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Št. zadetkov: 4
Overcoming barriers in hospital-based health technology assessment (HB-HTA): international expert panel consensus
Iga Lipska, Rok Hren
Izvirni znanstveni članek
Oznake: zdravstvo;vrednotenje zdravstvenih tehnologij;bolnišnice;healthcare;health technology assessment;hospitals;
The purpose of this article is to investigate the common facilitators and barriers associated with the implementation of hospital-based health technology assessment (HB-HTA) across diverse hospital settings in seven countries. Through a two-round Delphi study, insights were gathered from a panel of ...
Leto: 2024 Vir: Fakulteta za matematiko in fiziko (UL FMF)
Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency
Stefania Drovandi, Beata Lipska-Zietkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gülhan, Olivia Boyer, Agnes Trautmann, Hong Xu, Tanja Kersnik-Levart
Izvirni znanstveni članek
Oznake: coenzyme Q10;deficiency;supplementation therapy;end-stage kidney disease;ESKD;genetic kidney disease;hereditary;kidney survival;outcome;proteinuria reduction;
Primary Coenzyme Q10 (CoQ(10)) deficiency is an ultra-rare disorder caused by defects in genes involved in CoQ(10) biosynthesis leading to multidrug-resistant nephrotic syndrome as the hallmark kidney manifestation. Promising early results have been reported anecdotally with oral CoQ(10) supplementa ...
Leto: 2022 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy
Stefania Drovandi, Beata Lipska-Zietkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gülhan, Olivia Boyer, Agnes Trautmann, Szymon Ziętkiewicz, Tanja Kersnik-Levart
Izvirni znanstveni članek
Oznake: coenzyme Q10;mitochondria;steroid-resistant nephrotic syndrome;
PPrimary Coenzyme Q10 deficiency is a rare mitochondriopathy with a wide spectrum of organ involvement, including steroid-resistant nephrotic syndrome mainly associated with disease-causing variants in the genes COQ2, COQ6 or COQ8B. We performed a systematic literature review, PodoNet, mitoNET, and ...
Leto: 2022 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Diagnosis, management and treatment of the Alport syndrome
Roser Torra, Beata Lipska-Zietkiewicz, Frederic Acke, Corinne Antignac, Jan Ulrich Becker, Emilie Cornec-Le Gall, Albertien M van Eerde, Nicolas Feltgen, Matjaž Kopač
Pregledni znanstveni članek
Oznake: Alport syndrome;glomerular basement membrane;haematuria;
Glomerular nephropathy resulting from the genetic defects in COL4A3/4/5 genes including the classical Alport syndrome is the second most common hereditary kidney disease characterized by persistent haematuria progressing to the need for kidney replacement therapy, frequently associated with sensorin ...
Leto: 2025 Vir: Digitalni repozitorij raziskovalnih organizacij Slovenije
Št. zadetkov: 4
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