These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 7849710)
1. Identification of two mutant alleles of transcobalamin II in an affected family. Li N; Rosenblatt DS; Kamen BA; Seetharam S; Seetharam B Hum Mol Genet; 1994 Oct; 3(10):1835-40. PubMed ID: 7849710 [TBL] [Abstract][Full Text] [Related]
2. Nonsense mutations in human transcobalamin II deficiency. Li N; Rosenblatt DS; Seetharam B Biochem Biophys Res Commun; 1994 Nov; 204(3):1111-8. PubMed ID: 7980584 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Should transcobalamin deficiency be treated aggressively? Schiff M; Ogier de Baulny H; Bard G; Barlogis V; Hamel C; Moat SJ; Odent S; Shortland G; Touati G; Giraudier S J Inherit Metab Dis; 2010 Jun; 33(3):223-9. PubMed ID: 20352340 [TBL] [Abstract][Full Text] [Related]
5. Transcobalamin deficiency caused by compound heterozygosity for two novel mutations in the TCN2 gene: a study of two affected siblings, their brother, and their parents. Nissen PH; Nordwall M; Hoffmann-Lücke E; Sorensen BS; Nexo E J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S269-74. PubMed ID: 20607612 [TBL] [Abstract][Full Text] [Related]
6. Transcobalamin II Deficiency in Four Cases with Novel Mutations. Ünal Ş; Rupar T; Yetgin S; Yaralı N; Dursun A; Gürsel T; Çetin M Turk J Haematol; 2015 Dec; 32(4):317-22. PubMed ID: 25914105 [TBL] [Abstract][Full Text] [Related]
7. Transcobalamin II deficiency with methylmalonic aciduria in three sisters. Bibi H; Gelman-Kohan Z; Baumgartner ER; Rosenblatt DS J Inherit Metab Dis; 1999 Oct; 22(7):765-72. PubMed ID: 10518276 [TBL] [Abstract][Full Text] [Related]
8. Long-term Outcome of 4 Patients With Transcobalamin Deficiency Caused by 2 Novel TCN2 Mutations. Nashabat M; Maegawa G; Nissen PH; Nexo E; Al-Shamrani H; Al-Owain M; Alfadhel M J Pediatr Hematol Oncol; 2017 Nov; 39(8):e430-e436. PubMed ID: 28538514 [TBL] [Abstract][Full Text] [Related]
9. Transcobalamin deficiency due to activation of an intra exonic cryptic splice site. Namour F; Helfer AC; Quadros EV; Alberto JM; Bibi HM; Orning L; Rosenblatt DS; Jean-Louis G Br J Haematol; 2003 Dec; 123(5):915-20. PubMed ID: 14632784 [TBL] [Abstract][Full Text] [Related]
10. TC II deficiency: avoidance of false-negative molecular genetics by RNA-based investigations. Häberle J; Pauli S; Berning C; Koch HG; Linnebank M J Hum Genet; 2009 Jun; 54(6):331-4. PubMed ID: 19373259 [TBL] [Abstract][Full Text] [Related]
11. Expression of transcobalamin II mRNA in human tissues and cultured fibroblasts from normal and transcobalamin II-deficient patients. Li N; Seetharam S; Rosenblatt DS; Seetharam B Biochem J; 1994 Jul; 301 ( Pt 2)(Pt 2):585-90. PubMed ID: 7913804 [TBL] [Abstract][Full Text] [Related]
12. Congenital transcobalamin II deficiency due to errors in RNA editing. Qian L; Quadros EV; Regec A; Zittoun J; Rothenberg SP Blood Cells Mol Dis; 2002; 28(2):134-42; discussion 143-5. PubMed ID: 12064907 [TBL] [Abstract][Full Text] [Related]
13. Congenital disorders of vitamin B12 transport and their contributions to concepts. II. Hall CA Yale J Biol Med; 1981; 54(6):485-95. PubMed ID: 7342493 [TBL] [Abstract][Full Text] [Related]
14. Transcobalamin (TC) deficiency--potential cause of bone marrow failure in childhood. Prasad C; Rosenblatt DS; Corley K; Cairney AE; Rupar CA J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S287-92. PubMed ID: 18956254 [TBL] [Abstract][Full Text] [Related]
15. Uptake and metabolism of free cyanocobalamin by cultured human fibroblasts from controls and a patient with transcobalamin II deficiency. Berliner N; Rosenberg LE Metabolism; 1981 Mar; 30(3):230-6. PubMed ID: 7207198 [TBL] [Abstract][Full Text] [Related]
16. Genetic patterns of transcobalamin II and the relationships with congenital defects. Fràter-Schröder M Mol Cell Biochem; 1983; 56(1):5-31. PubMed ID: 6355816 [TBL] [Abstract][Full Text] [Related]
17. Seven Patients With Transcobalamin Deficiency Diagnosed Between 2010 and 2014: A Single-Center Experience. Yildirim ZK; Nexo E; Rupar T; Büyükavci M J Pediatr Hematol Oncol; 2017 Jan; 39(1):38-41. PubMed ID: 27824740 [TBL] [Abstract][Full Text] [Related]
18. Different Presentations of Patients with Transcobalamin II Deficiency: A Single-Center Experience from Turkey. Ünal S; Karahan F; Arıkoğlu T; Akar A; Kuyucu S Turk J Haematol; 2019 Feb; 36(1):37-42. PubMed ID: 30185401 [TBL] [Abstract][Full Text] [Related]
19. Transcobalamin deficiency - a rare genetic defect in transportation of cobalamin; case report. Iqbal N; Meghani MA; Khalid W; Ansari AH; Ansari MUH; Ansari SH Ann Hematol; 2024 Aug; 103(8):3243-3246. PubMed ID: 38976007 [TBL] [Abstract][Full Text] [Related]
20. New data supporting that early diagnosis and treatment are possible and necessary in intracellular cobalamin depletion: the case of transcobalamin II deficiency. Verónica B; Crespo C; Lochner N; Rossetti E; Tagliavini C; Bouso C; Eiroa H J Pediatr Endocrinol Metab; 2024 Apr; 37(4):380-386. PubMed ID: 38436354 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]