Thematische Bibliographien / Craniofacial growth

Inhaltsverzeichnis

  1. Zeitschriftenartikel
  2. Dissertationen
  3. Bücher
  4. Buchteile
  5. Konferenzberichte

Auswahl der wissenschaftlichen Literatur zum Thema „Craniofacial growth“

Autor: Grafiati
Veröffentlicht am 4. Juni 2021
Zuletzt aktualisiert am 12. Februar 2022

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Zeitschriftenartikel zum Thema "Craniofacial growth"

1

Figueroa, Alvaro A., und Hans Friede. „Craniofacial Growth in Unoperated Craniofacial Malformations“. Cleft Palate-Craniofacial Journal 37, Nr. 5 (September 2000): 1–15. http://dx.doi.org/10.1597/1545-1569_2000_037_0431_cgiucm_2.0.co_2.

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Figueroa, Alvaro A., und Hans Friede. „Craniofacial Growth in Unoperated Craniofacial Malformations“. Cleft Palate-Craniofacial Journal 37, Nr. 5 (September 2000): 431. http://dx.doi.org/10.1597/1545-1569(2000)037<0431:cgiucm>2.0.co;2.

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Friede, Hans. „Abnormal craniofacial growth“. Acta Odontologica Scandinavica 53, Nr. 3 (Januar 1995): 203–9. http://dx.doi.org/10.3109/00016359509005973.

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Sperber, Geoffrey H. „Fundamentals of Craniofacial Growth“. Cleft Palate-Craniofacial Journal 35, Nr. 3 (Mai 1998): 272–75. http://dx.doi.org/10.1597/1545-1569(1998)035<0272:focg>2.3.co;2.

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Ohman, James C., und Joan T. Richtsmeier. „Perspectives on Craniofacial Growth“. Clinics in Plastic Surgery 21, Nr. 4 (Oktober 1994): 489–99. http://dx.doi.org/10.1016/s0094-1298(20)30718-5.

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Castaldo, Gennaro, und Francesco Cerritelli. „Craniofacial growth: evolving paradigms“. CRANIO® 33, Nr. 1 (22.04.2014): 23–31. http://dx.doi.org/10.1179/0886963414z.00000000042.

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Laurenzo, J. F., J. W. Canady, B. Zimmerman, R. J. H. Smith und Barry L. Eppley. „Craniofacial Growth in Rabbits“. Journal of Craniofacial Surgery 8, Nr. 1 (Januar 1997): 81. http://dx.doi.org/10.1097/00001665-199701000-00027.

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Bradrick, J. P. „Perspectives on craniofacial growth“. Journal of Oral and Maxillofacial Surgery 53, Nr. 5 (Mai 1995): 631. http://dx.doi.org/10.1016/0278-2391(95)90096-9.

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Gans, Carl. „Craniofacial growth, evolutionary questions“. Development 103, Supplement (01.09.1988): 3–15. http://dx.doi.org/10.1242/dev.103.supplement.3.

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Understanding the growth of craniofacial systems in mammals, particularly in man, has always posed problems. Such craniofacial systems are formed ontogenetically of multiple tissue types, and the contributions of these tissues do not obviously match the divisions of adult skeletal elements (see Thorogood, this volume). Even the kind and number of segments in the head region continue to attract attention (Maderson, 1987). Furthermore, craniofacial systems appear to show trends toward an unusual number of developmental abnormalities or teratologies. Many of these teratologies suggest that we are not looking at a simple coordinated whole (Salinas, 1982; Shprintzen, 1982); rather, it seems as if multiple cranial and facial components incur differential growth either symmetrically or asymmetrically. It seems instructive to treat the basis of this curious array of complications from an evolutionary viewpoint, considering two aspects, adaptation and history.
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Funatsu, Minayo, Koshi Sato und Hideo Mitani. „Effects of Growth Hormone on Craniofacial Growth“. Angle Orthodontist 76, Nr. 6 (01.11.2006): 970–77. http://dx.doi.org/10.2319/011905-17.

