Ana Drole Torkar - Ljubljana University Medical Centre

基本信息

浏览量：0

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 19 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Case Report: the Success of Empagliflozin Therapy for Glycogen Storage Disease Type 1B

Ana Klinc,Urh Groselj,Matej Mlinaric,Matjaz Homan,Gasper Markelj, Ajda Mezek Novak,Andreja Sirca Campa,Jaka Sikonja,Tadej Battelino,Mojca Zerjav Tansek,Ana Drole Torkar

FRONTIERS IN ENDOCRINOLOGY (2024)

引用0浏览0WOS引用

Decreased physical fitness in children is associated with increased cardiovascular risk determined by increased carotid intima-media thickness

Ana Drole Torkar, Emil Plesnik,Klemen Dovc,Soncka Jazbinsek,Matej Mlinaric,Urh Groselj,Tadej Battelino, Grogor Starc,Primoz Kotnik

HORMONE RESEARCH IN PAEDIATRICS (2023): 231-232

引用0浏览0引用

Comparison of Tandem Mass Spectrometry and the Fluorometric Method—Parallel Phenylalanine Measurement on a Large Fresh Sample Series and Implications for Newborn Screening for Phenylketonuria

Dasa Perko,Urh Groselj,Vanja Cuk,Ziga Iztok Remec,Mojca Zerjav Tansek,Ana Drole Torkar,Blaz Krhin,Ajda Bicek,Adrijana Oblak,Tadej Battelino,Barbka Repic Lampret

International journal of molecular sciences（2023）

引用3浏览0WOS引用

Clinical and Genetic Characteristics of a Patient with Phosphoribosyl Pyrophosphate Synthetase 1 Deficiency and a Systematic Literature Review

Katarina Stajer,Neja Kovac,Jaka Sikonja,Matej Mlinaric,Sara Bertok,Jernej Brecelj,Marusa Debeljak,Jernej Kovac,Gasper Markelj,David Neubauer,Rina Rus,Mojca Zejav Tansek,Ana Drole Torkar,Aleksandra Zver,Tadej Battelino,Rosa Jimenez Torres,Urh Groselj

MOLECULAR GENETICS AND METABOLISM REPORTS (2023)

引用0浏览0引用

Newborn Screening in a Pandemic-Lessons Learned

Matej Mlinaric,James R Bonham,Viktor Kožich,Stefan Kölker,Ondrej Majek,Tadej Battelino,Ana Drole Torkar,Vanesa Koracin,Dasa Perko,Ziga Iztok Remec,Barbka Repic Lampret,Maurizio Scarpa,Peter C J I Schielen,Rolf H Zetterström,Urh Groselj

International journal of neonatal screeningno. 2 (2023): 21-21

引用0浏览0WOS引用

Early Discovery of Children with Lysosomal Acid Lipase Deficiency with the Universal Familial Hypercholesterolemia Screening Program

Ursa Sustar,Urh Groselj,Katarina Trebusak Podkrajsek,Matej Mlinaric,Jernej Kovac, Martin Thaler,Ana Drole Torkar,Ajda Skarlovnik,Tadej Battelino,Tinka Hovnik

Frontiers in Genetics（2022）

引用7浏览0WOS引用

Optimizing the Phenylalanine Cut-Off Value in a Newborn Screening Program

Dasa Perko,Barbka Repic Lampret,Ziga Iztok Remec,Mojca Zerjav Tansek,Ana Drole Torkar,Blaz Krhin,Ajda Bicek,Adrijana Oblak,Tadej Battelino,Urh Groselj

Genes（2022）

引用4浏览0WOS引用

Efficacy and Safety of Empagliflozin in Glycogen Storage Disease Type Ib: Data from an International Questionnaire

Sarah C. Gruenert,Terry G. J. Derks, Katarina Adrian,Khalid Al-Thihli,Diana Ballhausen,Joanna Bidiuk,Andrea Bordugo,Monica Boyer,Drago Bratkovic,Michaela Brunner-Krainz,Alberto Burlina,Anupam Chakrapani,Willemijn Corpeleijn,Alison Cozens,Charlotte Dawson, Helena Dhamko,Maja Djordjevic Milosevic,Hernan Eiroa,Yael Finezilber,Carolina Fischinger Moura de Souza,Maria Concepcion Garcia-Jimenez,Serena Gasperini,Dorothea Haas,Johannes Haeberle,Rebecca Halligan, Law Hiu Fung, Alexandra Hoerbe-Blindt, Laura Maria Horka,Martina Huemer,Sema Kalkan Ucar,Bozica Kecman,Sebile Kilavuz,Gergely Krivan,Martin Lindner, Natalia Luesebrink,Konstantinos Makrilakis,Anne Mei-Kwun Kwok,Esther M. Maier,Arianna Maiorana,Shawn E. McCandless,John James Mitchell,Hiroshi Mizumoto,Helen Mundy,Carlos Ochoa,Kathryn Pierce,Pilar Quijada Fraile,Debra Regier,Alessandro Rossi,Rene Santer, Hester C. Schuman,Piotr Sobieraj,Johannes Spenger,Ronen Spiegel,Karolina M. Stepien,Galit Tal,Mojca Zerjav Tansek,Ana Drole Torkar,Michel Tchan,Santhosh Thyagu,Samantha A. Schrier Vergano,Erika Vucko,Natalie Weinhold,Petra Zsidegh,Saskia B. Wortmann

Genetics in Medicine（2022）

引用21浏览0WOS引用

GENSKO ZDRAVLJENJE PRI MUKOPOLISAHARIDOZI TIPA IIIA: PREDSTAVITEV PRIMEROV

Benjamin Lah, Tadej Jalšovec,Ana Drole Torkar,Jana Kodrič,Saba Battelino,Mojca Žerjav Tanšek,Tadej Battelino,Urh Grošelj

Slovenska pediatrija, revija pediatrov Slovenije in specialistov šolske ter visokošolske medicine Slovenijeno. 2 (2022): 66-71

引用0浏览0引用

Compound Heterozygote Mutation in the SMPD1 Gene Leading to Nieman-Pick Disease Type A

Alja Kavcic,Matjaz Homan,Milanka Zivanovic,Marusa Debeljak,Tita Butenko,Ana Drole Torkar,Mojca Zerjav Tansek,Sara Bertok,Tadej Battelino,Urh Groselj

AMERICAN JOURNAL OF CASE REPORTS（2022）

引用1浏览0WOS引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn