Zobrazeno 1 - 10
of 45
pro vyhledávání: '"C. Montilla Morales"'
Autor:
J Narvaez, FJ López-Longo, C Galisteo, JA Hernandez-Beriain, A Olive, I Rua-Figueroa, E Raya, I Castellvi, A Fernández-Nebro, R Blanco, J Calvo-Alén, J Ibáñez, C Marras, A Boteanu, V Martínez-Taboada, JL Andreu, JM Pego-Reigosa, B Hernández-Cruz, E Uriarte Isacelaya, E Tomero Muriel, E Díez Álvarez, C Moriano, C Bermúdez, M Galindo-Izquierdo, M Freire González, O Fernández-Berrizbeitia, A Pérez Gómez, C Montilla-Morales, G Santos Soler, M Rodríguez-Gómez, P Vela-Casasempere, L Expósito, R Menor-Almagro, M Ibañez-Barceló, V Quevedo Vila, T Vázquez Rodríguez
Publikováno v:
Lupus Science and Medicine, Vol 9, Iss Suppl 2 (2022)
Externí odkaz:
https://doaj.org/article/3de8ad8238cc4479a39d5a2eacd04312
Akademický článek
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Autor:
C. Montilla Morales, C. Hidalgo Calleja, M.E. Acosta de la Vega, S. Pastor Navarro, L. Gómez-Lechón Quirós, O. Compán Fernández
Publikováno v:
Rheumatology International. 41:1869-1874
Alkaptonuria is a rare autosomal-recessive disorder that produces accumulation of homogentisic acid in body fluids. The accumulation in collagen tissues, mainly in the joint cartilage, produces ochronotic arthropathy. We report two clinical cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab5043a9d46617f25a5ba9e91213f2c1
https://doi.org/10.1007/s00296-020-04640-2
https://doi.org/10.1007/s00296-020-04640-2
Autor:
C. Montilla Morales, M.E. Acosta de la Vega, S. Pastor Navarro, O. Compán Fernández, D Moyano Bueno, J Martín Centellas, C. Hidalgo Calleja, L. Gómez-Lechón Quirós, A Santos-Briz Terrón
Publikováno v:
Rheumatology international. 40(8)
Crystalglobulinemia is an extremely rare pathology that is associated in most cases with plasma cell dyscrasia, mainly multiple myeloma. In most cases, it may be the manifestation of incipient gammopathy or it manifests shortly after diagnosis. We re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85b8736b6136bea60b696e317df5381d
https://pubmed.ncbi.nlm.nih.gov/32533290
https://pubmed.ncbi.nlm.nih.gov/32533290
Autor:
L, Gómez-Lechón Quirós, C, Hidalgo Calleja, M E, Acosta de la Vega, O, Compán Fernández, S, Pastor Navarro, C, Montilla Morales
Publikováno v:
Rheumatology international. 41(10)
Alkaptonuria is a rare autosomal-recessive disorder that produces accumulation of homogentisic acid in body fluids. The accumulation in collagen tissues, mainly in the joint cartilage, produces ochronotic arthropathy. We report two clinical cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b76412b33e3f6d66e1f2b10332e1af66
https://pubmed.ncbi.nlm.nih.gov/32642830
https://pubmed.ncbi.nlm.nih.gov/32642830
Autor:
G. Manzano Canabal, C. Montilla Morales, C. Hidalgo Calleja, M.E. Acosta de la Vega, J. del Pino-Montes
Publikováno v:
Medicine - Programa de Formación Médica Continuada Acreditado. 12:3542-3546
Resumen La osteomalacia es un defecto de la mineralizacion osea en el hueso maduro. La causa mas frecuente es el deficit severo de vitamina D, que en nuestro medio se da en situaciones de exclusion social o malabsorcion. El cuadro clinico suele ser a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::908239da90ee0286bad58584f621f34a
https://doi.org/10.1016/j.med.2018.06.024
https://doi.org/10.1016/j.med.2018.06.024
Autor:
A. Quesada Moreno, M.D. Sánchez González, C. Hidalgo Calleja, C. Montilla Morales, J. del Pino-Montes
Publikováno v:
Medicine - Programa de Formación Médica Continuada Acreditado. 12:909-914
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81ac40019422048d2818e8231eb9dfe5
https://doi.org/10.1016/j.med.2016.07.004
https://doi.org/10.1016/j.med.2016.07.004
Autor:
C. Aguilera Cros, S. Muñoz Fernández, V. Díaz, C Montilla Morales, C.T. Barbazán Álvarez, M. Arranz, M. Á. Belmonte Serrano, J.M. Ruiz Martín, D. Reina Sanz, J.R. Noguera Pons, E. de Miguel Mendieta
Publikováno v:
Spondyloarthritis – clinical aspects (other than treatment).
Background According to the 2009 ASAS classification criteria, a patient with chronic low back pain (CLBP) may be classified as axial spondyloarthritis (ax-SpA), with or without radiographic evidence of sacroiliitis, if at least one other SpA feature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af306639a437ec1f6db3c4b6379b19af
https://doi.org/10.1136/annrheumdis-2018-eular.1395
https://doi.org/10.1136/annrheumdis-2018-eular.1395
Autor:
J. A. Pinto Tasende, Rubén Queiro, A. Laiz Alonso, C Montilla Morales, S. Bustabad Reyes, E. Galindez Agirregoikoa, J.J. Bethencourt Baute, J Ramír, M. A. Belmonte, EA Blanco Morales, HS Park, P Menéndez Tejόn
Publikováno v:
Poster Presentations.
Background The natural history of psoriatic arthritis (PsA) is very little known and the information regarding prospective cohorts is very scarce worldwide, including our country. REAPSER (Spanish Rheumatology Society Registry of Psoriatic Arthritis)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67c8cbbdb722dd9df994eb3a562ede12
https://doi.org/10.1136/annrheumdis-2017-eular.4268
https://doi.org/10.1136/annrheumdis-2017-eular.4268
Autor:
A. Laiz Alonso, M. A. Belmonte, J Ramír, C Montilla Morales, S. Bustabad Reyes, Rubén Queiro, E. Galindez Agirregoikoa, HS Park, E Alonso Blanco Morales, J.J. Bethencourt Baute, J. A. Pinto Tasende, P Menéndez Tejόn
Publikováno v:
Abstracts Accepted for Publication.
Background The natural history of psoriatic arthritis (PsA) according to gender of patients is an aspect of the disease only partially studied. In prospective PsA cohorts such information is barely known. Objectives To analyze baseline gender differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06f490e809eca3bc270b196e6b99a83a
https://doi.org/10.1136/annrheumdis-2017-eular.5039
https://doi.org/10.1136/annrheumdis-2017-eular.5039