Tom J de Koning

51 – 60 of 200

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/person/10a3052d-93e9-4c0f-898c-1adb825f56a4?embed=1&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

« previous
1
…
5
6
7
8
…
20
next »

2018
Mark Treatable inherited rare movement disorders
Jinnah, H. A. ; Albanese, Alberto ; Bhatia, Kailash P. ; Cardoso, Francisco ; Da Prat, Gustavo ; de Koning, Tom J. ^LU ; Espay, Alberto J. ; Fung, Victor ; Garcia-Ruiz, Pedro J. and Gershanik, Oscar , et al. (2018) In Movement Disorders 33(1). p.21-35
- Contribution to journal › Scientific review
Mark Ketogenic Diet in Refractory Childhood Epilepsy : Starting With a Liquid Formulation in an Outpatient Setting
Weijenberg, Amerins ; van Rijn, Margreet ; Callenbach, Petra M C ; de Koning, Tom J ^LU and Brouwer, Oebele F (2018) In Child Neurology Open 5.
- Contribution to journal › Article
Mark Crossing barriers : a multidisciplinary approach to children and adults with young-onset movement disorders
van Egmond, Martje E ; Eggink, Hendriekje ; Kuiper, Anouk ; Sival, Deborah A ; Verschuuren-Bemelmans, Corien C ; Tijssen, Marina A J and de Koning, Tom J ^LU (2018) In Journal of clinical movement disorders 5.
- Contribution to journal › Article
2017
Mark Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation
Eggink, Hendriekje ; van Egmond, Martje E. ; Verschuuren-Bemelmans, Corien C. ; Schönherr, Marleen C. ; de Koning, Tom J. ^LU ; Oterdoom, D. L.Marinus ; van Dijk, J. Marc C. and Tijssen, Marina A.J. (2017) In Movement Disorders 32(1). p.162-165
- Contribution to journal › Debate/Note/Editorial
Mark Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation
Aldenhoven, Mieke ; Van Den Broek, Brigitte T.A. ; Wynn, Robert F. ; O'Meara, Anne ; Veys, Paul ; Rovelli, Attilio ; Jones, Simon A. ; Parini, Rossella ; Van Hasselt, Peter M. and Renard, Marleen , et al. (2017) In Blood Advances 1(24). p.2236-2242
- Contribution to journal › Article
Mark Non-motor symptoms and quality of life in dopa-responsive dystonia patients
Timmers, E. R. ; Kuiper, A. ; Smit, M. ; Bartels, A. L. ; Kamphuis, D. J. ; Wolf, N. I. ; Poll-The, B. T. ; Wassenberg, T. ; Peeters, E. A.J. and de Koning, T. J. ^LU , et al. (2017) In Parkinsonism and Related Disorders 45. p.57-62
- Contribution to journal › Article
Mark Rapid targeted genomics in critically ill newborns
Van Diemen, Cleo C. ; Kerstjens-Frederikse, Wilhelmina S. ; Bergman, Klasien A. ; De Koning, Tom J. ^LU ; Sikkema-Raddatz, Birgit ; Van Der Velde, Joeri K. ; Abbott, Kristin M. ; Herkert, Johanna C. ; Lohner, Katharina and Rump, Patrick , et al. (2017) In Pediatrics 140(4).
- Contribution to journal › Article
Mark Amino acid synthesis deficiencies
de Koning, T. J. ^LU (2017) In Journal of Inherited Metabolic Disease 40(4). p.609-620
- Contribution to journal › Scientific review
Mark The efficacy of the modified Atkins diet in North Sea Progressive Myoclonus Epilepsy : An observational prospective open-label study
Van Egmond, Martje E. ; Weijenberg, Amerins ; Van Rijn, Margreet E. ; Elting, Jan Willem J. ; Gelauff, Jeannette M. ; Zutt, Rodi ; Sival, Deborah A. ; Lambrechts, Roald A. ; Tijssen, Marina A.J. and Brouwer, Oebele F. , et al. (2017) In Orphanet Journal of Rare Diseases 12(1).
- Contribution to journal › Article
Mark The hidden Niemann-Pick type C patient : clinical niches for a rare inherited metabolic disease
Hendriksz, Christian J. ; Anheim, Mathieu ; Bauer, Peter ; Bonnot, Olivier ; Chakrapani, Anupam ; Corvol, Jean Christophe ; de Koning, Tom J. ^LU ; Degtyareva, Anna ; Dionisi-Vici, Carlo and Doss, Sarah , et al. (2017) In Current Medical Research and Opinion 33(5). p.877-890
- Contribution to journal › Article

« previous
1
…
5
6
7
8
…
20
next »