-
1
-
-
0033619201
-
Dehy-droepiandrosterone replacement in women with adrenal insufficiency
-
Arlt W, Callies F, van Vlijmen JC, et al (1999) Dehy-droepiandrosterone replacement in women with adrenal insufficiency. N Engl J Med 341:1013-1020
-
(1999)
N Engl J Med
, vol.341
, pp. 1013-1020
-
-
Arlt, W.1
Callies, F.2
Van Vlijmen, J.C.3
-
2
-
-
0035857957
-
Germline SDHD mutation in familial phaeochromocytoma
-
Astuti D, Douglas F, Lennard TWJ, et al (2001) Germline SDHD mutation in familial phaeochromocytoma. Lancet 357:1181-1182
-
(2001)
Lancet
, vol.357
, pp. 1181-1182
-
-
Astuti, D.1
Douglas, F.2
Lennard, T.W.J.3
-
3
-
-
0034964421
-
Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma
-
Astuti D, Latif F, Dallol A., et al (2001) Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am J Hum Genet 69:49-54
-
(2001)
Am J Hum Genet
, vol.69
, pp. 49-54
-
-
Astuti, D.1
Latif, F.2
Dallol, A.3
-
4
-
-
0036274254
-
Pheo-chromocytomas and paragangliomas in von hippel-lin-dau disease. A role for laparoscopic and cortical-sparing surgery
-
Baghai M, Thompson GB, Young W.F., et al (2002) Pheo-chromocytomas and paragangliomas in von Hippel-Lin-dau disease. A role for laparoscopic and cortical-sparing surgery. Arch Surg 137:682-689
-
(2002)
Arch Surg
, vol.137
, pp. 682-689
-
-
Baghai, M.1
Thompson, G.B.2
Young, W.F.3
-
5
-
-
0036712593
-
Hereditary paraganglioma targets diverse paraganglia
-
Baysal BE (2002) Hereditary paraganglioma targets diverse paraganglia. J Med Genet 39:617-622
-
(2002)
J Med Genet
, vol.39
, pp. 617-622
-
-
Baysal, B.E.1
-
6
-
-
0034602950
-
Mutations in SDHD, a mitochondrial complex II gene in hereditary paraganglioma
-
Baysal BE, Ferrell RE, Willett-Brozick JE, et al (2000) Mutations in SDHD, a mitochondrial complex II gene in hereditary paraganglioma. Science 287:848-851
-
(2000)
Science
, vol.287
, pp. 848-851
-
-
Baysal, B.E.1
Ferrell, R.E.2
Willett-Brozick, J.E.3
-
7
-
-
0034803010
-
Pheno-typic dichotomy in mitochondrial complex II genetic disorders
-
Baysal BE, Rubinstein WS, Taschner PEM (2001) Pheno-typic dichotomy in mitochondrial complex II genetic disorders. J Mol Med 79:495-503
-
(2001)
J Mol Med
, vol.79
, pp. 495-503
-
-
Baysal, B.E.1
Rubinstein, W.S.2
Taschner, P.E.M.3
-
8
-
-
0000077851
-
Macroglossia, omphalocoele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly
-
Beckwith JB (1969) Macroglossia, omphalocoele, adrenal cytomegaly, gigantism and hyperplastic visceromegaly. Birth Defects 5:188-196
-
(1969)
Birth Defects
, vol.5
, pp. 188-196
-
-
Beckwith, J.B.1
-
9
-
-
0037422207
-
Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas
-
Benn DE, Croxson MS, Tucker K, et al (2003) Novel succinate dehydrogenase subunit B (SDHB) mutations in familial phaeochromocytomas and paragangliomas, but an absence of somatic SDHB mutations in sporadic phaeochromocytomas. Oncogene 22:1358-1364
-
(2003)
Oncogene
, vol.22
, pp. 1358-1364
-
-
Benn, D.E.1
Croxson, M.S.2
Tucker, K.3
-
10
-
-
0030781576
-
Sporadic pheochromocytomas are rarely associated with germline mutations in the VHL tumor suppressor gene or the RET protooncogene
-
Brauch H, Hoppner W, Jahnig H., et al (1997) Sporadic pheochromocytomas are rarely associated with germline mutations in the VHL tumor suppressor gene or the RET protooncogene. J Clin Endocrinol Metab 82:4101-4104
-
(1997)
J Clin Endocrinol Metab
