-
1
-
-
0002541264
-
MEN I pathology and pathophysiology
-
Bi-Iczikian JP, Marcus R, Levine MA (eds), New York, Raven Press
-
Friedman E, Larsson C, Amorosi A, Brandi ML, Metz D, Jensen RT, Bale A, Skarulis MC, Eastman R, Nieman L, Norton J, Marx SJ: MEN I pathology and pathophysiology: in Bi-Iczikian JP, Marcus R, Levine MA (eds): The Parathyroids, Basic and Clinical Concepts, New York, Raven Press, 1994, voi 38, pp 647-680.
-
(1994)
The Parathyroids, Basic and Clinical Concepts
, vol.38
, pp. 647-680
-
-
Friedman, E.1
Larsson, C.2
Amorosi, A.3
Brandi, M.L.4
Metz, D.5
Jensen, R.T.6
Bale, A.7
Skarulis, M.C.8
Eastman, R.9
Nieman, L.10
Norton, J.11
Marx, S.J.12
-
2
-
-
0027787680
-
Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocal-ciuric hypcrcalcemia and neonatal severe HPT
-
Poliak MR, Brown EM, Chou YH, Hebert SC, Marx SJ, Steinmann B, Levi T, Scidmann CE, Scidmann JG: Mutations in the human Ca(2+)-sensing receptor gene cause familial hypocal-ciuric hypcrcalcemia and neonatal severe HPT, Cell 1993;75:1297-1303.
-
(1993)
Cell
, vol.75
, pp. 1297-1303
-
-
Poliak, M.R.1
Brown, E.M.2
Chou, Y.H.3
Hebert, S.C.4
Marx, S.J.5
Steinmann, B.6
Levi, T.7
Scidmann, C.E.8
Scidmann, J.G.9
-
3
-
-
0027517161
-
Genetic linkage analysis in familial benign (Hy-pocalciuric) hypercalcemia: Evidence for locus heterogeneity
-
Heath H, Jackson C, Otterud B, Leppcrt M: Genetic linkage analysis in familial benign (hy-pocalciuric) hypercalcemia: Evidence for locus heterogeneity, Am J Hum Genet 1993:53:193-200.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 193-200
-
-
Heath, H.1
Jackson, C.2
Otterud, B.3
Leppcrt, M.4
-
4
-
-
0025642521
-
Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: A clinically and genetically distinct syndrome
-
Jackson CE, Norum RA, Bovd SB, Talpos GB, Wilson SD, Taggart T, Mallctte LE: Hereditary hyperparathyroidism and multiple ossifying jaw fibromas: A clinically and genetically distinct syndrome, Surgery 1990:108:1006-1013.
-
(1990)
Surgery
, vol.108
, pp. 1006-1013
-
-
Jackson, C.E.1
Norum, R.A.2
Bovd, S.B.3
Talpos, G.B.4
Wilson, S.D.5
Taggart, T.6
Mallctte, L.E.7
-
5
-
-
0028958106
-
Hereditary hyperparathyroidism-jaw-tu-mor syndrome: The cndocrinc-tumor gene HRPT2 maps to chromosome I q2 l-q31
-
Szabo J, Heath B, Hill VM, Jackson CE, Zarbo RJ, Mallctte LE, Chew SL, Besser GM, Thak-ker RV, Huff V, Leppcrt MF, Heath H III: Hereditary hyperparathyroidism-jaw-tu-mor syndrome: The cndocrinc-tumor gene HRPT2 maps to chromosome I q2 l-q31, Am J Hum Genet 1995:56:944-950.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 944-950
-
-
Szabo, J.1
Heath, B.2
Hill, V.M.3
Jackson, C.E.4
Zarbo, R.J.5
Mallctte, L.E.6
Chew, S.L.7
Besser, G.M.8
Thak-Ker, R.V.9
Huff, V.10
Leppcrt, M.F.11
Heath, H.12
-
6
-
-
1842403802
-
Autosomal dominant primary hvperparathyroidism-jaw tumor syndrome associated with renal hamartomas and renal cysts: Linkage to Iq2l-q32 and loss of the wild-tvpe allele in hamartomas
-
press
-
Teh BT, Farnebo F, Kristoftcrsson U, Sundelin B, Cardinal J, Axelson R, Yap A, Epstein M, Heath H, Cameron D, Larsson C: Autosomal dominant primary hvperparathyroidism-jaw tumor syndrome associated with renal hamartomas and renal cysts: Linkage to Iq2l-q32 and loss of the wild-tvpe allele in hamartomas, J Clin Endocrinol Mctab 1996, in press.
