C BRITT, R OLIVARES-NAVARRETE, JK WILLIAMS… - 2011 - iadr.confex.com Introduction: Non-syndromic craniosynostosis is poorly understood and the molecular mechanisms are not known. We hypothesized that cells in fused suture express higher levels of osteogenic genes and produce paracrine factors that stimulate mesenchymal stem cells (MSCs) to ... Cached
P Nieminen, NV Morgan, AL Fenwick… - American journal of …, 2011 - ncbi.nlm.nih.gov Craniosynostosis and supernumerary teeth most often occur as isolated developmental anomalies, but they are also separately manifested in several malformation syndromes. Here, we describe a human syndrome featuring craniosynostosis, maxillary hypoplasia, ...
SA Rottgers, PD Kim, AR Kumar, JJ Cray… - Neurosurgical …, 2011 - medscape.com Object Sagittal craniosynostosis is the most common form of craniosynostosis and is commonly treated within the first year of life. Optimal treatment of patients older than 1 year of age is not well characterized. The authors reviewed cases of sagittal craniosynostosis involving ...
A Beenken… - 2011 - content.karger.com Abstract: Many craniosynostosis and dwarfism syndromes are attributable to gain-of-function mutations in FGFR1, FGFR2, and FGFR3. The molecular bases by which these pathogenic mutations over-activate FGFRs have been characterized extensively through the use of X-ray ... Related articles
JRW Kestle… - 2011 - content.lib.utah.edu Object. Childhood radiation exposure increases the lifetime risk of cancer from an estimated 0.07 to 0.35%. Neurological evaluation of patients after cranial vault reconstruction for synostosis repair is often complicated by pain medication, sedation, intubation, swelling, and ... Cached
C BRITT, R OLIVARES-NAVARRETE, JK WILLIAMS… - 2011 - iadr.confex.com Introduction: Non-syndromic craniosynostosis is poorly understood and the molecular mechanisms are not known. We hypothesized that cells in fused suture express higher levels of osteogenic genes and produce paracrine factors that stimulate mesenchymal stem cells (MSCs) to ... Cached
P Nieminen, NV Morgan, AL Fenwick… - American journal of …, 2011 - ncbi.nlm.nih.gov Craniosynostosis and supernumerary teeth most often occur as isolated developmental anomalies, but they are also separately manifested in several malformation syndromes. Here, we describe a human syndrome featuring craniosynostosis, maxillary hypoplasia, ...
SA Rottgers, PD Kim, AR Kumar, JJ Cray… - Neurosurgical …, 2011 - medscape.com Object Sagittal craniosynostosis is the most common form of craniosynostosis and is commonly treated within the first year of life. Optimal treatment of patients older than 1 year of age is not well characterized. The authors reviewed cases of sagittal craniosynostosis involving ...
A Beenken… - 2011 - content.karger.com Abstract: Many craniosynostosis and dwarfism syndromes are attributable to gain-of-function mutations in FGFR1, FGFR2, and FGFR3. The molecular bases by which these pathogenic mutations over-activate FGFRs have been characterized extensively through the use of X-ray ... Related articles
JRW Kestle… - 2011 - content.lib.utah.edu Object. Childhood radiation exposure increases the lifetime risk of cancer from an estimated 0.07 to 0.35%. Neurological evaluation of patients after cranial vault reconstruction for synostosis repair is often complicated by pain medication, sedation, intubation, swelling, and ... Cached