Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Songyun Zhang"'
Autor:
Yuanxiang Hu, Qing Teng, Jiahong Wu, Liyan Ma, Songyun Zhang, Weihao Li, Renjie Bi, Xinyang Wang, Ninglin Kang, Guiling Mo
Publikováno v:
Clinical Genetics. 101:116-121
A partial deficiency of the heme biosynthetic enzyme hydroxymethylbilane synthase (HMBS) leads to acute intermittent porphyria (AIP), a severe neurovisceral, autosomal dominant disorder with low penetrance. Even though in-depth investigations of the
Publikováno v:
Intractable Rare Dis Res
Acute intermittent porphyria (AIP) is a dominant inherited disorder with a low penetrance that is caused by mutations in the gene coding for hydroxymethylbilane synthase (HMBS). Information about the epidemiology and molecular genetic features of thi
Publikováno v:
Intractable Rare Dis Res
A very rare case of acute intermittent porphyria (AIP) co-existing Turner syndrome (TS) is reported for the first time. A 32-year-old woman was diagnosed with AIP due to recurrent acute abdominal pain, red urine and pathogenic mutation of Hydroxymeth
Publikováno v:
Neurological Research. 41:1024-1033
Objective: Diabetes-associated cognitive deficits is characterized by long-term potentiation (LTP) decline in the hippocampus. DL-3-n-butylphthalide (NBP) is a novel agent exerting protective effect against ischemic brain. However, the effects of NBP
Autor:
Ningzhen Ma, Yiran Zhang, Lanlan Zhao, Xiaoning Zhang, Xiantao Liu, Xinyang Wang, Songyun Zhang
Publikováno v:
Intractable Rare Dis Res
Acute intermittent porphyria (AIP) is an autosomal dominant disease caused by mutations in porphobilinogen deaminase (PBGD), the third enzyme of the heme synthesis pathway. Symptoms of AIP usually manifest as intermittent acute attacks with occasiona
Publikováno v:
Intractable Rare Dis Res
Acute intermittent porphyria (AIP) is a rare inherited metabolic disease associated with heme metabolism. Primary Sjogren's syndrome (PSS) is a common autoimmune disease. The combined presence of AIP and PSS complicates treatment. A rare case of conc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ddbeaa0d88aa945e816d0e9c9df1664
https://europepmc.org/articles/PMC7441034/
https://europepmc.org/articles/PMC7441034/
Publikováno v:
Metabolic brain disease. 34(1)
Numerous epidemiological studies have shown that diabetes mellitus (DM) is associated with dementia and cognition decline. However, there is currently no effective treatment for diabetes-induced cognitive dysfunction. The neuroprotective effect of L-
Publikováno v:
Behavioural Neurology, Vol 2018 (2018)
Behavioural Neurology
Behavioural Neurology
Background. With the change in lifestyle and the aging population, the incidence of cognitive dysfunction in diabetes mellitus is rising sharply. Oxidative stress is an important mechanism in the development of diabetic cognitive dysfunction. Nuclear
Publikováno v:
Cell Biochemistry and Biophysics. 71:315-322
Diabetes mellitus is associated with rapid cognitive decline. Currently, there is no effective treatment for cognitive dysfunction induced by diabetes. L-3-n-Butylphthalide (L-NBP) is a nerve protective drug extracted from seeds of celery, which has
Publikováno v:
SpringerPlus
Objectives This study aimed to investigate the alteration of Neuropeptide Y (NPY) in the hypothalamus and its correlation with insulin, leptin and ghrelin during the development of a rat model of type 2 diabetes mellitus. Methods The type 2 diabetes