Osvaldo Moutinho Pereira Soares
AuthID: R-002-E61
1
TITLE: INCIDENCE OF TP53 MUTATIONS IN PATIENTS WITH CANCER IN CENTRO HOSPITALAR DE TRAS-OS-MONTES E ALTO DOURO: A PRELIMINARY STUDY Full Text
AUTHORS: Arantes, Regina; Pinto, Catarina; Souto, Marta; Morais, Patricia; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Arantes, Regina; Pinto, Catarina; Souto, Marta; Morais, Patricia; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: 
WOS
WOS2
TITLE: CYTOGENETIC FINDINGS IN INFERTILE COUPLES FROM TRAS-OS-MONTES AND ALTO DOURO REGION: A GLIMPSE INTO THE GENETIC BASIS OF INFERTILITY Full Text
AUTHORS: Li, Fernanda; Arantes, Regina; Souto, Marta; Pinto, Catarina; Matos, Ana; Gomes, Zelia; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Li, Fernanda; Arantes, Regina; Souto, Marta; Pinto, Catarina; Matos, Ana; Gomes, Zelia; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS3
TITLE: IDENTIFICATION OF PATHOGENIC CDH1 MUTATION IN BILATERAL BREAST CANCER - A CASE REPORT Full Text
AUTHORS: Soares, Gabriela; Arantes, Regina; Souto, Marta; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Soares, Gabriela; Arantes, Regina; Souto, Marta; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS4
TITLE: TRISOMY 6 IN B-CELL LYMPHOMA: A RARE EVENT Full Text
AUTHORS: Sousa, Jose; Souto, Marta; Loureiro, Bruno; Arantes, Regina; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Sousa, Jose; Souto, Marta; Loureiro, Bruno; Arantes, Regina; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS5
TITLE: FAMILY STUDY OF A PERICENTRIC INVERSION IN CHROMOSOME 7 AND THE ANALYSIS IN SILICO OF THE BREAKPOINTS Full Text
AUTHORS: Morais, Patricia; Adega, Filomena; Souto, Marta; Arantes, Regina; Martins, Marcia; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Morais, Patricia; Adega, Filomena; Souto, Marta; Arantes, Regina; Martins, Marcia; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS6
TITLE: AN UNEXPECTABLE CYTOGENETIC RESULT IN A CHRONIC MYELOID LEUKEMIA CASE Full Text
AUTHORS: Souto, Marta; Sousa, Jose; Loureiro, Bruno; Arantes, Regina; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
AUTHORS: Souto, Marta; Sousa, Jose; Loureiro, Bruno; Arantes, Regina; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2023, SOURCE: 26th Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 102, ISSUE: 13
INDEXED IN: WOS
WOS7
TITLE: Two diseases, one patient. The importance of cytogenetic and FISH in Hematology
AUTHORS: Seixas, Filipa; Sousa, Pedro; Arantes, Regina; Souto, Marta; Ferraz, Patricia; Moutinho, Osvaldo; Cunha, Manuel; Leite, Rosario Pinto;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Seixas, Filipa; Sousa, Pedro; Arantes, Regina; Souto, Marta; Ferraz, Patricia; Moutinho, Osvaldo; Cunha, Manuel; Leite, Rosario Pinto;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
WOS8
TITLE: A rare duplication in 8p11 region
AUTHORS: Souto, Marta; Botelho, Pedro; Martins, Marcia; Moutinho, Osvaldo; Leite, Rosario Pinto;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
AUTHORS: Souto, Marta; Botelho, Pedro; Martins, Marcia; Moutinho, Osvaldo; Leite, Rosario Pinto;
PUBLISHED: 2022, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 30, ISSUE: SUPPL 1
INDEXED IN: WOS
WOS9
TITLE: A RARE CASE OF ACUTE MYELOID LEUKEMIA WITH DER(22)T(1;22)(Q21;P10): A CASE REPORT Full Text
AUTHORS: Ferreira, Tiago; Souto, Marta; Seixas, Filipa; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Ferreira, Tiago; Souto, Marta; Seixas, Filipa; Cunha, Manuel; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
WOS10
TITLE: 18P DELETION SYNDROME: A CASE REPORT Full Text
AUTHORS: Silva, Lucinda; Morais, Patricia; Soares, Gabriela; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
AUTHORS: Silva, Lucinda; Morais, Patricia; Soares, Gabriela; Moutinho, Osvaldo; Pinto Leite, Rosario;
PUBLISHED: 2022, SOURCE: MEDICINE, VOLUME: 101, ISSUE: 30
INDEXED IN: WOS
WOS