SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    M. R. Karolak, X. Yang, F. Elefteriou, FGFR1 signaling in hypertrophic chondrocytes is attenuated by the Ras-GAP neurofibromin during endochondral bone formation, Human Molecular Genetics, 2015, 24, 9, 2552

    CrossRef

  2. 2
    David A. Stevenson, David Little, Linlea Armstrong, Alvin H. Crawford, Deborah Eastwood, Jan M. Friedman, Tiziana Greggi, Gloria Gutierrez, Kim Hunter-Schaedle, David L. Kendler, Mateusz Kolanczyk, Fergal Monsell, Matthew Oetgen, B. Stephens Richards, Aaron Schindeler, Elizabeth K. Schorry, David Wilkes, David H. Viskochil, Feng-Chun Yang, Florent Elefteriou, Approaches to Treating NF1 Tibial Pseudarthrosis, Journal of Pediatric Orthopaedics, 2013, 33, 3, 269

    CrossRef

  3. 3
    R. Sharma, X. Wu, S. D. Rhodes, S. Chen, Y. He, J. Yuan, J. Li, X. Yang, X. Li, L. Jiang, E. T. Kim, D. A. Stevenson, D. Viskochil, M. Xu, F.-C. Yang, Hyperactive Ras/MAPK signaling is critical for tibial nonunion fracture in neurofibromin-deficient mice, Human Molecular Genetics, 2013, 22, 23, 4818

    CrossRef

  4. 4
    K. Bobotas, S. N. Lallos, V. S. Nikolaou, D. S. Κοrres, N. E. Efstathopoulos, Successful treatment of congenital pseudarthrosis of the tibia: still a challenge, European Journal of Orthopaedic Surgery & Traumatology, 2013, 23, S2, 303

    CrossRef

  5. 5
    K. Ono, M. R. Karolak, J. d. l. C. Ndong, W. Wang, X. Yang, F. Elefteriou, The Ras-GTPase activity of neurofibromin restrains ERK-dependent FGFR signaling during endochondral bone formation, Human Molecular Genetics, 2013, 22, 15, 3048

    CrossRef

  6. 6
    Donatella Granchi, Valentina Devescovi, Serena Rubina Baglio, Marina Magnani, Onofrio Donzelli, Nicola Baldini, A regenerative approach for bone repair in congenital pseudarthrosis of the tibia associated or not associated with type 1 neurofibromatosis: correlation between laboratory findings and clinical outcome, Cytotherapy, 2012, 14, 3, 306

    CrossRef

  7. 7
    Luigi Petramala, Sandra Giustini, Laura Zinnamosca, Cristiano Marinelli, Luciano Colangelo, Giuseppina Cilenti, Maria Chiara Formicuccia, Emilio D’Erasmo, Stefano Calvieri, Claudio Letizia, Bone mineral metabolism in patients with neurofibromatosis type 1 (von Recklingausen disease), Archives of Dermatological Research, 2012, 304, 4, 325

    CrossRef

  8. You have free access to this content8
    Junrong Ma, Mi Li, Janet Hock, Xijie Yu, Hyperactivation of mTOR critically regulates abnormal osteoclastogenesis in neurofibromatosis type 1, Journal of Orthopaedic Research, 2012, 30, 1
  9. You have free access to this content9
    Sang Min Lee, In Ho Choi, Dong Yeon Lee, Hye Ran Lee, Moon Seok Park, Won Joon Yoo, Chin Youb Chung, Tae-Joon Cho, Is double inactivation of the Nf1 gene responsible for the development of congenital pseudarthrosis of the tibia associated with NF1?, Journal of Orthopaedic Research, 2012, 30, 10
  10. 10
    Maria H. Alanne, Elina Siljamäki, Sirkku Peltonen, Kalervo Väänänen, Jolene J. Windle, Luis F. Parada, Jorma A. Määttä, Juha Peltonen, Phenotypic characterization of transgenic mice harboring Nf1+/− or Nf1−/− osteoclasts in otherwise Nf1+/+ background, Journal of Cellular Biochemistry, 2012, 113, 6
  11. 11
    Vivian Visnapuu, Sirkku Peltonen, Tapio Tammisalo, Juha Peltonen, Risto-Pekka Happonen, Radiographic Findings in the Jaws of Patients With Neurofibromatosis 1, Journal of Oral and Maxillofacial Surgery, 2012, 70, 6, 1351

