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 *

148 related articles for article (PubMed ID: 38269232)

  • 1. Absent Thumb and Radius in a Neonate With Tracheo-Esophageal Fistula and Ventricular Septal Defect: VACTERL Association.
    Sood A; Mishra GV; Khandelwal S; Suryadevara M; Manuja N
    Cureus; 2023 Dec; 15(12):e51058. PubMed ID: 38269232
    [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. Vertebral defect, anal atresia, cardiac defect, tracheoesophageal fistula/esophageal atresia, renal defect, and limb defect association with Mayer-Rokitansky-Küster-Hauser syndrome in co-occurrence: two case reports and a review of the literature.
    Bjørsum-Meyer T; Herlin M; Qvist N; Petersen MB
    J Med Case Rep; 2016 Dec; 10(1):374. PubMed ID: 28003020
    [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. Accompanied anomalies in anal atresia or tracheo-esophageal fistula: Comparison with or without VACTERL association.
    Ahn JH; Choi HJ
    Birth Defects Res; 2021 May; 113(9):696-701. PubMed ID: 33616304
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Esophageal atresia in newborns: a wide spectrum from the isolated forms to a full VACTERL phenotype?
    La Placa S; Giuffrè M; Gangemi A; Di Noto S; Matina F; Nociforo F; Antona V; Di Pace MR; Piccione M; Corsello G
    Ital J Pediatr; 2013 Jul; 39():45. PubMed ID: 23842449
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Right Pulmonary Artery Originating from Ascending Aorta (Hemitruncus Arteriosus) with VACTERL Association in a Neonate: A Case Report.
    Shin BS; Kim T; Lee HD; Ko H; Byun JH
    Children (Basel); 2022 Feb; 9(2):. PubMed ID: 35204915
    [TBL] [Abstract][Full Text] [Related]  

  • 8. VACTERL/VATER Association.
    Solomon BD
    Orphanet J Rare Dis; 2011 Aug; 6():56. PubMed ID: 21846383
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S.
    Amelot A; Cretolle C; de Saint Denis T; Sarnacki S; Catala M; Zerah M
    Eur J Pediatr; 2020 Jul; 179(7):1121-1129. PubMed ID: 32055959
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Congenital anal atresia with rectovestibular fistula, scoliosis, unilateral renal agenesis, and finger defect (VACTERL association) in a patient with partial bicornuate uterus and distal vaginal atresia: A case report.
    Kang J; Mao M; Zhang Y; Ai FF; Zhu L
    Medicine (Baltimore); 2018 Nov; 97(45):e12822. PubMed ID: 30407282
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association.
    Hilger A; Schramm C; Pennimpede T; Wittler L; Dworschak GC; Bartels E; Engels H; Zink AM; Degenhardt F; Müller AM; Schmiedeke E; Grasshoff-Derr S; Märzheuser S; Hosie S; Holland-Cunz S; Wijers CH; Marcelis CL; van Rooij IA; Hildebrandt F; Herrmann BG; Nöthen MM; Ludwig M; Reutter H; Draaken M
    Eur J Hum Genet; 2013 Dec; 21(12):1377-82. PubMed ID: 23549274
    [TBL] [Abstract][Full Text] [Related]  

  • 17. HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum.
    Kause F; Zhang R; Ludwig M; Schmiedeke E; Rissmann A; Thiele H; Altmueller J; Herms S; Hilger AC; Hildebrandt F; Reutter H
    Birth Defects Res; 2019 Jun; 111(10):591-597. PubMed ID: 30887706
    [TBL] [Abstract][Full Text] [Related]  

  • 18. VACTERL anomalies in patients with esophageal atresia: an updated delineation of the spectrum and review of the literature.
    Keckler SJ; St Peter SD; Valusek PA; Tsao K; Snyder CL; Holcomb GW; Ostlie DJ
    Pediatr Surg Int; 2007 Apr; 23(4):309-13. PubMed ID: 17377826
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Nonfamilial VACTERL-H Syndrome in a Dizygotic Twin: Prenatal Ultrasound and Postnatal 3D CT Findings.
    Hong SY; Kim SJ; Park MH; Lee KA
    Medicina (Kaunas); 2023 Jul; 59(8):. PubMed ID: 37629676
    [No Abstract]   [Full Text] [Related]  

  • 20. Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies.
    Brosens E; Ploeg M; van Bever Y; Koopmans AE; IJsselstijn H; Rottier RJ; Wijnen R; Tibboel D; de Klein A
    Eur J Med Genet; 2014 Aug; 57(8):440-52. PubMed ID: 24931924
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.