, vol.82
, pp. 4101-4104
-
-
Brauch, H.1
Hoppner, W.2
Jahnig, H.3
-
11
-
-
0030018392
-
Laparoscopic adrenalectomy compared to open adrenalectomy for benign adrenal neoplasms
-
Brunt LM, Doherty GM, Norton J.A., et al (1996) Laparoscopic adrenalectomy compared to open adrenalectomy for benign adrenal neoplasms. J Am Coll Surg 183:1-10
-
(1996)
J Am Coll Surg
, vol.183
, pp. 1-10
-
-
Brunt, L.M.1
Doherty, G.M.2
Norton, J.A.3
-
12
-
-
0036240747
-
Adrenalectomy for familial pheochromocytoma in the laparoscopic era
-
Brunt LM, Lairmore TC, Doherty G.M., et al (2001) Adrenalectomy for familial pheochromocytoma in the laparoscopic era. Ann Surg 235:713-721
-
(2001)
Ann Surg
, vol.235
, pp. 713-721
-
-
Brunt, L.M.1
Lairmore, T.C.2
Doherty, G.M.3
-
13
-
-
0029900871
-
Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1
-
Burgess JR, Harle RA, Tucker P, et al (1996) Adrenal lesions in a large kindred with multiple endocrine neoplasia type 1. Arch Surg 131:699-702
-
(1996)
Arch Surg
, vol.131
, pp. 699-702
-
-
Burgess, J.R.1
Harle, R.A.2
Tucker, P.3
-
14
-
-
0025217744
-
Somato-statin-producing duodenal carcinoids in patients with von recklinghausen's neurofibromatosis. A predilection for black patients
-
Burke AP, Sobin LH, Shekitka K.M., et al (1990) Somato-statin-producing duodenal carcinoids in patients with von Recklinghausen's neurofibromatosis. A predilection for black patients. Cancer 65:1591-1595
-
(1990)
Cancer
, vol.65
, pp. 1591-1595
-
-
Burke, A.P.1
Sobin, L.H.2
Shekitka, K.M.3
-
16
-
-
0027977002
-
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B
-
Carlson KM, Dou S, Chi D., et al (1994) Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B. Proc Natl Acad Sci USA 91: 1579-1583
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 1579-1583
-
-
Carlson, K.M.1
Dou, S.2
Chi, D.3
-
17
-
-
0017182358
-
Adrenal medullary disease in multiple endocrine neoplasia type 2: Pheochromocytoma and its precursors
-
Carney JA, Sizemore GW, Sheps S.G. (1976) Adrenal medullary disease in multiple endocrine neoplasia type 2: pheochromocytoma and its precursors. Am J Clin Pathol 66:279-290
-
(1976)
Am J Clin Pathol
, vol.66
, pp. 279-290
-
-
Carney, J.A.1
Sizemore, G.W.2
Sheps, S.G.3
-
18
-
-
0016427998
-
Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: The precursor of bilateral pheochromocytoma
-
Carney JA, Sizemore GW, Tyce G.M. (1975) Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: the precursor of bilateral pheochromocytoma. Mayo Clin Proc 50:3-10
-
(1975)
Mayo Clin Proc
, vol.50
, pp. 3-10
-
-
Carney, J.A.1
Sizemore, G.W.2
Tyce, G.M.3
-
19
-
-
0027297690
-
Phaeochromocytoma in multiple endocrine neoplasia type 2A: Survey of 100 cases
-
Casanova S, Rosenberg-Bourgin M, Farkas D., et al (1993) Phaeochromocytoma in multiple endocrine neoplasia type 2A: survey of 100 cases. Clin Endocrinol 38:531-537
-
(1993)
Clin Endocrinol
, vol.38
, pp. 531-537
-
-
Casanova, S.1
Rosenberg-Bourgin, M.2
Farkas, D.3
-
20
-
-
0035724034
-
Paraganglioma genes
-
Chew SL (2001) Paraganglioma genes. Clin Endocrinol 54:573-574
-
(2001)
Clin Endocrinol
, vol.54
, pp. 573-574
-
-
Chew, S.L.1
-
22
-
-
0027303248
-
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC
-
Donis-Keller H., Dou S, Chi D., et al (1993) Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. Hum Mol Genet 2:851-856
-
(1993)
Hum Mol Genet
