73 related articles for article (PubMed ID: 4182726)
1. Ketotic hyperglycinaemia.
Haworth JC; Ford JD
Lancet; 1969 Jun; 1(7606):1159. PubMed ID: 4182726
[No Abstract] [Full Text] [Related]
2. Methylmalonic acidemia. A disorder associated with acidosis, hyperglycinemia, and hyperlactatemia.
Lindblad B; Lindblad BS; Olin P; Svanberg B; Zetterström R
Acta Paediatr Scand; 1968 Sep; 57(5):417-24. PubMed ID: 5706053
[No Abstract] [Full Text] [Related]
3. Methylmalonic acidaemia and nonketotic hyperglycinaemia. Clinical and biochemical aspects.
Corbeel L; Tada K; Colombo JP; Eeckels R; Eggermont E; Jaeken J; Den Tandt W; Harvengt L; Delhaye J; Deloecker W
Arch Dis Child; 1975 Feb; 50(2):103-9. PubMed ID: 236734
[TBL] [Abstract][Full Text] [Related]
4. Defective propionate carboxylation in ketotic hyperglycinaemia.
Hsia YE; Scully KJ; Rosenberg LE
Lancet; 1969 Apr; 1(7598):757-8. PubMed ID: 4180220
[No Abstract] [Full Text] [Related]
5. Localisation of enzymic defect in propionicacidaemia.
Gompertz D; Storrs CN; Bau DC; Peters TJ; Hughes EA
Lancet; 1970 May; 1(7657):1140-3. PubMed ID: 4192098
[No Abstract] [Full Text] [Related]
6. Non-ketotic hyperglycinaemia in a family with an unusual phenotype.
Ando T; Nyhan WL; Bicknell J; Harris R; Stern J
J Inherit Metab Dis; 1978; 1(3):79-83. PubMed ID: 116082
[TBL] [Abstract][Full Text] [Related]
7. Methylmalonic-acidaemia-hyperglycinaemia.
Halvorsen S; Stokke O; Eldjarn L
Lancet; 1968 Apr; 1(7545):756. PubMed ID: 4170994
[No Abstract] [Full Text] [Related]
8. The oxidation of glycine and propionic acid in propionic acidemia with ketotic hyperglycinemia.
Ando T; Nyhan WL; Connor JD; Rasmussen K; Donnell G; Barnes N; Cottom D; Hull D
Pediatr Res; 1972 Jun; 6(6):576-83. PubMed ID: 5046977
[No Abstract] [Full Text] [Related]
9. Methylmalonic acid.
Barness LA
Pediatrics; 1973 Jun; 51(6):1012-5. PubMed ID: 4710435
[No Abstract] [Full Text] [Related]
10. The occurrence of beta-hydroxy-n-valeric acid in a patient with propionic and methylmalonic acidemia.
Stokke O; Jellum E; Eldjarn L; Schnitler R
Clin Chim Acta; 1973 May; 45(4):391-401. PubMed ID: 4730209
[No Abstract] [Full Text] [Related]
11. Ketotic hypoglycemia: an amino acid substrate limited disorder.
Haymond MW; Karl IE; Pagliara AS
J Clin Endocrinol Metab; 1974 Apr; 38(4):521-30. PubMed ID: 4820656
[No Abstract] [Full Text] [Related]
12. Amino acid loading tests in a patient with non-ketotic hyperglycinaemia.
Palmer T; Oberholzer VG
J Inherit Metab Dis; 1985; 8 Suppl 2():125-6. PubMed ID: 3930860
[No Abstract] [Full Text] [Related]
13. Familial chronic acidosis due to an error in lactate and pyruvate metabolism.
Haworth JC; Ford JD; Younoszai MK
Can Med Assoc J; 1967 Sep; 97(13):773-9. PubMed ID: 6050895
[No Abstract] [Full Text] [Related]
14. [Methyl malonic acidemia with hyperuricemic nephropathy].
Broyer M; Guesry P; Burgess EA; Charpentier C; Lemonnier A
Arch Fr Pediatr; 1974; 31(6):543-52. PubMed ID: 4441234
[No Abstract] [Full Text] [Related]
15. Non-ketotic hyperglycinaemia in a neonate. A case report.
De Ravel TJ; Smith CE; Scher LG; Davies VA; Rothberg AD
S Afr Med J; 1991 Aug; 80(4):201-2. PubMed ID: 1876959
[TBL] [Abstract][Full Text] [Related]
16. Recurrent attacks of ketotic acidosis associated with fructose-1,6-diphosphatase deficiency.
Corbeel L; Eggermont E; Eeckels R; Jaeken J; Casteels-Van Daele M; Devlieger H; Delmontte B
Acta Paediatr Belg; 1976; 29(1):29-34. PubMed ID: 189564
[No Abstract] [Full Text] [Related]
17. Sensitivity to carbohydrate in a patient with familial intermittent lactic acidosis and pyruvate dehydrogenase deficiency.
Cederbaum SD; Blass JP; Minkoff N; Brown WJ; Cotton ME; Harris SH
Pediatr Res; 1976 Aug; 10(8):713-20. PubMed ID: 821033
[TBL] [Abstract][Full Text] [Related]
18. Chronic congenital lactic acidosis. A fatal case with hyperphosphatemia and hyperlipemia.
Schärer K; Marty A; Mühlethaler JP
Helv Paediatr Acta; 1968 Apr; 23(2):107-27. PubMed ID: 5699019
[No Abstract] [Full Text] [Related]
19. Juvenile non-ketotic hyperglycinaemia in three siblings.
Cole DE; Meek DC
J Inherit Metab Dis; 1985; 8 Suppl 2():123-4. PubMed ID: 3930859
[No Abstract] [Full Text] [Related]
20. Thiamine-responsive lactice acidosis in a patient with deficient low-KM pyruvate carboxylase activity in liver.
Brunette MG; Delvin E; Hazel B; Scriver CR
Pediatrics; 1972 Nov; 50(5):702-11. PubMed ID: 4343503
[No Abstract] [Full Text] [Related]
[Next] [New Search]
