Zobrazeno 1 - 10
of 278
pro vyhledávání: '"polycystic kidneys"'
Publikováno v:
The Application of Clinical Genetics, Vol Volume 17, Pp 125-130 (2024)
Shuping Zhang,1,* Yamei Ma,1,* Xiu Zang,2 Hao Heng,2 Xuekui Liu,2 Gangshan Peng,3 Ran Liu,3 Jun Liang,1,2,* Houfa Geng1,2,* 1Graduate School, Bengbu Medical University, Bengbu, Anhui, People’s Republic of China; 2Department of Endoc
Externí odkaz:
https://doaj.org/article/017ada4496ca4d1dbdcb293437d3e84c
Autor:
Doviltyte Zina, Kiudeliene Rosita, Zviniene Kristina, Rutkauskiene Giedre, Masalskiene Jurate
Publikováno v:
Frontiers in Pediatrics, Vol 12 (2024)
BackgroundAutosomal dominant polycystic kidney disease (ADPKD) is rare but one of the most common inherited kidney diseases. Normal kidney function is maintained until adulthood in most patients. About 7 in 10 patients with ADPKD develop kidney failu
Externí odkaz:
https://doaj.org/article/3414bd10efc94215bd8610e4905409f0
Akademický článek
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Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Human ciliopathies are hereditary conditions caused by variants in ciliary-associated genes. Ciliopathies are often characterized by multiple system defects. However, it is not easy to make a definite diagnosis in the prenatal period only based on th
Externí odkaz:
https://doaj.org/article/874cecb5baa0414e9d51d15bfb976843
Publikováno v:
Frontiers in Physiology, Vol 12 (2021)
The orientation of cells in two-dimensional and three-dimensional space underpins how the kidney develops and responds to disease. The process by which cells orientate themselves within the plane of a tissue is termed planar cell polarity. In this Re
Externí odkaz:
https://doaj.org/article/f13255a95ad04f1a844a85b919f1a025
Publikováno v:
Iranian Journal of Neonatology, Vol 10, Iss 2, Pp 89-91 (2019)
Background: Meckel-Gruber Syndrome (MGS) is a rare autosomal recessive congenital syndrome with triad of encephalocele, polydactyly, and polycystic kidneys. The worldwide incidence of the MGS is 1 in 1.3-1 in 140,000 live births. The highest incidenc
Externí odkaz:
https://doaj.org/article/313d334789b14dc0847dd49e0a9dd684
Autor:
O.O. Melnyk
Publikováno v:
Počki, Vol 6, Iss 4.18, Pp 37-47 (2016)
In many diseases of the kidneys, N-acetyl-β-D-glucosaminidase (NAG) in the urine is excreted in large quantities. A significant increase in NAG activity is observed at the primary and secondary kidney damage, heavy metal poisoning, kidney transplant
Externí odkaz:
https://doaj.org/article/bffe74c231e34731bfd2817c2169d036
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 9, Pp TD01-TD02 (2016)
Renal Lymphangiectasia (RLM) is very rare benign lymphatic malformation. It can be misdiagnosed for other cystic renal masses, most commonly polycystic kidneys. Though incidentally found in most cases, it may be the cause for hypertension and renal
Externí odkaz:
https://doaj.org/article/bef9c6163c404829937d1cf6eb4b6d3e
Autor:
Hirotatsu Sato, Akihiko Kumamoto, Takao Koyama, Ryota Tanaka, Atsufumi Kamisako, Nobuyuki Higashino, Kodai Fukuda, Tetsuo Sonomura, Hiroki Furotani, Masataka Koike
Publikováno v:
CardioVascular and Interventional Radiology. 44:172-175
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad0397250c81ce63543f556876cd4ef9
https://doi.org/10.1007/s00270-020-02641-z
https://doi.org/10.1007/s00270-020-02641-z