, vol.2
, pp. 851-856
-
-
Donis-Keller, H.1
Dou, S.2
Chi, D.3
-
23
-
-
0024569718
-
The clinical and screening age-at-onset distribution for the MEN-2 syndrome
-
Easton DF, Ponder MA, Cummings T, et al (1989) The clinical and screening age-at-onset distribution for the MEN-2 syndrome. Am J Hum Genet 44:208-215
-
(1989)
Am J Hum Genet
, vol.44
, pp. 208-215
-
-
Easton, D.F.1
Ponder, M.A.2
Cummings, T.3
-
24
-
-
0033577985
-
Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von hippel-lindau disease and multiple endocrine neoplasia type 2
-
Eisenhofer G, Lenders JW, Linehan W.M., et al (1999) Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. N Engl J Med 340: 1872-1879
-
(1999)
N Engl J Med
, vol.340
, pp. 1872-1879
-
-
Eisenhofer, G.1
Lenders, J.W.2
Linehan, W.M.3
-
25
-
-
0028788184
-
Mutations in the RET proto-oncogene and the von hippel-lindau disease tumor suppressor gene in sporadic and syndromic pheochromocytomas
-
Eng C, Crossey PA, Mulligan L.M., et al (1995) Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumor suppressor gene in sporadic and syndromic pheochromocytomas. J Med Genet 32:934-937
-
(1995)
J Med Genet
, vol.32
, pp. 934-937
-
-
Eng, C.1
Crossey, P.A.2
Mulligan, L.M.3
-
26
-
-
0022535165
-
Familial medullary thyroid carcinoma without associated en-docrinopathies: A distinct clinical entity
-
Farndon JR, Leight GS, Dilley W.G., et al (1986) Familial medullary thyroid carcinoma without associated en-docrinopathies: a distinct clinical entity. Br J Surg 73: 278-281
-
(1986)
Br J Surg
, vol.73
, pp. 278-281
-
-
Farndon, J.R.1
Leight, G.S.2
Dilley, W.G.3
-
27
-
-
0030966414
-
Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1, 728 patients
-
Friedman JM, Birch P.H. (1997) Type 1 neurofibromatosis: a descriptive analysis of the disorder in 1, 728 patients. Am J Med Genet 70:138-143
-
(1997)
Am J Med Genet
, vol.70
, pp. 138-143
-
-
Friedman, J.M.1
Birch, P.H.2
-
28
-
-
0033569787
-
Von hippel-lindau syndrome. A pleomorphic condition
-
Friedrich CA (1999) Von Hippel-Lindau syndrome. A pleomorphic condition. Cancer 86:2478-2482
-
(1999)
Cancer
, vol.86
, pp. 2478-2482
-
-
Friedrich, C.A.1
-
29
-
-
0035054565
-
Genotype-phenotype correlation in von hippel-lindau syndrome
-
Friedrich CA (2001) Genotype-phenotype correlation in von Hippel-Lindau syndrome. Hum Mol Genet 10: 763-767
-
(2001)
Hum Mol Genet
, vol.10
, pp. 763-767
-
-
Friedrich, C.A.1
-
30
-
-
0026645968
-
Laparoscopic adrenalectomy in cushing's syndrome and pheochromocytoma
-
Gagner M, Lacroix A, Bolte E. (1992) Laparoscopic adrenalectomy in Cushing's syndrome and pheochromocytoma. N Engl J Med 327:1033
-
(1992)
N Engl J Med
, vol.327
, pp. 1033
-
-
Gagner, M.1
Lacroix, A.2
Bolte, E.3
-
31
-
-
0034671551
-
Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma
-
Gimm O, Armanios M, Dziema H., et al (2000) Somatic and occult germline mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res 60:6822-6825
-
(2000)
Cancer Res
, vol.60
, pp. 6822-6825
-
-
Gimm, O.1
Armanios, M.2
Dziema, H.3
-
32
-
-
0030957310
-
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
-
Gutmann DH, Aylsworth A, Carey J.C., et al (1997) The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA 278:51-57
-
(1997)
JAMA
, vol.278
, pp. 51-57
-
-
Gutmann, D.H.1
Aylsworth, A.2
Carey, J.C.3
-
33
-
-
0018225331
-
