Zobrazeno 1 - 10
of 121
pro vyhledávání: '"Jay R. Shapiro"'
Publikováno v:
AACE Clinical Case Reports, Vol 5, Iss 6, Pp e362-e364 (2019)
ABSTRACT: Objective: This case highlights the value of genetic screening for idiopathic osteoporosis with recurrent fractures. Methods: Case report and review of the literature. Results: A 52-year-old Caucasian female with idiopathic osteoporosis wit
Externí odkaz:
https://doaj.org/article/e9820f2c8d9b413d8c64a1d2efaf308e
Autor:
Amanda Jefferson, Helen Leonard, Aris Siafarikas, Helen Woodhead, Sue Fyfe, Leanne M Ward, Craig Munns, Kathleen Motil, Daniel Tarquinio, Jay R Shapiro, Torkel Brismar, Bruria Ben-Zeev, Anne-Marie Bisgaard, Giangennaro Coppola, Carolyn Ellaway, Michael Freilinger, Suzanne Geerts, Peter Humphreys, Mary Jones, Jane Lane, Gunilla Larsson, Meir Lotan, Alan Percy, Mercedes Pineda, Steven Skinner, Birgit Syhler, Sue Thompson, Batia Weiss, Ingegerd Witt Engerström, Jenny Downs
Publikováno v:
PLoS ONE, Vol 11, Iss 2, p e0146824 (2016)
OBJECTIVES:We developed clinical guidelines for the management of bone health in Rett syndrome through evidence review and the consensus of an expert panel of clinicians. METHODS:An initial guidelines draft was created which included statements based
Externí odkaz:
https://doaj.org/article/536bc8aa54354e409094505397797b8f
Autor:
Jay R Shapiro, Morten A. Karsdal, Lindsey Nicol, Kim Henriksen, Sandesh C.S. Nagamani, Ying Wang, Shu Sun, Brendan Lee, Rosamund C. Smith, Eric S. Orwoll, Patrick Morar
Publikováno v:
Bone. 120:70-74
Osteogenesis imperfecta [1] is a rare disorder of connective tissue caused by abnormalities in the synthesis or processing of type I collagen. Type I collagen is the most abundant type of collagen and is expressed in almost all connective tissues. Gi
Autor:
Jay R Shapiro
Publikováno v:
Marcus and Feldman's Osteoporosis ISBN: 9780128130735
Publisher Summary Osteoporosis is being recognized with increasing frequency in young adult women and men. The clinician is faced with a differential diagnosis that may range from an inherited disorder such as mild osteogenesis imperfecta, to acquire
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff2b8132b83d1cda73cd5284d1dc4706
https://doi.org/10.1016/b978-0-12-813073-5.00048-4
https://doi.org/10.1016/b978-0-12-813073-5.00048-4
Autor:
Bo Abrahamsen, Robert A. Adler, Sara Ajjour, Mohammad Mehdi Alemi, Dennis E. Anderson, Timothy R. Arnett, Mariam A. Assaad, Ghada T. Ballane, Roland Baron, J.H. Duncan Bassett, Douglas C. Bauer, William A. Bauman, Kristen M. Beavers, Sarah D. Berry, John P. Bilezikian, Emmanuel Biver, Dana Bliuc, Lynda F. Bonewald, Adele L. Boskey, Mary L. Bouxsein, Nathalie Bravenboer, Todd T. Brown, Susan V. Bukata, Katelyn Burkhart, Ernesto Canalis, Christopher Cardozo, Alesha B. Castillo, Jane A. Cauley, Jacqueline R. Center, Julia C. Chen, Roberto Civitelli, Adi Cohen, Felicia Cosman, Carolyn J. Crandall, Brooke M. Crawford, Natalie E. Cusano, Francisco J.A. de Paula, Kim Delbaere, David W. Dempster, Dima L. Diab, Ingrid