51
TÍTULO: Choosing not to know: accounts of non-engagement with pre-symptomatic testing for late onset-neurological disorders
AUTORES: Mendes, A; Paneque, M ; Clarke, A; Sequeiros, J;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
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TÍTULO: Choosing not to know: accounts of non-engagement with pre-symptomatic testing for Machado-Joseph disease
AUTORES: Alvaro Mendes ; Milena Paneque ; Angus Clarke; Jorge Sequeiros;
PUBLICAÇÃO: 2019, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27, NÚMERO: 3
INDEXADO EM: Scopus WOS CrossRef: 12
53
TÍTULO: Complementariness between medical geneticists and genetic counsellors: its added value in genetics services in Europe
AUTORES: Paneque P Herrera ; Serra Juhe, C; Pestoff, R; Cordier, C; Silva, J; Moldovan, R; Ingvoldstad, C;
PUBLICAÇÃO: 2019, FONTE: 51st Conference of the European-Society-of-Human-Genetics (ESHG) in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG) in EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27
INDEXADO EM: WOS
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TÍTULO: Patients' views: a new tool for quality assessment of genetic counselling  Full Text
AUTORES: Marcia Carvalho; Milena Paneque ; Fidjy Rodrigues; Jorge Saraiva; Alexandra Leonardo; Ana B Sousa; Vania Machado; Renata Oliveira; Miguel Rocha; Jorge Sequeiros; Marina S Lemos;
PUBLICAÇÃO: 2019, FONTE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, NÚMERO: 26
INDEXADO EM: WOS
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TÍTULO: Patients' Voices in Portugal - when rare becomes common  Full Text
AUTORES: Catarina Costa; Isabel Alonso; Jorge Sequeiros; Milena Paneque ;
PUBLICAÇÃO: 2019, FONTE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, NÚMERO: 26
INDEXADO EM: WOS
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TÍTULO: Psychiatric genetic counseling: A mapping exercise  Full Text
AUTORES: Ramona Moldovan; Kevin A McGhee; Domenico Coviello; Anniken Hamang; Angela Inglis; Charlotta I Ingvoldstad Malmgren; Maria Johansson Soller; Mercy Laurino; Bettina Meiser; Lauren Murphy; Milena Paneque ; Oleg Papsuev; Joanna Pawlak; Eulalia R Rovira Moreno; Clara Serra Juhe; Shiri Shkedi Rafid; Nakita Laing; Marie Antoinette Voelckel; Melanie Watson; Jehannine C Austin;
PUBLICAÇÃO: 2019, FONTE: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, VOLUME: 180, NÚMERO: 8
INDEXADO EM: Scopus WOS CrossRef: 28
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TÍTULO: Psychosocial experiences of young adults at risk for transthyretin familial amyloid polyneuropathy: early versus late-onset Portuguese case report  Full Text
AUTORES: Jose D Pereira; Marina S Lemos; Milena Paneque ;
PUBLICAÇÃO: 2019, FONTE: 22nd Annual Meeting of the Portuguese-Society-of-Human-Genetics (SPGH) in MEDICINE, VOLUME: 98, NÚMERO: 26
INDEXADO EM: WOS
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TÍTULO: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages
AUTORES: Jackson, L; O'Connor, A; Paneque, M ; Curtisova, V; Lunt, PW; Pourova, RK; Macek, M; Stefansdottir, V; Turchetti, D; Campos, M; Henneman, L; Godino, L; Skirton, H; Cornel, MC;
PUBLICAÇÃO: 2019, FONTE: GENETICS IN MEDICINE, VOLUME: 21, NÚMERO: 3
INDEXADO EM: WOS
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TÍTULO: The Gen-Equip Project: evaluation and impact of genetics e-learning resources for primary care in six European languages (vol 21, pg 718, 2018)
AUTORES: Jackson, L; O'Connor, A; Paneque, M ; Curtisova, V; Lunt, PW; Pourova, RK; Macek, M; Stefansdottir, V; Turchetti, D; Campos, M; Henneman, L; Godino, L; Skirton, H; Cornel, MC;
PUBLICAÇÃO: 2019, FONTE: GENETICS IN MEDICINE, VOLUME: 21, NÚMERO: 7
INDEXADO EM: Scopus WOS CrossRef: 1
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TÍTULO: The Global State of the Genetic Counseling Profession
AUTORES: MaryAnn Abacan; Lamia Alsubaie; Kristine Barlow Stewart; Beppy Caanen; Christophe Cordier; Eliza Courtney; Emeline Davoine; Janice Edwards; Niby J Elackatt; Kate Gardiner; Yue Guan; Lian Hua Huang; Charlotta Ingvoldstad Malmgren; Sahil Kejriwal; Hyon J Kim; Deborah Lambert; Paulina Araceli Lantigua Cruz; Juliana M H Lee; Marianne Lodahl; Ashild Lunde; Shelley Macaulay; Ivan Macciocca; Sonia Margarit; Anna Middleton; Ramona Moldovan; Joanne Ngeow; Alexandra J Obregon Tito; Kelly E Ormond; Milena Paneque ; Karen Powell; Kunal Sanghavi; Diana Scotcher; Jenna Scott; Clara Serra Juhe; Shiri Shkedi Rafid; Tina Marie Wessels; Sook Yee Yoon; Catherine Wicklund; ...Mais
PUBLICAÇÃO: 2019, FONTE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 27, NÚMERO: 2
INDEXADO EM: Scopus WOS CrossRef: 267
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