Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Zahir A. Bhuiyan"'
Publikováno v:
International Journal of Healthcare and Medical Sciences. :12-16
Castleman disease is a lymphoproliferative disorder and is easily confused with lymphoma or other lymphadenopathy. Castleman’s disease is divided into unicentric Castleman disease, which involved a single enlarged lymph node or region of lymph node
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4310eadff37e12aa9d0fae0f2dc05c3
https://doi.org/10.32861/ijhms.91.12.16
https://doi.org/10.32861/ijhms.91.12.16
Publikováno v:
European Journal of Clinical Medicine. 4:12-17
Background: The concept of giving out accolades and rewards has been there for centuries. When an individual is recognized for their good deed, they feel delighted. This inspires them to keep getting better and binds them to greater goals. First Annu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b17eef374824f0b7b948b7f8566501b
https://doi.org/10.24018/clinicmed.2023.4.2.257
https://doi.org/10.24018/clinicmed.2023.4.2.257
Autor:
Charles Antzelevitch, Amir Halkin, Raphael Rosso, Jitendra K. Vohra, Arnon Adler, Sami Viskin, Pieter G. Postema, Arthur A.M. Wilde, Manlio F. Márquez, Christian van der Werf, Zahir A. Bhuiyan, Jonathan M. Kalman, Jesaia Benhorin, Milton E Guevara-Valdivia
Publikováno v:
Heart rhythm, 9(6), 901-908. Elsevier
BACKGROUND Patients with long QT syndrome (LQTS) have inadequate shortening of the QT interval in response to the sudden heart rate accelerations provoked by standing-a phenomenon of diagnostic value. We now validate our original observations in a co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8f64279cdd210361f752b136efc6307
https://doi.org/10.1016/j.hrthm.2012.01.026
https://doi.org/10.1016/j.hrthm.2012.01.026
Autor:
Christian van der Werf, Jan D. H. Jongbloed, Maarten J. Cramer, Zahir A. Bhuiyan, Douwe E. Atsma, Irene M. van Langen, Ans C.P. Wiesfeld, Arjan C. Houweling, Maartje Noorman, Paul G.A. Volders, Jasper J. van der Smagt, Pieter A. Doevendans, Arthur A.M. Wilde, Dennis Dooijes, Paul A. van der Zwaag, Luc Jordaens, J. Peter van Tintelen, Moniek G.P.J. Cox, Arthur van den Wijngaard, Richard N.W. Hauer
Publikováno v:
Heart Rhythm. 7:S1-S44
Introduction: Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) is an autosomal dominantly inherited disease with incomplete penetrance and highly variable expression. Mutations in genes encoding 5 desmosomal proteins and TM
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ba1baefdf7b70829f3ae75c7ab59c99
https://doi.org/10.1016/j.hrthm.2010.03.028
https://doi.org/10.1016/j.hrthm.2010.03.028
Autor:
Pieter M. Kroonenberg, Josette Wulffaert, I. A. van Berckelaer-Onnes, Raoul C.M. Hennekam, Evert Scholte, Zahir A. Bhuiyan
Publikováno v:
Journal of Intellectual Disability Research. 53:604-619
Background Studies into the phenotype of rare genetic syndromes largely rely on bivariate analysis. The aim of this study was to describe the phenotype of Cornelia de Lange syndrome (CdLS) in depth by examining a large number of variables with varyin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2894a0d3845f9fb3664a28144c63b151
https://doi.org/10.1111/j.1365-2788.2009.01185.x
https://doi.org/10.1111/j.1365-2788.2009.01185.x
Autor:
L. C. Otterspoor, R. N. W. Hauer, A. A. M. Wilde, C. L. A. Reichert, Zahir A. Bhuiyan, M. J. M. Cramer
Publikováno v:
Netherlands heart journal, 15(10), 348-353. Bohn Stafleu van Loghum
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disorder of unknown cause that is characterised by fibrofatty replacement, primarily of the right ventricular myocardium, which can lead to life-threatening arrhythmias. It is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db517c94f88755c06dc844cd8cffe97b
https://doi.org/10.1007/bf03086013
https://doi.org/10.1007/bf03086013
Autor:
Tobias Opthof, Tamara T. Koopmann, Jeffrey R. Balser, Marcel M.A.M. Mannens, Ronald Wilders, Zahir A. Bhuiyan, Hanno L. Tan, Marieke W. Veldkamp, Arthur A.M. Wilde, Connie R. Bezzina, Jeroen P.P. Smits
Publikováno v:
Journal of molecular and cellular cardiology, 38(6), 969-981. Academic Press Inc.
