Ilan Golan

Summary

Affiliation: University of Regensburg
Country: Germany

Publications

  1. ncbi A novel missense mutation of the CBFA1 gene in a family with cleidocranial dysplasia (CCD) and variable expressivity
    I Golan
    Department of Orthodontics, University of Regensburg, Germany
    J Craniofac Genet Dev Biol 20:113-20. 2000
  2. ncbi [Anomalies of the skull in cleidocranial dysplasia]
    I Golan
    Poliklinik für Kieferorthopädie des Klinikum der Universität Regensburg, Regensburg
    HNO 52:1061-6. 2004
  3. ncbi [Inter- and intrafamilial expression of cleidocranial dysostosis]
    I Golan
    University of Regensburg, Department of Orthodontics, Germany
    Orthod Fr 74:7-13. 2003
  4. ncbi Dentomaxillofacial variability of cleidocranial dysplasia: clinicoradiological presentation and systematic review
    I Golan
    Department of Orthodontics, Division of Craniofacial Genetics, University of Regensburg, 93053 Regensburg, Germany
    Dentomaxillofac Radiol 32:347-54. 2003
  5. ncbi Early craniofacial signs of cleidocranial dysplasia
    I Golan
    Department of Orthodontics, Division Craniofacial Genetics, University of Regensburg, Germany
    Int J Paediatr Dent 14:49-53. 2004
  6. ncbi [Symptoms and signs in cleidocranial dysplasia (CCD)]
    I Golan
    Poliklinik für Kieferorthopädie, Klinikum der Universitat Regensburg
    Z Orthop Ihre Grenzgeb 141:336-40. 2003
  7. ncbi Evidence of intrafamilial variability of CBFA1/RUNX2 expression in cleidocranial dysplasia--a family study
    Ilan Golan
    Department of Orthodontics, University of Regensburg, Germany
    J Orofac Orthop 63:190-8. 2002
  8. ncbi Radiological findings and molecular genetic confirmation of cleidocranial dysplasia
    Ilan Golan
    Department of Orthodontics, Division Craniofacial Genetics
    Clin Radiol 57:525-9. 2002
  9. ncbi [Cleidocranial dysplasia. Description and analysis of a patient cohort]
    U Baumert
    AG Kraniofaziale Genetik Tissue Engineering, BioPark Regensburg, Zentrum für Medizinische Biotechnologie, Josef Engert Strasse 9, 93051 Regensburg, Germany
    Mund Kiefer Gesichtschir 10:385-93. 2006
  10. ncbi Pressure simulation of orthodontic force in osteoblasts: a pilot study
    U Baumert
    Department of Orthodontics, Center for Craniofacial Genetics, University of Regensburg, Germany
    Orthod Craniofac Res 7:3-9. 2004

