Zobrazeno 1 - 10
of 10
pro vyhledávání: '"G. M. Hulstijn-Dirkmaat"'
Het effect van multidisciplinaire groepsbehandeling bij kinderen met chronische defecatiestoornissen
Autor:
René S. V. M. Severijnen, G. M. Hulstijn-Dirkmaat, J. M. Th. Draaisma, A. T. M. Brugman-Boezeman, Marlou Essink, E. M. van Kuyk, H. P. A. van Kuppenveld, M. C. C. H. Steeghs
Publikováno v:
Tijdschrift voor Kindergeneeskunde. 76:157-164
Doel. Doel van dit onderzoek is het evalueren van het effect van multidisciplinaire groepsbehandeling bij kinderen met chronische defecatiestoornissen.
Autor:
G. M. Hulstijn-Dirkmaat
Publikováno v:
Tijdschrift voor kindergeneeskunde. 68:85-91
Het aantal familie-niertransplantaties neemt de laatste jaren mede op grond van positieve resultaten sterk toe. Bij kinderen is meestal een van de ouders donor. Psychologische overwegingen bij ouder-kindtransplantatie worden beschreven aan de hand va
Publikováno v:
Acta Paediatrica. 83:972-976
The burden placed on the parents of a child in dialysis treatment can induce negative effects on the medical treatment and on the psychological development of the child. To identify which families are at risk, both parents of 14 out of 16 eligible pa
Publikováno v:
Pediatric Dialysis ISBN: 9789401037709
Whereas the literature regarding the neurological of uremia and its treatment in children is scarce, a large body of published literature indicates delayed neuro-development in infants with end-stage renal disease (ESRD). The biochemical abnormalitie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1302228be3c94fb73d50adfd6efbdea7
https://doi.org/10.1007/978-94-007-1031-3_26
https://doi.org/10.1007/978-94-007-1031-3_26
Publikováno v:
American journal of medical genetics. 61(1)
Mental retardation (MR) is generally considered one of the main complications of congenital nephrogenic diabetes insipidus (NDI). However, psychometric studies of NDI patients are scarce and outdated. In the present study, 17 male NDI patients underw
Autor:
G. M. Hulstijn-Dirkmaat, J. A. Hoekstra, L.A.H. Monnens, V. V. A. M. Knoers, A.F. van Lieburg
Publikováno v:
American Journal of Medical Genetics, 61, 81-88
American Journal of Medical Genetics, 61, pp. 81-88
American Journal of Medical Genetics, 61, 1, pp. 81-88
American Journal of Medical Genetics, 61, pp. 81-88
American Journal of Medical Genetics, 61, 1, pp. 81-88
Mental retardation (MR) is generally considered one of the main complications of congenital nephrogenic diabetes insipidus (NDI). However, psychometric studies of NDI patients are scarce and outdated. In the present study, 17 male NDI patients underw
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64b63c09db4af5dd54c484cde31ff08b
http://hdl.handle.net/2066/23537
http://hdl.handle.net/2066/23537
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 136(46)
Medical and technical advances make it possible to treat young children with end-stage renal disease with far-reaching methods such as continuous ambulatory peritoneal dialysis (CAPD) and haemodialysis (HD). We investigated whether chronic renal fail
Publikováno v:
Tijdschrift voor kindergeneeskunde. 57(6)
In medicine medical decisions prove to be ethical issues. Whether treatment apart from being medically possible can also be meaningful, or can continue to be meaningful, is an ethical question, where interests, in nature different and sometimes contr
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 131(51)
Autor:
J. Vande Walle, C. M. L. van Dael, Elena Levtchenko, Marc R. Lilien, Elisabeth A.M. Cornelissen, R E A van der Rijken, Martine T.P. Besouw, G M Hulstijn-Dirkmaat
Publikováno v:
ResearcherID
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, 33(6), 787-793. SPRINGER
Journal of Inherited Metabolic Disease, 33, 787-93
Journal of Inherited Metabolic Disease, 33, 6, pp. 787-93
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, 33(6), 787-793. SPRINGER
Journal of Inherited Metabolic Disease, 33, 787-93
Journal of Inherited Metabolic Disease, 33, 6, pp. 787-93
Contains fulltext : 89600.pdf (Publisher’s version ) (Closed access) INTRODUCTION: Cystinosis is an autosomal recessive disorder leading to intralysosomal cystine accumulation in various tissues. It causes renal Fanconi syndrome and end stage renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ace8cad8d0dc9890ec0809fab328468
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000268584500218&KeyUID=WOS:000268584500218
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=ORCID&SrcApp=OrcidOrg&DestLinkType=FullRecord&DestApp=WOS_CPL&KeyUT=WOS:000268584500218&KeyUID=WOS:000268584500218