These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 30662209)

  • 1. VACTERL association - Ultrasound findings and autopsy correlation.
    Gaur NK; Gokhale S
    Indian J Radiol Imaging; 2018; 28(4):452-455. PubMed ID: 30662209
    [TBL] [Abstract][Full Text] [Related]  

  • 2. VACTERL (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, cardiac defects, renal and limb anomalies) association: disease spectrum in 25 patients ascertained for their upper limb involvement.
    Carli D; Garagnani L; Lando M; Fairplay T; Bernasconi S; Landi A; Percesepe A
    J Pediatr; 2014 Mar; 164(3):458-62.e1-2. PubMed ID: 24210691
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Vater or Vacterl syndrome (author's transl)].
    Baumann W; Greinacher I; Emmrich P; Spranger J
    Klin Padiatr; 1976 Jul; 188(4):328-37. PubMed ID: 988425
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of VACTERL and non-VACTERL association without the "V and L".
    Padma S; Sundaram PS; Sonik B
    Indian J Nucl Med; 2014 Jan; 29(1):46-9. PubMed ID: 24591785
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An Incidental Finding of Butterfly Vertebrae in a Case of Vertebral Defects, Anal Atresia, Cardiac Defects, Tracheo-Esophageal Fistula, Renal Anomalies, and Limb Abnormalities (VACTERL).
    Rao A; Gaikwad S; Taksande A; Wanjari MB
    Cureus; 2023 Jan; 15(1):e33401. PubMed ID: 36751248
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Network of Anomalies Prompting VACTERL Workup in a Trisomy 21 Newborn.
    Reinicke T; Costantino CL; Anderson DJ; Tran J; Griggs C
    Cureus; 2022 Jan; 14(1):e21290. PubMed ID: 35186552
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Non-VACTERL-type anomalies are frequent in patients with esophageal atresia/tracheo-esophageal fistula and full or partial VACTERL association.
    de Jong EM; Felix JF; Deurloo JA; van Dooren MF; Aronson DC; Torfs CP; Heij HA; Tibboel D
    Birth Defects Res A Clin Mol Teratol; 2008 Feb; 82(2):92-7. PubMed ID: 18186125
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Underlying genetic factors of the VATER/VACTERL association with special emphasis on the "Renal" phenotype.
    Reutter H; Hilger AC; Hildebrandt F; Ludwig M
    Pediatr Nephrol; 2016 Nov; 31(11):2025-33. PubMed ID: 26857713
    [TBL] [Abstract][Full Text] [Related]  

  • 9. VACTERL association with a rare vertebral anomaly (butterfly vertebra) in a case of monochorionic twin.
    Sandal G; Aslan N; Duman L; Ormeci AR
    Genet Couns; 2014; 25(2):231-5. PubMed ID: 25059024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Second study on the recurrence risk of isolated esophageal atresia with or without trachea-esophageal fistula among first-degree relatives: no evidence for increased risk of recurrence of EA/TEF or for malformations of the VATER/VACTERL association spectrum.
    Choinitzki V; Zwink N; Bartels E; Baudisch F; Boemers TM; Hölscher A; Turial S; Bachour H; Heydweiller A; Kurz R; Bartmann P; Pauly M; Brokmeier U; Leutner A; Nöthen MM; Schumacher J; Jenetzky E; Reutter H
    Birth Defects Res A Clin Mol Teratol; 2013 Dec; 97(12):786-91. PubMed ID: 24307608
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tracheal agenesis with anomalies found in both VACTERL and TACRD associations.
    Wei JL; Rodeberg D; Thompson DM
    Int J Pediatr Otorhinolaryngol; 2003 Sep; 67(9):1013-7. PubMed ID: 12907059
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Outcomes of kidney transplants in pediatric patients with the vertebral defects, anal atresia, cardiac defects, tracheoesophageal fistula, renal anomalies, limb abnormalities association.
    Diaz J; Chavers B; Chinnakotla S; Verghese P
    Pediatr Transplant; 2019 Mar; 23(2):e13341. PubMed ID: 30597716
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial Factors and VACTERL Association-Related Congenital Malformations.
    Siebel S; Solomon BD
    Mol Syndromol; 2013 Feb; 4(1-2):63-73. PubMed ID: 23653577
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies.
    Zeidler C; Woelfle J; Draaken M; Mughal SS; Große G; Hilger AC; Dworschak GC; Boemers TM; Jenetzky E; Zwink N; Lacher M; Schmidt D; Schmiedeke E; Grasshoff-Derr S; Märzheuser S; Holland-Cunz S; Schäfer M; Bartels E; Keppler K; Palta M; Leonhardt J; Kujath C; Rißmann A; Nöthen MM; Reutter H; Ludwig M
    Birth Defects Res A Clin Mol Teratol; 2014 Oct; 100(10):750-9. PubMed ID: 25131394
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association.
    Hilger AC; Halbritter J; Pennimpede T; van der Ven A; Sarma G; Braun DA; Porath JD; Kohl S; Hwang DY; Dworschak GC; Hermann BG; Pavlova A; El-Maarri O; Nöthen MM; Ludwig M; Reutter H; Hildebrandt F
    Hum Mutat; 2015 Dec; 36(12):1150-4. PubMed ID: 26294094
    [TBL] [Abstract][Full Text] [Related]  

  • 16. VACTERL associations in children undergoing surgery for esophageal atresia and anorectal malformations: Implications for pediatric surgeons.
    Lautz TB; Mandelia A; Radhakrishnan J
    J Pediatr Surg; 2015 Aug; 50(8):1245-50. PubMed ID: 25913268
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genes.
    Kolvenbach CM; van der Ven AT; Kause F; Shril S; Scala M; Connaughton DM; Mann N; Nakayama M; Dai R; Kitzler TM; Schneider R; Schierbaum L; Schneider S; Accogli A; Torella A; Piatelli G; Nigro V; Capra V; Hoppe B; Märzheuser S; Schmiedeke E; Rehm HL; Mane S; Lifton RP; Dworschak GC; Hilger AC; Reutter H; Hildebrandt F
    Am J Med Genet A; 2021 Dec; 185(12):3784-3792. PubMed ID: 34338422
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Array-based molecular karyotyping in 115 VATER/VACTERL and VATER/VACTERL-like patients identifies disease-causing copy number variations.
    Zhang R; Marsch F; Kause F; Degenhardt F; Schmiedeke E; Märzheuser S; Hoppe B; Bachour H; Boemers TM; Schäfer M; Spychalski N; Neser J; Leonhardt J; Kosch F; Ure B; Gómez B; Lacher M; Deffaa OJ; Palta M; Wittekindt B; Kleine K; Schmedding A; Grasshoff-Derr S; Ven AV; Heilmann-Heimbach S; Zwink N; Jenetzky E; Ludwig M; Reutter H
    Birth Defects Res; 2017 Jul; 109(13):1063-1069. PubMed ID: 28605140
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Familial recurrence of tracheoesophageal fistula and associated malformations.
    McMullen KP; Karnes PS; Moir CR; Michels VV
    Am J Med Genet; 1996 Jun; 63(4):525-8. PubMed ID: 8826429
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Report of a girl with vacterl syndrome and right pulmonary agenesis.
    Avcu S; Akgun C; Temel H; Arslan S; Akbayram S; Unal O
    Genet Couns; 2009; 20(4):379-83. PubMed ID: 20162874
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.