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pro vyhledávání: '"Bruges Armas J"'
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Autor:
Vergnaud, P, Lunt, M, Scheidt-Nave, C, Poor, G, Gennari, C, Hoszowski, K, Lopes Vaz, A, Reid, D.M, Benevolenskaya, L, Grazio, S, Weber, K, Miazgowski, T, Stepan, J.J, Masaryk, P, Galan, F, Bruges Armas, J, Lorenc, R, Havelka, S, Perez Cano, R, Seibel, M, Armbrecht, G, Kaptoge, S, O'Neill, T.W, Silman, A.J, Felsenberg, D, Reeve, J *, Delmas, P.D
Publikováno v:
In Clinica Chimica Acta 2002 322(1):121-132
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Publikováno v:
Tissue Antigens. Dec2008, Vol. 72 Issue 6, p593-598. 6p. 1 Diagram, 3 Charts, 1 Graph, 1 Map.
Autor:
Reeve, J., Lunt, M., Felsenberg, D., Silman, A.J., Scheidt-Nave, C., Poor, G., Gennari, C., Weber, K., Lorenc, R., Masaryk, P., Cannata, J.B., Dequeker, J., Reid, D.M., Pols, H.A., Benevolenskaya, L.I., Stepan, J.J., Miazgowski, T., Bhalla, A., Bruges, Armas J., Eastell, R., Lopes-Vaz, A., Lyritis, G., Jajić, Ivo, Woolf, A.D., Banzer, D., Reisinger, W., Todd, C.J., Felsch, B., Havelka, S., Hoszowski, K., Janott, J., Johnell, O., Raspe, H.H., Yershova, O.B., Kanis, J.A., Armbrecht, G., Finn, J.D., Gowin, W., O'Neill, T.W.
More severe vertebral fractures have more personal impact. In the European Prospective Osteoporosis Study, more severe vertebral collapse was predictable from prior fracture characteristics. Subjects with bi-concave or crush fractures at baseline had
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18a9589770f28de49cbb7031f6a32c21
https://ora.ox.ac.uk/objects/uuid:0cde5bc3-fcda-4413-bccc-c20431cba883
https://ora.ox.ac.uk/objects/uuid:0cde5bc3-fcda-4413-bccc-c20431cba883
Autor:
Bruges-Armas, J., Martinez-Laso, J., Martins, B., Allende, L., Gomez-Casado, E., Longas, J., Varela, P., Gonzalez-Granado, M., Arnaiz-Villena, A.
Publikováno v:
Tissue Antigens. Oct99, Vol. 54 Issue 4, p349. 11p.
Autor:
Raposo, M, Bettencourt, C, Maciel, P, Gao, F, Ramos, A, Kazachkova, N, Vasconcelos, J, Kay, T, Rodrigues, AJ, Bettencourt, B, Bruges-Armas, J, Geschwind, D, Coppola, G, Lima, M
Publikováno v:
Movement Disorders, vol 30, iss 7
Movement disorders : official journal of the Movement Disorder Society, vol 30, iss 7
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Movement disorders : official journal of the Movement Disorder Society, vol 30, iss 7
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
BACKGROUND: Machado-Joseph disease (or spinocerebellar ataxia type 3) is a late-onset polyglutamine neurodegenerative disorder caused by a mutation in the ATXN3 gene, which encodes for the ubiquitously expressed protein ataxin-3. Previous studies on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::88b355ef60befc165c694b3ea90fd8e5
https://escholarship.org/uc/item/8pq7j5cf
https://escholarship.org/uc/item/8pq7j5cf
Autor:
Uitterlinden, A. G., Ralston, S. H., Brandi, M. L., Carey, A. H., Grinberg, D., Langdahl, B. L., Lips, P., Lorenc, R., Obermayer-Pietsxch, B., Reeve, J., Reid, D. M., Amedei, A., Bassiti, A., Bustamante, M., Husted, L. B., Diez-Perez, A., Dobnig, H., Dunning, A. M., Enjuanes, A., Fahrleitner-Pammer, A., Fang, Y., Karczmarewicz, E., Kruk, M., Johannes van Leeuwen, Mavilia, C., Meurs, J. B. J., Mangion, J., Mcguigan, F. E. A., Pols, H. A. P., Renner, W., Rivadeneira, F., Schoor, N. M., Scollen, S., Sherlock, R. E., Ioannidis, J. P. A., Parsons, C., Bear, S., Farmer, R., Lukaszkiewicz, J., Bilinski, P., Czerwinski, E., Lewinski, A., Marcinowska-Suchowierska, E., Milewicz, A., Spaczynski, M., Jaworski, M., Nuti, R., Grazio, S., Miazgowski, T., Boonen, R., Masaryk, P., Stepan, J. J., Lopes Vaz, A., Cannata, J., Weber, K., Benevolenskaya, L. I., Todd, C., Khaw, K. -T, Da Silva, J., Bhalla, A., Poor, G., Bruges Armas, J., Lyritis, G., O Neill, T. W., Lunt, M., Compston, J., Cooper, C., Duncan, E., Keen, R., Mclellan, A., Wass, J., Dekema, E., Essen, H., Pluijm, S., Bravenboer, N., Hofman, A., Duijn, C. M., Jong, P. J., Breteler, M. M., Stricker, B. H., Witteman, J. C.
