Search Results - "Agyei Wiafe, Samuel"

Competence in professional psychology practice in Ghana: Qualitative insights from practicing clinical health psychologists by de-Graft Aikins, Ama, Osei-Tutu, Annabella, Agyei, Francis, Asante, Paapa Yaw, Aboyinga, Hannah, Adjei, Alexandra, Ahulu, Linda Dede, Botchway, Irene, Britwum, Marian, Agyei Wiafe, Samuel, Edu-Ansah, Kofi, Nkrumah, Rita, Ohenewaa, Esther, Vogelsang, Joycelyn Kalitsi, Ketor, Robert

“…Issues concerning competence of practicing psychologists have not been critically investigated in Ghana. This study used the three-dimensional cube model of…”
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Unlocking sociocultural and community factors for the global adoption of genomic medicine by Chediak, Lynsey, Bedlington, Nicola, Gadson, Ayesha, Kent, Alastair, Khalek, Aiedah Abdul, Rosen, Luke, Rust, Malisa, Shaikh, Mohd Farooq, Tan, Meng Yoe, Wiafe, Samuel Agyei, Baynam, Gareth, Steward, Charles A

“…Advances in genomic sequencing and genetic testing are increasingly transforming the diagnosis and treatment of diseases-specifically, rare diseases. However,…”
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Pfeiffer syndrome type 3 with FGR2 c.1052C>G (p.Ser351Cys) variant in West Africa: a case report by Danso, Kwadwo Apeadu, Akuaku, Rosemary Sefakor, Young, Florence Naa Adoley, Wiafe, Samuel Agyei

“…Pfeiffer syndrome is a rare genetic condition that includes anomalies of the head, hands, and feet. It was originally described by Rudolf Pfeiffer in 1964. As…”
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Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon by Delgado-Vega, Angelica Maria, Cederroth, Helene, Taylan, Fulya, Ekholm, Katja, Ek, Marlene, Thonberg, Håkan, Jemt, Anders, Nilsson, Daniel, Eisfeldt, Jesper, Bilgrav Saether, Kristine, Höijer, Ida, Akgun-Dogan, Ozlem, Asano, Yui, Barakat, Tahsin Stefan, Batkovskyte, Dominyka, Baynam, Gareth, Bodamer, Olaf, Chetruengchai, Wanna, Corcoran, Pádraic, Couse, Madeline, Danis, Daniel, Dohi, Eisuke, Erhardsson, Mattias, Fernandez-Luna, Luis, Fujiwara, Toyofumi, Garg, Neha, Giugliani, Roberto, Gonzaga-Jauregui, Claudia, Groza, Tudor, Gunnarsson, Cecilia, Hammarsjö, Anna, Hammond, Charles Kumi, Hatirnaz Ng, Özden, Hesketh, Sirisha, Hettiarachchi, Dineshani, Johansson Soller, Maria, Kirmani, Umn Ahmed, Kjellberg, Martin, Kvarnung, Malin, Kvlividze, Oleg, Lagerstedt-Robinson, Kristina, Lasko, Paul, Lassmann, Timo, Lau, Lynette Y. S., Laurie, Steven, Lim, Weng Khong, Liu, Zhandong, Lysenkova Wiklander, Mariya, Makay, Prince, Maiga, Alassane Baneye, Maya-González, Carolina, Meyn, M. Stephen, Neethiraj, Ramprasad, Nigro, Vincenzo, Nordgren, Felix, Nordlund, Jessica, Orrsjö, Sara, Ottosson, Jesper, Ozbek, Ugur, Özdemir, Özkan, Partin, Clyde, Pearce, David A., Peck, Raquel, Pettersson, Maria, Pongpanich, Monnat, Posada de la Paz, Manuel, Ramani, Arun, Romero, Juan Andres, Romero, Vanessa I., Rosenquist, Richard, Saw, Aung Min, Spencer, Matthew, Stattin, Eva-Lena, Srichomthong, Chalurmpon, Tapia-Paez, Isabel, Taruscio, Domenica, Taylor, Julie P., Tkemaladze, Tinatin, Tully, Ian, Tümer, Zeynep, van Zelst-Stams, Wendy A. G., Verloes, Alain, Västerviga, Emma, Wang, Sailan, Yang, Rachel, Yamamoto, Shinya, Yépez, Vicente A., Zhang, Qing, Shotelersuk, Vorasuk, Alanay, Yasemin, Botto, Lorenzo D., Kirmani, Salman, Lumaka, Aimé, Palmer, Elizabeth Emma, Puri, Ratna Dua, Wirta, Valtteri, Lindstrand, Anna, Buske, Orion J., Cederroth, Mikk, Nordgren, Ann

“…In the first-ever Undiagnosed Hackathon, nearly 100 experts from 28 countries combined advanced phenotyping and genomic techniques for 48 hours, ultimately…”
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Global health for rare diseases through primary care by Baynam, Gareth, Hartman, Adam L, Letinturier, Mary Catherine V, Bolz-Johnson, Matt, Carrion, Prescilla, Grady, Alice Chen, Dong, Xinran, Dooms, Marc, Dreyer, Lauren, Graessner, Holm, Granados, Alicia, Groza, Tudor, Houwink, Elisa, Jamuar, Saumya Shekhar, Vasquez-Loarte, Tania, Tumiene, Biruté, Wiafe, Samuel Agyei, Bjornson-Pennell, Heidi, Groft, Stephen

“…Rare diseases affect over 300 million people worldwide and are gaining recognition as a global health priority. Their inclusion in the UN Sustainable…”
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Digit-all: Rare Diseases by Baynam, Gareth, Chediak, Lynsey, Bilkey, Gemma, Gration, Dylan, Wiafe, Samuel Agyei

“…Rare diseases are increasingly recognised as a global public health priority and contribute to significant and disproportionately high health system impacts…”
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Digit-all: Rare Diseases by Gareth Baynam, Lynsey Chediak, Gemma Bilkey, Dylan Gration, Samuel Agyei Wiafe

“…Rare diseases are increasingly recognised as a global public health priority and contribute to significant and disproportionately high health system impacts…”
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Pfeiffer syndrome type 3 with FGR2 c.1052C>G (p.Ser351Cys) variant in West Africa: a case report by Danso, Kwadwo Apeadu, Akuaku, Rosemary Sefakor, Young, Florence Naa Adoley, Wiafe, Samuel Agyei

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