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Kevelam, H. J.
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1

Kinetik der oxidativen Polymerisation von 1,8-Nonadiin:

Kevelam, H. J. ; de Jong, K. P. ; Meinders, H. C..
Colloid and Polymer Science.  255 (1977)  8 - p. 817-817 , 1977
Link: https://doi.org/10.1007/..
 
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2

A novel polycyclic triamine derivative of tridehydro[12]ann..:

van Roosmalen, J.H. ; Jones, E. ; Kevelam, H.J.
Tetrahedron Letters.  13 (1972)  19 - p. 1865-1868 , 1972
Link: https://doi.org/10.1016/..
 
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3

Author response: Acute intermittent porphyria-related leuko..:

van der Knaap, Marjo S. ; Kevelam, Sietske H.
Neurology.  88 (2017)  7 - p. 718-719 , 2017
Link: https://doi.org/10.1212/..
 
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4

Author response: Cathepsin A–related arteriopathy with stro..:

van der Knaap, Marjo S. ; Bugiani, Marianna ; Kevelam, Sietske H.
Neurology.  88 (2017)  18 - p. 1776-1776 , 2017
Link: https://doi.org/10.1212/..
 
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5

Cathepsin A–related arteriopathy with strokes and leukoence..:

Bugiani, Marianna ; Kevelam, Sietske H. ; Bakels, Hannah S....
Neurology.  87 (2016)  17 - p. 1777-1786 , 2016
Link: https://doi.org/10.1212/..
 
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6

Acute intermittent porphyria-related leukoencephalopathy:

Kevelam, Sietske H. ; Neeleman, Rochus A. ; Waisfisz, Quinten...
Neurology.  87 (2016)  12 - p. 1258-1265 , 2016
Link: https://doi.org/10.1212/..
 
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7

OP49 – 2560: PLP1 mutations affecting PLP1/DM20 alternative..:

Kevelam, S.H. ; Taube, J.R. ; van Spaendonk, R.M.L....
European Journal of Paediatric Neurology.  19 (2015)  - p. S16 , 2015
Link: https://doi.org/10.1016/..
 
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8

AlteredPLP1splicing causes hypomyelination of early myelina..:

Kevelam, Sietske H. ; Taube, Jennifer R. ; van Spaendonk, Rosalina M. L....
Annals of Clinical and Translational Neurology.  2 (2015)  6 - p. 648-661 , 2015
Link: https://doi.org/10.1002/..
 
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9

Recessive ITPA mutations cause an early infantile encephalo..:

Kevelam, Sietske H. ; Bierau, Jörgen ; Salvarinova, Ramona...
Annals of Neurology.  78 (2015)  4 - p. 649-658 , 2015
Link: https://doi.org/10.1002/..
 
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10

LAMA2 mutations in adult-onset muscular dystrophy with leuk..:

Kevelam, Sietske H. ; van Engelen, Baziel G.M. ; van Berkel, Carola G.M...
Muscle & Nerve.  49 (2014)  4 - p. 616-617 , 2014
Link: https://doi.org/10.1002/..
 
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11

Novel (ovario) leukodystrophy related toAARS2mutations:

Dallabona, Cristina ; Diodato, Daria ; Kevelam, Sietske H....
Neurology.  82 (2014)  23 - p. 2063-2071 , 2014
Link: https://doi.org/10.1212/..
 
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12

Reply: Infantile Leigh-like syndrome caused by SLC19A3 muta..:

van der Knaap, Marjo S. ; Kevelam, Sietske H.
Brain.  137 (2014)  9 - p. e297-e297 , 2014
Link: https://doi.org/10.1093/..
 
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13

NUBPLmutations in patients with complex I deficiency and a ..:

Kevelam, Sietske H. ; Rodenburg, Richard J. ; Wolf, Nicole I....
Neurology.  80 (2013)  17 - p. 1577-1583 , 2013
Link: https://doi.org/10.1212/..
 
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14

Exome sequencing reveals mutated SLC19A3 in patients with a..:

Kevelam, Sietske H. ; Bugiani, Marianna ; Salomons, Gajja S....
Brain.  136 (2013)  5 - p. 1534-1543 , 2013
Link: https://doi.org/10.1093/..
 
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15

Copy Number Variations in Patients With Electrical Status E..:

Kevelam, Sietske H.G. ; Jansen, Floor E. ; Binsbergen, Ellen van...
Journal of Child Neurology.  27 (2011)  2 - p. 178-182 , 2011
Link: https://doi.org/10.1177/..
 
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