van der Smagt, JJ
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2

Heterogeneity in the origin of recurrent complete hydatidif..:

Van Der Smagt, JJ ; Scheenjes, E ; Kremer, JAM..
BJOG: An International Journal of Obstetrics & Gynaecology.  113 (2006)  6 - p. 725-728 , 2006
 
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3

The Netherlands Arrhythmogenic Cardiomyopathy Registry: des..:

Bosman, LP ; Verstraelen, TE ; van Lint, FHM...
https://discovery.ucl.ac.uk/id/eprint/10084457/1/Bosman2019_Article_TheNetherlandsArrhythmogenicCa.pdf.  , 2019
 
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4

The Netherlands Arrhythmogenic Cardiomyopathy Registry: des..:

Bosman, LP ; Verstraelen, TE ; van Lint, FHM...
Bosman , LP , Verstraelen , TE , van Lint , FHM , Cox , M , Groeneweg , JA , Mast , TP , van der Zwaag , PA , Volders , PG , Evertz , R , Wong , L , de Groot , N , Zeppenfeld , K , van der Heijden , JF , Van Den Berg , MP , Wilde , AA , Asselbergs , FW , Hauer , RN , te Riele , A , Tintelen , JP , Baas , AE , Barge-Schaapveld , D , Boekholdt , SM , Cramer , MJM , Dooijes , D , Jongbloed , JD , Loh , P , Planken , RN , Prakken , NHJ , van der Smagt , JJ , v.d. Wal , AC , Teske , AJ , van Veen , TA , Velthuis , BK , Vink , A & Yap , S 2019 , ' The Netherlands Arrhythmogenic Cardiomyopathy Registry: design and status update ' , Netherlands Heart Journal , vol. 27 , no. 10 , pp. 480-486 . https://doi.org/10.1007/s12471-019-1270-1.  , 2019
 
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5

The first titin (c.59926 + 1G > A) founder mutation associa..:

Hoorntje, ET ; van Spaendonck-Zwarts, KY ; te Rijdt, WP...
https://discovery.ucl.ac.uk/id/eprint/10053314/1/ejhf.1030.pdf.  , 2018
 
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7

Juvenile interleukin-36 receptor antagonist deficiency (DIT..:

Cuperus, Edwin ; Koevoets, R ; van der Smagt, JJ...
Cuperus , E , Koevoets , R , van der Smagt , JJ , Toonstra , J , de Graaf , M , Frenkel , J & Pasmans , S 2018 , ' Juvenile interleukin-36 receptor antagonist deficiency (DITRA) with c.80T >C (p.Leu27Pro) mutation successfully treated with etanercept and acitretin ' , JAAD Case Reports , vol. 4 , no. 2 , pp. 192-195 . https://doi.org/10.1016/j.jdcr.2017.08.019.  , 2018
 
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8

Lack of evidence for a causal role of CALR3 in monogenic ca..:

Verhagen, Judith ; Veldman, JH (Job) ; van der Zwaag, PA...
Verhagen , J , Veldman , JH , van der Zwaag , PA , von der Thüsen , J , Brosens , E , Christiaans , M , Dooijes , D , Helderman-van d Enden , A , Deprez , RHL , Michels , M , Mil , AM , Oldenburg , R , van der Smagt , JJ , van den Wijngaard , A , Wessels , M , Hofstra , R , van Slegtenhorst , M , Jongbloed , JDH & De Graaf - van de Laar , I 2018 , ' Lack of evidence for a causal role of CALR3 in monogenic cardiomyopathy ' , European Journal of Human Genetics , vol. 26 , no. 11 , pp. 1603-1610 . https://doi.org/10.1038/s41431-018-0208-1.  , 2018
 
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9

Next-generation sequencing of a large gene panel in patient..:

Visser, M ; Dooijes, D ; van der Smagt, JJ...
https://discovery.ucl.ac.uk/id/eprint/10051667/1/Next%20Generation%20Sequencing%20of%20a%20large%20gene%20panel%20in%20patients%20initially%20d.pdf.  , 2017
 
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10

Distinct fibrosis pattern in desmosomal and phospholamban m..:

Sepehrkhouy, S ; Gho, JMIH ; van Es, R...
https://discovery.ucl.ac.uk/id/eprint/10054467/1/Asselbergs_Distinct%20fibrosis%20pattern%20manuscript.pdf.  , 2017
 
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11

A consanguineous family with Hirschsprung disease, microcep..:

Brooks, Alice ; Breuning, MH ; Osinga, J...
Brooks , A , Breuning , MH , Osinga , J , van der Smagt , JJ , Catsman - Berrevoets , C , Buys , CHCM , Meijers , C & Hofstra , RMW 1999 , ' A consanguineous family with Hirschsprung disease, microcephaly, and mental retardation (Goldberg-Shprintzen syndrome) ' , Journal of Medical Genetics , vol. 36 , pp. 485-489 ..  , 1999
 
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