Prescriptions for Antipsychotics: Youth with Intellectual/Developmental Disabilities Compared to Youth without Intellectual/Developmental Disabilities
Marquis, Sandra, Marquis, N Esmé, Lunsky, Yona, McGrail, Kimberlyn M, Baumbusch, Jennifer
Published in Journal of autism and developmental disorders (28.04.2024)
Published in Journal of autism and developmental disorders (28.04.2024)
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Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
Mignot, Cyril, von Stülpnagel, Celina, Nava, Caroline, Ville, Dorothée, Sanlaville, Damien, Lesca, Gaetan, Rastetter, Agnès, Gachet, Benoit, Marie, Yannick, Korenke, G Christoph, Borggraefe, Ingo, Hoffmann-Zacharska, Dorota, Szczepanik, Elżbieta, Rudzka-Dybała, Mariola, Yiş, Uluç, Çağlayan, Hande, Isapof, Arnaud, Marey, Isabelle, Panagiotakaki, Eleni, Korff, Christian, Rossier, Eva, Riess, Angelika, Beck-Woedl, Stefanie, Rauch, Anita, Zweier, Christiane, Hoyer, Juliane, Reis, André, Mironov, Mikhail, Bobylova, Maria, Mukhin, Konstantin, Hernandez-Hernandez, Laura, Maher, Bridget, Sisodiya, Sanjay, Kuhn, Marius, Glaeser, Dieter, Weckhuysen, Sarah, Myers, Candace T, Mefford, Heather C, Hörtnagel, Konstanze, Biskup, Saskia, Lemke, Johannes R, Héron, Delphine, Kluger, Gerhard, Depienne, Christel, Craiu, Dana, De Jonghe, Peter, Helbig, Ingo, Guerrini, Renzo, Lehesjoki, Anna-Elina, Marini, Carla, Muhle, Hiltrud, Møller, Rikke S, Neubauer, Bernd, Pal, Deb, Selmer, Kaja, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Talvik, Tiina, von Spiczak, Sarah
Published in Journal of medical genetics (01.08.2016)
Published in Journal of medical genetics (01.08.2016)
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China and intellectual property rights: A challenge to the rule of law
Brander, James A, Cui, Victor, Vertinsky, Ilan
Published in Journal of international business studies (01.09.2017)
Published in Journal of international business studies (01.09.2017)
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Journal Article
Reliability and validity of the dynamic risk outcome scales—short version for clients with mild intellectual disabilities or borderline intellectual functioning
Delforterie, M. J., Turhan, A., Driessen, M., Neijmeijer, L., Hesper, B., Didden, R.
Published in Journal of applied research in intellectual disabilities (01.05.2024)
Published in Journal of applied research in intellectual disabilities (01.05.2024)
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FOXP1-related intellectual disability syndrome: a recognisable entity
Meerschaut, Ilse, Rochefort, Daniel, Revençu, Nicole, Pètre, Justine, Corsello, Christina, Rouleau, Guy A, Hamdan, Fadi F, Michaud, Jacques L, Morton, Jenny, Radley, Jessica, Ragge, Nicola, García-Miñaúr, Sixto, Lapunzina, Pablo, Bralo, Maria Palomares, Mori, Maria Ángeles, Moortgat, Stéphanie, Benoit, Valérie, Mary, Sandrine, Bockaert, Nele, Oostra, Ann, Vanakker, Olivier, Velinov, Milen, de Ravel, Thomy JL, Mekahli, Djalila, Sebat, Jonathan, Vaux, Keith K, DiDonato, Nataliya, Hanson-Kahn, Andrea K, Hudgins, Louanne, Dallapiccola, Bruno, Novelli, Antonio, Tarani, Luigi, Andrieux, Joris, Parker, Michael J, Neas, Katherine, Ceulemans, Berten, Schoonjans, An-Sofie, Prchalova, Darina, Havlovicova, Marketa, Hancarova, Miroslava, Budisteanu, Magdalena, Dheedene, Annelies, Menten, Björn, Dion, Patrick A, Lederer, Damien, Callewaert, Bert
Published in Journal of medical genetics (01.09.2017)
Published in Journal of medical genetics (01.09.2017)
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Journal Article
Defects in tRNA Anticodon Loop 2′-O-Methylation Are Implicated in Nonsyndromic X-Linked Intellectual Disability due to Mutations in FTSJ1
Guy, Michael P., Shaw, Marie, Weiner, Catherine L., Hobson, Lynne, Stark, Zornitza, Rose, Katherine, Kalscheuer, Vera M., Gecz, Jozef, Phizicky, Eric M.