Measurement of urinary epinephrine in screening for pheochromocytoma in multiple endocrine neoplasia type II
-
Hamilton BP, Landsberg L, Levine R.J. (1978) Measurement of urinary epinephrine in screening for pheochromocytoma in multiple endocrine neoplasia type II. Am J Med 65:1027-1032
-
(1978)
Am J Med
, vol.65
, pp. 1027-1032
-
-
Hamilton, B.P.1
Landsberg, L.2
Levine, R.J.3
-
34
-
-
0033729031
-
Multiple endocrine neoplasia type 2 (MEN 2) and RET: From neoplasia to neurogenesis
-
Hansford JR, Mulligan L.M. (2000) Multiple endocrine neoplasia type 2 (MEN 2) and RET: from neoplasia to neurogenesis. J Med Genet 37:817-827
-
(2000)
J Med Genet
, vol.37
, pp. 817-827
-
-
Hansford, J.R.1
Mulligan, L.M.2
-
36
-
-
0025738681
-
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
-
Henry I, Bonaiti-Pellie C, Chehensse V., et al (1991) Uniparental paternal disomy in a genetic cancer-predisposing syndrome. Nature 351:665-667
-
(1991)
Nature
, vol.351
, pp. 665-667
-
-
Henry, I.1
Bonaiti-Pellie, C.2
Chehensse, V.3
-
37
-
-
0028174024
-
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma
-
Hofstra RM, Landsvater RM, Ceccherini I, et al (1994) A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma. Nature 367:375-376
-
(1994)
Nature
, vol.367
, pp. 375-376
-
-
Hofstra, R.M.1
Landsvater, R.M.2
Ceccherini, I.3
-
38
-
-
0027136050
-
Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: Results of long-term follow-up
-
Howe JR, Norton JA, Wells SA Jr (1993) Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up. Surgery 114:1070-1077
-
(1993)
Surgery
, vol.114
, pp. 1070-1077
-
-
Howe, J.R.1
Norton, J.A.2
Wells Jr., S.A.3
-
39
-
-
0033675895
-
Pheochromocytoma: Inherited associations, bilaterality, and cortex preservation
-
Inabnet W, Caragliano P, Pertsemlidis D. (2000) Pheochromocytoma: inherited associations, bilaterality, and cortex preservation. Surgery 128:1007-1012
-
(2000)
Surgery
, vol.128
, pp. 1007-1012
-
-
Inabnet, W.1
Caragliano, P.2
Pertsemlidis, D.3
-
40
-
-
0033935327
-
Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma
-
Janetschek G, Finkenstedt G, Gasser R., et al (1998) Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma. J Urol 164:14-17
-
(1998)
J Urol
, vol.164
, pp. 14-17
-
-
Janetschek, G.1
Finkenstedt, G.2
Gasser, R.3
-
41
-
-
0034693757
-
The RET protooncogene in human cancers
-
Jhiang SM (2000) The RET protooncogene in human cancers. Oncogene 19:5590-5597
-
(2000)
Oncogene
, vol.19
, pp. 5590-5597
-
-
Jhiang, S.M.1
-
42
-
-
0021043434
-
Carcinoid tumour of ampulla of vater associated with viscero-cuta-neous neurofibromatosis
-
Kapur BM, Sarin SK, Anand C.S., et al (1983) Carcinoid tumour of ampulla of Vater associated with viscero-cuta-neous neurofibromatosis. Postgrad Med 59:734-735
-
(1983)
Postgrad Med
, vol.59
, pp. 734-735
-
-
Kapur, B.M.1
Sarin, S.K.2
Anand, C.S.3
-
44
-
-
0000671591
-
Genetic Abnormalities in multiple endocrine neoplasia type 2
-
Doherty GM, Skogseid B (eds) Lippincott Williams & Wilkins, Philadelphia
-
Kikumori T, Evans D, Lee J.E., et al (2001) Genetic abnormalities in multiple endocrine neoplasia type 2. In: Doherty GM, Skogseid B (eds) Surgical endocrinology. Lippincott Williams & Wilkins, Philadelphia, pp 531-540
-
(2001)
Surgical Endocrinology
, pp. 531-540
-
-
Kikumori, T.1
Evans, D.2
Lee, J.E.3
-
45
-
-
0033812849
-
Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the carney complex
