PubMed (OMIM) for id: 78687

Year	Number of Results
1961	1
1964	1
1967	2
1970	1
1973	1
1976	2
1978	3
1979	1
1980	1
1981	1
1984	1
1986	2
1988	2
1989	1
1990	2
1991	3
1992	1
2002	2
2024	0

1

Argininosuccinic aciduria, an inborn error of amino acid metabolism.

LEVIN B, MACKAY HM, OBERHOLZER VG. LEVIN B, et al. Arch Dis Child. 1961 Dec;36(190):622-32. doi: 10.1136/adc.36.190.622. Arch Dis Child. 1961. PMID: 14464548 Free PMC article. No abstract available.

2

Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families.

Kleijer WJ, Garritsen VH, Linnebank M, Mooyer P, Huijmans JG, Mustonen A, Simola KO, Arslan-Kirchner M, Battini R, Briones P, Cardo E, Mandel H, Tschiedel E, Wanders RJ, Koch HG. Kleijer WJ, et al. J Inherit Metab Dis. 2002 Sep;25(5):399-410. doi: 10.1023/a:1020108002877. J Inherit Metab Dis. 2002. PMID: 12408190

3

Argininosuccinate lyase (ASL) deficiency: mutation analysis in 27 patients and a completed structure of the human ASL gene.

Linnebank M, Tschiedel E, Häberle J, Linnebank A, Willenbring H, Kleijer WJ, Koch HG. Linnebank M, et al. Hum Genet. 2002 Oct;111(4-5):350-9. doi: 10.1007/s00439-002-0793-4. Epub 2002 Aug 14. Hum Genet. 2002. PMID: 12384776

4

Neonatal argininosuccinic aciduria-survival after early diagnosis and dietary management.

Collins FS, Summer GK, Schwartz RP, Parke JC Jr. Collins FS, et al. J Pediatr. 1980 Mar;96(3 Pt 1):429-31. doi: 10.1016/s0022-3476(80)80688-3. J Pediatr. 1980. PMID: 7359236 No abstract available.

5

Studies on complementation in argininosuccinate synthetase and argininosuccinate lyase deficiencies in human fibroblasts.

Cathelineau L, Pham Dinh D, Briand P, Kamoun P. Cathelineau L, et al. Hum Genet. 1981;57(3):282-4. doi: 10.1007/BF00278945. Hum Genet. 1981. PMID: 7250970

6

Interallelic complementation in an inborn error of metabolism: genetic heterogeneity in argininosuccinate lyase deficiency.

McInnes RR, Shih V, Chilton S. McInnes RR, et al. Proc Natl Acad Sci U S A. 1984 Jul;81(14):4480-4. doi: 10.1073/pnas.81.14.4480. Proc Natl Acad Sci U S A. 1984. PMID: 6589607 Free PMC article.

7

Argininosuccinic aciduria. Report of two new cases and demonstration of intermittent elevation of blood ammonia.

Moser HW, Efron ML, Brown H, Diamond R, Neumann CG. Moser HW, et al. Am J Med. 1967 Jan;42(1):9-26. doi: 10.1016/0002-9343(67)90003-4. Am J Med. 1967. PMID: 6016480 No abstract available.

8

Arginosuccine aciduria.

Levin B. Levin B. Am J Dis Child. 1967 Jan;113(1):162-5. Am J Dis Child. 1967. PMID: 6015896 No abstract available.

9

A familial study of a human enzyme defect, argininosuccinic aciduria.

Coryell ME, Hall WK, Thevaos TG, Welter DA, Gatz AJ, Horton BF, Sisson BD, Looper JW Jr, Farrow RT. Coryell ME, et al. Biochem Biophys Res Commun. 1964;14:307-12. doi: 10.1016/s0006-291x(64)80001-2. Biochem Biophys Res Commun. 1964. PMID: 5836520 No abstract available.

10

Argininosuccinic aciduria. Case report with neuropathological findings.

Lewis PD, Miller AL. Lewis PD, et al. Brain. 1970;93(2):413-22. doi: 10.1093/brain/93.2.413. Brain. 1970. PMID: 5422414 No abstract available.

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