BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

273 related articles for article (PubMed ID: 38180355)

  • 21. [Unilateral renal agenesis. New arguments about the genetic relationship between kidney malformations and urolithiasis].
    Garcia Nieto V; Huertes Díaz B; Escribano Subias J; Alarcón Alacio MT; Gonzalez Rodríguez JD; Cabrera Sevilla JE; Peralta Aros C; Luis Yanes MI
    An Pediatr (Barc); 2016 Nov; 85(5):240-246. PubMed ID: 26669685
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Etiology and management of early pregnancy renal anhydramnios: Is there a place for serial amnioinfusions?
    Jelin AC; Sagaser KG; Forster KR; Ibekwe T; Norton ME; Jelin EB
    Prenat Diagn; 2020 Apr; 40(5):528-537. PubMed ID: 32003482
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prenatal diagnosis of bilateral renal agenesis.
    Kaffe S; Godmilow L; Walker BA; Hirschhorn K
    Obstet Gynecol; 1977 Apr; 49(4):478-80. PubMed ID: 857212
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Familial kidney agenesis: renal adysplasia as a cause of urogenital abnormalities in 3 generations].
    Schwyzer U; Litschgi M; Schinzel A
    Geburtshilfe Frauenheilkd; 1989 Aug; 49(8):759-61. PubMed ID: 2676695
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformations.
    Loo CK; Pereira TN; Ramm GA
    Birth Defects Res A Clin Mol Teratol; 2012 Feb; 94(2):116-22. PubMed ID: 22246978
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
    Sanna-Cherchi S; Khan K; Westland R; Krithivasan P; Fievet L; Rasouly HM; Ionita-Laza I; Capone VP; Fasel DA; Kiryluk K; Kamalakaran S; Bodria M; Otto EA; Sampson MG; Gillies CE; Vega-Warner V; Vukojevic K; Pediaditakis I; Makar GS; Mitrotti A; Verbitsky M; Martino J; Liu Q; Na YJ; Goj V; Ardissino G; Gigante M; Gesualdo L; Janezcko M; Zaniew M; Mendelsohn CL; Shril S; Hildebrandt F; van Wijk JAE; Arapovic A; Saraga M; Allegri L; Izzi C; Scolari F; Tasic V; Ghiggeri GM; Latos-Bielenska A; Materna-Kiryluk A; Mane S; Goldstein DB; Lifton RP; Katsanis N; Davis EE; Gharavi AG
    Am J Hum Genet; 2017 Nov; 101(5):789-802. PubMed ID: 29100090
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A pedigree study of perinatally lethal renal disease.
    Bankier A; de Campo M; Newell R; Rogers JG; Danks DM
    J Med Genet; 1985 Apr; 22(2):104-11. PubMed ID: 3886908
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans.
    Vivante A; Kohl S; Hwang DY; Dworschak GC; Hildebrandt F
    Pediatr Nephrol; 2014 Apr; 29(4):695-704. PubMed ID: 24398540
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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. PubMed ID: 31098643
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus.
    Hogge WA; Vick DJ; Schnatterly PA; MacMillan RH
    Am J Med Genet; 1989 Jun; 33(2):242-3. PubMed ID: 2669483
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Renal agenesis, associated genital malformations, and responsible genes.
    Acién P; Acién M
    Fertil Steril; 2021 Nov; 116(5):1370-1371. PubMed ID: 34548168
    [No Abstract]   [Full Text] [Related]  

  • 32. Prenatal diagnosis of dysmorphic syndromes by routine fetal ultrasound examination across Europe.
    Stoll C; Clementi M;
    Ultrasound Obstet Gynecol; 2003 Jun; 21(6):543-51. PubMed ID: 12808670
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: a systematic review.
    Hofmann AD; Duess JW; Puri P
    Pediatr Surg Int; 2014 Aug; 30(8):757-61. PubMed ID: 24974188
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Dilemma after termination of pregnancy due to urogenital fetal anomalies: Discrepancy between prenatal ultrasonographic diagnosis and autopsy.
    Ozdemir O; Aksoy F; Sen C
    Int J Gynaecol Obstet; 2022 Oct; 159(1):223-228. PubMed ID: 34951011
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital unilateral renal agenesis: Prevalence, prenatal diagnosis, associated anomalies. Data from two birth-defect registries.
    Laurichesse Delmas H; Kohler M; Doray B; Lémery D; Francannet C; Quistrebert J; Marie C; Perthus I
    Birth Defects Res; 2017 Sep; 109(15):1204-1211. PubMed ID: 28722320
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Screening for Mullerian anomalies in patients with unilateral renal agenesis: Leveraging early detection to prevent complications.
    Friedman MA; Aguilar L; Heyward Q; Wheeler C; Caldamone A
    J Pediatr Urol; 2018 Apr; 14(2):144-149. PubMed ID: 29459133
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Hereditary renal agenesis . Report of a case].
    Stella A
    Minerva Ginecol; 1998 Jun; 50(6):255-9. PubMed ID: 9763817
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Bilateral renal agenesis in three consecutive siblings.
    Morse RP; Rawnsley E; Crowe HC; Marin-Padilla M; Graham JM
    Prenat Diagn; 1987 Oct; 7(8):573-9. PubMed ID: 3317388
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Evaluation of prenatally diagnosed structural congenital anomalies.
    Gagnon A;
    J Obstet Gynaecol Can; 2009 Sep; 31(9):875-881. PubMed ID: 19941713
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Obstructed hemivagina and ipsilateral renal agenesis (OHVIRA) syndrome should be redefined as ipsilateral renal anomalies: cases of symptomatic atrophic and dysplastic kidney with ectopic ureter to obstructed hemivagina.
    Schlomer B; Rodriguez E; Baskin L
    J Pediatr Urol; 2015 Apr; 11(2):77.e1-6. PubMed ID: 25797857
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.