459 related articles for article (PubMed ID: 24856029)
1. Rare inherited kidney diseases: challenges, opportunities, and perspectives.
Devuyst O; Knoers NV; Remuzzi G; Schaefer F;
Lancet; 2014 May; 383(9931):1844-59. PubMed ID: 24856029
[TBL] [Abstract][Full Text] [Related]
2. Key challenges in the treatment of rare pediatric skeletal genetic disorders: from bench to bedside.
Lorget F; Legeai-Mallet L
Drug Discov Today; 2015 Jul; 20(7):781-3. PubMed ID: 25943098
[No Abstract] [Full Text] [Related]
3. Monogenic renal diseases: a clinical introduction.
Grünfeld JP
J Nephrol; 2002; 15 Suppl 6():S43-6. PubMed ID: 12515373
[TBL] [Abstract][Full Text] [Related]
4. Recent Developments in Using
Oriel C; Lasko P
Int J Mol Sci; 2018 Jul; 19(7):. PubMed ID: 30011838
[TBL] [Abstract][Full Text] [Related]
5. Unexpectedly high prevalence of rare genetic disorders in kidney transplant recipients with an unknown causal nephropathy.
Quaglia M; Musetti C; Ghiggeri GM; Fogazzi GB; Settanni F; Boldorini RL; Lazzarich E; Airoldi A; Izzo C; Giordano M; Stratta P
Clin Transplant; 2014 Sep; 28(9):995-1003. PubMed ID: 24961278
[TBL] [Abstract][Full Text] [Related]
6. Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research.
Wangler MF; Yamamoto S; Chao HT; Posey JE; Westerfield M; Postlethwait J; ; Hieter P; Boycott KM; Campeau PM; Bellen HJ
Genetics; 2017 Sep; 207(1):9-27. PubMed ID: 28874452
[TBL] [Abstract][Full Text] [Related]
7. [Application of Next-Generation Sequencing in Rare Renal Diseases].
Cai ZY; Zhao JR
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2022 Jun; 44(3):484-490. PubMed ID: 35791948
[TBL] [Abstract][Full Text] [Related]
8. Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
Aymé S; Bockenhauer D; Day S; Devuyst O; Guay-Woodford LM; Ingelfinger JR; Klein JB; Knoers NVAM; Perrone RD; Roberts J; Schaefer F; Torres VE; Cheung M; Wheeler DC; Winkelmayer WC;
Kidney Int; 2017 Oct; 92(4):796-808. PubMed ID: 28938953
[TBL] [Abstract][Full Text] [Related]
9. Orphan kidney diseases.
Soliman NA
Nephron Clin Pract; 2012; 120(4):c194-9. PubMed ID: 22922418
[TBL] [Abstract][Full Text] [Related]
10. Editorial of Special Issue "Rare Kidney Diseases: New Translational Research Approach to Improve Diagnosis and Therapy".
Zaza G; Gambaro G
Int J Mol Sci; 2020 Jun; 21(12):. PubMed ID: 32545922
[TBL] [Abstract][Full Text] [Related]
11. From the Editors Desk: Angela Zawacki-Downing Writing to Professor Illana Gozes, Editor-in-Chief Journal of Molecular Neuroscience-Speaking from a Mother's Heart, AD's ADNP Syndrome.
Zawacki-Downing A
J Mol Neurosci; 2019 Aug; 68(4):511-514. PubMed ID: 31201656
[No Abstract] [Full Text] [Related]
12. [Together for patients with hereditary neuromuscular conditions].
Arntzen KA; Lund I; Rasmussen M; Rønningen KE; Torp TI; Ørstavik K
Tidsskr Nor Laegeforen; 2016 Aug; 136(14-15):1198-9. PubMed ID: 27554555
[No Abstract] [Full Text] [Related]
13. Fighting rare diseases: the model of the telethon research institutes in Italy.
Ballabio A; Naldini L
Hum Gene Ther; 2015 Apr; 26(4):183-5. PubMed ID: 25901396
[No Abstract] [Full Text] [Related]
14. Managing drugs for rare genetic diseases: trends and insights.
Zitter M
Manag Care; 2005 Feb; 14(2):52-4, 57-60, 63-4; quiz 66-7. PubMed ID: 15782848
[TBL] [Abstract][Full Text] [Related]
15. Establishing a second-generation artificial intelligence-based system for improving diagnosis, treatment, and monitoring of patients with rare diseases.
Hurvitz N; Azmanov H; Kesler A; Ilan Y
Eur J Hum Genet; 2021 Oct; 29(10):1485-1490. PubMed ID: 34276056
[TBL] [Abstract][Full Text] [Related]
16. 2016 Curt Stern Award Address: From Rare to Common Diseases: Translating Genetic Discovery to Therapy.
Lee B
Am J Hum Genet; 2017 Mar; 100(3):397-400. PubMed ID: 28257687
[No Abstract] [Full Text] [Related]
17. Solving the unsolved rare diseases in Europe.
Graessner H; Zurek B; Hoischen A; Beltran S
Eur J Hum Genet; 2021 Sep; 29(9):1319-1320. PubMed ID: 34140650
[No Abstract] [Full Text] [Related]
18. Inherited and congenital malformations of the kidneys in the neonatal period.
Kaplan BS; Kaplan P; Ruchelli E
Clin Perinatol; 1992 Mar; 19(1):197-211. PubMed ID: 1576768
[TBL] [Abstract][Full Text] [Related]
19. [Introduction to Genetic/Rare Disease and the Application of Genetic Counseling].
Chu SY; Weng CY
Hu Li Za Zhi; 2017 Oct; 64(5):11-17. PubMed ID: 28948586
[TBL] [Abstract][Full Text] [Related]
20. Rare genetic diseases: update on diagnosis, treatment and online resources.
Pogue RE; Cavalcanti DP; Shanker S; Andrade RV; Aguiar LR; de Carvalho JL; Costa FF
Drug Discov Today; 2018 Jan; 23(1):187-195. PubMed ID: 29129805
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]