Dick-de-Paula, Linda A. DiMeglio, Matthew T. Drake, Alanna M.K. Dubrovsky, Luca D’Onofrio, Richard Eastell, Grahame J. Elder, Ghada A. El-Hajj Fuleihan, Kristine E. Ensrud, Serge Ferrari, Bernard Freudenthal, Harry K. Genant, Louis C. Gerstenfeld, Lora Giangregorio, Evelien Gielen, Deborah T. Gold, Steven R. Goldring, Catherine M. Gordon, Francesca Gori, Gail A. Greendale, James F. Griffith, Peyman Hadji, Christopher J. Hernandez, Jonathan Hoggatt, Denise K. Houston, Amira I. Hussein, Christopher R. Jacobs, Xuezhi Jiang, James D. Johnston, Risa Kagan, Lamya Karim, Carrie Karvonen-Gutierrez, Wendy B. Katzman, Masanobu Kawai, Sundeep Khosla, Douglas P. Kiel, Saija A. Kontulainen, Paul Kostenuik, Alexandra Krez, Henry Kronenberg, Rajiv Kumar, Nancy E. Lane, Lisa Langsetmo, Michaël R. Laurent, L. Lawenius, Sergey Leikin, William D. Leslie, E. Michael Lewiecki, Minghao Liu, Yi Liu, Stephen R. Lord, Joseph Lorenzo, Nina S. Ma, Naim M. Maalouf, Robert Marcus, Michael R. McClung, Marcela Moraes Mendes, Paul D. Miller, Madhusmita Misra, Mahshid Mohseni, Elise F. Morgan, Suzanne N. Morin, Mona Al Mukaddam, Chris J.J. Mulder, Nandini Nair, Nicola Napoli, Nat Nasomyont, Dorothy A. Nelson, Jeri W. Nieves, Robert Nissenson, Claes Ohlsson, Christina V. Oleson, Laura Ortinau, Eric Orwoll, Susan M. Ott, Roberto Pacifici, Andrea Palermo, A.M. Parfitt, Dongsu Park, Sylvain Provot, Sonia Bhandari Randhawa, John F. Randolph, Fernando Rivadeneira, Pamela Gehron Robey, Lauren Robinson, Tara Rogers-Soeder, G. David Roodman, Clifford J. Rosen, Kenneth G. Saag, Shivani Sahni, Khashayar Sakhaee, David T. Scadden, Anne L. Schafer, Ernestina Schipani, Monica C. Serra, Jay R. Shapiro, Catherine Sherrington, James M. Shikany, Shonni J. Silverberg, Andrea J. Singer, K. Sjögren, Peter J. Snyder, Emily M. Stein, Christine M. Swanson, Pawel Szulc, Pamela Taxel, Peter J. Tebben, Sarah E. Twardowski, André G. Uitterlinden, Rachana Vaidya, Cristianna Vallera, Adriaan A. van Bodegraven, Bram C.J. van der Eerden, Marjolein C.H. van der Meulen, André J. van Wijnen, Dirk Vanderschueren, Jean Wactawski-Wende, Laura Watts, Nelson B. Watts, Ashley A. Weaver, Robert S. Weinstein, Graham R. Williams, Joy Wu, Karin C. Wu, Michael T. Yin, Elaine W. Yu, Hua Zhou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cce6be4ef85b41d83683049082f9d16
https://doi.org/10.1016/b978-0-12-813073-5.00087-3
https://doi.org/10.1016/b978-0-12-813073-5.00087-3
Autor:
Nicholas Mikolajewicz, Bettina M. Willie, Anthony Hall, Michael Molloy-Bland, Pauline T. Lukey, Nick Bishop, Amaka C. Offiah, Andrew J. Burghardt, Francis H. Glorieux, Lars Folkestad, Jay R. Shapiro, Suzanne N Morin, Svetlana V. Komarova, Kenneth M. Kozloff, Bert van Rietbergen, Kim Wager
Publikováno v:
Journal of Bone and Mineral Research, 35(3), 446-459. Wiley-Blackwell
Mikolajewicz, N, Bishop, N, Burghardt, A J, Folkestad, L, Hall, A, Kozloff, K M, Lukey, P T, Molloy-Bland, M, Morin, S N, Offiah, A C, Shapiro, J, van Rietbergen, B, Wager, K, Willie, B M, Komarova, S V & Glorieux, F H 2020, ' HR-pQCT Measures of Bone Microarchitecture Predict Fracture : Systematic Review and Meta-Analysis ', Journal of Bone and Mineral Research, vol. 35, no. 3, pp. 446-459 . https://doi.org/10.1002/jbmr.3901