Published in Human mutation (01.12.2015)
Published in Human mutation (01.12.2015)
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Executive functions and their relationship with intellectual capacity and age in schoolchildren with intellectual disability
Erostarbe‐Pérez, M., Reparaz‐Abaitua, C., Martínez‐Pérez, L., Magallón‐Recalde, S.
Published in Journal of intellectual disability research (01.01.2022)
Published in Journal of intellectual disability research (01.01.2022)
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Intellectual capital and firm performance: evidence from certified firms from the EFQM excellence model
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Book Review
Intellectual capital, absorptive capacity and product innovation
Engelman, Raquel Machado, Fracasso, Edi Madalena, Schmidt, Serje, Zen, Aurora Carneiro
Published in Management decision (01.01.2017)
Published in Management decision (01.01.2017)
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Exploring the impacts of intellectual property on intellectual capital and company performance: The case of Iranian computer and electronic organizations
Namvar, Morteza, Fathian, Mohammad, Akhavan, Peyman, Reza Gholamian, Mohammad
Published in Management decision (01.01.2010)
Published in Management decision (01.01.2010)
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A missense mutation in the catalytic domain of O‐GlcNAc transferase links perturbations in protein O‐GlcNAcylation to X‐linked intellectual disability
Pravata, Veronica M., Gundogdu, Mehmet, Bartual, Sergio G., Ferenbach, Andrew T., Stavridis, Marios, Õunap, Katrin, Pajusalu, Sander, Žordania, Riina, Wojcik, Monica H., Aalten, Daan M. F.
Published in FEBS letters (01.02.2020)
Published in FEBS letters (01.02.2020)
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IQSEC2-Associated Intellectual Disability and Autism
Levy, Nina S, Umanah, George K E, Rogers, Eli J, Jada, Reem, Lache, Orit, Levy, Andrew P
Published in International journal of molecular sciences (21.06.2019)
Published in International journal of molecular sciences (21.06.2019)
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Journal Article
Foreign actors and intellectual property protection regulations in developing countries
Brandl, Kristin, Darendeli, Izzet, Mudambi, Ram
Published in Journal of international business studies (01.07.2019)
Published in Journal of international business studies (01.07.2019)
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Journal Article
Intellectual disability‐associated gene ftsj1 is responsible for 2′‐O‐methylation of specific tRNAs
Li, Jing, Wang, Yan‐Nan, Xu, Bei‐Si, Liu, Ya‐Ping, Zhou, Mi, Long, Tao, Li, Hao, Dong, Han, Nie, Yan, Chen, Peng R, Wang, En‐Duo, Liu, Ru‐Juan
Published in EMBO reports (05.08.2020)
Published in EMBO reports (05.08.2020)
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Journal Article
PTRHD1 (C2orf79) mutations lead to autosomal‐recessive intellectual disability and parkinsonism
Khodadadi, Hamidreza, Azcona, Luis J., Aghamollaii, Vajiheh, Omrani, Mir Davood, Garshasbi, Masoud, Taghavi, Shaghayegh, Tafakhori, Abbas, Shahidi, Gholam Ali, Jamshidi, Javad, Darvish, Hossein, Paisán‐Ruiz, Coro
Published in Movement disorders (01.02.2017)
Published in Movement disorders (01.02.2017)
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