-
Kirschner LS, Carney JA, Pack S.D., et al (2000) Mutations of the gene encoding the protein kinase A type I-alpha regulatory subunit in patients with the Carney complex. Nat Genet 26:89-92
-
(2000)
Nat Genet
, vol.26
, pp. 89-92
-
-
Kirschner, L.S.1
Carney, J.A.2
Pack, S.D.3
-
47
-
-
0035986364
-
Pheochromocytoma in von hippel-lindau disease: Distinct histopathologic phenotype compared to pheochromo cytoma in multiple endocrine neoplasia type 2
-
Koch C, Mauro D, McClellan M.W., et al (2002) Pheochromocytoma in von Hippel-Lindau disease: distinct histopathologic phenotype compared to pheochromo cytoma in multiple endocrine neoplasia type 2. Endocrine Pathol 13:17-27
-
(2002)
Endocrine Pathol
, vol.13
, pp. 17-27
-
-
Koch, C.1
Mauro, D.2
McClellan, M.W.3
-
48
-
-
0031015524
-
Octreotide scintigraphy and catecholamine response to an octreotide challenge in Malignant phaeochromocytoma
-
Kopf D, Bockisch A, Steinert H., et al (1997) Octreotide scintigraphy and catecholamine response to an octreotide challenge in malignant phaeochromocytoma. Clin Endocrinol 46:39-44
-
(1997)
Clin Endocrinol
, vol.46
, pp. 39-44
-
-
Kopf, D.1
Bockisch, A.2
Steinert, H.3
-
49
-
-
0033674591
-
Malignancy in neurofibromatosis type 1
-
Korf BR (2000) Malignancy in neurofibromatosis type 1. The Oncologist 5:477-485
-
(2000)
The Oncologist
, vol.5
, pp. 477-485
-
-
Korf, B.R.1
-
50
-
-
0027238246
-
Management of pheochromocytomas in patients with multiple endocrine neoplasia type 2 syndromes
-
Lairmore TC, Ball DW, Baylin S.B., et al (1993) Management of pheochromocytomas in patients with multiple endocrine neoplasia type 2 syndromes. Ann Surg 217: 595-603
-
(1993)
Ann Surg
, vol.217
, pp. 595-603
-
-
Lairmore, T.C.1
Ball, D.W.2
Baylin, S.B.3
-
51
-
-
0029906124
-
Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma
-
Lee JE, Curley SA, Gagel R.F., et al (1996) Cortical-sparing adrenalectomy for patients with bilateral pheochromocytoma. Surgery 120:1064-1071
-
(1996)
Surgery
, vol.120
, pp. 1064-1071
-
-
Lee, J.E.1
Curley, S.A.2
Gagel, R.F.3
-
52
-
-
0014587529
-
Soft-tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome?
-
Li FP, Fraumeni J.F. (1969) Soft-tissue sarcomas, breast cancer, and other neoplasms: a familial syndrome? Ann Int Med 71:747-752
-
(1969)
Ann Int Med
, vol.71
, pp. 747-752
-
-
Li, F.P.1
Fraumeni, J.F.2
-
53
-
-
0019522340
-
Bilateral occurrence of pheochromocytoma in patients with the multiple endocrine neoplasia syndrome type 2A (Sipple's syndrome)
-
Lips KJ, Van der Sluys Veer J, Struyvenberg A, et al. (1981) Bilateral occurrence of pheochromocytoma in patients with the multiple endocrine neoplasia syndrome type 2A (Sipple's syndrome). Am J Med 70:1051-1060
-
(1981)
Am J Med
, vol.70
, pp. 1051-1060
-
-
Lips, K.J.1
Van Der Sluys Veer, J.2
Struyvenberg, A.3
-
54
-
-
0025741681
-
Von hippel-lindau disease: A genetic study
-
Maher ER, Iselius L, Yates J.R., et al (1991) Von Hippel-Lindau disease: a genetic study. J Med Genet 28:443-447
-
(1991)
J Med Genet
, vol.28
, pp. 443-447
-
-
Maher, E.R.1
Iselius, L.2
Yates, J.R.3
-
55
-
-
0026530299
-
Germline mutations of the p53 tumor-suppressor gene in children and young adults with second Malignant neoplasms
-
Malkin D, Jolly KW, Barbier N, et al (1992) Germline mutations of the p53 tumor-suppressor gene in children and young adults with second malignant neoplasms. N Engl J Med 326:1309-1315
