa Ferreira, Giuseppe Indolfi, Ruben E. Quiros‐Tejeira, Pinar Bulut, Pier Luigi Calvo, Zerrin Önal, Pamela L. Valentino, Dev M. Desai, John Eshun, Maria Rogalidou, Antal Dezsőfi, Sabina Wiecek, Gabriella Nebbia, Raquel Borges Pinto, Victorien M. Wolters, María Legarda Tamara, Andréanne N. Zizzo, Jennifer Garcia, Kathleen Schwarz, Marisa Beretta, Thomas Damgaard Sandahl, Carolina Jimenez‐Rivera, Nanda Kerkar, Jernej Brecelj, Quais Mujawar, Nathalie Rock, Cristina Molera Busoms, Wikrom Karnsakul, Eberhard Lurz, Ermelinda Santos‐Silva, Niviann Blondet, Luis Bujanda, Uzma Shah, Richard J. Thompson, Bettina E. Hansen, Binita M. Kamath, The Global ALagille Alliance (GALA) Study Group   +93 more
wiley   +1 more source

Prevalencia de desnutrición en menores de cinco años de Tabasco Malnutrition prevalence in children under 5 years old in Tabasco, Mexico

Salud Pública de México, 1998
Objetivo. Evaluar la prevalencia de desnutrición que se presentó en niños tabasqueños menores de cinco años en 1996, y su evolución entre 1991 y 1996. Material y métodos.
Lucio G. Lastra-Escudero, Silvia G. Roldán-Fernández, Enrique Hernández-Martínez, Alma Patricia Hernández-Torres, Félix Gerardo Lechuga-Padrón   +4 more
doaj  

Human Milk-Derived Fortifier to Reduce Hospital-Acquired Malnutrition in Uncomplicated Gastroschisis: A Case Report

American Journal of Perinatology Reports
Gastroschisis is one of the most common congenital gastrointestinal disorders, occurring in about one in 1,953 infants born each year in the United States.
Anna Strle, Sarah M. Reyes, Megan Schmidt, Mary Frances Lynch   +3 more
doaj   +1 more source

Strategies for reversing the effects of metabolic disorders induced as a consequence of developmental programming

Frontiers in Physiology, 2012
Obesity and the metabolic syndrome have reached epidemic proportions worldwide with far-reaching health care and economic implications. The rapid increase in the prevalence of these disorders suggests that environmental and behavioural influences, rather
Mark H Vickers, Deborah M Sloboda
doaj   +1 more source

Lactoferrin Deficiency During Lactation Causes Adult Obesity‐Related Metabolic Disease Through Persistent Adipose Dysfunction Driven by Impaired Adipocyte Development

Advanced Science, EarlyView.
Lactational lactoferrin deficiency exerts lasting effects on epididymal adipose tissue development from lactation into adulthood: it impairs adipocyte hyperplasia and induces pathological hypertrophy, resulting in lower body weight yet exacerbated metabolic dysfunction under a high‐fat diet in adulthood.
Qin An, Yunxia Zou, Wenli Wang, Zhimei Cheng, Zhuoxing Zhang, Ruwei Liu, Xiong Wang, Kunlun Huang, Fangrong Ding, Yunping Dai, Qingyong Meng, Yali Zhang   +11 more
wiley   +1 more source

Probiotics for the Management of Pediatric Gastrointestinal Disorders: Position Paper of the ESPGHAN Special Interest Group on Gut Microbiota and Modifications

