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Literature DB >> 20833328

Prologue to the volume: Endocrine tumors and their genetics, a perspective.

Constantine A Stratakis¹.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 2010 PMID： 20833328 PMCID： PMC2939060 DOI： 10.1016/j.beem.2010.07.004

Source DB: PubMed Journal: Best Pract Res Clin Endocrinol Metab ISSN： 1521-690X Impact factor: 4.690

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13 in total

1. Evidence for a 7000-year-old case of primary hyperparathyroidism.

Authors: Albert R Zink; Stephanie Panzer; Martinus Fesq-Martin; Eva Burger-Heinrich; Joachim Wahl; Andreas G Nerlich
Journal: JAMA Date: 2005-01-05 Impact factor: 56.272

2. Multiple endocrine neoplasias in the era of translational medicine.

Authors: C A Stratakis; S J Marx
Journal: Horm Metab Res Date: 2005-06 Impact factor: 2.936

3. Possible case of hyperparathyroidism in a Roman period skeleton from the Dakhleh Oasis, Egypt, diagnosed using bone histomorphometry.

Authors: M Cook; E Molto; C Anderson
Journal: Am J Phys Anthropol Date: 1988-01 Impact factor: 2.868

Review 4. Endocrine tumours in neurofibromatosis type 1, tuberous sclerosis and related syndromes.

Authors: Maya B Lodish; Constantine A Stratakis
Journal: Best Pract Res Clin Endocrinol Metab Date: 2010-06 Impact factor: 4.690

Review 5. SDH-related pheochromocytoma and paraganglioma.

Authors: Vitaly Kantorovich; Kathryn S King; Karel Pacak
Journal: Best Pract Res Clin Endocrinol Metab Date: 2010-06 Impact factor: 4.690

Review 6. MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations.

Authors: Marianthi Georgitsi
Journal: Best Pract Res Clin Endocrinol Metab Date: 2010-06 Impact factor: 4.690

Prologue to the volume: Endocrine tumors and their genetics, a perspective.

1. Evidence for a 7000-year-old case of primary hyperparathyroidism.

2. Multiple endocrine neoplasias in the era of translational medicine.

3. Possible case of hyperparathyroidism in a Roman period skeleton from the Dakhleh Oasis, Egypt, diagnosed using bone histomorphometry.

Review 4. Endocrine tumours in neurofibromatosis type 1, tuberous sclerosis and related syndromes.

Review 5. SDH-related pheochromocytoma and paraganglioma.

Review 6. MEN-4 and other multiple endocrine neoplasias due to cyclin-dependent kinase inhibitors (p27(Kip1) and p18(INK4C)) mutations.

Review 7. Multiple endocrine neoplasia--introduction.

Review 8. Familial multiple endocrine neoplasia: the first 100 years.

9. Evidence of MEN-2 in the original description of classic pheochromocytoma.

Review 10. Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4).