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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 21, 2015
Lactate and its many faces
Marjan Taher, Wilhelmina G Leen, Ron A Wevers, et al.
Experimental Physiology
|
May 1, 1995
The effects of MM-creatine kinase deficiency on sustained force production of mouse fast skeletal muscle
A de Haan, J C Koudijs, R A Wevers, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 21, 2009
[The right medicine for cerebrotendinous xanthomatosis]
Aad Verrips, Ron A Wevers, Francjan J van Spronsen, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
Dorus Kouwenberg, Thatjana Gardeitchik, Ron A Wevers, et al.
Clinical Chemistry
|
June 1, 1992
Measuring urinary glycosaminoglycans in the presence of protein: an improved screening procedure for mucopolysaccharidoses based on dimethylmethylene blue
J G de Jong, R A Wevers, R Liebrand-van Sambeek
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1978
Post-synthetic changes in creatine kinase isozymes (EC 2.7.3.2)
R A Wevers, M Delsing, J A Klein Gebbink, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2023
A framework for evaluating long-term impact of newborn screening
Shona Kalkman, Ron A Wevers, Frits A Wijburg, et al.
Zeitschrift Fur Hautkrankheiten
|
May 1, 1990
[Increased expression of proliferation keratins K 6 and K 16 in unaffected skin in exacerbated psoriasis]
A Wevers, H G Arnold, B Bonnekoh, et al.
Molecular Genetics and Metabolism
|
March 19, 2013
Thrombotic complications in patients with PMM2-CDG
M Linssen, M Mohamed, R A Wevers, et al.
Annals of Human Genetics
|
January 31, 2003
Seven novel acid sphingomyelinase gene mutations in Niemann-Pick type A and B patients
J Sikora, H Pavlu-Pereira, M Elleder, et al.
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of 55
Search research articles
Search
Showing results (51-60 of 543) with videos related to
Sort By:
Page
of 55
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 21, 2015
Lactate and its many faces
Marjan Taher, Wilhelmina G Leen, Ron A Wevers, et al.
Experimental Physiology
|
May 1, 1995
The effects of MM-creatine kinase deficiency on sustained force production of mouse fast skeletal muscle
A de Haan, J C Koudijs, R A Wevers, et al.
Nederlands Tijdschrift Voor Geneeskunde
|
May 21, 2009
[The right medicine for cerebrotendinous xanthomatosis]
Aad Verrips, Ron A Wevers, Francjan J van Spronsen, et al.
American Journal of Medical Genetics. Part A
|
August 12, 2011
Recognizable phenotype with common occurrence of microcephaly, psychomotor retardation, but no spontaneous bone fractures in autosomal recessive cutis laxa type IIB due to PYCR1 mutations
Dorus Kouwenberg, Thatjana Gardeitchik, Ron A Wevers, et al.
Clinical Chemistry
|
June 1, 1992
Measuring urinary glycosaminoglycans in the presence of protein: an improved screening procedure for mucopolysaccharidoses based on dimethylmethylene blue
J G de Jong, R A Wevers, R Liebrand-van Sambeek
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 15, 1978
Post-synthetic changes in creatine kinase isozymes (EC 2.7.3.2)
R A Wevers, M Delsing, J A Klein Gebbink, et al.
European Journal of Human Genetics : EJHG
|
October 3, 2023
A framework for evaluating long-term impact of newborn screening
Shona Kalkman, Ron A Wevers, Frits A Wijburg, et al.
Zeitschrift Fur Hautkrankheiten
|
May 1, 1990
[Increased expression of proliferation keratins K 6 and K 16 in unaffected skin in exacerbated psoriasis]
A Wevers, H G Arnold, B Bonnekoh, et al.
Molecular Genetics and Metabolism
|
March 19, 2013
Thrombotic complications in patients with PMM2-CDG
M Linssen, M Mohamed, R A Wevers, et al.
Annals of Human Genetics
|
January 31, 2003
Seven novel acid sphingomyelinase gene mutations in Niemann-Pick type A and B patients
J Sikora, H Pavlu-Pereira, M Elleder, et al.
Page
of 55