-
(1996)
J Clin Endocrinol Mctab
-
-
Teh, B.T.1
Farnebo, F.2
Kristoftcrsson, U.3
Sundelin, B.4
Cardinal, J.5
Axelson, R.6
Yap, A.7
Epstein, M.8
Heath, H.9
Cameron, D.10
Larsson, C.11
-
7
-
-
0029854297
-
Sporadic primary hyperparathyroidism in the setting of multiple endocrine neoplasia type I
-
Teh BT, McArdlc J, Paramcswaran V, David R, Hayward N, Larsson C, Shepherd J: Sporadic primary hyperparathyroidism in the setting of multiple endocrine neoplasia type I, Arch Surg 1996:131:1230-1232.
-
(1996)
Arch Surg
, vol.131
, pp. 1230-1232
-
-
Teh, B.T.1
McArdlc, J.2
Paramcswaran, V.3
David, R.4
Hayward, N.5
Larsson, C.6
Shepherd, J.7
-
8
-
-
0017274578
-
Familial hyperparathyroidism: Description of a large kindred with physiologic observations and a review of the literature
-
Goldsmith RE, Sizemore GW, Chen I-W, Zalme F., Altemcier WA: Familial hyperparathyroidism: Description of a large kindred with physiologic observations and a review of the literature, Ann Intern Med 1976:84:36—43.
-
(1976)
Ann Intern Med
, vol.84
, pp. 36-43
-
-
Goldsmith, R.E.1
Sizemore, G.W.2
Chen, I.-W.3
Zalme, F.4
Altemcier, W.A.5
-
9
-
-
0027930956
-
Familial isolated primary hyperparathyroidism
-
Kassem M, Zhang X, Brask S, Eriksen EF, Mosekilde L, Kruse TA: Familial isolated primary hyperparathyroidism, Clin Endocrinol 1994:41:415-420.
-
(1994)
Clin Endocrinol
, vol.41
, pp. 415-420
-
-
Kassem, M.1
Zhang, X.2
Brask, S.3
Eriksen, E.F.4
Mosekilde, L.5
Kruse, T.A.6
-
10
-
-
0027140277
-
Familial isolated hyperparathyroidism: A distinct genetic entity with an increased risk of parathyroid cancer
-
Wassif W, Motiiz CF, Friedman E, Weber G, Wong S, Nordenskjöld M, Peters T, Larsson C: Familial isolated hyperparathyroidism: A distinct genetic entity with an increased risk of parathyroid cancer, J Clin Endocrinol Metab 1993:77:1485-1489.
-
(1993)
J Clin Endocrinol Metab
, vol.77
, pp. 1485-1489
-
-
Wassif, W.1
Motiiz, C.F.2
Friedman, E.3
Weber, G.4
Wong, S.5
Nordenskjöld, M.6
Peters, T.7
Larsson, C.8
-
11
-
-
0023828816
-
Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma
-
Larsson C, Skogseid B, Öbcrg K, Nakamura Y, Nordenskjöld M: Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma, Nature 1988,332:85-87.
