170 related articles for article (PubMed ID: 24355766)
21. Thiamine Responsive Megaloblastic Anaemia, Diabetes Mellitus and Sensorineural Hearing Loss in a Child.
Khurshid A; Fatimah S; Altaf C; Malik HS; Sajjad Z; Khadim MT
J Coll Physicians Surg Pak; 2018 Sep; 28(9):S169-S171. PubMed ID: 30173687
[TBL] [Abstract][Full Text] [Related]
22. TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case report.
Li X; Cheng Q; Ding Y; Li Q; Yao R; Wang J; Wang X
BMC Pediatr; 2019 Jul; 19(1):233. PubMed ID: 31296181
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. 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]
26. 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]
27. Novel nonsense mutation (p.Ile411Metfs*12) in the SLC19A2 gene causing Thiamine Responsive Megaloblastic Anemia in an Indian patient.
Manimaran P; Subramanian VS; Karthi S; Gandhimathi K; Varalakshmi P; Ganesh R; Rathinavel A; Said HM; Ashokkumar B
Clin Chim Acta; 2016 Jan; 452():44-9. PubMed ID: 26549656
[TBL] [Abstract][Full Text] [Related]
28. A Novel Mutation of SLC19A2 in a Chinese Zhuang Ethnic Family with Thiamine-Responsive Megaloblastic Anemia.
Xian X; Liao L; Shu W; Li H; Qin Y; Yan J; Luo J; Lin FQ
Cell Physiol Biochem; 2018; 47(5):1989-1997. PubMed ID: 29969779
[TBL] [Abstract][Full Text] [Related]
29. Thiamine responsive megaloblastic anemia.
Mathews L; Narayanadas K; Sunil G
Indian Pediatr; 2009 Feb; 46(2):172-4. PubMed ID: 19242038
[TBL] [Abstract][Full Text] [Related]
30. Identification of novel compound heterozygous variants in SLC19A2 and the genotype-phenotype associations in thiamine-responsive megaloblastic anemia.
Zhang S; Qiao Y; Wang Z; Zhuang J; Sun Y; Shang X; Li G
Clin Chim Acta; 2021 May; 516():157-168. PubMed ID: 33571483
[TBL] [Abstract][Full Text] [Related]
31. [Thiamine-responsive megaloblastic anemia or Rogers syndrome: A literature review].
Lu H; Lu H; Vaucher J; Tran C; Vollenweider P; Castioni J
Rev Med Interne; 2019 Jan; 40(1):20-27. PubMed ID: 30031565
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Thiamine-responsive megaloblastic anemia syndrome.
Bay A; Keskin M; Hizli S; Uygun H; Dai A; Gumruk F
Int J Hematol; 2010 Oct; 92(3):524-6. PubMed ID: 20835854
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia.
Shaw-Smith C; Flanagan SE; Patch AM; Grulich-Henn J; Habeb AM; Hussain K; Pomahacova R; Matyka K; Abdullah M; Hattersley AT; Ellard S
Pediatr Diabetes; 2012 Jun; 13(4):314-21. PubMed ID: 22369132
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Thiamine responsive megaloblastic anemia: the puzzling phenotype.
Beshlawi I; Al Zadjali S; Bashir W; Elshinawy M; Alrawas A; Wali Y
Pediatr Blood Cancer; 2014 Mar; 61(3):528-31. PubMed ID: 24249281
[TBL] [Abstract][Full Text] [Related]
38. Leber congenital amaurosis as an initial manifestation in a Chinese patient with thiamine-responsive megaloblastic anemia syndrome.
Wu S; Yuan Z; Sun Z; Yao F; Sui R
Am J Med Genet A; 2022 Mar; 188(3):948-952. PubMed ID: 34821467
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine-responsive megaloblastic anemia in an Egyptian family.
Amr K; Pawlikowska P; Aoufouchi S; Rosselli F; El-Kamah G
Mol Genet Genomic Med; 2019 Jul; 7(7):e00777. PubMed ID: 31144472
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
