156 related articles for article (PubMed ID: 16227032)
1. Prenatal and postnatal treatment in cobalamin C defect.
Huemer M; Simma B; Fowler B; Suormala T; Bodamer OA; Sass JO
J Pediatr; 2005 Oct; 147(4):469-72. PubMed ID: 16227032
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. Practical management of combined methylmalonicaciduria and homocystinuria.
Smith DL; Bodamer OA
J Child Neurol; 2002 May; 17(5):353-6. PubMed ID: 12150582
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of methylmalonic aciduria by analysis of organic acids and total homocysteine in amniotic fluid.
Zhang Y; Yang YL; Hasegawa Y; Yamaguchi S; Shi CY; Song JQ; Sayami S; Liu P; Yan R; Dong JH; Qin J
Chin Med J (Engl); 2008 Feb; 121(3):216-9. PubMed ID: 18298912
[TBL] [Abstract][Full Text] [Related]
5. Cobalamin and folate deficiency: acquired and hereditary disorders in children.
Rosenblatt DS; Whitehead VM
Semin Hematol; 1999 Jan; 36(1):19-34. PubMed ID: 9930566
[TBL] [Abstract][Full Text] [Related]
6. Cobalamin C defect presenting with isolated pulmonary hypertension.
Iodice FG; Di Chiara L; Boenzi S; Aiello C; Monti L; Cogo P; Dionisi-Vici C
Pediatrics; 2013 Jul; 132(1):e248-51. PubMed ID: 23753090
[TBL] [Abstract][Full Text] [Related]
7. Vitamin B12 in health and disease: part I--inherited disorders of function, absorption, and transport.
Kapadia CR
Gastroenterologist; 1995 Dec; 3(4):329-44. PubMed ID: 8775094
[TBL] [Abstract][Full Text] [Related]
8. Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy.
Van Hove JL; Van Damme-Lombaerts R; Grünewald S; Peters H; Van Damme B; Fryns JP; Arnout J; Wevers R; Baumgartner ER; Fowler B
Am J Med Genet; 2002 Aug; 111(2):195-201. PubMed ID: 12210350
[TBL] [Abstract][Full Text] [Related]
9. Hereditary partial transcobalamin II deficiency with neurologic, mental and hematologic abnormalities in children and adults.
Teplitsky V; Huminer D; Zoldan J; Pitlik S; Shohat M; Mittelman M
Isr Med Assoc J; 2003 Dec; 5(12):868-72. PubMed ID: 14689755
[TBL] [Abstract][Full Text] [Related]
10. Two newborns with nutritional vitamin B12 deficiency: challenges in newborn screening for vitamin B12 deficiency.
Campbell CD; Ganesh J; Ficicioglu C
Haematologica; 2005 Dec; 90(12 Suppl):ECR45. PubMed ID: 16464760
[TBL] [Abstract][Full Text] [Related]
11. [Measurement of methylmalonic acid, homocysteine and methionine in cobalamin and folate deficiencies and homocysteinuria].
Ueland PM; Schneede J
Tidsskr Nor Laegeforen; 2008 Mar; 128(6):690-3. PubMed ID: 18337849
[TBL] [Abstract][Full Text] [Related]
12. Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism.
Allen RH; Stabler SP; Lindenbaum J
Metabolism; 1993 Nov; 42(11):1448-60. PubMed ID: 7694037
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria.
Bartholomew DW; Batshaw ML; Allen RH; Roe CR; Rosenblatt D; Valle DL; Francomano CA
J Pediatr; 1988 Jan; 112(1):32-9. PubMed ID: 3257264
[TBL] [Abstract][Full Text] [Related]
15. Clinical and biochemical outcome after hydroxocobalamin dose escalation in a series of patients with cobalamin C deficiency.
Matos IV; Castejón E; Meavilla S; O'Callaghan M; Garcia-Villoria J; López-Sala A; Ribes A; Artuch R; Garcia-Cazorla A
Mol Genet Metab; 2013 Aug; 109(4):360-5. PubMed ID: 23746552
[TBL] [Abstract][Full Text] [Related]
16. Accumulation of odd-numbered long-chain fatty acids in fetuses and neonates with inherited disorders of propionate metabolism.
Wendel U; Baumgartner R; van der Meer SB; Spaapen LJ
Pediatr Res; 1991 Apr; 29(4 Pt 1):403-5. PubMed ID: 1852536
[TBL] [Abstract][Full Text] [Related]
17. COBALAMIN C DEFICIENCY WITH INFANTILE SPASM AND CUTANEOUS FINDINGS: A UNIQUE CASE.
Öztürk Z; Arhan E; Aydin K; Hirfanoğlu T; Tümer L; Okur I; Serdaroğlu A; Akbaş Y; Karaoğlu B
Genet Couns; 2016; 27(3):399-403. PubMed ID: 30204970
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Acquired and inherited disorders of cobalamin and folate in children.
Whitehead VM
Br J Haematol; 2006 Jul; 134(2):125-36. PubMed ID: 16846473
[TBL] [Abstract][Full Text] [Related]
20. How can cobalamin injections be spaced in long-term therapy for inborn errors of vitamin B(12) absorption?
Boina Abdallah A; Ogier de Baulny H; Kozyraki R; Passemard S; Fenneteau O; Lebon S; Rigal O; Mesples B; Yacouben K; Giraudier S; Benoist JF; Schiff M
Mol Genet Metab; 2012 Sep; 107(1-2):66-71. PubMed ID: 22854512
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
