Zobrazeno 1 - 8
of 8
pro vyhledávání: '"J. H. A. M. TUERLINGS"'
Publikováno v:
Tijdschrift voor psychiatrie. 59(12)
The most recent information about the use of ECT in the Netherlands dates from 2008. An update version of the guideline for the use of ECT in the Netherlands was issued in 2010.To obtain insight into the practice of ECT in the Netherlands five years
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6e6425279d020a1ea5187fcbb76ac1bf
https://pubmed.ncbi.nlm.nih.gov/29251750
https://pubmed.ncbi.nlm.nih.gov/29251750
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 161
Two independent, home-dwelling geriatric patients presented with apathy at a general practice in the Netherlands and were seen by an elderly care physician after (non-)medical interventions had failed. Both patients were treated with low-dose methylp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf643d0b038573782aefd8ee8ff89bc0
https://pubmed.ncbi.nlm.nih.gov/28914218
https://pubmed.ncbi.nlm.nih.gov/28914218
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 152(36)
Patients with severe psychiatric and somatic disorders may require admission to a combined psychiatric-somatic care unit. These units provide specialised psychiatric and somatic care as well as palliative care. This is illustrated by two case reports
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::324d068fc276e3706171d6e99945dafd
https://pubmed.ncbi.nlm.nih.gov/18807328
https://pubmed.ncbi.nlm.nih.gov/18807328
Publikováno v:
Tijdschrift voor psychiatrie. 48(10)
Over the last few decades much research has been done into the raised level of psychiatric comorbidity in epilepsy. On the basis of a case study of a patient suffering from post-ictal psychoses we explain the psychiatric differential diagnosis within
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2117817f100e4892be2f5f4c15fb7d79
https://pubmed.ncbi.nlm.nih.gov/17086946
https://pubmed.ncbi.nlm.nih.gov/17086946
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(31)
Prevention of deliberate self-harm, especially suicide attempts, remains difficult and this puts a great burden on the family as well as on the health-care professionals. The risk of a subsequent suicide attempt or a successful suicide is high while
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d56d98afa2bd9da5c9551127d137f5c
https://pubmed.ncbi.nlm.nih.gov/15646867
https://pubmed.ncbi.nlm.nih.gov/15646867
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 146(38)
Three women, aged 21, 34 and 32 and with a family history of mental retardation said to be caused by perinatal asphyxia, each gave birth to a child with mental retardation. A chromosomal translocation, fragile X syndrome, and myotonic dystrophy could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8f80a6745f0f42998a846b258f35289
https://pubmed.ncbi.nlm.nih.gov/12369434
https://pubmed.ncbi.nlm.nih.gov/12369434
Autor:
P. E. JIRA, R. J. A. WANDERS, J. A. M. SMEITINK, J. JONG, R. A. WEVERS, W. OOSTHEIM, J. H. A. M. TUERLINGS, R. C. M. HENNEKAM, R. C. A. SENGERS, H. R. WATERHAM
Publikováno v:
Annals of human genetics, 65(Part 3), 229-236. Wiley-Blackwell
Annals of Human Genetics, 65, Pt 3, pp. 229--36
Annals of Human Genetics, 65, 229--36
Annals of Human Genetics, 65, Pt 3, pp. 229--36
Annals of Human Genetics, 65, 229--36
Item does not contain fulltext Smith--Lemli--Opitz syndrome (SLOS) is caused by mutations in the DHCR7 gene leading to deficient activity of 7-dehydrocholesterol reductase (DHCR7; EC 1.3.1.21), the final enzyme of the cholesterol biosynthetic pathway
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68cf521b99e5269ceac5d7dcec78aec4
https://doi.org/10.1046/j.1469-1809.2001.6530229.x
https://doi.org/10.1046/j.1469-1809.2001.6530229.x
Publikováno v:
Prenatal diagnosis. 13(4)
A 70,XXX,+18 karyotype was found by chorionic villus sampling, while the fetal fibroblast culture of the affected fetus revealed a 47,XX,+18 karyotype. From several possible mechanisms, we assume that a second gamete fusion occurred after the first c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32fd456d52c64650f61bd17c662ae498
https://pubmed.ncbi.nlm.nih.gov/8506231
https://pubmed.ncbi.nlm.nih.gov/8506231