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Journal Abstract Search
265 related items for PubMed ID: 7393687
1. [Vitamin B 12 responsive methylmalenic aciduria. Apropos of a new case]. Sann L, Divry P, Rolland MO, Bourgeois J, Bethenod M. Pediatrie; 1980; 35(3):205-12. PubMed ID: 7393687 [No 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 16; 311(7):451-4. PubMed ID: 6749192 [No Abstract] [Full Text] [Related]
5. [A case of metabolic encephalopathy caused by vitamin B 12-dependent methylmalonicaciduria]. Capece G, Giliberti P, Militerni R, Pignero A. Acta Neurol Quad (Napoli); 1981 Aug 16; 42():254-9. PubMed ID: 7270059 [No Abstract] [Full Text] [Related]
6. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. Baumgartner ER, Wick H, Maurer R, Egli N, Steinmann B. Helv Paediatr Acta; 1979 Aug 16; 34(5):465-82. PubMed ID: 528229 [Abstract] [Full Text] [Related]
7. Methylmalonic aciduria (1 case report). Yuan LF, Zhao SM, Luo HY, Huang XH, Guo YZ, Xu JZ, Xu YY. Proc Chin Acad Med Sci Peking Union Med Coll; 1987 Aug 16; 2(3):183-5. PubMed ID: 3444838 [No Abstract] [Full Text] [Related]
9. Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria. Coulombe JT, Shih VE, Levy HL. Pediatrics; 1981 Jan 16; 67(1):26-31. PubMed ID: 7243433 [Abstract] [Full Text] [Related]
10. 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 16; 149(6):412-5. PubMed ID: 2332011 [Abstract] [Full Text] [Related]
14. Epileptiform ocular movements with methylmalonic aciduria and homocystinuria. Cogan DG, Schulman J, Porter RJ, Mudd SH. Am J Ophthalmol; 1980 Aug 16; 90(2):251-3. PubMed ID: 7425038 [Abstract] [Full Text] [Related]
15. [Methylmalonic aciduria - diagnosis and therapy using as example 2 cases of this genetic metabolic disorder]. Lubs H, Seidlitz G, Pfau E. Padiatr Grenzgeb; 1982 Aug 16; 21(4):319-26. PubMed ID: 7177670 [No Abstract] [Full Text] [Related]
19. [Pharmacologic and dietetic treatment of 2 siblings with atypical methylmalonic aciduria]. Duillo MT, Poggi L, Cortese M, de Toni T, Di Rocco M. Minerva Pediatr; 1984 Oct 31; 36(20):999-1002. PubMed ID: 6531009 [No Abstract] [Full Text] [Related]