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Št. zadetkov: 5
European human granulocytic anaplasmosis is caused by a subcluster of Anaplasma phagocytophilum Ecotype I
Paulina M. Lesiczka, Friederike D. von Loewenich, Robert Kohl, Aleksandra I. Krawczyk, Ron P. Dirks, Pierre H. Boyer, Benoit Jaulhac, Anna Moniuszko-Malinowska, Tina Uršič, Franc Strle, Stanka Lotrič-Furlan, Tatjana Avšič-Županc, Miroslav Petrovec, Miroslav Petrovec, Hein Sprong, Hein Sprong
Izvirni znanstveni članek
Oznake: Anaplasma phagocytophilum;groEL;human granulocytic anaplasmosis;Ixodes ricinus;multilocus sequence typing;ecotypes;whole genome sequence;ticks;
Anaplasma phagocytophilum causes human granulocytic anaplasmosis. However, despite its ubiquitous presence in animals and ticks, human cases are rarely reported in Europe. We generated genetic data from A. phagocytophilum from patients and compared them with sequences from wild and domestic animals ...
Leto: 2025 Vir: Repozitorij Univerze v Ljubljani (RUL)
Old whine in new bottles?
Mark A. Boyer
Pregledni znanstveni članek
Oznake: Politične vede;Mednarodni odnosi;Raziskovanje;
Old whine in new bottles?
Leto: 2003 Vir: Fakulteta za družbene vede (UL FDV)
Comparing magnetism in isostructural oxides A[sub](0.8)La[sub](1.2)MnO[sub](4.1)
Mirela Dragomir, Paul A. Dube, Iztok Arčon, Chad Boyer, Meghan Rutherford, Christopher Wiebe, Graham King, Hanna Dabkowska, John E. Greedan
Izvirni znanstveni članek
Oznake: antiferomagnetiki;Mn XANES;struktura;
This study presents the strikingly distinct magnetic properties of two isostructural compounds, Ba0.8La1.2MnO4.1 and Sr0.8La1.2MnO4.1 (K2NiF4 type, I4/mmm). Spectroscopic studies have shown that Mn is in a +3.0(1) oxidation state only, in both compounds; therefore, the charge is balanced by acco ...
Leto: 2019 Vir: Univerza v Novi Gorici (UNG)
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
Št. zadetkov: 5
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