-
1
-
-
85047682409
-
Guidelines for diagnosis and therapy of MEN type 1 and type 2
-
Brandi ML, Gagel RF, Angeli A, Bilezikian JP, Beck-Peccoz P, Bordi C, Conte-Devolx B, Falchetti A, Gheri RG, Libroia A, Lips CJ, Lombardi G, Mannelli M, Pacini F, Ponder BA, Raue F, Skogseid B, Tamburrano G, Thakker RV, Thompson NW, Tomassetti P, Tonelli F, Wells SA Jr & Marx SJ. Guidelines for diagnosis and therapy of MEN type 1 and type 2. Journal of Clinical Endocrinology and Metabolism 2001 86 5658-5671.
-
(2001)
Journal of Clinical Endocrinology and Metabolism
, vol.86
, pp. 5658-5671
-
-
Brandi, M.L.1
Gagel, R.F.2
Angeli, A.3
Bilezikian, J.P.4
Beck-Peccoz, P.5
Bordi, C.6
Conte-Devolx, B.7
Falchetti, A.8
Gheri, R.G.9
Libroia, A.10
Lips, C.J.11
Lombardi, G.12
Mannelli, M.13
Pacini, F.14
Ponder, B.A.15
Raue, F.16
Skogseid, B.17
Tamburrano, G.18
Thakker, R.V.19
Thompson, N.W.20
Tomassetti, P.21
Tonelli, F.22
Wells Jr, S.A.23
Marx, S.J.24
more..
-
2
-
-
18344380647
-
Molecular genetics of multiple endocrine neoplasia types 1 and 2
-
Marx SJ. Molecular genetics of multiple endocrine neoplasia types 1 and 2. Nature Reviews. Cancer 2005 5 367-375.
-
(2005)
Nature Reviews. Cancer
, vol.5
, pp. 367-375
-
-
Marx, S.J.1
-
3
-
-
0030963446
-
Positional cloning of the gene for multiple endocrine neoplasia type 1
-
Chandrasekharappa SC, Guru SC, Manickam P, Olufemi SE, Collins FS, Emmert-Buck MR, Debelenko LV, Zhuang Z, Lubensky IA, Liotta LA, Crabtree JS, Wang Y, Roe BA, Weisemann J, Boguski MS, Agarwal SK, Kester MB, Kim YS, Hcppner C, Dong Q, Spiegel AM, Burns AL & Marx SJ. Positional cloning of the gene for multiple endocrine neoplasia type 1. Science 1997 276 404-407.
-
(1997)
Science
, vol.276
, pp. 404-407
-
-
Chandrasekharappa, S.C.1
Guru, S.C.2
Manickam, P.3
Olufemi, S.E.4
Collins, F.S.5
Emmert-Buck, M.R.6
Debelenko, L.V.7
Zhuang, Z.8
Lubensky, I.A.9
Liotta, L.A.10
Crabtree, J.S.11
Wang, Y.12
Roe, B.A.13
Weisemann, J.14
Boguski, M.S.15
Agarwal, S.K.16
Kester, M.B.17
Kim, Y.S.18
Hcppner, C.19
Dong, Q.20
Spiegel, A.M.21
Burns, A.L.22
Marx, S.J.23
more..
-
4
-
-
8544266010
-
Identification of the multiple endocrine neoplasia type 1 (MEN1) gene
-
Lemmens I, Van de Ven WJ, Kas K, Zhang CX, Giraud S, Wautout V, Buisson N, De Witte K, Salandre J, Lenoir G, Pugeat M, Calender A, Parente F, Quincey D, Gaudray P, De Wit MJ, Lips CJ, Hoppener JW, Khodaei S, Grant AL, Weber G, Kytola S, Teh BT, Farnebo F, Phelan C, Hayward N, Larsson C, Pannet AA, Forbes SA, Bassett JH & Thakker RV. Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. Human Molecular Genetics 1997 6 1177-1183.
-
(1997)
Human Molecular Genetics
, vol.6
, pp. 1177-1183
-
-
Lemmens, I.1
Van de Ven, W.J.2
Kas, K.3
Zhang, C.X.4
Giraud, S.5
Wautout, V.6
Buisson, N.7
De Witte, K.8
Salandre, J.9
Lenoir, G.10
Pugeat, M.11
Calender, A.12
Parente, F.13
Quincey, D.14
Gaudray, P.15
De Wit, M.J.16
Lips, C.J.17
Hoppener, J.W.18
Khodaei, S.19
Grant, A.L.20
Weber, G.21
Kytola, S.22
Teh, B.T.23
Farnebo, F.24
Phelan, C.25
Hayward, N.26
Larsson, C.27
Pannet, A.A.28
Forbes, S.A.29
Bassett, J.H.30
Thakker, R.V.31
more..
