Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India.

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Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India.

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2012 nî lūn-bûn

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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2012年论文

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2012年论文

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Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India.

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Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India.

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Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India.

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P1476

Congenital Hyperferritinemia Diagnosed in A 2 Month Old-A Case Report from India.

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P2093

Joshi Anand Kerketta

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Moushumi Lodh

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P2860

Serum ferritin: Past, present and future

The evaluation of hyperferritinemia: an updated strategy based on advances in detecting genetic abnormalities.

A new missense mutation in the L ferritin coding sequence associated with elevated levels of glycosylated ferritin in serum and absence of iron overload.

Hyperferritinaemia-cataract syndrome: worldwide mutations and phenotype of an increasingly diagnosed genetic disorder.

Hyperferritinemia without iron overload in patients with bilateral cataracts: a case series

A child with hyperferritinemia: case report.

Interpretation of serum ferritin concentrations as indicators of total-body iron stores in survey populations: the role of biomarkers for the acute phase response.

Hereditary Hyperferritinemia-Cataract Syndrome

Hereditary hyperferritinemia-cataract syndrome: relationship between phenotypes and specific mutations in the iron-responsive element of ferritin light-chain mRNA

P304

51-54

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scholarly article

case report

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P577

2012-07-18T00:00:00Z

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27683412

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P921

birth defect

P932

4975243

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