-
(1992)
N Engl J Med
, vol.326
, pp. 1309-1315
-
-
Malkin, D.1
Jolly, K.W.2
Barbier, N.3
-
56
-
-
0030792719
-
Adrenal masses in patients with familial adenomatous polyposis
-
Marchesa P, Fazio VW, Church J.M., et al (1997) Adrenal masses in patients with familial adenomatous polyposis. Dis Colon Rectum 40:1023-1028
-
(1997)
Dis Colon Rectum
, vol.40
, pp. 1023-1028
-
-
Marchesa, P.1
Fazio, V.W.2
Church, J.M.3
-
57
-
-
0028783824
-
Pheochromocytoma in multiple endocrine neoplasia type 2: European study
-
Modigliani E, Vasen HM, Raue K, et al (1995) Pheochromocytoma in multiple endocrine neoplasia type 2: European study. J Internal Med 238:363-367
-
(1995)
J Internal Med
, vol.238
, pp. 363-367
-
-
Modigliani, E.1
Vasen, H.M.2
Raue, K.3
-
58
-
-
0038360493
-
Medullary thyroid carcinoma and the multiple endocrine neoplasia type 2 syndromes
-
Doherty GM, Skogseid B (eds) Lippincott Williams & Wilkins, Philadelphia
-
Moley JF, Albinson C. (2001) Medullary thyroid carcinoma and the multiple endocrine neoplasia type 2 syndromes. In: Doherty GM, Skogseid B (eds) Surgical endocrinology. Lippincott Williams & Wilkins, Philadelphia, pp 541-557
-
(2001)
Surgical Endocrinology
, pp. 541-557
-
-
Moley, J.F.1
Albinson, C.2
-
59
-
-
0027231568
-
Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A
-
Mulligan LM, Kwok JB, Healey C.S., et al (1993) Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Nature 363:458-460
-
(1993)
Nature
, vol.363
, pp. 458-460
-
-
Mulligan, L.M.1
Kwok, J.B.2
Healey, C.S.3
-
60
-
-
0023530559
-
A case of von recklinghausen's disease associated with pheochromo-cytoma and papillary carcinoma of the thyroid gland
-
Nakamura H, Koga M, Higa S., et al (1987) A case of von Recklinghausen's disease associated with pheochromo-cytoma and papillary carcinoma of the thyroid gland. Endocrinol Jpn 34:545-551
-
(1987)
Endocrinol Jpn
, vol.34
, pp. 545-551
-
-
Nakamura, H.1
Koga, M.2
Higa, S.3
-
61
-
-
0027508442
-
Pheochromocytomas, multiple endocrine neoplasia type 2, and von hippel-lindau disease
-
Neumann HPH, Berger DP, Sigmund G, et al (1993) Pheochromocytomas, multiple endocrine neoplasia type 2, and von Hippel-Lindau disease. N Engl J Med 329:1531-1538.
-
(1993)
N Engl J Med
, vol.329
, pp. 1531-1538
-
-
Neumann, H.P.H.1
Berger, D.P.2
Sigmund, G.3
-
62
-
-
84885783005
-
-
Erratum
-
Erratum (1994) N Engl J Med 331: 1535
-
(1994)
N Engl J Med
, vol.331
, pp. 1535
-
-
-
63
-
-
0029090153
-
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia type 2
-
Neumann HPH, Eng C, Mulligan L.M., et al (1995) Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia type 2. JAMA 274:1149-1151
-
(1995)
JAMA
, vol.274
, pp. 1149-1151
-
-
Neumann, H.P.H.1
Eng, C.2
Mulligan, L.M.3
-
64
-
-
0032893034
-
Adrenal-sparing surgery for phaeochromocytoma
-
Neumann HPH, Bender BU, Reincke M, et al (1999) Adrenal-sparing surgery for phaeochromocytoma. Br J Surg 86:94-97
-
(1999)
Br J Surg
, vol.86
, pp. 94-97
-
-
Neumann, H.P.H.1
Bender, B.U.2
Reincke, M.3
-
65
-
-
0037046659
-
Germ-line mutations in nonsyndromic pheochromocy-toma
-
Neumann HPH, Bausch B, McWhinney S.R., et al (2002) Germ-line mutations in nonsyndromic pheochromocy-toma. N Engl J Med 346:1459-1466
-
(2002)
N Engl J Med
, vol.346
, pp. 1459-1466
-
-
Neumann, H.P.H.1
Bausch, B.2