-
5
-
-
22444445436
-
Menin molecular interactions: Insights into normal functions and tumorigenesis
-
Agarwal SK, Kennedy PA, Scacheri PC, Novotny EA, Hickman AB, Cerrato A, Rice TS, Moore JB, Rao S, Ji Y, Mateo C, Libutti SK, Oliver B, Chandrasekharappa SC, Burns A, Collins FS, Spiegel AM & Marx SJ. Menin molecular interactions: insights into normal functions and tumorigenesis. Hormone and Metabolic Research 2005 37 369-374.
-
(2005)
Hormone and Metabolic Research
, vol.37
, pp. 369-374
-
-
Agarwal, S.K.1
Kennedy, P.A.2
Scacheri, P.C.3
Novotny, E.A.4
Hickman, A.B.5
Cerrato, A.6
Rice, T.S.7
Moore, J.B.8
Rao, S.9
Ji, Y.10
Mateo, C.11
Libutti, S.K.12
Oliver, B.13
Chandrasekharappa, S.C.14
Burns, A.15
Collins, F.S.16
Spiegel, A.M.17
Marx, S.J.18
-
6
-
-
0036269867
-
Genotype-phenotype analysis in multiple endocrine neoplasia type 1
-
Kouvaraki MA, Lee JR, Shapiro SE, Gagel RF. Sherman SI, Sellin RV, Cote GJ & Evans DB. Genotype-phenotype analysis in multiple endocrine neoplasia type 1. Archives of Surgery 2002 137 641-647.
-
(2002)
Archives of Surgery
, vol.137
, pp. 641-647
-
-
Kouvaraki, M.A.1
Lee, J.R.2
Shapiro, S.E.3
Gagel, R.F.4
Sherman, S.I.5
Sellin, R.V.6
Cote, G.J.7
Evans, D.B.8
-
7
-
-
0036301097
-
Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: Search for correlation between phenotype and the functional domains of the MEN1 protein
-
Wautot V, Vercherat C, Lespinasse J, Chambe B, Lenoir GM, Zhang CX, Porchet N, Cordler M, Beroud C & Calender A. Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein. Human Mutation 2002 20 35-47.
-
(2002)
Human Mutation
, vol.20
, pp. 35-47
-
-
Wautot, V.1
Vercherat, C.2
Lespinasse, J.3
Chambe, B.4
Lenoir, G.M.5
Zhang, C.X.6
Porchet, N.7
Cordler, M.8
Beroud, C.9
Calender, A.10
-
8
-
-
13444304438
-
Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing
-
Ellard S, Hattersley AT, Brewer CM & Vaidya B. Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing. Clinical Endocrinology 2005 62 169-175.
-
(2005)
Clinical Endocrinology
, vol.62
, pp. 169-175
-
-
Ellard, S.1
Hattersley, A.T.2
Brewer, C.M.3
Vaidya, B.4
-
9
-
-
38149112594
-
Multiple endocrine neoplasia type 1 (MEN1): Analysis of 1336 mutations reported in the first decade following identification of the gene
-
Lemos MC & Thakker RV. Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene. Human Mutation 2008 29 22-32.
-
(2008)
Human Mutation
, vol.29
, pp. 22-32
-
-
Lemos, M.C.1
Thakker, R.V.2
-
10
-
-
0023633709
-
Hyperparathyroidism presenting as the first lesion in multiple endocrine neoplasia type 1
-
Benson L, Ljunghall S, Akerstrom G & Oberg K. Hyperparathyroidism presenting as the first lesion in multiple endocrine neoplasia type 1. American Journal of Medicine 1987 82 731-737.
-
(1987)
American Journal of Medicine
, vol.82
, pp. 731-737
-
-
Benson, L.1
Ljunghall, S.2
Akerstrom, G.3
Oberg, K.4
-
11
-
-
0031730065
-
The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1
-
Carty SE, Helm AK, Amico JA, Clarke MR, Foley TP, Watson CG & Mulvihill JJ. The variable penetrance and spectrum of manifestations of multiple endocrine neoplasia type 1. Surgery 1998 124 1106-1113.
-
(1998)
Surgery
, vol.124
, pp. 1106-1113
-
-
Carty, S.E.1
Helm, A.K.2
Amico, J.A.3
Clarke, M.R.4
Foley, T.P.5
Watson, C.G.6
Mulvihill, J.J.7
-
12
-
-
0008405857
-
MEN-1 (Burin): Update on a unique phenotypic variant. (Abstract)
-
Green JS, Rigatto C, Parfrey PS, Kaiser SM, Galway AB, Joyce CJ, Galway A, Joyce C & Ur E. MEN-1 (Burin): update on a unique phenotypic variant. (Abstract) American Journal of Human Genetics 1999 65 (Suppl 1) A128.
