133 related articles for article (PubMed ID: 7357085)
1. Congenital methylmalonic aciduria--homocystinuria with megaloblastic anemia: observations on response to hydroxocobalamin and on the effect of homocysteine and methionine on the deoxyuridine suppression test.
Carmel R; Bedros AA; Mace JW; Goodman SI
Blood; 1980 Apr; 55(4):570-9. PubMed ID: 7357085
[No Abstract] [Full Text] [Related]
2. Methylmalonic aciduria with homocystinuria.
Ribes A; Vilaseca MA; Briones P; Maya A; Sabater J; Pascual P; Alvarez L; Ros J; Gonzalez Pascual E
J Inherit Metab Dis; 1984; 7 Suppl 2():129-30. PubMed ID: 6434865
[No Abstract] [Full Text] [Related]
3. Abnormal deoxyuridine suppression test in congenital methylmalonic aciduria-homocystinuria without megaloblastic anemia: divergent biochemical and morphological bone marrow manifestations of disordered cobalamin metabolism in man.
Carmel R; Goodman SI
Blood; 1982 Feb; 59(2):306-11. PubMed ID: 7055641
[TBL] [Abstract][Full Text] [Related]
4. Cobalamin C mutation (methylmalonic aciduria and homocystinuria) in adolescence. A treatable cause of dementia and myelopathy.
Shinnar S; Singer HS
N Engl J Med; 1984 Aug; 311(7):451-4. PubMed ID: 6749192
[No Abstract] [Full Text] [Related]
5. Retinal degeneration in vitamin B12 disorder associated with methylmalonic aciduria and sulfur amino acid abnormalities.
Robb RM; Dowton SB; Fulton AB; Levy HL
Am J Ophthalmol; 1984 Jun; 97(6):691-6. PubMed ID: 6731535
[TBL] [Abstract][Full Text] [Related]
6. Vitamin B12-responsive megaloblastic anemia, homocystinuria, and transient methylmalonic aciduria in cb1E disease.
Tuchman M; Kelly P; Watkins D; Rosenblatt DS
J Pediatr; 1988 Dec; 113(6):1052-6. PubMed ID: 3193313
[No Abstract] [Full Text] [Related]
7. Maculopathy and retinal degeneration in cobalamin C methylmalonic aciduria and homocystinuria.
Tsina EK; Marsden DL; Hansen RM; Fulton AB
Arch Ophthalmol; 2005 Aug; 123(8):1143-6. PubMed ID: 16087854
[No Abstract] [Full Text] [Related]
8. [A rare inborn error of intracellular processing of cobalamine presenting with microcephalus and megaloblastic anemia: a report of 3 children].
Müller P; Horneff G; Hennermann JB
Klin Padiatr; 2007; 219(6):361-7. PubMed ID: 18050048
[TBL] [Abstract][Full Text] [Related]
9. Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria.
Mitchell GA; Watkins D; Melançon SB; Rosenblatt DS; Geoffroy G; Orquin J; Homsy MB; Dallaire L
J Pediatr; 1986 Mar; 108(3):410-5. PubMed ID: 3950820
[TBL] [Abstract][Full Text] [Related]
10. A cobalamin metabolic defect with homocystinuria, methylmalonic aciduria and macrocytic anemia.
Mamlok RJ; Isenberg JN; Rassin DK; Norcross K; Tallan HH
Neuropediatrics; 1986 May; 17(2):94-9. PubMed ID: 2873525
[TBL] [Abstract][Full Text] [Related]
11. Biochemical diagnosis and outcome of 2 years treatment in a patient with combined methylmalonic aciduria and homocystinuria.
Bellini C; Cerone R; Bonacci W; Caruso U; Magliano CP; Serra G; Fowler B; Romano C
Eur J Pediatr; 1992 Nov; 151(11):818-20. PubMed ID: 1468456
[TBL] [Abstract][Full Text] [Related]
12. EEG in assessing hydroxycobalamin therapy in neonatal methylmalonic aciduria with homocystinuria.
Bellieni CV; Ferrari F; De Felice C; Bagnoli F; Cioni M; Farnetani M; Gatti MG; Buonocore G
Biol Neonate; 2000 Nov; 78(4):327-30. PubMed ID: 11093015
[TBL] [Abstract][Full Text] [Related]
13. CblC/D defect combined with haemodynamically highly relevant VSD.
Tomaske M; Bosk A; Heinemann MK; Sieverding L; Baumgartner ER; Fowler B; Trefz FK
J Inherit Metab Dis; 2001 Aug; 24(4):511-2. PubMed ID: 11596656
[TBL] [Abstract][Full Text] [Related]
14. Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.
Rosenblatt DS; Thomas IT; Watkins D; Cooper BA; Erbe RW
Am J Med Genet; 1987 Feb; 26(2):377-83. PubMed ID: 3812589
[TBL] [Abstract][Full Text] [Related]
15. Homocystinuria with methylmalonic aciduria: two cases in a sibship.
Goodman SI; Moe PG; Hammond KB; Mudd SH; Uhlendorf BW
Biochem Med; 1970 Dec; 4(5):500-15. PubMed ID: 5524089
[No Abstract] [Full Text] [Related]
16. Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism.
Schuh S; Rosenblatt DS; Cooper BA; Schroeder ML; Bishop AJ; Seargeant LE; Haworth JC
N Engl J Med; 1984 Mar; 310(11):686-90. PubMed ID: 6700644
[TBL] [Abstract][Full Text] [Related]
17. Epileptiform ocular movements with methylmalonic aciduria and homocystinuria.
Cogan DG; Schulman J; Porter RJ; Mudd SH
Am J Ophthalmol; 1980 Aug; 90(2):251-3. PubMed ID: 7425038
[TBL] [Abstract][Full Text] [Related]
18. [Outcomes of patients with combined methylmalonic acidemia and homocystinuria after treatment].
Huang Z; Han LS; Ye J; Qiu WJ; Zhang HW; Gao XL; Wang Y; Ji WJ; Li XY; Gu XF
Zhonghua Er Ke Za Zhi; 2013 Mar; 51(3):194-8. PubMed ID: 23751581
[TBL] [Abstract][Full Text] [Related]
19. [Neonatal onset methylmalonic aciduria and homocystinuria:Biochemical and clinical improvement with betaine therapy].
Urbón Artero A; Aldana Gómez J; Reig Del Moral C; Nieto Conde C; Merinero Cortés B
An Esp Pediatr; 2002 Apr; 56(4):337-41. PubMed ID: 11927078
[TBL] [Abstract][Full Text] [Related]
20. Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patient.
Ribes A; Briones P; Vilaseca MA; Lluch M; Rodes M; Maya A; Campistol J; Pascual P; Suormala T; Baumgartner R
Eur J Pediatr; 1990 Mar; 149(6):412-5. PubMed ID: 2332011
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]