Zobrazeno 1 - 10
of 607
pro vyhledávání: '"Adolescent onset"'
Autor:
Zhihua Liu, Dali Lv, Jianfeng Li, Fuwei Li, Yanhua Zhang, Yongjie Liu, Chao Gao, Yafeng Qiu, Jun Ma, Ruiling Zhang
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
BackgroundInflammation is associated with the pathophysiology of schizophrenia. The blood markers for systemic inflammation include neutrophil-lymphocyte ratio (NLR), systemic immune-inflammation index (SII), lymphocyte-monocyte ratio (LMR), system i
Externí odkaz:
https://doaj.org/article/774083ee5b4b484188f998a1ab9baf21
Akademický článek
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Autor:
Kun Zhang, Xingyue Jin, Yuqiong He, Shuxian Wu, Xilong Cui, Xueping Gao, Chunxiang Huang, Xuerong Luo
Publikováno v:
Frontiers in Psychiatry, Vol 14 (2023)
BackgroundFrontotemporal cortex dysfunction has been found to be associated with cognitive impairment in patients with schizophrenia (SCZ). In patients with adolescent-onset SCZ, a more serious type of SCZ with poorer functional outcome, cognitive im
Externí odkaz:
https://doaj.org/article/833c76d6f7b44161bc26d7c1e89fe7f4
Publikováno v:
Heliyon, Vol 8, Iss 10, Pp e10818- (2022)
Objectives: Cognitive insight (CI), the ability to perceive erroneous beliefs and correcting them based on safe experiences, is a common cognitive manifestation among schizophrenic individuals. Even though the functional morphology of the default mod
Externí odkaz:
https://doaj.org/article/b64e9a05d36944a6b2925808f4b14181
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Publikováno v:
BMC Psychiatry, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Objective Numerous studies have identified impaired decision making (DM) under both ambiguity and risk in adult patients with schizophrenia. However, the assessment of DM in patients with adolescent-onset schizophrenia (AOS) has been challen
Externí odkaz:
https://doaj.org/article/19af7a77de7c46ab85113806a5eeb66f
Autor:
Zhengxia Zhong, Xiaoyong Yan, Zhengying Fang, Yijun Dong, Jiaxing Tan, Jingyuan Xie, Linhong Hu, Shibin Zhang, Wei Qin
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Objective: Nephronophthisis (NPHP) is a rare autosomal recessive inherited kidney disease that can cause cystic enlargement of the kidneys, and lead to end-stage renal disease (ESRD) before the age of 30 years. Herein we describe a case of adolescent
Externí odkaz:
https://doaj.org/article/ef9c2fd6c5994026b70427257f8493a6
Autor:
Yamei Yang, Jie Liu, Kan Deng, Lin Lu, Huijuan Zhu, Xiaolan Lian, Xinjie Bao, Lian Duan, Yong Yao
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundThyrotropin-secreting adenoma (TSH-oma) is a very rare kind of functional pituitary adenoma, especially that which occurs in adolescents. However, its potential clinical and therapeutic characteristics are still unknown.ObjectivesThe study
Externí odkaz:
https://doaj.org/article/7660d03fabb64915bd86f43037fcdbb7
Autor:
Waldemar Brola, Barbara Steinborn, Marek Żak, Maria Mazurkiewicz-Bełdzińska, Sergiusz Jóźwiak, Piotr Sobolewski, Maciej Wilski, Małgorzata Bilska, Magdalena Siedlarska, Iwona Puzio-Bochen, Agnieszka Wencel-Warot, Małgorzata Lemka, Sławomir Kroczka, Elżbieta Czyżyk, Małgorzata Bocheńska, Ewa Emich-Widera, Jerzy Pietruszewski, Leszek Boćkowski, Katarzyna Kapica-Topczewska, Agata Czarnowska, Alina Kułakowska, Barbara Ujma-Czapska, Agata Gruna-Ożarowska, Łukasz Przysło, Katarzyna Połatyńska, Magdalena Dudzińska, Krystyna Mitosek-Szewczyk, Aleksandra Melnyk, Monika Adamczyk-Sowa, Katarzyna Kotulska
Publikováno v:
Journal of Clinical Medicine, Vol 11, Iss 24, p 7494 (2022)
Background. Paediatric-onset MS (POMS) has a unique clinical profile compared to the more prevalent adult-onset MS. For this study, we aimed to determine the demographic and clinical characteristics of POMS in Poland as well as addressing some of its
Externí odkaz:
https://doaj.org/article/8474abeda82d40aca3681abc891a57da
Autor:
Meghan Corrigan Nelson, Shanmuganathan Chandrakasan, Lori Ponder, Ignacio Sanz, Baruch Goldberg, Ekemini A. Ogbu, Kelly Rouster-Stevens, Sampath Prahalad
Publikováno v:
Children, Vol 9, Iss 12, p 1865 (2022)
Introduction: Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease that is associated with significant morbidity and mortality. SLE disproportionately affects women and minorities. Childhood-onset SLE (cSLE) in particular tends to b
Externí odkaz:
https://doaj.org/article/4d721eb6d6634957a74d2beb4ec50723