McWhinney, S.R.3
-
67
-
-
0035151026
-
Pheochromocytoma in multiple endocrine neoplasia type 2: A prospective study
-
Nguyen L, Niccoli-Sire P, Caron P., et al (2001) Pheochromocytoma in multiple endocrine neoplasia type 2: a prospective study. Eur J Endocrinol 144:37-44
-
(2001)
Eur J Endocrinol
, vol.144
, pp. 37-44
-
-
Nguyen, L.1
Niccoli-Sire, P.2
Caron, P.3
-
68
-
-
0033767445
-
Mutations in SDHC cause autosomal dominant paraganglioma, type 3
-
Niemann S, Müller U (2000) Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat Genet 26:268-270
-
(2000)
Nat Genet
, vol.26
, pp. 268-270
-
-
Niemann, S.1
Müller, U.2
-
69
-
-
0028850669
-
Multiple endocrine neoplasia type 2B: More than an endocrine disorder
-
O'Riordain D.S., O'Brien T, Crotty TB, et al (1995) Multiple endocrine neoplasia type 2B: more than an endocrine disorder. Surgery 118:936-942
-
(1995)
Surgery
, vol.118
, pp. 936-942
-
-
O'Riordain, D.S.1
O'Brien, T.2
Crotty, T.B.3
-
70
-
-
0031657522
-
Neurofibromatosis type 1 (NF1): A protein truncation assay yielding identification of mutations in 73% of patients
-
Park VM, Pivnick E.K. (1998) Neurofibromatosis type 1 (NF1): A protein truncation assay yielding identification of mutations in 73% of patients. J Med Genet 35:813-820
-
(1998)
J Med Genet
, vol.35
, pp. 813-820
-
-
Park, V.M.1
Pivnick, E.K.2
-
71
-
-
0031889547
-
Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma
-
Pomares FJ, Canas R, Rodriguez J.M., et al (1998) Differences between sporadic and multiple endocrine neoplasia type 2A phaeochromocytoma. Clin Endocrinol 48:195-200
-
(1998)
Clin Endocrinol
, vol.48
, pp. 195-200
-
-
Pomares, F.J.1
Canas, R.2
Rodriguez, J.M.3
-
72
-
-
0026876355
-
Neurofibromatosis: From gene to phe-notype
-
Ponder BA (1992) Neurofibromatosis: from gene to phe-notype. Semin Cancer Biol 3:115-120
-
(1992)
Semin Cancer Biol
, vol.3
, pp. 115-120
-
-
Ponder, B.A.1
-
73
-
-
0028149096
-
Pheochromocytoma as the first manifestation of von hippel-lindau disease
-
Richard S, Beigelman C, Duclos J.M., et al (1994) Pheochromocytoma as the first manifestation of von Hippel-Lindau disease. Surgery 116:1076-1081
-
(1994)
Surgery
, vol.116
, pp. 1076-1081
-
-
Richard, S.1
Beigelman, C.2
Duclos, J.M.3
-
74
-
-
0026695967
-
PET scanning with hydroxyephedrine: An approach to the localization of pheochromocytoma
-
Shulkin BL, Wieland DM, Schwaiger M, et al (1992) PET scanning with hydroxyephedrine: an approach to the localization of pheochromocytoma. J Nucl Med 33: 1125-1131
-
(1992)
J Nucl Med
, vol.33
, pp. 1125-1131
-
-
Shulkin, B.L.1
Wieland, D.M.2
Schwaiger, M.3
-
75
-
-
0035683789
-
Von hippel-lindau disease: Gene to bedside
-
Sims KB (2001) Von Hippel-Lindau disease: gene to bedside. Curr Opin Neurol 14:695-703
-
(2001)
Curr Opin Neurol
, vol.14
, pp. 695-703
-
-
Sims, K.B.1
-
76
-
-
0001251788
-
The association of pheochromocytoma with carcinoma of the thyroid gland
-
Sipple JH (1961) The association of pheochromocytoma with carcinoma of the thyroid gland. Am J Med 31:163-166
-
(1961)
Am J Med
, vol.31
, pp. 163-166
-
-
Sipple, J.H.1
-
77
-
-
0019417415
-
Scintigraphic localization of pheochromocytoma
-
Sisson JC, Frager MS, Valk T.W., et al (1981) Scintigraphic localization of pheochromocytoma. N Engl J Med 305: 12-17
-
(1981)
N Engl J Med
, vol.305
, pp. 12-17
-
-
Sisson, J.C.1
Frager, M.S.2
Valk, T.W.3
