Zobrazeno 1 - 10
of 390
pro vyhledávání: '"homocysteinemia"'
Autor:
Wenting Shi, Jing Zhang, Wairong Zhao, Meiyan Yue, Jie Ma, Silu Zeng, Jingyi Tang, Yu Wang, Zhongyan Zhou
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2301 (2024)
Background/Objectives: Homocysteine (Hcy) and iron are factors co-related with the progression of cardiovascular diseases. The vascular endothelium is an important barrier for physiological homeostasis, and its impairment initiates cardiovascular inj
Externí odkaz:
https://doaj.org/article/961adf6e0dc8450f9af3bbc95bff9b54
Autor:
Qian Zhang, Peilin Cong, Li Tian, Tingmei Wu, Xinwei Huang, Yuxin Zhang, Huanghui Wu, Huazheng Liang, Lize Xiong
Publikováno v:
Brain Research Bulletin, Vol 209, Iss , Pp 110913- (2024)
The perioperative neurocognitive disorder (PND) is a severe complication that affects millions of surgical patients each year. Homocysteine (Hcy) is known to increase the risk of developing PND in both young and elderly mice. However, whether Hcy alo
Externí odkaz:
https://doaj.org/article/0ab910918d264193885f36f7e169e78b
Autor:
Deepak Sharma, Jay Tewari, Shubhajeet Roy, Paras Sisodia, Anadika Rana, Virendra Atam, Md Al Hasibuzzaman
Publikováno v:
Clinical Case Reports, Vol 12, Iss 3, Pp n/a-n/a (2024)
Key Clinical Message Cerebral Venous Sinus Thrombosis (CVST) is a subtype of venous thromboembolism, which occurs in the dural venous sinuses. Blockage of the venous drainage of the brain leads to the development of hemorrhages. Strokes can hence dev
Externí odkaz:
https://doaj.org/article/2525dd152d194ec68a9867a9fb4fb198
Akademický článek
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Autor:
Yu-Peng Liu, Ru-Xuan He, Zhe-Hui Chen, Lu-Lu Kang, Jin-Qing Song, Yi Liu, Chun-Yan Shi, Jun-Ya Chen, Hui Dong, Yao Zhang, Meng-Qiu Li, Ying Jin, Jiong Qin, Yan-Ling Yang
Publikováno v:
Frontiers in Nutrition, Vol 10 (2023)
BackgroundThe most common disorder of the intracellular cobalamin metabolism pathway is the combined methylmalonic acidemia and homocysteinemia, cblC type (cblC). There is a variation in its clinical spectrum ranging from severe neonatal-onset forms
Externí odkaz:
https://doaj.org/article/5a32ad0b2ce74b7fb1f2cdb5bd154301
Akademický článek
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Akademický článek
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Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Methylmalonic acidemia is a severe heterogeneous disorder of methylmalonate and cobalamin (Cbl; vitamin B12) metabolism with poor prognosis. Around 90% of reported patients with methylmalonic acidemia (MMA) are severe infantile early onset, while cas
Externí odkaz:
https://doaj.org/article/b701a7d7f2d84280a6f9b153468485a8
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Methylmalonic acidemia is a rare autosomal recessive metabolic disease. However, because of the atypical clinical symptoms, the type of late-onset methylmalonic academia is often misdiagnosed. Especially when the blood vitamin B12 and folic acid leve
Externí odkaz:
https://doaj.org/article/18205927c38e4a438eb4f0df686466a7
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Methylmalonic acidemia (MMA) can display many clinical manifestations, among which acute lymphoblastic leukemia (ALL) has not been reported, and congenital heart disease (CHD) is also rare.Case presentation: We report an MMA case with ALL
Externí odkaz:
https://doaj.org/article/8f6f7a3209ff4045a1f16b91b9a9ec95