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  1. 1
    Evaluation and management of nonsyndromic craniosynostosis

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

    Baskı/Yayın Bilgisi 2011
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  2. 2
    Three‐dimensional analysis of mandibular growth and tooth eruption

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

    Baskı/Yayın Bilgisi 2005
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  3. 3
    Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras.

    Constitutive receptor activation by Crouzon syndrome mutations in fibroblast growth factor receptor (FGFR)2 and FGFR2/Neu chimeras. Yazar: Brendan D. Galvin, Kristen C. Hart, April N. Meyer, Melanie K. Webster, Daniel J. Donoghue

    Baskı/Yayın Bilgisi 1996
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  4. 4
    Comparison of periodontal parameters in individuals with syndromic craniosynostosis

    Comparison of periodontal parameters in individuals with syndromic craniosynostosis Yazar: Paula Simões Múfalo, Rosane de Oliveira Fortes Kaizer, Gisele da Silva Dalben, Ana Lúcia Pompéia Fraga de Almeida

    Baskı/Yayın Bilgisi 2009
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  5. 5
    Intellectual development in Apert's syndrome: a long term follow up of 29 patients.

    Intellectual development in Apert's syndrome: a long term follow up of 29 patients. Yazar: M A Patton, Judith Goodship, Richard Hayward, Richard Lansdown

    Baskı/Yayın Bilgisi 1988
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  6. 6
    Apert syndrome: skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery

    Apert syndrome: skull abnormalities, brain malformations, neuropsychological evaluation and timing for surgery Yazar: Adriano Yacubian Fernandes

    Baskı/Yayın Bilgisi 2002
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  7. 7
    Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly.

    Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly. Yazar: Maria Rita Passos‐Bueno, A. Richieri‐Costa, Andréa L. Sertié, Alexander L.J. Kneppers

    Baskı/Yayın Bilgisi 1998
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  8. 8
    Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice

    Activation of p38 MAPK pathway in the skull abnormalities of Apert syndrome Fgfr2+P253R mice Yazar: Yingli Wang, Miao Sun, Victoria L Uhlhorn, Xueyan Zhou, Inga Peter, Neus Martínez‐Abadías, Cheryl A. Hill, Christopher J. Percival, Joan T. Richtsmeier, David L. Huso, Ethylin Wang Jabs

    Baskı/Yayın Bilgisi 2010
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  9. 9
    Beyond the closed suture in apert syndrome mouse models: Evidence of primary effects of FGFR2 signaling on facial shape at birth

    Beyond the closed suture in apert syndrome mouse models: Evidence of primary effects of FGFR2 signaling on facial shape at birth Yazar: Neus Martínez‐Abadías, Christopher J. Percival, Kristina Aldridge, Cheryl A. Hill, Timothy M. Ryan, Satama Sirivunnabood, Yingli Wang, Ethylin Wang Jabs, Joan T. Richtsmeier

    Baskı/Yayın Bilgisi 2010
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  10. 10
    FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models

    FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Yazar: Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier

    Baskı/Yayın Bilgisi 2011
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  11. 11
    06-P007 Different functional roles of FGF2 and FGF10 signaling in S252W FGFR2 cells: Impact in the Apert phenotype?

    06-P007 Different functional roles of FGF2 and FGF10 signaling in S252W FGFR2 cells: Impact in the Apert phenotype? Yazar: Erika Yeh, Daniele Yumi Sunaga, Roberto D. Fanganiello, Maria Rita Passos‐Bueno

    Baskı/Yayın Bilgisi 2009
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  12. 12
    Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome

    Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome Yazar: Erika Yeh, Roberto D. Fanganiello, Daniele Yumi Sunaga, Xueyan Zhou, G.H. Holmes, Kátia M. Rocha, Nivaldo Alonso, Hamilton Matushita, Yingli Wang, Ethylin Wang Jabs, Maria Rita Passos‐Bueno

    Baskı/Yayın Bilgisi 2013
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  13. 13
    Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses

    Impact of genetics on the diagnosis and clinical management of syndromic craniosynostoses Yazar: Nneamaka B. Agochukwu, Benjamin D. Solomon, Maximilian Muenke

    Baskı/Yayın Bilgisi 2012
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  14. 14
    ACROCEPHALY AND SCAPHOCEPHALY WITH SYMMETRICALLY DISTRIBUTED MALFORMATIONS OF THE EXTREMITIES

    ACROCEPHALY AND SCAPHOCEPHALY WITH SYMMETRICALLY DISTRIBUTED MALFORMATIONS OF THE EXTREMITIES Yazar: Edwards A. Park, G. Powers

    Baskı/Yayın Bilgisi 1920
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  15. 15
    Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome

    Loss of fibroblast growth factor receptor 2 ligand-binding specificity in Apert syndrome Yazar: Kai Yu, Andrew B. Herr, Gabriel Waksman, David M. Ornitz

    Baskı/Yayın Bilgisi 2000
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  16. 16
    Craniosynostosis genetics: The mystery unfolds

    Craniosynostosis genetics: The mystery unfolds Yazar: Inusha Panigrahi

    Baskı/Yayın Bilgisi 2011
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  17. 17
    Neuropsychological and phonological evaluation in the Apert's syndrome: study of two cases

    Neuropsychological and phonological evaluation in the Apert's syndrome: study of two cases Yazar: Sylvia Maria Ciasca, Ana Paula Serra de Araújo, Adriana Nobre de Paula Simão, Simone Aparecida Capellini, Paula Scalla Chiaratti, Edwaldo E. Camargo, Allan O. Santos, Elba Cristina Sá de Camargo

    Baskı/Yayın Bilgisi 2001
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  18. 18
    De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome

    De Novo Alu-Element Insertions in FGFR2 Identify a Distinct Pathological Basis for Apert Syndrome Yazar: Michael Oldridge, Elaine H. Zackai, Donna M. McDonald‐McGinn, Sachiko Iseki, Gillian Morriss‐Kay, Stephen R.F. Twigg, David Johnson, Steven A. Wall, Wen G. Jiang, Christiane Theda, Ethylin Wang Jabs, Andrew O.M. Wilkie

    Baskı/Yayın Bilgisi 1999
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  19. 19
    Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology

    Early onset of craniosynostosis in an Apert mouse model reveals critical features of this pathology Yazar: Greg Holmes, Gerson Rothschild, Upal Roy, Chu‐Xia Deng, Alka Mansukhani, Claudio Basilico

    Baskı/Yayın Bilgisi 2009
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  20. 20
    Mesodermal expression of Fgfr2 is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome

    Mesodermal expression of Fgfr2 is necessary and sufficient to induce craniosynostosis in a mouse model of Apert syndrome Yazar: Greg Holmes, Claudio Basilico

    Baskı/Yayın Bilgisi 2012
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