Results 171 to 180 of about 1,981,808 (273)

Acute Febrile Illness With Triple Co-Infection: A Case Report on the Diagnostic Challenges of Overlapping Febrile Illnesses. [PDF]

Clin Case Rep
Basyal S, Parajuli R, Yadav DP, Bhattarai S, Bhandari K, Basyal S, Zaman G, Parajuli R.   +7 more
europepmc   +1 more source

Presumptive necrotising fasciitis with concurrent pyothorax in a 9‐month‐old Great Dane

Veterinary Record Case Reports, Volume 14, Issue 4, November 2026.
Abstract A 9‐month‐old, entire, male Great Dane presented with rapid multi‐limb swelling, pyrexia and diarrhea following initial treatment for presumed gastroenteritis. Diagnostic evaluation revealed septic pleuropneumonia concurrent with rapidly progressive soft tissue infection affecting three limbs.
Christopher Ponticello
wiley   +1 more source

Measles Without Rash During Acute Febrile Illness Surveillance in Tanzania, 2023-2024. [PDF]

Clin Infect Dis
Lukumay S, Augustino D, Naumanga QS, Payne ST, Guga G, Mungi J, Temu M, Msoka K, Mosha R, Becker L, Liu J, Mduma E, Houpt ER.   +12 more
europepmc   +1 more source

Prospective Study of Targeted Busulfan–Fludarabine Conditioning for Hematopoietic Stem Cell Transplantation in Genetic Rare Diseases

European Journal of Haematology, Volume 117, Issue 5, Page 1369-1377, November 2026.
ABSTRACT Objectives Genetic rare diseases (GRDs), including chronic granulomatous disease, familial hemophagocytic lymphohistiocytosis, and congenital neutropenia, often require hematopoietic stem cell transplantation (HSCT) as the only curative option.
Bo Kyung Kim, Kyung Taek Hong, Jung Yoon Choi, Hyun Jin Park, Kyung‐Sang Yu, In‐Jin Jang, Hyoung Jin Kang   +6 more
wiley   +1 more source

Lessons from the field: implementing an electronic clinical decision support app for acute febrile illness in rural Cambodia. [PDF]

Trans R Soc Trop Med Hyg
Mishra A, Wynberg E, Liverani M, Vanna M, Chanpheakdey P, Nguon C, Callery JJ, Adhikari B, Tripura R, Chandna A, Fegan G, Waithira N, Peto TJ, Voeurng B, Davoeng C, Rekol H, Dysoley L, Day NPJ, Lubell Y, Chew R.   +19 more
europepmc   +1 more source

A Case of Disseminated Encephalitozoon cuniculi in a Lung Transplant Recipient: Microsporidiosis in the Era of Molecular Diagnostics

Transplant Infectious Disease, EarlyView.
Lee S. Gottesdiener, Clare DeLaurentis, Marcus R. Pereira   +2 more
wiley   +1 more source

Secretory Phospholipase A2 in Patients With Sickle Cell Disease Hospitalized for Vaso‐Occlusive Pain Episodes

Pediatric Blood &Cancer, Volume 73, Issue 10, October 2026.
ABSTRACT Background Secretory phospholipase A2 (sPLA2) is an inflammatory mediator linked to acute chest syndrome (ACS) in sickle cell disease (SCD), a serious complication that can develop during an acute vaso‐occlusive pain episode (VOE). Plasma sPLA2 levels have been proposed as a potential biomarker for predicting ACS onset.
Rawan Korman, Maria Yasmine, Dunia Hatabah, Noor Alzraikat, Frank Harris, Lou Ann Brown, Satheesh Chonat, Nitya Bakshi, Chris A. Rees, Carlton Dampier, Claudia R. Morris   +10 more
wiley   +1 more source

Host-derived immune signatures as biomarkers to differentiate arboviral acute febrile illness from other causes of acute fever. [PDF]

Front Microbiol
Tiberti N, Bertoli G, Mazzi C, Vezzelli E, Sanfilippo L, Valerio M, Ancillotti L, Accordini S, Piubelli C, Buonfrate D, Castilletti C, Gobbi FG.   +11 more
europepmc   +1 more source

Changing Etiologies of Febrile Illness in Areas of Differing Malaria Transmission in Rural Kenya

, 2014
Thesis (Ph.D.)--University of Washington, 2014"Background": As malaria continues to decline in many parts of sub-Saharan African (SSA) and malaria rapid diagnostic tests become increasingly used; a growing number of febrile children are now being ...
Onchiri, Frankline Magaki
core  

Histidine Supplementation Stabilizes Hearing and Vision and Improves Growth in HARS1‐Related Autosomal Recessive Disorder Associated With Usher‐Like Symptoms

American Journal of Medical Genetics Part A, Volume 200, Issue 10, Page 2289-2308, October 2026.
ABSTRACT Autosomal recessive HARS1‐related disorder (originally described as Usher syndrome type 3B) caused by a homozygous Y454S variant in the histidyl‐tRNA synthetase gene (HARS1) is characterized by progressive sensorineural hearing and vision loss and respiratory deterioration with risk for sudden death following febrile illnesses.
Victoria Mok Siu, Rosan Kenana, Rana Chakrabarti, Sarah D. P. Wilhelm, Joseph Andrews, Susan J. Leat, Christina Parker, Michael Miller, Leslie A. Nangle, Wendy McCaul, Ashfia Chowdhury, Natalie Hutchings, Ryan A. Adams, Lauren Guy, Mandy Rhody, Verena Juncal, Marisa I. Mendes, Desiree E. C. Smith, Gajja S. Salomons, Angelica A. Moresco, Daphne L. McCulloch, D. Holmes Morton, Ilka U. Heinemann, C. Anthony Rupar   +23 more
wiley   +1 more source