Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Teresa Collazo-Mesa"'
Autor:
Bárbara Torres-Rives, Goitybell Martínez-Téllez, Minerva Matarán-Valdés, Lisi Osorio-Ilas, Daysi Vilches-Lescaille, Cira Rodríguez-Pelier, Yaíma Zúñiga-Rosales, Teresa Collazo-Mesa
Publikováno v:
VacciMonitor, Vol 30, Iss 1, Pp 10-17 (2021)
La uveítis anterior no infecciosa es una enfermedad inflamatoria del ojo que afecta al tracto uveal y que puede causar ceguera total y otras discapacidades visuales. Esta enfermedad se ubica en el espectro de enfermedades autoinmunes y autoinflamato
Externí odkaz:
https://doaj.org/article/45e2cfd6240145d69edd30360f1bba6d
Autor:
Antonio Alejandro Esperón Álvarez, Inés Virginia Noa Hechavarría, Ixchel López Reyes, Teresa Collazo Mesa
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 25, Iss 1, Pp 1-6 (2024)
Abstract Background Von Hippel-Lindau (VHL) syndrome is an autosomal dominantly inherited disorder that predisposes to multiple neoplasms. Patients may develop hemangioblastomas of the central nervous system and retina, multiple cysts in the pancreas
Externí odkaz:
https://doaj.org/article/e7c46c747fb44a9d834bb6caef3cb0ae
Autor:
Yaixa Piloto-Roque, Arlet Acanda de la Rocha, Ismael Cervera García, Yulia Clark Feoktistova, Teresa Collazo-Mesa
Publikováno v:
Revista Habanera de Ciencias Médicas, Vol 9, Iss 1 (2010)
La hemofilia A se caracteriza por ser una enfermedad congénita del trastorno de la coagulación y constituye un desorden recesivo ligado al cromosoma X. El estudio molecular se realiza por estudio indirecto, por ser causada por mutaciones heterogén
Externí odkaz:
https://doaj.org/article/e5412d5f70304f75a9fd70db2f75ba3f
Autor:
Juan E Figueredo-Lago, Anny Armas-Cayarga, Yaimé J González-González, Teresa Collazo-Mesa, Iria García de la Rosa, Yenitse Perea-Hernández, Elvia N Santos-González
Publikováno v:
Biotecnología Aplicada, Vol 32, Iss 4, Pp 4301-4306
Externí odkaz:
https://doaj.org/article/ccf3d421d697419893d5749925425c1d
Autor:
Tania Mayvel Espinosa Reyes, Teresa Collazo Mesa, Paulina Arasely Lantigua Cruz, Adriana Agramonte Machado, Emma Domínguez Alonso, Henrik Falhammar
Publikováno v:
International Journal of Endocrinology, Vol 2021 (2021)
Background. There are several studies that show a good genotype-phenotype correlation in congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD). However, there is well-documented evidence of inconsistency in some cases. Objecti
Externí odkaz:
https://doaj.org/article/015947750cf04b57b602c0fb2f5aa2d2
Autor:
Estela Morales Peralta, Yaíma Zúñiga Rosales, Teresa Collazo Mesa, Elvia Nelemi Santos González, Yadira Hernández Pérez, María de los Angeles González Torres, Hilda Roblejo Balbuena, Beatriz Marcheco Teruel
Publikováno v:
Bionatura. 7:1-5
COVID-19 has had severe consequences worldwide. It has been estimated that the contribution of genetic factors to the disease is about 50%. The A16974C polymorphism of the IL-12 p40 gene has been described as being related to resistance or susceptibi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c289153a3ba2dcd8235f4d939258a6f
https://doi.org/10.21931/rb/2022.07.01.34
https://doi.org/10.21931/rb/2022.07.01.34
Autor:
Bárbara Torres Rives, Isabel Frutos Ambou, Teresa Collazo Mesa, Rosa Colás González, Minerva Mataran Valdés, Goitybell Martínez Téllez
Publikováno v:
Reumatología Clínica. 17:575-581
Resumen Objetivo Identificar la relacion entre los niveles sericos de inmunoglobulinas, los componentes 3 y 4 del complemento, la presencia del alelo HLA-B27 y el diagnostico de espondiloartropatia en pacientes con uveitis anterior no infecciosa. Mat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7439b8f0c021bd34c816a3742ba015fc
https://doi.org/10.1016/j.reuma.2020.07.007
https://doi.org/10.1016/j.reuma.2020.07.007
Autor:
Minerva Mataran Valdés, Isabel Frutos Ambou, Rosa Colás González, Bárbara Torres Rives, Goitybell Martínez Téllez, Teresa Collazo Mesa
Publikováno v:
Reumatología Clínica (English Edition). 17:575-581
Objective To identify the relationship between serum immunoglobulin levels, complement components 3 and 4, the presence of the HLA-B27 allele and diagnosis of spondyloarthropathies in patients with non-infectious anterior uveitis. Materials and metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d4852beb6ae3b960e41d92c5241f6ea3
https://doi.org/10.1016/j.reumae.2020.07.007
https://doi.org/10.1016/j.reumae.2020.07.007
Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Autor:
Adriana Agramonte Machado, Henrik Falhammar, Emma Domínguez Alonso, Teresa Collazo Mesa, Tania Mayvel Espinosa Reyes, Paulina Arasely Lantigua Cruz
Publikováno v:
BMC Endocrine Disorders, Vol 20, Iss 1, Pp 1-8 (2020)
BMC Endocrine Disorders
BMC Endocrine Disorders
Background Congenital adrenal hyperplasia (CAH) is an autosomal recessive group of diseases. 21-Hydroxylase deficiency (21OHD) accounts for between 95 and 99% of all CAH cases. Objectives To characterize the genotype of patients clinically diagnosed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0040d364eaa6793c8d58b9e47c47aafb
http://link.springer.com/article/10.1186/s12902-020-00643-z
http://link.springer.com/article/10.1186/s12902-020-00643-z
Autor:
Teresa Collazo Mesa, Yaíma Zúñiga Rosales, Yadira Hernández Pérez, Estela Morales Peralta, Elvia Nelmi Santos González, Hilda Roblejo Balbuena, Beatriz Marcheco Teruel, María de los Ángeles González Torres
Publikováno v:
The Egyptian Journal of Medical Human Genetics
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-4 (2021)
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-4 (2021)
Purpose To determine the relationship between the genotypes of the TaqI polymorphism of VDR gene and the clinical forms of COVID-19 in Cuban patients. Methods TaqI polymorphism was determined by the PCR in 104 Cuban patients, who suffered different c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e11e1f555c5960032f5754b98d341a1c
https://doi.org/10.1186/s43042-021-00206-4
https://doi.org/10.1186/s43042-021-00206-4