AMASS
发表于 2025-3-21 19:39:51
书目名称Neuroacanthocytosis Syndromes影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0663842<br><br> <br><br>书目名称Neuroacanthocytosis Syndromes读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0663842<br><br> <br><br>
ARBOR
发表于 2025-3-21 23:27:41
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防锈
发表于 2025-3-22 01:01:21
Acanthocytes and Disorders of Lipoprotein Metabolismntury ago to describe the dysmorphic erythrocytes seen in abetalipoproteinemia (ABL), a complex metabolic disorder that is characterised by fat malabsorption, atypical retinitis pigmentosa and spinocerebellar ataxia. ABL results from mutation in the gene encoding microsomal triglyceride transfer pro
eardrum
发表于 2025-3-22 06:28:10
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慎重
发表于 2025-3-22 12:40:09
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CON
发表于 2025-3-22 16:22:33
McLeod Syndrome: A Clinical Reviewe encoding the XK protein, a membrane transport protein of yet unknown function. Hematologically, McLeod syndrome is characterized by an absent Kx erythrocyte antigen, weak expression of Kell antigens, acanthocytosis, and compensated hemolysis. Asymptomatic male McLeod carriers have elevated serum c
课程
发表于 2025-3-22 18:34:49
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万花筒
发表于 2025-3-22 23:41:26
Acanthocytes in Pantothenate Kinase Associated Neurodegeneration shown to be due to mutations in the gene for pantothenate kinase 2 (.). It was suggested that this group of disorders should now be referred to as pantothenate kinase associated neurodegeneration (PKAN). . is a key regulatory enzyme in the biosynthesis of coenzyme A, which in turn is pivotal in pho
祖先
发表于 2025-3-23 01:25:41
Diagnostic Test for Neuroacanthocytosis: Quantitative Measurement of Red Blood Cell Morphologyn and distribution. These morphological changes occur normally because of ultrastructural abnormalities of the erythrocyte membrane due to lipid or membrane skeleton alterations. Since genetic analyses and/or specific laboratory tests are available only for a minority of disorders associated with ac
CANON
发表于 2025-3-23 08:42:57
Differential Diagnosis of Serum Creatine Kinase Elevationated creatine kinase levels are identified. General practitioners, anesthesiologists, surgeons and neurologists might be confronted with such an unexplained non-cardiac hyperCKemia. Although this problem is not uncommon, it has been the subject of only a few studies. We provide a clinical review of