Mikolajewicz, N, Bishop, N, Burghardt, A J, Folkestad, L, Hall, A, Kozloff, K M, Lukey, P T, Molloy-Bland, M, Morin, S N, Offiah, A C, Shapiro, J, van Rietbergen, B, Wager, K, Willie, B M, Komarova, S V & Glorieux, F H 2020, ' HR-pQCT Measures of Bone Microarchitecture Predict Fracture : Systematic Review and Meta-Analysis ', Journal of Bone and Mineral Research, vol. 35, no. 3, pp. 446-459 . https://doi.org/10.1002/jbmr.3901
High-resolution peripheral quantitative computed tomography (HR-pQCT) is a noninvasive imaging modality for assessing volumetric bone mineral density (vBMD) and microarchitecture of cancellous and cortical bone. The objective was to (1) assess fractu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef7872ee822dac7c438ff333abd1367c
https://research.tue.nl/nl/publications/f9896051-8a64-4b38-8e91-3a217b6e0d3b
https://research.tue.nl/nl/publications/f9896051-8a64-4b38-8e91-3a217b6e0d3b
Autor:
Sandesh C.S. Nagamani, Ying Wang, Rosamund C. Smith, Eric S. Orwoll, Lindsey Nicol, Jay R. Shapiro, Brendan Lee, John H. Sloan
Publikováno v:
Journal of Bone and Mineral Research. 33:307-315
Sclerostin (SOST), a glycoprotein primarily derived from osteocytes, is an important regulator of bone remodeling. Osteogenesis imperfecta (OI) is a heritable disorder of bone characterized by low bone mass, bone fragility, recurrent fractures, and b
Autor:
E. Michael Lewiecki, Jay R Shapiro
Publikováno v:
Journal of Bone and Mineral Research. 32:1977-1980
Hypophosphatasia (HPP) is a rare inherited disorder of bone affecting approximately 500 to 600 known individuals in the United States. HPP is the result of mutations involving the gene for tissue nonspecific alkaline phosphatase. Five clinical types
Autor:
Nikia Stinson, Kathryn R. Wagner, Genila Bibat, Hema Chagarlamudi, Alastair Corbett, Carla Grosmann, Marion Stoll, Jay R. Shapiro, Carly Matichak Stock
Publikováno v:
Muscle & Nerve. 56:1108-1113
Introduction: Herein we provide a comprehensive overview of bone health in facioscapulohumeral muscular dystrophy (FSHD). Methods: Ninety-four adult individuals with FSHD type 1 from 2 sites were included in this cross-sectional study. Clinical chara
Autor:
Jake Schmidt, Michaela Durigova, Francis H. Glorieux, Cathleen L. Raggio, Robert D. Steiner, Chloe Citron, Peter H. Byers, Keren Machol, Jay R Shapiro, Erin Carter, Brendan Lee, David Cuthbertson, Rodrigo C. Silva, Michael B. Bober, Sandesh C.S. Nagamani, Sobiah Khan, Henri Traboulsi, Trevor D. Hadley, Vernon R. Sutton, Kenneth Brookler, Peter A. Smith, Kate Citron
Publikováno v:
Am J Med Genet A
BACKGROUND: Osteogenesis imperfecta (OI) is a genetic connective tissue disorder characterized by increased bone fragility and recurrent fractures. The phenotypic severity of OI has a significant influence on the ability to walk but little is known a