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Three-decade investigation of familial pheochromocytoma. An allele of von Hippel-Lindau disease?
Arch Intern Med. 1993 Nov 22;153(22):2550-6.
Arch Intern Med. 1993.
PMID: 8239848
Familial pheochromocytoma due to mutant von Hippel-Lindau disease gene.
Mulvihill JJ, Ferrell RE, Carty SE, Tisherman SE, Zbar B.
Mulvihill JJ, et al. Among authors: tisherman se.
Arch Intern Med. 1997 Jun 23;157(12):1390-1.
Arch Intern Med. 1997.
PMID: 9201016
No abstract available.
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Genotype-phenotype correlation in von Hippel-Lindau disease: identification of a mutation associated with VHL type 2A.
Chen F, Slife L, Kishida T, Mulvihill J, Tisherman SE, Zbar B.
Chen F, et al. Among authors: tisherman se.
J Med Genet. 1996 Aug;33(8):716-7. doi: 10.1136/jmg.33.8.716.
J Med Genet. 1996.
PMID: 8863170
Free PMC article.
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Familial pheochromocytoma.
TISHERMAN SE, GREGG FJ, DANOWSKI TS.
TISHERMAN SE, et al.
JAMA. 1962 Oct 13;182:152-6. doi: 10.1001/jama.1962.03050410048010.
JAMA. 1962.
PMID: 13985160
No abstract available.
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Pathogenesis and pharmacologic management of pseudo-obstruction of the bowel in pheochromocytoma.
Mullen JP, Cartwright RC, Tisherman SE, Misage JR, Shapiro AP.
Mullen JP, et al. Among authors: tisherman se.
Am J Med Sci. 1985 Oct;290(4):155-8. doi: 10.1097/00000441-198510000-00004.
Am J Med Sci. 1985.
PMID: 2866712
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