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Quoted phrase not found in phrase index: "Renal hypodysplasia/aplasia 1"
Page 1
Effect of Renal Reconstruction on Renal Function After Partial Nephrectomy.
Bahler CD, Sundaram CP. Bahler CD, et al. J Endourol. 2016 May;30 Suppl 1:S37-41. doi: 10.1089/end.2016.0055. Epub 2016 Mar 3. J Endourol. 2016. PMID: 26864480 Review.
Newer biomarkers of renal injury should be used when studying predictors of renal injury....
Newer biomarkers of renal injury should be used when studying predictors of renal injury....
Renal agenesis: A meta-analysis of its prevalence and clinical characteristics based on 15 641 184 patients.
Plutecki D, Kozioł T, Bonczar M, Ostrowski P, Skorupa A, Matejuk S, Walocha J, Pękala J, Musiał A, Pasternak A, Koziej M. Plutecki D, et al. Nephrology (Carlton). 2023 Oct;28(10):525-533. doi: 10.1111/nep.14190. Epub 2023 May 30. Nephrology (Carlton). 2023. PMID: 37254584 Review.
There appears to be universal disease and symptom prevalence with minor differences between world regions, although quality of future observational research should include genomic data. This will provide even further insight into the prognosis of various renal anomalies an …
There appears to be universal disease and symptom prevalence with minor differences between world regions, although quality of future obs …
Clinical and mutational spectrum of hypoparathyroidism, deafness and renal dysplasia syndrome.
Belge H, Dahan K, Cambier JF, Benoit V, Morelle J, Bloch J, Vanhille P, Pirson Y, Demoulin N. Belge H, et al. Nephrol Dial Transplant. 2017 May 1;32(5):830-837. doi: 10.1093/ndt/gfw271. Nephrol Dial Transplant. 2017. PMID: 27387476
Hypoparathyroidism was present in six patients (with hypocalcaemia and inaugural seizures in two out of six). Renal abnormalities observed in six patients were diverse and of dysplastic nature. Three patients displayed nephrotic-range proteinuria and reached end-stage rena …
Hypoparathyroidism was present in six patients (with hypocalcaemia and inaugural seizures in two out of six). Renal abnormalities observe …
Mutations in Uroplakin IIIA are a rare cause of renal hypodysplasia in humans.
Schönfelder EM, Knüppel T, Tasic V, Miljkovic P, Konrad M, Wühl E, Antignac C, Bakkaloglu A, Schaefer F, Weber S; ESCAPE Trial Group. Schönfelder EM, et al. Am J Kidney Dis. 2006 Jun;47(6):1004-12. doi: 10.1053/j.ajkd.2006.02.177. Am J Kidney Dis. 2006. PMID: 16731295
De novo UPIIIA mutations recently were identified in 4 of 17 patients with severe bilateral renal adysplasia. METHODS: To evaluate the overall role of UPIIIA in human renal hypodysplasia pathogenesis, we performed UPIIIA mutation analysis in a cohort of 170 pediatri …
De novo UPIIIA mutations recently were identified in 4 of 17 patients with severe bilateral renal adysplasia. METHODS: To eval …
Perinatal and infant outcome of fetuses with prenatally diagnosed hyperechogenic kidneys.
Yulia A, Napolitano R, Aiman A, Desai D, Johal N, Whitten M, Ushakov F, Pandya PP, Winyard PJD. Yulia A, et al. Ultrasound Obstet Gynecol. 2021 Jun;57(6):953-958. doi: 10.1002/uog.22121. Ultrasound Obstet Gynecol. 2021. PMID: 32530118 Free article.
Considering renal outcome alone, kidney function was abnormal in 13 (21.7%), 10 (17.9%) and 0 (0%) infants in these three groups, respectively, although concurrent pathology clearly affected global outcome in the more complex cases. Neonatal mortality of 1.6% was observed …
Considering renal outcome alone, kidney function was abnormal in 13 (21.7%), 10 (17.9%) and 0 (0%) infants in these three groups, respective …
2022 Recommendations of the AFU Lithiasis Committee: Endoscopic description of renal papillae and stones.
Almeras C, Estrade V, Meria P; lithiasis committee of the French Association of Urology (CLAFU). Almeras C, et al. Prog Urol. 2023 Nov;33(14):766-781. doi: 10.1016/j.purol.2023.08.012. Prog Urol. 2023. PMID: 37918978 Review.
