Enfermedad de Gaucher, un abordaje terapéutico moderno

Autores:
Solano, María Helena
Ramírez C., Carlos
Parra, Lucía
Loboguerrero, José
Tipo de recurso:
Article of journal
Fecha de publicación:
2001
Institución:
Fundación Universitaria de Ciencias de la Salud - FUCS
Repositorio:
Repositorio Digital Institucional ReDi
Idioma:
spa
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oai:repositorio.fucsalud.edu.co:001/2165
Acceso en línea:
https://repositorio.fucsalud.edu.co/handle/001/2165
https://doi.org/10.31260/RepertMedCir.v10.n2.2001.251
Palabra clave:
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openAccess
License
Fundación Universitaria de Ciencias de la Salud FUCS - 2018
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network_name_str Repositorio Digital Institucional ReDi
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dc.title.spa.fl_str_mv Enfermedad de Gaucher, un abordaje terapéutico moderno
dc.title.translated.eng.fl_str_mv Gaucher disease, a modern therapeutic approach
title Enfermedad de Gaucher, un abordaje terapéutico moderno
spellingShingle Enfermedad de Gaucher, un abordaje terapéutico moderno
title_short Enfermedad de Gaucher, un abordaje terapéutico moderno
title_full Enfermedad de Gaucher, un abordaje terapéutico moderno
title_fullStr Enfermedad de Gaucher, un abordaje terapéutico moderno
title_full_unstemmed Enfermedad de Gaucher, un abordaje terapéutico moderno
title_sort Enfermedad de Gaucher, un abordaje terapéutico moderno
dc.creator.fl_str_mv Solano, María Helena
Ramírez C., Carlos
Parra, Lucía
Loboguerrero, José
dc.contributor.author.spa.fl_str_mv Solano, María Helena
Ramírez C., Carlos
Parra, Lucía
Loboguerrero, José
publishDate 2001
dc.date.accessioned.none.fl_str_mv 2001-08-01 00:00:00
2022-02-21T20:34:46Z
dc.date.issued.none.fl_str_mv 2001-08-01
dc.date.available.none.fl_str_mv 2001-08-01 00:00:00
2022-02-21T20:34:46Z
dc.type.spa.fl_str_mv Artículo de revista
dc.type.eng.fl_str_mv Journal article
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dc.identifier.doi.none.fl_str_mv 10.31260/RepertMedCir.v10.n2.2001.251
dc.identifier.issn.none.fl_str_mv 0121-7372
dc.identifier.uri.none.fl_str_mv https://repositorio.fucsalud.edu.co/handle/001/2165
dc.identifier.eissn.none.fl_str_mv 2462-991X
dc.identifier.url.none.fl_str_mv https://doi.org/10.31260/RepertMedCir.v10.n2.2001.251
identifier_str_mv 10.31260/RepertMedCir.v10.n2.2001.251
0121-7372
2462-991X
url https://repositorio.fucsalud.edu.co/handle/001/2165
https://doi.org/10.31260/RepertMedCir.v10.n2.2001.251
dc.language.iso.spa.fl_str_mv spa
language spa
dc.relation.references.spa.fl_str_mv Charrow J, Anderson HC, Kaplan P, et al. The Gaucher registry: demographics and disease characteristics of 1698 patients with
Gaucher disease. Arch Intern Med. 2000; 160: 2835-43.
Giraldo P, Pocovi M, Pérez-Calvo J, et al. Report of the spanisch Gaucher's disease registry: clinical and genetic characteristics. Heamatologica. 2000; 85: 792-9.
Pérez-Calvo J, Bernal M, Giraldo P, et al. Co-morbidity in Gaucher's disease: results of a natinowide enquiry in Spain.
EurJ Med Res. 2000; 5: 231-5. Elstein D, Abrahamov a, Hadas-Halpern I, Zimran A.
Recommendations for diagnosis, evaluation and monitoring of patients with Gaucher disease. Arch Intern Med. 1999; 159: 1254-5.
Charrow J, Esplin JA, Griggle TJ, et al. Gaucher disease: recommendations on diagnosis, evaluation and monitoring.
