Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Tuerlings, J.H.A.M."'
Publikováno v:
Journal of the International Neuropsychological Society, 22, 2, pp. 99
Journal of the International Neuropsychological Society, 22, 99
Journal of the International Neuropsychological Society, 22, 99
Item does not contain fulltext Objectives: The 22q11.2 deletion syndrome (22qDS), mostly caused by the common deletion (LCR-A-D) including TBX and COMT genes, is highly associated with congenital anomalies and endocrine dysfunctions accompanied by sc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b6aeb7d3769ce00932e96416dfecd58a
https://hdl.handle.net/2066/166224
https://hdl.handle.net/2066/166224
Publikováno v:
Nederlands Tijdschrift voor Geneeskunde, 146, 1765-8
Nederlands Tijdschrift voor Geneeskunde, 146, 38, pp. 1765-8
Nederlands Tijdschrift voor Geneeskunde, 146, 38, pp. 1765-8
Item does not contain fulltext 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 syndrom
Autor:
Golde, R.J.T. van, Tuerlings, J.H.A.M., Kremer, J.A.M., Braat, D.D.M., Schoute, F., Hoefsloot, L.H.
Publikováno v:
Journal of Assisted Reproduction and Genetics, 18, 7, pp. 395--9
Journal of Assisted Reproduction and Genetics, 18, 395--9
Journal of Assisted Reproduction and Genetics, 18, 395--9
Item does not contain fulltext PURPOSE: To study the role of the autosomal candidate gene DAZLA (Deleted in AZoospermia Like Autosome) in male subfertility. METHODS: We reviewed clinical data of subfertile men with oligozoospermia or azoospermia, mos
Autor:
Engelen, J.J.M., Tuerlings, J.H.A.M., Albrechts, J.C.M., Schrander-Stumpel, C.T.R.M., Hamers, A.J.H., Die, C.E. van
Publikováno v:
Genetic Counseling, 11, 13-17
Genetic Counseling, 11, 1, pp. 13-17
Genetic Counseling, 11, 1, pp. 13-17
Item does not contain fulltext
Autor:
Kremer, J.A.M., Tuerlings, J.H.A.M., Borm, G.F., Hoefsloot, L.H., Meuleman, E.J.H., Braat, D.D.M., Brunner, H.G., Merkus, J.M.W.M.
Publikováno v:
Human Reproduction, 13, pp. 2808-2811
Human Reproduction, 13, 2808-2811
Human Reproduction, 13, 2808-2811
Item does not contain fulltext 4 p.
Publikováno v:
Prenatal Diagnosis, 16, 554-558
Prenatal Diagnosis, 16, pp. 554-558
Prenatal Diagnosis, 16, pp. 554-558
Item does not contain fulltext
Publikováno v:
Journal of ECT, 26(4), 248-252
Objectives: Electroconvulsive therapy (ECT) has been described as an effective treatment option for catatonia in retrospective case series. We aimed to investigate treatment characteristics and outcomes of patients with catatonia who were treated wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8345fc9c0327f1ad8c7f09490c95d93a
https://hdl.handle.net/1887/117706
https://hdl.handle.net/1887/117706
Publikováno v:
The European Journal of Psychiatry, 22, 195-199
The European Journal of Psychiatry, 22, 4, pp. 195-199
The European Journal of Psychiatry, 22, 4, pp. 195-199
Contains fulltext : 77413.pdf (Publisher’s version ) (Open Access) Background and Objectives: Testosterone deficiency has been implicated in the etiology of depression although there is an ongoing debate on the nature of this association. There is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b6892ebd572120ac0791953146666f6b
http://hdl.handle.net/2066/77413
http://hdl.handle.net/2066/77413
Publikováno v:
Journal of Intellectual Disability Research, 50, 11, pp. 797
Journal of Intellectual Disability Research, 50, 797
Journal of Intellectual Disability Research, 50, 797
Item does not contain fulltext 1 p.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::de6482784f9f5f7768eb86b0a240f12b
https://hdl.handle.net/2066/55675
https://hdl.handle.net/2066/55675