280,88 €
312,09 €
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Pheochromocytoma, Paraganglioma and Neuroblastoma
Pheochromocytoma, Paraganglioma and Neuroblastoma
280,88
312,09 €
  • We will send in 10–14 business days.
Pheochromocytoma, paraganglioma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. These neoplasms are associated with significant morbidity and mortality. Some international studies currently underway are researching and evaluating the presence of any similarities and differences between these tumors. Hopefully, future results will reveal several potential novel genes and pathways that might have major roles in the pathogenesis and progressi…
  • Publisher:
  • Year: 2021
  • Pages: 130
  • ISBN-10: 1839689471
  • ISBN-13: 9781839689475
  • Format: 17 x 24.4 x 1 cm, hardcover
  • Language: English
  • SAVE -10% with code: EXTRA

Pheochromocytoma, Paraganglioma and Neuroblastoma (e-book) (used book) | bookbook.eu

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Pheochromocytoma, paraganglioma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. These neoplasms are associated with significant morbidity and mortality. Some international studies currently underway are researching and evaluating the presence of any similarities and differences between these tumors. Hopefully, future results will reveal several potential novel genes and pathways that might have major roles in the pathogenesis and progression of these neoplasms. This book discusses epidemiology, genetics, and treatment of these malignancies.

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  • Publisher:
  • Year: 2021
  • Pages: 130
  • ISBN-10: 1839689471
  • ISBN-13: 9781839689475
  • Format: 17 x 24.4 x 1 cm, hardcover
  • Language: English English

Pheochromocytoma, paraganglioma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. These neoplasms are associated with significant morbidity and mortality. Some international studies currently underway are researching and evaluating the presence of any similarities and differences between these tumors. Hopefully, future results will reveal several potential novel genes and pathways that might have major roles in the pathogenesis and progression of these neoplasms. This book discusses epidemiology, genetics, and treatment of these malignancies.

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