Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Miguel A Garcia-Gonzalez"'
Autor:
Mahtab Mohammadpoor Faskhodi, Miguel A Garcia-Gonzalez, Mireya Fernandez-Chimeno, Federico Guede-Fernández, Marc Mateu-Mateus, Lluis Capdevila, Juan J Ramos-Castro
Publikováno v:
PLoS ONE, Vol 19, Iss 2, p e0298354 (2024)
The pulse arrival time (PAT) has been considered a surrogate measure for pulse wave velocity (PWV), although some studies have noted that this parameter is not accurate enough. Moreover, the inter-beat interval (IBI) time series obtained from success
Externí odkaz:
https://doaj.org/article/7678f4223b3f4f89b912524bb5b3b526
Autor:
Miguel A Garcia-Gonzalez, Patricia Outeda, Qin Zhou, Fang Zhou, Luis F Menezes, Feng Qian, David L Huso, Gregory G Germino, Klaus B Piontek, Terry Watnick
Publikováno v:
PLoS ONE, Vol 5, Iss 9 (2010)
Autosomal dominant polycystic kidney disease (ADPKD) is a common cause of inherited renal failure that results from mutations in PKD1 and PKD2. The disorder is characterized by focal cyst formation that involves somatic mutation of the wild type alle
Externí odkaz:
https://doaj.org/article/5625a3686f1e4e759055e408742f7e50
Autor:
Manuel Heras Benito, Miguel A. Garcia-Gonzalez, María Valdenebro Recio, Álvaro Molina Ordás, Ramiro Callejas Martínez, María Astrid Rodríguez Gómez, Leonardo Calle García, Lisbeth Sousa Silva, María José Fernández-Reyes Luis
Publikováno v:
Nefrología (English Edition), Vol 36, Iss 5, Pp 552-555 (2016)
We describe the case of a young woman who was diagnosed with advanced kidney disease, with an incidental finding of nephrocalcinosis of unknown aetiology, having been found asymptomatic throughout her life. The genetic study by panels of known genes
Externí odkaz:
https://doaj.org/article/eea27117cf63430fab68f1aeb5f89aa7
Autor:
Miguel Angel Garcia-Gonzalez, Veronica Vallejo-Ruiz, Fausto Atonal-Flores, Jorge Flores-Hernandez, Oswaldo Torres-Ramírez, Alfonso Diaz-Fonsecae, Francisco Perez Vizcaino, Jose Gustavo Lopez-Lopez
Publikováno v:
Clinical and Experimental Hypertension. 44:355-365
Chronic treatment with sildenafil (SILD) is an effective protector on the development of cardiovascular complications of pulmonary hypertension (PH) and diabetes. However, to date, no studies have evaluated the effect of SILD on cardiopulmonary patho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b939d19f560111ddcfc9b29805c6bc4
https://doi.org/10.1080/10641963.2022.2050743
https://doi.org/10.1080/10641963.2022.2050743
Publikováno v:
Computing in Cardiology Conference (CinC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b25d7a4eff0d7ff7fa2cf362d8af44e8
https://doi.org/10.22489/cinc.2022.009
https://doi.org/10.22489/cinc.2022.009
Autor:
Adrian Cordido, Marta Vizoso-Gonzalez, Laura Nuñez-Gonzalez, Alberto Molares-Vila, Maria del Pilar Chantada-Vazquez, Susana B. Bravo, Miguel A. Garcia-Gonzalez
Publikováno v:
Biomedicines; Volume 10; Issue 2; Pages: 290
(1) Background: Polycystic liver disease (PLD) is a heterogeneous group of congenital disorders characterized by bile duct dilatation and cyst development derived from cholangiocytes. Nevertheless, the cystogenesis mechanism is currently unknown and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef6eb3a15f8b537b8354be49e4f3c64c
https://pubmed.ncbi.nlm.nih.gov/35203500
https://pubmed.ncbi.nlm.nih.gov/35203500
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 11414, p 11414 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 11414, p 11414 (2021)
Gitelman and Bartter syndromes are rare inherited diseases that belong to the category of renal tubulopathies. The genes associated with these pathologies encode electrolyte transport proteins located in the nephron, particularly in the Distal Convol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a8b5bd6a11c65191d9bb24bbef3d1cf
http://europepmc.org/articles/PMC8584233
http://europepmc.org/articles/PMC8584233
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 6523, p 6523 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Autosomal recessive polycystic kidney disease (ARPKD) is a rare disorder and one of the most severe forms of polycystic kidney disease, leading to end-stage renal disease (ESRD) in childhood. PKHD1 is the gene that is responsible for the vast majorit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f665a96b15874ae9b1ff7a2e15c4fc22
https://www.mdpi.com/1422-0067/22/12/6523
https://www.mdpi.com/1422-0067/22/12/6523
Publikováno v:
PLoS Computational Biology, Vol 16, Iss 10, p e1008337 (2020)
PLoS Computational Biology
PLoS Computational Biology
The Polycystic Kidney Disease (PKD) is characterized by progressive renal cyst development and other extrarenal manifestation including Polycystic Liver Disease (PLD). Phenotypical characterization of animal models mimicking human diseases are common
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b0a23ce051c7f6ee4c3732d6e6da23e
https://doaj.org/article/d2df838b583e4c88821ec175d2a1444e
https://doaj.org/article/d2df838b583e4c88821ec175d2a1444e
Autor:
Marco Chiaravalli, Miguel A. Garcia-Gonzalez, Diego Martin-Sanchez, Patricia Outeda, Olaya Lamas-Gonzalez, Candido Diaz, Maria Vanessa Perez-Gomez, Laura Rodriguez-Osorio, Terry Watnick, Alessandra Boletta, Alberto Ortiz, Ana Belen Sanz, Laura Nuñez-Gonzalez, Adrián Cordido, Julio M. Martinez-Moreno, Angel Carracedo
Publikováno v:
J Am Soc Nephrol
Background In autosomal dominant polycystic kidney disease (ADPKD), cyst development and enlargement lead to ESKD. Macrophage recruitment and interstitial inflammation promote cyst growth. TWEAK is a TNF superfamily (TNFSF) cytokine that regulates in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9f93766d56f4fbc9921c463fec27148
https://pubmed.ncbi.nlm.nih.gov/34155062
https://pubmed.ncbi.nlm.nih.gov/34155062