, 2022
Background: Probiotics, defined as live microorganisms that, when administered in adequate amounts, confer a health benefit on the host, are widely used despite uncertainty regarding their efficacy and discordant recommendations about their use.
van Goudoever, Johannes B., Chris H. P. van den Akker, Iva Hojsak, Orel, Rok,, Flavia Indrio, Hojsak, Iva,, Guarino, Alfredo, Szajewska, Hania,, van Goudoever, Johannes B, van Goudoever, Johannes B.,, Orel, Rok, van den Akker, Chris H. P., Szajewska, Hania, Domellöf, Magnus,, Weizman, Zvi,, Raanan Shamir, Domellöf, Magnus, Van den Akker, Chris H., Shamir, Raanan,, Canani, Roberto Berni, Mosca, Alexis,, Alexis Mosca, ESPGHAN Special Interest Group on Gut Microbiota and Modificat., Silvia Salvatore, Lo Vecchio, Andrea,, Lo Vecchio, Andrea, Hania Szajewska, Mihatsch, Walter A, Guarino, Alfredo,, Weizman, Zvi, Indrio, Flavia, Alfredo Guarino, Vandenplas, Yvan,, Vandenplas, Yvan, Indrio, Flavia,, Hojsak, Iva, Salvatore, Silvia,, Mihatsch, Walter A.,, Zvi Weizman, Domell?f, Magnus, Andrea Lo Vecchio, Johannes B. van Goudoever, Salvatore, Silvia, van den Akker, Chris H P,, Canani, Roberto B., Mosca, Alexis, Berni Canani, Roberto,, Mihatsch, Walter A., Berni Canani, Roberto, Rok Orel, Roberto Berni Canani, Yvan Vandenplas, Magnus Domellöf, Shamir, Raanan, Walter A. Mihatsch   +54 more
core   +1 more source

35 Individuals With HUWE1‐Related Neurodevelopmental Disorder and Suggested Clinical Evaluations

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT HUWE1 (HECT, UBA, and WWE Domain Containing E3 Ubiquitin Protein Ligase1, OMIM 300697), located at Xp11.22, encodes a ubiquitin ligase that is highly conserved across species. Genetic variants in HUWE1 described in multiple independent studies cause X‐linked intellectual disability, including in the patients identified by Juberg, Marsidi, and ...
Mindy H. Li, Deziree L. Coleman, Kelsey Hogan, Danielle Luz, Lindsay Bhandari, Newell Belnap, Tiffany Busa, Charles Coutton, Klaus Dieterich, Svetlana Gorokhova, Clara Hildebrandt, Rachel Logan, Milena Mariani, Manuela Morleo, Vincenzo Nigro, John Pappas, Rachel Rabin, Kelly Schoch, Angelo Selicorni, Vandana Shashi, Rebecca Spillmann, Jennifer Sullivan, Charlotte Tardy, Samantha A. Schrier Vergano, Brock Grill, Kristin Baranano   +25 more
wiley   +1 more source

The use of choline supplementation in premature newborns: a systematic review

Revista Paulista de Pediatria
Objective: To identify the routes and doses of choline supplementation required to meet the metabolic demands of preterm infants. Data Source: The information was searched in three databases: US National Library of Medicine National Institute of ...
Ligia Modelli Rodrigues, Allan Chiaratti de Oliveira, Tulio Konstantyner   +2 more
doaj   +1 more source

Nutritional Deficiencies in Children of the First 3 Years of Life, According to a Multicenter Study in Ukraine

Zdorovʹe Rebenka, 2013
Taking into account the fact that in Ukraine today there is not enough researches that summarize the data on the nutritional status of young children, the prevalence of eating disorders and lack of basic macro- and micronutrients in children, the ...
S.L. Nyankovsky, O.G. Shadrin, V.A. Klymenko, D.O. Dobriansky, O.S. Ivakhnenko, M.O. Yavorska, O.M. Platonova, G.L. Solodovnik, V.V. Zayets   +8 more
doaj   +1 more source

Functional gastrointestinal disorders in infants: to treat, observe or correct?

Zdorovʹe Rebenka, 2020
The article discusses the functional disorders of the gastrointestinal tract in infants. The prevalence of functional gastrointestinal disorders is extremely high in all age groups, but in young children, functional diseases are actually a normal variant:
O.Yu. Belousova, L.V. Kazaryan
doaj   +1 more source