-
(1988)
Nature
, vol.332
, pp. 85-87
-
-
Larsson, C.1
Skogseid, B.2
Öbcrg, K.3
Nakamura, Y.4
Nordenskjöld, M.5
-
12
-
-
0030298007
-
Definition of the MEN! candidate area based on a 5 Mb integrated map of proximal I lql3
-
European Consortium of MEN 1: Definition of the MEN! candidate area based on a 5 Mb integrated map of proximal I lql3, Genomics 1996:37:354-365.
-
(1996)
Genomics
, vol.37
, pp. 354-365
-
-
-
13
-
-
15844383259
-
Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11 pi 3-1 lq 13 and exclusion of p-calpain as the multiple endocrine neoplasia type 1 gene
-
Pang JT, Lloyd SE, Wooding C, Farrcn B, Pöttinger B, Harding B, Leigh SAE, Pook MA, Benham FJ, Gillett GT, Taggart RT, Thakker RJ: Genetic mapping studies of 40 loci and 23 cosmids in chromosome 11 pi 3-1 lq 13 and exclusion of p-calpain as the multiple endocrine neoplasia type 1 gene, Hum Gen 1996:97:732-741.
-
(1996)
Hum Gen
, vol.97
, pp. 732-741
-
-
Pang, J.T.1
Lloyd, S.E.2
Wooding, C.3
Farrcn, B.4
Pöttinger, B.5
Harding, B.6
Leigh, S.7
Pook, M.A.8
Benham, F.J.9
Gillett, G.T.10
Taggart, R.T.11
Thakker, R.J.12
-
14
-
-
0027532174
-
Exclusion of fau as the multiple endocrine neoplasia type I (MEN 1) gene
-
Kas K, Weber G, Michicls L, Mcrrcgaert J, Sandclin K, Skogseid B, Thompson N, Nordenskjöld M, Larsson C, Friedman E: Exclusion of fau as the multiple endocrine neoplasia type I (MEN 1) gene, Hum Mol Genet 1993;2: 349-353.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 349-353
-
-
Kas, K.1
Weber, G.2
Michicls, L.3
McRrcgaert, J.4
Sandclin, K.5
Skogseid, B.6
Thompson, N.7
Nordenskjöld, M.8
Larsson, C.9
Friedman, E.10
-
15
-
-
0028913540
-
Exclusion of the l3kD rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1
-
Grimmond S, Weber G, Larsson C, Walters M, Teh B, Shepherd J, Nordenskjöld M, Hayward N: Exclusion of the l3kD rapamycin binding protein gene (FKBP2) as a candidate gene for multiple endocrine neoplasia type 1, Hum Genet 1995;95:455-458.
-
(1995)
Hum Genet
, vol.95
, pp. 455-458
-
-
Grimmond, S.1
Weber, G.2
Larsson, C.3
Walters, M.4
Teh, B.5
Shepherd, J.6
Nordenskjöld, M.7
Hayward, N.8
-
16
-
-
0031060656
-
Exclusion of the phosphoinositidc-specific phospho-lipase Cß3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1
-
Weber G, Grimmond S, Lagercrantz J, Friedman E, Phelan C, Carson E, Hayward N, Jaco-bovitz O, Nordenskjöld M, Larsson C: Exclusion of the phosphoinositidc-specific phospho-lipase Cß3 (PLCB3) gene as a candidate for multiple endocrine neoplasia type 1, Hum Genet 1997;99:130-132.
-
(1997)
Hum Genet
, vol.99
, pp. 130-132
-
-
Weber, G.1
Grimmond, S.2
Lagercrantz, J.3
Friedman, E.4
Phelan, C.5
Carson, E.6
Hayward, N.7
Jaco-Bovitz, O.8
Nordenskjöld, M.9
Larsson, C.10
-
17
-
-
0030026141
-
Isolation and characterization of a novel gene close to the human phos-phoinositide-specific phospholipase C (53 gene on chromosomc Ilql3
-
Lagercrantz J, Carson E, Larsson C, Nordcn-skjold M, Weber G: Isolation and characterization of a novel gene close to the human phos-phoinositide-specific phospholipase C 53 gene on chromosomc Ilql3, Genomics 1996:31: 380-384.