Background. - Mutations in the gene encoding the human cardiac sodium channel (SCN5A) have been associated with three distinct cardiac arrhythmia disorders: the long QT syndrome, the Brugada syndrome and cardiac conduction disease. Here we report the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2053ab9c13c8a59569007b8b97731d8a
https://doi.org/10.1016/j.yjmcc.2005.02.024
https://doi.org/10.1016/j.yjmcc.2005.02.024
Autor:
Jeroen P.P. Smits, H. Wedekind, Connie R. Bezzina, Marieke W. Veldkamp, Arthur A.M. Wilde, Eric Schulze-Bahr, Zahir A. Bhuiyan
Publikováno v:
Cardiovascular research, 67(3), 459-466. Oxford University Press
Objective: Congenital long QT syndrome type 3 (LQT3) is an inherited cardiac arrhythmia disorder due to mutations in the cardiac sodium channel gene, SCN5A. Although most LQT3 mutations cause a persistent sodium current, increasing diversity in the d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::978ae87e5aeba9f119baab00ff9d130f
https://doi.org/10.1016/j.cardiores.2005.01.017
https://doi.org/10.1016/j.cardiores.2005.01.017
Publikováno v:
Heart Rhythm. 8:1952-1954
t The U.S. Food and Drug Administration (FDA) recently recommended that propoxyphene (an opioid analgesic drug used for the relief of moderate pain) be withdrawn from the U.S. market. This FDA recommendation followed concerns of possible propoxyphene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af37077733ae902dcd6c026388e2495c
https://doi.org/10.1016/j.hrthm.2011.07.015
https://doi.org/10.1016/j.hrthm.2011.07.015
Autor:
Jacques M.T. de Bakker, Maarten J. Cramer, Jasper J. van der Smagt, Irene M. van Langen, Paul G.A. Volders, Christian van der Werf, Arjan C. Houweling, Dennis Dooijes, Moniek G.P.J. Cox, Maartje Noorman, J. Peter van Tintelen, Jan D. H. Jongbloed, Richard N.W. Hauer, Ans C.P. Wiesfeld, Arthur van den Wijngaard, Arthur A.M. Wilde, Paul A. van der Zwaag, Douwe E. Atsma, Luc Jordaens, Zahir A. Bhuiyan, Pieter A. Doevendans
Publikováno v:
Circulation, 123(23), 2690-2700. LIPPINCOTT WILLIAMS & WILKINS
Circulation, 123(23), 2690-U87
Cox, M G P J, van der Zwaag, P A, van der Werf, C, van der Smagt, J J, Noorman, M, Bhuiyan, Z A, Wiesfeld, A C P, Volders, P G A, van Langen, I M, Atsma, D E, Dooijes, D, van den Wijngaard, A, Houweling, A C, Jongbloed, J D H, Jordaens, L, Cramer, M J, Doevendans, P A, de Bakker, J M T, Wilde, A A M, van Tintelen, J P & Hauer, R N W 2011, ' Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study ', Circulation, vol. 123, no. 23, pp. 2690-2U87 . https://doi.org/10.1161/CIRCULATIONAHA.110.988287
Circulation, 123(23), 2690-U87. LIPPINCOTT WILLIAMS & WILKINS
Circulation, 123(23), 2690-U87. Lippincott Williams & Wilkins
Circulation, 123(23), 2690-2U87. Lippincott Williams and Wilkins
Circulation, 123(23), 2690-U87. Lippincott Williams and Wilkins
Circulation, 123(23), 2690-U87
Cox, M G P J, van der Zwaag, P A, van der Werf, C, van der Smagt, J J, Noorman, M, Bhuiyan, Z A, Wiesfeld, A C P, Volders, P G A, van Langen, I M, Atsma, D E, Dooijes, D, van den Wijngaard, A, Houweling, A C, Jongbloed, J D H, Jordaens, L, Cramer, M J, Doevendans, P A, de Bakker, J M T, Wilde, A A M, van Tintelen, J P & Hauer, R N W 2011, ' Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Pathogenic Desmosome Mutations in Index-Patients Predict Outcome of Family Screening: Dutch Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Genotype-Phenotype Follow-Up Study ', Circulation, vol. 123, no. 23, pp. 2690-2U87 . https://doi.org/10.1161/CIRCULATIONAHA.110.988287
Circulation, 123(23), 2690-U87. LIPPINCOTT WILLIAMS & WILKINS
Circulation, 123(23), 2690-U87. Lippincott Williams & Wilkins
Circulation, 123(23), 2690-2U87. Lippincott Williams and Wilkins
Circulation, 123(23), 2690-U87. Lippincott Williams and Wilkins
Background— Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an autosomal dominant inherited disease with incomplete penetrance and variable expression. Causative mutations in genes encoding 5 desmosomal proteins are found in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34eb64150a79307bd233f39a9c75e225
https://cris.maastrichtuniversity.nl/en/publications/304c728d-57b3-426b-beb1-53d568810cb9
https://cris.maastrichtuniversity.nl/en/publications/304c728d-57b3-426b-beb1-53d568810cb9
