Found: 12
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Capillary electrophoresis with capacitively coupled contactless conductivity detection for the determination of urinary ethylmalonic acid for the diagnosis of ethylmalonic aciduria.
- Published in:
- Journal of Separation Science, 2020, v. 43, n. 7, p. 1365, doi. 10.1002/jssc.201901044
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- Article
Separation and quantification of the urinary enantiomers of 2‐hydroxyglutaric acid by capillary electrophoresis with capacitively coupled contactless conductivity detection: Application to the diagnosis of D‐ and L‐2‐hydroxyglutaric aciduria
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- Journal of Separation Science, 2023, v. 46, n. 16, p. 1, doi. 10.1002/jssc.202300145
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- Article
Telemedicine Applications in a Tertiary Pediatric Hospital in Turkey During COVID-19 Pandemic.
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- Telemedicine & e-Health, 2021, v. 27, n. 10, p. 1180, doi. 10.1089/tmj.2020.0381
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- Article
Vitamin D levels in children and adolescents with autism.
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- Journal of International Medical Research, 2020, v. 48, n. 7, p. 1, doi. 10.1177/0300060520934638
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- Article
Maternal Inborn Errors of Metabolism Detected in Expanded Newborn Metabolic Screening.
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- Turkish Archives of Pediatrics, 2023, v. 58, n. 4, p. 382, doi. 10.5152/TurkArchPediatr.2023.23009
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- Article
An Overview of Acute Hepatic Porphyrias: Clinical Implications, Diagnostic Approaches, and Management Strategies.
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- Turkish Archives of Pediatrics, 2023, v. 58, n. 1, p. 3, doi. 10.5152/TurkArchPediatr.2022.22301
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- Article
Tanınız nedir?
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- Archives of the Turkish Dermatology & Venerology / Turkderm, 2014, v. 48, n. 2, p. 111
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- Article
L-2-hidroksiglutarik asidüri hastalarında klinik, nöroradyolojik ve genetik bulguların değerlendirilmesi.
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- Türk Pediatri Arşivi, 2020, v. 55, n. 3, p. 290, doi. 10.14744/TurkPediatriArs.2019.06926
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- Article
Treatment of maple syrup urine disease with high flow hemodialysis in a neonate.
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- Turkish Journal of Pediatrics, 2019, v. 61, n. 1, p. 107, doi. 10.24953/turkjped.2019.01.017
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- Article
Serum Neopterin, Biopterin, Tryptophan, and Kynurenine Levels in Patients with Fabry Disease.
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- Balkan Medical Journal, 2024, v. 41, n. 2, p. 113, doi. 10.4274/balkanmedj.galenos.2024.2023-10-98
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- Article
Screening Inherited Metabolic Disorders in Patients with Familial Mediterranean Fever.
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- Journal of Pediatric Research, 2015, v. 2, n. 4, p. 201, doi. 10.4274/jpr.44227
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- Article
Spondyloocular Syndrome: Novel Mutations in XYLT2 Gene and Expansion of the Phenotypic Spectrum.
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- Journal of Bone & Mineral Research, 2016, v. 31, n. 8, p. 1577, doi. 10.1002/jbmr.2834
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- Article