Zobrazeno 1 - 10
of 271
pro vyhledávání: '"Parma, J"'
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1987 May . 84(10), 3181-3184.
Externí odkaz:
https://www.jstor.org/stable/29356
Publikováno v:
Intas Polivet. Jan-Jun2020, Vol. 21 Issue 1, p120-121. 2p.
Autor:
Metral, And Aberle, E., And Assmann, O., And Baglin, R. W., And Barnes, V., And Berrig, M. J., And Bertarelli, O. E., And Bregliozzi, A., And Calatroni, G., Carra, Federico, And Caspers, F., And Day, F., And Ferro luzzi, H. A., And Gallilee, M., And Garion, M. A., And Garlasche, C., And Grudiev, M., And Jimenez, A., And Jones, J. M., And Kononenko, R., And Losito, O., And Nougaret, R., And Parma, J. L., And Redaelli, V., And Salvant, S., And Strubin, B., And Veness, P., And Vollinger, R., And Weterings, C.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2153::81ec7675a61225fe8d981d48e1b40222
http://hdl.handle.net/11583/2686859
http://hdl.handle.net/11583/2686859
Publikováno v:
Acta clinica Belgica, 66(2), 129-131. Taylor and Francis Ltd.
A tired 32-year-old woman complaining of tiredness was referred for work-up of a possible immune deficiency. She had a history of recurrent infections since birth, which usually responded to antibiotics within a few days. Her mother, a nurse, had rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::d6b4bd6e94e70d192e880f447e4bf7bb
https://pure.amc.nl/en/publications/a-woman-with-recurrent-infections-since-birtha-new-mevalonate-kinase-mutation(c62b4ded-9d34-4dbe-b982-e72102503bae).html
https://pure.amc.nl/en/publications/a-woman-with-recurrent-infections-since-birtha-new-mevalonate-kinase-mutation(c62b4ded-9d34-4dbe-b982-e72102503bae).html
Autor:
Santoro M., Thomas G. A., Williams G. H., Chiappetta G., Pozcharskaya V., Bogdonova T. I., Demidchick E. P., Cherstvoy E. D., Voskoboinik L., Tronko N. D., Carss A., Bunnel H., Tonnachera M., Parma J., Dumont J. E., Keller G., Hofler H., Williams E. D., VECCHIO, GIANCARLO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::c649ff017ca9def5780fb34d42665593
http://hdl.handle.net/11588/167408
http://hdl.handle.net/11588/167408
Autor:
Gonzalez-Merino E, Emiliani S, Pichon B, Parma J, As, Vannin, Delbaere A, Vassart G, Marc Abramowicz, Englert Y
Publikováno v:
Europe PubMed Central
The clinical activity of the preimplantation genetic diagnosis (PGD) at Erasme Hospital was carried out since September 1999 for a 47,XYY patient. Up to 31 December 2007, 79 PGD cycles were carried out (45 couples) for either chromosomal structural a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7973e080c937f7e4ec9b735176b6503c
https://pubmed.ncbi.nlm.nih.gov/19202707
https://pubmed.ncbi.nlm.nih.gov/19202707
Autor:
Vilain C, Rydlewski C, Duprez L, Heinrichs C, Marc Abramowicz, Malvaux P, Renneboog B, Parma J, Costagliola S, Vassart G
Publikováno v:
Europe PubMed Central
Congenital hypothyroidism (CH) is a relatively frequent and potentially severe disease. It is classically subdivided into: 1) thyroid dysgenesis (TD), a defect in the organogenesis of the gland leading to hypoplastic, ectopic, or absent thyroid gland
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5dce8ce2945e8cbf4726516458db79af
https://pubmed.ncbi.nlm.nih.gov/11232006
https://pubmed.ncbi.nlm.nih.gov/11232006