Publikováno v:
Annals of Internal Medicine, 145(4), 255-264. American College of Physicians
Scopus-Elsevier
Uitterlinden, A G, Ralston, S H, Brandi, M L, Carey, A H, Grinberg, D, Langdahl, B L, Lips, P, Lorenc, R, Obermayer-Pietsxch, B, Reeve, J, Reid, D M, Amedei, A, Bassiti, A, Bustamante, M, Husted, L B, Diez-Perez, A, Dobnig, H, Dunning, A M, Enjuanes, A, Fahrleitner-Pammer, A, Fang, Y, Karczmarewicz, E, Kruk, M, Van Leeuwen, J P T M, Mavilia, C, Van Meurs, J B J, Mangion, J, McGuigan, F E A, Pols, H A P, Renner, W, Rivadeneira, F, Van Schoor, N M, Scollen, S, Sherlock, R E, Ioannidis, J P A, Parsons, C, Bear, S, Farmer, R, Lukaszkiewicz, J, Bilinski, P, Czerwinski, E, Lewinski, A, Marcinowska-Suchowierska, E, Milewicz, A, Spaczynski, M, Jaworski, M, Nuti, R, Grazio, S, Miazgowski, T, Boonen, R, Masaryk, P, Stepan, J J, Lopes Vaz, A, Cannata, J, Weber, K, Benevolenskaya, L I, Todd, C, Khaw, K T, Da Silva, J, Bhalla, A, Poor, G, Bruges Armas, J, Lyritis, G, O'Neill, T W, Lunt, M, Compston, J, Cooper, C, Duncan, E, Keen, R, McLellan, A, Wass, J, Dekema, E, Van Essen, H, Pluijm, S, Bravenboer, N, Hofman, A, Van Duijn, C M, De Jong, P J, Breteler, M M, Stricker, B H & Witteman, J C 2006, ' The association between common vitamin D receptor gene variations and osteoporosis : A participant-level meta-analysis ', Annals of Internal Medicine, vol. 145, no. 4, pp. 255-264 . https://doi.org/10.7326/0003-4819-145-4-200608150-00005
Uitterlinden, A G, Ralston, S H, Brandi, M L, Carey, A H, Grinberg, D, Langdahl, B L, Lips, P, Lorenc, R, Obermayer-Pietsch, B, Reeve, J, Reid, D M, Amedei, A, Bassiti, A, Bustamante, M, Husted, L B, Diez-Perez, A, Dobnig, H, Dunning, A M, Enjuanes, A, Fahrleitner-Pammer, A, Fang, Y, Karczmarewicz, E, Kruk, M, van Leeuwen, J P, Mavilia, C, van Meurs, J B, Mangion, J, McGuigan, F E, Pols, H A, Renner, W, Rivadeneira, F, van Schoor, N M, Scollen, S, Sherlock, R E & Ioannidis, J P 2006, ' The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis ', Annals of Internal Medicine, vol. 145, no. 4, pp. 255-264 .
Scopus-Elsevier
Uitterlinden, A G, Ralston, S H, Brandi, M L, Carey, A H, Grinberg, D, Langdahl, B L, Lips, P, Lorenc, R, Obermayer-Pietsxch, B, Reeve, J, Reid, D M, Amedei, A, Bassiti, A, Bustamante, M, Husted, L B, Diez-Perez, A, Dobnig, H, Dunning, A M, Enjuanes, A, Fahrleitner-Pammer, A, Fang, Y, Karczmarewicz, E, Kruk, M, Van Leeuwen, J P T M, Mavilia, C, Van Meurs, J B J, Mangion, J, McGuigan, F E A, Pols, H A P, Renner, W, Rivadeneira, F, Van Schoor, N M, Scollen, S, Sherlock, R E, Ioannidis, J P A, Parsons, C, Bear, S, Farmer, R, Lukaszkiewicz, J, Bilinski, P, Czerwinski, E, Lewinski, A, Marcinowska-Suchowierska, E, Milewicz, A, Spaczynski, M, Jaworski, M, Nuti, R, Grazio, S, Miazgowski, T, Boonen, R, Masaryk, P, Stepan, J J, Lopes Vaz, A, Cannata, J, Weber, K, Benevolenskaya, L I, Todd, C, Khaw, K T, Da Silva, J, Bhalla, A, Poor, G, Bruges Armas, J, Lyritis, G, O'Neill, T W, Lunt, M, Compston, J, Cooper, C, Duncan, E, Keen, R, McLellan, A, Wass, J, Dekema, E, Van Essen, H, Pluijm, S, Bravenboer, N, Hofman, A, Van Duijn, C M, De Jong, P J, Breteler, M M, Stricker, B H & Witteman, J C 2006, ' The association between common vitamin D receptor gene variations and osteoporosis : A participant-level meta-analysis ', Annals of Internal Medicine, vol. 145, no. 4, pp. 255-264 . https://doi.org/10.7326/0003-4819-145-4-200608150-00005
Uitterlinden, A G, Ralston, S H, Brandi, M L, Carey, A H, Grinberg, D, Langdahl, B L, Lips, P, Lorenc, R, Obermayer-Pietsch, B, Reeve, J, Reid, D M, Amedei, A, Bassiti, A, Bustamante, M, Husted, L B, Diez-Perez, A, Dobnig, H, Dunning, A M, Enjuanes, A, Fahrleitner-Pammer, A, Fang, Y, Karczmarewicz, E, Kruk, M, van Leeuwen, J P, Mavilia, C, van Meurs, J B, Mangion, J, McGuigan, F E, Pols, H A, Renner, W, Rivadeneira, F, van Schoor, N M, Scollen, S, Sherlock, R E & Ioannidis, J P 2006, ' The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis ', Annals of Internal Medicine, vol. 145, no. 4, pp. 255-264 .
Background: Polymorphisms of the vitamin D receptor (VDR) gene have been implicated in the genetic regulation of bone mineral density (BMD). However, the clinical impact of these variants remains unclear. Objective: To evaluate the relation between V
Akademický článek
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