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For: Westland R, Renkema KY, Knoers NVAM. Clinical Integration of Genome Diagnostics for Congenital Anomalies of the Kidney and Urinary Tract. Clin J Am Soc Nephrol 2020;16:128-37. [PMID: 32312792 DOI: 10.2215/CJN.14661119] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
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1 Fei YF, Smith YR, Wan J, Dendrinos ML, Winfrey OK, Quint EH. Should we screen for Müllerian anomalies following diagnosis of a congenital renal anomaly? Journal of Pediatric Urology 2022. [DOI: 10.1016/j.jpurol.2022.04.017] [Reference Citation Analysis]
2 Tanudisastro HA, Holman K, Ho G, Farnsworth E, Fisk K, Gayagay T, Hackett E, Jenkins G, Krishnaraj R, Lai T, Wong K, Patel C, Mallawaarachchi A, Mallett AJ, Bennetts B, Alexander SI, McCarthy HJ. Australia and New Zealand renal gene panel testing in routine clinical practice of 542 families. NPJ Genom Med 2021;6:20. [PMID: 33664247 DOI: 10.1038/s41525-021-00184-x] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Knoers NVAM. The term CAKUT has outlived its usefulness: the case for the defense. Pediatr Nephrol 2022. [PMID: 35867161 DOI: 10.1007/s00467-022-05678-z] [Reference Citation Analysis]
4 Narikot A, Pardeshi VC, Shubha AM, Iyengar A, Vasudevan A. Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract. BMC Nephrol 2022;23:1. [PMID: 34979951 DOI: 10.1186/s12882-021-02628-z] [Reference Citation Analysis]
5 Woolf AS. The term CAKUT has outlived its usefulness: the case for the prosecution. Pediatr Nephrol 2022. [PMID: 35575937 DOI: 10.1007/s00467-022-05576-4] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Khan K, Ahram DF, Liu YP, Westland R, Sampogna RV, Katsanis N, Davis EE, Sanna-Cherchi S. Multidisciplinary approaches for elucidating genetics and molecular pathogenesis of urinary tract malformations. Kidney Int 2021:S0085-2538(21)01060-7. [PMID: 34780871 DOI: 10.1016/j.kint.2021.09.034] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Groen In 't Woud S, Westland R, Feitz WFJ, Roeleveld N, van Wijk JAE, van der Zanden LFM, Schreuder MF. Clinical Management of Children with a Congenital Solitary Functioning Kidney: Overview and Recommendations. Eur Urol Open Sci 2021;25:11-20. [PMID: 34337499 DOI: 10.1016/j.euros.2021.01.003] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 La Scola C, Ammenti A, Bertulli C, Bodria M, Brugnara M, Camilla R, Capone V, Casadio L, Chimenz R, Conte ML, Conversano E, Corrado C, Guarino S, Luongo I, Marsciani M, Marzuillo P, Meneghesso D, Pennesi M, Pugliese F, Pusceddu S, Ravaioli E, Taroni F, Vergine G, Peruzzi L, Montini G. Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology. Pediatr Nephrol 2022. [PMID: 35713730 DOI: 10.1007/s00467-022-05528-y] [Reference Citation Analysis]