Zobrazeno 1 - 10
of 303
pro vyhledávání: '"J. E k"'
Publikováno v:
Kidney International Reports, Vol 6, Iss 4, Pp S167-S168 (2021)
Externí odkaz:
https://doaj.org/article/267d23997f5f4a3f9b178e063cb76468
Akademický článek
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Autor:
A Luojus, M Lehto, O Halminen, J Haukka, A L Aro, J Putaala, M Linna, P Mustonen, J Kinnunen, M Niemi, J Hartikainen, J E K Airaksinen
Publikováno v:
Europace. 25
Funding Acknowledgements Type of funding sources: Public hospital(s). Main funding source(s): Helsinki and Uusimaa Hospital District (TYH2019309) and The Finnish Foundation for Cardiovascular Research Background and aims Elderly patients with atrial
Autor:
null J. E. K., null E. U.
Publikováno v:
Pollution and Policy ISBN: 9780520329829
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60b5f2c7dbc264d69dc2e40d90b53cbf
https://doi.org/10.2307/jj.2430492.3
https://doi.org/10.2307/jj.2430492.3
Publikováno v:
Scholedge International Journal of Multidisciplinary & Allied Studies. 2020, Vol. 7 Issue 1, p45-73. 29p.
Publikováno v:
Scholedge International Journal of Multidisciplinary & Allied Studies. 2019, Vol. 6 Issue 12, p137-155. 19p.
Autor:
Secada, J. E. K.
Publikováno v:
The Philosophical Review, 1990 Jan 01. 99(1), 45-72.
Externí odkaz:
https://www.jstor.org/stable/2185203
Publikováno v:
African Arts, 1970 Apr 01. 3(3), 36-80.
Externí odkaz:
https://www.jstor.org/stable/3334494
Autor:
J. E. K. Aroh
Publikováno v:
Sustainable Intensification for Agroecosystem Services and Management ISBN: 9789811632068
Mangrove forests are globally distributed, including Nigeria with the third largest mangrove area in the world. Mangroves perform diverse ecological and productive functions wherever they exist. They are considered to be the most efficient ecosystem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2d74b8e206deb128a8eede729c31163a
https://doi.org/10.1007/978-981-16-3207-5_16
https://doi.org/10.1007/978-981-16-3207-5_16
Autor:
Ivanovski I., Djuric O., Broccoli S., Caraffi S. G., Accorsi P., Adam M. P., Avela K., Badura-Stronka M., Bayat A., Clayton-Smith J., Cocco I., Cordelli D. M., Cuturilo G., Di Pisa V., Dupont Garcia J., Gastaldi R., Giordano L., Guala A., Hoei-Hansen C., Inaba M., Iodice A., Nielsen J. E. K., Kuburovic V., Lazalde-Medina B., Malbora B., Mizuno S., Moldovan O., Moller R. S., Muschke P., Otelli V., Pantaleoni C., Piscopo C., Poch-Olive M. L., Prpic I., Marin Reina P., Raviglione F., Ricci E., Scarano E., Simonte G., Smigiel R., Tanteles G., Tarani L., Trimouille A., Valera E. T., Schrier Vergano S., Writzl K., Callewaert B., Savasta S., Street M. E., Iughetti L., Bernasconi S., Giorgi Rossi P., Garavelli L.
Publikováno v:
Ivanovski, I, Djuric, O, Broccoli, S, Caraffi, S G, Accorsi, P, Adam, M P, Avela, K, Badura-Stronka, M, Bayat, A, Clayton-Smith, J, Cocco, I, Cordelli, D M, Cuturilo, G, Di Pisa, V, Dupont Garcia, J, Gastaldi, R, Giordano, L, Guala, A, Hoei-Hansen, C, Inaba, M, Iodice, A, Nielsen, J E K, Kuburovic, V, Lazalde-Medina, B, Malbora, B, Mizuno, S, Moldovan, O, Møller, R S, Muschke, P, Otelli, V, Pantaleoni, C, Piscopo, C, Poch-Olive, M L, Prpic, I, Marín Reina, P, Raviglione, F, Ricci, E, Scarano, E, Simonte, G, Smigiel, R, Tanteles, G, Tarani, L, Trimouille, A, Valera, E T, Schrier Vergano, S, Writzl, K, Callewaert, B, Savasta, S, Street, M E, Iughetti, L, Bernasconi, S, Giorgi Rossi, P & Garavelli, L 2020, ' Mowat-Wilson syndrome : growth charts ', Orphanet Journal of Rare Diseases, vol. 15, 151 . https://doi.org/10.1186/s13023-020-01418-4
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Orphanet Journal of Rare Diseases
ORPHANET JOURNAL OF RARE DISEASES
Volume 15
Issue 1
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-12 (2020)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Orphanet Journal of Rare Diseases
ORPHANET JOURNAL OF RARE DISEASES
Volume 15
Issue 1
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Background: Mowat–Wilson syndrome (MWS; OMIM #235730) is a genetic condition caused by heterozygous mutations or deletions of the ZEB2 gene. It is characterized by moderate-severe intellectual disability, epilepsy, Hirschsprung disease and multiple
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36eb6ffaf0310403b7e7418f5c8baafa
https://curis.ku.dk/portal/da/publications/mowatwilson-syndrome(958dfaa0-b4f4-4afb-bc1b-f587e943a8f5).html
https://curis.ku.dk/portal/da/publications/mowatwilson-syndrome(958dfaa0-b4f4-4afb-bc1b-f587e943a8f5).html