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Page 1
Clinical and community genetics services in the Dutch Caribbean.
J Community Genet. 2021 Jul;12(3):497-501. doi: 10.1007/s12687-021-00515-6. Epub 2021 Mar 10.
J Community Genet. 2021.
PMID: 33751485
Free PMC article.
Severe Pediatric COVID-19 and Multisystem Inflammatory Syndrome in Children From Wild-type to Population Immunity: A Prospective Multicenter Cohort Study With Real-time Reporting.
Tulling AJ, Lugthart G, Mooij MG, Brackel CLH, Terheggen-Lagro SWJ, Oostenbrink R, Buysse CMP, Hashimoto S, Armbrust W, Bannier MAGE, Bekhof J, van Gameren-Oosterom HB, Hendriks H, van Houten MA, van der Linden JW, Lebon A, van Onzenoort-Bokken L, Tramper-Stranders GA, van Veen M, von Asmuth EGJ, Buddingh EP; COPP-study group.
Tulling AJ, et al.
Pediatr Infect Dis J. 2023 Dec 1;42(12):1077-1085. doi: 10.1097/INF.0000000000004098. Epub 2023 Oct 12.
Pediatr Infect Dis J. 2023.
PMID: 37823702
Free PMC article.
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Genetic care in geographically isolated small island communities: 8 years of experience in the Dutch Caribbean.
Verberne EA, Westermann JM, de Vries TI, Ecury-Goossen GM, Lo-A-Njoe SM, Manshande ME, Faries S, Veenhuis HD, Philippi P, Falix FA, Rosina-Angelista I, Ponson-Wever M, Rafael-Croes L, Thorsen P, Arends E, de Vroomen M, Nagelkerke SQ, Tilanus M, van der Veken LT, Huijsdens-van Amsterdam K, van der Kevie-Kersemaekers AM, Alders M, Mannens MMAM, van Haelst MM.
Verberne EA, et al. Among authors: manshande me.
Am J Med Genet A. 2022 Jun;188(6):1777-1791. doi: 10.1002/ajmg.a.62708. Epub 2022 Mar 7.
Am J Med Genet A. 2022.
PMID: 35253369
Free PMC article.
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Neurologic sequelae of severe chikungunya infection in the first 6 months of life: a prospective cohort study 24-months post-infection.
van Ewijk R, Huibers MHW, Manshande ME, Ecury-Goossen GM, Duits AJ, Calis JC, van Wassenaer-Leemhuis AG.
van Ewijk R, et al. Among authors: manshande me.
BMC Infect Dis. 2021 Feb 16;21(1):179. doi: 10.1186/s12879-021-05876-4.
BMC Infect Dis. 2021.
PMID: 33593326
Free PMC article.
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PDE3A gene screening improves diagnostics for patients with Bilginturan syndrome (hypertension and brachydactyly syndrome).
Renkema KY, Westermann JM, Nievelstein RAJ, Lo-A-Njoe SM, van der Zwaag B, Manshande ME, van Haelst MM.
Renkema KY, et al. Among authors: manshande me.
Hypertens Res. 2018 Nov;41(11):981-988. doi: 10.1038/s41440-018-0094-5. Epub 2018 Sep 12.
Hypertens Res. 2018.
PMID: 30209282
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Genetic diagnosis for rare diseases in the Dutch Caribbean: a qualitative study on the experiences and associated needs of parents.
Verberne EA, van den Heuvel LM, Ponson-Wever M, de Vroomen M, Manshande ME, Faries S, Ecury-Goossen GM, Henneman L, van Haelst MM.
Verberne EA, et al. Among authors: manshande me.
Eur J Hum Genet. 2022 May;30(5):587-594. doi: 10.1038/s41431-022-01039-4. Epub 2022 Jan 28.
Eur J Hum Genet. 2022.
PMID: 35087185
Free PMC article.
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Limb anomalies, microcephaly, dysmorphic facial features and fibroma of the tongue after failed abortion with methotrexate and misoprostol.
Verberne EA, Manshande ME, Wagner-Buitenweg NF, Elhage W, Holtsema H, van Haelst MM.
Verberne EA, et al. Among authors: manshande me.
Clin Dysmorphol. 2020 Oct;29(4):182-185. doi: 10.1097/MCD.0000000000000331.
Clin Dysmorphol. 2020.
PMID: 32541333
No abstract available.
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