Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Łukasz Obołończyk"'
Autor:
Wojciech Wolyniec, Sonia Kaniuka- Jakubowska, Mato Nagel, Zuzanna Wolyniec, Lukasz Obolonczyk, Renata Swiatkowska-Stodulska, Krzysztof Sworczak, Marcin Renke
Publikováno v:
Nefrología (English Edition), Vol 36, Iss 3, Pp 304-309 (2016)
Introduction: Hypokalaemia is a common clinical problem. A potential but commonly overlooked cause of hypokalaemia is Gitelman syndrome. Material and methods: A 26-year-old man was admitted to the hospital due to syncope with general and muscular wea
Externí odkaz:
https://doaj.org/article/6b90c3dd2ebe472ba26ddc92520921ea
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
BackgroundRenal cell cancer may cause various paraneoplastic syndromes; however, paraneoplastic hypereosinophilia occurs exceedingly rare. Thus far, only two cases of clear cell renal cell carcinoma (CCRCC) associated with hypereosinophilia have been
Externí odkaz:
https://doaj.org/article/7a5862df264d47edad97d476383b9619
Publikováno v:
Biomedicines, Vol 10, Iss 1, p 123 (2022)
Introduction. Primary hyperparathyroidism (PHPT) is a condition characterized by disorders of calcium–phosphate metabolism and bone metabolism caused by pathological overproduction of parathyroid hormone (PTH). The diagnosis of overt PHPT is based
Externí odkaz:
https://doaj.org/article/ed71bc04885c4511adf2337d2f39fabd
Autor:
Izabela Karwacka, Łukasz Obołończyk, Sonia Kaniuka-Jakubowska, Michał Bohdan, Krzysztof Sworczak
Publikováno v:
Biomedicines, Vol 9, Iss 11, p 1708 (2021)
Primary aldosteronism (PA) is a heterogeneous group of disorders caused by the autonomous overproduction of aldosterone with simultaneous suppression of plasma renin activity (PRA). It is considered to be the most common endocrine cause of secondary
Externí odkaz:
https://doaj.org/article/fa1f82f2f734431ab5daddcf1a8c0822
Publikováno v:
Biomedicines, Vol 9, Iss 2, p 98 (2021)
Adrenocortical carcinoma (ACC) is a rare epithelial neoplasm, with a high tendency for local invasion and distant metastases, with limited treatment options. Surgical treatment is the method of choice. For decades, the mainstay of pharmacological tre
Externí odkaz:
https://doaj.org/article/34206bddd62b4632bc2c2492f1d3d057
Publikováno v:
Arterial Hypertension. 27:56-62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::980ee40fc19023e42e292d7ac82b69d4
https://doi.org/10.5603/ah.a2023.0005
https://doi.org/10.5603/ah.a2023.0005
Autor:
Krzysztof Sworczak, Katarzyna Sikorska, Łukasz Obołończyk, Katarzyna Banaszkiewicz, Damian Panas
Publikováno v:
Endokrynologia Polska. 72:126-132
Introduction: Hereditary haemochromatosis (HH) is a disease characterised by the excessive absorption of iron and its deposition in various organs. Late complications of this disease include cirrhosis, hepatocellular carcinoma, and endocrine disorder
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c686076026739fc38635865293c1b2dd
https://doi.org/10.5603/ep.a2021.0008
https://doi.org/10.5603/ep.a2021.0008
Publikováno v:
Psychiatria Polska. 55:397-404
Przedstawiamy przypadek kliniczny pacjentki z zaburzeniami psychiatrycznym u której w 63 roku życia postawiono rozpoznanie zespołu DiGeorga, zespołu Fahra oraz zespołu Turnera. Według naszej wiedzy jest to pierwszy na świecie opisany przypadek
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f847cdf53fe7540e3b1225841cc6e07
https://doi.org/10.12740/pp/119376
https://doi.org/10.12740/pp/119376
Autor:
Jarosław B. Ćwikła, Łukasz Obołończyk, Krzysztof Sworczak, Elżbieta A. Zych, Katarzyna Chełmińska, Piotr Wiśniewski, Aleksandra Jaruszewska
Publikováno v:
Arterial Hypertension. 24:38-44
The rarity of malignant pheochromocytoma coupled with the lack of definitive predictors of malignancy and the variability of clinical course, poses a significant diagnostic and therapeutic challenge. Since data on treatment is so scarce, case reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b6e904c6e03f7b8e05bd5dddaa8c4cf
https://doi.org/10.5603/ah.a2020.0001
https://doi.org/10.5603/ah.a2020.0001
Autor:
Łukasz Obołończyk, Izabela Karwacka, Krzysztof Sworczak, Michał Bohdan, Sonia Kaniuka-Jakubowska
Publikováno v:
Biomedicines, Vol 9, Iss 1708, p 1708 (2021)
Biomedicines
Biomedicines
Primary aldosteronism (PA) is a heterogeneous group of disorders caused by the autonomous overproduction of aldosterone with simultaneous suppression of plasma renin activity (PRA). It is considered to be the most common endocrine cause of secondary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcc8f0d62e1aaee27a687f6b176f3af4
https://www.mdpi.com/2227-9059/9/11/1708
https://www.mdpi.com/2227-9059/9/11/1708