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Abstract Objective: This study determined the effects of growth hormone (GH) therapy on craniofacial growth in idiopathic growth hormone deficiency (GHD). Materials and Methods: Fifty-seven patients (33 boys and 24 girls; age range 4.5 to 16.7 years) with GHD were investigated and categorized into three groups according to the duration of GH therapy: the untreated group, the short-term therapy group, and the long-term therapy group. Their lateral cephalometric radiographs were studied, and craniofacial measurements were assessed by age and sex by using matched standard deviation scores. Results: In the untreated group, the anterior cranial base, total facial height, maxillary length, mandibular total length, mandibular body length, and ramus height were smaller than the standard values. In comparison with the untreated group, the long-term therapy group had a significantly larger upper facial height (P &lt; .05), maxillary length (P &lt; .01), and ramus height (P &lt; .01) measurements. Conclusions: Children who received long-term GH replacement therapy showed increased growth of the craniofacial skeleton, especially the maxilla and ramus. These findings suggest that GH accelerates craniofacial development, which improves occlusion and the facial profile.
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Dissertationen zum Thema "Craniofacial growth"

1

Meyer, Crystal Rose Foster. „Craniofacial growth and development in the Arikara“. Laramie, Wyo. : University of Wyoming, 2008. http://proquest.umi.com/pqdweb?did=1663116451&sid=1&Fmt=2&clientId=18949&RQT=309&VName=PQD.

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Khonsari, Roman Hossein. „Mechanical forces in craniofacial development and growth“. Thesis, King's College London (University of London), 2013. http://kclpure.kcl.ac.uk/portal/en/theses/mechanical-forces-in-craniofacial-development-and-growth(12bf47d0-2a8a-4b18-9f87-c88978619f36).html.

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Mechanical forces are known to interact with developmental dynamics and post-natal growth processes. The aim of this thesis was to investigate the role of mechanical force in craniofacial development and growth at the molecular, cellular and organ levels by using di erent models. The craniofacial phenotype of mice with a mesenchymal conditional deletion of Pkd2 (Pkd2fl=fl;Wnt1-Cre) was examined using histology, -CT imaging, in situ hybridisation and synchrotron X-ray microtomography. It was shown that Pkd2fl=fl;Wnt1-Cre mice present growth anomalies mostly located in organs subjected to post-natal mechanical stress. The facial features of patients with PKD1 mutations were then studied by 3D photography and dense surface modelling. Speci c facial features in these patients were identi ed and indicated that PKD genes may be involved in human craniofacial growth. In order to further illustrate the interactions between craniofacial growth and external constraints, the craniofacial structure of a series of skulls with intentional deformations was examined by 3D cephalometry, wall thickness analysis and haptic-aided semi-automatic segmentation. Intentional modi cations of the skull vault induced changes in the shape of the orbits and the maxillary sinuses, as well as local changes in vault bone thickness. The e ects of external constraints on soft-tissues were studied through the brain anomalies in four fetuses with extreme skull malformations occurring in FGFR2-related craniosynostoses. Characteristic brain anomalies were described in FGFR2-related craniosynostoses, that were related both to FGFR2 hyperactivation and to abnormal mechanical stress. Mechanotransduction at the cellular level was investigated using a mathematical model for bone deposition in sutures taking into account the data provided by synchrotron X-ray microtomography. Based on these theoretical investigations, it was found that bone deposition in sutures was driven by a mechanics-dependent non-linear instability also giving account for the appearance of sutural interdigitations. Synchrotron microtomography also appeared as a reliable tool for the study of bone microanatomy. Finally, the evolution and development the bucco-hypophyseal canal, an organ that may be involved in mechanosensation, was studied using sonic-pathway related mutant mice, and the maintenance of this canal in development and evolution was related to modulations in sonic-hedgehog pathway related genes. A new technique for the high-resolution imaging of embryonic soft-tissues was also described. Together, these results show that mechanical forces shape craniofacial development and growth at the molecular, cellular and organ levels. The understanding of the processes involved in the recording and the transduction of external forces is of interest in the treatment of congenital and acquired craniofacial disorders.
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Frederickson, Joseph Alexander. „Craniofacial Ontogeny In Centrosaurus apertus“. Master's thesis, Temple University Libraries, 2013. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/229570.

