Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Maria Isabel Achatz

Showing results (1-10 of 71) with videos related to

Pageof 8
Sort By:
Cold Spring Harbor Perspectives in Medicine|September 25, 2016
The Inherited p53 Mutation in the Brazilian PopulationMaria Isabel Achatz, Gerard P Zambetti
Lancet Regional Health. Americas|February 13, 2023
Cancer surveillance for patients with Li-Fraumeni Syndrome in Brazil: A cost-effectiveness analysisIsadora A Frankenthal, Mariana Cartaxo Alves, Casey Tak, et al.
Case Reports in Oncology|October 21, 2020
Complete Clinical Response in Stage IVB Endometrioid Endometrial Carcinoma after First-Line Pembrolizumab Therapy: Report of a Case with Isolated Loss of PMS2 ProteinJesus Paula Carvalho, Auro Del Giglio, Maria Isabel Achatz, et al.
Familial Cancer|December 24, 2025
Description of six cases of melanoma in 512 patients with germline pathogenic variants in the TP53 geneElisabeth de A C Callegaro, Janina Pontes Pisani, Vanessa Monteleone, et al.
Frontiers in Oncology|August 25, 2022
Double heterozygous pathogenic variants prevalence in a cohort of patients with hereditary breast cancerThais Baccili Cury Megid, Mateus C Barros-Filho, Janina Pontes Pisani, et al.
JAMA Oncology|January 24, 2017
Frequency of Thyroid Carcinoma in Brazilian TP53 p.R337H Carriers With Li Fraumeni SyndromeMaria Nirvana da Cruz Formiga, Kelvin César de Andrade, Luiz Paulo Kowalski, et al.
JCO Global Oncology|March 11, 2020
Recommendations for Advancing the Diagnosis and Management of Hereditary Breast and Ovarian Cancer in BrazilMaria Isabel Achatz, Maira Caleffi, Rodrigo Guindalini, et al.
International Journal of Molecular Sciences|April 28, 2015
Xeroderma pigmentosum: low prevalence of germline XPA mutations in a Brazilian XP populationKarina Miranda Santiago, Amanda França de Nóbrega, Rafael Malagoli Rocha, et al.
Cancer Imaging : the Official Publication of the International Cancer Imaging Society|August 16, 2018
Whole-body magnetic resonance imaging of Li-Fraumeni syndrome patients: observations from a two rounds screening of Brazilian patientsDaniele Paixão, Marcos Duarte Guimarães, Kelvin César de Andrade, et al.
Orphanet Journal of Rare Diseases|April 30, 2014
The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutationsAmanda G Silva, Ana C V Krepischi, Peter L Pearson, et al.
Pageof 8

Showing results (1-10 of 71) with videos related to

Sort By:
Pageof 8
Cold Spring Harbor Perspectives in Medicine|September 25, 2016
The Inherited p53 Mutation in the Brazilian PopulationMaria Isabel Achatz, Gerard P Zambetti
Lancet Regional Health. Americas|February 13, 2023
Cancer surveillance for patients with Li-Fraumeni Syndrome in Brazil: A cost-effectiveness analysisIsadora A Frankenthal, Mariana Cartaxo Alves, Casey Tak, et al.
Case Reports in Oncology|October 21, 2020
Complete Clinical Response in Stage IVB Endometrioid Endometrial Carcinoma after First-Line Pembrolizumab Therapy: Report of a Case with Isolated Loss of PMS2 ProteinJesus Paula Carvalho, Auro Del Giglio, Maria Isabel Achatz, et al.
Familial Cancer|December 24, 2025
Description of six cases of melanoma in 512 patients with germline pathogenic variants in the TP53 geneElisabeth de A C Callegaro, Janina Pontes Pisani, Vanessa Monteleone, et al.
Frontiers in Oncology|August 25, 2022
Double heterozygous pathogenic variants prevalence in a cohort of patients with hereditary breast cancerThais Baccili Cury Megid, Mateus C Barros-Filho, Janina Pontes Pisani, et al.
JAMA Oncology|January 24, 2017
Frequency of Thyroid Carcinoma in Brazilian TP53 p.R337H Carriers With Li Fraumeni SyndromeMaria Nirvana da Cruz Formiga, Kelvin César de Andrade, Luiz Paulo Kowalski, et al.
JCO Global Oncology|March 11, 2020
Recommendations for Advancing the Diagnosis and Management of Hereditary Breast and Ovarian Cancer in BrazilMaria Isabel Achatz, Maira Caleffi, Rodrigo Guindalini, et al.
International Journal of Molecular Sciences|April 28, 2015
Xeroderma pigmentosum: low prevalence of germline XPA mutations in a Brazilian XP populationKarina Miranda Santiago, Amanda França de Nóbrega, Rafael Malagoli Rocha, et al.
Cancer Imaging : the Official Publication of the International Cancer Imaging Society|August 16, 2018
Whole-body magnetic resonance imaging of Li-Fraumeni syndrome patients: observations from a two rounds screening of Brazilian patientsDaniele Paixão, Marcos Duarte Guimarães, Kelvin César de Andrade, et al.
Orphanet Journal of Rare Diseases|April 30, 2014
The profile and contribution of rare germline copy number variants to cancer risk in Li-Fraumeni patients negative for TP53 mutationsAmanda G Silva, Ana C V Krepischi, Peter L Pearson, et al.
Pageof 8