-
(1999)
American Journal of Human Genetics
, vol.65
, Issue.SUPPL. 1
-
-
Green, J.S.1
Rigatto, C.2
Parfrey, P.S.3
Kaiser, S.M.4
Galway, A.B.5
Joyce, C.J.6
Galway, A.7
Joyce, C.8
Ur, E.9
-
13
-
-
0022533505
-
Multiple endocrine neoplasia type I: Assessment of laboratory tests to screen for the gene in a large kindred
-
Marx SJ, Vinik AI, Santen RJ, Floyd JC Jr, Mills JL & Green J III. Multiple endocrine neoplasia type I: assessment of laboratory tests to screen for the gene in a large kindred. Medicine 1986 65 226-241.
-
(1986)
Medicine
, vol.65
, pp. 226-241
-
-
Marx, S.J.1
Vinik, A.I.2
Santen, R.J.3
Floyd Jr, J.C.4
Mills, J.L.5
Green III, J.6
-
14
-
-
7144229389
-
Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland
-
Olufemi SE, Green JS, Manickam P, Guru SC, Agarwal SK, Kester MB, Dong Q, Burns AL, Spiegel AM, Marx SJ, Collins FS & Chandrasekharappa SC. Common ancestral mutation in the MEN1 gene is likely responsible for the prolactinoma variant of MEN1 (MEN1Burin) in four kindreds from Newfoundland. Human Mutation 1998 11 264-269.
-
(1998)
Human Mutation
, vol.11
, pp. 264-269
-
-
Olufemi, S.E.1
Green, J.S.2
Manickam, P.3
Guru, S.C.4
Agarwal, S.K.5
Kester, M.B.6
Dong, Q.7
Burns, A.L.8
Spiegel, A.M.9
Marx, S.J.10
Collins, F.S.11
Chandrasekharappa, S.C.12
-
15
-
-
0024853151
-
Screening for the multiple endocrine neoplasia syndrome type I. A study of 11 kindreds in The Netherlands
-
Vasen HF, Lamers CB & Lips CJ. Screening for the multiple endocrine neoplasia syndrome type I. A study of 11 kindreds in The Netherlands. Archives of Internal Medicine 1989 149 2717-2722.
-
(1989)
Archives of Internal Medicine
, vol.149
, pp. 2717-2722
-
-
Vasen, H.F.1
Lamers, C.B.2
Lips, C.J.3
-
16
-
-
0025997106
-
Multiple endocrine neoplasia type 1: A 10-year prospective screening study in four kindreds
-
Skogseid B, Eriksson B, Lundqvist G, Lorelius LE, Rastad J, Wide L, Akerstrom G & Oberg K. Multiple endocrine neoplasia type 1: a 10-year prospective screening study in four kindreds. Journal of Clinical Endocrinology and Metabolism 1991 73 281-287.
-
(1991)
Journal of Clinical Endocrinology and Metabolism
, vol.73
, pp. 281-287
-
-
Skogseid, B.1
Eriksson, B.2
Lundqvist, G.3
Lorelius, L.E.4
Rastad, J.5
Wide, L.6
Akerstrom, G.7
Oberg, K.8
-
17
-
-
0001710006
-
Clinical studies of multiple endocrine neoplasia. type 1 (MEN1)
-
Trump D, Farren B, Wooding C, Pang JT, Besser GM, Buchanan KD, Edwards CR, Heath DA, Jackson CE, Jansen S, Lips K, Monson JP, O'Halloran D, Sampson J, Shalet SM, Wheeler MH, Zink A & Thakker RV. Clinical studies of multiple endocrine neoplasia. type 1 (MEN1). Quarterly Journal of Medicine 1996 89 653-669.
-
(1996)
Quarterly Journal of Medicine
, vol.89
, pp. 653-669
-
-
Trump, D.1
Farren, B.2
Wooding, C.3
Pang, J.T.4
Besser, G.M.5
Buchanan, K.D.6
Edwards, C.R.7
Heath, D.A.8
Jackson, C.E.9
Jansen, S.10
Lips, K.11
Monson, J.P.12
O'Halloran, D.13
Sampson, J.14
Shalet, S.M.15
Wheeler, M.H.16
Zink, A.17
Thakker, R.V.18
-
18
-
-
0035025614
-
Predictive genetic screening and clinical findings in multiple endocrine neoplasia type I families
-
Kopp I, Bartsch D, Wild A, Schilling T, Nies C, Bergenfelz A, Rieder H, Simon B & Rothmund M. Predictive genetic screening and clinical findings in multiple endocrine neoplasia type I families. World Journal of Surgery 2001 25 610-616.
-
(2001)
World Journal of Surgery
, vol.25
, pp. 610-616
-
-
Kopp, I.1
Bartsch, D.2
Wild, A.3
Schilling, T.4
Nies, C.5
Bergenfelz, A.6
Rieder, H.7
Simon, B.8
Rothmund, M.9
-
19
-
-
18244392974
-
Pituitary disease in MEN type 1 (MEN1): Data from the France - Belgium MEN1 multicenter study
-
Verges B, Boureille F, Goudet P, Murat A, Beckers A, Sassolas G, Cougard P, Chambe B, Montvernay C & Calender A. Pituitary disease in MEN type 1 (MEN1): data from the France - Belgium MEN1 multicenter study. Journal of Clinical Endocrinology and Metabolism 2002 87 457-465.
