Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Erik Fjellstedt"'
Publikováno v:
International Journal of Nephrology and Renovascular Disease. 13:273-280
Purpose: Conventional hemodialysis (HD) treatment has an acceptable removal of small uremic molecules, but so-called middle molecules in the range of 0.5-60 kDa are poorly cleared with HD compared to a native kidney, which may contribute to morbidity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8961aaef1ee78a59beba1d72487cd65e
https://doi.org/10.2147/ijnrd.s263110
https://doi.org/10.2147/ijnrd.s263110
Autor:
Bengt Zöller, Erik Fjellstedt, Xinjun Li, Delshad Saleh Akrawi, Kristina Sundquist, Jan Sundquist
Publikováno v:
Annals of Medicine. 48:313-322
Familial risks of glomerulonephritis (acute, chronic and unspecified glomerulonephritis) have not been studied. This study aims to determine the familial risks of glomerulonephritis.Individuals born from1932 onwards diagnosed with glomerulonephritis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e4f69034efb01a2ea5c6d1eca461384
https://doi.org/10.3109/07853890.2016.1169316
https://doi.org/10.3109/07853890.2016.1169316
Autor:
Erik Fjellstedt, Bengt Zöller, Delshad Saleh Akrawi, Mir Nabi PirouziFard, Jan Sundquist, Kristina Sundquist
Publikováno v:
European journal of clinical investigation. 49(8)
Background: Glomerulonephritis clusters in families. However, infections are common inducers of glomerulonephritis and may also cluster in families. Studies of adoptees and their biological and adoptive parents may disentangle genetic from environmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ef3296a05c244983e15ee117f91c376
https://pubmed.ncbi.nlm.nih.gov/31172510
https://pubmed.ncbi.nlm.nih.gov/31172510
Autor:
Bengt Zöller, Delshad Saleh Akrawi, Erik Fjellstedt, Mir Nabi PirouziFard, Jan Sundquist, Kristina Sundquist
Publikováno v:
Nephron. 138(2)
Background/Aims: The heritability of end-stage renal disease (ESRD) among adoptees has not been examined so far. By studying adoptees and their biological and adoptive parents, it is possible to differentiate between the genetic causes and environmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b39c81633e9797545bb9efc429a9369
https://pubmed.ncbi.nlm.nih.gov/29131054
https://pubmed.ncbi.nlm.nih.gov/29131054
Autor:
Eric Verbeken, Yumi Noda, Paula Specht, Angels Betriu, Ahad A. Abdalla, Bogusław Okopień, Isabelle Jaussent, Magdalena Olszanecka-Glinianowicz, MariaJose Soler, Krzysztof Labuzek, Tuan Ismail, Soo Bong Lee, Mai Sugahara, Izumi Sugimoto, Jung Eun Lee, Mohammad Ibrahim Anan, Olle Melander, Naobumi Mise, Yasuhisa Sakurai, Ailish Hannigan, Kazuko Suzuki, Cornelius J. Cronin, Isao Kubota, Harin Rhee, Nihil Chitalia, Tomokazu Okado, Amir E.L. Okely, Ludomir Stefańczyk, Masanori Emoto, Esam Lotfy Harash, Francesca Mallamaci, Magdalena Kaczmarska, Markus Ketteler, Célia Brugueirolle, Rafał Ficek, Sei Sasaki, Ghislain Opdenakker, Toshihide Naganuma, Göran Berglund, Erik Fjellstedt, Tetsuo Shoji, Jürgen Floege, Kristien Daenen, Sung Kyu Ha, Mikio Okamura, Hoon Young Choi, Hélène Leray-Moragues, Anne-Marie Dupuy, Michał Nowicki, Kenichi Ishizawa, Anna Faura, Marc Hoylaerts, Sol Otero, Tatsuya Nakatani, Il Young Kim, Astrid Weiland, Masaaki Inaba, Daniela Leonardis, Piotr Grzelak, Malaka Yehya Fouad, Inge Fourneau, Austin G. Stack, Wael Fouad Nassar, Jerzy Chudek, Byeong Yun Yang, Ilona Kurnatowska, Rika Miura, In Hye Hwang, Elvira Fernández, David Goldsmith, Jean-Paul Cristol, Hyeong Cheon Park, Bert Bammens, Julio Pascual, Hideaki Shima, Mohammad Hany Hafez, Silvia