Results 41 to 50 of about 21,660 (161)

On TRacK With Larotrectinib in a Neonate With a Giant Congenital ETV6::NTRK3 Fusion‐Positive Infantile Fibrosarcoma of the Head and Neck

Head &Neck, Volume 47, Issue 5, Page E50-E57, May 2025.
ABSTRACT Background Infantile fibrosarcoma (IFS) is a rare pediatric tumor of intermediate malignancy with high local aggressiveness that typically presents in young infants. Its occurrence in the head and neck region is rare. Complete non‐mutilating surgical resection is often not possible, requiring multimodal treatment.
Teresa M. Cardesa‐Salzmann, Monika Sparber‐Sauer, Peter Hingst, Andreas Erbersdobler, Bjoern Schneider, Maja Hühns, Andre Jakob, Friederike Terpe, Christian Spang, Dorothea Stalmann, Claudia Bierwirth, Christina Hauenstein, Stefanie Märzheuser, Manfred Ballmann, Carl Friedrich Classen   +14 more
wiley   +1 more source

Circulating αKlotho influences phosphate handling by controlling FGF23 production [PDF]

, 2012
The FGF23 coreceptor αKlotho (αKL) is expressed as a membrane-bound protein (mKL) that forms heteromeric complexes with FGF receptors (FGFRs) to initiate intracellular signaling.
Allen, Matthew R., Breyer, Matthew D, Broderick, Carol, Burr, David B., Cass, Taryn A, Clinkenbeard, Erica L., Farrow, Emily G, Guo, Qianxu, Kharitonenkov, Alexei, Ma, Y Linda, O'Bryan, Linda M, Roberts, Jessica L, Saha, Joy, Smith, Rosamund C, Summers, Lelia J, Sun, Haijun, White, Kenneth E, Wilson, Jonathan M, Zeng, Qing Qiang   +18 more
core   +1 more source

Extreme hypercalcemia secondary to parathyroid adenoma obscured by excessive coffee consumption and premature ventricular complexes

Journal of General and Family Medicine, Volume 26, Issue 3, Page 263-266, May 2025.
Diagnostic biases are potentially life‐threatening. We present a case of extreme hypercalcemia falsely diagnosed as premature ventricular complexes attributed to heavy coffee consumption, while symptoms and electrocardiographic findings of hypercalcemia were disregarded. Abstract Severe hypercalcemia has an arrhythmogenic effect. We present a case of a
Yuval Avidan, Sameer Kassem
wiley   +1 more source

Association between early phosphate intake and refeeding syndrome in extremely low‐birth‐weight infants: A retrospective cohort study

Journal of Parenteral and Enteral Nutrition, Volume 49, Issue 4, Page 460-467, May 2025.
Abstract Background Preterm infants are at risk of refeeding syndrome, a constellation of biochemical changes associated with nutrition. We aimed to determine whether increased early phosphate intake with routine biochemical monitoring is associated with a reduction in refeeding syndrome.
Thomas B. Wright, Frank H. Bloomfield, Tanith Alexander, Barbara E. Cormack   +3 more
wiley   +1 more source

Renal phosphate handling in Gitelman syndrome—the results of a case-control study [PDF]

, 2018
Background: Patients with Gitelman syndrome, a hereditary salt-wasting tubulopathy, have loss-of-function mutations in the SLC12A3 gene coding for the thiazide-sensitive sodium chloride co-transporter in the distal convoluted tubule.
Albisetti, Walter, Amoruso, Chiara, Barretta, Francesco, Bettinelli, Alberto, Bianchetti, Mario, Minnici, Giuseppe, Syrèn, Marie-Louise, Viganò, Cristina   +7 more
core  

Clinical, Electroencephalogram and Imaging Characteristics of Patients With Anti‐LGI1 Antibody Encephalitis: A Multicenter Cohort Study

CNS Neuroscience &Therapeutics, Volume 31, Issue 5, May 2025.
To summarize and analyze the general clinical manifestations, laboratory tests, electroencephalography and imaging characteristics, treatment and prognosis of 88 patients with anti‐leucine‐rich glioma inactivated protein 1 antibody encephalitis (LGI1‐AE) at baseline, discharge, and follow‐up in China, aiming to identify risk factors affecting disease ...
Yang Zhao, Yue Yuan, Rong‐Ze Wang, Mei Cui, Shu‐Fen Chen, Ke‐Liang Chen, Meng‐Meng Li, Yu‐Yuan Huang, Hai‐Ning Zhang, Yan Zhang, Meng Zhao, Hui Tian, Li Sun, Jin‐Tai Yu   +13 more
wiley   +1 more source

Description and pilot evaluation of the Metabolic Irregularities Narrowing down Device software: a case analysis of physician programming [PDF]

, 2015
Background: There is a gap between the abilities and the everyday applications of Computerized Decision Support Systems (CDSSs). This gap is further exacerbated by the different ‘worlds’ between the software designers and the clinician end-users ...
Albrecht, III, Charles, Goldberg, Andrew D., Herasevich, Vitaly, Kashiouris, Markos G., Miljković, Miloš   +4 more
core   +3 more sources

X‐Linked Hypophosphataemia and Burosumab: A Systemic Disease With a New Treatment

Journal of Paediatrics and Child Health, Volume 61, Issue 5, Page 685-700, May 2025.
ABSTRACT X linked hypophosphataemia (XLH) is a systemic, chronic condition that significantly impairs quality of life. In XLH, a phosphate regulating endopeptidase homologue X‐linked (PHEX) gene mutation leads to excess fibroblast growth factor 23 (FGF23), causing hypophosphataemia and subsequent rickets, lower limb deformity, pain and other sequelae ...
Jessica L. Sandy, Andrew Biggin, Aris Siafarikas, Peter J. Simm, Christine P. Rodda, Craig F. Munns   +5 more
wiley   +1 more source

Effectiveness and Safety of Oral Azvudine for Elderly Hospitalized Patients With COVID‐19: A Multicenter, Retrospective, Real‐World Study

Advanced Science, Volume 12, Issue 13, April 3, 2025.
This multicenter, retrospective, real‐world study enrolls the largest hospitalized elderly cohort of COVID‐19 patients from nine hospitals in Henan Province to investigate the effectiveness and safety of Azvudine. The results show that compared controls, Azvudine treatment can reduce the rate of all‐cause death in elderly patients with COVID‐19, and ...
Ranran Sun, Haiyu Wang, Junyi Sun, Mengzhao Yang, Shixi Zhang, Xinjun Hu, Bo Yu, Zhan Song, Na Han, Hong Luo, Ming Cheng, Guangming Li, Guotao Li, Yiqiang Yuan, Lili Liang, Yanyang Zhang, Donghua Zhang, Silin Li, Quancheng Kan, Hongxia Liang, Zhigang Ren   +20 more
wiley   +1 more source

Genetic and clinical peculiarities in a new family with hereditary hypophosphatemic rickets with hypercalciuria: a case report [PDF]

, 2010
Hereditary hypophosphatemic rickets with hypercalciuria is a rare autosomal recessive disorder (OMIM #241530), characterized by decreased renal phosphate reabsorption that leads to hypophosphatemia, rickets, and bone pain; hypophosphatemia is believed to
Coto, Eliecer, Gil-Peña, Helena, Pérez-Menéndez, Teresa M, Santos, Fernando   +3 more
core