Suchergebnisse

Pfeiffer syndrome type 2: case report von Oyamada, Maria Kiyoko, Ferreira, Haideé Salgado Alonso, Hoff, Marcelo

Volltext

Long-term developmental follow-up in children with nonsyndromic craniosynostosis von Maggie Bellew, Paul Chumas

Volltext Volltext

Roles of FGF signaling in skeletal development and human genetic diseases von Chen Lin

Volltext Volltext

Evaluation and management of nonsyndromic craniosynostosis von Fabiana Ursitti, Teresa Fadda, Laura Papetti, Mario Pagnoni, Francesco Nicita, Gian Domenico Iannetti, Alberto Spalice

Volltext Volltext

Molecular aspects of craniosynostoses: implications in diagnosis and genetic counseling von Maria Rita Passos‐Bueno, Fernanda Sarquis Jehee, Lúcia Maria Libório Armelin

Volltext Volltext

Growth of the normal skull vault and its alteration in craniosynostosis: insights from human genetics and experimental studies von Gillian Morriss‐Kay, Andrew O.M. Wilkie

Volltext Volltext

Early treatment of coronal synostosis with endoscopy-assisted craniectomy and postoperative cranial orthosis therapy: 16-year experience von David F. Jimenez, Constance M. Barone

Volltext Volltext

Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability von Stephen R.F. Twigg, Jennifer Forecki, Jacqueline A.C. Goos, Ivy C A Richardson, A. Jeannette M. Hoogeboom, Ans M.W. van den Ouweland, Sigrid M.A. Swagemakers, Maarten H. Lequin, Daniel Van Antwerp, Simon J. McGowan, Isabelle Westbury, Kerry A. Miller, Steven A. Wall, Peter J. van der Spek, Irene M.J. Mathijssen, Erwin Pauws, Christa Merzdorf, Andrew O.M. Wilkie

Volltext Volltext

Duration of exposure to cranial vault surgery: associations with neurodevelopment among children with single‐suture craniosynostosis von Heather Naumann, Charles M. Haberkern, Kristen E. Pietila, Craig B. Birgfeld, Jacqueline R. Starr, Kathleen A. Kapp‐Simon, Richard A. Hopper, Matthew L. Speltz

Volltext

<i>FGFR2</i>mutation in 46,XY sex reversal with craniosynostosis von Stefan Bagheri‐Fam, Makoto Ono, Li Li, Liang Zhao, Janelle Ryan, Raymond Lai, Y Katsura, Fernando J. Rossello, Peter Koopman, Gerd Scherer, Oliver Bartsch, Jacob V.P. Eswarakumar, Vincent R. Harley

Volltext Volltext

Three‐dimensional analysis of mandibular growth and tooth eruption von Søren Krarup, Tron A. Darvann, P. Larsen, Jeffrey L. Marsh, Sven Kreiborg

Volltext Volltext

Augmentation of smad-dependent BMP signaling in neural crest cells causes craniosynostosis in mice von Yoshihiro Komatsu, Paul B. Yu, Nobuhiro Kamiya, Haichun Pan, Tomokazu Fukuda, Gregory J. Scott, Manas K. Ray, Ken–ichi Yamamura, Yuji Mishina

Volltext Volltext

A Genetic-Pathophysiological Framework for Craniosynostosis von Stephen R.F. Twigg, Andrew O.M. Wilkie

Volltext Volltext

The preoperative incidence of raised intracranial pressure in nonsyndromic sagittal craniosynostosis is underestimated in the literature von Steven A. Wall, Gregory P.L. Thomas, David Johnson, Jo C. Byren, Jayaratnam Jayamohan, Shailendra Magdum, David J. McAuley, Peter G. Richards

Volltext Volltext

Attention and executive function in children with and without single-suture craniosynostosis von Brent R. Collett, Kathleen A. Kapp‐Simon, Erin R. Wallace, Mary Michaeleen Cradock, Lauren Buono, Matthew L. Speltz

Volltext

Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families von Ramy M. Hanna, Sarah Marsh, D. Swistun, Lihadh Al‐Gazali, Maha S. Zaki, Ghada M. H. Abdel‐Salam, Asma Al-Tawari, Lailá Bastaki, Hülya Kayserili, A Rajab, B. Boglárka, Ralf Dietrich, William B. Dobyns, C. L. Truwit, Shifteh Sattar, Nathaniel A. Chuang, Elliott H. Sherr, Joseph G. Gleeson

Volltext

FGF signaling: its role in bone development and human skeleton diseases von Nan Su

Volltext Volltext

Tissue‐specific responses to aberrant FGF signaling in complex head phenotypes von Neus Martínez‐Abadías, Susan M. Motch, Talia L. Pankratz, Yingli Wang, Kristina Aldridge, Ethylin Wang Jabs, Joan T. Richtsmeier

Volltext

Familial incidence and associated symptoms in a population of individuals with nonsyndromic craniosynostosis von Jaclyn Greenwood, Pamela Flodman, Kathryn Osann, Simeon A. Boyadjiev, Virginia Kimonis

Volltext Volltext

Further Analysis of the Crouzon Mouse: Effects of the FGFR2C342Y Mutation Are Cranial Bone–Dependent von Jin Liu, Hwa Kyung Nam, Estee Wang, Nan Hatch

Volltext