Inicio
Información del autor
Autor Luis Vicente Syro Moreno
Comentario :
Médico Neurocirujano, Hospital Pablo Tobón Uribe
|
Documentos disponibles escritos por este autor (77)
Refinar búsqueda
Arginine vasopressin (AVP): a review of its historical perspectives, current research and multifunctional role in the hypothalamo-hypophysial system / Luis Vicente Syro Moreno
Título : Arginine vasopressin (AVP): a review of its historical perspectives, current research and multifunctional role in the hypothalamo-hypophysial system Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2016 Títulos uniformes : Pituitary Idioma : Inglés (eng) Palabras clave : Arginine vasopressin corticotroph cells hypothalamus pituitary receptors Resumen : Introduction: This publication reviews the function of arginine vasopressin and focuses on the morphologic and functional correlation between the hormone and its effect on stress, the hypophysial–adrenocortical axis, neuroimmune responses, renal function and corticotroph pituitary tumors. Materials and methods: A literature review was performed using various search engines for information regarding the morphology and the multifunctional role of arginine vasopressin. Results: Although a large number of studies were published discussing these interactions, there are several important areas that are still obscure. Conclusion: The questions of how does arginine vasopressin affect the morphology and function of these various areas, and how does the secretion of ACTH and adreno-cortical hormones influence the morphology of arginine vasopressin-producing cells and their hormone secretion requires further investigation. Mención de responsabilidad : Fabio Rotondo, Henriett Butz, Luis V Syro, George M Yousef, Antonio Di Ieva, Lina M Restrepo, Andres Quintanar-Stephano, Istvan Berczi, Kalman Kovacs Referencia : Pituitary. 2016 Aug;19(4):345-55. DOI (Digital Object Identifier) : 10.1007/s11102-015-0703-0 PMID : 26762848 En línea : https://link.springer.com/article/10.1007%2Fs11102-015-0703-0 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3948 Arginine vasopressin (AVP): a review of its historical perspectives, current research and multifunctional role in the hypothalamo-hypophysial system [documento electrónico] / Luis Vicente Syro Moreno, . - 2016.
Obra : Pituitary
Idioma : Inglés (eng)
Palabras clave : Arginine vasopressin corticotroph cells hypothalamus pituitary receptors Resumen : Introduction: This publication reviews the function of arginine vasopressin and focuses on the morphologic and functional correlation between the hormone and its effect on stress, the hypophysial–adrenocortical axis, neuroimmune responses, renal function and corticotroph pituitary tumors. Materials and methods: A literature review was performed using various search engines for information regarding the morphology and the multifunctional role of arginine vasopressin. Results: Although a large number of studies were published discussing these interactions, there are several important areas that are still obscure. Conclusion: The questions of how does arginine vasopressin affect the morphology and function of these various areas, and how does the secretion of ACTH and adreno-cortical hormones influence the morphology of arginine vasopressin-producing cells and their hormone secretion requires further investigation. Mención de responsabilidad : Fabio Rotondo, Henriett Butz, Luis V Syro, George M Yousef, Antonio Di Ieva, Lina M Restrepo, Andres Quintanar-Stephano, Istvan Berczi, Kalman Kovacs Referencia : Pituitary. 2016 Aug;19(4):345-55. DOI (Digital Object Identifier) : 10.1007/s11102-015-0703-0 PMID : 26762848 En línea : https://link.springer.com/article/10.1007%2Fs11102-015-0703-0 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3948 Reserva
Reservar este documentoEjemplares(1)
Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000533 AC-2016-008 Archivo digital Producción Científica Artículos científicos Disponible
Título : Biomarkers of pituitary carcinomas Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2016 Títulos uniformes : Expert Review of Endocrinology and Metabolism Idioma : Inglés (eng) Palabras clave : Angiogenesis Galectin-3 HIF-1 H-ras Ki-67 microRNA P27/KIP1 P53 pituitary carcinoma telomerase Resumen : Pituitary carcinoma is a rare tumor originating from adenohypophyseal cells. Currently, diverse pathogenetic mechanisms, i.e. de novo versus malignant transformation from pituitary adenoma, remain obscure and require further investigation. During the last two decades, scientific research added new horizons not only in regards to general tumor concepts but also in next generation biomarker armamentarium that sheds light on alternate pathways in carcinogenesis. Areas covered: In this review, the impact of apoptotic and proliferative markers, angiogenesis, telomerase activity, H-ras, HIF-1, HER-2/neu, Rb gene, and microRNAs in pathogenetic mechanisms of pituitary carcinomas were revised. Expert commentary: It is becoming increasingly important for the need of standardization of new biomarkers but also for better comprehension of the diverse pathways in tumorigenesis. This can only be accomplished by tapping into the continuously expanding spectrum of new biomarkers. Mención de responsabilidad : Aydin Sav, Fabio Rotondo, Luis V Syro, Antonio Di Ieva, Michael D Cusimano, Kalman Kovacs Referencia : Expert Rev Endocrinol Metab. 2016 May;11(3):253-261. DOI (Digital Object Identifier) : 10.1080/17446651.2016.1179110 PMID : 30058931 En línea : https://www.tandfonline.com/doi/abs/10.1080/17446651.2016.1179110 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4611 Biomarkers of pituitary carcinomas [documento electrónico] / Luis Vicente Syro Moreno, . - 2016.