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Geology
M.S.
Centrosaurus apertus, a large bodied ceratopsid from the Late Cretaceous of North America, is one of the most common fossils recovered from the Belly River Group of Canada. This fossil record shows a wide diversity in morphology and size, with specimens ranging from putative juveniles to fully-grown individuals. The goal of this study was to reconstruct the ontogenetic changes that occur in the craniofacial skeleton of C. apertus through a quantitative cladistic analysis. Forty-seven cranial specimens were independently coded in separate data matrices for 80 hypothetical multistate growth characters and 130 binary growth characters. Analyses were executed under heuristic searches with all characters unordered and equally weighted. Both analyses yielded the max-limit of 100,000 most parsimonious saved trees and the strict consensus collapsed into large polytomies, so a 50% majority rule consensus was obtained to recover structure in the data. In order to reduce conflict resulting from missing data, fragmentary individuals were removed from the data matrices and the analyses were rerun under a branch and bound search for both multistate and binary data sets. The multistate analysis yielded a single most parsimonious tree, while the binary analysis yielded thirteen equally most parsimonious trees. A strict consensus of the thirteen trees collapsed into a polytomy in the most mature individuals, but the resolved portion is consistent with the tree recovered in the multistate analysis. Among both the complete and the reduced data sets the multistate analyses recovered a shorter tree with a higher consistency index (CI) than the additive binary data sets. The arrangement within the trees show a progression of specimens with a recurved nasal horn in the least mature individuals, followed by specimens with straight nasal horns in relatively more mature individuals, and finally specimens with procurved nasal horns in the most mature individuals. The supraorbital unit, however, shows no consistent pattern of development. The parietal horns develop relatively early, becoming long and curved in some of the least mature skulls. In relatively mature individuals these structures resorb, leaving the horns with a withered appearance. This resorption continues in the most mature individuals until much of the horn is gone. The development of the parietal and nasal horns may represent a heterochronic process (i.e. peramorphosis) in centrosaurine evolution, where juvenile morphology is similar to that of basal neoceratopsians, whereas the adult condition is comparable to that of derived centrosaurines. Bone textural changes were found to be sufficient proxies for relative maturity in individuals that have not reached adult size. Additionally, frill size is congruent with relative maturity status and makes an acceptable proxy for ontogenetic status, especially in smaller individuals. In adult-sized individuals, the fusion of the epoccipitals and the orientation of the nasal horn are the best indicators of relative maturity. There is no clear evidence for sexually specific characters or sexual size dimorphism in C. apertus.
Temple University--Theses
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Britto, Jonathan Anthony. „Syndromic craniofacial dysostosis : from genotype to phenotype: studies of FGFR gene expression in human craniofacial development and craniosynostosis“. Thesis, University College London (University of London), 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268446.

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Yamanaka, Shigeki. „Circulatory CNP rescues craniofacial hypoplasia in achondroplasia“. Kyoto University, 2017. http://hdl.handle.net/2433/228228.

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Stewart, Amanda Lynn. „Timing of Protein Malnutrition and its Effects on Craniofacial Growth“. University of Cincinnati / OhioLINK, 2005. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1115750961.

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Wong, Hoi-leong Xavier, und 王凱亮. „The functional crosstalk between MT1-MMP and ADAMs in craniofacial & vascular development“. Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2013. http://hdl.handle.net/10722/197072.

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Chan, Kui-ming. „MT1-MMP in craniofacial development and FGF signaling“. Click to view the E-thesis via HKUTO, 2007. http://sunzi.lib.hku.hk/hkuto/record/b40203645.

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Patterson, Jennifer. „Regenerative matrices for oriented bone growth in craniofacial and dental repair /“. Thesis, Connect to this title online; UW restricted, 2007. http://hdl.handle.net/1773/8018.

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Bandeen, Timothy C. „Effects of sickle cell disease on growth of the craniofacial complexes. /“. View the abstract Download the full-text PDF version View the full-text HTML version, 2005. http://etd.utmem.edu/ABSTRACTS/2005%5F001%5Fbandeen%5Findex.html.

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Thesis (M.S.)--University of Tennessee Health Sciences Center, 2005.
Spine title: Effects of sickle cell disease on growth of the craniofacial complexes. Appendices: leaves 162-414 Bibliography: leaves 145-161.
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Bücher zum Thema "Craniofacial growth"

1

G, Sarnat Bernard. Craniofacial biology and craniofacial surgery. Hackensack, N.J: World Scientific, 2010.

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G, Sarnat Bernard. Craniofacial biology and craniofacial surgery. New Jersey: World Scientific, 2009.

