Literature DB >> 13811705

Peculiar familial and malignant pheochromocytomas of the organs of Zuckerkandl.

J E COOK, R W URICH, H G SAMPLE, N W FAWCETT.   

Abstract

Entities:  

Keywords:  PARAGANGLIOMA/case reports

Mesh:

Year:  1960        PMID: 13811705     DOI: 10.7326/0003-4819-52-1-126

Source DB:  PubMed          Journal:  Ann Intern Med        ISSN: 0003-4819            Impact factor:   25.391


× No keyword cloud information.
  5 in total

1.  SECRETING TUMORS OF CHROMAFFIN TISSUE.

Authors:  G D HUEBNER; P A REED
Journal:  Ann Surg       Date:  1963-08       Impact factor: 12.969

2.  [The pheochromocytoma as a dominant hereditary dysgenetic tumor].

Authors:  C von DOEPP
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1962

3.  [Pulmonary artery pressure in a clinical case of pheochromyocytoma].

Authors:  F H Degenring; B May
Journal:  Klin Wochenschr       Date:  1970-04-15

4.  Functional tumors of the organ of Zuckerkandl.

Authors:  F Glenn; G F Gray
Journal:  Ann Surg       Date:  1976-05       Impact factor: 12.969

5.  Functionless non-chromaffin retroperitoneal paraganglioma causing cauda equina compression.

Authors:  P Ciappetta; G Perrino; M Albrizio
Journal:  Acta Neurochir (Wien)       Date:  1980       Impact factor: 2.216

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.