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Year Number of Results
2007 1
2008 1
2012 2
2013 1
2015 2
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2019 2
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2022 3
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2024 2

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Page 1
Editorial: Treatment of psychopathological and neurocognitive disorders in genetic syndromes: In need of multidisciplinary phenotyping and treatment design.
Egger J, Egger C, Woodcock K, De Witte L, Van Den Bree M, Van Dongen L, Wingbermühle E, Kleefstra T. Egger J, et al. Among authors: wingbermuhle e. Front Psychiatry. 2022 Sep 2;13:1009376. doi: 10.3389/fpsyt.2022.1009376. eCollection 2022. Front Psychiatry. 2022. PMID: 36117652 Free PMC article. No abstract available.
The 8th International RASopathies Symposium: Expanding research and care practice through global collaboration and advocacy.
Pierpont EI, Bennett AM, Schoyer L, Stronach B, Anschutz A, Borrie SC, Briggs B, Burkitt-Wright E, Castel P, Cirstea IC, Draaisma F, Ellis M, Fear VS, Frone MN, Flex E, Gelb BD, Green T, Gripp KW, Khoshkhoo S, Kieran MW, Kleemann K, Klein-Tasman BP, Kontaridis MI, Kruszka P, Leoni C, Liu CZ, Merchant N, Magoulas PL, Moertel C, Prada CE, Rauen KA, Roelofs R, Rossignol R, Sevilla C, Sevilla G, Sheedy R, Stieglitz E, Sun D, Tiemens D, White F, Wingbermühle E, Wolf C, Zenker M, Andelfinger G. Pierpont EI, et al. Among authors: wingbermuhle e. Am J Med Genet A. 2024 Apr;194(4):e63477. doi: 10.1002/ajmg.a.63477. Epub 2023 Nov 15. Am J Med Genet A. 2024. PMID: 37969032
The most important problems and needs of rasopathy patients with a noonan syndrome spectrum disorder.
Tiemens DK, Kleimeier L, Leenders E, Wingbermühle E, Roelofs RL, Sibbles B, Oostwegel FSM, Vroonland E, van Leeuwen C, Niessen H, Sonnega P, Duursma A, Willemsen MAAP, Draaisma JMT, Pittens CACM. Tiemens DK, et al. Among authors: wingbermuhle e. Orphanet J Rare Dis. 2023 Jul 21;18(1):198. doi: 10.1186/s13023-023-02818-y. Orphanet J Rare Dis. 2023. PMID: 37480127 Free PMC article.
Behavior and cognitive functioning in Witteveen-Kolk syndrome.
van Dongen LCM, Wingbermühle E, Dingemans AJM, Bos-Roubos AG, Vermeulen K, Pop-Purceleanu M, Kleefstra T, Egger JIM. van Dongen LCM, et al. Among authors: wingbermuhle e. Am J Med Genet A. 2020 Oct;182(10):2384-2390. doi: 10.1002/ajmg.a.61775. Epub 2020 Aug 11. Am J Med Genet A. 2020. PMID: 32783353 Free PMC article.
Personality and Psychopathology in Adults with Noonan Syndrome.
Roelofs RL, Wingbermühle E, van der Heijden PT, Jonkers R, de Haan M, Kessels RPC, Egger JIM. Roelofs RL, et al. Among authors: wingbermuhle e. J Clin Psychol Med Settings. 2020 Jun;27(2):256-267. doi: 10.1007/s10880-019-09659-7. J Clin Psychol Med Settings. 2020. PMID: 31560100 Free PMC article.
Intellectual Profiles in KBG-Syndrome: A Wechsler Based Case-Control Study.
van Dongen LCM, Wingbermühle E, Oomens W, Bos-Roubos AG, Ockeloen CW, Kleefstra T, Egger JIM. van Dongen LCM, et al. Among authors: wingbermuhle e. Front Behav Neurosci. 2017 Dec 19;11:248. doi: 10.3389/fnbeh.2017.00248. eCollection 2017. Front Behav Neurosci. 2017. PMID: 29311865 Free PMC article.
Noonan syndrome: psychological and psychiatric aspects.
Verhoeven W, Wingbermühle E, Egger J, Van der Burgt I, Tuinier S. Verhoeven W, et al. Among authors: wingbermuhle e. Am J Med Genet A. 2008 Jan 15;146A(2):191-6. doi: 10.1002/ajmg.a.32115. Am J Med Genet A. 2008. PMID: 18080322
19 results