Found: 15
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Comparison of Liquid Chromatography-Tandem Mass Spectrometry and Sandwich ELISA for Determination of Keratan Sulfate in Plasma and Urine.
- Published in:
- Biomarker Insights, 2011, n. 6, p. 69, doi. 10.4137/BMI.S7451
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- Publication type:
- Article
A Region-based Fault-Tolerant Routing Algorithmfor 2D Irregular Mesh Network-on-Chip.
- Published in:
- Journal of Electronic Testing, 2013, v. 29, n. 3, p. 415, doi. 10.1007/s10836-013-5377-9
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- Publication type:
- Article
An Efficient Framework for Scalable Defect Isolation in Large Scale Networks of DNA Self-Assembly.
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- Journal of Electronic Testing, 2009, v. 25, n. 1, p. 11, doi. 10.1007/s10836-008-5086-y
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- Publication type:
- Article
Guidelines for Newborn Screening of Congenital Hypothyroidism (2021 Revision).
- Published in:
- Clinical Pediatric Endocrinology, 2023, v. 32, n. 1, p. 26, doi. 10.1297/cpe.2022-0063
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- Publication type:
- Article
Clinical guidelines for the diagnosis and treatment of 21-hydroxylase deficiency (2021 revision).
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- Clinical Pediatric Endocrinology, 2022, v. 31, n. 3, p. 116, doi. 10.1297/cpe.2022-0009
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- Publication type:
- Article
Results from 28 years of newborn screening for congenital adrenal hyperplasia in Sapporo City.
- Published in:
- 2013
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- Publication type:
- Abstract
Postpartum thyroid dysfunction in women with normal thyroid function during pregnancy.
- Published in:
- Clinical Endocrinology, 2000, v. 53, n. 4, p. 487, doi. 10.1046/j.1365-2265.2000.01107.x
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- Publication type:
- Article
Gestational transient hyperthyroxinaemia (GTH): screening for thyroid function in 23 163 pregnant women using dried blood spots.
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- Clinical Endocrinology, 1998, v. 49, n. 3, doi. 10.1046/j.1365-2265.1998.00540.x
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- Publication type:
- Article
Presymptomatic diagnosis of Wilson disease associated with a novel mutation of the ATP7B gene.
- Published in:
- 2002
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- Publication type:
- case study
Validation of keratan sulfate level in mucopolysaccharidosis type IVA by liquid chromatography–tandem mass spectrometry.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 35, doi. 10.1007/s10545-009-9013-x
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- Publication type:
- Article
Dermatan sulfate and heparan sulfate as a biomarker for mucopolysaccharidosis I.
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- Journal of Inherited Metabolic Disease, 2010, v. 33, n. 2, p. 141, doi. 10.1007/s10545-009-9036-3
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- Publication type:
- Article
Design of an extended 2D mesh network‐on‐chip and development of A fault‐tolerantrouting method.
- Published in:
- IET Computers & Digital Techniques (Wiley-Blackwell), 2019, v. 13, n. 3, p. 224, doi. 10.1049/iet-cdt.2018.5032
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- Publication type:
- Article
Neonatal mass screening for 21-hydroxylase deficiency.
- Published in:
- Clinical Pediatric Endocrinology, 2016, v. 25, n. 1, p. 1, doi. 10.1297/cpe.25.1
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- Publication type:
- Article
Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision).
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 107
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- Publication type:
- Article
Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision).
- Published in:
- Clinical Pediatric Endocrinology, 2015, v. 24, n. 3, p. 77
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- Publication type:
- Article