V Nunziata, R Giannattasio, G Di Giovanni, MR … - Clin …, 1989 - interscience.wiley.com We describe a kindred with medullary thyroid carcinoma and phaeochromocy-toma (MEN 2A
or Sipple's syndrome) in which a cutaneous manifestation is only present in affected
members. These members felt an intense itching in an area 5–10 cm in length and ... Cited by 48 - Related articles - All 3 versions
MF Robinson, EJ Furst, V Nunziata, ML … - Henry Ford Hospital …, 1992 - be-md.ncbi.nlm.nih.gov The hereditary conditions of primary cutaneous lichen amyloidosis and multiple endocrine neoplasia
type 2 (MEN 2) are rare clinical entities. The initial reports of two families in which the two conditions
coincided have led to the identification of at least eight additional families with this clinical ... Cited by 25 - Related articles - BL Direct - All 2 versions
I Ceccherini, C Romei, V Barone, F Pacini, E … - Journal of …, 1994 - cat.inist.fr Identification of the Cys 634 →Tyr mutation of the RET proto-oncogene in a pedigree
with multiple endocrine neoplasia type 2 A and localized cutaneous lichen
amyloidosis. I CECCHERINI, C ROMEI, V BARONE, F PACINI, E ... Cited by 36 - Related articles - BL Direct - All 3 versions
BG Kousseff, C Espinoza, GA Zamore - Journal of the American Academy of …, 1991 - Elsevier A five-generation white family with multiple endocrine neoplasia type 2A had six affected
members. Two, a mother and her daughter, had interscapular cutaneous pruritic lesions resembling
macular/lichen amyloidosis. In the daughter, light microscopy showed homogeneous ... Cited by 17 - Related articles - All 5 versions
M Verdy, AM Weber, CC Roy, CL Morin, M … - Journal of pediatric …, 1982 - journals.lww.com Journal oi " ' onittfttitfiolitxv orni Nutrition к''ч'п I'rcss. New York Case Report Hirschsprung's Disease
in a Family with Multiple Endocrine Neoplasia Type 2 Maurice Verdy, Andrée M. Weber, Claude
С Roy, Claude L. Morin, Marcel Cadotte, and Pierre Brochu Departements Je Médecine, ... Cited by 61 - Related articles - All 4 versions
V Nunziata, G Di Giovanni, AM Lettera, M D' … - Henry Ford Hospital …, 1989 - ncbi.nlm.nih.gov We have previously described a kindred with hereditary medullary thyroid carcinoma and pheochromocytoma
(multiple endocrine neoplasia type 2A [MEN 2A]) with localized pruritic cutaneous manifestations
present only in affected members. Although the initial skin biopsies reported did not show ... Cited by 21 - Related articles
JR Farndon, GS Leight, WG Dilley, SB Baylin, RC … - Br J Surg, 1986 - interscience.wiley.com In an evaluation of 213 patients from 15 kindreds with familial medullary thyroid carcinoma
(MTC), we detected 41 subjects from two kindreds (L and O) who had MTC but no extra-thyroidal
manifestations (hyperparathyroidism, phaeochromocytomas or mucosal neuromas) of ... Cited by 172 - Related articles - All 4 versions
A Bolino, I Schuffenecker, Y Luo, M Seri, M Silengo, T … - Oncogene, 1995 - ncbi.nlm.nih.gov RET is a receptor tyrosine kinase gene which is responsible for three different inherited cancer
syndromes namely multiple endocrine neoplasia type 2A (MEN 2A), type 2B (MEN 2B) and familial
medullary thyroid carcinoma (FMTC) as well as for Hirschsprung disease (HSCR), a ... Cited by 180 - Related articles - BL Direct - All 3 versions
BAJ Ponder, R Coffey, RF Gagel, P Semple, MA … - The Lancet, 1988 - Elsevier Many gene carriers for multiple endocrine neoplasia type 2a (MEN 2a) do not manifest the
disease, even into old age. Thus, a negative family history in a patient presenting with medullary
thyroid carcinoma does not reliably exclude familial disease. Data are reported for the ... Cited by 117 - Related articles - All 7 versions
