124 related articles for article (PubMed ID: 31714439)
1. Two Novel TMPRSS6 Variants in a Compound Heterozygous Child With Iron Refractory Iron Deficiency Anemia.
Allison J; Drury L; Ford JB
J Pediatr Hematol Oncol; 2020 May; 42(4):e238-e239. PubMed ID: 31714439
[TBL] [Abstract][Full Text] [Related]
2. Iron-refractory iron deficiency anemia (IRIDA) cases with 2 novel TMPRSS6 mutations.
Sal E; Keskin EY; Yenicesu I; Bruno M; De Falco L
Pediatr Hematol Oncol; 2016 Apr; 33(3):226-32. PubMed ID: 27120435
[TBL] [Abstract][Full Text] [Related]
3. Two novel mutations in the tmprss6 gene associated with iron-refractory iron-deficiency anaemia (irida) and partial expression in the heterozygous form.
Pellegrino RM; Coutinho M; D'Ascola D; Lopes AM; Palmieri A; Carnuccio F; Costa M; Zecchina G; Saglio G; Costa E; Barbot J; Porto G; Pinto JP; Roetto A
Br J Haematol; 2012 Sep; 158(5):668-72. PubMed ID: 22765023
[No Abstract] [Full Text] [Related]
4. Iron refractory iron deficiency anemia: presentation with hyperferritinemia and response to oral iron therapy.
Khuong-Quang DA; Schwartzentruber J; Westerman M; Lepage P; Finberg KE; Majewski J; Jabado N
Pediatrics; 2013 Feb; 131(2):e620-5. PubMed ID: 23319530
[TBL] [Abstract][Full Text] [Related]
5. A child with severe iron-deficiency anemia and a complex TMPRSS6 genotype.
Capra AP; Ferro E; Cannavò L; La Rosa MA; Zirilli G
Hematology; 2017 Oct; 22(9):559-564. PubMed ID: 28447549
[TBL] [Abstract][Full Text] [Related]
6. Iron Refractory Iron Deficiency Anemia Due to 374 Base Pairs Deletion in the TMPRSS6 Gene.
Çakmakli S; Acipayam C; Yenmiş İnan MN; Doğan H
J Pediatr Hematol Oncol; 2019 Jul; 41(5):e333-e335. PubMed ID: 30130276
[TBL] [Abstract][Full Text] [Related]
7. The role of TMPRSS6 polymorphisms in iron deficiency anemia partially responsive to oral iron treatment.
Poggiali E; Andreozzi F; Nava I; Consonni D; Graziadei G; Cappellini MD
Am J Hematol; 2015 Apr; 90(4):306-9. PubMed ID: 25557470
[TBL] [Abstract][Full Text] [Related]
8. Two novel mutations in TMPRSS6 associated with iron-refractory iron deficiency anemia in a mother and child.
Yaish HM; Farrell CP; Christensen RD; MacQueen BC; Jackson LK; Trochez-Enciso J; Kaplan J; Ward DM; Salah WK; Phillips JD
Blood Cells Mol Dis; 2017 Jun; 65():38-40. PubMed ID: 28460265
[TBL] [Abstract][Full Text] [Related]
9. Responsiveness to oral iron and ascorbic acid in a patient with IRIDA.
Cau M; Galanello R; Giagu N; Melis MA
Blood Cells Mol Dis; 2012 Feb; 48(2):121-3. PubMed ID: 22169218
[TBL] [Abstract][Full Text] [Related]
10. Novel mutation in the TMPRSS6 gene with iron-refractory iron deficiency anemia.
Kodama K; Noguchi A; Adachi H; Hebiguchi M; Yano M; Takahashi T
Pediatr Int; 2014 Aug; 56(4):e41-4. PubMed ID: 25252070
[TBL] [Abstract][Full Text] [Related]
11. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA).
