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3-Methylcrotonyl-coenzyme A carboxylase deficiency in Amish/Mennonite adults identified by detection of increased acylcarnitines in blood spots of their children.
Gibson KM, Bennett MJ, Naylor EW, Morton DH. Gibson KM, et al. J Pediatr. 1998 Mar;132(3 Pt 1):519-23. doi: 10.1016/s0022-3476(98)70032-0. J Pediatr. 1998. PMID: 9544913
A simple screening test for reduced glutathione in filter paper spots of blood.
Garrick MD, Orfanos AP, Rogers L, Naylor EW, Guthrie R. Garrick MD, et al. J Pediatr. 1981 Feb;98(2):265-7. doi: 10.1016/s0022-3476(81)80656-7. J Pediatr. 1981. PMID: 7463226 No abstract available.
Newborn screening of urea cycle disorders.
Naylor EW. Naylor EW. Pediatrics. 1981 Sep;68(3):453-7. Pediatrics. 1981. PMID: 7279482 No abstract available.
Urine screening for metabolic disease in newborn infants.
Paul TD, Naylor EW, Guthrie R. Paul TD, et al. J Pediatr. 1980 Apr;96(4):653-6. doi: 10.1016/s0022-3476(80)80732-3. J Pediatr. 1980. PMID: 7359269
An improved screening test for adenosine deaminase deficiency.
Naylor EW, Orfanos AP, Guthrie R. Naylor EW, et al. J Pediatr. 1978 Sep;93(3):473-6. doi: 10.1016/s0022-3476(78)81168-8. J Pediatr. 1978. PMID: 690770 No abstract available.
Combined transient and peripheral defects in tetrahydrobiopterin synthesis.
Allanson J, McInnes R, Bradley L, Tarby T, Naylor E, Nardella M. Allanson J, et al. J Pediatr. 1991 Feb;118(2):261-3. doi: 10.1016/s0022-3476(05)80498-6. J Pediatr. 1991. PMID: 1993959 No abstract available.
Biopterin synthesis defects: problems in diagnosis.
Hoganson G, Berlow S, Kaufman S, Milstien S, Schuett V, Matalon R, Naylor E, Seifert W. Hoganson G, et al. Pediatrics. 1984 Dec;74(6):1004-11. Pediatrics. 1984. PMID: 6150460
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