Zobrazeno 1 - 10
of 189
pro vyhledávání: '"tubulopathies"'
Autor:
Víctor M. Garcia-Nieto, Félix Claverie-Martin, Teresa Moraleda-Mesa, Ana Perdomo-Ramírez, Gloria Mª Fraga-Rodríguez, María Isabel Luis-Yanes, Elena Ramos-Trujillo
Publikováno v:
Nefrología (English Edition), Vol 44, Iss 1, Pp 23-31 (2024)
Renal diseases associated with hypomagnesemia are a complex and diverse group of tubulopathies caused by mutations in genes encoding proteins that are expressed in the thick ascending limb of the loop of Henle and in the distal convoluted tubule. In
Externí odkaz:
https://doaj.org/article/1c9bd7e83fa546cd8868b7cc5cdd51a5
Autor:
Víctor M. Garcia-Nieto, Félix Claverie-Martin, Teresa Moraleda-Mesa, Ana Perdomo-Ramírez, Gloria Ma Fraga-Rodríguez, María Isabel Luis-Yanes, Elena Ramos-Trujillo
Publikováno v:
Nefrología, Vol 44, Iss 1, Pp 23-31 (2024)
Resumen: Las enfermedades renales que cursan con hipomagnesemia son un grupo complejo y variopinto de tubulopatías producidas por mutaciones en genes que codifican proteínas que se expresan en la rama gruesa ascendente del asa de Henle y en el túb
Externí odkaz:
https://doaj.org/article/aaa77f6be77346e3bf5f2affb17d063a
Publikováno v:
Архивъ внутренней медицины, Vol 13, Iss 1, Pp 5-13 (2023)
Uromodulin is a unique protein produced in the kidneys by epithelial cells of the ascending thick portion of the loop of Henle. It implements physiological mechanisms not only at the tubular level, but also participates in the coordination of general
Externí odkaz:
https://doaj.org/article/e7d443b1150647d8b00109acc7fa70ff
Autor:
Judy Savige, B. André Weinstock
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Previously, genetic kidney disease was often recognised when family members shared clinical features. Now, many genetic kidney diseases are diagnosed when testing demonstrates a pathogenic variant in a gene associated with the disease. Detection of a
Externí odkaz:
https://doaj.org/article/545f4d9ac3bc45219aef7a1c7e5bc43b
Autor:
Rakhtan K. Qasba, Anna Carolina Flumignan Bucharles, Maria Victoria Ferreira Piccoli, Pranjal Sharma, Akshat Banga, Balakrishnan Kamaraj, Faisal A. Nawaz, Harshadayani Jagadish Kumar, Mahika Afrin Happy, Ruman K. Qasba, Gowthami Sai Kogilathota Jagirdhar, Mohammad Yasir Essar, Piyush Garg, Shiva Teja Reddy, Kaanthi Rama, Salim Surani, Rahul Kashyap
Publikováno v:
Medicina, Vol 59, Iss 9, p 1638 (2023)
Background and Objectives: Bartter syndrome (BS) is a rare group of autosomal-recessive disorders that usually presents with hypokalemic metabolic alkalosis, occasionally with hyponatremia and hypochloremia. The clinical presentation of BS is heterog
Externí odkaz:
https://doaj.org/article/23cc7bf5d75a4d01a482a1d984e65038
Publikováno v:
Kidney Research and Clinical Practice, Vol 40, Iss 4, Pp 512-526 (2021)
In the kidney, a set of proteins expressed in the epithelial cells of the thick ascending loop of Henle and the distal convoluted tubule directly or indirectly play important roles in the regulation of serum magnesium levels. Magnesium reabsorption i
Externí odkaz:
https://doaj.org/article/a4f0f70a65a44018b161bfc5a314792c
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Cristina Julia Blázquez Gómez, Helena Gil-Peña, Flor A. Ordóñez Álvarez, Fernando Santos Rodríguez
Publikováno v:
Nefrología, Vol 41, Iss 2, Pp 182-190 (2021)
Resumen: Antecedentes y objetivo: Las tubulopatías primarias son raras y se presentan habitualmente en la edad pediátrica. Avances recientes en diagnóstico genético y tratamiento han cambiado su historia natural. Este estudio presenta el espectro
Externí odkaz:
https://doaj.org/article/328ce1d6f1d84b1fbff0f2d1117b120e
Autor:
Alexander A. Baranov, Leyla S. Namazova-Baranova, Tatyana V. Sergeeva, Olga V. Chumakova, Svetlana S. Paunova, Nurali Z. Zokirov, Olga V. Komarova, Tea V. Margieva, Vladimir K. Tatochenko, Maya D. Bakradze, Elena N. Tsygina, Olga I. Zrobok, Tatiana V. Vashurina, Irina N. Lupan, Mikhail Yu. Kagan, Alexey N. Tsygin
Publikováno v:
Педиатрическая фармакология, Vol 16, Iss 2, Pp 85-90 (2019)
The authors provide a review of current clinical guidelines regarding medical care provided to children with Bartter’s syndrome — impaired renal tubular function (loop of Henle) with the development of hypokalemia, hypochloremia, metabolic alkalo
Externí odkaz:
https://doaj.org/article/846b8deb1e164b068bb58c895ef61a6b
Autor:
Ignazio Verzicco, Giuseppe Regolisti, Federico Quaini, Pietro Bocchi, Irene Brusasco, Massimiliano Ferrari, Giovanni Passeri, Valentina Cannone, Pietro Coghi, Enrico Fiaccadori, Alessandro Vignali, Riccardo Volpi, Aderville Cabassi
Publikováno v:
Frontiers in Oncology, Vol 10 (2020)
The use of antineoplastic drugs has a central role in treatment of patients affected by cancer but is often associated with numerous electrolyte derangements which, in many cases, could represent life-threatening conditions. In fact, while several an
Externí odkaz:
https://doaj.org/article/95490b8ca4ba409090359377787e88af