Obra : Expert Review of Endocrinology and Metabolism
Idioma : Inglés (eng)
Palabras clave : Angiogenesis Galectin-3 HIF-1 H-ras Ki-67 microRNA P27/KIP1 P53 pituitary carcinoma telomerase Resumen : Pituitary carcinoma is a rare tumor originating from adenohypophyseal cells. Currently, diverse pathogenetic mechanisms, i.e. de novo versus malignant transformation from pituitary adenoma, remain obscure and require further investigation. During the last two decades, scientific research added new horizons not only in regards to general tumor concepts but also in next generation biomarker armamentarium that sheds light on alternate pathways in carcinogenesis. Areas covered: In this review, the impact of apoptotic and proliferative markers, angiogenesis, telomerase activity, H-ras, HIF-1, HER-2/neu, Rb gene, and microRNAs in pathogenetic mechanisms of pituitary carcinomas were revised. Expert commentary: It is becoming increasingly important for the need of standardization of new biomarkers but also for better comprehension of the diverse pathways in tumorigenesis. This can only be accomplished by tapping into the continuously expanding spectrum of new biomarkers. Mención de responsabilidad : Aydin Sav, Fabio Rotondo, Luis V Syro, Antonio Di Ieva, Michael D Cusimano, Kalman Kovacs Referencia : Expert Rev Endocrinol Metab. 2016 May;11(3):253-261. DOI (Digital Object Identifier) : 10.1080/17446651.2016.1179110 PMID : 30058931 En línea : https://www.tandfonline.com/doi/abs/10.1080/17446651.2016.1179110 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=4611 Reserva
Reservar este documentoEjemplares(1)
Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD001109 AC-2016-090 Archivo digital Producción Científica Artículos científicos Disponible
Título : Clinicopathologic features of familial pituitary adenomas Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2016 Títulos uniformes : Diagnostic Histopathology Idioma : Inglés (eng) Palabras clave : AIP Carney complex classification diagnosis DICER1 familial isolated familial syndromes genetics McCune–Albright syndrome multiple endocrine neoplasia type 1 pathology pituitary adenoma pituitary blastoma X-linked acrogigantism syndrome Resumen : Pituitary adenomas are common neoplasms. Initially considered as sporadic tumours, some of them are associated with familial syndromes such as familial isolated pituitary adenoma, multiple endocrine neoplasia type 1 and type 4, X-linked acrogigantism syndrome, Carney complex, pheochromocytoma/paraganglioma–pituitary adenoma, pituitary blastoma and McCune–Albright syndrome. They represent a group of diseases with different genetic background and variable phenotype. Here, we summarize the clinicopathological features of pituitary adenomas associated with these familial syndromes. Mención de responsabilidad : Luis V. Syro, Fabio Rotondo, Kalman Kovacs, Márta Korbonits Referencia : Diag Histop. 2016;22(3):85-91. DOI (Digital Object Identifier) : 10.1016/j.mpdhp.2016.02.004 En línea : http://www.diagnostichistopathology.co.uk/article/S1756-2317(16)00022-0/fulltext Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3958 Clinicopathologic features of familial pituitary adenomas [documento electrónico] / Luis Vicente Syro Moreno, . - 2016.
