Zobrazeno 1 - 10
of 300
pro vyhledávání: '"Mc, Gubler"'
Autor:
M Zivna, H Hulkova, M Matignon, K Hodanova, P Vylet'al, M Kalbacova, V Baresova, J Sikora, H Blazkova, J Zivny, R Ivanek, V Stranecky, J Sovova, K Claes, E Lerut, JP Fryns, PS Hart, TC Hart, JN Adams, A Pawtowski, M Clemessy, JM Gasc, MC Gubler, C Antignac, M Elleder, K Kapp, P Grimbert, AJ Bleyer, S Kmoch
Publikováno v:
Clinical Journal of the American Society of Nephrology. 5:563-567
Publikováno v:
CIÊNCIAVITAE
Europe PubMed Central
Europe PubMed Central
Autor:
Heidet L, Cai Y, Sado Y, Ninomiya Y, Thorner P, Guicharnaud L, Boye E, Chauvet V, Lc, Solal, Beziau A, Rg, Torres, Corinne ANTIGNAC, Mc, Gubler
Publikováno v:
Europe PubMed Central
CIÊNCIAVITAE
CIÊNCIAVITAE
Inherited diffuse esophageal leiomyomatosis a benign tumor involving smooth muscle cells of the whole esophagus, is frequently associated with X-linked Alport syndrome, a hereditary disease of type IV collagen. Families with this condition are consis
Autor:
MC Gubler, C Antignac
Publikováno v:
Archives de Pédiatrie. 3:S341-S342
Autor:
Heidet L, Boye E, Cai Y, Sado Y, Zhang X, Jf, Fléjou, Fékété F, Ninomiya Y, Mc, Gubler, Corinne ANTIGNAC
Publikováno v:
Europe PubMed Central
CIÊNCIAVITAE
CIÊNCIAVITAE
Leiomyomata of the esophagus are sporadic benign tumors of unknown etiology. We studied a collection of nine tumors for the expression of extracellular matrix components and found the same aberrant expression pattern as previously observed in inherit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::36db866f27269eb1bfd7633e910a59a5
http://europepmc.org/abstract/med/9502408
http://europepmc.org/abstract/med/9502408
Autor:
Tsimaratos M, Bérard E, Sigaudy S, Almahana T, Delarue A, Roquelaure B, Costet C, Corinne ANTIGNAC, Mc, Gubler, Picon G, Philip N, Sarles J
Publikováno v:
Europe PubMed Central
CIÊNCIAVITAE
CIÊNCIAVITAE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0fc1107e9f52eb9dc0b6b13c3b5ac287
http://europepmc.org/abstract/med/9438667
http://europepmc.org/abstract/med/9438667
Autor:
Jaubert F, Vasiliu V, Patey-Mariaud de Serre N, Auber F, cecile Jeanpierre, Mc, Gubler, Nihoul-Fékété C, Fellous M
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::76f8e97537627bf802d2f687f85e435c
http://europepmc.org/abstract/med/15357247
http://europepmc.org/abstract/med/15357247
Autor:
Mc, Gubler, Corinne ANTIGNAC, Deschênes G, Knebelmann B, Mc, Hors-Cayla, Jp, Grünfeld, Broyer M, Habib R
Publikováno v:
CIÊNCIAVITAE
Europe PubMed Central
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::87426e9c9ab4b3d204a3f967bff6e07f
http://europepmc.org/abstract/med/8427057
http://europepmc.org/abstract/med/8427057
Autor:
Knebelmann B, Breillat C, Forestier L, Arrondel C, Jacassier D, Giatras I, Drouot L, Deschênes G, Jp, Grünfeld, Broyer M, Mc, Gubler, Corinne ANTIGNAC
Publikováno v:
Europe PubMed Central
CIÊNCIAVITAE
CIÊNCIAVITAE
Alport syndrome is a mainly X-linked hereditary disease of basement membranes that is characterized by progressive renal failure, deafness, and ocular lesions. It is associated with mutations of the COL4A5 gene located at Xq22 and encoding the alpha5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::26e8dc39f053890509ce273d2ff03b3f
http://europepmc.org/abstract/med/8940267
http://europepmc.org/abstract/med/8940267
Publikováno v:
Europe PubMed Central
CIÊNCIAVITAE
CIÊNCIAVITAE
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::222adf10db1398c452466bb1576cec27
http://europepmc.org/abstract/med/8381254
http://europepmc.org/abstract/med/8381254