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 *

141 related articles for article (PubMed ID: 38329589)

  • 1. SALL4 deletion and kidney and cardiac defects associated with VACTERL association.
    Watanabe D; Nakato D; Yamada M; Suzuki H; Takenouchi T; Miya F; Kosaki K
    Pediatr Nephrol; 2024 Aug; 39(8):2347-2349. PubMed ID: 38329589
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Phenotypic diversity of patients diagnosed with VACTERL association.
    Husain M; Dutra-Clarke M; Lemieux B; Wencel M; Solomon BD; Kimonis V
    Am J Med Genet A; 2018 Sep; 176(9):1830-1837. PubMed ID: 30152190
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. An approach to the identification of anomalies and etiologies in neonates with identified or suspected VACTERL (vertebral defects, anal atresia, tracheo-esophageal fistula with esophageal atresia, cardiac anomalies, renal anomalies, and limb anomalies) association.
    Solomon BD; Baker LA; Bear KA; Cunningham BK; Giampietro PF; Hadigan C; Hadley DW; Harrison S; Levitt MA; Niforatos N; Paul SM; Raggio C; Reutter H; Warren-Mora N
    J Pediatr; 2014 Mar; 164(3):451-7.e1. PubMed ID: 24332453
    [No Abstract]   [Full Text] [Related]  

  • 6. Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
    van de Putte R; van Rooij IALM; Marcelis CLM; Guo M; Brunner HG; Addor MC; Cavero-Carbonell C; Dias CM; Draper ES; Etxebarriarteun L; Gatt M; Haeusler M; Khoshnood B; Klungsoyr K; Kurinczuk JJ; Lanzoni M; Latos-Bielenska A; Luyt K; O'Mahony MT; Miller N; Mullaney C; Nelen V; Neville AJ; Perthus I; Pierini A; Randrianaivo H; Rankin J; Rissmann A; Rouget F; Schaub B; Tucker D; Wellesley D; Wiesel A; Zymak-Zakutnia N; Loane M; Barisic I; de Walle HEK; Roeleveld N; Bergman JEH
    Pediatr Res; 2020 Feb; 87(3):541-549. PubMed ID: 31499513
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. Congenital Great Toe Hypoplasia Equivalent to a Grade 3 Hypoplastic Thumb in a Patient with VACTERL Association.
    Mende K; Tonkin MA
    J Hand Surg Asian Pac Vol; 2018 Dec; 23(4):605-606. PubMed ID: 30428812
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The genetic landscape and clinical implications of vertebral anomalies in VACTERL association.
    Chen Y; Liu Z; Chen J; Zuo Y; Liu S; Chen W; Liu G; Qiu G; Giampietro PF; Wu N; Wu Z
    J Med Genet; 2016 Jul; 53(7):431-7. PubMed ID: 27084730
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PCSK5 mutation in a patient with the VACTERL association.
    Nakamura Y; Kikugawa S; Seki S; Takahata M; Iwasaki N; Terai H; Matsubara M; Fujioka F; Inagaki H; Kobayashi T; Kimura T; Kurahashi H; Kato H
    BMC Res Notes; 2015 Jun; 8():228. PubMed ID: 26055999
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. 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]  

  • 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. VATER/VACTERL Association and Caudal Regression with Xq25-q27.3 Microdeletion: A Case Report.
    Puvabanditsin S; Van Gurp J; February M; Khalil M; Mayne J; Ai McConnell J; Mehta R
    Fetal Pediatr Pathol; 2016; 35(2):133-41. PubMed ID: 26881326
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association.
    Winberg J; Gustavsson P; Papadogiannakis N; Sahlin E; Bradley F; Nordenskjöld E; Svensson PJ; Annerén G; Iwarsson E; Nordgren A; Nordenskjöld A
    PLoS One; 2014; 9(1):e85313. PubMed ID: 24416387
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.