51
52
53
54
van Lith, Bas J. H., Kerstens, Hans C. J. W., van den Bemd, Laura A. C., Nijhuis-van der Sanden, Maria W. G., Weerdesteyn, Vivian, Smeets, Rob J. E. M., Fheodoroff, Klemens, van de Warrenburg, Bart P. C., Geurts, Alexander C. H.
Veröffentlicht in: van Lith , B J H , Kerstens , H C J W , van den Bemd , L A C , Nijhuis-van der Sanden , M W G , Weerdesteyn , V , Smeets , R J E M , Fheodoroff , K , van de Warrenburg , B P C & Geurts , A C H 2020 , ' Experienced complaints, activity limitations and loss of motor capacities in patients with pure hereditary spastic paraplegia : a web-based survey in the Netherlands ' , Orphanet Journal of Rare Diseases , vol. 15 , no. 1 , 64 . https://doi.org/10.1186/s13023-020-1338-4;
2020
Veröffentlicht in: van Lith , B J H , Kerstens , H C J W , van den Bemd , L A C , Nijhuis-van der Sanden , M W G , Weerdesteyn , V , Smeets , R J E M , Fheodoroff , K , van de Warrenburg , B P C & Geurts , A C H 2020 , ' Experienced complaints, activity limitations and loss of motor capacities in patients with pure hereditary spastic paraplegia : a web-based survey in the Netherlands ' , Orphanet Journal of Rare Diseases , vol. 15 , no. 1 , 64 . https://doi.org/10.1186/s13023-020-1338-4;
2020
55
Wijnen, Petal, Drent, Marjolein, Bekers, Otto, Verschakelen, Johny, Bast, Aalt
Veröffentlicht in: Wijnen , P , Drent , M , Bekers , O , Verschakelen , J & Bast , A 2019 , ' VKORC1 and CYP2C9 Polymorphisms : A Case Report in a Dutch Family with Pulmonary Fibrosis ' , International journal of molecular sciences , vol. 20 , no. 5 , 1160 . https://doi.org/10.3390/ijms20051160;
2019
Veröffentlicht in: Wijnen , P , Drent , M , Bekers , O , Verschakelen , J & Bast , A 2019 , ' VKORC1 and CYP2C9 Polymorphisms : A Case Report in a Dutch Family with Pulmonary Fibrosis ' , International journal of molecular sciences , vol. 20 , no. 5 , 1160 . https://doi.org/10.3390/ijms20051160;
2019
56
58
59
60