161 related articles for article (PubMed ID: 22576805)
41. The spectrum of mutations, including four novel ones, in the thiamine-responsive megaloblastic anemia gene SLC19A2 of eight families.
Raz T; Labay V; Baron D; Szargel R; Anbinder Y; Barrett T; Rabl W; Viana MB; Mandel H; Baruchel A; Cayuela JM; Cohen N
Hum Mutat; 2000; 16(1):37-42. PubMed ID: 10874303
[TBL] [Abstract][Full Text] [Related]
42. An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment.
Di Candia F; Di Iorio V; Tinto N; Bonfanti R; Iovino C; Rosanio FM; Fedi L; Iafusco F; Arrigoni F; Malesci R; Simonelli F; Rigamonti A; Franzese A; Mozzillo E
Ital J Pediatr; 2023 Nov; 49(1):158. PubMed ID: 38037112
[TBL] [Abstract][Full Text] [Related]
43. Thiamine responsive megaloblastic anemia in three Indian children.
Raju K N Gowda V; Shivananda GM; Sankhyan N
Indian J Pediatr; 2011 Jul; 78(7):888-9. PubMed ID: 21340725
[No Abstract] [Full Text] [Related]
44. 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]
45. Does early treatment prevent deafness in thiamine-responsive megaloblastic anaemia syndrome?
Akın L; Kurtoğlu S; Kendirci M; Akın MA; Karakükçü M
J Clin Res Pediatr Endocrinol; 2011; 3(1):36-9. PubMed ID: 21448333
[TBL] [Abstract][Full Text] [Related]
46. Loss-of-Function Mutation in Thiamine Transporter 1 in a Family With Autosomal Dominant Diabetes.
Jungtrakoon P; Shirakawa J; Buranasupkajorn P; Gupta MK; De Jesus DF; Pezzolesi MG; Panya A; Hastings T; Chanprasert C; Mendonca C; Kulkarni RN; Doria A
Diabetes; 2019 May; 68(5):1084-1093. PubMed ID: 30833467
[TBL] [Abstract][Full Text] [Related]
47. Cochlear implant and thiamine-responsive megaloblastic anemia syndrome.
Hagr AA
Ann Saudi Med; 2014; 34(1):78-80. PubMed ID: 24658560
[TBL] [Abstract][Full Text] [Related]
48. 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]
49. Arrhythmia in thiamine responsive megaloblastic anemia syndrome.
Argun M; Baykan A; Hatipoğlu N; Akın L; Şahin Y; Narin N; Kurtoğlu S
Turk J Pediatr; 2018; 60(3):348-351. PubMed ID: 30511554
[TBL] [Abstract][Full Text] [Related]
50. Thiamine-responsive megaloblastic anaemia.
Veetil VM; Pachat D; Nikitha K; Kutty JM
Natl Med J India; 2023; 36(5):314-315. PubMed ID: 38759983
[TBL] [Abstract][Full Text] [Related]
51. Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome.
Diaz GA; Banikazemi M; Oishi K; Desnick RJ; Gelb BD
Nat Genet; 1999 Jul; 22(3):309-12. PubMed ID: 10391223
[TBL] [Abstract][Full Text] [Related]
52. 50 Years Ago in The Journal of Pediatrics: Thiamine-Responsive Megaloblastic Anemia.
Mullikin D; Grimes AB
J Pediatr; 2019 Apr; 207():53. PubMed ID: 30922504
[No Abstract] [Full Text] [Related]
53. Thiamine transporter mutation: an example of monogenic diabetes mellitus.
Alzahrani AS; Baitei E; Zou M; Shi Y
Eur J Endocrinol; 2006 Dec; 155(6):787-92. PubMed ID: 17132746
[TBL] [Abstract][Full Text] [Related]
54. Thiamine responsive megaloblastic anemia syndrome.
Ganesh R; Ezhilarasi S; Vasanthi T; Gowrishankar K; Rajajee S
Indian J Pediatr; 2009 Mar; 76(3):313-4. PubMed ID: 19347672
[TBL] [Abstract][Full Text] [Related]
55. Thiamine-responsive megaloblastic anaemia syndrome: long-term follow-up and mutation analysis of seven families.
Ricketts CJ; Minton JA; Samuel J; Ariyawansa I; Wales JK; Lo IF; Barrett TG
Acta Paediatr; 2006 Jan; 95(1):99-104. PubMed ID: 16373304
[TBL] [Abstract][Full Text] [Related]
56. Thiamine-responsive megaloblastic anemia syndrome: a disorder of high-affinity thiamine transport.
Neufeld EJ; Fleming JC; Tartaglini E; Steinkamp MP
Blood Cells Mol Dis; 2001; 27(1):135-8. PubMed ID: 11358373
[TBL] [Abstract][Full Text] [Related]
57. Diabetes mellitus, thiamine-dependent megaloblastic anemia, and sensorineural deafness associated with deficient alpha-ketoglutarate dehydrogenase activity.
Abboud MR; Alexander D; Najjar SS
J Pediatr; 1985 Oct; 107(4):537-41. PubMed ID: 4045602
[TBL] [Abstract][Full Text] [Related]
58. Male infertility and thiamine-dependent erythroid hypoplasia in mice lacking thiamine transporter Slc19a2.
Fleming JC; Tartaglini E; Kawatsuji R; Yao D; Fujiwara Y; Bednarski JJ; Fleming MD; Neufeld EJ
Mol Genet Metab; 2003; 80(1-2):234-41. PubMed ID: 14567973
[TBL] [Abstract][Full Text] [Related]
59. Rare case with megaloblastic anaemia.
Saleem M; Shah SS; Mehmood T
J Ayub Med Coll Abbottabad; 2014; 26(1):104-5. PubMed ID: 25358233
[TBL] [Abstract][Full Text] [Related]
60. Monogenic diabetes syndromes: Locus-specific databases for Alström, Wolfram, and Thiamine-responsive megaloblastic anemia.
Astuti D; Sabir A; Fulton P; Zatyka M; Williams D; Hardy C; Milan G; Favaretto F; Yu-Wai-Man P; Rohayem J; López de Heredia M; Hershey T; Tranebjaerg L; Chen JH; Chaussenot A; Nunes V; Marshall B; McAfferty S; Tillmann V; Maffei P; Paquis-Flucklinger V; Geberhiwot T; Mlynarski W; Parkinson K; Picard V; Bueno GE; Dias R; Arnold A; Richens C; Paisey R; Urano F; Semple R; Sinnott R; Barrett TG
Hum Mutat; 2017 Jul; 38(7):764-777. PubMed ID: 28432734
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]