Obra : Diagnostic Histopathology
Idioma : Inglés (eng)
Palabras clave : AIP Carney complex classification diagnosis DICER1 familial isolated familial syndromes genetics McCune–Albright syndrome multiple endocrine neoplasia type 1 pathology pituitary adenoma pituitary blastoma X-linked acrogigantism syndrome Resumen : Pituitary adenomas are common neoplasms. Initially considered as sporadic tumours, some of them are associated with familial syndromes such as familial isolated pituitary adenoma, multiple endocrine neoplasia type 1 and type 4, X-linked acrogigantism syndrome, Carney complex, pheochromocytoma/paraganglioma–pituitary adenoma, pituitary blastoma and McCune–Albright syndrome. They represent a group of diseases with different genetic background and variable phenotype. Here, we summarize the clinicopathological features of pituitary adenomas associated with these familial syndromes. Mención de responsabilidad : Luis V. Syro, Fabio Rotondo, Kalman Kovacs, Márta Korbonits Referencia : Diag Histop. 2016;22(3):85-91. DOI (Digital Object Identifier) : 10.1016/j.mpdhp.2016.02.004 En línea : http://www.diagnostichistopathology.co.uk/article/S1756-2317(16)00022-0/fulltext Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3958 Reserva
Reservar este documentoEjemplares(1)
Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000544 AC-2016-019 Archivo digital Producción Científica Artículos científicos Disponible
Título : Autophagy in endocrine tumors Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2015 Títulos uniformes : Endocrine Related Cancer Idioma : Inglés (eng) Palabras clave : Autophagy autophagy modulation endocrine disease neoplasia therapeutic potential Resumen : Autophagy is an important intracellular process involving the degradation of cytoplasmic components. It is involved in both physiological and pathological conditions, including cancer. The role of autophagy in cancer is described as a ‘double-edged sword,’ a term that reflects its known participation in tumor suppression, tumor survival and tumor cell proliferation. Available research regarding autophagy in endocrine cancer supports this concept. Autophagy shows promise as a novel therapeutic target in different types of endocrine cancer, inhibiting or increasing treatment efficacy in a context- and cell-type dependent manner. At present, however, there is very little research concerning autophagy in endocrine tumors. No research was reported connecting autophagy to some of the tumors of the endocrine glands such as the pancreas and ovary. This review aims to elucidate the roles of autophagy in different types of endocrine cancer and highlight the need for increased research in the field. Mención de responsabilidad : Andrea Weckman, Fabio Rotondo, Antonio Di Ieva, Luis V Syro, Henriett Butz, Michael D Cusimano and Kalman Kovacs Referencia : Endoc Rel Cancer. 2015;22(4):205-18. DOI (Digital Object Identifier) : 10.1530/ERC-15-0042 En línea : https://erc.bioscientifica.com/view/journals/erc/22/4/R205.xml Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3901 Autophagy in endocrine tumors [documento electrónico] / Luis Vicente Syro Moreno, . - 2015.
Obra : Endocrine Related Cancer
Idioma : Inglés (eng)
Palabras clave : Autophagy autophagy modulation endocrine disease neoplasia therapeutic potential Resumen : Autophagy is an important intracellular process involving the degradation of cytoplasmic components. It is involved in both physiological and pathological conditions, including cancer. The role of autophagy in cancer is described as a ‘double-edged sword,’ a term that reflects its known participation in tumor suppression, tumor survival and tumor cell proliferation. Available research regarding autophagy in endocrine cancer supports this concept. Autophagy shows promise as a novel therapeutic target in different types of endocrine cancer, inhibiting or increasing treatment efficacy in a context- and cell-type dependent manner. At present, however, there is very little research concerning autophagy in endocrine tumors. No research was reported connecting autophagy to some of the tumors of the endocrine glands such as the pancreas and ovary. This review aims to elucidate the roles of autophagy in different types of endocrine cancer and highlight the need for increased research in the field. Mención de responsabilidad : Andrea Weckman, Fabio Rotondo, Antonio Di Ieva, Luis V Syro, Henriett Butz, Michael D Cusimano and Kalman Kovacs Referencia : Endoc Rel Cancer. 2015;22(4):205-18. DOI (Digital Object Identifier) : 10.1530/ERC-15-0042 En línea : https://erc.bioscientifica.com/view/journals/erc/22/4/R205.xml Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3901 Reserva
Reservar este documentoEjemplares(1)
Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000481 AC-2015-034 Archivo digital Producción Científica Artículos científicos Disponible
Título : Biomarkers of acromegaly Tipo de documento : documento electrónico Autores : Luis Vicente Syro Moreno, Fecha de publicación : 2015 Títulos uniformes : Endocrine Idioma : Inglés (eng) Mención de responsabilidad : Luis V Syro, Fabio Rotondo, Kalman Kovacs Referencia : Endocrine. 2015 May;49(1):4-5. DOI (Digital Object Identifier) : 10.1007/s12020-015-0579-9 PMID : 25784390 En línea : https://link.springer.com/article/10.1007%2Fs12020-015-0579-9 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3902 Biomarkers of acromegaly [documento electrónico] / Luis Vicente Syro Moreno, . - 2015.
Obra : Endocrine
Idioma : Inglés (eng)
Mención de responsabilidad : Luis V Syro, Fabio Rotondo, Kalman Kovacs Referencia : Endocrine. 2015 May;49(1):4-5. DOI (Digital Object Identifier) : 10.1007/s12020-015-0579-9 PMID : 25784390 En línea : https://link.springer.com/article/10.1007%2Fs12020-015-0579-9 Enlace permanente : https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=3902 Reserva
Reservar este documentoEjemplares(1)
Código de barras Número de Ubicación Tipo de medio Ubicación Sección Estado DD000483 AC-2015-036 Archivo digital Producción Científica Artículos científicos Disponible PermalinkPermalinkHuman kallikrein 10 expression in surgically removed human pituitary corticotroph adenomas: an immunohistochemical study / Luis Vicente Syro MorenoPermalinkPermalinkPermalinkPermalinkPermalinkTreatment of invasive silent somatotroph pituitary adenoma with temozolomide. Report of a case and review of the literature / Luis Vicente Syro MorenoPermalinkPermalinkPermalink