Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Weinreich Stephanie"'
Autor:
Weinreich Stephanie S, Vrinten Charlotte, Verschuuren Jan JGM, Uyl-de Groot Carin A, Kuijpers Marja R, Sterrenburg Ellen, Scholten Rob JPM, van Bezooijen Cees FRM, Timmen Marcel FTH, van Weely Sonja, Cornel Martina C
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 7, Iss Suppl 2, p A29 (2012)
Externí odkaz:
https://doaj.org/article/ff2b10a8f30d4adfad7c2dca85708df9
Autor:
Weinreich Stephanie, Rigter Tessel, van El Carla, Dondorp Wybo, Kostense Pieter, van der Ploeg Ans T, Reuser Arnold JJ, Cornel Martina, Hagemans Marloes
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 7, Iss 1, p 15 (2012)
Abstract Background Neonatal screening for Pompe disease has been introduced in Taiwan and a few U.S. states, while other jurisdictions including some European countries are piloting or considering this screening. First-tier screening flags both clas
Externí odkaz:
https://doaj.org/article/30ddceeea42742cf91564d3918c48f3a
Autor:
Cornel Martina C, Rijmen Frank, de Lange-de Klerk Elly SM, Weinreich Stephanie S, de Kinderen Marja, Plass Anne
Publikováno v:
BMC Public Health, Vol 9, Iss 1, p 338 (2009)
Abstract Background In the Netherlands no formal recommendations exist concerning preconceptional or antenatal testing for carriership of hereditary haemoglobinopathies. Those at highest risk may be unaware of the possibility of carrier screening. Wh
Externí odkaz:
https://doaj.org/article/1bfb4fae74934a05ae0b2ef54bfe7970
Autor:
Lipka, Alexander F. *, Vrinten, Charlotte, van Zwet, Erik W., Schimmel, Kirsten J.M., Cornel, Martina C., Kuijpers, Marja R., Hekster, Yechiel A., Weinreich, Stephanie S., Verschuuren, Jan J.G.M.
Publikováno v:
In Neuromuscular Disorders March 2017 27(3):259-265
Autor:
van Teeffelen, Sarah R., Douglas, Conor M.W., van El, Carla G., Weinreich, Stephanie S., Henneman, Lidewij, Radstake, Maud, Cornel, Martina C.
Publikováno v:
Public Health Genomics, 2016 Jan 01. 19(1), 25-33.
Externí odkaz:
https://www.jstor.org/stable/26778228
Autor:
van der Zwaag, Angeli M., Weinreich, Stephanie S., Bosma, Astrid R., Rigter, Tessel, Losekoot, Monique, Henneman, Lidewij, Cornel, Martina C.
Publikováno v:
Public Health Genomics, 2015 Jan 01. 18(1), 52-59.
Externí odkaz:
https://www.jstor.org/stable/26778165
Autor:
Weinreich, Stephanie
Publikováno v:
Community Genetics, 2006 Jan 01. 9(4), 279-280.
Externí odkaz:
https://www.jstor.org/stable/26679546
Akademický článek
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Autor:
Weinreich, Stephanie S.1,2 s.weinreich@vumc.nl, Vrinten, Charlotte1,3, Kuijpers, Marja R.2, Lipka, Alexander F.4, Schimmel, Kirsten J. M.5, van Zwet, Erik W.6, Gispen-de Wied, Christine7, Verschuuren, Jan J. G. M.4, Cornel, Martina C.1, Hekster, Yechiel A7 (AUTHOR)
Publikováno v:
Orphanet Journal of Rare Diseases. 5/12/2017, Vol. 12, p1-18. 18p.
Autor:
Weinreich, Stephanie S1, Bosma, Astrid1, Henneman, Lidewij1, Rigter, Tessel1, Spruijt, Carla MJ2, Grimbergen, Anneliese JEMA2, Breuning, Martijn H2, de Koning, Eelco JP3, Losekoot, Monique2, Cornel, Martina C1
Publikováno v:
European Journal of Human Genetics. Jan2015, Vol. 23 Issue 1, p29-33. 5p.