Zobrazeno 1 - 7
of 7
pro vyhledávání: '"H. A. van Kooten"'
Autor:
J. J. A. van den Dorpel, E. Poelman, L. Harlaar, H. A. van Kooten, L. J. van der Giessen, P. A. van Doorn, A. T. van der Ploeg, J. M. P. van den Hout, N. A. M. E. van der Beek
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Enzyme replacement therapy (ERT; alglucosidase alfa) has improved the prospects for patients with classic infantile Pompe disease considerably. However, over time we noticed that many of these children exhibit distal muscle weakne
Externí odkaz:
https://doaj.org/article/271819d21b264ee4ac3cfc5060e9e962
Autor:
A.T. van der Ploeg, C.H.A. Roelen, P.A. van Doorn, H. A. van Kooten, Esther Brusse, Margreet A E M Wagenmakers, N.A.M.E. van der Beek, Michelle Michels
Publikováno v:
Neuromuscular Disorders, 31(2), 79-90. Elsevier Ltd.
Pompe disease is a rare inherited metabolic and neuromuscular disorder, presenting as a spectrum, with the classic infantile form on one end and the more slowly progressive non-classic form on the other end. While being a hallmark in classic infantil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::971d3839072f267c9aa426ac96071aa6
http://www.scopus.com/inward/record.url?scp=85098668931&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85098668931&partnerID=8YFLogxK
Autor:
Esther Poelman, A.T. van der Ploeg, J. M. P. van den Hout, L. J. van der Giessen, J. van den Dorpel, N.A.M.E. van der Beek, L. Harlaar, P.A. van Doorn, H. A. van Kooten
Publikováno v:
Orphanet Journal of Rare Diseases, 15(1):247. BioMed Central Ltd.
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Orphanet Journal of Rare Diseases
Background Enzyme replacement therapy (ERT; alglucosidase alfa) has improved the prospects for patients with classic infantile Pompe disease considerably. However, over time we noticed that many of these children exhibit distal muscle weakness at an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326be033ab928243efcbdb890524b2a8
https://pure.eur.nl/en/publications/ba162367-65ef-42bb-8306-31bcfb409449
https://pure.eur.nl/en/publications/ba162367-65ef-42bb-8306-31bcfb409449
Autor:
A.T. van der Ploeg, N.A.M.E. van der Beek, E. Brusse, P.A. van Doorn, H. A. van Kooten, L. Harlaar
Publikováno v:
Neuromuscular Disorders. 29:S61
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e217d80e4685a2761cd92b1c67a9649
https://doi.org/10.1016/j.nmd.2019.06.099
https://doi.org/10.1016/j.nmd.2019.06.099
Publikováno v:
Drugs. 46:183-188
The relationship between insulin resistance and hyperinsulinaemia on one hand and hypertension on the other hand has become apparent during the last few years. Insulin resistance, which may be genetically determined, is, according to our present unde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d460aac4aab12077cb08b6af1c570a2a
https://doi.org/10.2165/00003495-199300462-00028
https://doi.org/10.2165/00003495-199300462-00028
Publikováno v:
Archiv f�r die gesamte Virusforschung. 24:312-318
The preparation of a combined CF antigen derived from parainfluenza virus types 1, 2, 3 and 4 was described. Similar but triple antigens made from types 1–3, were put to tests with paired serum samples of 84 patients who excreted parainfluenza viru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::212aa67ad8e972d0a18d27a9a77e36f3
https://doi.org/10.1007/bf01243072
https://doi.org/10.1007/bf01243072
Publikováno v:
The Journal of infectious diseases. 126(2)
Two types of hepatitis-associated antigen (HAA), AB and AC, and the corresponding antibodies were distinguished by immunodiffusion, blocking of antigens with type-specific antibodies, and absorption of antibodies by saturation with heterotypic antige
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::869f26c9864f9e2eee534a3e339943f6
https://pubmed.ncbi.nlm.nih.gov/4115467
https://pubmed.ncbi.nlm.nih.gov/4115467