Repeat Intracranial Expansion After Skull Regrowth in Hyperostotic Disease: Technical Note.
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[1] Yi-Ping Li,et al. TGF-β and BMP signaling in osteoblast, skeletal development, and bone formation, homeostasis and disease , 2016, Bone Research.
[2] Tariq Alam,et al. Visual and otologic manifestation of Camurati–Engelmann's disease: a case report , 2015, Radiology case reports.
[3] T. Kauko,et al. Outcomes of cranioplasty with synthetic materials and autologous bone grafts. , 2015, World neurosurgery.
[4] Muh-Shi Lin,et al. 3-D titanium mesh reconstruction of defective skull after frontal craniectomy in traumatic brain injury. , 2015, Injury.
[5] G. Mortier,et al. Camurati–Engelmann Disease (Progressive Diaphyseal Dysplasia): Reports of an Indian Kindred , 2013, Calcified Tissue International.
[6] R. Goodman,et al. Internal cranial expansion surgery for the treatment of refractory idiopathic intracranial hypertension. , 2012, Journal of neurosurgery. Pediatrics.
[7] C. Deng,et al. TGF-β and BMP Signaling in Osteoblast Differentiation and Bone Formation , 2012, International journal of biological sciences.
[8] B. Abuzayed,et al. Cranioplasty: Review of materials and techniques , 2011, Journal of Neurosciences in Rural Practice.
[9] S. Shintani,et al. Enhancement of bone morphogenetic protein-2-induced ectopic bone formation by transforming growth factor-β1. , 2011, Tissue engineering. Part A.
[10] M. Carlson,et al. Skull base manifestations of Camurati-Engelmann disease. , 2010, Archives of otolaryngology--head & neck surgery.
[11] P. Reilly,et al. Syndrome of the trephined. , 2009, Journal of neurosurgery.
[12] J. Choi,et al. The First Korean Case of Camurati-Engelmann Disease (Progressive Diaphyseal Dysplasia) Confirmed by TGFB1 Gene Mutation Analysis , 2009, Journal of Korean medical science.
[13] J. Mocco,et al. Aggressive Cranial Vault Decompression for Cranial Hyperostosis: Technical Case Report of Two Cases , 2005, Neurosurgery.
[14] S. Wientroub,et al. Camurati-Engelmann Disease : review of the clinical , radiological and molecular data of 24 families and implications towards diagnostics and treatment , 2005 .
[15] S. Wallace,et al. Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati–Engelmann disease): Report of a four‐generation pedigree, identification of a mutation in TGFB1, and review , 2004, American journal of medical genetics. Part A.
[16] D. Friedland,et al. Cochlear Implantation for Auditory Rehabilitation in Camurati-Engelmann Disease , 2000, The Annals of otology, rhinology, and laryngology.
[17] C. Wirth,et al. Camurati-Engelmann disease (progressive hereditary craniodiaphyseal dysplasia). Case report. , 1978, Journal of neurosurgery.
[18] G. Krohel,et al. Engelmann's disease. , 1977, American journal of ophthalmology.