Zobrazeno 1 - 10
of 2 534
pro vyhledávání: '"Late diagnosis"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)
Abstract This study investigated the association between serum albumin concentration and 12-weeks mortality of HIV/AIDS with late diagnosis in China. This retrospective cohort study included, 1079 inpatients diagnosis with late HIV/AIDS between Janua
Externí odkaz:
https://doaj.org/article/94eaed0104bb4c5aa7669d1f40576dc3
Autor:
Pušica Irena Lj, Lapčević Mirjana R., Ratković Stojanka N., Manić Marina N., Arapović Mirjana D.
Publikováno v:
Opšta Medicina, Vol 30, Iss 1-2, Pp 29-40 (2024)
Introduction. Early diagnosis and treatment improve clinical outcomes, especially in chronic arthritis (CA) and systemic connective tissue disorders (SCTD). Thanks to clinical research from the 1990s on and innovative drugs, 55 million life-years hav
Externí odkaz:
https://doaj.org/article/67266acc7bd5466eb6332c65499a9ae3
Autor:
Valdemir Kim, Gulnur Zhakhina, Arnur Gusmanov, Yesbolat Sakko, Mariyam Kim, Meruyert Madikenova, Zhannat Kuanshaliyeva, Alpamys Issanov, Ainur Assan, Marina Khvan, Altay Nabiyev, Sholpan Altynova, Abduzhappar Gaipov
Publikováno v:
Renal Failure, Vol 46, Iss 2 (2024)
Chronic kidney disease (CKD) presents a significant global health challenge, often progressing to end-stage renal disease (ESRD) necessitating renal replacement therapy (RRT). Late referral (LR) to nephrologists before RRT initiation is linked with a
Externí odkaz:
https://doaj.org/article/55c744ce77ff484c9513d4d84ba959d2
Autor:
Irene Garcia-Molina
Publikováno v:
Frontiers in Psychology, Vol 15 (2024)
Family and friends may play an important role both in the identification and diagnosis of any condition, as well as in the provision of support afterwards. However, when the diagnosis is autism and it arrives late, as is often the case with autistic
Externí odkaz:
https://doaj.org/article/0be574bd51a542e28cb0ec81819324a6
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Congenital adrenal hyperplasia (CAH) and Williams Syndrome (WS; MIM # 194050) are distinct genetic conditions characterized by unique clinical features. 21-Hydroxylase deficiency (21-OHD; MIM #201910), the most common form of CAH, arises from mutatio
Externí odkaz:
https://doaj.org/article/06ece388f0a3487a960289fa5cd75253
Autor:
Valerian Mwenda, Martin Mwangi, Gladwell Gathecha, Joseph Kibachio, Robert Too, Zeinab Gura, Marleen Temmerman
Publikováno v:
Gynecologic Oncology Reports, Vol 52, Iss , Pp 101355- (2024)
Background: Cervical cancer is the leading cause of cancer mortality among women in Kenya. Two thirds of cervical cancer cases in Kenya are diagnosed in advanced stages. We aimed to identify factors associated with late diagnosis of cervical cancer,
Externí odkaz:
https://doaj.org/article/ccec188d2ee74c4ea45dd5ef4cf08fa9
Publikováno v:
Shanghai yufang yixue, Vol 35, Iss 12, Pp 1187-1191 (2023)
ObjectiveTo investigate the late diagnosis of HIV infection and associated factors in Jiading District between 1998 and 2022, and to provide the information for the development of AIDS prevention and control strategy.MethodsInformation of newly rep
Externí odkaz:
https://doaj.org/article/4c832c47622d4b328d9ccfab82592fbd
Autor:
Alejandro G. García-Ruiz de Morales, María Jesús Vivancos, Jorge Lázaro, Beatriz Romero Hernández, Beatriz Mateos, Pilar Pérez-Elías, Margarita Herrero Delgado, Laura Villanova Cuadra, Santiago Moreno, Javier Martínez-Sanz, María Jesús Pérez-Elías
Publikováno v:
Biomedicines, Vol 12, Iss 8, p 1846 (2024)
Despite remarkable improvement in the human immunodeficiency virus (HIV) and hepatitis C virus (HCV) care continuum, the rate of late diagnosis of HIV and HCV in high-income countries remains unacceptably high. Testing relies mainly on primary care p
Externí odkaz:
https://doaj.org/article/bd96d538550841f99b0ad787b3d3de48
Autor:
Dulce Quelhas, Sandra D.K. Kingma, An I. Jonckheere, Claudia S. Smeets-Peels, Daniel Costa Gomes, José Duro, Anabela Oliveira, Gert Matthijs, Laura K.M. Steinbusch, Jaak Jaeken, Isabel Rivera, Estela Rubio-Gozalbo
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 38, Iss , Pp 101057- (2024)
The authors report the natural history of three patients with late-diagnosed Classic Galactosemia (CG) (at 16, 19 and 28 years). This was due to a combination of factors: absence of neonatal screening, absence of some typical acute neonatal symptoms,
Externí odkaz:
https://doaj.org/article/6931300d149b424894c7347156a86442
Publikováno v:
International Journal of General Medicine, Vol Volume 16, Pp 4227-4234 (2023)
Aslıhan Candevir,1 Ferit Kuscu,1 Behice Kurtaran,1 Süheyla Kömür,1 Ayşe Seza İnal,1 Damla Ertürk,2 Yeşim Taşova1 1Infectious Diseases, Çukurova University, Adana, Türkiye; 2Infectious Diseases, Health Sciences U
Externí odkaz:
https://doaj.org/article/ec5a063a09d342fb9f5f853d0f1a386e