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  1. 1
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  2. 2
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  3. 3
    Sing-Ling Liao, Pei-Yin Tsai, Yueh-Chin Cheng, Chiung-Hsin Chang, Huei-Chen Ko, Fong-Ming Chang, Prenatal Diagnosis of Fetal Encephalocele Using Three-dimensional Ultrasound, Journal of Medical Ultrasound, 2012, 20, 3, 150

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  4. 4
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  5. 5
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  6. 6
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  7. 7
    Faiz U. Ahmad, Ashok K. Mahapatra, Neural tube defects at separate sites: further evidence in support of multi-site closure of the neural tube in humans, Surgical Neurology, 2009, 71, 3, 353

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  8. 8
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  9. 9
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  10. 10
    Jason R. Guercio, Lois J. Martyn, Congenital Malformations of the Eye and Orbit, Otolaryngologic Clinics of North America, 2007, 40, 1, 113

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  11. 11
    J.-B. Charrier, E. Racy, C. Nowak, B. Lemaire, S. Bobin, Embriologia e anomalie congenite del naso, EMC - Otorinolaringoiatria, 2007, 6, 3, 1

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  12. 12
    J.-B. Charrier, E. Racy, C. Nowak, B. Lemaire, S. Bobin, Embriología y anomalías congénitas de la nariz, EMC - Otorrinolaringología, 2007, 36, 3, 1

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  13. 13
    J.-B. Charrier, E. Racy, C. Nowak, B. Lemaire, S. Bobin, Embryologie et anomalies congénitales du nez, EMC - Oto-rhino-laryngologie, 2007, 2, 2, 1

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  14. 14
    Maria Trovato, Maria D’Armiento, Luca Lavra, Alessandra Ulivieri, Roberto Dominici, Enrica Vitarelli, Maddalena Grosso, Raffaella Vecchione, Gaetano Barresi, Salvatore Sciacchitano, Expression of p53/hgf/c-met/STAT3 signal in fetuses with neural tube defects, Virchows Archiv, 2007, 450, 2, 203

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  15. 15
    Ashley J. Robinson, Susan Blaser, Ants Toi, David Chitayat, William Halliday, Sophie Pantazi, Munire Gundogan, Suzanne Laughlin, Greg Ryan, The Fetal Cerebellar Vermis, Ultrasound Quarterly, 2007, 23, 3, 211

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  16. 16
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  17. 17
    V. de P. Djientcheu, A. Wonkam, A.K. Njamnshi, P. Ongolo-Zogo, B. Rilliet, M.A. Morris, Discordant encephalocele in monozygotic twins, American Journal of Medical Genetics Part A, 2006, 140A, 5
  18. 18
    M. Michael Cohen, Holoprosencephaly: Clinical, anatomic, and molecular dimensions, Birth Defects Research Part A: Clinical and Molecular Teratology, 2006, 76, 9
  19. 19
    A. Tejerizo-García, M. de Marino, M. Belloso, A. Villalba, S.P. González-Rodríguez, M.A. Ruiz, A. Henríquez, R. Alcántara, J.L. Lanchares, L.C. Tejerizo-López, Iniencefalia, Clínica e Investigación en Ginecología y Obstetricia, 2006, 33, 4, 130

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  20. 20
    Imaging the Central Nervous System of the Fetus and Neonate, 2006,

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  21. 21
    Takafumi Hasegawa, Naoto Sugeno, Yusei Shiga, Atsushi Takeda, Hiroshi Karibe, Teiji Tominaga, Yasuto Itoyama, Transethmoidal intranasal meningoencephalocele in an adult with recurrent meningitis, Journal of Clinical Neuroscience, 2005, 12, 6, 702

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  22. 22
    Mariarosaria Di Tommaso, Andrea L Tranquilli, A checklist to identify the origin of cerebral palsy, Journal of Maternal-Fetal and Neonatal Medicine, 2004, 15, 5, 281