-
(2002)
Journal of Clinical Endocrinology and Metabolism
, vol.87
, pp. 457-465
-
-
Verges, B.1
Boureille, F.2
Goudet, P.3
Murat, A.4
Beckers, A.5
Sassolas, G.6
Cougard, P.7
Chambe, B.8
Montvernay, C.9
Calender, A.10
-
20
-
-
0032231883
-
A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors
-
Teh BT, Esapa CT, Houlston R, Grandell U, Farnebo F, Nordenskjold M, Pearce CJ, Carmichael D, Larsson C & Harris PE. A family with isolated hyperparathyroidism segregating a missense MEN1 mutation and showing loss of the wild-type alleles in the parathyroid tumors. American Journal of Human Genetics 1998 63 1544-1549.
-
(1998)
American Journal of Human Genetics
, vol.63
, pp. 1544-1549
-
-
Teh, B.T.1
Esapa, C.T.2
Houlston, R.3
Grandell, U.4
Farnebo, F.5
Nordenskjold, M.6
Pearce, C.J.7
Carmichael, D.8
Larsson, C.9
Harris, P.E.10
-
21
-
-
0034457762
-
Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree
-
Kassem M, Kruse TA, Wong FK, Larsson C & Teh BT. Familial isolated hyperparathyroidism as a variant of multiple endocrine neoplasia type 1 in a large Danish pedigree. Journal of Clinical Endocrinology and Metabolism 2000 85 165-167.
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, pp. 165-167
-
-
Kassem, M.1
Kruse, T.A.2
Wong, F.K.3
Larsson, C.4
Teh, B.T.5
-
22
-
-
0036739679
-
Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism
-
Villablanca A, Wassif WS, Smith T, Hoog A, Vierimaa O, Kassem M, Dwight T, Du Forsberg LQ, Learoyd D, Jones K, Stranks S, Juhlin C, Teh BT, Carling T, Robinson B & Larsson C. Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism. European Journal of Endocrinology 2002 147 313-322.
-
(2002)
European Journal of Endocrinology
, vol.147
, pp. 313-322
-
-
Villablanca, A.1
Wassif, W.S.2
Smith, T.3
Hoog, A.4
Vierimaa, O.5
Kassem, M.6
Dwight, T.7
Du Forsberg, L.Q.8
Learoyd, D.9
Jones, K.10
Stranks, S.11
Juhlin, C.12
Teh, B.T.13
Carling, T.14
Robinson, B.15
Larsson, C.16
-
23
-
-
37349016937
-
Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene
-
Hannan FM, Nesbit MA, Christie PT, Fratter C, Dudley NE, Sadler GP & Thakker RV. Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene. Nature Clinical Practice. Endocrinology & Metabolism 2008 4 53-58.
-
(2008)
Nature Clinical Practice. Endocrinology & Metabolism
, vol.4
, pp. 53-58
-
-
Hannan, F.M.1
Nesbit, M.A.2
Christie, P.T.3
Fratter, C.4
Dudley, N.E.5
Sadler, G.P.6
Thakker, R.V.7
-
24
-
-
4043111906
-
Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma
-
Hao W Skarulis MC, Simonds WE, Weinstein LS, Agarwal SK, Mateo C, James-Newton L, Hobbs GR, Gibril F, Jensen RT & Marx SJ. Multiple endocrine neoplasia type 1 variant with frequent prolactinoma and rare gastrinoma. Journal of Clinical Endocrinology and Metabolism 2004 89 3776-3784.
-
(2004)
Journal of Clinical Endocrinology and Metabolism
, vol.89
, pp. 3776-3784
-
-
Hao, W.1
Skarulis, M.C.2
Simonds, W.E.3
Weinstein, L.S.4
Agarwal, S.K.5
Mateo, C.6
James-Newton, L.7
Hobbs, G.R.8
Gibril, F.9
Jensen, R.T.10
Marx, S.J.11
-
25
-
-
0026394553
-
The natural history of multiple endocrine neoplasia type 1
-
Shepherd JJ. The natural history of multiple endocrine neoplasia type 1. Archives of Surgery 1991 126 935-952.
-
(1991)
Archives of Surgery
, vol.126
, pp. 935-952
-
-
Shepherd, J.J.1
-
26
-
-
35349015699
-
Multiple endocrine neoplasia type 1 in Northern Finland; clinical features and genotype phenotype correlation
-
Vierimaa O, Ebeling TM, Kytölä S, Bloigu R, Eloranta E, Salmi J, Korpi-Hyövälti E, Niskanen L, Orvola A, Elovaara E, Gynther A, Sane T, Välimäki M, Ignatius J, Leisti J & Salmela PI. Multiple endocrine neoplasia type 1 in Northern Finland; clinical features and genotype phenotype correlation. European Journal of Endocrinology 2007 157 285-294.
