Results 71 to 80 of about 3,053 (170)

European Consensus on Malabsorption—UEG & SIGE, LGA, SPG, SRGH, CGS, ESPCG, EAGEN, ESPEN, and ESPGHAN. Part 1: Definitions, Clinical Phenotypes, and Diagnostic Testing for Malabsorption

United European Gastroenterology Journal, Volume 13, Issue 4, Page 599-613, May 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

Clinical impact and safety of brain biopsy in unexplained central nervous system disorders: a real‐world cohort study

Annals of Clinical and Translational Neurology, Volume 12, Issue 4, Page 792-804, April 2025.
Abstract Objective A substantial part of central nervous system (CNS) disorders remains unexplained, despite various new and minimally invasive diagnostic techniques. Within this rapidly developing diagnostic field, the precise role of brain biopsy is unknown.
Robin W. van Steenhoven, Saan Salih, Juna M. de Vries, Ide Smets, Rob M. Verdijk, Mayke Gardeniers, Jeroen Kerstens, Juliette Brenner, Yvette S. Crijnen, Marjolein Geurts, Jacoline E. C. Bromberg, Corine H. GeurtsvanKessel, Peter A. E. Sillevis Smitt, Rutger K. Balvers, Maarten J. Titulaer   +14 more
wiley   +1 more source

Back from the brink of obscurity

eLife, 2018
A mutation in a transcription factor makes people susceptible to Tropheryma whipplei, the bacterium that causes a rare condition called Whipple's disease.
Donald C Vinh
doaj   +1 more source

Spondylodiscitis as the first manifestation of Whipple's disease -a removal worker with chronic low back pain [PDF]

, 2018
Whipple's disease is a rare systemic infectious disease caused by the actinobacterium Tropheryma whipplei. Spondylodiscitis is an extremely rare manifestation of the infection and has previously been described in only three case reports.
Altwegg, M., Gubler, J., Maibach, R., Morf, M., Weber, U.   +4 more
core  

Analysis of Pathogenic Bacteria and Associated Risk Factors of Bloodstream Infections in ICU Patients Undergoing ECMO Support Using mNGS Technology

International Journal of Clinical Practice, Volume 2025, Issue 1, 2025.
Objective: To analyze the characteristics of pathogens and related risk factors of bloodstream infections (BSI) in patients undergoing ECMO support using mNGS technology. Methods: A retrospective analysis was conducted on 59 patients who received ECMO support in the Emergency Intensive Care Unit (EICU) of the Affiliated Hospital of Xuzhou Medical ...
Jie Kang, Yi Hang, Zheng Liu, Man Yuan, Xiaosong Qiu, Ying Ye, Yuzhu Zang, Xiaobo Huang, Siyuan Song, Yi Wang, Tun-Chieh Chen   +10 more
wiley   +1 more source

Deadly Carousel or Difficult Interpretation of New Diagnostic Tools for Whipple's Disease: Case Report and Review of the Literature [PDF]

, 2018
: Whipple's disease is a rare systemic disorder classically presenting with weight loss, arthralgias, and diarrhea, which was first described in 1907. The causative bacterium Tropheryma whipplei, is a fastidious organism not growing on conventional media.
Altwegg, M., Müller, S., Seebach, J., Vogt, P.   +3 more
core  

Unraveling the Genetic Predisposition on Respiratory Infections: From Single Nucleotide Polymorphisms to Inborn Errors of Immunity

Interdisciplinary Perspectives on Infectious Diseases, Volume 2025, Issue 1, 2025.
Background: The complex interplay between the human genome and microbial pathogens has captured scientific interest, leading to profound insights into the genetic basis of host’s susceptibility to infections. Objective: Here, we explore the spectrum of genetic susceptibility in infectious diseases, ranging from common single nucleotide polymorphisms ...
Francesca Conti, Mattia Moratti, Bianca Laura Cinicola, Riccardo Castagnoli, Riccardo Papa, Silvia Federici, Giuliana Giardino, Lucia Leonardi, Maria Sangerardi, Annarosa Soresina, Gian Luigi Marseglia, Michele Miraglia Del Giudice, Marcello Lanari, Caterina Cancrini, Vassilios Lougaris, Fabio Cardinale, on behalf of the Immunology Committee of the Italian Society of Pediatric Allergology and Immunology (SIAIP), Suraiya Saleem   +17 more
wiley   +1 more source

Delayed Diagnosis of Whipple’s Disease Complicated by Jarisch–Herxheimer Reaction to Ceftriaxone Treatment: A Case Report and Literature Review

Tropical Medicine and Infectious Disease, 2022
Whipple’s disease is a rare chronic infection caused by the actinomycete Tropheryma whipplei. Patients commonly present with gastrointestinal symptoms. We present a case of classic Whipple’s disease complicated by a probable Jarisch–Herxheimer reaction ...
Marcus C. C. Clarke, Ric N. Price
doaj   +1 more source

Whipple's disease: rare disorder and late diagnosis [PDF]

, 2012
Whipple's disease is a rare systemic infectious disorder caused by the bacterium Tropheryma whipplei. We report the case of a 61-year-old male patient who presented to emergency room complaining of asthenia, arthralgia, anorexia, articular complaints ...
Abreu P, Anderson M, Bai JC, Baisden BL, Bruno Galperim, Carneiro AC, Cosme Á, Dobbins WO III, Fenollar F, Feurle GE, Feurle GE, Gerard A, Iqbal T, Jackuliak P, Lagier JC, Lepidi H, Longman RS, Louis ED, Luciana Schmidt Kirschnick, Marcelo Campos Appel-da-Silva, Marth T, Marth T, Martinetti M, Naegeli B, Oliveira L, Rafael Bergesch D'Incao, Rodrigo Mayer Lul, Schijf LJ, Schneider T, Viviane Plasse Renon, Von Herbay A   +30 more
core   +2 more sources

Resistance to trimethoprim/sulfamethoxazole and Tropheryma whipplei [PDF]

International Journal of Antimicrobial Agents, 2009
Whipple's disease (WD) is a chronic infection caused by Tropheryma whipplei. A 1-year treatment of oral trimethoprim/sulfamethoxazole (SXT) is commonly used. Advances in the culture of T. whipplei have allowed for full genome sequencing and antibiotic susceptibility testing, which has demonstrated resistance of T. whipplei to trimethoprim.
Fenollar, F., Rolain, J. M., Alric, L., Papo, T., Chauveheid, M. P., van de Beek, D., /Raoult, Didier   +6 more
openaire   +4 more sources