SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Eric F Lock, Karen L Soldano, Melanie E Garrett, Heidi Cope, Christina A Markunas, Herbert Fuchs, Gerald Grant, David B Dunson, Simon G Gregory, Allison E Ashley-Koch, Joint eQTL assessment of whole blood and dura mater tissue from individuals with Chiari type I malformation, BMC Genomics, 2015, 16, 1

    CrossRef

  2. 2
    M.S. Thøfner, C.L. Stougaard, U. Westrup, A.A. Madry, C.S. Knudsen, H. Berg, C.S.E. Jensen, R.M.L. Handby, H. Gredal, M. Fredholm, M. Berendt, Prevalence and Heritability of Symptomatic Syringomyelia in Cavalier King Charles Spaniels and Long-term Outcome in Symptomatic and Asymptomatic Littermates, Journal of Veterinary Internal Medicine, 2015, 29, 1
  3. 3
    Alper Cesmebasi, Marios Loukas, Elizabeth Hogan, Sara Kralovic, R. Shane Tubbs, Aaron A. Cohen-gadol, The Chiari malformations: A review with emphasis on anatomical traits, Clinical Anatomy, 2015, 28, 1
  4. 4
    Christina A. Markunas, David S. Enterline, Kaitlyn Dunlap, Karen Soldano, Heidi Cope, Jeffrey Stajich, Gerald Grant, Herbert Fuchs, Simon G. Gregory, Allison E. Ashley-Koch, Genetic Evaluation and Application of Posterior Cranial Fossa Traits as Endophenotypes for Chiari Type I Malformation, Annals of Human Genetics, 2014, 78, 1
  5. 5
    Aintzane Urbizu, Maria-Antonia Poca, Xavier Vidal, Alex Rovira, Juan Sahuquillo, Alfons Macaya, MRI-based Morphometric Analysis of Posterior Cranial Fossa in the Diagnosis of Chiari Malformation Type I, Journal of Neuroimaging, 2014, 24, 3
  6. 6
    Hiroshi Kuroki, Naoki Inomata, Hideaki Hamanaka, Kiyoshi Higa, Etsuo Chosa, Naoya Tajima, Two siblings with neuropathic scoliosis caused by Chiari malformation type I with syringomyelia, Journal of Orthopaedic Science, 2014,

    CrossRef

  7. 7
    Tetsunari Nishikawa, Toshiro Yamamoto, Ken-ichi Honjo, Hiroaki Ichioka, Kenta Yamamoto, Narisato Kanamura, Hirohito Kato, Masahiro Wato, Toshikazu Kubo, Masahiko Mori, Akio Tanaka, Marfan's syndrome: Clinical manifestations in the oral-craniofacial area, biophysiological roles of fibrillins and elastic extracellular microfibers, and disease control of the fibrillin gene, Journal of Oral and Maxillofacial Surgery, Medicine, and Pathology, 2013, 25, 4, 374

    CrossRef

  8. 8
    Gaetano Terrone, Alessandra D'Amico, Floriana Imperati, Massimo Carella, Orazio Palumbo, Mattia Gentile, Roberto Berni Canani, Daniela Melis, Alfonso Romano, Iolanda Parente, Marina Riccitelli, Ennio Del Giudice, A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients, European Journal of Medical Genetics, 2012, 55, 8-9, 466

    CrossRef

  9. 9
    Alan L. Shanske, James T. Goodrich, Leena Ala-Kokko, Stuart Baker, Barbara Frederick, Brynn Levy, Germline mosacism in Shprintzen–Goldberg syndrome, American Journal of Medical Genetics Part A, 2012, 158A, 7
  10. 10
    Christian P Schaaf, Robin P Goin-Kochel, Kerri P Nowell, Jill V Hunter, Kirk A Aleck, Sarah Cox, Ankita Patel, Carlos A Bacino, Marwan Shinawi, Expanding the clinical spectrum of the 16p11.2 chromosomal rearrangements: three patients with syringomyelia, European Journal of Human Genetics, 2011, 19, 2, 152

    CrossRef

  11. 11
    B. Hebing, C.H. Wiegand, K. Wesseler, Konnataler Stridor, muskuläre Hypotonie und Hydrocephalus occlusus, Monatsschrift Kinderheilkunde, 2011, 159, 6, 526

    CrossRef

  12. 12
    Rita Bertalan, Ágnes Sallai, János Sólyom, Gábor Lotz, István Szabó, Balázs Kovács, Éva Szabó, Attila Patócs, Károly Rácz, Hyperthyroidism Caused by a Germline Activating Mutation of the Thyrotropin Receptor Gene: Difficulties in Diagnosis and Therapy, Thyroid, 2010, 20, 3, 327

    CrossRef

  13. 13
    Dharmendra Ganesan, Richard D. Hayward, Dominic N. Thompson, Evolution of tonsillar ectopia associated with frontal encephalocoele, Child's Nervous System, 2009, 25, 7, 889

    CrossRef

  14. 14
    Arnold H. Menezes, Timothy W. Vogel, Specific entities affecting the craniocervical region: syndromes affecting the craniocervical junction, Child's Nervous System, 2008, 24, 10, 1155

    CrossRef

  15. 15
    R. Shane Tubbs, Mark Hill, Marios Loukas, Mohammadali M. Shoja, W. Jerry Oakes, Volumetric analysis of the posterior cranial fossa in a family with four generations of the Chiari malformation Type I, Journal of Neurosurgery: Pediatrics, 2008, 1, 1, 21

    CrossRef

  16. 16
    Maisa Seppala, Michael J. Depew, David C. Martinelli, Chen-Ming Fan, Paul T. Sharpe, Martyn T. Cobourne, Gas1 is a modifier for holoprosencephaly and genetically interacts with sonic hedgehog , Journal of Clinical Investigation, 2007, 117, 6, 1575

    CrossRef

  17. 17
    R. Shane Tubbs, Michael J. Lyerly, Marios Loukas, Mohammadali M. Shoja, W. Jerry Oakes, The pediatric Chiari I malformation: a review, Child's Nervous System, 2007, 23, 11, 1239

    CrossRef

  18. 18
    John D Heiss, Edward H Oldfield, Syringomyelia and Related Diseases, eLS,