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1988
2025

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 1
1990 1
1992 1
1994 1
1996 1
1997 2
1998 1
1999 2
2000 3
2001 2
2002 2
2003 5
2004 2
2005 3
2006 2
2007 1
2008 3
2009 1
2011 3
2012 1
2013 2
2014 8
2015 4
2017 1
2018 1
2019 2
2020 2
2022 1
2023 1
2024 1
2025 0

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54 results

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Page 1
Retroperitoneoscopic heminephrectomy.
Taghavi K, Mushtaq I. Taghavi K, et al. J Pediatr Urol. 2018 Apr;14(2):196-197. doi: 10.1016/j.jpurol.2018.02.010. Epub 2018 Mar 7. J Pediatr Urol. 2018. PMID: 29551554 Review.
The vital first step is a 'critical view' of the collecting system/vascular supply of both upper/lower moieties. Dividing the lateral renal attachments later in the dissection allows passive retraction of the hilum, facilitating this dissection....
The vital first step is a 'critical view' of the collecting system/vascular supply of both upper/lower moieties. Dividing the …
Antenatally detected hydronephrosis.
Piepsz A. Piepsz A. Semin Nucl Med. 2007 Jul;37(4):249-60. doi: 10.1053/j.semnuclmed.2007.02.008. Semin Nucl Med. 2007. PMID: 17544625 Review.
Hydronephrosis is defined as a dilation of the renal collecting system, and several entirely different clinical entities can be considered this general heading, whereas early detection may have a different impact depending on the entity considered. The presen …
Hydronephrosis is defined as a dilation of the renal collecting system, and several entirely different clinical entitie …
Renal dysplasia.
Chen RY, Chang H. Chen RY, et al. Arch Pathol Lab Med. 2015 Apr;139(4):547-51. doi: 10.5858/arpa.2013-0660-RS. Arch Pathol Lab Med. 2015. PMID: 25822765 Free article. Review.
Prevalence is estimated at 0.1% of infants (via ultrasound screening) and 4% of fetuses and infants (via autopsy study). Occurrences may be combined with abnormalities in the collecting system or associated with complex syndromes. Histopathology shows primiti …
Prevalence is estimated at 0.1% of infants (via ultrasound screening) and 4% of fetuses and infants (via autopsy study). Occurrences may be …
Fetal genitourinary imaging.
Chapman T. Chapman T. Pediatr Radiol. 2012 Jan;42 Suppl 1:S115-23. doi: 10.1007/s00247-011-2172-6. Epub 2012 Mar 6. Pediatr Radiol. 2012. PMID: 22395724 Review.
Fetal MR might be indicated to further clarify abnormalities found sonographically. The primary imaging modality for evaluation of the fetal kidney is US, which plays an important role in the detection of collecting system dilatation and parenchymal diseases …
Fetal MR might be indicated to further clarify abnormalities found sonographically. The primary imaging modality for evaluation of th …
Prenatal imaging features and postnatal outcomes of isolated fetal duplex renal collecting system: A systematic review and meta-analysis.
Bascietto F, Khalil A, Rizzo G, Makatsariya A, Buca D, Silvi C, Ucci M, Liberati M, Familiari A, D'Antonio F. Bascietto F, et al. Prenat Diagn. 2020 Mar;40(4):424-431. doi: 10.1002/pd.5622. Epub 2020 Jan 28. Prenat Diagn. 2020. PMID: 31834636
OBJECTIVES: To perform a systematic review of studies reporting the outcome of fetuses with a prenatal diagnosis of isolated duplex collecting system (DCS). METHODS: Inclusion criteria were studies reporting the outcome of fetuses with a prenatal diagnosis of isolat …
OBJECTIVES: To perform a systematic review of studies reporting the outcome of fetuses with a prenatal diagnosis of isolated duplex colle
Overlapping Machinery in Lysosome-Related Organelle Trafficking: A Lesson from Rare Multisystem Disorders.
Banushi B, Simpson F. Banushi B, et al. Cells. 2022 Nov 21;11(22):3702. doi: 10.3390/cells11223702. Cells. 2022. PMID: 36429129 Free PMC article. Review.
The formation, maturation and secretion of specific LROs are compromised in a number of hereditary rare multisystem disorders, including Hermansky-Pudlak syndromes, Griscelli syndrome and the Arthrogryposis, Renal dysfunction and Cholestasis syndrome. Each of these disorde …
The formation, maturation and secretion of specific LROs are compromised in a number of hereditary rare multisystem disorders, including Her …
The duplicated collecting system of the urinary tract: embryology, imaging appearances and clinical considerations.
Didier RA, Chow JS, Kwatra NS, Retik AB, Lebowitz RL. Didier RA, et al. Pediatr Radiol. 2017 Oct;47(11):1526-1538. doi: 10.1007/s00247-017-3904-z. Epub 2017 Sep 21. Pediatr Radiol. 2017. PMID: 29043421 Review.
Duplication anomalies of the urinary collecting system are common and can be discovered and characterized with multiple imaging modalities. The embryology, imaging manifestations and clinical ramifications of duplicated ureters and renal collecting
Duplication anomalies of the urinary collecting system are common and can be discovered and characterized with multiple imagin …
Renal branching morphogenesis: morphogenetic and signaling mechanisms.
Blake J, Rosenblum ND. Blake J, et al. Semin Cell Dev Biol. 2014 Dec;36:2-12. doi: 10.1016/j.semcdb.2014.07.011. Epub 2014 Jul 28. Semin Cell Dev Biol. 2014. PMID: 25080023 Review.
The renal collecting system is formed in utero, completed by the 34th week of gestation in humans, and dictates final nephron complement. ...The ureteric bud subsequently undergoes a series of iterative branching and remodeling events in a process called r
The renal collecting system is formed in utero, completed by the 34th week of gestation in humans, and dictates final n …
The normal and pathologic renal medulla: a comprehensive overview.
López JI, Larrinaga G, Kuroda N, Angulo JC. López JI, et al. Pathol Res Pract. 2015 Apr;211(4):271-80. doi: 10.1016/j.prp.2014.12.009. Epub 2014 Dec 24. Pathol Res Pract. 2015. PMID: 25595996 Review.
The renal medulla comprises an intricate system of tubules, blood vessels and interstitium that is not well understood by most general pathologists. We conducted an extensive review of the literature on the renal medulla, in both normal and pathologic conditi …
The renal medulla comprises an intricate system of tubules, blood vessels and interstitium that is not well understood by most …
Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT).
Renkema KY, Winyard PJ, Skovorodkin IN, Levtchenko E, Hindryckx A, Jeanpierre C, Weber S, Salomon R, Antignac C, Vainio S, Schedl A, Schaefer F, Knoers NV, Bongers EM; EUCAKUT consortium. Renkema KY, et al. Nephrol Dial Transplant. 2011 Dec;26(12):3843-51. doi: 10.1093/ndt/gfr655. Nephrol Dial Transplant. 2011. PMID: 22121240 Review.
Congenital anomalies of the kidney and urinary tract (CAKUT) are the commonest cause of chronic kidney disease in children. Structural anomalies within the CAKUT spectrum include renal agenesis, kidney hypo-/dysplasia, multicystic kidney dysplasia, duplex collect
Congenital anomalies of the kidney and urinary tract (CAKUT) are the commonest cause of chronic kidney disease in children. Structura
54 results