Zobrazeno 1 - 10
of 115
pro vyhledávání: '"Croxen, R."'
Publikováno v:
The Journal of Cell Biology, 1970 Feb 01. 44(2), 329-339.
Externí odkaz:
https://www.jstor.org/stable/1605967
Autor:
Spelbrink JN, Li FY, Tiranti V, Nikali K, Yuan QP, Tariq M, Wanrooij S, Garrido N, Comi G, Morandi L, Toscano A, Fabrizi GM, Somer H, Croxen R, Beeson D, Poulton J, Suomalainen A, Jacobs HT, Zeviani M, Larsson C., SANTORO, LUCIO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::835723dd793122797266eab40a4c3acd
http://hdl.handle.net/11588/398360
http://hdl.handle.net/11588/398360
Publikováno v:
Pediatric Endocrinology Reviews, 1, 518-524. YS Medical Media Ltd.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::8cae95708dfcae80c4949cf56ed3ae72
https://pure.eur.nl/en/publications/d943603c-68e3-4772-b212-58cdbcf3338c
https://pure.eur.nl/en/publications/d943603c-68e3-4772-b212-58cdbcf3338c
Autor:
Besson, D, Croxen, R, Hatton, C, Shelley, C, Colquhoun, D, Chauplannaz, G, Oosterhuis, H, Newsom-Davis, J, Vincent, A
Publikováno v:
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY. 73(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::10e127373f0bbb3d4473852cd1cae403
http://ora.ox.ac.uk/objects/uuid:4bb10c85-560a-410e-afcd-16318b9c65d1
http://ora.ox.ac.uk/objects/uuid:4bb10c85-560a-410e-afcd-16318b9c65d1
Autor:
Croxen, R, Hatton, C, Shelley, C, Brydson, M, Chauplannaz, G, Oosterhuis, H, Vincent, A, Newsom-Davis, J, Colquhoun, D, Beeson, D
Publikováno v:
NEUROLOGY. 59(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d69dfa658fc5d6a761945e3029a39931
http://ora.ox.ac.uk/objects/uuid:8ade7f2b-7e15-4b42-b86b-c21b363e4f99
http://ora.ox.ac.uk/objects/uuid:8ade7f2b-7e15-4b42-b86b-c21b363e4f99
Publikováno v:
JOURNAL OF PHYSIOLOGY-LONDON. 527
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::92812b2fac8489e33a3b4270471a3294
http://ora.ox.ac.uk/objects/uuid:ebd5ebd8-8c20-4af8-b15f-0dca69774bb2
http://ora.ox.ac.uk/objects/uuid:ebd5ebd8-8c20-4af8-b15f-0dca69774bb2
Publikováno v:
EUROPEAN JOURNAL OF NEUROSCIENCE. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2297270cc5b2112cdc828b3ea0540cc9
http://ora.ox.ac.uk/objects/uuid:e090d2b5-0869-4cd0-a21a-a5163dcf8444
http://ora.ox.ac.uk/objects/uuid:e090d2b5-0869-4cd0-a21a-a5163dcf8444
Publikováno v:
Human Molecular Genetics, 6(5), 767-774. Oxford University Press
Congenital myasthenic syndromes are a group of rare genetic disorders that compromise neuromuscular transmission. A subset of these disorders, the slow-channel congenital myasthenic syndrome (SCCMS), is dominantly inherited and has been shown to invo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::94296bf78bf54ece9c5db9e431104801
https://research.rug.nl/en/publications/f00fe919-0bc2-4f4a-bca6-c18c67d81a43
https://research.rug.nl/en/publications/f00fe919-0bc2-4f4a-bca6-c18c67d81a43