Results 151 to 160 of about 181,370 (308)
Chao Chen,1,* Yan Tian,2,* Fengshun Jia,1,* Mingkun Feng,1 Guoqiang Zhang,2 Qian Li,2 Yanwei Zhang,3 Ningling Sun,4 Songnian Hu,5,6 Zheng Ji1 1Department of Cardiology, Tangshan Gongren Hospital, Tangshan, Hebei, People’s Republic of China ...
Chen C +9 more
doaj
An 8-week experiment was carried out to investigate the effects of light intensity on growth, survival and skin color of Chinese longsnout catfish juveniles.
Xie, SQ, Chinese Acad Sci, State Key Lab Freshwater Ecol & Biotechnol, Inst Hydrobiol, Wuhan 430072, Peoples R China +5 more
core
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source
Low anxiety disorder comorbidity rate in bipolar disorders in Han Chinese in Taiwan.
[[abstract]]OBJECTIVES: Studies report high comorbidity of lifetime anxiety disorders with bipolar disorders in Western patients, but it is unclear in Taiwan.
Yun-Hsuan Chang;Shiou-Lan Chen;Shih-Heng Chen;Chun-Hsieh Chu;Sheng-Yu Lee;Hsin-Fen Yang;Nian-Sheng Tzeng;I Hui Lee;Po See Chen;Tzung Lieh Yeh;San-Yuan Huangf, Kuei-Ru Chou;Yen Kuang Yang;Hui-Chen Ko;Ru-Band Lu;Jules Angst
core
ABSTRACT Objective Considerable efforts have been dedicated to developing effective treatments for post‐stroke executive impairment (PSEI), among which repetitive transcranial magnetic stimulation (rTMS) has shown great potential. This study aimed to investigate the therapeutic effects of high‐frequency rTMS on working memory (WM) and response ...
Mengting Lao +6 more
wiley +1 more source
RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu +21 more
wiley +1 more source
The Genetic Progress of Psoriasis in the Han Chinese Population [PDF]
Gao, Jinping +2 more
openaire +2 more sources
ABSTRACT Objective High‐resolution MRI enables detailed assessment of intracranial vessel wall pathology in moyamoya vasculopathy. We aimed to classify adult moyamoya vasculopathy etiologies using high‐resolution MRI and to examine subtype‐specific associations between high‐resolution MRI features and ischemic infarction.
Guangsong Han +8 more
wiley +1 more source
Choroid Plexus Enlargement and USPIO‐Based Inflammatory Feature in Cerebral Small Vessel Disease
ABSTRACT Objective The choroid plexus (CP) is a key component of the blood–cerebrospinal fluid barrier (BCSFB), but its mechanism of action in cerebral small vessel disease (CSVD) remains unclear. This study investigated CP volume (CPV) alterations and their association with conventional imaging markers in CSVD and explored the underlying role of ...
Yongqiang Qu +11 more
wiley +1 more source
The Sleep Quality of Han Chinese and Tibetan Firefighters at High Altitude: A Field Study. [PDF]
Tang X +8 more
europepmc +1 more source

