Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Luciane Kalakun"'
1
Akademický článek
Population prevalence of hereditary breast cancer phenotypes and implementation of a genetic cancer risk assessment program in southern Brazil
Autor: Edenir I. Palmero, Maira Caleffi, Lavínia Schüler-Faccini, Fernanda L. Roth, Luciane Kalakun, Cristina Brinkmann Oliveira Netto, Giovana Skonieski, Juliana Giacomazzi, Bernadete Weber, Roberto Giugliani, Suzi A. Camey, Patricia Ashton-Prolla
Publikováno v: Genetics and Molecular Biology, Vol 32, Iss 3, Pp 447-455 (2009)
In 2004, a population-based cohort (the Núcleo Mama Porto Alegre - NMPOA Cohort) was started in Porto Alegre, southern Brazil and within that cohort, a hereditary breast cancer study was initiated, aiming to determine the prevalence of hereditary br
Externí odkaz: https://doaj.org/article/c0c640b4078949199f7dc6945aa124a9
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2
Akademický článek
White matter lesions in Fabry disease before and after enzyme replacement therapy: a 2-year follow-up Lesões da substância branca na doença de Fabry antes e depois da terapia de reposição enzimática: um seguimento de 2 anos
Autor: Laura B. Jardim, Flávio Aesse, Leonardo M. Vedolin, Cláudio Pitta-Pinheiro, João Marconato, Maira G. Burin, Cláudia Cecchin, Cristina B.O. Netto, Ursula S. Matte, Fernanda Pereira, Luciane Kalakun, Roberto Giugliani
Publikováno v: Arquivos de Neuro-Psiquiatria, Vol 64, Iss 3b, Pp 711-717 (2006)
PURPOSE: To report the clinical and neuroimaging, central nervous system (CNS) findings of patients with Fabry disease (FD) during 24 months of enzyme replacement therapy (ERT) with agalsidase-alpha. METHOD: Eight patients were included. Six complete
Externí odkaz: https://doaj.org/article/710f3a84363d4619a672cb8bc518f0ca
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3
Population prevalence of hereditary breast cancer phenotypes and implementation of a genetic cancer risk assessment program in southern Brazil
Autor: Bernadete Weber, Patricia Ashton-Prolla, Lavinia Schuler-Faccini, Cristina Brinkmann Oliveira Netto, Juliana Giacomazzi, Fernanda Lenara Roth, Suzi Alves Camey, Maira Caleffi, Roberto Giugliani, Luciane Kalakun, Edenir Inêz Palmero, Giovana Skonieski
Publikováno v: Genetics and Molecular Biology, Vol 32, Iss 3, Pp 447-455 (2009)
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Scopus-Elsevier
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 32, Issue: 3, Pages: 447-455, Published: 10 JUL 2009
Genetics and Molecular Biology v.32 n.3 2009
Sociedade Brasileira de Genética (SBG)
instacron:SBG
In 2004, a population-based cohort (the Núcleo Mama Porto Alegre - NMPOA Cohort) was started in Porto Alegre, southern Brazil and within that cohort, a hereditary breast cancer study was initiated, aiming to determine the prevalence of hereditary br
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8742ce8b830c271a95ccdf50b27001ed
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1415-47572009000300004
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4
Clinical Characterization and Risk Profile of Individuals Seeking Genetic Counseling for Hereditary Breast Cancer in Brazil
Autor: Fernando Regla Vargas, Patricia Ashton-Prolla, Sergio J Azevedo, José Claudio Casali da Rocha, Lavinia Schuler-Faccini, Roberto Giugliani, Maira Caleffi, Melissa Brauner Blom, Edenir Inêz Palmero, Luciane Kalakun
Publikováno v: Journal of Genetic Counseling. 16:363-371
Hereditary breast cancer (HBC) accounts for 5-10% of breast cancer cases and it significantly increases the lifetime risk of cancer. Our objective was to evaluate the sociodemographic variables, family history of cancer, breast cancer (BC) screening
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce1f417b74d3d754400748af8a50acb9
https://doi.org/10.1007/s10897-006-9073-0
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5
Lesões da substância branca na doença de Fabry antes e depois da terapia de reposição enzimática: um seguimento de 2 anos
Autor: Luciane Kalakun, Cláudia Rafaela Cecchin, Roberto Giugliani, Ursula da Silveira Matte, Laura Bannach Jardim, Cristina Brinckmann Oliveira Netto, Cláudio de Faria Pitta-Pinheiro, Fernanda dos Santos Pereira, Leonardo Modesti Vedolin, Flávio Franciosi Aesse, João Marconato, Maira Graeff Burin
Publikováno v: Arquivos de Neuro-Psiquiatria v.64 n.3b 2006
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 64, Issue: 3b, Pages: 711-717, Published: SEP 2006
Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
