Boot, Erik
103  Ergebnisse:
Personensuche X
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1

Parkinsonism in Genetic Neurodevelopmental Disorders:A Syst..:

von Scheibler, Emma N.M.M ; van Eeghen, Agnies M ; de Koning, Tom J...
https://research.rug.nl/en/publications/d8ab84b3-ff1c-4c7b-bebf-95f530653249.  , 2023
 
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2

Rapporteur summaries of plenary, symposia, and oral session..:

Zai, Gwyneth ; Alberry, Bonnie ; Arloth, Janine...
https://journals.lww.com/psychgenetics/Fulltext/2016/12000/Rapporteur_summaries_of_plenary,_symposia,_and.1.aspx.  , 2023
 
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8

Post-traumatic stress in adults with 22q11.2 deletion syndr..:

von Scheibler, Emma N M M ; van Amelsvoort, Thérèse A M J ; Vingerhoets, Claudia..
von Scheibler , E N M M , van Amelsvoort , T A M J , Vingerhoets , C , van Eeghen , A M & Boot , E 2022 , ' Post-traumatic stress in adults with 22q11.2 deletion syndrome ' , Bjpsych open , vol. 8 , no. 4 , 126 , pp. e126 . https://doi.org/10.1192/bjo.2022.525.  , 2022
 
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11

Possible underreporting of pathogenic variants in RAI1 caus..:

Boot, Erik ; Linders, Cathelijne C ; Tromp, Sterre H..
Boot , E , Linders , C C , Tromp , S H , van den Boogaard , M-J & van Eeghen , A M 2021 , ' Possible underreporting of pathogenic variants in RAI1 causing Smith–Magenis syndrome ' , American Journal of Medical Genetics, Part A , vol. 185 , no. 10 , pp. 3167-3169 . https://doi.org/10.1002/ajmg.a.62380.  , 2021
 
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12

Systematic Review of N-of-1 Studies in Rare Genetic Neurode..:

Mueller, Annelieke R ; Brands, Marion M. M. G ; van de Ven, Peter M...
Mueller , A R , Brands , M M M G , van de Ven , P M , Roes , K C B , Cornel , M C , van Karnebeek , C D M , Wijburg , F A , Daams , J G , Boot , E & van Eeghen , A M 2021 , ' Systematic Review of N-of-1 Studies in Rare Genetic Neurodevelopmental Disorders The Power of 1 ' , Neurology , vol. 96 , no. 11 , pp. 529-540 . https://doi.org/10.1212/WNL.0000000000011597.  , 2021
 
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Ocular findings in 22q11.2 deletion syndrome: A systematic ..:

von Scheibler, Emma N. M. M ; van der Valk Bouman, Emy S ; Nuijts, Myrthe A...
von Scheibler , E N M M , van der Valk Bouman , E S , Nuijts , M A , Bauer , N J C , Berendschot , T T J M , Vermeltfoort , P , Bok , L A , van Eeghen , A M , Houben , M L , van Amelsvoort , T A M J , Boot , E & van Egmond-Ebbeling , M B 2021 , ' Ocular findings in 22q11.2 deletion syndrome: A systematic literature review and results of a Dutch multicenter study ' , American Journal of Medical Genetics, Part A . https://doi.org/10.1002/ajmg.a.62556.  , 2021
 
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14

Ocular findings in 22q11.2 deletion syndrome:A systematic l..:

von Scheibler, Emma N. M. M ; van der Valk Bouman, Emy S ; Nuijts, Myrthe A...
von Scheibler , E N M M , van der Valk Bouman , E S , Nuijts , M A , Bauer , N J C , Berendschot , T T J M , Vermeltfoort , P , Bok , L A , van Eeghen , A M , Houben , M L , van Amelsvoort , T A M J , Boot , E & van Egmond-Ebbeling , M B 2021 , ' Ocular findings in 22q11.2 deletion syndrome : A systematic literature review and results of a Dutch multicenter study ' , American Journal of Medical Genetics, Part A . https://doi.org/10.1002/ajmg.a.62556.  , 2021
 
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15

Genetic contributors to risk of schizophrenia in the presen..:

Cleynen, Isabelle ; Engchuan, Worrawat ; Hestand, Matthew...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41380-020-0654-3.  , 2020
 
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