    CrossRef

  12. 12
    Dong Yeon Lee, Tae-Joon Cho, Hye Ran Lee, Kang Lee, Hyuk Joo Moon, Moon Seok Park, Won Joon Yoo, Chin Youb Chung, In Ho Choi, Disturbed Osteoblastic Differentiation of Fibrous Hamartoma Cell from Congenital Pseudarthrosis of the Tibia Associated with Neurofibromatosis Type I, Clinics in Orthopedic Surgery, 2011, 3, 3, 230

    CrossRef

  13. 13
    W. Wang, J. S. Nyman, K. Ono, D. A. Stevenson, X. Yang, F. Elefteriou, Mice lacking Nf1 in osteochondroprogenitor cells display skeletal dysplasia similar to patients with neurofibromatosis type I, Human Molecular Genetics, 2011, 20, 20, 3910

    CrossRef

  14. 14
    Wei Zhang, Steven D. Rhodes, Liming Zhao, Yongzheng He, Yingze Zhang, Yong Shen, Dalong Yang, Xiaohua Wu, Xiaohong Li, Xianlin Yang, Su-Jung Park, Shi Chen, Charles Turner, Feng-Chun Yang, Primary osteopathy of vertebrae in a neurofibromatosis type 1 murine model, Bone, 2011, 48, 6, 1378

    CrossRef

  15. 15
    Eetu Heervä, Sirkku Peltonen, Pertti Pirttiniemi, Risto-Pekka Happonen, Vivian Visnapuu, Juha Peltonen, Short mandible, maxilla and cranial base are common in patients with neurofibromatosis 1, European Journal of Oral Sciences, 2011, 119, 2
  16. 16
    David A. Stevenson, Feng-Chun Yang, The musculoskeletal phenotype of the RASopathies, American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2011, 157, 2
  17. 17
    Eeva-Mari Jouhilahti, Sirkku Peltonen, Anthony M. Heape, Juha Peltonen, The Pathoetiology of Neurofibromatosis 1, The American Journal of Pathology, 2011, 178, 5, 1932

    CrossRef

  18. 18
    Donatella Granchi, Valentina Devescovi, Serena Rubina Baglìo, Elisa Leonardi, Onofrio Donzelli, Marina Magnani, Stefano Stilli, Armando Giunti, Nicola Baldini, Biological basis for the use of autologous bone marrow stromal cells in the treatment of congenital pseudarthrosis of the tibia, Bone, 2010, 46, 3, 780

    CrossRef

  19. 19
    Eetu Heervä, Maria H. Alanne, Sirkku Peltonen, Tommi Kuorilehto, Teuvo Hentunen, Kalervo Väänänen, Juha Peltonen, Osteoclasts in neurofibromatosis type 1 display enhanced resorption capacity, aberrant morphology, and resistance to serum deprivation, Bone, 2010, 47, 3, 583

    CrossRef

  20. 20
    Mohamed Lotfy, Risheng Xu, Matthew McGirt, Sameh Sakr, Basim Ayoub, Ali Bydon, Reconstruction of skull base defects in sphenoid wing dysplasia associated with neurofibromatosis I with titanium mesh, Clinical Neurology and Neurosurgery, 2010, 112, 10, 909

    CrossRef

  21. 21
    S. Pannier, Conférences d'enseignement 2010, 2010,

    CrossRef

  22. 22
    Hannu-Ville Leskelä, Tommi Kuorilehto, Juha Risteli, Jussi Koivunen, Marja Nissinen, Sirkku Peltonen, Pentti Kinnunen, Ludwine Messiaen, Petri Lehenkari, Juha Peltonen, Congenital pseudarthrosis of neurofibromatosis type 1: Impaired osteoblast differentiation and function and altered NF1 gene expression, Bone, 2009, 44, 2, 243

    CrossRef

  23. You have free access to this content23
    Florent Elefteriou, Mateusz Kolanczyk, Aaron Schindeler, David H. Viskochil, Janet M. Hock, Elizabeth K. Schorry, Alvin H. Crawford, Jan M. Friedman, David Little, Juha Peltonen, John C. Carey, David Feldman, Xijie Yu, Linlea Armstrong, Patricia Birch, David L. Kendler, Stefan Mundlos, Feng-Chun Yang, Gina Agiostratidou, Kim Hunter-Schaedle, David A. Stevenson, Skeletal abnormalities in neurofibromatosis type 1: Approaches to therapeutic options, American Journal of Medical Genetics Part A, 2009, 149A, 10
  24. 24
    Ozgur Duman, Sebahat Ozdem, Doga Turkkahraman, Nihal Dundar Olgac, Firat Gungor, Senay Haspolat, Bone metabolism markers and bone mineral density in children with neurofibromatosis type-1, Brain and Development, 2008, 30, 9, 584

