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.
5. Unusual case of thiamine responsive megaloblastic anemia. Tinsa F; Ben Amor S; Kaabachi N; Ben Lasouad M; Boussetta K; Bousnina S Tunis Med; 2009 Feb; 87(2):159-63. PubMed ID: 19522453 [TBL] [Abstract][Full Text] [Related]
6. Five years followup of diabetes mellitus in two siblings with thiamine responsive megaloblastic anemia. Bappal B; Nair R; Shaikh H; AI Khusaiby SM; de Silva V Indian Pediatr; 2001 Nov; 38(11):1295-8. PubMed ID: 11721072 [No Abstract] [Full Text] [Related]
8. Thiamine-responsive megaloblastic anaemia: a cause of syndromic diabetes in childhood. Olsen BS; Hahnemann JM; Schwartz M; Østergaard E Pediatr Diabetes; 2007 Aug; 8(4):239-41. PubMed ID: 17659067 [TBL] [Abstract][Full Text] [Related]
9. Thiamine-responsive megaloblastic anemia syndrome: long term follow-up. Borgna-Pignatti C; Azzalli M; Pedretti S J Pediatr; 2009 Aug; 155(2):295-7. PubMed ID: 19619756 [TBL] [Abstract][Full Text] [Related]
10. Thiamine-responsive megaloblastic anemia: early diagnosis may be effective in preventing deafness. Onal H; Bariş S; Ozdil M; Yeşil G; Altun G; Ozyilmaz I; Aydin A; Celkan T Turk J Pediatr; 2009; 51(3):301-4. PubMed ID: 19817279 [TBL] [Abstract][Full Text] [Related]
11. Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness. Labay V; Raz T; Baron D; Mandel H; Williams H; Barrett T; Szargel R; McDonald L; Shalata A; Nosaka K; Gregory S; Cohen N Nat Genet; 1999 Jul; 22(3):300-4. PubMed ID: 10391221 [TBL] [Abstract][Full Text] [Related]
12. Studies on thiamine metabolism in thiamine-responsive megaloblastic anaemia. Poggi V; Rindi G; Patrini C; De Vizia B; Longo G; Andria G Eur J Pediatr; 1989 Jan; 148(4):307-11. PubMed ID: 2540004 [TBL] [Abstract][Full Text] [Related]
13. Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations. Banka S; de Goede C; Yue WW; Morris AA; von Bremen B; Chandler KE; Feichtinger RG; Hart C; Khan N; Lunzer V; Mataković L; Marquardt T; Makowski C; Prokisch H; Debus O; Nosaka K; Sonwalkar H; Zimmermann FA; Sperl W; Mayr JA Mol Genet Metab; 2014 Dec; 113(4):301-6. PubMed ID: 25458521 [TBL] [Abstract][Full Text] [Related]
14. Thiamine transport by erythrocytes and ghosts in thiamine-responsive megaloblastic anaemia. Rindi G; Casirola D; Poggi V; De Vizia B; Patrini C; Laforenza U J Inherit Metab Dis; 1992; 15(2):231-42. PubMed ID: 1326679 [TBL] [Abstract][Full Text] [Related]