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Year Number of Results
1980 1
1981 1
1982 2
1983 2
1984 2
1985 4
1986 5
1987 2
1988 7
1989 4
1990 7
1991 5
1992 3
1993 5
1994 1
1995 5
1996 3
1997 8
1998 5
1999 4
2000 5
2001 3
2002 2
2003 4
2004 4
2005 8
2006 7
2007 3
2008 12
2009 11
2010 6
2011 2
2012 6
2013 7
2014 5
2015 3
2016 9
2017 7
2018 7
2019 8
2020 6
2021 9
2022 7
2023 7
2024 1

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203 results

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Page 1
An international consensus approach to the management of atypical hemolytic uremic syndrome in children.
Loirat C, Fakhouri F, Ariceta G, Besbas N, Bitzan M, Bjerre A, Coppo R, Emma F, Johnson S, Karpman D, Landau D, Langman CB, Lapeyraque AL, Licht C, Nester C, Pecoraro C, Riedl M, van de Kar NC, Van de Walle J, Vivarelli M, Frémeaux-Bacchi V; HUS International. Loirat C, et al. Among authors: langman cb. Pediatr Nephrol. 2016 Jan;31(1):15-39. doi: 10.1007/s00467-015-3076-8. Epub 2015 Apr 11. Pediatr Nephrol. 2016. PMID: 25859752 Review.
Structural and non-coding variants increase the diagnostic yield of clinical whole genome sequencing for rare diseases.
Pagnamenta AT, Camps C, Giacopuzzi E, Taylor JM, Hashim M, Calpena E, Kaisaki PJ, Hashimoto A, Yu J, Sanders E, Schwessinger R, Hughes JR, Lunter G, Dreau H, Ferla M, Lange L, Kesim Y, Ragoussis V, Vavoulis DV, Allroggen H, Ansorge O, Babbs C, Banka S, Baños-Piñero B, Beeson D, Ben-Ami T, Bennett DL, Bento C, Blair E, Brasch-Andersen C, Bull KR, Cario H, Cilliers D, Conti V, Davies EG, Dhalla F, Dacal BD, Dong Y, Dunford JE, Guerrini R, Harris AL, Hartley J, Hollander G, Javaid K, Kane M, Kelly D, Kelly D, Knight SJL, Kreins AY, Kvikstad EM, Langman CB, Lester T, Lines KE, Lord SR, Lu X, Mansour S, Manzur A, Maroofian R, Marsden B, Mason J, McGowan SJ, Mei D, Mlcochova H, Murakami Y, Németh AH, Okoli S, Ormondroyd E, Ousager LB, Palace J, Patel SY, Pentony MM, Pugh C, Rad A, Ramesh A, Riva SG, Roberts I, Roy N, Salminen O, Schilling KD, Scott C, Sen A, Smith C, Stevenson M, Thakker RV, Twigg SRF, Uhlig HH, van Wijk R, Vona B, Wall S, Wang J, Watkins H, Zak J, Schuh AH, Kini U, Wilkie AOM, Popitsch N, Taylor JC. Pagnamenta AT, et al. Among authors: langman cb. Genome Med. 2023 Nov 9;15(1):94. doi: 10.1186/s13073-023-01240-0. Genome Med. 2023. PMID: 37946251 Free PMC article.
Fertility Management in Cystinosis: A Clinical Perspective.
Langman CB, Delos Santos RB, Ghossein C, Atherton AM, Levtchenko EN, Servais A. Langman CB, et al. Kidney Int Rep. 2023 Nov 3;9(2):214-224. doi: 10.1016/j.ekir.2023.10.030. eCollection 2024 Feb. Kidney Int Rep. 2023. PMID: 38344731 Free PMC article. Review.
Clinical Outcomes of Patients with C3G or IC-MPGN Treated with the Factor D Inhibitor Danicopan: Final Results from Two Phase 2 Studies.
Nester C, Appel GB, Bomback AS, Bouman KP, Cook HT, Daina E, Dixon BP, Rice K, Najafian N, Hui J, Podos SD, Langman CB, Lightstone L, Parikh SV, Pickering MC, Sperati CJ, Trachtman H, Tumlin J, de Vries AP, Wetzels JFM, Remuzzi G. Nester C, et al. Among authors: langman cb. Am J Nephrol. 2022;53(10):687-700. doi: 10.1159/000527167. Epub 2022 Nov 24. Am J Nephrol. 2022. PMID: 36423588 Free article. Clinical Trial.
L-carnitine treatment of anemia.
Golper TA, Goral S, Becker BN, Langman CB. Golper TA, et al. Among authors: langman cb. Am J Kidney Dis. 2003 Apr;41(4 Suppl 4):S27-34. doi: 10.1016/s0272-6386(03)00114-8. Am J Kidney Dis. 2003. PMID: 12751051 Review.
Bone Complications of Cystinosis.
Langman CB. Langman CB. J Pediatr. 2017 Apr;183S:S2-S4. doi: 10.1016/j.jpeds.2016.12.052. J Pediatr. 2017. PMID: 28343472 No abstract available.
Pathophysiology and Treatment of Enteric Hyperoxaluria.
Witting C, Langman CB, Assimos D, Baum MA, Kausz A, Milliner D, Tasian G, Worcester E, Allain M, West M, Knauf F, Lieske JC. Witting C, et al. Among authors: langman cb. Clin J Am Soc Nephrol. 2021 Mar 8;16(3):487-495. doi: 10.2215/CJN.08000520. Epub 2020 Sep 8. Clin J Am Soc Nephrol. 2021. PMID: 32900691 Free PMC article.
The primary hyperoxalurias.
Bobrowski AE, Langman CB. Bobrowski AE, et al. Among authors: langman cb. Semin Nephrol. 2008 Mar;28(2):152-62. doi: 10.1016/j.semnephrol.2008.01.008. Semin Nephrol. 2008. PMID: 18359396 Review.
203 results