    CrossRef

  25. 25
    Aaron Schindeler, David G. Little, Recent insights into bone development, homeostasis, and repair in type 1 neurofibromatosis (NF1), Bone, 2008, 42, 4, 616

    CrossRef

  26. 26
    S. Alwan, L. Armstrong, H. Joe, P.H. Birch, J. Szudek, J.M. Friedman, Associations of osseous abnormalities in Neurofibromatosis 1, American Journal of Medical Genetics Part A, 2007, 143A, 12
  27. 27
    David A. Stevenson, David H. Viskochil, John C. Carey, Neurofibromatosis type 1 is a genetic skeletal disorder, American Journal of Medical Genetics Part A, 2007, 143A, 17
  28. 28
    Vivian Visnapuu, Sirkku Peltonen, Tero Ellilä, Eero Kerosuo, Kalervo Väänänen, Risto-Pekka Happonen, Juha Peltonen, Periapical cemental dysplasia is common in women with NF1, European Journal of Medical Genetics, 2007, 50, 4, 274

    CrossRef

  29. 29
    Marwan Shinawi, Millan S. Patel, Preaxial polydactyly in neurofibromatosis 1, Clinical Dysmorphology, 2007, 16, 3, 193

    CrossRef

  30. 30
    Florent Elefteriou, M. Douglas Benson, Hideaki Sowa, Michael Starbuck, Xiuyun Liu, David Ron, Luis F. Parada, Gerard Karsenty, ATF4 mediation of NF1 functions in osteoblast reveals a nutritional basis for congenital skeletal dysplasiae, Cell Metabolism, 2006, 4, 6, 441

    CrossRef

  31. 31
    Paul C. Edwards, John E. Fantasia, Tarnjit Saini, Tracey J. Rosenberg, Stephen A. Sachs, Salvatore Ruggiero, Clinically aggressive central giant cell granulomas in two patients with neurofibromatosis 1, Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology, 2006, 102, 6, 765

    CrossRef

  32. 32
    David A. Stevenson, Holly Zhou, Shadi Ashrafi, Ludwine M. Messiaen, John C. Carey, Jacques L. D’Astous, Stephen D. Santora, David H. Viskochil, Double Inactivation of NF1 in Tibial Pseudarthrosis, The American Journal of Human Genetics, 2006, 79, 1, 143

    CrossRef

  33. 33
    AB Trovó-Marqui, EH Tajara, Neurofibromin: a general outlook, Clinical Genetics, 2006, 70, 1
  34. 34
    Aaron Schindeler, David G Little, Ras-MAPK Signaling in Osteogenic Differentiation: Friend or Foe?, Journal of Bone and Mineral Research, 2006, 21, 9
  35. 35
    Tommi Kuorilehto, Pentti Kinnunen, Marja Nissinen, Maria Alanne, Hannu-Ville Leskelä, Petri Lehenkari, Juha Peltonen, Vasculopathy in two cases of NF1-related congenital pseudarthrosis, Pathology - Research and Practice, 2006, 202, 9, 687

    CrossRef

  36. 36
    T. Kuorilehto, M. Pöyhönen, R. Bloigu, J. Heikkinen, K. Väänänen, Juha Peltonen, Decreased bone mineral density and content in neurofibromatosis type 1: Lowest local values are located in the load-carrying parts of the body, Osteoporosis International, 2005, 16, 8, 928

    CrossRef

  37. 37
    Marga Lammert, Martin Kappler, Victor-Felix Mautner, Kurt Lammert, Stephan Störkel, Jan M. Friedman, Derek Atkins, Decreased bone mineral density in patients with neurofibromatosis 1, Osteoporosis International, 2005, 16, 9, 1161

    CrossRef

  38. 38
    Joseph R Tucci, Paget disease of bone, Current Opinion in Endocrinology & Diabetes, 2004, 11, 6, 321

    CrossRef