Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Teresa Żak"'
Autor:
Agnieszka Lecka-Ambroziak, Marta Wysocka-Mincewicz, Katarzyna Doleżal-Ołtarzewska, Agata Zygmunt-Górska, Teresa Żak, Anna Noczyńska, Dorota Birkholz-Walerzak, Renata Stawerska, Maciej Hilczer, Monika Obara-Moszyńska, Barbara Rabska-Pietrzak, Elżbieta Gołębiowska, Adam Dudek, Elżbieta Petriczko, Mieczysław Szalecki, on behalf of the Polish Coordination Group for rhGH Treatment
Publikováno v:
Diagnostics, Vol 11, Iss 5, p 798 (2021)
Genotype–phenotype correlation in patients with Prader–Willi syndrome (PWS) has still not been fully described. We retrospectively analysed data of 147 patients and compared groups according to genetic diagnosis: paternal deletion of chromosome 1
Externí odkaz:
https://doaj.org/article/1b4e6c7c88e8489294f0bdb9a0cb38d0
Autor:
Richard Pebody, Maria D Van Kerkhove, Mahmoud Hassan, Thierno Balde, Olivier Le Polain de Waroux, Sandra Adele, Kazuki Shimizu, Charlotte Christiane Hammer, Lisa Owen, Villyen Motaze, Michael Höhle, Piers Mook, Masaya Kato, Kathleen Ryan, Tanja Schmidt, Marjam Esmail, Jessica Lee Abbate, Opeayo Ogundiran, Sophie Maes, Victoria D Bélorgeot, Ana Riviere-Cinnamond, Martina McMenamin, Jessica Kolmer, Irena Djordjevic, Finlay Campbell, Henry Laurenson-Schafer, Basma Mostafa Abdelgawad, Amarnath Babu, Neale Batra, Hannah Brindle, Tshewang Dorji, Ingrid Hammermeister Nezu, Lucía Hernández-García, Friday Idoko, Sarah Karmin, Zyleen A Kassamali, Tamano Matsui, Mengjuan Duan, Boris I Pavlin, Tika Sedai, Teresa Zakaria, Abdi R Mahamud, Dominic Cocciolone, Christian Gapp, Kayla King, Aimee Latta, Sandra Lindmark, Ihor Perehinets, Amy Gimma, Jason McKnight, Margaux Mesle, Maarten Van Haverbeke, Tamar Amar, Ka Yeung Cheng, Silviu Ciobanu, Lauren E MacDonald, Jeff Pires, Jukka Pukkila, Celine Roman, Laila Skrowny, Ara Tadevosyan, Catherine Smallwood, Juniorcaius Ikejezie, Blanche Johanna Greene-Cramer, Adedoyin Abiola Awofisayo-Okuyelu, Bernadette Mirembe, Tondri Noe Guinko, Homa Attar-Cohen, Stephen Leshan Koyie, Samuel Mesfin, Veronica Cristea, Nikola Sklenovska, Mostafa Mahran, Emily Meyer, Grace Brough, Harsh Lata, Alessandro Miglietta, Sydel Parikh, Eri Togami, Yurie Izawa, Aura Rocio Escobar Corado Waeber, Anahi Rico Chinchilla, Yeo Won Jin, Raquel Medialdea Carrera, Amaia Artazcoz Glaria, Hyo Jeong Kim, Muhammed Tayyab
Publikováno v:
BMJ Global Health, Vol 8, Iss 7 (2023)
Background Globally, since 1 January 2020 and as of 24 January 2023, there have been over 664 million cases of COVID-19 and over 6.7 million deaths reported to WHO. WHO developed an evidence-based alert system, assessing public health risk on a weekl
Externí odkaz:
https://doaj.org/article/71885beb338f4dc781555f0fc9ee1d3b
Publikováno v:
Pediatria Polska. 86:664-666
The described patient since the infancy period presented macrosomy: body high and weight over the 97 percentile, thickened face features, macroglossia, big hands and feet. Additionally, defect of the posture and deformed knees were observed. At 5 yea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::05d57ed17ca3e1e3b21dcd64f93f3784
https://doi.org/10.1016/s0031-3939(11)70586-8
https://doi.org/10.1016/s0031-3939(11)70586-8
Autor:
Anna Noczyńska, Teresa Żak, Joanna Bladowska, Leszek Noga, Anna Zimny, Anna Zacharzewska-Gondek, Paweł Szewczyk, Tomasz Maciej Gondek, Marek Sąsiadek
Publikováno v:
Braindevelopment. 36(9)
The pathogenesis of idiopathic growth hormone deficiency (GHD) in children, including possible cerebral metabolic alterations, remains unclear. The aim of the study was to evaluate metabolic changes within the normal appearing brain in children with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ffba2a35f88a6526b48cbc873ad4054
https://pubmed.ncbi.nlm.nih.gov/24360094
https://pubmed.ncbi.nlm.nih.gov/24360094