Apert syndrome: magnetic resonance imaging (MRI) of associated intracranial anomalies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/article/10.1007/s00381-017-3670-0/fulltext.html
Reference60 articles.
1. Yu K, Herr AB, Waksman G, Ornitz DM (2000) Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome. Proc Natl Acad Sci U S A 97:14536–14541. https://doi.org/10.1073/pnas.97.26.14536
2. Blaser SI, Padfield N, Chitayat D, Forrest CR (2015) Skull base development and craniosynostosis. Pediatr Radiol 45(Suppl 3):S485–S496. https://doi.org/10.1007/s00247-015-3320-1
3. Breik O, Mahindu A, Moore MH, Molloy CJ, Santoreneos S et al (2016) Central nervous system and cervical spine abnormalities in Apert syndrome. Childs Nerv Syst 32:833–838. https://doi.org/10.1007/s00381-016-3036-z
4. Patton MA, Goodship J, Hayward R, Lansdown R (1988) Intellectual development in Apert’s syndrome: a long term follow up of 29 patients. J Med Genet 25:164–167
5. Murovic JA, Posnick JC, Drake JM, Humphreys RP, Hoffman HJ et al (1993) Hydrocephalus in Apert syndrome: a retrospective review. Pediatr Neurosurg 19:151–155
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