PURPOSE: To report the clinical and neuroimaging, central nervous system (CNS) findings of patients with Fabry disease (FD) during 24 months of enzyme replacement therapy (ERT) with agalsidase-alpha. METHOD: Eight patients were included. Six complete
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::510be8815c618f8e71430331df171db7
https://doi.org/10.1590/s0004-282x2006000500002
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6
Improvement of sympathetic skin responses under enzyme replacement therapy in Fabry disease
Autor: Jefferson Becker, Irenio Gomes, F. Pereira, Laura Bannach Jardim, R. Giugliani, Cristina Brinckmann Oliveira Netto, Ursula da Silveira Matte, Maira Graeff Burin, Daniel Bocchese Nora, Luciane Kalakun
Publikováno v: Journal of Inherited Metabolic Disease. 29:653-659
Aim To report the effect of enzyme replacement therapy (ERT) in sympathetic skin responses (SSR) of patients with Fabry disease. Patients and methods Seven male patients were included in an open-label protocol using agalsidase-alfa, continued at regu
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20329c9375fce67218bc936ead48eb81
https://doi.org/10.1007/s10545-006-0339-3
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7
Development and validation of a simple questionnaire for the identification of hereditary breast cancer in primary care
Autor: Érica Batassini, Maira Caleffi, Susana Mayer Moreira, Lavinia Schuler-Faccini, Juliana Giacomazzi, Vanessa Belo-Reyes, Ernestina Silva de Aguiar, Patricia Ashton-Prolla, Fernanda Lenara Roth, Roberto Giugliani, Suzi Alves Camey, Luciane Kalakun, Edenir Inêz Palmero, Aishameriane Venes Schmidt
Publikováno v: Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
BMC Cancer
BMC Cancer, Vol 9, Iss 1, p 283 (2009)
Background Breast cancer is a significant public health problem worldwide and the development of tools to identify individuals at-risk for hereditary breast cancer syndromes, where specific interventions can be proposed to reduce risk, has become inc
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8374a28162b5e536a78346d6054f34d2
https://doi.org/10.1186/1471-2407-9-283
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8
Consistency of self-reported first-degree family history of cancer in a population-based study
Autor: Edenir Inêz Palmero, Luciane Kalakun, Maira Caleffi, Fernanda Lenara Roth, Roberto Giugliani, Susana Mayer Moreira, Lavinia Schuler-Faccini, Suzi Alves Camey, Carla Bochi, Patricia Ashton-Prolla
Publikováno v: Familial cancer. 8(3)
The aim of this study was to assess the preva- lence and consistency of self-reported family history of cancer among first-degree relatives (FDR) in a population- based study. Women at primary care units (PCU) were submitted to a questionnaire about
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc0a6d4a895e04bb849eda852a3592b5
https://pubmed.ncbi.nlm.nih.gov/19153822
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9
Evolution of uterine cervical cancer mortality from 1979 to 1998 in the state of Rio Grande do Sul, Brazil
Autor: Mary Clarisse Bozzetti, Luciane Kalakun
Publikováno v: Repositório Institucional da UFRGS
Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
Cadernos de Saúde Pública v.21 n.1 2005
Cadernos de Saúde Pública
Fundação Oswaldo Cruz (FIOCRUZ)
instacron:FIOCRUZ
Cadernos de Saúde Pública, Vol 21, Iss 1, Pp 299-309 (2005)
A mortalidade por câncer de colo de útero tem diminuído em países desenvolvidos. Entretanto, no Brasil, os dados apontam o câncer de colo de útero como uma das mais freqüentes causas de morte por neoplasia em mulheres, estando em quarto lugar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf1d17ab618c4d01c9773477643a5afc
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10
CNS involvement in Fabry disease: clinical and imaging studies before and after 12 months of enzyme replacement therapy
Autor: Leonardo Modesti Vedolin, C. Pitta-Pinheiro, Roberto Giugliani, Ursula da Silveira Matte, Flávio Franciosi Aesse, Laura Bannach Jardim, José Augusto Marconato, Cláudia Rafaela Cecchin, Ida Vanessa Doederlein Schwartz, Maira Graeff Burin, Luciane Kalakun
Publikováno v: Journal of inherited metabolic disease. 27(2)
We report the clinical and radiological central nervous system (CNS) findings of 8 Fabry disease patients, before (8/8) and after (7/8) 12 months of enzyme replacement therapy (ERT) with agalsidase-alpha. Eight biochemically proven Fabry disease pati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9f66a56da775b6368a34dc4423eaab9
https://pubmed.ncbi.nlm.nih.gov/15159654
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