-
(2007)
European Journal of Endocrinology
, vol.157
, pp. 285-294
-
-
Vierimaa, O.1
Ebeling, T.M.2
Kytölä, S.3
Bloigu, R.4
Eloranta, E.5
Salmi, J.6
Korpi-Hyövälti, E.7
Niskanen, L.8
Orvola, A.9
Elovaara, E.10
Gynther, A.11
Sane, T.12
Välimäki, M.13
Ignatius, J.14
Leisti, J.15
Salmela, P.I.16
-
27
-
-
0029977338
-
-
Burgess JR, Shepherd JJ, Parameswaran V, Hoffman L & Greenaway TM. Somatotrophinomas in multiple endocrine neoplasia type 1: a review of clinical phenotype and insulin-like growth factor-1 levels in a large multiple endocrine neoplasia type 1 kindred. American Journal of Medicine 1996 100 544-547.
-
Burgess JR, Shepherd JJ, Parameswaran V, Hoffman L & Greenaway TM. Somatotrophinomas in multiple endocrine neoplasia type 1: a review of clinical phenotype and insulin-like growth factor-1 levels in a large multiple endocrine neoplasia type 1 kindred. American Journal of Medicine 1996 100 544-547.
-
-
-
-
28
-
-
7144253116
-
Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families
-
Agarwal SK, Debelenko LV, Kester MB, Guru SC, Manickam P, Olufemi SE, Skarulis MC, Heppner C, Crabtree JS, Lubensky IA, Zhuang Z, Kim YS, Chandrasekharappa SC, Collins FS, Liotta LA, Spiegel AM, Burns AL, Emmert-Buck MR & Marx SJ. Analysis of recurrent germline mutations in the MEN1 gene encountered in apparently unrelated families. Human Mutation 1998 12 75-82.
-
(1998)
Human Mutation
, vol.12
, pp. 75-82
-
-
Agarwal, S.K.1
Debelenko, L.V.2
Kester, M.B.3
Guru, S.C.4
Manickam, P.5
Olufemi, S.E.6
Skarulis, M.C.7
Heppner, C.8
Crabtree, J.S.9
Lubensky, I.A.10
Zhuang, Z.11
Kim, Y.S.12
Chandrasekharappa, S.C.13
Collins, F.S.14
Liotta, L.A.15
Spiegel, A.M.16
Burns, A.L.17
Emmert-Buck, M.R.18
Marx, S.J.19
-
29
-
-
0033870521
-
Phenotype and phenocopy: The relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1)
-
Burgess JR, Nord B, David R, Greenaway TM, Parameswaran V, Larsson C, Shepherd JJ & Teh BT. Phenotype and phenocopy: the relationship between genotype and clinical phenotype in a single large family with multiple endocrine neoplasia type 1 (MEN 1). Clinical Endocrinology 2000 53 205-211.
-
(2000)
Clinical Endocrinology
, vol.53
, pp. 205-211
-
-
Burgess, J.R.1
Nord, B.2
David, R.3
Greenaway, T.M.4
Parameswaran, V.5
Larsson, C.6
Shepherd, J.J.7
Teh, B.T.8
-
30
-
-
0035078625
-
Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland
-
Kytölä S, Villablanca A, Ebeling T, Nord B, Larsson C, Höög A, Wong FK, Välimäki M, Vierimaa O, Teh BT, Salmela PI & Leisti J. Founder effect in multiple endocrine neoplasia type 1 (MEN 1) in Finland. Journal of Medical Genetics 2001 38 185-189.
-
(2001)
Journal of Medical Genetics
, vol.38
, pp. 185-189
-
-
Kytölä, S.1
Villablanca, A.2
Ebeling, T.3
Nord, B.4
Larsson, C.5
Höög, A.6
Wong, F.K.7
Välimäki, M.8
Vierimaa, O.9
Teh, B.T.10
Salmela, P.I.11
Leisti, J.12
-
31
-
-
0032860796
-
Osteoporosis in multiple endocrine neoplasia type 1
-
Burgess JR, David R, Greenaway TM, Parameswaran V & Shepherd JJ. Osteoporosis in multiple endocrine neoplasia type 1. Archives of Surgery 1999 134 1119-1123.
-
(1999)
Archives of Surgery
, vol.134
, pp. 1119-1123
-
-
Burgess, J.R.1
David, R.2
Greenaway, T.M.3
Parameswaran, V.4
Shepherd, J.J.5
-
32
-
-
33646559510
-
Management of pancreatic endocrine tumors in multiple endocrine neoplasia. type 1
-
Kouvaraki MA, Shapiro SE, Cote GJ, Lee JE, Yao IC, Waguespack SG, Gagel RF, Evans DB & Perrier ND. Management of pancreatic endocrine tumors in multiple endocrine neoplasia. type 1. World Journal of Surgery 2006 30 643-653.
