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381by Marcello Scala, Irene Schiavetti, Francesca Madia, Cristina Chelleri, Gianluca Piccolo, Andrea Accogli, Antonella Riva, Vincenzo Salpietro, Renata Bocciardi, Guido Morcaldi, Marco Di Duca, Francesco Caroli, Antonio Verrico, Claudia Milanaccio, Gianmaria Viglizzo, Monica Traverso, Simona Baldassari, Paolo Scudieri, Michele Iacomino, Gianluca Piatelli, Carlo Minetti, Pasquale Striano, Maria Luisa Garrè, Patrizia De Marco, Maria Cristina Diana, Valeria Capra, Marco Pavanello, Federico Zara“...Neurofibromatosis type 1 (NF1) is a proteiform genetic condition caused by pathogenic variants...”
Published 2021-04-01
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382by Timm Greulich, Alan Altraja, Miriam Barrecheguren, Robert Bals, Jan Chlumsky, Joanna Chorostowska-Wynimko, Christian Clarenbach, Luciano Corda, Angelo Guido Corsico, Ilaria Ferrarotti, Cristina Esquinas, Caroline Gouder, Ana Hećimović, Aleksandra Ilic, Yavor Ivanov, Sabina Janciauskiene, Wim Janssens, Malcolm Kohler, Alvils Krams, Beatriz Lara, Ravi Mahadeva, Gerry McElvaney, Jean-François Mornex, Karen O'Hara, David Parr, Eava Piitulainen, Karin Schmid-Scherzer, Niels Seersholm, Robert A. Stockley, Jan Stolk, Maria Sucena, Hanan Tanash, Alice Turner, Ruxandra Ulmeanu, Marion Wilkens, Arzu Yorgancioğlu, Ana Zaharie, Marc Miravitlles“...Rationale and objectives Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads...”
Published 2020-03-01
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383by Taqueda, Maria Stela Melo Santos“..., and potentialize an eventual genetic condition. Prevalence in the western countries is about 10-15% of adults...”
Published 2017
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384by Almeida, Juliana Pereira“... === Abstract: Hereditary Gingival Fibromatosis (HGF) is a rare genetic condition clinically manifested by a...”
Published 2004
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385by Chris Stinton, Mary Jordan, Hannah Fraser, Peter Auguste, Rachel Court, Lena Al-Khudairy, Jason Madan, Dimitris Grammatopoulos, Sian Taylor-Phillips“...Background: Lynch syndrome is an inherited genetic condition that is associated with an increased...”
Published 2021-06-01
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386by Henricson, Cecilia“... the area of cognitive psychology. Usher syndrome is a rare genetic condition causing a combination...”
Published 2015
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Doctoral Thesis -
387by Oliveira, Érika Assunção de“...), which is a genetic condition that affects the formation of the dentin, and involves primary...”
Published 2010
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388by Gomes, Mayara Emmily Chaves“... it as secondary and, so, to decrease the importance of the speech of those who have the genetic condition, what...”
Published 2018
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389by Nuno Sepúlveda, Nuno Sepúlveda, Lynn Grignard, Jonathan Curry, Laleta Mahey, Guido J. H. Bastiaens, Alfred B. Tiono, Joseph Okebe, Sam A. Coulibaly, Bronner P. Gonçalves, Bronner P. Gonçalves, Muna Affara, Alphonse Ouédraogo, Edith C. Bougouma, Guillaume S. Sanou, Issa Nébié, Kjerstin Lanke, Sodiomon B. Sirima, Alassane Dicko, Umberto d’Alessandro, Umberto d’Alessandro, Taane G. Clark, Taane G. Clark, Susana Campino, Ingrid Chen, Alice C. Eziefula, Alice C. Eziefula, Roly Gosling, Teun Bousema, Teun Bousema, Chris Drakeley“... in individuals suffering from Glucose-6-phospate dehydrogenase (G6PD) deficiency, a genetic condition determined...”
Published 2021-04-01
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390by Ivan Ivanovski, Olivera Djuric, Serena Broccoli, Stefano Giuseppe Caraffi, Patrizia Accorsi, Margaret P. Adam, Kristina Avela, Magdalena Badura-Stronka, Allan Bayat, Jill Clayton-Smith, Isabella Cocco, Duccio Maria Cordelli, Goran Cuturilo, Veronica Di Pisa, Juliette Dupont Garcia, Roberto Gastaldi, Lucio Giordano, Andrea Guala, Christina Hoei-Hansen, Mie Inaba, Alessandro Iodice, Jens Erik Klint Nielsen, Vladimir Kuburovic, Brissia Lazalde-Medina, Baris Malbora, Seiji Mizuno, Oana Moldovan, Rikke S. Møller, Petra Muschke, Valeria Otelli, Chiara Pantaleoni, Carmelo Piscopo, Maria Luisa Poch-Olive, Igor Prpic, Purificación Marín Reina, Federico Raviglione, Emilia Ricci, Emanuela Scarano, Graziella Simonte, Robert Smigiel, George Tanteles, Luigi Tarani, Aurelien Trimouille, Elvis Terci Valera, Samantha Schrier Vergano, Karin Writzl, Bert Callewaert, Salvatore Savasta, Maria Elisabeth Street, Lorenzo Iughetti, Sergio Bernasconi, Paolo Giorgi Rossi, Livia Garavelli“...Abstract Background Mowat–Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused...”
Published 2020-06-01
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391by Hannum, Juliana Santos de Souza“... of a genetic condition. The main objective of the GC is to guide individual comprehension of condition...”
Published 2016
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392by Chachlaki, Konstantina“... rare congenital genetic condition presenting a unique combination of GnRH deficiency, arising from a...”
Published 2016
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393by Schweinberger, Bruna Martins“... for new studies regarding the effects caused by exposure to excess methionine due to a genetic condition...”
Published 2017
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394by Schweinberger, Bruna Martins“... for new studies regarding the effects caused by exposure to excess methionine due to a genetic condition...”
Published 2017
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395by Schweinberger, Bruna Martins“... for new studies regarding the effects caused by exposure to excess methionine due to a genetic condition...”
Published 2017
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396by Bonne, Nicolas-Xavier“... inactivation of the NF2 gene is linked to the onset of Neurofibromatosis type 2 (NF2), a genetic condition...”
Published 2018
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397by Assis, Alexandro Mangueira Lima de“... of Brazil s population. The current genetic condition is a result of the interbreeding process between...”
Published 2015
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398by Maciel, Mariza Araujo Marinho“... of an associated genetic condition and gender. Two collection instruments were used. The first questionnaire...”
Published 2018
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399by Jafri, Syed Hussain“...Introduction: Prenatal diagnosis for genetic conditions has been available in Pakistan since 1994...”
Published 2017
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400“..., according to which the «cause» concept includes the causative agent of infectious disease, genetic...”
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Article