-
(1996)
Genomics
, vol.31
, pp. 380-384
-
-
Lagercrantz, J.1
Carson, E.2
Larsson, C.3
Nordcn-Skjold, M.4
Weber, G.5
-
18
-
-
0029871284
-
Expression of the VEGF Related Factor (Vrf) gene in the pre-and postnatal mouse
-
Lagercrantz J, Larsson C, Grimmond S, Fre-driksson M, Weber G, Piehl F: Expression of the VEGF Related Factor (vrf) gene in the pre-and postnatal mouse, Biochcm Biophys Res Commun 1996;220:147-152.
-
(1996)
Biochcm Biophys Res Commun
, vol.220
, pp. 147-152
-
-
Lagercrantz, J.1
Larsson, C.2
Grimmond, S.3
Fre-Driksson, M.4
Weber, G.5
Piehl, F.6
-
19
-
-
0027491108
-
Homozygotes for the autosomal dominant neoplasia syndrome MEN1
-
Brandi M-L, Weber G, Svensson A, Falchetti A, Tonelli F, Castello R, Furlani L, Scappaticci S, Fraccaro M, Larsson C: Homozygotes for the autosomal dominant neoplasia syndrome MEN1, Am J Hum Genet 1993;53:1167-1172.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 1167-1172
-
-
Brandi, M.-L.1
Weber, G.2
Svensson, A.3
Falchetti, A.4
Tonelli, F.5
Castello, R.6
Furlani, L.7
Fraccaro, S.M.8
Larsson, C.9
-
20
-
-
0023522307
-
Ahcrcd Gs and adenylate cyclase activity in human GH-sccrcting pituitary adenomas
-
Vallar L, Spada A, Giannattasio G: Ahcrcd Gs and adenylate cyclase activity in human GH-sccrcting pituitary adenomas, Nature 1987; 330:566-568.
-
(1987)
Nature
, vol.330
, pp. 566-568
-
-
Vallar, L.1
Spada, A.2
Giannattasio, G.3
-
21
-
-
0025724116
-
Transforming DNA sequences present in human prolactin-secreting pituitary tumors
-
Gonsky R, Herman V, Mclmed S, Fagin J: Transforming DNA sequences present in human prolactin-secreting pituitary tumors, Mol End 1991:5:1687-1695.
-
(1991)
Mol End
, vol.5
, pp. 1687-1695
-
-
Gonsky, R.1
Herman, V.2
McLmed, S.3
Fagin, J.4
-
22
-
-
0026064404
-
Rearrangement and over-expression of D11S287E, a candidate oncogene on chromosomc llql3 in benign parathyroid adenoma
-
Rosenberg CL, Kim HG, Shows TB, Kronen-berg HM, Arnold A: Rearrangement and over-expression of D11S287E, a candidate oncogene on chromosomc llql3 in benign parathyroid adenoma, Oncogene 1991;6:449-453.
-
(1991)
Oncogene
, vol.6
, pp. 449-453
-
-
Rosenberg, C.L.1
Kim, H.G.2
Shows, T.B.3
Kronen-Berg, H.M.4
Arnold, A.5
-
23
-
-
0025850979
-
Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type I
-
Scappaticci S, Maraschio P, del Ciotto N, Fossati GS, Zonta A, Fraccaro M: Chromosome abnormalities in lymphocytes and fibroblasts of subjects with multiple endocrine neoplasia type I, Cancer Genet Cytogenet 1991:52:85-92
-
(1991)
Cancer Genet Cytogenet
, vol.52
, pp. 85-92
-
-
Scappaticci, S.1
Maraschio, P.2
Del Ciotto, N.3
Fossati, G.S.4
Zonta, A.5
Fraccaro, M.6
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