Zobrazeno 1 - 10
of 2 444
pro vyhledávání: '"Peterlin, P."'
Publikováno v:
Zdravniški Vestnik, Vol 93, Iss 7-8, Pp 236-244 (2024)
Izhodišča: Bolezenska stanja novorojenčkov pogosto motijo fiziološke procese, ki uravnavajo tekočinsko ravnovesje. Zato je ocena tekočinskega stanja pri bolnih novorojenčkih pomembna. V klinični praksi si pomagamo z vrednotenjem kliničnih zn
Externí odkaz:
https://doaj.org/article/43cfe68b1d9a4023b6f766079b2b761f
Autor:
Lenko, Helena, Peterlin, Primož
Publikováno v:
J Radioth Pract 17(2018): 104-113
Aim: To examine and quantify set-up errors in patient positioning in head-and-neck radiotherapy and to investigate the impact of the choice of reference isocentre -- on the patient neck or patient skull -- on the magnitude of set-up errors. Materials
Externí odkaz:
http://arxiv.org/abs/2302.13801
Autor:
Pierre Peterlin, Joëlle Gaschet, Pascal Turlure, Marie-Pierre Gourin, Pierre-Yves Dumas, Sylvain Thepot, Ana Berceanu, Sophie Park, Marie-Anne Hospital, Thomas Cluzeau, Jose-Miguel Torregrosa-Diaz, Louis Drevon, Rosa Sapena, Fatiha Chermat, Lionel Ades, Sophie Dimicoli-Salazar, Maxime Jullien, Pierre Fenaux, Patrice Chevallier.
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Not available.
Externí odkaz:
https://doaj.org/article/fdb35f6dc1a84d53a039d44847a7287b
Autor:
Volk M, Writzl K, Veble A, Jaklič H, Teran N, Prosenc B, Štimpfel M, Virant Klun I, Vrtačnik Bokal E, Ban Frangež H, Peterlin B
Publikováno v:
Balkan Journal of Medical Genetics, Vol 26, Iss 2, Pp 5-10 (2024)
Preimplantation genetic testing (PGT) is the earliest form of prenatal diagnosis that has become an established procedure for couples at risk of passing a severe genetic disease to their offspring. At UMC Ljubljana, we conducted a retrospective regis
Externí odkaz:
https://doaj.org/article/6c96e592e7ff4b3d998ebf6d0eaa66d8
Autor:
Ana Peterlin, Sara Bertok, Karin Writzl, Luca Lovrečić, Aleš Maver, Borut Peterlin, Maruša Debeljak, Gregor Nosan
Publikováno v:
Life, Vol 14, Iss 9, p 1118 (2024)
Congenital heart disease (CHD) is the most commonly detected congenital anomaly and affects up to 1% of all live-born neonates. Current guidelines support the use of chromosomal microarray analysis (CMA) and next-generation sequencing (NGS) as diagno
Externí odkaz:
https://doaj.org/article/c8de490009d64f8a8114c8222891020a
Autor:
Valentin Letailleur, Amandine Le Bourgeois, Thierry Guillaume, Alice Garnier, Pierre Peterlin, Maxime Jullien, Chloe Antier, Marie-Christine Béné, Patrice Chevallier
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 20, Iss 1 (2024)
The impact of pre-graft COVID-19 vaccinations in donor or recipient as well as pre-graft infection has been studied in 157 adults having received allogeneic stem cell transplantation (Allo-SCT) for various hematological diseases during the delta/omic
Externí odkaz:
https://doaj.org/article/7a0e67596beb4c6ea0bc7e8047040371
Akademický článek
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Autor:
Prelog Tomaz, Bucek Simon, Brozic Andreja, Peterlin Jakob, Kavcic Marko, Omerzel Masa, Markelc Bostjan, Jesenko Tanja, Prevodnik Veronika Kloboves
Publikováno v:
Radiology and Oncology, Vol 58, Iss 1, Pp 133-144 (2024)
Flow cytometry plays is important in the diagnosis of acute lymphoblastic leukaemia (ALL) and when antigen-specific immunotherapy is indicated. We have investigated the effects of prednisolone, vincristine, daunorubicin, asparaginase and methotrexate
Externí odkaz:
https://doaj.org/article/dc828b633786449ba8c30cc50bdb358a
Publikováno v:
Clinical and Translational Radiation Oncology, Vol 46, Iss , Pp 100751- (2024)
Background and purpose: Radiation-induced damage to the hippocampi can cause cognitive decline. International recommendations for nasopharyngeal cancer (NPC) radiotherapy (RT) lack specific guidelines for protecting the hippocampi. Our study evaluate
Externí odkaz:
https://doaj.org/article/1c28487be36042d299c4f14561eb35ff
Autor:
Pierre Peterlin, Julia Bonnelye, Alice Garnier, Amandine Le Bourgeois, Thierry Guillaume, Maxime Jullien, Hervé Dutartre, Marie Le Moigne, Caroline Schmitt, Laurent Gouya, Antoine Poli, Sebastien Barbarot, Patrice Chevallier
Publikováno v:
Skin Health and Disease, Vol 4, Iss 2, Pp n/a-n/a (2024)
Abstract Congenital erythropoietic porphyria (CEP), or Gunther disease, is a rare genetic disease responsible for severe dermatologic, hepatic and/or haematological damages related to the deficient activity of the uroporphyrinogen III synthase. Allog
Externí odkaz:
https://doaj.org/article/ac9c6284044848508d9dfc030f859de4