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SPEED-RELATED TRAFFIC ACCIDENT ANALYSIS USING GIS-BASED DBSCAN AND NNH CLUSTERING.
- Published in:
- International Archives of the Photogrammetry, Remote Sensing & Spatial Information Sciences, 2022, n. 4/W1, p. 487, doi. 10.5194/isprs-archives-XLVIII-4-W1-2022-487-2022
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- Article
Interaction of melatonin and Bmal1 in the regulation of PI3K/AKT pathway components and cellular survival.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-55663-0
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- Article
Identification of candidate biomarkers in converting and non-converting clinically isolated syndrome by proteomics analysis of cerebrospinal fluid.
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- Acta Neurologica Belgica, 2019, v. 119, n. 1, p. 101, doi. 10.1007/s13760-018-0954-4
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- Article
Changes in serum proteins after endotoxin administration in healthy and cholinetreated calves.
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- BMC Veterinary Research, 2016, v. 12, p. 1, doi. 10.1186/s12917-016-0837-y
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- Article
Asymptomatic adults and older siblings with biotinidase deficiency ascertained by family studies of index cases.
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- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 6, p. 903, doi. 10.1007/s10545-005-0161-3
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- Article
Breastfeeding experience in inborn errors of metabolism other than phenylketonuria.
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- Journal of Inherited Metabolic Disease, 2005, v. 28, n. 4, p. 457, doi. 10.1007/s10545-005-0457-3
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- Article
Consanguineous 3-methylcrotonyl-CoA carboxylase deficiency: Early-onset necrotizing encephalopathy with lethal outcome.
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- 2005
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- Publication type:
- Report
Hyperhydroxyprolinaemia detected in newborn screening with tandem mass spectrometry.
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- Journal of Inherited Metabolic Disease, 2004, v. 27, n. 6, p. 781, doi. 10.1023/B:BOLI.0000045839.08631.9d
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- Article
Silent and symptomatic primary carnitine deficiency within the same family due toidentical mutations in the organic cation/carnitine transporter OCTN2.
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- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 6, p. 613, doi. 10.1023/A:1025968502527
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- Article
Molecular analyses of the HGO gene mutations in Turkish alkaptonuria patients suggest that the R58fs mutation originated from Central Asia and was spread throughout Europe and Anatolia by human migrations.
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- Journal of Inherited Metabolic Disease, 2003, v. 26, n. 1, p. 17, doi. 10.1023/A:1024063126954
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- Article
Novel mutations cause biotinidase deficiency in Turkish children.
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- Journal of Inherited Metabolic Disease, 2000, v. 23, n. 2, p. 120, doi. 10.1023/A:1005609614443
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- Article
Incidence of biotinidase deficiency in Turkish newborns.
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- 1998
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- Publication type:
- letter
Molecular aspects of glycogen storage disease type Ia in Turkish patients: A novel mutation in the glucose-6-phosphatase gene.
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- Journal of Inherited Metabolic Disease, 1998, v. 21, n. 4, p. 445, doi. 10.1023/A:1005339616074
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- Article