Endoscopic observation is performed during treatments by flexible ureteroscopy to differentiate in situ between renal papillary abnormalities and stones based on their concordance with Daudon's morphological/composition descriptions adapted to endoscopy. ...
Endoscopic observation is performed during treatments by flexible ureteroscopy to differentiate in situ between renal papillary abnor …
Non-papillary prone percutaneous nephrolithotomy for renal abnormalities: single-institution experience.
Tsaturyan A, Faitatziadis S, Peteinaris A, Adamou C, Pagonis K, Natsos A, Vrettos T, Liatsikos E, Kallidonis P. Tsaturyan A, et al. World J Urol. 2023 Feb;41(2):581-587. doi: 10.1007/s00345-022-04254-2. Epub 2022 Dec 22. World J Urol. 2023. PMID: 36547678
PURPOSE: To evaluate the effectiveness and safety of non-papillary prone PCNL for the treatment of patients with renal abnormalities. METHODS: An observational retrospective cohort study including PCNL cases of patients with renal abnormalities was performed. ...
PURPOSE: To evaluate the effectiveness and safety of non-papillary prone PCNL for the treatment of patients with renal abnormalities. METHOD …
Prenatal and Early Postnatal Outcomes for Fetuses with Anatomic or Functional Renal Agenesis.
Ogundipe EA, Behrendt N, Leavitt C, Reynolds R, Vemulakonda VM. Ogundipe EA, et al. Fetal Diagn Ther. 2022;49(9-10):411-418. doi: 10.1159/000526820. Epub 2022 Oct 5. Fetal Diagn Ther. 2022. PMID: 36198283
Developmentally, she is on track with cognitive and language skills but is behind with general motor skills. We observed a 30-day mortality of 60% and 1-year mortality of 80%. CONCLUSIONS: Individuals carrying a pregnancy complicated by CAKUT anomalies face a difficult cho …
Developmentally, she is on track with cognitive and language skills but is behind with general motor skills. We observed a 30-day mor …
Histopathology in Ureteropelvic Junction Obstruction With and Without Crossing Vessels.
Cancian M, Pareek G, Caldamone A, Aguiar L, Wang H, Amin A. Cancian M, et al. Urology. 2017 Sep;107:209-213. doi: 10.1016/j.urology.2017.05.013. Epub 2017 May 16. Urology. 2017. PMID: 28526243
The degrees of muscle hypertrophy (P = .89) and fibrosis (P = .17) were not predictive of etiology. The odds of a crossing vessel increased by 4.3 times (95% confidence interval 1.8-9.9) when edema was present (P = .009) and by 4.4 (95% confidence interval 1.4-13.7) times …
The degrees of muscle hypertrophy (P = .89) and fibrosis (P = .17) were not predictive of etiology. The odds of a crossing vessel inc …
A null founder variant in NPNT, encoding nephronectin, causes autosomal recessive renal agenesis.
Al-Hamed MH, Altuwaijri N, Alsahan N, Ali W, Abdulwahab F, Alzahrani F, Majrashi N, Alkuraya FS. Al-Hamed MH, et al. Clin Genet. 2022 Jul;102(1):61-65. doi: 10.1111/cge.14128. Epub 2022 Mar 22. Clin Genet. 2022. PMID: 35246978
We report two families in whom genome-wide linkage analysis showed an autozygous locus linked to BRA (at least one member has unilateral renal agenesis) at 4q24, with an LOD score of ~3. Exome sequencing detected a nonsense variant in NPNT in both families within the linka …
We report two families in whom genome-wide linkage analysis showed an autozygous locus linked to BRA (at least one member has unilateral ren …
38 results