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Meikle, Murray C. Craniofacial development, growth and evolution. Bressingham: Bateson, 2002.

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A synopsis of craniofacial growth. 2. Aufl. Norwalk, Ct: Appleton & Lange, 1988.

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1965-, Bradley James P., Hrsg. Craniofacial biology and craniofacial surgery. New Jersey: World Scientific, 2009.

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G, Sarnat Bernard. Essays on craniofacial biology and craniofacial surgery. New Jersey: World Scientific, 2009.

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Behrents, Rolf Gordon. Growth in the aging craniofacial skeleton. Ann Arbor, Mich: Center for Human Growth and Development, University of Michigan, 1985.

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Sperber, Geoffrey H. Craniofacial embryogenetics and development. 2. Aufl. Shelton, CT: People's Medical Pub. House USA, 2010.

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Kent, Raymond D. Development of the craniofacial-oral-laryngeal anatomy. San Diego: Singular Pub. Group, 1995.

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Behrents, Rolf Gordon. An Atlas of growth in the aging craniofacial skeleton. Ann Arbor, Mich: Center for Human Growth and Development, University of Michigan, 1985.

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Buchteile zum Thema "Craniofacial growth"

1

Cohen, Steven R., und Andrew Wexler. „Craniofacial Growth“. In Fundamentals of Maxillofacial Surgery, 28–52. New York, NY: Springer New York, 1997. http://dx.doi.org/10.1007/978-1-4612-1898-2_2.

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David, David J., David C. Hemmy und Rodney D. Cooter. „Growth Disorders“. In Craniofacial Deformities, 101–9. New York, NY: Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3232-2_7.

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Rawlins, Joseph T., und Lynne A. Opperman. „Tgf-&Bg;; Regulation of Suture Morphogenesis and Growth“. In Craniofacial Sutures, 178–96. Basel: KARGER, 2008. http://dx.doi.org/10.1159/000115038.

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Ramirez-Yañez, German O. „Craniofacial Growth and Development“. In Sleep Disorders in Pediatric Dentistry, 39–56. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-13269-9_3.

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Colcleugh, Robert G., und Oleh Antonyshin. „Vascularized Cranial Bone Grafts and Growth — An Experimental Study“. In Craniofacial Surgery, 390–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-82875-1_71.

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Hajihosseini, Mohammad K. „Fibroblast Growth Factor Signaling in Cranial Suture Development and Pathogenesis“. In Craniofacial Sutures, 160–77. Basel: KARGER, 2008. http://dx.doi.org/10.1159/000115037.

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Koerich, Leonardo, Eser Tufekci und Steven J. Lindauer. „3D Imaging to Assess Growth and Treatment Effects“. In Craniofacial 3D Imaging, 51–69. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-00722-5_3.

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Kim, Su-Jung. „Craniofacial Growth Modification for OSA Children“. In Orthodontics in Obstructive Sleep Apnea Patients, 41–58. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-24413-2_4.

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Gill, Daljit S., und Farhad B. Naini. „An Introduction to Human Craniofacial Growth and Development“. In Orthodontics: Principles and Practice, 1–16. West Sussex, UK: John Wiley & Sons, Ltd,., 2013. http://dx.doi.org/10.1002/9781118785041.ch1.

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Lee, Christopher S. D., Christopher D. Hermann, Rolando Gittens, Rene Olivares-Navarrete, Zvi Schwartz und Barbara D. Boyan. „Bone Bioengineering: Scaffolds, Growth Factors, and Stem Cells“. In Stem Cells in Craniofacial Development and Regeneration, 339–66. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118498026.ch19.

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Konferenzberichte zum Thema "Craniofacial growth"

1

Salama, Mostafa A., und Basma Hathout. „An Ensemble Feature Ranking Technique for the Analysis of the Craniofacial Growth“. In 2020 IEEE 5th International Conference on Signal and Image Processing (ICSIP). IEEE, 2020. http://dx.doi.org/10.1109/icsip49896.2020.9339386.

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Friess, Martin. „The study of craniofacial growth patterns using 3D laser scanning and geometric morphometrics“. In Electronic Imaging 2006, herausgegeben von Brian D. Corner, Peng Li und Matthew Tocheri. SPIE, 2006. http://dx.doi.org/10.1117/12.654898.

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