LATE-ONSET

作品数：77被引量：167H指数：6
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相关机构：复旦大学苏州大学首都医科大学附属北京世纪坛医院广东医科大学更多>>
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  • 期刊=World Journal of Clinical Casesx
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Elabela is a reliable biomarker for predicting early onset preeclampsia:A comparative study
《World Journal of Clinical Cases》2023年第17期3993-4002,共10页Eham Amer Ali Wassan Nori Alea Farhan Salman Taghreed S Saeed Al-Rawi Ban H Hameed Raid M Al-Ani 
approved by the Scientific-Ethical Committee of the Mustansiriyah University(Approval No.IRB126).
BACKGROUND Preeclampsia(PE)is a multisystemic metabolic disease with an undetermined etiology.PE is a worldwide cause of maternal and perinatal morbidity,subdivided into early(EoPE)and late-onset(LoPE)according to 34 ...
关键词：Early onset preeclampsia Late-onset preeclampsia PREDICTION Elabela PREECLAMPSIA Pregnant women 
Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with mitochondrial DNA 3243A>G mutation masquerading as autoimmune encephalitis:A case report
《World Journal of Clinical Cases》2023年第14期3275-3281,共7页Jian-Wei Wang Xiao-Bo Yuan Hong-Fang Chen 
Supported by the Science and Technology Plan of Jinhua City,No.2020-3-026。
BACKGROUND Here,we present a unique case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes(MELAS)syndrome,which initially appeared to be autoimmune encephalitis and was ultimately confir...
关键词：MELAS Mitochondrial DNA mutation ENCEPHALITIS Case report 
Liver transplantation for late-onset ornithine transcarbamylase deficiency:A case report被引量：4
《World Journal of Clinical Cases》2022年第18期6156-6162,共7页Xiao-Hui Fu Yu-Hui Hu Jian-Xiang Liao Li Chen Zhan-Qi Hu Jia-Lun Wen Shu-Li Chen 
Supported by the Sanming Project of Medicine in Shenzhen,No.SZSM201812005。
BACKGROUND Ornithine transcarbamylase deficiency(OTCD)is an X-linked inherited disorder and characterized by marked elevation of blood ammonia.The goal of treatment is to minimize the neurological damage caused by hyp...
关键词：Ornithine transcarbamylase deficiency Urea cycle disorder Hyperammonemic encephalopathy Liver transplantation Case report 
Screw penetration of the iliopsoas muscle causing late-onset pain after total hip arthroplasty: A case report被引量：1
《World Journal of Clinical Cases》2021年第32期10006-10012,共7页Hyung-Seok Park Sang-Hong Lee Hong-Man Cho Hyun-Bai Choi Suenghwan Jo 
by Research Fund from Chosun University Hospital,2019。
BACKGROUND Postoperative pain following total hip arthroplasty(THA)may occur in a few patients but may pose a significant challenge to surgeons if the etiology is not identified.Herein,we report the case of a patient ...
关键词：Acetabular cup Iliopsoas impingement Para-rectus approach Screw penetration Total hip arthroplasty Case report 
Late-onset Leigh syndrome without delayed development in China:A case report被引量：2
《World Journal of Clinical Cases》2021年第24期7133-7138,共6页Jian-Min Liang Cui-Juan Xin Guang-Liang Wang Xue-Mei Wu 
the National Natural Science Foundation of China,No.81801284 and No.81771396.
BACKGROUND Leigh syndrome(LS)is one of the most common mitochondrial diseases in infants and children.LS often manifests as early-onset with delayed phenotypic development.However,late-onset LS with normal development...
关键词：Leigh syndrome 9176 mutation LATE-ONSET Case report 
Late-onset non-islet cell tumor hypoglycemia: A case report
《World Journal of Clinical Cases》2021年第1期163-169,共7页Shunichi Matsumoto Eijiro Yamada Yasuyo Nakajima Naoki Yamaguchi Takashi Okamura Toshiki Yajima Satoshi Yoshino Kazuhiko Horiguchi Emi Ishida Masashi Yoshikawa Jun Nagaoka Sho Sekiguchi Mai Sue Shuichi Okada Izumi Fukuda Ken Shirabe Masanobu Yamada 
BACKGROUND Hypoglycemia due to non-insulin-producing tumors is referred to as non-islet cell tumor hypoglycemia(NICTH).As NICTH is a rare lesion,the natural course of NICTH is not well understood.We report a case of N...
关键词：HYPOGLYCEMIA Non-islet cell tumor hypoglycemia Blood glucose Solitary tumor Late onset Case report Insulin-like growth factor II 
Late-onset multiple acyl-CoA dehydrogenase deficiency with cardiac syncope: A case report被引量：3
《World Journal of Clinical Cases》2020年第5期995-1001,共7页Xue-Qi Pan Xue-Li Chang Wei Zhang Hua-Xing Meng Jing Zhang Jia-Ying Shi Jun-Hong Guo 
BACKGROUND Multiple acyl-CoA dehydrogenase deficiency(MADD)is an uncommon autosomal recessive disorder of mitochondrial fatty acid beta-oxidation.Syncope is a transient loss of consciousness due to acute global cerebr...
关键词：Late-onset multiple acyl-CoA dehydrogenase deficiency ETFDH Cardiac syncope Supraventricular tachycardia MITOCHONDRION CARNITINE Case report 
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