-
(2006)
World Journal of Surgery
, vol.30
, pp. 643-653
-
-
Kouvaraki, M.A.1
Shapiro, S.E.2
Cote, G.J.3
Lee, J.E.4
Yao, I.C.5
Waguespack, S.G.6
Gagel, R.F.7
Evans, D.B.8
Perrier, N.D.9
-
33
-
-
34548009103
-
Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1
-
Toledo RA, Lourenco DM, Coutinho FL, Quedas E, Mackowiack I, Machado MC, Montenegro F, Cunha-Neto MB, Liberman B Pereira MA, Correa PH & Toledo SP. Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1. Clinical Endocrinology 2007 67 377-384.
-
(2007)
Clinical Endocrinology
, vol.67
, pp. 377-384
-
-
Toledo, R.A.1
Lourenco, D.M.2
Coutinho, F.L.3
Quedas, E.4
Mackowiack, I.5
Machado, M.C.6
Montenegro, F.7
Cunha-Neto, M.B.8
Liberman, B.9
Pereira, M.A.10
Correa, P.H.11
Toledo, S.P.12
-
34
-
-
34548788937
-
The impact of clinical and genetic screenings on the management of the multiple endocrine neoplasia type 1
-
Lourenço-Jr DM, Toledo RA, Coutinho FL, Margarido LC, Siqueira SA, dos Santos MA, Montenegro FL, Machado MC & Toledo SP. The impact of clinical and genetic screenings on the management of the multiple endocrine neoplasia type 1. Clinics 2007 62 465-476.
-
(2007)
Clinics
, vol.62
, pp. 465-476
-
-
Lourenço-Jr, D.M.1
Toledo, R.A.2
Coutinho, F.L.3
Margarido, L.C.4
Siqueira, S.A.5
dos Santos, M.A.6
Montenegro, F.L.7
Machado, M.C.8
Toledo, S.P.9
-
35
-
-
53349151101
-
-
WHO. Technical Report Series
-
WHO. Technical Report Series 1994 843 5-48.
-
(1994)
, vol.843
, pp. 5-48
-
-
-
36
-
-
0032801294
-
Type 1 multiple endocrine neoplasia (MENI): Contribution of genetic analysis to the screening and follow-up of a large French kindred
-
Waterlot C, Porchet N, Bauters C, Decoulx M, Wemeau JL, Proye C, Degand PM, Aubert JP, Cortet C & Dewailly D. Type 1 multiple endocrine neoplasia (MENI): contribution of genetic analysis to the screening and follow-up of a large French kindred. Clinical Endocrinology 1999 51 101-107.
-
(1999)
Clinical Endocrinology
, vol.51
, pp. 101-107
-
-
Waterlot, C.1
Porchet, N.2
Bauters, C.3
Decoulx, M.4
Wemeau, J.L.5
Proye, C.6
Degand, P.M.7
Aubert, J.P.8
Cortet, C.9
Dewailly, D.10
-
37
-
-
9844226196
-
A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation
-
Giraud S, Choplin H, Tch BT, Lespinasse J, Jouvet A, Labat-Moleur F, Lenoir G, Hamon B, Hamon P & Calender A. A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation. Journal of Clinical Endocrinology and Metabolism 1997 82 3487-3492.
-
(1997)
Journal of Clinical Endocrinology and Metabolism
, vol.82
, pp. 3487-3492
-
-
Giraud, S.1
Choplin, H.2
Tch, B.T.3
Lespinasse, J.4
Jouvet, A.5
Labat-Moleur, F.6
Lenoir, G.7
Hamon, B.8
Hamon, P.9
Calender, A.10
-
38
-
-
0034453841
-
An unusual kindred of the multiple endocrine neoplasia type 1 in Japanese
-
Abe T, Yoshimoto K, Taniyama M, Hanakawa K, Izumiyama H, Itakura M & Matsumoto K. An unusual kindred of the multiple endocrine neoplasia type 1 in Japanese. Journal of Clinical Endocrinology and Metabolism 2000 85 1327-1330.
-
(2000)
Journal of Clinical Endocrinology and Metabolism
, vol.85
, pp. 1327-1330
-
-
Abe, T.1
Yoshimoto, K.2
Taniyama, M.3
Hanakawa, K.4
Izumiyama, H.5
Itakura, M.6
Matsumoto, K.7
-
41
-
-
33749392405
-
Sporadic versus hereditary gastrinomas of the duodenum and pancreas: Distinct clinico-pathological and epidemiological features
-
Anlauf M, Garbrecht N, Henopp T, Schmitt A, Schlenger R, Raffel A, Krausch M, Gimm O, Eisenberger CF, Knoefel WT, Dralle H, Komminoth P, Heitz PU, Perren A & Klöppel G. Sporadic versus hereditary gastrinomas of the duodenum and pancreas: distinct clinico-pathological and epidemiological features. World Journal of Gastroenterology 2006 12 5440-5446.
