Intraoperative and postoperative complications in the surgical treatment of craniosynostosis: minimally invasive versus open surgical procedures

S Arts, H Delye, EJ van Lindert - Journal of Neurosurgery: Pediatrics, 2017 - thejns.org
OBJECTIVE To compare minimally invasive endoscopic and open surgical procedures, to
improve informed consent of parents, and to establish a baseline for further targeted …

Modelling human skull growth: a validated computational model

J Libby, A Marghoub, D Johnson… - Journal of the …, 2017 - royalsocietypublishing.org
During the first year of life, the brain grows rapidly and the neurocranium increases to about
65% of its adult size. Our understanding of the relationship between the biomechanical …

Regulation of cranial morphogenesis and cell fate at the neural crest-mesoderm boundary by engrailed 1

RA Deckelbaum, G Holmes, Z Zhao, C Tong… - …, 2012 - journals.biologists.com
The characterization of mesenchymal progenitors is central to understanding development,
postnatal pathology and evolutionary adaptability. The precise identity of the mesenchymal …

[HTML][HTML] Functional craniology and brain evolution: from paleontology to biomedicine

E Bruner, JM De la Cuétara, M Masters… - Frontiers in …, 2014 - frontiersin.org
Anatomical systems are organized through a network of structural and functional
relationships among their elements. This network of relationships is the result of evolution, it …

Developmental anatomy of craniofacial sutures

DP Rice - Craniofacial sutures, 2008 - karger.com
Sutures are fibrous joints in the vertebrate skull. They consist of two bone ends and
intervening fibrous tissue which differentiates from embryonic mesenchyme. Sutures are not …

Noonan syndrome is associated with enhanced pERK activity, the repression of which can prevent craniofacial malformations

T Nakamura, J Gulick, R Pratt… - Proceedings of the …, 2009 - National Acad Sciences
A gain of function mutation in SHP2, a protein phosphatase encoded by PTPN11, causes
Noonan syndrome (NS), which is characterized in part by developmental deficits in both the …

Visualizing the lateral somitic frontier in the Prx1Cre transgenic mouse

JL Durland, M Sferlazzo, M Logan… - Journal of …, 2008 - Wiley Online Library
Abstract Changes in the organization of the musculoskeletal system have accounted for
many evolutionary adaptations in the vertebrate body plan. The musculoskeletal system …

[HTML][HTML] Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology

G Holmes, G Rothschild, UB Roy, CX Deng… - Developmental …, 2009 - Elsevier
Activating mutations of FGFRs1–3 cause craniosynostosis (CS), the premature fusion of
cranial bones, in man and mouse. The mechanisms by which such mutations lead to CS …

Prx1 and 3.2 kb Col1a1 promoters target distinct bone cell populations in transgenic mice

Z Ouyang, Z Chen, M Ishikawa, X Yue, A Kawanami… - Bone, 2014 - Elsevier
Bones consist of a number of cell types including osteoblasts and their precursor cells at
various stages of differentiation. To analyze cellular organization within the bone, we …

The relationship between brachycephalic head features in modern Persian cats and dysmorphologies of the skull and internal hydrocephalus

MJ Schmidt, M Kampschulte… - Journal of veterinary …, 2017 - Wiley Online Library
Background Cat breeders observed a frequent occurrence of internal hydrocephalus in
Persian cats with extreme brachycephalic head morphology. Objective To investigate a …