المؤلفون: Boeckhaus, Jan, Gross, Oliver^{Aff1, IDs11560023006653_cor2}

المصدر: Die Nephrologie: Zeitschrift für Nephrologie und Hypertensiologie. 18(5):276-283

المؤلفون: Margareta Fistrek Prlic, Sanda Huljev Frkovic, Bodo Beck, Ivana Tonkovic Durisevic, Stela Bulimbasic, Marijana Coric, Lovro Lamot, Ema Ivandic, Ivana Vukovic Brinar

المصدر: Frontiers in Pediatrics, Vol 11 (2023)

مصطلحات موضوعية: hereditary kidney disease, autosomal dominant inheritance, tubulointerstitial kidney disease, kidney cyst, renal failure, case report, Pediatrics, RJ1-570

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fped.2023.1283325/full; https://doaj.org/toc/2296-2360

URL الوصول: https://doaj.org/article/87de7d133de64c65a9214404dda0a93a

المؤلفون: ZHANG Yanqin, WANG Fang, DING Jie

المصدر: 罕见病研究, Vol 1, Iss 3, Pp 233-237 (2022)

مصطلحات موضوعية: rare kidney disease, hereditary kidney disease, children, diagnosis, therapy, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2097-0501

URL الوصول: https://doaj.org/article/b1446b99925a466d8acd3be230afb2e3

المؤلفون: Torimitsu, Takuto, Yoshida, Tadashi^{Aff2, IDs1373002100621x_cor2}, Nishi, Satomi, Itoh, Hiroshi, Oya, Mototsugu^{Aff2, Aff4}

المصدر: CEN Case Reports: Official Publication of the Japanese Society of Nephrology. 11(1):11-16

المؤلفون: Riedhammer, Korbinian M.^{Aff1, IDs11560021005476_cor1}, Schmaderer, Christoph, Heemann, Uwe, Bockenhauer, Detlef

المصدر: Der Nephrologe: Zeitschrift für Nephrologie und Hypertensiologie. 16(6):397-410

المؤلفون: Riedhammer, Korbinian Maria^Aff1, Schmaderer, Christoph, Heemann, Uwe, Hoefele, Julia

المصدر: Der Nephrologe: Zeitschrift für Nephrologie und Hypertensiologie. 15(6):381-398

المؤلفون: Ana Marta Gomes, Daniela Lopes, Clara Almeida, Sofia Santos, Jorge Malheiro, Irina Lousa, Alberto Caldas Afonso, Idalina Beirão

المصدر: International Journal of Molecular Sciences, Vol 23, Iss 13, p 7276 (2022)

مصطلحات موضوعية: Alport syndrome, hereditary kidney disease, COL4A, biomarkers, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/23/13/7276; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/f0dd9d6fb19e4ec19736eb3f58cd2fd8

المؤلفون: Marijn F. Stokman, Sophie Saunier, Alexandre Benmerah

المصدر: Frontiers in Cell and Developmental Biology, Vol 9 (2021)

مصطلحات موضوعية: hereditary kidney disease, ciliopathy, nephronophthisis, signaling, cell cycle, drug screen, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fcell.2021.653138/full; https://doaj.org/toc/2296-634X

URL الوصول: https://doaj.org/article/0d23257401bb4940810ceca00da65f06

المؤلفون: Raquel Martínez-Pulleiro, María García-Murias, Manuel Fidalgo-Díaz, Miguel Ángel García-González

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 20, p 11063 (2021)

مصطلحات موضوعية: Alport syndrome, hereditary kidney disease, chronic kidney disease, collagen, COL4A, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/22/20/11063; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/e7954bd4458c4aa39dba491d721e7aa7

المؤلفون: Diana Rubel, Yanqin Zhang, Nenja Sowa, Rainer Girgert, Oliver Gross

المصدر: Journal of Clinical Medicine, Vol 10, Iss 13, p 2958 (2021)

مصطلحات موضوعية: hereditary kidney disease, progressive kidney fibrosis, nephroprotective therapy, type IV collagen, Medicine

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2077-0383/10/13/2958; https://doaj.org/toc/2077-0383

URL الوصول: https://doaj.org/article/2c426fc381dc471d991df81c5aab6c57