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Spectrum of Organic Aciduria Diseases in Tunisia: A 35-year Retrospective Study.
- Published in:
- Saudi Journal of Medicine & Medical Sciences, 2024, v. 12, n. 1, p. 27, doi. 10.4103/sjmms.sjmms_437_23
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- Article
Analysis of Branched Amino Acids by UPLC as an Alternative Method for the Management of Patients with MUSD.
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- Clinical Laboratory, 2023, v. 69, n. 12, p. 2509, doi. 10.7754/Clin.Lab.2023.230613
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- Article
Effects of high-intensity interval training on body composition, aerobic and anaerobic performance and plasma lipids in overweight/obese and normal-weight young men.
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- Biology of Sport, 2017, v. 34, n. 4, p. 385, doi. 10.5114/biolsport.2017.69827
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- Article
Effect of High-Intensity Interval Training on Plasma Omentin-1 Concentration in Overweight/Obese and Normal-Weight Youth.
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- Obesity Facts: The European Journal of Obesity, 2017, v. 10, n. 4, p. 323, doi. 10.1159/000471882
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- Article
Association of plasma 25-hydroxyvitamin D with physical performance in physically active children.
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- Applied Physiology, Nutrition & Metabolism, 2016, v. 41, n. 11, p. 1124, doi. 10.1139/apnm-2016-0097
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- Article
Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population.
- Published in:
- Biochemical Genetics, 2016, v. 54, n. 5, p. 653, doi. 10.1007/s10528-016-9744-y
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- Article
Lack of association between FokI polymorphism in vitamin D receptor gene (VDR) & type 2 diabetes mellitus in the Tunisian population.
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- Indian Journal of Medical Research, 2016, v. 144, n. 1, p. 46, doi. 10.4103/0971-5916.193282
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- Article
Autism in Phenylketonuria Patients.
- Published in:
- Journal of Child Neurology, 2016, v. 31, n. 7, p. 843, doi. 10.1177/0883073815623636
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- Publication type:
- Article
Association between paraoxonase-1 gene promoter -108C/T polymorphism and myocardial infarction in the Tunisian male population / Tunuslu erkek populasyonunda miyokard enfarktüs ile paraoksonaz -1 gen başlatıcı -108C/T polimorfizmi arasındaki ilişki
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- Turkish Journal of Biochemistry / Turk Biyokimya Dergisi, 2016, v. 41, n. 2, p. 65, doi. 10.1515/tjb-2016-0012
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- Article
Plasma arachidonic and docosahexaenoic acids in Tunisian very low birth weight infants: status and association with selected neonatal morbidities.
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- 2015
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- Publication type:
- journal article
Effects of a high-intensity intermittent training program on aerobic capacity and lipid profile in trained subjects.
- Published in:
- Open Access Journal of Sports Medicine, 2014, v. 5, p. 243, doi. 10.2147/OAJSM.S68701
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- Publication type:
- Article
Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 4, p. 216, doi. 10.1038/jhg.2014.4
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- Article
Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III.
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- Molecular Biology Reports, 2013, v. 40, n. 7, p. 4197, doi. 10.1007/s11033-013-2500-z
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- Publication type:
- Article
Adiponectin and Metabolic Syndrome in a Tunisian Population.
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- Inflammation, 2012, v. 35, n. 3, p. 828, doi. 10.1007/s10753-011-9383-8
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- Publication type:
- Article
Screening of three Mediterranean phenylketonuria mutations in Tunisian families.
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- Journal of Genetics, 2012, v. 91, n. 1, p. 91, doi. 10.1007/s12041-012-0140-z
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- Publication type:
- Article
Status of vitamins A and E in schoolchildren in the centre west of Tunisia: a population-based study.
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- Public Health Nutrition, 2011, v. 14, n. 2, p. 255, doi. 10.1017/S1368980010001631
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- Publication type:
- Article
HLA Class II Alleles Susceptibility Markers of Type 1 Diabetes Fail to Specify Phenotypes of Ketosis-Prone Diabetes in Adult Tunisian Patients.
- Published in:
- Experimental Diabetes Research, 2011, p. 1, doi. 10.1155/2011/964160
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- Publication type:
- Article
Association between the 2756A> G variant in the gene encoding methionine synthase and myocardial infarction in Tunisian patients.
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- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 10, p. 1364, doi. 10.1515/CCLM.2008.306
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- Publication type:
- Article
Association of the insertion/deletion gene polymorphism of the apolipoprotein B signal peptide with myocardial infarction in Tunisian patients.
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- Clinical Chemistry & Laboratory Medicine, 2008, v. 46, n. 8, p. 1097, doi. 10.1515/CCLM.2008.215
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- Publication type:
- Article
Association of a 27-bp repeat polymorphism in intron 4 of endothelial constitutive nitric oxide synthase gene with myocardial infarction in Tunisian patients.
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- Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 11, p. 1476, doi. 10.1515/CCLM.2007.312
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- Publication type:
- Article
Dihydropteridine Reductase Deficiency in a Large Consanguineous Tunisian Family: Clinical,...
- Published in:
- Journal of Child Neurology, 1998, v. 13, n. 10, p. 475, doi. 10.1177/088307389801301002
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- Publication type:
- Article