Finberg KE; Heeney MM; Campagna DR; Aydinok Y; Pearson HA; Hartman KR; Mayo MM; Samuel SM; Strouse JJ; Markianos K; Andrews NC; Fleming MD
Nat Genet; 2008 May; 40(5):569-71. PubMed ID: 18408718
[TBL] [Abstract][Full Text] [Related]
12. Microcytic anaemia with low transferrin saturation, increased serum hepcidin and non-synonymous TMPRSS6 variants: not always iron-refractory iron deficiency anaemia.
Donker AE; Brons PP; Swinkels DW
Br J Haematol; 2015 Apr; 169(1):150-1. PubMed ID: 25312922
[No Abstract] [Full Text] [Related]
13. Iron Refractory Iron Deficiency Anaemia: A Rare Cause of Iron Deficiency Anaemia.
McGrath T; Cotter M
Ir Med J; 2018 Jan; 111(1):678. PubMed ID: 29869859
[TBL] [Abstract][Full Text] [Related]
14. A novel splicing mutation of TMPRSS6 in a Chinese child with iron-refractory iron deficiency anaemia.
Xiong Y; Wu Z; Yang W; Zhao X; Peng G; Tang K; Tian Z; Xing H; Rao Q; Wang M; Wang J; Zhang F
Br J Haematol; 2015 Nov; 171(4):647-9. PubMed ID: 25873000
[No Abstract] [Full Text] [Related]
15. Is the acronym IRIDA acceptable for slow responders to iron in the presence of TMPRSS6 mutations?
Yilmaz-Keskin E; Sal E; de Falco L; Bruno M; Iolascon A; Koçak U; Yenicesu I
Turk J Pediatr; 2013; 55(5):479-84. PubMed ID: 24382527
[TBL] [Abstract][Full Text] [Related]
16. Novel missense mutation in the TMPRSS6 gene in a Japanese female with iron-refractory iron deficiency anemia.
Sato T; Iyama S; Murase K; Kamihara Y; Ono K; Kikuchi S; Takada K; Miyanishi K; Sato Y; Takimoto R; Kobune M; Kato J
Int J Hematol; 2011 Jul; 94(1):101-103. PubMed ID: 21643693
[TBL] [Abstract][Full Text] [Related]
17. Functional and clinical impact of novel TMPRSS6 variants in iron-refractory iron-deficiency anemia patients and genotype-phenotype studies.
De Falco L; Silvestri L; Kannengiesser C; Morán E; Oudin C; Rausa M; Bruno M; Aranda J; Argiles B; Yenicesu I; Falcon-Rodriguez M; Yilmaz-Keskin E; Kocak U; Beaumont C; Camaschella C; Iolascon A; Grandchamp B; Sanchez M
Hum Mutat; 2014 Nov; 35(11):1321-9. PubMed ID: 25156943
[TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the CUB sequence of matriptase-2 (TMPRSS6) is implicated in iron-resistant iron deficiency anaemia (IRIDA).
Jaspers A; Caers J; Le Gac G; Ferec C; Beguin Y; Fillet G
Br J Haematol; 2013 Feb; 160(4):564-5. PubMed ID: 23216605
[No Abstract] [Full Text] [Related]
19. A novel homozygous nonsense mutation (p.Y78*) in TMPRSS6 gene causing iron-refractory iron deficiency anemia (IRIDA) in two siblings.
Çakmaklı S; Kaplan Ç; Uzunoğlu M; Büyükbayram M; Görgülü E; Zarif NÖ; Keskin EY
Turk J Pediatr; 2020; 62(1):103-108. PubMed ID: 32253873
[TBL] [Abstract][Full Text] [Related]
20. A mutation in the TMPRSS6 gene, encoding a transmembrane serine protease that suppresses hepcidin production, in familial iron deficiency anemia refractory to oral iron.
Melis MA; Cau M; Congiu R; Sole G; Barella S; Cao A; Westerman M; Cazzola M; Galanello R
Haematologica; 2008 Oct; 93(10):1473-9. PubMed ID: 18603562
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
