Similar Papers

Paper Title
Journal
Date
Author
Rapid diagnosis of medium‐chain acyl CoA dehydrogenase deficiency by measurement ofcis‐4‐decenoic acid in plasma
S J R Heales ... P Robinson
Journal of Inherited Metabolic Disease | VOL. 14
S J R Heales, et. al.S J R Heales ... P Robinson
13 Feb 1991
Metabolic Disorders Associated With Neonatal Hypoglycemia
Stephen G Kahler
NeoReviews | VOL. 5
Stephen G KahlerStephen G Kahler
01 Sep 2004
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype–phenotype relationship
Niels Gregersen ... Thomas J Corydon
Human Mutation | VOL. 18
Niels Gregersen, et. al.Niels Gregersen ... Thomas J Corydon
01 Sep 2001
Mutation analysis in mitochondrial fatty acid oxidation defects: Exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship
Niels Gregersen ... Rikke K.J Olsen
Human Mutation | VOL. 18
Niels Gregersen, et. al.Niels Gregersen ... Rikke K.J Olsen
01 Jan 2001
View more papers

More From: Clinical Biochemistry

Paper Title
Journal
Date
Author
Assessing the predictive value of elevated triglycerides, triglyceride-glucose index (TyG), and TG/HDL ratios for cardiovascular disease and mortality during 20 years of follow-up: Tehran lipid and glucose study.
Shayesteh Khalili ... Aryan Salahi-Niri
Clinical biochemistry | VOL. -
Shayesteh Khalili, et. al.Shayesteh Khalili ... Aryan Salahi-Niri
23 Jan 2025
Utility of the combination of high fluorescence cells and tumor markers for the diagnosis of malignant pleural effusions.
Elisa Nuez-Zaragoza ... Vicente Aguadero
Clinical biochemistry | VOL. -
Elisa Nuez-Zaragoza, et. al.Elisa Nuez-Zaragoza ... Vicente Aguadero
21 Jan 2025
Clinical significance of fecal Syndecan-2 gene methylation combined with blood tumor abnormal protein detection in the diagnosis of colorectal cancer and precancerous lesions.
Xuanjun Liu ... Gan He
Clinical biochemistry | VOL. 136
Xuanjun Liu, et. al.Xuanjun Liu ... Gan He
18 Jan 2025
KNG1 mutations (c.618 T > G and c.1165C > T) cause disruption of the Cys206-Cys218 disulfide bond and truncation of the D5 domain leading to hereditary high molecular weight kininogen deficiency.
Xiaoying Lv ... Fuyong Zhang
Clinical biochemistry | VOL. -
Xiaoying Lv, et. al.Xiaoying Lv ... Fuyong Zhang
10 Jan 2025
View more papers

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.