Collado, Dong Won Lee, Frances Boa, Andrzej Wiecek, Anders Christensson, Min Ji Shin, Seung Kyo Park, Kosuke Kudo, Katarzyna Wyskida, Ayako Tsuchiya, Sergi Mojal, Liam F. Casserly, Ihm Soo Kwak, Laura Tooth, Tatemitsu Rai, Eva Rodríguez, Leila Chenine, Bernard Canaud, Soichiro Iimori, Lisa Uchida, Davide Bolignano, Anna Masajtis-Zagajewska, Rocco Tripepi, Mahmoud E.L. Temraz, Marion Morena, Takafumi Kanemitsu, Muriel Giansily-Blaizot, Juan C. Kaski, Katsuhito Mori, Eiji Ishimura, Maria Andersson-Ohlsson, Nagaaki Kotera, Shinichi Uchida, Kazunobu Ichikawa, Eun Young Seong, Shinya Nakatani, Masatomo Chikamori, Kyung Nam Lee, Shotaro Naito, Tsuneo Konta, Agnieszka Zak-Gołab, Masafumi Kobayashi, Clara Barrios, Mostafa Abdelaziz Mostafa, Debasish Banerjee, Vincent Brandenburg, Hoang T. Nguyen, Tomoko Honda, Jean-François Schved, Yaser Mohammad Hendi, Kornel Pośpiech, Carmine Zoccali
Publikováno v:
Nephrology Dialysis Transplantation. 28:i352-i357
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e7ba50558e8701991c64c207714e3d75
https://doi.org/10.1093/ndt/gft130
https://doi.org/10.1093/ndt/gft130
Publikováno v:
Genetic Testing. 7:13-20
Cystinuria is an autosomal recessive disorder characterized by increased urinary excretion of cystine and dibasic amino acids, which cause recurrent stone formation in affected individuals. Three subtypes of cystinuria have been described (type I, II
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2275d82720b9da541fea2e00b99f99dd
https://doi.org/10.1089/109065703321560886
https://doi.org/10.1089/109065703321560886
Autor:
Erik Fjellstedt, Peter Söderkvist, Lotta Harnevik, Annette Molbaek, Torsten Denneberg, Hans-Göran Tiselius
Publikováno v:
Human Mutation. 18:516-525
Cystinuria is an autosomal recessive disorder that affects luminal transport of cystine and dibasic amino acids in the kidneys and the small intestine. Three subtypes of cystinuria can be defined b ...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de116822534defe8d499af83ce5f96ba
https://doi.org/10.1002/humu.1228
https://doi.org/10.1002/humu.1228
Publikováno v:
Urological Research. 29:295-302
For many years, urine alkalinization has been one of the cornerstones in the treatment of homozygous cystinuria. Because of the relationship found between the excretion of urinary sodium and cystine, potassium citrate has emerged as the preferred sod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5dfefa769287cb883a5bb0f878381834
https://doi.org/10.1007/s002400100200
https://doi.org/10.1007/s002400100200
Publikováno v:
American Journal of Nephrology; 39(2), pp 85-91 (2014)
Background/Aims: Chronic kidney disease (CKD) is common in the general population, may lead to end-stage renal disease, and is most frequently found among males. Familial clustering of kidney diseases has been observed. We aimed to study a potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2651349dd901c8686fb8445fa14e5609
https://pubmed.ncbi.nlm.nih.gov/24481112
https://pubmed.ncbi.nlm.nih.gov/24481112
Autor:
Torsten Denneberg, Jan-Olof Jeppsson, Lotta Harnevik, Peter Söderkvist, Hans-Göran Tiselius, Erik Fjellstedt
Publikováno v:
Urological research. 31(6)
Advances in molecular genetics have brought a deeper understanding of cystinuria. This autosomal recessive disease, which is caused by a defective tubular reabsorption of cystine and the three dibasic amino acids arginine, lysine and ornithine, resul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fc9057c62d7c38dfb508a60a4899007
https://pubmed.ncbi.nlm.nih.gov/14586528
https://pubmed.ncbi.nlm.nih.gov/14586528