Zobrazeno 1 - 10
of 191
pro vyhledávání: '"Agaath Been"'
Autor:
Marieke J. H. Begemann, Ilse A. Thompson, Wim Veling, Shiral S. Gangadin, Chris N. W. Geraets, Erna van ‘t Hag, Sanne J. Müller-Kuperus, Priscilla P. Oomen, Alban E. Voppel, Mark van der Gaag, Martijn J. Kikkert, Jim Van Os, H. Filip E. Smit, Rikus H. Knegtering, Sybren Wiersma, Luyken H. Stouten, Harm J. Gijsman, Lex Wunderink, Anton B. P. Staring, Selene R. T. Veerman, Amrita G. S. Mahabir, Jörg Kurkamp, Gerdina H. M. Pijnenborg, Natalie D. Veen, Machteld Marcelis, Koen P. Grootens, Gunnar Faber, Nico J. van Beveren, Agaath Been, Truus van den Brink, Maarten Bak, Therese A. M. J. van Amelsvoort, Andrea Ruissen, Christine Blanke, Karin Groen, Lieuwe de Haan, Iris E. C. Sommer
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-19 (2020)
Abstract Background Antipsychotic medication is effective for symptomatic treatment in schizophrenia-spectrum disorders. After symptom remission, continuation of antipsychotic treatment is associated with lower relapse rates and lower symptom severit
Externí odkaz:
https://doaj.org/article/9656afbed63342b7995e44fd4b046096
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Advanced Pharmaceutical Bulletin, Vol 12, Iss 4, Pp 649-657 (2022)
Purpose: Cancer is the leading challenge to human health since the dawn of early Egyptianmanuscripts, where they found tumour from fossils in the modernized 20th century. Increasingrate of incidence and death from cancer in the past few years is thou
Externí odkaz:
https://doaj.org/article/0ace810089564110b3419c076cdaf588
Publikováno v:
Clinical Case Reports, Vol 9, Iss 8, Pp n/a-n/a (2021)
Abstract Raynaud's phenomenon is a rare side effect of CGRP monoclonal antibodies. These molecular treatments are a relatively new class of drugs for the prevention of migraine. It is likely that we will see this side effect more often in the future.
Externí odkaz:
https://doaj.org/article/d012f358859e4983a7badeb37478a275
Publikováno v:
Neurology India. Jul/Aug2021, Vol. 69 Issue 4, p808-816. 9p.
Autor:
Martin de Jonge, Albert Batalla, Gerdina H. M. Pijnenborg, Jim van Os, Iris E. C. Sommer, Elske Willemse, Sybren Wiersma, Therese van Amelsvoort, Truus van den Brink, Marieke J. H. Begemann, Joran Lokkerbol, Shiral S. Gangadin, Maarten Bak, Sinan Guloksuz, Amrita G.S. Mahabir, P. Roberto Bakker, Martijn J. Kikkert, G. Faber, Nynke Boonstra, Marinte van den Bosch, Koen P. Grootens, Agaath Been, Franciska de Beer, Yudith R A Haveman, Wim Veling, Bodyl A Brand, Jörg Kurkamp, Sanne Koops, Filip Smit, Tonnie Staring, Nico J.M. van Beveren, Erna van ‘t Hag, Machteld Marcelis, Chris N W Geraets, A E Voppel, Natalie D. Veen, Inge van der Heijden, Selene R. T. Veerman, Priscilla P. Oomen, Lieuwe de Haan, Rikus Knegtering, Ellen Graveland, Bram-Sieben Rosema, Joelle Hoornaar
Publikováno v:
Psychological Medicine, 53(6), 2317-2327. Cambridge University Press
BackgroundCognitive deficits may be characteristic for only a subgroup of first-episode psychosis (FEP) and the link with clinical and functional outcomes is less profound than previously thought. This study aimed to identify cognitive subgroups in a
Autor:
Kathelijne van Dongen, Katinka van Dongen, Hans Bom, Agaath Koudstaal, Robert Vermeiren, Anne Krabbendam
Publikováno v:
Kind & Adolescent Praktijk. 22:6-12
Publikováno v:
Indian Journal of Ophthalmology, Vol 65, Iss 11, Pp 1087-1092 (2017)
Leber's hereditary optic neuropathy (LHON) is a common inherited mitochondrial disorder that is characterized by the degeneration of the optic nerves, leading to vision loss. The major mutations in the mitochondrial genes ND1, ND4, and ND6 of LHON su
Externí odkaz:
https://doaj.org/article/e447613fe2534bb8b75fcd24b501255e
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Manickam, Agaath Hedina1 hedina03@gmail.com, Buture, Alina2, Tomkins, Esther3, Ruttledge, Martin3
Publikováno v:
Clinical Case Reports. Aug2021, Vol. 9 Issue 8, p1-4. 4p.