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Aceruloplasminemia - Durga Kumawat - Bog

Bag om Aceruloplasminemia

"Aceruloplasminemia: Understanding the Rare Genetic Disorder" is an informative and insightful book that delves into the complex world of a rare genetic disorder that affects iron metabolism and can lead to neurodegeneration. This comprehensive guide provides an in-depth understanding of the clinical manifestations, biochemical features, genetic variants, and advanced imaging techniques used for diagnosis. The book also explores the mechanisms of iron-induced neurotoxicity and the role of ceruloplasmin in iron metabolism. This book is an invaluable resource for researchers, clinicians, and patients alike, providing a thorough understanding of the disease and its impact on the global population. With its concise yet comprehensive coverage of the subject matter, this book is sure to be a must-read for anyone seeking to deepen their knowledge of this rare genetic disorder.

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  • Sprog:
  • Engelsk
  • ISBN:
  • 9789357333450
  • Indbinding:
  • Paperback
  • Sideantal:
  • 176
  • Udgivet:
  • 6. juni 2023
  • Størrelse:
  • 152x10x229 mm.
  • Vægt:
  • 265 g.
  • 2-3 uger.
  • 9. december 2024
På lager

Normalpris

  • BLACK NOVEMBER

Medlemspris

Prøv i 30 dage for 45 kr.
Herefter fra 79 kr./md. Ingen binding.

Beskrivelse af Aceruloplasminemia

"Aceruloplasminemia: Understanding the Rare Genetic Disorder" is an informative and insightful book that delves into the complex world of a rare genetic disorder that affects iron metabolism and can lead to neurodegeneration. This comprehensive guide provides an in-depth understanding of the clinical manifestations, biochemical features, genetic variants, and advanced imaging techniques used for diagnosis. The book also explores the mechanisms of iron-induced neurotoxicity and the role of ceruloplasmin in iron metabolism. This book is an invaluable resource for researchers, clinicians, and patients alike, providing a thorough understanding of the disease and its impact on the global population. With its concise yet comprehensive coverage of the subject matter, this book is sure to be a must-read for anyone seeking to deepen their knowledge of this rare genetic disorder.

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