Bilateral recurrent phaeochromocytoma associated with a growth hormone- secreting pituitary tumour

British Journal of Surgery

Volumn 83, Issue 8, 1996, Pages 1132-

  Teh, B T ^a,b   Hansen, J ^a   Svensson, P J ^b   Hartley, L ^a  

^a PRINCESS ALEXANDRA HOSPITAL   (Australia)

^b KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

BIGUANIDE DERIVATIVE; GROWTH HORMONE;

ADRENALECTOMY; ADULT; ARTICLE; CASE REPORT; DISEASE ASSOCIATION; EXON; HUMAN; HYPOPHYSECTOMY; HYPOPHYSIS TUMOR; MALE; PHEOCHROMOCYTOMA; PRIORITY JOURNAL; PROTO ONCOGENE; RECURRENT DISEASE; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0029766137     PISSN: 00071323     EISSN: None     Source Type: Journal    
DOI: 10.1002/bjs.1800830832     Document Type: Article

References (5)

1. Lips CJM, Vasen HFA, Lamers CBHW. Multiple endocrine neoplasia syndromes. Crit Rev Oncol Hematol 1984; 2: 117-84.
2. Mulligan LM, Marsh DJ, Robinson BG et al. Genotype-phenotype correlation in multiple endocrine neoplasia 2: report of the International RET Mutation Consortium. J Intern Met 1995; 238: 343-6.
3. Larsson C, Skogseid B, Oberg K, Nakamura Y, Nordenskjöld M. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 1988; 332: 85-7.
4. Lips CJM, Landsvater RM, Höppener JWM et al. Clinical screening as compared with DNA analysis in families with multiple endocrine neoplasia type 2A. N Engl J Med 1994; 331: 828-35.
5. Wells SA Jr, Chi DD, Toshima K et al. Predictive DNA testing and prophylactic thyroidectomy in patients at risk for multiple endocrine neoplasia type 2A. Ann Surg 1994; 220: 237-50.