Mutation of a Putative Mitochondrial Iron Transporter Gene (ABC7) in X-Linked Sideroblastic Anemia and Ataxia (XLSA/A) [PDF]
, 1999 Rando Allikmets +5 more
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Cloning and chromosomal mapping of a novel ABC transporter gene (hABC7), a candidate for X-linked sideroblastic anemia with spinocerebellar ataxia [PDF]
, 1998 Yoshikazu Shimada +11 more
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A novel mutation of the erythroid-specific ?-aminolevulinate synthase gene in a patient with non-inherited pyridoxine-responsive sideroblastic anemia [PDF]
, 1999 Hideo Harigae +6 more
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Red cell aspartate aminotransferase saturation with oral pyridoxine intake
São Paulo Medical JournalCONTEXT AND OBJECTIVE: The coenzyme of aspartate aminotransferase is pyridoxal phosphate, generated from fresh vegetables containing pyridoxine. Vitamin B6-responsive sideroblastic anemia, myelofibrosis and Peyronie’s syndrome respond to high pyridoxine ...
Marilena Oshiro +3 more
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先天性鉄芽球性貧血の原因遺伝子の同定及びin vitroでの鉄芽球の解析 [PDF]
, 2010 平成11年度-平成13年度科学研究費補助金(基盤研究(C)(2))研究成果報告書,課題番号 ...
張替 秀郎
core +1 more source
Interaction between succinyl CoA synthetase and the heme-biosynthetic enzyme ALAS-E is disrupted in sideroblastic anemia [PDF]
, 2000 Kazumichi Furuyama, Shigeru Sassa
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Abnormalities of flavin monooxygenase as an etiology for sideroblastic anemia [PDF]
, 2000 Matthew Barber +4 more
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Case report of sideroblastic anemia caused by ingestion of coins [PDF]
, 2001 Ashok Kumar, Abdul Rahman Jazieh
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Clinical Immunology CommunicationsSyndrome of Congenital Sideroblastic Anemia, B-cell Immunodeficiency, Periodic Fevers, and Developmental Delay (SIFD) is caused by mutations in the tRNA nucleotidyltransferase 1 (TRNT1) gene.
Amer Khojah +5 more
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