Zobrazeno 1 - 10
of 188
pro vyhledávání: '"N. Haites"'
Autor:
Hans W. Müller, Ueli Suter, Christine Van Broeckhoven, O. Haneman, E. Nelis, V. Timmerman, S. Sancho, L. Barrio, P. Bolhuis, R. Dermietzel, M. Frank, A. Gabreëls-Festen, C. Gillen, N. Haites, G. Levi, E. Mariman, R. Martini, K. Nave, B. Rautenstrauss, M. Schachner, A. Schenone, C. Schneider, M. Schröder, K. Willecke
Publikováno v:
Neurobiology of Disease, Vol 4, Iss 3, Pp 215-220 (1997)
The First Workshop of the European Consortium on Charcot–Marie–Tooth (CMT) disease brought together neuroscientists, molecular and cell biologists, neuropathologists, neurologists, and geneticists with a common interest in the understanding of th
Externí odkaz:
https://doaj.org/article/9f049ec01c554906b50a3476d82e1efa
Autor:
A.A.W.M. Gabreëls-Festen, C. Van Broeckhoven, G. Levi, Hans Werner Müller, A. Schenone, M. Frank, K. Willecke, R. Martini, Vincent Timmerman, B. Rautenstrauss, R. Dermietzel, C. Schneider, N. Haites, O. Haneman, Edwin C. M. Mariman, Ueli Suter, C. Gillen, M. Schröder, Eva Nelis, M. Schachner, S. Sancho, Klaus-Armin Nave, L. Barrio, P.A. Bolhuis
Publikováno v:
Neurobiology of disease
Neurobiology of Disease, 4, pp. 215-220
Neurobiology of Disease, 4, 3, pp. 215-220
Neurobiology of Disease, 4, 215-220
Neurobiology of Disease, Vol 4, Iss 3, Pp 215-220 (1997)
Neurobiology of Disease, 4, pp. 215-220
Neurobiology of Disease, 4, 3, pp. 215-220
Neurobiology of Disease, 4, 215-220
Neurobiology of Disease, Vol 4, Iss 3, Pp 215-220 (1997)
The First Workshop of the European Consortium on Charcot–Marie–Tooth (CMT) disease brought together neuroscientists, molecular and cell biologists, neuropathologists, neurologists, and geneticists with a common interest in the understanding of th
Publikováno v:
Familial cancer. 1(2)
The purpose of this study was to retrospectively compare the outcomes of treatment in 304 women with familial and sporadic breast cancer to clarify the options for the primary management of familial breast cancer. The majority of women were consecuti
Publikováno v:
Clinical genetics. 64(4)
Communication about genetic risk in families is an important issue for genetic counsellors. The objective of this study was to explore the barriers and facilitators in family communication about genetic risk. Semi-structured interviews were undertake
Autor:
N Haites
Publikováno v:
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP). 11(1)
IntroductionDNA for studying gene–nutrient or other interactions and for testing hypotheses relating to the causes of human diseases can be obtained from a wide range of tissue types. The main limitation to obtaining DNA is, in fact, the availabili
Publikováno v:
BMJ (Clinical research ed.). 322(7293)
Publikováno v:
The Journal of clinical endocrinology and metabolism. 85(12)
The period of Leydig cell hyperplasia (14-18 weeks gestation) in human fetal testis is crucial for normal gonad development. We have studied the spatio-temporal distribution of key developmental and functional markers in human fetal testis between 13
Autor:
P, Møller, M M, Reis, G, Evans, H, Vasen, N, Haites, E, Anderson, C M, Steel, J, Apold, F, Lalloo, L, Maehle, P, Preece, H, Gregory, K, Heimdal
Publikováno v:
Disease Markers
BACKGROUND: Surveillance programmes for women at increased genetic risk of breast cancer are being established worldwide but little is known of their efficacy in early detection of cancers and hence reduction in mortality. METHODS: Data were contribu