Zobrazeno 1 - 10
of 160
pro vyhledávání: '"Rodney Grahame"'
Publikováno v:
Rambam Maimonides Medical Journal, Vol 7, Iss 4, p e0334 (2016)
Ehlers–Danlos syndrome (EDS)—hypermobility type (HT) is considered to be the most common subtype of EDS and the least severe one; EDS-HT is considered to be identical to the joint hypermobility syndrome and manifests with musculoskeletal complain
Externí odkaz:
https://doaj.org/article/4867a7794403424791b9c4cd43f0752f
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 175:148-157
In the last decade, growing attention has been placed on joint hypermobility and related disorders. The new nosology for Ehlers-Danlos syndrome (EDS), the best-known and probably the most common of the disorders featuring joint hypermobility, identif
Publikováno v:
Clinical Rheumatology. 39:2481-2482
Autor:
Piyush Gampawar, Penny J. Norsworthy, Rodney Grahame, Christina Kanonidou, Ruwan A. Weerakkody, Michael Mueller, Holly A. Black, Hanadi Kazkaz, Neeti Ghali, Jana Vandrovcova, Timothy J. Aitman, F. Michael Pope, David Ross, Yousef Ibrahim, Anthony Vandersteen, Jennifer Biggs, Nicholas J.W. Cheshire, David J. P. Ferguson, Abdulshakur Abdullah
Publikováno v:
Weerakkody, R, Vandrovcova, J, Kanonidou, C, Mueller, M, Gampawar, P, Ibrahim, Y, Norsworthy, P J, Biggs, J, Abdullah, A, Ross, D, Black, H, Ferguson, D J P, Cheshire, N, Kazkaz, H, Grahame, R, Ghali, N, Vandersteen, A, Pope, F M & Aitman, T J 2016, ' Targeted next generation sequencing makes new molecular diagnoses and expands genotype-phenotype relationship in Ehlers-Danlos syndrome ', Genetics in Medicine . https://doi.org/10.1038/gim.2016.14
Ehlers–Danlos syndrome (EDS) comprises a group of overlapping hereditary disorders of connective tissue with significant morbidity and mortality, including major vascular complications. We sought to identify the diagnostic utility of a next-generat
Autor:
Rodney Grahame, Rubina Aktar, Joan K. Morris, Qasim Aziz, Alan Hakim, Asma Fikree, Charles H. Knowles
Publikováno v:
Neurogastroenterology & Motility. 27:569-579
The overlap of unexplained gastrointestinal (GI) and somatic symptoms is well established in patients with functional gastrointestinal disorders (FGID). Joint hypermobility syndrome (JHS) is a non-inflammatory connective tissue disorder associated wi
Autor:
Rodney, Grahame
Publikováno v:
Rheumatology (Oxford, England). 56(12)
Autor:
Brad T. Tinkle, Tomoki Kosho, Clair A. Francomano, Eyal Reinstein, Neeti Ghali, Jessica M Bowen, Johannes Zschocke, Marianne Rohrbach, James H. Black, Roberto Mendoza-Londono, Michael Frank, Marco Castori, Serwet Demirdas, Angela F. Brady, Helen Cohen, Diana Johnson, Nicol C. Voermans, Birgit Juul-Kristensen, F. Michael Pope, Mark E. Lavallee, Sylvie Fournel-Gigleux, John W. Belmont, Nigel Wheeldon, Anne De Paepe, Rodney Grahame, Fransiska Malfait, Cecilia Giunta, Peter H. Byers, Leema Robert, Ines Kapferer-Seebacher, Nigel Burrows, Anthony Vandersteen, Caroline van Mourik, Melanie Pepin, Lara Bloom, Glenda Sobey, Howard P. Levy, Tim Van Damme, Britta Berglund, Lynn Sanders, Marina Colombi, Alan Hakim, Hanadi Kazkaz, Xavier Jeunemaitre, Julie De Backer
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 1, pp. 8-26
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 8-26
Malfait, F, Francomano, C, Byers, P H, Belmont, J, Berglund, B, Black, J, Bloom, L, Bowen, J M, Brady, A F, Burrows, N P, Castori, M, Cohen, H, Colombi, M, Demirdas, S, De Backer, J, De Paepe, A, Fournel-Gigleux, S, Frank, M, Ghali, N, Giunta, C, Grahame, R, Hakim, A, Jeunemaitre, X, Johnson, D, Juul-Kristensen, B, Kapferer-Seebacher, I, Kazkaz, H, Kosho, T, Lavallee, M E, Levy, H, Mendoza-Londono, R, Pepin, M, Pope, F M, Reinstein, E, Robert, L, Rohrbach, M, Sanders, L, Sobey, G J, Van Damme, T, Vandersteen, A, van Mourik, C, Voermans, N, Wheeldon, N, Zschocke, J & Tinkle, B 2017, ' The 2017 international classification of the Ehlers-Danlos syndromes ', American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, vol. 175, no. 1, pp. 8-26 . https://doi.org/10.1002/ajmg.c.31552
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 1, pp. 8-26
American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2017, 175 (1), pp.8-26. ⟨10.1002/ajmg.c.31552⟩
American Journal of Medical Genetics Part C : Seminars in Medical Genetics, 175, 8-26
Malfait, F, Francomano, C, Byers, P H, Belmont, J, Berglund, B, Black, J, Bloom, L, Bowen, J M, Brady, A F, Burrows, N P, Castori, M, Cohen, H, Colombi, M, Demirdas, S, De Backer, J, De Paepe, A, Fournel-Gigleux, S, Frank, M, Ghali, N, Giunta, C, Grahame, R, Hakim, A, Jeunemaitre, X, Johnson, D, Juul-Kristensen, B, Kapferer-Seebacher, I, Kazkaz, H, Kosho, T, Lavallee, M E, Levy, H, Mendoza-Londono, R, Pepin, M, Pope, F M, Reinstein, E, Robert, L, Rohrbach, M, Sanders, L, Sobey, G J, Van Damme, T, Vandersteen, A, van Mourik, C, Voermans, N, Wheeldon, N, Zschocke, J & Tinkle, B 2017, ' The 2017 international classification of the Ehlers-Danlos syndromes ', American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, vol. 175, no. 1, pp. 8-26 . https://doi.org/10.1002/ajmg.c.31552
Item does not contain fulltext The Ehlers-Danlos syndromes (EDS) are a clinically and genetically heterogeneous group of heritable connective tissue disorders (HCTDs) characterized by joint hypermobility, skin hyperextensibility, and tissue fragility
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6f0b002b28d94b1fa69a6762a4a7db7
https://www.zora.uzh.ch/id/eprint/145775/
https://www.zora.uzh.ch/id/eprint/145775/
Publikováno v:
British Journal of Pain. 9:157-166
Background: The model of activity avoidance prompted by fear of increased pain and/or harm dominates understanding and research into activity limitation in chronic pain. Yet, the accounts of people with chronic pain on decisions about activity limita
Autor:
Rodney Grahame
Publikováno v:
Rheumatology. 57:2250-2251
Publikováno v:
Rambam Maimonides Medical Journal
Rambam Maimonides Medical Journal, Vol 7, Iss 4, p e0334 (2016)
Rambam Maimonides Medical Journal, Vol 7, Iss 4, p e0334 (2016)
Ehlers-Danlos syndrome (EDS)-hypermobility type (HT) is considered to be the most common subtype of EDS and the least severe one; EDS-HT is considered to be identical to the joint hypermobility syndrome and manifests with musculoskeletal complaints,