    CrossRef

  23. 23
    Hélène Dollfus, Alain Verloes, Dysmorphology and the orbital region: a practical clinical approach, Survey of Ophthalmology, 2004, 49, 6, 547

    CrossRef

  24. 24
    Gary D. Clark, The classification of cortical dysplasias through molecular genetics, Brain and Development, 2004, 26, 6, 351

    CrossRef

  25. 25
    Nicola Brunetti-Pierri, Roberto Mendoza-Londono, Maulik R. Shah, Lefkothea Karaviti, Brendan Lee, von Voss-Cherstvoy syndrome with transient thrombocytopenia and normal psychomotor development, American Journal of Medical Genetics Part A, 2004, 126A, 3
  26. 26
    Gary D Clark, Brain development and the genetics of brain development, Neurologic Clinics, 2002, 20, 4, 917

    CrossRef

  27. 27
    Jeffrey C. Posnick, Bernard J. Costello, Dermoid cysts, gliomas, and encephaloceles: evaluation and treatment, Atlas of the Oral and Maxillofacial Surgery Clinics, 2002, 10, 1, 85

    CrossRef

  28. 28
    Taosheng Huang, Mark S. Korson, Celeste Krauss, Lewis B. Holmes, Four cases with hypoplastic thumbs and encephaloceles, American Journal of Medical Genetics, 2002, 111, 2
  29. 29
    EK Pivnick, ML Rivas, EA Tolley, SD Smith, GJ Presbury, Interpupillary distance in a normal black population, Clinical Genetics, 1999, 55, 3
  30. 30
    Inger Kjær, Henrik Mygind, Birgit Fischer Hansen, Notochordal remnants in human iniencephaly suggest disturbed dorsoventral axis signaling, American Journal of Medical Genetics, 1999, 84, 5
  31. 31
    Juan F. Martínez-Lage, Máximo Poza, Teresa Lluch, Craniosynostosis in neural tube defects: A theory on its pathogenesis, Surgical Neurology, 1996, 46, 5, 465

    CrossRef

  32. 32
    Maria Leine Guion-Almeida, Antonio Richieri-Costa, Dolores Saavedra, M. Michael Cohen, Frontonasal dysplasia: analysis of 21 cases and literature review, International Journal of Oral and Maxillofacial Surgery, 1996, 25, 2, 91

    CrossRef

  33. 33
    M. Michael Cohen, Antonio Richieri-Costa, Maria Leine Guion-Almeida, Dolores Saavedra, Hypertelorism: interorbital growth, measurements, and pathogenetic considerations, International Journal of Oral and Maxillofacial Surgery, 1995, 24, 6, 387

    CrossRef

  34. 34
    Miguel Urioste, Luis Paisán, María Luisa Martínez-Frías, DK-phocomelia syndrome in a child with a long follow-up, American Journal of Medical Genetics, 1994, 52, 3
  35. 35
    M. Rita Passos-Bueno, Suely K. Marie, Mario Monteiro, Isaac Neustein, Martin R. Whittle, Mariz Vainzof, Mayana Zatz, Knobloch syndrome in a large Brazilian consanguineous family: Confirmation of autosomal recessive inheritance, American Journal of Medical Genetics, 1994, 52, 2
  36. 36
    Edward E.C. Angtuaco, Teresita L. Angtuaco, Edgardo J.C. Angtuaco, Prenatal diagnosis of central nervous system abnormalities, Current Problems in Diagnostic Radiology, 1994, 23, 3, 71

    CrossRef

  37. 37
    Steven J. Wininger, Alan E. Donnenfeld, Syndromes identified in fetuses with prenatally diagnosed cephaloceles, Prenatal Diagnosis, 1994, 14, 9
  38. 38
    V.A. Adetiloye, F.O. Dare, O.A. Oyelami, A ten-year review of encephalocele in a teaching hospital, International Journal of Gynecology & Obstetrics, 1993, 41, 3, 241

