Coexistence of Pheochromocytoma and Renal Artery Stenosis in a Pediatric Patient with Hypertension

Autor: Serras, I, Baeta Baptista, R, Francisco, T, Casimiro, A, Lito, D, Alves, R, Abranches, M

Publikováno v: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Pheochromocytoma and renal artery stenosis are surgically treatable causes of hypertension. Although rare, the coexistence of pheochromocytoma and renal artery stenosis has been described in case reports. Common pathophysiological mechanisms other th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::92c2092614b5ecae5f0a8e7b83c4a50b

Conjuntivite Neonatal. Que PROFILAXIA ?

Autor: Serras, I, Candeias, F, Brito, MJ

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______2340::8c61b12588d05518a10ae1da9a9e02f5
https://hdl.handle.net/10400.17/2528

Urinary Tract Effects of HPSE2 Mutations

Autor: Stuart, H. M., Roberts, N. A., Hilton, E. N., Mckenzie, E. A., Daly, S. B., Hadfield, K. D., Rahal, J. S., Gardiner, N. J., Tanley, S. W., Lewis, M. A., Sites, E., Angle, B., Alves, C., Lourenço, T., Rodrigues, M., Calado, A., Amado, M., Guerreiro, N., Serras, I., Beetz, C., Varga, R. -E., Silay, M. S., Darlow, J. M., Dobson, M. G., Barton, D. E., Hunziker, M., Puri, P., Feather, S. A., Goodship, J. A., Goodship, T. H. J., Lambert, H. J., Cordell, H. J., Saggar, A., Kinali, M., Lorenz, C, Moeller, K, Schaefer, F, Bayazit, Ak, Weber, S, Newman, Wg, Woolf, As, Beattie, J, Bradbuty, M, Coad, N, Coulthard, M, Cuckow, P, Dossetor, J, Dudley, J, Hughes, D, Feather, S, Fitzpatrick, M, Goodship, Ja, Goodship, Th, Griffin, N, Gullett, Am, Haycock, G, Hodes, D, Houtman, P, Hughes, A, Hulton, S, Hunter, E, Iqbal, J, Inward, C, Jackson, J, Jadresic, L, Jaswon, M, Jones, C, Jones, R, Judd, B, Kier, M, Kilby, A, Lambert, H, Lewis, M, Malcolm, S, Marks, S, Maxwell, H, Mcgraw, M, Milford, D, Moghal, N, O'Connor, M, O'Donoghue, Dj, Ognanovic, M, Plant, N, Postlethwaite, R, Rees, L, Reid, C, Rfidah, E, Rigdon, S, Sandford, R, Savage, M, Scanlan, J, Sinha, S, Stephens, S, Stewart, A, Storr, J, Taheri, S, Taylor, Cm, Tizard, J, Trompeter, R, Tullus, K, Verber, I, Van't Hoff, W, Vernon, S, Verrier-Jones, K, Watson, A, Webb, N, Wilcox, D, Aksu, N, Alpay, H, Anarat, A, Arbeiter, K, Ardissino, Gl, Balat, A, Baskin, E, Bayazit, A, Büscher, R, Cakar, N, Caldas Afonso, A, Caliskan, S, Candan, C, Canpolat, N, Donmez, O, Doyon, A, Drozdz, D, Dusek, J, Duzova, A, Emre, S, Erdogan, H, Feldkötter, M, Fischbach, M, Galiano, G, Haffner, D, Harambat, J, Jankauskiene, A, Jeck, N, John, U, Jungraithmair, T, Kemper, M, Kiyak, A, Kracht, D, Kranz, B, Laube, G, Litwin, M, Matteucci, Cm, Montini, G, Melk, A, Mir, S, Niemirska, A, Peco-Antic, A, Ozcelik, G, Pelan, E, Picca, S, Pohl, M, Querfeld, U, Ranchin, B, Shroff, R, Simonetti, G, Sözeri, B, Soylemezoglu, O, Tabel, Y, Testa, S, Trivelli, A, Vidal, E, Wigger, M, Wühl, E, Wygoda, S, Yalcinkaya, F, Yilmaz, E, Zeller, R, Zurowska, Am.

Publikováno v: Europe PubMed Central
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

PubMedID: 25145936 Urofacial syndrome (UFS) is an autosomal recessive congenital disease featuring grimacing and incomplete bladder emptying. Mutations of HPSE2, encoding heparanase 2, a heparanase 1 inhibitor, occur in UFS, but knowledge about the H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4796319029029e10fd14a07767d3d461
http://europepmc.org/abstract/med/25145936

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