Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.

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Iron metabolism in erythroid cells and patients with congenital sideroblastic anemia.How Surrogate and Chemical Genetics in Model Organisms Can Suggest Therapies for Human Genetic Diseases.

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Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Study of Glycine and Folic Aci ...... Mutated Sideroblastic Anemia.

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Amanda Bettle

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Chantale Pambrun

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Christopher R McMaster

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Conrad V Fernandez

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Jason N Berman

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Marilyn Tiller

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Marissa A LeBlanc

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Victoria E Price

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Zhijie Yu

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P2860

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Molecular basis of inherited microcytic anemia due to defects in iron acquisition or heme synthesis

Erythroid heme biosynthesis and its disorders

Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia

Pyridoxine-refractory congenital sideroblastic anaemia with evidence for autosomal inheritance: exclusion of linkage to ALAS2 at Xp11.21 by polymorphism analysis.

Efficacy of high-dose glycine in the treatment of enduring negative symptoms of schizophrenia.

Hereditary sideroblastic anemias: pathophysiology, diagnosis, and treatment.

Compartmentalization of Mammalian folate-mediated one-carbon metabolism.

Beneficial effects of L-serine and glycine in the management of seizures in 3-phosphoglycerate dehydrogenase deficiency.

Isovaleric acidemia: response to a leucine load after three weeks of supplementation with glycine, L-carnitine, and combined glycine-carnitine therapy.

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Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.

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P2860

P2860

Study of Glycine and Folic Acid Supplementation to Ameliorate Transfusion Dependence in Congenital SLC25A38 Mutated Sideroblastic Anemia.

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