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1.
Ned Tijdschr Geneeskd ; 150(44): 2410-4, 2006 Nov 04.
Artigo em Holandês | MEDLINE | ID: mdl-17131697

RESUMO

In the Netherlands, the practice of private freezing and banking of umbilical-cord blood is increasing. In a questionnaire, Dutch midwives and gynaecologists were asked about their attitude towards cord-blood collection if asked to perform this after delivery. The response rate was 35% (125/356) and 71% (71/100), respectively. Two-thirds of those asked responded that they would comply. The most common application of cord blood is in the treatment of (malignant) blood disorders. The use of autologous cord blood is, however, often not the best choice for treating leukaemia in young children and the number of stem cells is often too low in a single-cord blood sample to treat older children and adults. Although frequently suggested in the lay press, there is no proven effect in other indications, such as amyotrophic lateral sclerosis, multiple sclerosis and myocardial infarction. Information on therapeutic applications of cord blood from companies with commercial interests is leading to the exploitation ofpregnantwomen. The government should consider limiting this practice and prohibiting the activities of these companies in the Netherlands pending scientific evidence for their claims.


Assuntos
Células da Medula Óssea , Transplante de Células-Tronco de Sangue do Cordão Umbilical , Sangue Fetal , Conhecimentos, Atitudes e Prática em Saúde , Gestantes/psicologia , Bancos de Sangue , Feminino , Neoplasias Hematológicas/terapia , Histocompatibilidade , Humanos , Países Baixos , Gravidez , Coleta de Tecidos e Órgãos , Transplante Autólogo
2.
Ned Tijdschr Geneeskd ; 147(19): 898-900, 2003 May 10.
Artigo em Holandês | MEDLINE | ID: mdl-12768802

RESUMO

In 1999, the Dutch Medical Research Involving Human Subjects Act came into force. The principal aim of this Act is to provide protection for human subjects who take part in medical research. Medical research involving human subjects may only be carried out after it has been approved by a recognised medical ethics committee. A central committee (Dutch acronym: CCMO) regulates the recognition of the local medical ethics committees and monitors their performance. For some types of research the protocol has to be reviewed by the CCMO itself. These are: non-therapeutic research involving children and mentally incompetent patients and research on gene therapy, xenotransplantation and embryos. The CCMO has recently published a guide for the local medical ethics committees. It presents an excellent overview of all the legal and practical aspects of the work of medical ethics committees. The guide is highly recommended.


Assuntos
Comitês de Ética em Pesquisa/legislação & jurisprudência , Ética em Pesquisa , Experimentação Humana/legislação & jurisprudência , Pesquisa/normas , Revisão Ética , Regulamentação Governamental , Experimentação Humana/ética , Humanos , Países Baixos , Pesquisa/legislação & jurisprudência , Sujeitos da Pesquisa/legislação & jurisprudência , Experimentação Humana Terapêutica/ética , Experimentação Humana Terapêutica/legislação & jurisprudência
11.
BMJ ; 306(6872): 226, 1993 Jan 23.
Artigo em Inglês | MEDLINE | ID: mdl-8443519
14.
CMAJ ; 140(7): 788, 1989 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-2924224
16.
Br Med J (Clin Res Ed) ; 295(6612): 1563-4, 1987 Dec 12.
Artigo em Inglês | MEDLINE | ID: mdl-3122904
17.
J Clin Pathol ; 32(6): 528-33, 1979 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-469009

RESUMO

A patient with systemic lupus erythematosus was studied whose blood serum on repeated occasions showed undetectable levels of haemolytic omplement (C). A detailed investigation of individual C components in the serum of the proposita and her family revealed the absence of functional C2 in the patient and half-normal values in the relatives. C4 levels in the family, but not in the patient, were above normal, whereas the levels of factor B were low in all cases. No abnormalities were noted in C3, C9, or C1INH. Tissue typing showed linkage of the C2-deficiency gene with the HLA-A10/B18 and A9/B18 haplotypes. No linkage with red cell antigens and no relationship with plasma kallikrein levels was found.


Assuntos
Complemento C2/deficiência , Antígenos HLA/genética , Lúpus Eritematoso Sistêmico/imunologia , Adolescente , Adulto , Idoso , Antígenos de Grupos Sanguíneos , Complemento C2/genética , Feminino , Antígenos HLA/análise , Homozigoto , Humanos , Lúpus Eritematoso Sistêmico/sangue , Lúpus Eritematoso Sistêmico/genética , Masculino , Pessoa de Meia-Idade , Linhagem
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