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Bilateral Cavernous Internal Carotid Aneurysms in a Child with Juvenile Paget Disease and Osteoprotegerin Deficiency

C.A. Allen, B.L. Hart, C.L. Taylor and C.L. Clericuzio
American Journal of Neuroradiology January 2008, 29 (1) 7-8; DOI: https://doi.org/10.3174/ajnr.A0755
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C.L. Clericuzio
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American Journal of Neuroradiology: 29 (1)
American Journal of Neuroradiology
Vol. 29, Issue 1
January 2008
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C.A. Allen, B.L. Hart, C.L. Taylor, C.L. Clericuzio
Bilateral Cavernous Internal Carotid Aneurysms in a Child with Juvenile Paget Disease and Osteoprotegerin Deficiency
American Journal of Neuroradiology Jan 2008, 29 (1) 7-8; DOI: 10.3174/ajnr.A0755

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Bilateral Cavernous Internal Carotid Aneurysms in a Child with Juvenile Paget Disease and Osteoprotegerin Deficiency
C.A. Allen, B.L. Hart, C.L. Taylor, C.L. Clericuzio
American Journal of Neuroradiology Jan 2008, 29 (1) 7-8; DOI: 10.3174/ajnr.A0755
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This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • Juvenile Paget's disease with heterozygous duplication within TNFRSF11A encoding RANK
    Michael P. Whyte, Cristina Tau, William H. McAlister, Xiafang Zhang, Deborah V. Novack, Virginia Preliasco, Eduardo Santini-Araujo, Steven Mumm
    Bone 2014 68
  • Juvenile Paget disease
    Stergios A. Polyzos, Tim Cundy, Christos S. Mantzoros
    Metabolism 2018 80
  • Osteoprotegerin and kidney disease
    Alejandra Montañez-Barragán, Isaias Gómez-Barrera, Maria D. Sanchez-Niño, Alvaro C. Ucero, Liliana González-Espinoza, Alberto Ortiz
    Journal of Nephrology 2014 27 6
  • Rare Inherited forms of Paget’s Disease and Related Syndromes
    Stuart H. Ralston, J. Paul Taylor
    Calcified Tissue International 2019 104 5
  • Juvenile Paget's Disease From Heterozygous Mutation of SP7 Encoding Osterix (Specificity Protein 7, Transcription Factor SP7)
    Michael P. Whyte, Philippe M. Campeau, William H. McAlister, G. David Roodman, Nori Kurihara, Angela Nenninger, Shenghui Duan, Gary S. Gottesman, Vinieth N. Bijanki, Homer Sedighi, Deborah J. Veis, Steven Mumm
    Bone 2020 137
  • Novel homozygous mutations in the osteoprotegerin gene TNFRSF11B in two unrelated patients with juvenile Paget's disease
    Dorit Naot, Ally Choi, David Shaun Musson, Pelin Özlem Simsek Kiper, Gulen Eda Utine, Koray Boduroglu, Munro Peacock, Linda A. DiMeglio, Tim Cundy
    Bone 2014 68
  • Auricular ossification: A newly recognized feature of osteoprotegerin‐deficiency juvenile Paget disease
    Gary S. Gottesman, Katherine L. Madson, William H. McAlister, Angela Nenninger, Deborah Wenkert, Steven Mumm, Michael P. Whyte
    American Journal of Medical Genetics Part A 2016 170 4
  • Osteoprotegerin Prevents Intracranial Aneurysm Progression by Promoting Collagen Biosynthesis and Vascular Smooth Muscle Cell Proliferation
    Takeshi Miyata, Manabu Minami, Hiroharu Kataoka, Kosuke Hayashi, Taichi Ikedo, Tao Yang, Yu Yamamoto, Masayuki Yokode, Susumu Miyamoto
    Journal of the American Heart Association 2020 9 17
  • Angiotensin II Induces Aortic Rupture and Dissection in Osteoprotegerin‐Deficient Mice
    Toshihiro Tsuruda, Atsushi Yamashita, Misa Otsu, Masanori Koide, Yuko Nakamichi, Yoko Sekita‐Hatakeyama, Kinta Hatakeyama, Taro Funamoto, Etsuo Chosa, Yujiro Asada, Nobuyuki Udagawa, Johji Kato, Kazuo Kitamura
    Journal of the American Heart Association 2022 11 8
  • Treatment of Symptomatic Bilateral Cavernous Carotid Aneurysms: Long-term Results of 6 Cases
    Yoichi Uozumi, Sho Okamoto, Yoshio Araki, Takashi Izumi, Noriaki Matsubara, Kinya Yokoyama, Masaki Sumitomo, Shigeru Miyachi, Toshihiko Wakabayashi
    Journal of Stroke and Cerebrovascular Diseases 2015 24 5

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