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Quoted phrase not found in phrase index: "Abnormal ureter physiology"
Page 1
Organ Abnormalities Caused by Turner Syndrome.
Yoon SH, Kim GY, Choi GT, Do JT. Yoon SH, et al. Cells. 2023 May 11;12(10):1365. doi: 10.3390/cells12101365. Cells. 2023. PMID: 37408200 Free PMC article. Review.
Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-linked genes, affects multiple organ systems, leading to hypogonadotropic hypogonadism, short stature, cardiovascular and vascular abnormalities, liver disease, renal abnormalities, …
Turner syndrome (TS), a genetic disorder due to incomplete dosage compensation of X-linked genes, affects multiple organ systems, leading to …
Dysplastic kidneys.
Winyard P, Chitty LS. Winyard P, et al. Semin Fetal Neonatal Med. 2008 Jun;13(3):142-51. doi: 10.1016/j.siny.2007.10.009. Epub 2007 Dec 11. Semin Fetal Neonatal Med. 2008. PMID: 18065301 Review.
Dysplastic kidneys are common malformations affecting up to 1 in 1000 of the general population. They are part of the spectrum of Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) and an increasing number of children are being diagnosed on antenatal u …
Dysplastic kidneys are common malformations affecting up to 1 in 1000 of the general population. They are part of the spectrum of Congeni …
The term CAKUT has outlived its usefulness: the case for the prosecution.
Woolf AS. Woolf AS. Pediatr Nephrol. 2022 Nov;37(11):2785-2791. doi: 10.1007/s00467-022-05576-4. Epub 2022 May 16. Pediatr Nephrol. 2022. PMID: 35575937 Free PMC article. Review.
CAKUT stands for Congenital Anomalies of the Kidney and Urinary Tract, and the acronym first appeared in a review article published in 1998. ...To reach these conclusions, I focus on the complex of research observations that led to the theory behind CAKUT, and then …
CAKUT stands for Congenital Anomalies of the Kidney and Urinary Tract, and the acronym first appeared in a review article published i …
Peristalsis prevents ureteral dilation.
Kalayeh K, Fowlkes JB, Xie H, Schultz WW, Sack BS. Kalayeh K, et al. Neurourol Urodyn. 2024 Jan;43(1):258-266. doi: 10.1002/nau.25332. Epub 2023 Nov 13. Neurourol Urodyn. 2024. PMID: 37961019
In doing so, we treated ureteral peristalsis as an infinite train of sinusoidal waves. We then analyzed antegrade and retrograde flows in the ureter under different bladder-kidney differential pressure and peristalsis conditions. ...We theorize that this retrograde flow ca …
In doing so, we treated ureteral peristalsis as an infinite train of sinusoidal waves. We then analyzed antegrade and retrograde flows in th …
Plumbing in the embryo: developmental defects of the urinary tracts.
Uetani N, Bouchard M. Uetani N, et al. Clin Genet. 2009 Apr;75(4):307-17. doi: 10.1111/j.1399-0004.2009.01175.x. Clin Genet. 2009. PMID: 19419410 Review.
Gene inactivation studies in mice provided invaluable information on the formation of the Wolffian duct, a central component of embryonic renal development, on ureter and kidney induction as well as on distal ureter maturation. ...This review is aimed at bridging th …
Gene inactivation studies in mice provided invaluable information on the formation of the Wolffian duct, a central component of embryonic re …
Cerebro-costo-mandibular syndrome.
Plötz FB, van Essen AJ, Bosschaart AN, Bos AP. Plötz FB, et al. Am J Med Genet. 1996 Mar 29;62(3):286-92. doi: 10.1002/(SICI)1096-8628(19960329)62:3<286::AID-AJMG16>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8882789 Review.
His chest roentgenographs showed marked hypoplasia of the first to tenth rib, multiple posterior rib-gaps in the only four ossified ribs. Tracheomalacia and stenosis of the left ureter was observed during autopsy. No structural cerebral anomalies were observed …
His chest roentgenographs showed marked hypoplasia of the first to tenth rib, multiple posterior rib-gaps in the only four ossified ribs. Tr …
Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging.
Ezawa N, Katoh N, Oguchi K, Yoshinaga T, Yazaki M, Sekijima Y. Ezawa N, et al. Eur J Nucl Med Mol Imaging. 2018 Mar;45(3):452-461. doi: 10.1007/s00259-017-3814-1. Epub 2017 Sep 10. Eur J Nucl Med Mol Imaging. 2018. PMID: 28891012
Physiological tracer uptake was universally observed in the urinary tract (kidney, renal pelvis, ureter and bladder) and enterohepatic circulatory system (liver, gallbladder, bile duct and small intestine) in all participants. ...Histological amyloid deposition was …
Physiological tracer uptake was universally observed in the urinary tract (kidney, renal pelvis, ureter and bladder) and enter …
Pacemakers in the upper urinary tract.
Di Benedetto A, Arena S, Nicotina PA, Mucciardi G, Galì A, Magno C. Di Benedetto A, et al. Neurourol Urodyn. 2013 Apr;32(4):349-53. doi: 10.1002/nau.22310. Epub 2012 Sep 21. Neurourol Urodyn. 2013. PMID: 23002060 Review.
DISCUSSION: Alterations in ICC-LCs are closely associated with a variety of motility disorders and many congenital urological diseases of the UUT such as primary obstructive megaureter, congenital ureteropelvic junction obstruction, and vesicoureteral reflux. CONCLU …
DISCUSSION: Alterations in ICC-LCs are closely associated with a variety of motility disorders and many congenital urological disease …
Renin-angiotensin system in ureteric bud branching morphogenesis: insights into the mechanisms.
Yosypiv IV. Yosypiv IV. Pediatr Nephrol. 2011 Sep;26(9):1499-512. doi: 10.1007/s00467-011-1820-2. Epub 2011 Feb 26. Pediatr Nephrol. 2011. PMID: 21359618 Review.
Moreover, mutations in the genes encoding components of the RAS in mice or humans cause diverse types of CAKUT which include renal papillary hypoplasia, hydronephrosis, duplicated collecting system, renal tubular dysgenesis, renal vascular abnormalities, abnormal gl …
Moreover, mutations in the genes encoding components of the RAS in mice or humans cause diverse types of CAKUT which include renal papillary …
Renin-angiotensin system in ureteric bud branching morphogenesis: implications for kidney disease.
Yosypiv IV. Yosypiv IV. Pediatr Nephrol. 2014 Apr;29(4):609-20. doi: 10.1007/s00467-013-2616-3. Epub 2013 Sep 7. Pediatr Nephrol. 2014. PMID: 24061643 Review.
Failure of normal branching morphogenesis of the ureteric bud (UB), a key ontogenic process that controls organogenesis of the metanephric kidney, leads to congenital anomalies of the kidney and urinary tract (CAKUT), the leading cause of end-stage kidney disease in childr …
Failure of normal branching morphogenesis of the ureteric bud (UB), a key ontogenic process that controls organogenesis of the metanephric k …
104 results