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pregnancy combined with hereditary renal disease相关文献:
Neonatal Life-Threatening Nonoliguric Hyperkalemia Under Therapeutic Hypothermia.
Piastra M, Tempera A, De Carolis MP, Pezza L, Genovese O, Benassi C, Morena TC, Picconi E, Zito G, De Rosa G, Conti G, De Luca D.
Ther Hypothermia Temp Manag. 2021 Dec;11(4):238-241. doi: 10.1089/ther.2021.0009. Epub 2021 Aug 17.
PMID:34619071
Hereditary Nephrogenic Diabetes Insipidus.
Knoers N, Lemmink H.
2000 Feb 12 [updated 2020 Feb 27]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
PMID:20301356
Pregnancy in women with Alport syndrome.
Crovetto F, Moroni G, Zaina B, Acaia B, Ossola MW, Fedele L.
Int Urol Nephrol. 2013 Aug;45(4):1223-7. doi: 10.1007/s11255-012-0154-8. Epub 2012 Mar 15.
PMID:22418765
Association of prenatal renal ultrasound abnormalities with pathogenic copy number variants in a large Chinese cohort.
Su J, Qin Z, Fu H, Luo J, Huang Y, Huang P, Zhang S, Liu T, Lu W, Li W, Jiang T, Wei S, Yang S, Shen Y.
Ultrasound Obstet Gynecol. 2022 Feb;59(2):226-233. doi: 10.1002/uog.23702.
PMID:34090309
Update on the Prenatal Diagnosis and Outcomes of Fetal Bilateral Renal Agenesis.
Huber C, Shazly SA, Blumenfeld YJ, Jelin E, Ruano R.
Obstet Gynecol Surv. 2019 May;74(5):298-302. doi: 10.1097/OGX.0000000000000670.
PMID:31098643
Abstracts from the 3rd International Genomic Medicine Conference (3rd IGMC 2015) : Jeddah, Kingdom of Saudi Arabia. 30 November - 3 December 2015.
Shay JW, Homma N, Zhou R, Naseer MI, Chaudhary AG, Al-Qahtani M, Hirokawa N, Goudarzi M, Fornace AJ Jr, Baeesa S, Hussain D, Bangash M, Alghamdi F, Schulten HJ, Carracedo A, Khan I, Qashqari H, Madkhali N, Saka M, Saini KS, Jamal A, Al-Maghrabi J, Abuzenadah A, Chaudhary A, Al Qahtani M, Damanhouri G, Alkhatabi H, Goodeve A, Crookes L, Niksic N, Beauchamp N, Abuzenadah AM, Vaught J, Budowle B, Assidi M, Buhmeida A, Al-Maghrabi J, Buhmeida A, Assidi M, Merdad L, Kumar S, Miura S, Gomez K, Carracedo A, Rasool M, Rebai A, Karim S, Eldin HFN, Abusamra H, Alhathli EM, Salem N, Al-Qahtani MH, Kumar S, Faheem H, Agarwa A, Nieschlag E, Wistuba J, Damm OS, Beg MA, Abdel-Meguid TA, Mosli HA, Bajouh OS, Abuzenadah AM, Al-Qahtani MH, Coskun S, Abu-Elmagd M, Buhmeida A, Dallol A, Al-Maghrabi J, Hakamy S, Al-Qahtani W, Al-Harbi A, Hussain S, Assidi M, Al-Qahtani M, Abuzenadah A, Ozkosem B, DuBois R, Messaoudi SS, Dandana MT, Mahjoub T, Almawi WY, Abdalla S, Al-Aama MN, Elzawahry A, Takahashi T, Mimaki S, Furukawa E, Nakatsuka R, Kurosaka I, Nishigaki T, Nakamura H, Serada S, Naka T, Hirota S, Shibata T, Tsuchihara K, Nishida T, Kato M, Mehmood S, Ashraf NM, Asif A, Bilal M, Mehmood MS, Hussain …
BMC Genomics. 2016 Jul 20;17 Suppl 6(Suppl 6):487. doi: 10.1186/s12864-016-2858-0.
PMID:27454254
Combined Preimplantation Genetic Testing for Autosomal Dominant Polycystic Kidney Disease: Consequences for Embryos Available for Transfer.
Mir Pardo P, Martínez-Conejero JA, Martín J, Simón C, Cervero A.
Genes (Basel). 2020 Jun 24;11(6):692. doi: 10.3390/genes11060692.
PMID:32599795
Clinical features of 102 patients with different types of Herlyn-Werner-Wunderlich syndrome.
Jiang J, Yi S.
Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2023 Apr 28;48(4):550-556. doi: 10.11817/j.issn.1672-7347.2023.220336.
PMID:37385617
Unilateral macrocystic dysplasia and contralateral agenesis in a monoamniotic twin.
Ostatníková Michaela, Doležal Pavel, Gábor Martin, Záhumenský Jozef.
Ceska Gynekol. 2022;87(4):278-281. doi: 10.48095/cccg2022278.
PMID:36055789
Harboyan Syndrome: A Novel SLC4A11 Variant With Unique Genotype-Phenotype Correlation.
Magan T, Hammersmith KM, Viaene AN, Kumar P, Eagle RC Jr, Milman T.
Cornea. 2022 Aug 1;41(8):1053-1057. doi: 10.1097/ICO.0000000000003023. Epub 2022 Apr 8.
PMID:35439766
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