Zobrazeno 1 - 10
of 153
pro vyhledávání: '"Petrò E"'
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/10e92c9dbd7d41deadaab76204795532
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
IntroductionThere is a dearth of knowledge in South Africa about the incidence, prevalence, and effect of autism spectrum disorder (ASD). Consequently, national autism data is outdated, and World Health Organization (WHO) prevalence rates are being u
Externí odkaz:
https://doaj.org/article/e02307f77df74874beb4a516ba29daa0
Publikováno v:
African Journal of Career Development, Vol 6, Iss 1, Pp e1-e11 (2024)
Background: Academic performance has been perceived as an element, which can change the lives of youth, while emotional intelligence (EI) often relates to adolescents’ well-being and, in turn, can influence academic performance. Emotional intellige
Externí odkaz:
https://doaj.org/article/a2299283ac7e4233871bd03c3dd91573
Publikováno v:
African Journal of Psychological Assessment, Vol 6, Iss 0, Pp e1-e14 (2024)
This qualitative research study emerged from the essential need for reliable and valid intelligence test instruments for South African school learners, who are characterised as a diverse population with their variety in culture, ethnicity, and langua
Externí odkaz:
https://doaj.org/article/a369dec6a00046b0b0b85b64c61de01c
Autor:
Marine Delamare, Amandine Le Roy, Mathilde Pacault, Loïc Schmitt, Céline Garrec, Nada Maaziz, Matti Myllykoski, Antoine Rimbert, Valéna Karaghiannis, Bernard Aral, Mark Catherwood, Fabrice Airaud, Lamisse Mansour-Hendili, David Hoogewijs, Edoardo Peroni, Salam Idriss, Valentine Lesieur, Amandine Caillaud, Karim Si-Tayeb, Caroline Chariau, Anne Gaignerie, Minke Rab, Torsten Haferlach, Manja Meggendorfer, Stéphane Bézieau, Andrea Benetti, Nicole Casadevall, Pierre Hirsch, Christian Rose, Mathieu Wemeau, Frédéric Galacteros, Bruno Cassinat, Beatriz Bellosillo, Celeste Bento, Richard van Wijk, Petro E. Petrides, Maria Luigia Randi, Mary Frances McMullin, Peppi Koivunen, François Girodon, Betty Gardie, ECYT consortium
Publikováno v:
Haematologica, Vol 108, Iss 11 (2023)
Hereditary erythrocytosis is a rare hematologic disorder characterized by an excess of red blood cell production. Here we describe a European collaborative study involving a collection of 2,160 patients with erythrocytosis sequenced in ten different
Externí odkaz:
https://doaj.org/article/3f9446a9e07d45d496f7af7a30c39bce
Autor:
Petro E. Petrides
Publikováno v:
Diagnostics, Vol 12, Iss 7, p 1618 (2022)
Heme, iron protoporphyrin IX, is one of life’s most central molecules. Hence, availability of the enzymatic machinery necessary for its synthesis is crucial for every cell. Consequently, inborn errors of porphyrin metabolism that compromise normal
Externí odkaz:
https://doaj.org/article/c416a319ebff45a7abcedbfa4ab7497a
Publikováno v:
Proteomes, Vol 7, Iss 2, p 20 (2019)
Extracellular vesicles (EVs), e.g., exosomes and microvesicles, are one of the main networks of intercellular communication. In myeloproliferative neoplasms, such as polycythemia vera (PV), excess of EVs originating from overabundant blood cells can
Externí odkaz:
https://doaj.org/article/f30d54762e714fee8004e426c4fd6024
Autor:
Petro E. Mabeyo, Mkabwa L. K. Manoko, Amra Gruhonjic, Paul A. Fitzpatrick, Göran Landberg, Máté Erdélyi, Stephen S. Nyandoro
Publikováno v:
International Journal of Food Science, Vol 2015 (2015)
Selenium deficiency in humans has been associated with various diseases, the risks of which can be reduced through dietary supplementation. Selenium accumulating plants may provide a beneficial nutrient for avoiding such illnesses. Thus, leafy vegeta
Externí odkaz:
https://doaj.org/article/6d261280ab7c4111aa7613d844d2be43
Publikováno v:
Haematologica, Vol 95, Iss 7 (2010)
Externí odkaz:
https://doaj.org/article/d0f364ed6cd942d3bb477c27abd6d9a4
Autor:
Vytautas Ivaskevicius, Arijit Biswas, Carville Bevans, Verena Schroeder, Hans Peter Kohler, Hannelore Rott, Susan Halimeh, Petro E. Petrides, Harald Lenk, Manuele Krause, Bruno Miterski, Ursula Harbrecht, Johannes Oldenburg
Publikováno v:
Haematologica, Vol 95, Iss 6 (2010)
Background Severe hereditary coagulation factor XIII deficiency is a rare homozygous bleeding disorder affecting one person in every two million individuals. In contrast, heterozygous factor XIII deficiency is more common, but usually not associated
Externí odkaz:
https://doaj.org/article/6e5b12b4e8814299832a7d0527145f99