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Literature DB >> 16790714

Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma.

Birke Bausch, Wiktor Borozdin, Hartmut P H Neumann.

Abstract

Entities: Disease Gene Species

Mesh：

Year: 2006 PMID： 16790714 DOI： 10.1056/NEJMc066006

Source DB: PubMed Journal: N Engl J Med ISSN： 0028-4793 Impact factor: 91.245

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41 in total

Review 1. An update on the genetics of pheochromocytoma.

Authors: D Karasek; U Shah; Z Frysak; C Stratakis; K Pacak
Journal: J Hum Hypertens Date: 2012-05-31 Impact factor: 3.012

2. High prevalence of elevated blood pressure among children with neurofibromatosis type 1.

Authors: Tom Dubov; Hagit Toledano-Alhadef; Gil Chernin; Shlomi Constantini; Roxana Cleper; Shay Ben-Shachar
Journal: Pediatr Nephrol Date: 2015-08-28 Impact factor: 3.714

Review 3. Pheochromocytoma/Paraganglioma: Is This a Genetic Disorder?

Authors: Lauren Fishbein
Journal: Curr Cardiol Rep Date: 2019-07-31 Impact factor: 2.931

Review 4. Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.

Authors: Lauren Fishbein; Katherine L Nathanson
Journal: Cancer Genet Date: 2012 Jan-Feb

5. Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas.

Authors: Johan Kugelberg; Jenny Welander; Francesca Schiavi; Ambrogio Fassina; Martin Bäckdahl; Catharina Larsson; Giuseppe Opocher; Peter Söderkvist; Patricia L Dahia; Hartmut P H Neumann; Oliver Gimm
Journal: World J Surg Date: 2014-03 Impact factor: 3.352

Review 6. Mosaic RASopathies.

Authors: Christian Hafner; Leopold Groesser
Journal: Cell Cycle Date: 2012-12-19 Impact factor: 4.534

Clinical and genetic characteristics of patients with neurofibromatosis type 1 and pheochromocytoma.

Review 1. An update on the genetics of pheochromocytoma.

2. High prevalence of elevated blood pressure among children with neurofibromatosis type 1.

Review 3. Pheochromocytoma/Paraganglioma: Is This a Genetic Disorder?

Review 4. Pheochromocytoma and paraganglioma: understanding the complexities of the genetic background.

5. Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas.

Review 6. Mosaic RASopathies.

Review 7. [Adrenalectomy for preservation of adrenocortical function. Indication and results].

8. Copy number variations and cancer.

Review 9. Update on the management of familial central nervous system tumor syndromes.

Review 10. [Pheochromocytoma - still a challenge].