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Glutamic acid decarboxylase (GAD) in mammalian tissue outside the central nervous system, and its possible relevance to hereditary vitamin B6 dependency with seizures.
Scriver CR, Whelan DT. Scriver CR, et al. Among authors: whelan dt. Ann N Y Acad Sci. 1969 Sep 30;166(1):83-96. doi: 10.1111/j.1749-6632.1969.tb54259.x. Ann N Y Acad Sci. 1969. PMID: 5262035 No abstract available.
Glutamic acid decarboxylase and gamma-aminobutyric acid in mammalian kidney.
Whelan DT, Scriver CR, Mohyuddin F. Whelan DT, et al. Nature. 1969 Nov 29;224(5222):916-7. doi: 10.1038/224916a0. Nature. 1969. PMID: 5389396 No abstract available.
A -aminobutyrate pathway in mammalian kidney cortex.
Lancaster G, Mohyuddin F, Scriver CR, Whelan DT. Lancaster G, et al. Among authors: whelan dt. Biochim Biophys Acta. 1973 Feb 28;297(2):229-40. doi: 10.1016/0304-4165(73)90069-x. Biochim Biophys Acta. 1973. PMID: 4705464 No abstract available.
Novel mutations (Asn 484 Lys, Thr 500 Ala, Gly 438 Glu) in Morquio B disease.
Bagshaw RD, Zhang S, Hinek A, Skomorowski MA, Whelan D, Clarke JT, Callahan JW. Bagshaw RD, et al. Among authors: whelan d. Biochim Biophys Acta. 2002 Dec 12;1588(3):247-53. doi: 10.1016/s0925-4439(02)00172-2. Biochim Biophys Acta. 2002. PMID: 12393180
Novel (cys152 > arg) missense mutation in an Arab patient with Canavan disease.
Kaul R, Gao GP, Michals K, Whelan DT, Levin S, Matalon R. Kaul R, et al. Among authors: whelan dt. Hum Mutat. 1995;5(3):269-71. doi: 10.1002/humu.1380050313. Hum Mutat. 1995. PMID: 7599639 No abstract available.
Vitamin D dependency: an inherited postnatal syndrome with secondary hyperparathyroidism.
Arnaud C, Maijer R, Reade T, Scriver CR, Whelan DT. Arnaud C, et al. Among authors: whelan dt. Pediatrics. 1970 Dec;46(6):871-80. Pediatrics. 1970. PMID: 5491441 No abstract available.
L-Glutaric acidemia: investigation of a patient and his family.
Whelan DT, Hill R, Ryan ED, Spate M. Whelan DT, et al. Pediatrics. 1979 Jan;63(1):88-93. Pediatrics. 1979. PMID: 440804
Citrullinemia: phenotypic variations.
Whelan DT, Brusso T, Spate M. Whelan DT, et al. Pediatrics. 1976 Jun;57(6):935-41. Pediatrics. 1976. PMID: 934749
Variability of the de Lange syndrome: report of 3 cases and genetic analysis of 54 families.
Pashayan H, Whelan D, Guttman S, Fraser FC. Pashayan H, et al. Among authors: whelan d. J Pediatr. 1969 Nov;75(5):853-8. doi: 10.1016/s0022-3476(69)80310-0. J Pediatr. 1969. PMID: 5347434 No abstract available.
Paternal transmission of fragile X syndrome.
Zeesman S, Zwaigenbaum L, Whelan DT, Hagerman RJ, Tassone F, Taylor SA. Zeesman S, et al. Among authors: whelan dt. Am J Med Genet A. 2004 Aug 30;129A(2):184-9. doi: 10.1002/ajmg.a.30191. Am J Med Genet A. 2004. PMID: 15316964
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