-
1
-
-
0023828816
-
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
-
Larsson C, Skogseid B, Oberg K, Nakamura Y, Nordenskjold M. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature 1988; 332: 85.
-
(1988)
Nature
, vol.332
, pp. 85
-
-
Larsson, C.1
Skogseid, B.2
Oberg, K.3
Nakamura, Y.4
Nordenskjold, M.5
-
2
-
-
0028170327
-
The phospholipase Cβ3 gene allocated in the MEN1 region shows loss of expression in endocrine tumours
-
Weber G, Friedman E, Grimond S et al. The phospholipase Cβ3 gene allocated in the MEN1 region shows loss of expression in endocrine tumours. Human Molec. Gen. 1994; 3: 1775-81.
-
(1994)
Human Molec. Gen.
, vol.3
, pp. 1775-1781
-
-
Weber, G.1
Friedman, E.2
Grimond, S.3
-
3
-
-
0024853151
-
Screening for the Multiple Endocrine Neoplasia Syndrome Type I
-
Vasen HFA, Lamers CBHW, Lips CJM. Screening for the Multiple Endocrine Neoplasia Syndrome Type I. Arch. Int. Med. 1989; 149: 2712-22.
-
(1989)
Arch. Int. Med.
, vol.149
, pp. 2712-2722
-
-
Vasen, H.F.A.1
Lamers, C.B.H.W.2
Lips, C.J.M.3
-
4
-
-
0021814901
-
Latent familial multiple endocrine neoplasia in Tasmania
-
Shepherd JJ. Latent familial multiple endocrine neoplasia in Tasmania. Med. J. Aust. 1985; 142: 395-7.
-
(1985)
Med. J. Aust.
, vol.142
, pp. 395-397
-
-
Shepherd, J.J.1
-
5
-
-
0026394553
-
The natural history of Multiple Endocrine Neoplasia Type 1. Highly uncommon or highly unrecognized
-
Shepherd JJ. The natural history of Multiple Endocrine Neoplasia Type 1. Highly uncommon or highly unrecognized. Arch. Surg. 1991; 126: 935-52.
-
(1991)
Arch. Surg.
, vol.126
, pp. 935-952
-
-
Shepherd, J.J.1
-
6
-
-
0024422566
-
Hypercalcemia in the multiple endocrine neoplasia syndromes
-
Fitzpatrick LA. Hypercalcemia in the multiple endocrine neoplasia syndromes. Endo. Met. Clin. N. Amer. 1989; 18: 741-52.
-
(1989)
Endo. Met. Clin. N. Amer.
, vol.18
, pp. 741-752
-
-
Fitzpatrick, L.A.1
-
7
-
-
0015258396
-
Five families with multiple endocrine adenomatosis
-
Snyder N, Scurry MT, Deiss WP. Five families with multiple endocrine adenomatosis. Ann. Int. Med. 1972; 76: 53-8.
-
(1972)
Ann. Int. Med.
, vol.76
, pp. 53-58
-
-
Snyder, N.1
Scurry, M.T.2
Deiss, W.P.3
-
9
-
-
1542574823
-
Pluriglandular syndrome
-
Berdjis CC. Pluriglandular syndrome. Oncologia 1962; 15: 288-311.
-
(1962)
Oncologia
, vol.15
, pp. 288-311
-
-
Berdjis, C.C.1
-
10
-
-
0018918911
-
Primary hyperparathyroidism - Incidence, morbidity, and potential economic impact in a community
-
Heath H, Hodgson SF, Kennedy MA. Primary hyperparathyroidism - Incidence, morbidity, and potential economic impact in a community. N. Engl. J. Med. 1980; 302: 189-93.
-
(1980)
N. Engl. J. Med.
, vol.302
, pp. 189-193
-
-
Heath, H.1
Hodgson, S.F.2
Kennedy, M.A.3
-
11
-
-
0015060986
-
Serum calcium: Survey for hyperparathyroidism: Results in 50 000 clinic patients
-
Boonstra CE, Jackson CE. Serum calcium: Survey for hyperparathyroidism: Results in 50 000 clinic patients. Am. J. Clin. Pathol. 1971; 55: 523-6.
-
(1971)
Am. J. Clin. Pathol.
, vol.55
, pp. 523-526
-
-
Boonstra, C.E.1
Jackson, C.E.2
-
13
-
-
0025372687
-
Clonal loss of Int-2 alleles in sporadic and familial pancreatic endocrine tumours
-
Teh BT, Hayward NK, Wilkinson S, Woods GM, Cameron D, Shepherd JJ. Clonal loss of Int-2 alleles in sporadic and familial pancreatic endocrine tumours. Br. J. Cancer 1990; 62: 253-4.
-
(1990)
Br. J. Cancer
, vol.62
, pp. 253-254
-
-
Teh, B.T.1
Hayward, N.K.2
Wilkinson, S.3
Woods, G.M.4
Cameron, D.5
Shepherd, J.J.6
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