-
(2006)
World Journal of Gastroenterology
, vol.12
, pp. 5440-5446
-
-
Anlauf, M.1
Garbrecht, N.2
Henopp, T.3
Schmitt, A.4
Schlenger, R.5
Raffel, A.6
Krausch, M.7
Gimm, O.8
Eisenberger, C.F.9
Knoefel, W.T.10
Dralle, H.11
Komminoth, P.12
Heitz, P.U.13
Perren, A.14
Klöppel, G.15
-
42
-
-
33644903223
-
Groupe dcs Tumeurs Endocrines (GTE). Prospective endoscopic ultrasonographic evaluation of the frequency of nonfunctioning pancreaticoduodenal endocrine tumors in patients with multiple endocrine neoplasia type 1
-
Thomas-Marques L, Murat A, Delemer B, Penfornis A, Cardot-Bauters C, Baudin E, Niccoli-Sire P, Levoir D, Choplin Hdu B, Chabre O, Jovenin N & Cadiot G. Groupe dcs Tumeurs Endocrines (GTE). Prospective endoscopic ultrasonographic evaluation of the frequency of nonfunctioning pancreaticoduodenal endocrine tumors in patients with multiple endocrine neoplasia type 1. American Journal of Gastroenterology 2006 101 266-273.
-
(2006)
American Journal of Gastroenterology
, vol.101
, pp. 266-273
-
-
Thomas-Marques, L.1
Murat, A.2
Delemer, B.3
Penfornis, A.4
Cardot-Bauters, C.5
Baudin, E.6
Niccoli-Sire, P.7
Levoir, D.8
Choplin Hdu, B.9
Chabre, O.10
Jovenin, N.11
Cadiot, G.12
-
43
-
-
29644442002
-
Acromegaly in a multiple endocrine neoplasia type 1 (MEN1) family with low penetrance of the disease
-
Dreijerink KM, Van Beek AP, Lentjes EG, Post JG, Van der Luijt RB, Canninga-Van Dijk MR & Lips CJ. Acromegaly in a multiple endocrine neoplasia type 1 (MEN1) family with low penetrance of the disease. European Journal of Endocrinology 2005 153 741-746.
-
(2005)
European Journal of Endocrinology
, vol.153
, pp. 741-746
-
-
Dreijerink, K.M.1
Van Beek, A.P.2
Lentjes, E.G.3
Post, J.G.4
Van der Luijt, R.B.5
Canninga-Van Dijk, M.R.6
Lips, C.J.7
-
44
-
-
0024346202
-
Skeletal disease in primary hyperparathyroidism
-
Silverberg SJ, Shane E, De La Cruz L, Dempster DW, Feldman F, Seldin D, Jacobs TP, Siris ES, Cafferty M, Parisien MV, Lindsay R, Clemens TL & Bilezikian JP. Skeletal disease in primary hyperparathyroidism. Journal of Bone and Mineral Research 1989 4 283-291.
-
(1989)
Journal of Bone and Mineral Research
, vol.4
, pp. 283-291
-
-
Silverberg, S.J.1
Shane, E.2
De La Cruz, L.3
Dempster, D.W.4
Feldman, F.5
Seldin, D.6
Jacobs, T.P.7
Siris, E.S.8
Cafferty, M.9
Parisien, M.V.10
Lindsay, R.11
Clemens, T.L.12
Bilezikian, J.P.13
-
45
-
-
12344280973
-
Primary hyperparathyroidism: New concepts in clinical, densitometric and biochemical features
-
Bilezikian JP, Brandi ML, Rubin M & Silverberg SJ. Primary hyperparathyroidism: new concepts in clinical, densitometric and biochemical features. Journal of Internal Medicine 2005 257 6-17.
-
(2005)
Journal of Internal Medicine
, vol.257
, pp. 6-17
-
-
Bilezikian, J.P.1
Brandi, M.L.2
Rubin, M.3
Silverberg, S.J.4
-
47
-
-
0038756727
-
Inactivation of menin, the product of the multiple endocrine neoplasia type 1 gene, inhibits the commitment of multipotential mesenchymal stem cells into the osteoblast lineage
-
Sowa H, Kaji H, Canaff L, Hendy GN, Tsukamoto T, Yamaguchi T, Miyazono K, Sugimoto T & Chihara K. Inactivation of menin, the product of the multiple endocrine neoplasia type 1 gene, inhibits the commitment of multipotential mesenchymal stem cells into the osteoblast lineage. Journal of Biological Chemistry 2003 278 21058-21069.
-
(2003)
Journal of Biological Chemistry
, vol.278
, pp. 21058-21069
-
-
Sowa, H.1
Kaji, H.2
Canaff, L.3
Hendy, G.N.4
Tsukamoto, T.5
Yamaguchi, T.6
Miyazono, K.7
Sugimoto, T.8
Chihara, K.9
-
48
-
-
0034087665
-
MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1
-
Morelli A, Falchetti A, Martineti V, Becherini L, Mark M, Friedman E & Brandi ML. MEN1 gene mutation analysis in Italian patients with multiple endocrine neoplasia type 1. European Journal of Endocrinology 2000 142 131-137.
