Found: 12
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Simple Analysis of Plasmalogens in Erythrocytes Using Gas Chromatography/Mass Spectrometry with Selected-ion Monitoring Acquisition.
- Published in:
- Rapid Communications in Mass Spectrometry: RCM, 1996, v. 10, n. 10, p. 1283, doi. 10.1002/(SICI)1097-0231(19960731)10:10<1283::AID-RCM298>3.0.CO;2-N
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- Publication type:
- Article
Color Tuning in the Luminescence of Two Oligomers Derived from N,N′-(Naphthalenediyl)bis-phenylimine Containing Oligomers.
- Published in:
- International Journal of Optics, 2020, p. 1, doi. 10.1155/2020/3672198
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- Publication type:
- Article
Hyperplasia of Antral G Cells in Uraemic Patients.
- Published in:
- Digestion, 1984, v. 29, n. 1, p. 26, doi. 10.1159/000199004
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- Publication type:
- Article
Tyrosinemia type III: diagnosis and ten-year follow-up.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Severe complex I deficiency in a case of neonatal-onset lactic acidosis and fatal liver failure.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Isolated sulphite oxidase deficiency: clinical and biochemical features in an Italian patient.
- Published in:
- Journal of Inherited Metabolic Disease, 2004, v. 27, n. 1, p. 101
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- Publication type:
- Article
Glycine N -methyltransferase deficiency: A novel inborn error causing persistent isolated hypermethioninaemia.
- Published in:
- Journal of Inherited Metabolic Disease, 2001, v. 24, n. 4, p. 448, doi. 10.1023/A:1010577512912
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- Publication type:
- Article
Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D.
- Published in:
- Journal of Inherited Metabolic Disease, 2001, v. 24, n. 3, p. 411, doi. 10.1023/A:1010525206818
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- Publication type:
- Article
3-Methylglutaconic aciduria and hypermethioninaemia in a child with clinical and neuroradiological findings of Leigh disease.
- Published in:
- Journal of Inherited Metabolic Disease, 1999, v. 22, n. 5, p. 593, doi. 10.1023/A:1005565610613
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- Publication type:
- Article
Minor facial anomalies in combined methylmalonic aciduria and homocystinuria due to a defect in cobalamin metabolism.
- Published in:
- Journal of Inherited Metabolic Disease, 1999, v. 22, n. 3, p. 247, doi. 10.1023/A:1005521702298
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- Publication type:
- Article
Fumarate hydratase deficiency.
- Published in:
- Journal of Inherited Metabolic Disease, 1998, v. 21, n. 4, p. 435, doi. 10.1023/A:1005379330187
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- Publication type:
- Article
Monozygotic twins with X-linked adrenoleukodystrophy and different phenotypes.
- Published in:
- 2001
- By:
- Publication type:
- case study