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47. Genetic and biochemical analysis of human cobalamin mutants in cell culture. Fenton WA; Rosenberg LE Annu Rev Genet; 1978; 12():223-48. PubMed ID: 371525 [No Abstract] [Full Text] [Related]
48. [Combined exchange transfusion and peritoneal dialysis treatment in a neonatal case of methylmalonic acidemia with severe hyperammonemia]. Sanjurjo P; Jaquotot C; Vallo A; Uriarte R; Prats JM; Ugarte M; RodrÃguez Soriano J An Esp Pediatr; 1982 Oct; 17(4):317-20. PubMed ID: 6818879 [TBL] [Abstract][Full Text] [Related]
49. Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases. Bodemer C; De Prost Y; Bachollet B; Poggi F; Teillac-Hamel D; Fraitag S; Saudubray JM Br J Dermatol; 1994 Jul; 131(1):93-8. PubMed ID: 8043426 [TBL] [Abstract][Full Text] [Related]
50. [Report of a case with methylmalonic acidemia]. Lin HH; Wu C; Dong Y Zhonghua Er Ke Za Zhi; 2008 Jul; 46(7):557-8. PubMed ID: 19099824 [No Abstract] [Full Text] [Related]
51. Abnormal patterns of urine and serum amino acids in methylmalonic acidemia. Halvorsen S; Stokke O; Eldjarn L Acta Paediatr Scand; 1970 Jan; 59(1):28-32. PubMed ID: 5422739 [No Abstract] [Full Text] [Related]
52. Response to dietary therapy in B 12 unresponsive methylmalonic acidemia. Nyhan WL; Fawcett N; Ando T; Rennert OM; Julius RL Pediatrics; 1973 Mar; 51(3):539-48. PubMed ID: 4707869 [No Abstract] [Full Text] [Related]
53. [Inherited metabolic disorders accompanied with epileptic manifestations]. Sasaki M; Sakuragawa N Ryoikibetsu Shokogun Shirizu; 2002; (37 Pt 6):278-82. PubMed ID: 12483881 [No Abstract] [Full Text] [Related]
54. The natural history of the inherited methylmalonic acidemias. Matsui SM; Mahoney MJ; Rosenberg LE N Engl J Med; 1983 Apr; 308(15):857-61. PubMed ID: 6132336 [TBL] [Abstract][Full Text] [Related]
55. An evaluation of protein requirements in methylmalonic acidaemia. Ney D; Bay C; Saudubray JM; Kelts DG; Kulovich S; Sweetman L; Nyhan WL J Inherit Metab Dis; 1985; 8(3):132-42. PubMed ID: 3939589 [TBL] [Abstract][Full Text] [Related]
56. Dietary therapy in two patients with vitamin B12-unresponsive methylmalonic acidemia. Satoh T; Narisawa K; Igarashi Y; Saitoh T; Hayasaka K; Ichinohazama Y; Onodera H; Tada K; Oohara K Eur J Pediatr; 1981 Feb; 135(3):305-12. PubMed ID: 7227387 [TBL] [Abstract][Full Text] [Related]
57. [Methylmalonic acidemia: classification, diagnosis and therapy]. Cantani A Klin Padiatr; 1983; 195(6):388-93. PubMed ID: 6361367 [TBL] [Abstract][Full Text] [Related]
59. Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis. Oberholzer VG; Levin B; Burgess EA; Young WF Arch Dis Child; 1967 Oct; 42(225):492-504. PubMed ID: 6061291 [No Abstract] [Full Text] [Related]
60. Substrate disposal in metabolic disease: a comparison between rates of in vivo propionate oxidation and urinary metabolite excretion in children with methylmalonic acidemia. Thompson GN; Walter JH; Bresson JL; Ford GC; Bonnefont JP; Chalmers RA; Saudubray JM; Leonard JV; Halliday D J Pediatr; 1989 Nov; 115(5 Pt 1):735-9. PubMed ID: 2809905 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]