Similar articles for PMID: 5010106

Year	Number of Results
1959	1
1960	1
1961	3
1963	4
1964	3
1966	4
1967	6
1968	1
1969	2
1970	5
1971	5
1972	7
1973	5
1974	3
1975	2
1976	2
1977	2
1978	4
1979	1
1980	2
1982	3
1983	2
1984	3
1985	4
1986	1
1987	2
1988	2
1989	2
1990	1
1991	1
1992	2
1993	3
1994	2
1995	3
1996	1
1997	2
1999	3
2000	2
2001	1
2002	1
2003	2
2004	2
2005	1
2007	3
2008	2
2009	2
2010	2
2011	1
2012	2
2013	1
2014	2
2016	1
2017	1
2018	2
2019	2
2024	0

1

Maple syrup urine disease (branched-chain keto-aciduria) variant type manifesting as hyperkinetic behaviour and mental retardation. Report of two cases.

Kalyanaraman K, Chamukuttan S, Arjundas G, Gajanan N, Ramamurthi B. Kalyanaraman K, et al. J Neurol Sci. 1972 Feb;15(2):209-17. doi: 10.1016/0022-510x(72)90008-1. J Neurol Sci. 1972. PMID: 5010106 No abstract available.

2

A variant form of branched-chain keto aciduria.

van der Horst JL, Wadman SK. van der Horst JL, et al. Acta Paediatr Scand. 1971 Sep;60(5):594-9. doi: 10.1111/j.1651-2227.1971.tb06996.x. Acta Paediatr Scand. 1971. PMID: 5125167 No abstract available.

3

Intermittent branched chain ketonuria (variant of maple syrup urine disease).

Irwin WC, Martel SB, Goluboff N. Irwin WC, et al. Clin Biochem. 1971 Jun;4(2):52-8. doi: 10.1016/s0009-9120(71)90611-4. Clin Biochem. 1971. PMID: 5128296 No abstract available.

4

A new variant of maple syrup urine disease (branched chain ketoaciduria). Clinical and biochemical evaluation.

Schulman JD, Lustberg TJ, Kennedy JL, Museles M, Seegmiller JE. Schulman JD, et al. Am J Med. 1970 Jul;49(1):118-24. doi: 10.1016/s0002-9343(70)80121-8. Am J Med. 1970. PMID: 5431474 No abstract available.

5

Family with intermittent maple syrup urine disease.

Valman HB, Patrick AD, Seakins JW, Platt JW, Gompertz D. Valman HB, et al. Arch Dis Child. 1973 Mar;48(3):225-8. doi: 10.1136/adc.48.3.225. Arch Dis Child. 1973. PMID: 4693464 Free PMC article.

6

[On the clinical picture and pathological anatomy of the maple syrup disease ("branded chain ketoaciduria"). Report on 2 cases in 1 family].

Sander C, Clotten R, Noetzel H, Wehinger H. Sander C, et al. Dtsch Med Wochenschr. 1968 May 3;93(18):895-903 passim. doi: 10.1055/s-0028-1105160. Dtsch Med Wochenschr. 1968. PMID: 5650843 German. No abstract available.

7

Plasma amino acid analyses in two cases of maple syrup urine disease.

Surarit R, Srisomsap C, Wasant P, Svasti J, Suthatvoravut U, Chokchaichamnankit D, Liammongkolkul S. Surarit R, et al. Southeast Asian J Trop Med Public Health. 1999;30 Suppl 2:138-9. Southeast Asian J Trop Med Public Health. 1999. PMID: 11400750

8

Biochemical studies on a variant of branched chain ketoaciduria in a 19-year-old female.

Fischer MH, Gerritsen T. Fischer MH, et al. Pediatrics. 1971 Nov;48(5):795-801. Pediatrics. 1971. PMID: 5125877 No abstract available.

9

M aple syrup urine disease. A review with a report of an additional case.

Schwartz JF, Kolendrianos ET. Schwartz JF, et al. Dev Med Child Neurol. 1969 Aug;11(4):460-70. Dev Med Child Neurol. 1969. PMID: 5805351 No abstract available.

10

[Leucinose. II. Study of heterozygotes].

Fontaine G, Dautrevaux M, Farriaux JP, Biserte G. Fontaine G, et al. Lille Med. 1967 Apr;12(4):480-3. Lille Med. 1967. PMID: 5619112 French. No abstract available.

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