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Journal Abstract Search
299 related items for PubMed ID: 35970429
1. Adult-Onset Focal Segmental Glomerulosclerosis With Steroid-Dependent Nephrotic Syndrome Caused by a Novel TBC1D8B Variant: A Case Report and Literature Review. Fang Z, Zhang C, Jin Y, Tong J, Liu J, Hao X, Weng Q, Yu S, Du W, Cai Y, Zheng Q, Yang L, Ren H, Pan X, Xie J. Am J Kidney Dis; 2023 Feb; 81(2):240-244. PubMed ID: 35970429 [Abstract] [Full Text] [Related]
2. Nephrotic Syndrome Gene TBC1D8B Is Required for Endosomal Maturation and Nephrin Endocytosis in Drosophila. Milosavljevic J, Lempicki C, Lang K, Heinkele H, Kampf LL, Leroy C, Chen M, Gerstner L, Spitz D, Wang M, Knob AU, Kayser S, Helmstädter M, Walz G, Pollak MR, Hermle T. J Am Soc Nephrol; 2022 Dec; 33(12):2174-2193. PubMed ID: 36137753 [Abstract] [Full Text] [Related]
3. TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways. Dorval G, Kuzmuk V, Gribouval O, Welsh GI, Bierzynska A, Schmitt A, Miserey-Lenkei S, Koziell A, Haq S, Benmerah A, Mollet G, Boyer O, Saleem MA, Antignac C. Am J Hum Genet; 2019 Feb 07; 104(2):348-355. PubMed ID: 30661770 [Abstract] [Full Text] [Related]
4. TBC1D8B Mutations Implicate RAB11-Dependent Vesicular Trafficking in the Pathogenesis of Nephrotic Syndrome. Kampf LL, Schneider R, Gerstner L, Thünauer R, Chen M, Helmstädter M, Amar A, Onuchic-Whitford AC, Loza Munarriz R, Berdeli A, Müller D, Schrezenmeier E, Budde K, Mane S, Laricchia KM, Rehm HL, MacArthur DG, Lifton RP, Walz G, Römer W, Bergmann C, Hildebrandt F, Hermle T. J Am Soc Nephrol; 2019 Dec 07; 30(12):2338-2353. PubMed ID: 31732614 [Abstract] [Full Text] [Related]
5. Genetic basis of adult-onset nephrotic syndrome and focal segmental glomerulosclerosis. Liu J, Wang W. Front Med; 2017 Sep 07; 11(3):333-339. PubMed ID: 28776307 [Abstract] [Full Text] [Related]
6. NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review. Franceschini N, North KE, Kopp JB, McKenzie L, Winkler C. Genet Med; 2006 Feb 07; 8(2):63-75. PubMed ID: 16481888 [Abstract] [Full Text] [Related]
7. Novel TBC1D8B Variant in a 6-Month-Old Boy With Steroid-Sensitive Nephrotic Syndrome: A Case Report. Hou L, Yin L, Wu Y, Zhao C, Du Y. Front Pediatr; 2021 Feb 07; 9():732512. PubMed ID: 34858901 [Abstract] [Full Text] [Related]
8. A girl with MIRAGE syndrome who developed steroid-resistant nephrotic syndrome: a case report. Ishiwa S, Kamei K, Tanase-Nakao K, Shibata S, Matsunami K, Takeuchi I, Sato M, Ishikura K, Narumi S. BMC Nephrol; 2020 Aug 12; 21(1):340. PubMed ID: 32787808 [Abstract] [Full Text] [Related]
9. Nephrotic syndrome with focal segmental glomerulosclerosis after an insect bite. Révai T, Kaszás I, Márton C, Arpási G, Winkler G. Clin Nephrol; 2006 Aug 12; 66(2):128-30. PubMed ID: 16939069 [Abstract] [Full Text] [Related]
14. A combined low-density lipoprotein apheresis and prednisone therapy for steroid-resistant primary focal segmental glomerulosclerosis in children. Hattori M, Chikamoto H, Akioka Y, Nakakura H, Ogino D, Matsunaga A, Fukazawa A, Miyakawa S, Khono M, Kawaguchi H, Ito K. Am J Kidney Dis; 2003 Dec 12; 42(6):1121-30. PubMed ID: 14655182 [Abstract] [Full Text] [Related]
15. Precise clinicopathologic findings for application of genetic testing in pediatric kidney transplant recipients with focal segmental glomerulosclerosis/steroid-resistant nephrotic syndrome. Miura K, Kaneko N, Hashimoto T, Ishizuka K, Shirai Y, Hisano M, Chikamoto H, Akioka Y, Kanda S, Harita Y, Yamamoto T, Hattori M. Pediatr Nephrol; 2023 Feb 12; 38(2):417-429. PubMed ID: 35655039 [Abstract] [Full Text] [Related]
16. Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis. Nagano C, Hara S, Yoshikawa N, Takeda A, Gotoh Y, Hamada R, Matsuoka K, Yamamoto M, Fujinaga S, Sakuraya K, Kamei K, Hamasaki Y, Oguchi H, Araki Y, Ogawa Y, Okamoto T, Ito S, Tanaka S, Kaito H, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagase H, Iijima K, Nozu K. Kidney360; 2022 Aug 25; 3(8):1384-1393. PubMed ID: 36176665 [Abstract] [Full Text] [Related]