Arch Intern Med. 1998; 158: 1754-60. Pérez-Calvo J, Giraldo P, GiraltM. Type I Gaucher's disease: clinical, evolutive and therapeutic features in 8 cases. Sangre (Barc). 1994; 39: 3-7.
Beighton J, S acks S. Bone involvement in Gaucher disease. En Deskink RJ, Gatts, Grabowski GA eds. Gaucher Disease: a century of deliniation and reseach. Proceedings of the First International Symposium on Gaucher Disease. New York. NYAlan R Liss Inc. 1982; 107-129.
Herman G, Shapiro RS. Abdelwahab f, et al. MR imaging in adult with Gaucer disease Type 1. Evaluation of marrow involvement and disease activity. Skeletal Radiol 1993; 22: 247- 251.
Esplin JA, Mc Pherson EJ. Treatment of bone complication in patients with Gaucer disease. Gaucher Clinical Perspectives. 1994; 2: 7-11
Pastores GM, Sibille A, Grabowski GA. Enzyme therapy in Gaucher Disease Type 1. Dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months. Blood. 1993; 32: 408- 16.
Niederau C, Holderer A, Heintges T, Stronhmeyer G. Gucocerebrosidase for treatment of Gaucher Disease. First longterm results. J Hepatol. 1994; 21: 610-7.
Rosenthal D, Smith MW, Goodsitt M, Doppelt S. Bone and bone marrow changes in Gaucher Disease. Evaluation in cuantitative MR. Radiology. 1989; 170: 143-6.
Mankin H, Dopplet S, Rosemberg A, Barranger J. Metabolic bone disease in patients with Gaucher disease. En: Avioli L,
Krane S. eds. Metabolic bone disease and clinically related disorders. WB Saunders, 1990.
Grabowski G. Enzimology, Genetics and treatment in Gaucher disease. En: Harris H, Hirsch K. eds. Advances in Human Genetics. New York Plenum Press. 1993.
Bimal T, Latham T, Grabowski G. Gaucher disease: molecular heterogenety and phenotype—genotype correlations. Am J Hum Genet. 1989; 45: 212-25.
Sidranski E, Shaoji T, Martin B, Stubblefield B. DNA mutation analysis of Gaucher patients. Am J Med Genetics. 1992; 42: 331-6.
dc.relation.bitstream.none.fl_str_mv https://revistas.fucsalud.edu.co/index.php/repertorio/article/download/251/249
dc.relation.citationedition.spa.fl_str_mv Núm. 2 , Año 2001 : Mayo – Agosto
dc.relation.citationendpage.none.fl_str_mv 28
dc.relation.citationissue.spa.fl_str_mv 2
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dc.relation.citationvolume.spa.fl_str_mv 10
dc.relation.ispartofjournal.spa.fl_str_mv Revista Repertorio de Medicina y Cirugía
dc.rights.spa.fl_str_mv Fundación Universitaria de Ciencias de la Salud FUCS - 2018
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dc.publisher.spa.fl_str_mv Sociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la Salud
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institution Fundación Universitaria de Ciencias de la Salud - FUCS
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spelling Solano, María Helenacfbd69f8e4d28c6e6c3d2a032972d1fc500Ramírez C., Carlos37c9c397457308f305c3601c09b7d56a300Parra, Lucíacc1ce440f207fd2fa04f85ae8587a733300Loboguerrero, Joséfc05d2bcfc5951850343590a10e369bd3002001-08-01 00:00:002022-02-21T20:34:46Z2001-08-012001-08-01 00:00:002022-02-21T20:34:46ZSociedad de Cirugía de Bogotá, Hospital de San José y Fundación Universitaria de Ciencias de la SaludFundación Universitaria de Ciencias de la Salud FUCS - 2018info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/4.0/http://purl.org/coar/access_right/c_abf2https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/251Enfermedad de Gaucher, un abordaje terapéutico modernoGaucher disease, a modern therapeutic approachapplication/pdfArtículo de revistaJournal articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionTexthttp://purl.org/coar/version/c_970fb48d4fbd8a8510.31260/RepertMedCir.v10.n2.2001.2510121-7372https://repositorio.fucsalud.edu.co/handle/001/21652462-991Xhttps://doi.org/10.31260/RepertMedCir.v10.n2.2001.251spaCharrow J, Anderson HC, Kaplan P, et al. The Gaucher registry: demographics and disease characteristics of 1698 patients withGaucher disease. Arch Intern Med. 2000; 160: 2835-43.Giraldo P, Pocovi M, Pérez-Calvo J, et al. Report of the spanisch Gaucher's disease registry: clinical and genetic characteristics. Heamatologica. 2000; 85: 792-9.Pérez-Calvo J, Bernal M, Giraldo P, et al. Co-morbidity in Gaucher's disease: results of a natinowide enquiry in Spain.EurJ Med Res. 2000; 5: 231-5. Elstein D, Abrahamov a, Hadas-Halpern I, Zimran A.Recommendations for diagnosis, evaluation and monitoring of patients with Gaucher disease. Arch Intern Med. 1999; 159: 1254-5.Charrow J, Esplin JA, Griggle TJ, et al. Gaucher disease: recommendations on diagnosis, evaluation and monitoring.Arch Intern Med. 1998; 158: 1754-60. Pérez-Calvo J, Giraldo P, GiraltM. Type I Gaucher's disease: clinical, evolutive and therapeutic features in 8 cases. Sangre (Barc). 1994; 39: 3-7.Beighton J, S acks S. Bone involvement in Gaucher disease. En Deskink RJ, Gatts, Grabowski GA eds. Gaucher Disease: a century of deliniation and reseach. Proceedings of the First International Symposium on Gaucher Disease. New York. NYAlan R Liss Inc. 1982; 107-129.Herman G, Shapiro RS. Abdelwahab f, et al. MR imaging in adult with Gaucer disease Type 1. Evaluation of marrow involvement and disease activity. Skeletal Radiol 1993; 22: 247- 251.Esplin JA, Mc Pherson EJ. Treatment of bone complication in patients with Gaucer disease. Gaucher Clinical Perspectives. 1994; 2: 7-11Pastores GM, Sibille A, Grabowski GA. Enzyme therapy in Gaucher Disease Type 1. Dosage efficacy and adverse effects in 33 patients treated for 6 to 24 months. Blood. 1993; 32: 408- 16.Niederau C, Holderer A, Heintges T, Stronhmeyer G. Gucocerebrosidase for treatment of Gaucher Disease. First longterm results. J Hepatol. 1994; 21: 610-7.Rosenthal D, Smith MW, Goodsitt M, Doppelt S. Bone and bone marrow changes in Gaucher Disease. Evaluation in cuantitative MR. Radiology. 1989; 170: 143-6.Mankin H, Dopplet S, Rosemberg A, Barranger J. Metabolic bone disease in patients with Gaucher disease. En: Avioli L,Krane S. eds. Metabolic bone disease and clinically related disorders. WB Saunders, 1990.Grabowski G. Enzimology, Genetics and treatment in Gaucher disease. En: Harris H, Hirsch K. eds. Advances in Human Genetics. New York Plenum Press. 1993.Bimal T, Latham T, Grabowski G. Gaucher disease: molecular heterogenety and phenotype—genotype correlations. Am J Hum Genet. 1989; 45: 212-25.Sidranski E, Shaoji T, Martin B, Stubblefield B. DNA mutation analysis of Gaucher patients. Am J Med Genetics. 1992; 42: 331-6.https://revistas.fucsalud.edu.co/index.php/repertorio/article/download/251/249Núm. 2 , Año 2001 : Mayo – Agosto2822410Revista Repertorio de Medicina y CirugíaPublicationOREORE.xmltext/xml2487https://repositorio.fucsalud.edu.co/bitstreams/bcb5577b-ebb9-44bf-abb7-9c7347531e3c/downloade1df5073a5966537c3983eef99cf67a2MD51001/2165oai:repositorio.fucsalud.edu.co:001/21652024-02-02 13:08:52.686https://creativecommons.org/licenses/by-nc-sa/4.0/Fundación Universitaria de Ciencias de la Salud FUCS - 2018metadata.onlyhttps://repositorio.fucsalud.edu.coRepositorio Digital de la Fundación Universitaria de Ciencias de la Saludredi@fucsalud.edu.co

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