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Scientifica
Volume 2017, Article ID 5364827, 29 pages
https://doi.org/10.1155/2017/5364827
Review Article

Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans

1Department of Parasitology, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia
2Laboratory for Fetal and Regenerative Biology, Colorado Fetal Care Center, Division of Pediatric Surgery, Children’s Hospital Colorado, University of Colorado, Anschutz Medical Campus, 12700 E 17th Ave, Aurora, CO 80045, USA
3Training and Technical Division, Islamic Hospital, Abdali, Amman 2414, Jordan
4Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia

Correspondence should be addressed to Noraishah M. Abdul-Aziz; ym.ude.cmmu@ahsion

Received 20 June 2016; Revised 14 November 2016; Accepted 1 December 2016; Published 13 February 2017

Academic Editor: Heinz Hofler

Copyright © 2017 Siti W. Mohd-Zin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [7 citations]

The following is the list of published articles that have cited the current article.

  • Nor Linda Abdullah, Siti W. Mohd-Zin, Azlina Ahmad-Annuar, and Noraishah M. Abdul-Aziz, “A Novel Occulta-Type Spina Bifida Mediated by Murine Double Heterozygotes EphA2 and EphA4 Receptor Tyrosine Kinases,” Frontiers in Cell and Developmental Biology, vol. 5, 2017. View at Publisher · View at Google Scholar
  • Adibah Sahmat, Renuka Gunasekaran, Siti W. Mohd-Zin, Lohis Balachandran, Meow-Keong Thong, Julia P. Engkasan, Dharmendra Ganesan, Zaliha Omar, Abu Bakar Azizi, Azlina Ahmad-Annuar, and Noraishah M. Abdul-Aziz, “The Prevalence and Distribution of Spina Bifida in a Single Major Referral Center in Malaysia,” Frontiers in Pediatrics, vol. 5, 2017. View at Publisher · View at Google Scholar
  • Sebastian Ocklenburg, and Onur Güntürkünpp. 1–368, 2017. View at Publisher · View at Google Scholar
  • Pardo Vargas, Bustos, and Díaz Sanhueza, “Neurological manifestations associated with spina bifida in adults,” Semergen, 2017. View at Publisher · View at Google Scholar
  • Przemyslaw Kosinski, Robert Brawura Biskupski Samaha, Michal Lipa, Thomas Kohl, and Miroslaw Wielgos, “Contemporary management of prenatally diagnosed spina bifida aperta - an update,” Ginekologia Polska, vol. 89, no. 11, pp. 637–641, 2018. View at Publisher · View at Google Scholar
  • Marie Beaumont, Linda Akloul, Wilfrid Carré, Chloé Quélin, Hubert Journel, Laurent Pasquier, Mélanie Fradin, Sylvie Odent, Houda Hamdi-Rozé, Erwan Watrin, Valérie Dupé, Christèle Dubourg, and Véronique David, “Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders,” Human Genetics, 2019. View at Publisher · View at Google Scholar
  • Alessio Pirino, Maria Alessandra Sotgiu, Erich Cosmi, Andrea Montella, and Pasquale Bandiera, “Association of Klippel-Feil syndrome, Dandy-Walker malformation, spina bifida: A case report,” Radiology Case Reports, vol. 14, no. 3, pp. 415–418, 2019. View at Publisher · View at Google Scholar