Results 41 to 50 of about 565,186 (153)

Micronutrient deficiencies after pancreatico‐duodenectomy: A narrative review of the literature and recommendations for clinical practice

Nutrition in Clinical Practice, Volume 40, Issue 5, Page 1073-1092, October 2025.
Abstract Micronutrient uptake is impaired after pancreatico‐duodenectomy (PD) because of malabsorption, reduced absorptive capacity, and poor oral intake. Biochemical depletion is reported in cohort studies, but deficiency states are predominantly reported in case reports, making it difficult to assess occurrence rates.
Mary E. Phillips, Callum Livingstone, Adam E. Frampton, Kathryn H. Hart   +3 more
wiley   +1 more source

Revisiting Vitamin and Trace Mineral Nutrition in Atlantic Salmon Farming With Emphasis on Fish Health

Reviews in Aquaculture, Volume 17, Issue 4, September 2025.
ABSTRACT Atlantic salmon farming is faced with numerous environmental and production‐related challenges affecting fish health and welfare, globally and in Norway. An animal's requirement for a nutrient is the sum of the required supply of available nutrients for maintenance, growth, reproduction, health, and disease resistance.
Antony J. P. Philip, Trond M. Kortner, Pauline Wischhusen, Kristin Hamre, Åshild Krogdahl, Kaja H. Skjærven, Guro Løkka, Gerd M. Berge, Marit Espe, Nini H. Sissener   +9 more
wiley   +1 more source

Thiamine-responsive megaloblastic anemia

Pediatric Hematology/Oncology and Immunopathology
Thiamine-responsive megaloblastic anemia (TRMA), also known as Rogers syndrome, is a rare autosomal recessive disorder first described by Dr. Lon E. Rogers et al. in 1969. This condition is defined by a classic triad of symptoms comprising megaloblastic anemia, diabetes mellitus and sensorineural hearing loss, although clinically it can still exhibit ...
Medina Kh. Gurzhikhanova, M. A. Maschan
openaire   +1 more source

Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness – a case report for dual diagnosis

BMC Pediatrics, 2019
Background Phenotypic difference is general in Mendelian disease. Due to the extremely low incidence for a single disease, phenotype spectrum needs to be expanded.
Yan Zhang, Yi Zhang, Victor Wei Zhang, Chunyi Zhang, Hongke Ding, Aihua Yin   +5 more
doaj   +1 more source

Thiamine withdrawal can lead to diabetic ketoacidosis in thiamine responsive megaloblastic anemia: Report of two siblings

, 2008
Thiamine responsive megaloblastic anemia syndrome (TRMA), an autosomal recessive disorder caused by the deficiency of thiamine transporter protein, is the association of diabetes mellitus, anemia and deafness.
Keskin, Mehmet, M. Kendirci, Kurtoglu, Selim, S. Kurtoglu, M. Keskin, N. Hatipoglu, M. Akcakus, Akçakuş, Mustafa, Hatipoğlu, Nihal, Kendirci, Mustafa   +9 more
core   +1 more source

European Consensus on Malabsorption—UEG & SIGE, LGA, SPG, SRGH, CGS, ESPCG, EAGEN, ESPEN, and ESPGHAN

United European Gastroenterology Journal, Volume 13, Issue 5, Page 773-797, June 2025.
ABSTRACT Malabsorption is a complex and multifaceted condition characterised by the defective passage of nutrients into the blood and lymphatic streams. Several congenital or acquired disorders may cause either selective or global malabsorption in both children and adults, such as cystic fibrosis, exocrine pancreatic insufficiency (EPI), coeliac ...
Marco Vincenzo Lenti, Heinz Florian Hammer, Ilja Tacheci, Rosa Burgos, Stephane Schneider, Anastasiou Foteini, Aleksejs Derovs, Jutta Keller, Ilse Broekaert, Marianna Arvanitakis, Dan Lucian Dumitrascu, Oscar Segarra‐Cantón, Željko Krznarić, Juris Pokrotnieks, Gonçalo Nunes, Johann Hammer, Loris Pironi, Marc Sonyi, Cristina Maria Sabo, Juan Mendive, Adrien Nicolau, Jernej Dolinsek, Denisa Kyselova, Lucrezia Laterza, Antonio Gasbarrini, Teodora Surdea‐Blaga, Jorge Fonseca, Christos Lionis, Gino Roberto Corazza, Antonio Di Sabatino   +29 more
wiley   +1 more source

L’anémie mégaloblastique thiamine dépendante ou syndrome de Rogers : une revue de la littérature [Thiamine-responsive megaloblastic anemia or Rogers syndrome: A literature review]

, 2019
Thiamine-responsive megaloblastic anemia (TRMA), also known as Rogers syndrome, is a rare autosomal recessive disease characterized by three main components: megaloblastic anemia, diabetes mellitus and sensorineural deafness.
Lu, Hortense, Vollenweider, P., Lu, Henri, Vaucher, J., Tran, C., Castioni, J., Lu H, Tran C, Vollenweider P, Vaucher J, Castioni J   +10 more
core   +1 more source

Inherited microcytic anemias due to disorders of iron and heme metabolism: An updated clinical review [PDF]

Hemasphere
Abstract Microcytic anemia is among the most common hematological abnormalities in clinical practice and is usually attributable to iron deficiency, thalassemia traits, or anemia of inflammation. A small but clinically important subset of patients, however, has inherited disorders of iron metabolism or heme synthesis presenting with persistent ...
Makis A, Saougou I, Hatzimichael E.
europepmc   +2 more sources

What do we know about micronutrients in critically ill patients? A narrative review

Journal of Parenteral and Enteral Nutrition, Volume 49, Issue 1, Page 33-58, January 2025.
Abstract Micronutrient (MN) status alterations (both depletion and deficiency) are associated with several complications and worse outcomes in critically ill patients. On the other side of the spectrum, improving MN status has been shown to be a potential co‐adjuvant therapy.
Angelique M.E. de Man, Christian Stoppe, Kristine W.A.C. Koekkoek, George Briassoulis, Lilanthi S.D.P. Subasinghe, Cristian Cobilinschi, Adam M. Deane, William Manzanares, Ioana Grințescu, Liliana Mirea, Ashraf Roshdy, Antonella Cotoia, Danielle E. Bear, Sabrina Boraso, Vincent Fraipont, Kenneth B. Christopher, Michael P. Casaer, Jan Gunst, Olivier Pantet, Muhammed Elhadi, Giuliano Bolondi, Xavier Forceville, Matthias W.A. Angstwurm, Mohan Gurjar, Rodrigo Biondi, Arthur R.H. van Zanten, Mette M. Berger, ESICM/FREM MN group   +27 more
wiley   +1 more source

Recurrent stroke in a child with TRMA syndrome and SLC19A2 gene mutation [PDF]

, 2018
Here we report a 5-month-old boy with thiamine Responsive Megaloblastic Anemia syndrome (TRMA syndrome) with several attacks of stroke. In addition to the cardinal clinical manifestations of the syndrome (thiamine-responsive megaloblastic anemia ...
Karimzadeh, Parvaneh, Moosavian, Toktam, Moosavian, Hamidreza, kiumarsi, Azadeh   +3 more
core   +1 more source