    CrossRef

  39. 39
    A. E. Czeizel, P. Göblyös, G. Kustos, E. Mester, E. Paraicz, The second report of Knobloch syndrome, American Journal of Medical Genetics, 1992, 42, 6
  40. 40
    J. Camón, D. Sabaté, J. Franch, M. A. López-Béjar, J. Pastor, J. Rutllant, J. Ordeig, E. Degollada, J. Verdu, Associated Multiple Congenital Malformations in Domestic Animals. Contribution of Four Cases, Journal of Veterinary Medicine Series A, 1990, 37, 1-10
  41. 41
    David A. Nyberg, The fetal central nervous system, Seminars in Roentgenology, 1990, 25, 4, 317

    CrossRef

  42. 42
    William B. Dobyns, Roberta A. Pagon, Dawna Armstrong, Cynthia J. R. Curry, Frank Greenberg, Arthur Grix, Lewis B. Holmes, Renata Laxova, Virginia V. Michels, Meinhard Robinow, Roberta L. Zimmerman, John M. Opitz, James F. Reynolds, Diagnostic criteria for Walker-Warburg syndrome, American Journal of Medical Genetics, 1989, 32, 2
  43. 43
    M. Michael Cohen, Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology, Teratology, 1989, 40, 3
  44. 44
    M. Michael Cohen, Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities, American Journal of Medical Genetics, 1989, 34, 2
  45. 45
    David Bick, Richard I. Markowitz, Arthur Horwich, John M. Opitz, James F. Reynolds, Trisomy 18 associated with ectopia cordis and occipital meningocele, American Journal of Medical Genetics, 1988, 30, 3
  46. 46
    Ntinos C. Myrianthopoulos, Michael Melnick, John M. Opitz, James F. Reynolds, Studies in neural tube defects I. Epidemiologic and etiologic aspects, American Journal of Medical Genetics, 1987, 26, 4
  47. 47
    Gianluigi Pilu, Nicola Rizzo, Luigi Filippo Orsini, Luciano Bovicelli, Antenatal recognition of cerebral anomalies, Ultrasound in Medicine & Biology, 1986, 12, 4, 319

    CrossRef

  48. 48
    L. Rebecca Campbell, Delbert H. Dayton, G. S. Sohal, Neural tube defects: A review of human and animal studies on the etiology of neural tube defects, Teratology, 1986, 34, 2
  49. 49
    John R. Waterson, Michael A. DiPietro, Mason Barr, John M. Opitz, James F. Reynolds, Apert syndrome with frontonasal encephalocele, American Journal of Medical Genetics, 1985, 21, 4
  50. 50
    G. A. Machin, G. H. Sperber, J. Wootliffe, Monozygotic twin aborted fetuses discordant for holoprosencephaly/synotia, Teratology, 1985, 31, 2
  51. 51
    William B. Dobyns, Joel B. Kirkpatrick, Helen M. Hittner, Frank L. Kretzer, Richard M. Roberts, John M. Opitz, James F. Reynolds, Syndromes with lissencephaly. II: Walker-Warburg and Cerebro-Oculo-Muscular syndromes and a new syndrome with type II lissencephaly, American Journal of Medical Genetics, 1985, 22, 1
  52. 52
    G. Alfieri, G. Campana, G. Valentini, M. L. Giovannucci-Uzielli, E. Lapi, The Anterior Segment Anomalies in the Warburg Syndrome: A Study of New Cases, Ophthalmic Genetics, 1985, 6, 3, 141

    CrossRef

  53. 53
    Chester B. Whitley, Theodore R. Thompson, Angeline R. Mastri, Robert J. Gorlin, Warburg syndrome: Lethal neurodysplasia with autosomal recessive inheritance, The Journal of Pediatrics, 1983, 102, 4, 547

    CrossRef