-
(2000)
European Journal of Endocrinology
, vol.142
, pp. 131-137
-
-
Morelli, A.1
Falchetti, A.2
Martineti, V.3
Becherini, L.4
Mark, M.5
Friedman, E.6
Brandi, M.L.7
-
49
-
-
0032231708
-
Germline mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders
-
Giraud S, Zhang CX, Serova-Sinilnikova O, Wautot V, Salandre J, Buisson N, Waterlot C, Bauters C, Porchet N, Aubert JP, Emy P, Cadiot G, Delcmer B, Chabre O, Niccoli P, Leprat F, Duron F, Emperauger B, Cougard P, Goudet P, Sarfati E, Riou JP, Guichard S, Rodier M & Calender A. Germline mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders. American Journal of Human Genetics 1998 63 455-467.
-
(1998)
American Journal of Human Genetics
, vol.63
, pp. 455-467
-
-
Giraud, S.1
Zhang, C.X.2
Serova-Sinilnikova, O.3
Wautot, V.4
Salandre, J.5
Buisson, N.6
Waterlot, C.7
Bauters, C.8
Porchet, N.9
Aubert, J.P.10
Emy, P.11
Cadiot, G.12
Delcmer, B.13
Chabre, O.14
Niccoli, P.15
Leprat, F.16
Duron, F.17
Emperauger, B.18
Cougard, P.19
Goudet, P.20
Sarfati, E.21
Riou, J.P.22
Guichard, S.23
Rodier, M.24
Calender, A.25
more..
-
50
-
-
19944430556
-
A report of a national mutation testing service for the MEN1 gene: Clinical presentations and implications for mutation testing
-
Cardinal JW, Bergman L, Hayward N, Sweet A, Warner J, Marks L, Learoyd D, Dwight T, Robinson B, Epstein M, Smith M, Teh BT, Cameron DP & Prins JB. A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing. Journal of Medical Genetics 2005 42 69-74.
-
(2005)
Journal of Medical Genetics
, vol.42
, pp. 69-74
-
-
Cardinal, J.W.1
Bergman, L.2
Hayward, N.3
Sweet, A.4
Warner, J.5
Marks, L.6
Learoyd, D.7
Dwight, T.8
Robinson, B.9
Epstein, M.10
Smith, M.11
Teh, B.T.12
Cameron, D.P.13
Prins, J.B.14
-
51
-
-
34548805701
-
Clinical testing for mutations in the MEN1 gene in Sweden: A report on 200 unrelated cases
-
Tham E, Grandell U, Lindgren E, Toss G, Skogseid B & Nordenskjöld M. Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases. Journal of Clinical Endocrinology and Metabolism 2007 92 3389-3395.
-
(2007)
Journal of Clinical Endocrinology and Metabolism
, vol.92
, pp. 3389-3395
-
-
Tham, E.1
Grandell, U.2
Lindgren, E.3
Toss, G.4
Skogseid, B.5
Nordenskjöld, M.6
-
52
-
-
0033021488
-
A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1
-
Cetani F, Pardi E, Cianferotti L, Vignali E, Picone A, Miccoli P, Pinchera A & Marcocci C. A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1. European Journal of Endocrinology 1999 140 429-433.
-
(1999)
European Journal of Endocrinology
, vol.140
, pp. 429-433
-
-
Cetani, F.1
Pardi, E.2
Cianferotti, L.3
Vignali, E.4
Picone, A.5
Miccoli, P.6
Pinchera, A.7
Marcocci, C.8
-
53
-
-
0035289633
-
Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: Additional information for mutational screening
-
Asteria C, Faglia G, Roncoroni R, Borretta G, Ribotto P & Beck-Peccoz P. Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: additional information for mutational screening. Human Mutation 2001 17 237.
-
(2001)
Human Mutation
, vol.17
, pp. 237
-
-
Asteria, C.1
Faglia, G.2
Roncoroni, R.3
Borretta, G.4
Ribotto, P.5
Beck-Peccoz, P.6
-
54
-
-
33745925858
-
MEN1 family with a novel frameshift mutation
-
Nuzzo V, Tauchmanová L, Falchetti A, Faggiano A, Marini F, Piantadosi S, Brandi ML, Leopaldi L & Colao A. MEN1 family with a novel frameshift mutation. Journal of Endocrinological Investigation 2006 29 450-456.
-
(2006)
Journal of Endocrinological Investigation
, vol.29
, pp. 450-456
-
-
Nuzzo, V.1
Tauchmanová, L.2
Falchetti, A.3
Faggiano, A.4
Marini, F.5
Piantadosi, S.6
Brandi, M.L.7
Leopaldi, L.8
Colao, A.9
|