Zobrazeno 1 - 10
of 238
pro vyhledávání: '"Enlarged kidney"'
Autor:
Tatsuya Suwabe, Yoshifumi Ubara, Daisuke Ikuma, Naoki Sawa, Hiroki Mizuno, Masayuki Yamanouchi, Noriko Hayami
Publikováno v:
Internal Medicine. 61:49-52
Polycystic liver disease (PLD) is the most common extrarenal manifestation of autosomal dominant polycystic kidney disease (ADPKD). However, current treatments for PLD are only supportive. We experienced a case of enlarged kidneys and liver in a 53-y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05c8ae0d31d6edb3bacc83ea3fb0341b
https://doi.org/10.2169/internalmedicine.7441-21
https://doi.org/10.2169/internalmedicine.7441-21
Autor:
Amrit Tuteja, Femitha Pournami, Naveen Jain, Gopala Krishna Madhavilatha, Sajina Sathyan, Anand Nandakumar, Jyothi Prabhakar
Publikováno v:
Journal of Child Science. 11:e70-e73
Autosomal recessive polycystic kidney disease, described as a congenital hepatorenal fibrocystic syndrome, is a significant inherited cause of end stage renal failure in children with reported incidence of 1 in 20,000 live births. The clinical spectr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83241691150187f18f5a9d905a2ddcfb
https://doi.org/10.1055/s-0041-1725175
https://doi.org/10.1055/s-0041-1725175
Autor:
Jean V. Varghese, Antriya Annie Tom
Publikováno v:
Indian Journal of Case Reports. :339-341
Autosomal dominant polycystic kidney disease (ADPKD) is an inherited condition that causes small fluid-filled sacs called cysts to develop in the kidneys. ADPKD affects 1 in 500–1000 people. We report the case of a 70-year-old male patient with com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a139e1aaf09383b83410d195b0a4db59
https://doi.org/10.32677/ijcr.v7i8.2965
https://doi.org/10.32677/ijcr.v7i8.2965
Publikováno v:
Open Access Macedonian Journal of Medical Sciences; Vol. 8 No. C (2020): C-Case Reports; 160-163
BACKGROUND: URCD is a rare disease characterized by cysts with various sizes in a diffusely enlarged kidney without forming a distinct encapsulated mass. We present literature review and report a case of URCD in our center. The aim of the study was t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68b05eec9a3c8a98a459c69dcf9bbfd4
https://doi.org/10.3889/oamjms.2020.5031
https://doi.org/10.3889/oamjms.2020.5031
Autor:
Chenyang Qi, Jian Kang Chen, Feng Wang, Huijuan Wu, Zhonghua Zhao, Zhigang Zhang, Xing Mao, Yili Fang, Fang Li
Publikováno v:
Cell Death Discovery, Vol 6, Iss 1, Pp 1-16 (2020)
Cell Death Discovery
Cell Death Discovery
Tuberous sclerosis complex (TSC) is characterized by hamartomatous lesions in multiple organs, with most patients developing polycystic kidney disease and leading to a decline of renal function. TSC is caused by loss-of-function mutations in either T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3754fed37ffba648673ab9816807659e
http://link.springer.com/article/10.1038/s41420-020-0285-0
http://link.springer.com/article/10.1038/s41420-020-0285-0
Autor:
Nathalie Boddaert, Laurence Heidet, Caroline Rutten, Laureline Berteloot, Nicolas Garcelon, Rémi Salomon, Pauline Iorio, Marie-Pierre Audrézet, Vincent Morinière
Publikováno v:
Pediatric Nephrology. 35:1033-1040
While typical ultrasound patterns of ciliopathy-related cystic kidney diseases have been described in children, ultrasound findings can overlap between different diseases and atypical patterns exist. In this study, we assessed the presence of the “
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8a711431300ee5f0dfe4c3d6427801e
https://doi.org/10.1007/s00467-020-04480-z
https://doi.org/10.1007/s00467-020-04480-z
Publikováno v:
Biology
Volume 10
Issue 7
Biology, Vol 10, Iss 633, p 633 (2021)
Volume 10
Issue 7
Biology, Vol 10, Iss 633, p 633 (2021)
Simple Summary The worldwide prevalence of diabetes mellitus (DM) in 2020 has been estimated at 463 million patients. About 90% of patients with diabetes have type 2 diabetes mellitus (T2D), caused primarily by insulin resistance and insufficiency. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9260765fc2aca69db9efbb2c1a067b84
http://europepmc.org/articles/PMC8301011
http://europepmc.org/articles/PMC8301011
Autor:
Ying Gao, Chris E. Freise, Oana L. Klein, Jonathan Freise, Mehdi Tavakol, Meyeon Park, Brian K. Lee
Publikováno v:
Kidney International Reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7c1e8580acd6ae5b36f0563f3de8f9a
https://doi.org/10.1016/j.ekir.2019.01.003
https://doi.org/10.1016/j.ekir.2019.01.003
Autor:
Juliette Garel, Hubert Ducou Le Pointe, Marie Cassart, Valeria Della Valle, Mathilde Lefebvre, Jean-Marie Jouannic, Eléonore Blondiaux, Lucie Guilbaud, Catherine Garel
Publikováno v:
Pediatric Radiology. 49:906-912
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disease. This pathology has been increasingly diagnosed in utero and several sonographic patterns are well described in the literature. To present a series of fet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d66ec61570ca435428e3a33b5abaefdd
https://doi.org/10.1007/s00247-018-4325-3
https://doi.org/10.1007/s00247-018-4325-3
Publikováno v:
Indian Journal of Nephrology
Indian Journal of Nephrology, Vol 29, Iss 2, Pp 111-115 (2019)
Indian Journal of Nephrology, Vol 29, Iss 2, Pp 111-115 (2019)
Xanthogranulomatous pyelonephritis (XGP) is an uncommon and distinct type of chronic infective pyelonephritis causing destruction of the kidney, severely affecting the renal function. The perinephric adipose tissue and peritoneum is not uncommonly in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::026dd1502b8a82b7823eda3757db2c1b
http://europepmc.org/articles/PMC6440323
http://europepmc.org/articles/PMC6440323