Detail Information

Publications16

  1. ncbi A novel missense mutation of the CBFA1 gene in a family with cleidocranial dysplasia (CCD) and variable expressivity
    I Golan
    Department of Orthodontics, University of Regensburg, Germany
    J Craniofac Genet Dev Biol 20:113-20. 2000
    ..To conclude, a missense mutation in the CBFA1 gene was detected in a family with variably expressed CCD syndrome. A detailed clinical examination is necessary to detect minimally affected gene mutation carriers...
  2. ncbi [Anomalies of the skull in cleidocranial dysplasia]
    I Golan
    Poliklinik für Kieferorthopädie des Klinikum der Universität Regensburg, Regensburg
    HNO 52:1061-6. 2004
    ..The description of the otorhinolaryngeal and craniofacial anomalies in patients with cleidocranial dysplasia...
  3. ncbi [Inter- and intrafamilial expression of cleidocranial dysostosis]
    I Golan
    University of Regensburg, Department of Orthodontics, Germany
    Orthod Fr 74:7-13. 2003
    ..The results of our craniofacial examination are in agreement with the numerous descriptions in the literature. This study accents the difficulty in establishing a clinical based diagnosis due to the wide variability...
  4. ncbi Dentomaxillofacial variability of cleidocranial dysplasia: clinicoradiological presentation and systematic review
    I Golan
    Department of Orthodontics, Division of Craniofacial Genetics, University of Regensburg, 93053 Regensburg, Germany
    Dentomaxillofac Radiol 32:347-54. 2003
    ..The aim of this study was to determine the clinical and radiological presentation of cleidocranial dysplasia (CCD) in our patient group and to compare them with other reported cases by a systematic review (SR) of the literature...
  5. ncbi Early craniofacial signs of cleidocranial dysplasia
    I Golan
    Department of Orthodontics, Division Craniofacial Genetics, University of Regensburg, Germany
    Int J Paediatr Dent 14:49-53. 2004
    ..The aim of this study is to describe the initial craniofacial findings in patients with CCD in order to categorise their reliability for early detection...
  6. ncbi [Symptoms and signs in cleidocranial dysplasia (CCD)]
    I Golan
    Poliklinik für Kieferorthopädie, Klinikum der Universitat Regensburg
    Z Orthop Ihre Grenzgeb 141:336-40. 2003
    ..Occurrence of main symptoms and the rate of spontaneous mutations in patients with cleidocranial dysplasia...
  7. ncbi Evidence of intrafamilial variability of CBFA1/RUNX2 expression in cleidocranial dysplasia--a family study
    Ilan Golan
    Department of Orthodontics, University of Regensburg, Germany
    J Orofac Orthop 63:190-8. 2002
    ..To investigate the phenotypical expression of an identical mutation of the CBFA1/RUNX2 gene within a family with cleidocranial dysplasia...
  8. ncbi Radiological findings and molecular genetic confirmation of cleidocranial dysplasia
    Ilan Golan
    Department of Orthodontics, Division Craniofacial Genetics
    Clin Radiol 57:525-9. 2002
  9. ncbi [Cleidocranial dysplasia. Description and analysis of a patient cohort]
    U Baumert
    AG Kraniofaziale Genetik Tissue Engineering, BioPark Regensburg, Zentrum für Medizinische Biotechnologie, Josef Engert Strasse 9, 93051 Regensburg, Germany
    Mund Kiefer Gesichtschir 10:385-93. 2006
    ..CCD is possibly the only general syndrome that can be diagnosed based on the dental findings alone. CCD correlates with mutations in the RUNX2 gene...
  10. ncbi Pressure simulation of orthodontic force in osteoblasts: a pilot study
    U Baumert
    Department of Orthodontics, Center for Craniofacial Genetics, University of Regensburg, Germany
    Orthod Craniofac Res 7:3-9. 2004
    ..To elucidate the RUNX2 gene expression induction in human osteoblasts after mechanical loading...
  11. ncbi Atypical expression of cleidocranial dysplasia: clinical and molecular-genetic analysis
    I Golan
    Department of Orthodontics, University of Regensburg, Germany
    Orthod Craniofac Res 5:243-9. 2002
    ..We conclude that molecular-genetic analysis may be a helpful tool in the differential diagnosis of many congenital diseases such as CCD and RTS...
  12. ncbi Cleidocranial dysplasia: molecular genetic analysis and phenotypic-based description of a Middle European patient group
    Uwe Baumert
    Department of Orthodontics, Center for Craniofacial Genetics, University of Regensburg, Regensburg, Germany
    Am J Med Genet A 139:78-85. 2005
    ..Analysis of the mutation patterns revealed that mutational frequency and types of mutations found can be attributed to the gene's structure and function...
  13. ncbi Common mutations and independent assortment of CCD
    Uwe Baumert
    J Oral Pathol Med 31:567-8. 2002
  14. ncbi Clarification of data reported in "cleidocranial dysplasia: molecular genetic analysis and phenotypic-based description of a Middle European patient group" (AJMG 139A:78-85)
    Uwe Baumert
    Am J Med Genet A 140:1030. 2006
  15. ncbi [On the effect of mutations of the fibroblast growth factor receptors as exemplified by three cases of craniosynostoses]
    Markus N Preising
    Abteilung für Kinderophthalmologie, Strabismologie und Ophthalmogenetik, Klinikum der Universitat Regensburg
    Klin Monbl Augenheilkd 220:669-81. 2003
    ....
  16. ncbi Expression of tropoelastin in human periodontal ligament fibroblasts after simulation of orthodontic force
    Meir Redlich
    Department of Orthodontics, Hadassah Faculty of Dental Medicine, Hebrew University, founded by the Alpha Omega Fraternity, PO Box 12277, Jerusalem 91220, Israel
    Arch Oral Biol 49:119-24. 2004
    ....