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Results: 1-5 |
Results: 5
HEREDITARY DISORDERS OF PURINE AND PYRIMIDINE METABOLISM (VOL 72, PG 719, 1997)
Authors: VALIK D
Citation: D. Valik, HEREDITARY DISORDERS OF PURINE AND PYRIMIDINE METABOLISM (VOL 72, PG 719, 1997), Mayo Clinic proceedings, 73(2), 1998, pp. 200-200
ENCEPHALOPATHY, LACTIC-ACIDOSIS, HYPERAMMONEMIA AND 5-FLUOROURACIL TOXICITY
Authors: VALIK D
Citation: D. Valik, ENCEPHALOPATHY, LACTIC-ACIDOSIS, HYPERAMMONEMIA AND 5-FLUOROURACIL TOXICITY, British Journal of Cancer, 77(10), 1998, pp. 1710-1711
FIRST US CASE OF ADENYLOSUCCINATE LYASE DEFICIENCY WITH SEVERE HYPOTONIA
Authors: VALIK D MINER PT JONES JD
Citation: D. Valik et al., FIRST US CASE OF ADENYLOSUCCINATE LYASE DEFICIENCY WITH SEVERE HYPOTONIA, Pediatric neurology, 16(3), 1997, pp. 252-255
HEREDITARY DISORDERS OF PURINE AND PYRIMIDINE METABOLISM - IDENTIFICATION OF THEIR BIOCHEMICAL PHENOTYPES IN THE CLINICAL LABORATORY
Authors: VALIK D JONES JD
Citation: D. Valik et Jd. Jones, HEREDITARY DISORDERS OF PURINE AND PYRIMIDINE METABOLISM - IDENTIFICATION OF THEIR BIOCHEMICAL PHENOTYPES IN THE CLINICAL LABORATORY, Mayo Clinic proceedings, 72(8), 1997, pp. 719-725
ADENYLOSUCCINASE DEFICIENCY AND DISORDERS OF CARBOHYDRATE-METABOLISM - THE INTEGRATED SCREENING-TEST
Authors: VALIK D JONES JD
Citation: D. Valik et Jd. Jones, ADENYLOSUCCINASE DEFICIENCY AND DISORDERS OF CARBOHYDRATE-METABOLISM - THE INTEGRATED SCREENING-TEST, Pediatric research, 37(4), 1995, pp. 154-154
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