-
78
-
-
0026762788
-
Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1
-
Skogseid B, Larsson C, Lindgren P.G., et al (1992) Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1. J Clin Endocrinol Metab 75:76-81
-
(1992)
J Clin Endocrinol Metab
, vol.75
, pp. 76-81
-
-
Skogseid, B.1
Larsson, C.2
Lindgren, P.G.3
-
79
-
-
0028806115
-
Adrenal lesion in multiple endocrine neoplasia type 1
-
Skogseid B, Rastad J, Gobl A., et al (1995) Adrenal lesion in multiple endocrine neoplasia type 1. Surgery 118: 1077-1082
-
(1995)
Surgery
, vol.118
, pp. 1077-1082
-
-
Skogseid, B.1
Rastad, J.2
Gobl, A.3
-
80
-
-
0031938588
-
A family with hereditary extra-adrenal paragangliomas without evidence for mutations in the von hippel-lindau disease or ret genes
-
Sköldberg F., Grimelius L, Woodward E.R., et al (1998) A family with hereditary extra-adrenal paragangliomas without evidence for mutations in the von Hippel-Lindau disease or ret genes. Clin Endocrinol 48:11-16
-
(1998)
Clin Endocrinol
, vol.48
, pp. 11-16
-
-
Sköldberg, F.1
Grimelius, L.2
Woodward, E.R.3
-
81
-
-
0025648762
-
Germ-line transmission of a mutated p53 gene in a cancer-prone family with li-fraumeni syndrome
-
Srivastava S, Zou Z, Pirollo K., et al (1990) Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature 348:747-749
-
(1990)
Nature
, vol.348
, pp. 747-749
-
-
Srivastava, S.1
Zou, Z.2
Pirollo, K.3
-
82
-
-
0035001830
-
Clinical genetics of multiple endocrine neoplasias, carney complex and related syndromes
-
Stratakis CA (2001) Clinical genetics of multiple endocrine neoplasias, Carney complex and related syndromes. J Endocrinol Invest 24:370-383
-
(2001)
J Endocrinol Invest
, vol.24
, pp. 370-383
-
-
Stratakis, C.A.1
-
83
-
-
0034853288
-
Genetics of endocrine disease. Clinical and molecular features of the carney complex: Diagnostic criteria and recommendations for patient evaluation
-
Stratakis CA, Kirschner LS, Carney J.A. (2001) Genetics of endocrine disease. Clinical and molecular features of the Carney complex: diagnostic criteria and recommendations for patient evaluation. J Clin Endocrinol Metab 86:4041-4046
-
(2001)
J Clin Endocrinol Metab
, vol.86
, pp. 4041-4046
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Carney, J.A.3
-
84
-
-
0001926360
-
A refined genetic, radiation hybrid, and physical map of the carney complex (CNC) locus on chromosome 2p16; evidence for genetic heterogeneity in the syndrome
-
Taymans SE, Macrae CA, Casey M, et al (1997) A refined genetic, radiation hybrid, and physical map of the Carney complex (CNC) locus on chromosome 2p16; evidence for genetic heterogeneity in the syndrome. Am J Hum Genet 61 Suppl A84.
-
(1997)
Am J Hum Genet
, vol.61
, Issue.SUPPL. A84
-
-
Taymans, S.E.1
Macrae, C.A.2
Casey, M.3
-
85
-
-
0028817229
-
Comparison of radiolabeled octreotide and meta-iodobenzylguanidine (MIBG) scintigraphy in Malignant pheochromocytoma
-
Tenenbaum F, Lumbroso J, Schlumberger M., et al (1995) Comparison of radiolabeled octreotide and meta-iodobenzylguanidine (MIBG) scintigraphy in malignant pheochromocytoma. J Nucl Med 36:1-6
-
(1995)
J Nucl Med
, vol.36
, pp. 1-6
-
-
Tenenbaum, F.1
Lumbroso, J.2
Schlumberger, M.3
-
86
-
-
0031444499
-
Laparoscopic versus open posterior adrenalectomy: A case-control study of 100 patients
-
Thompson GB, Grant CS, van Heerden JA, et al (1997) Laparoscopic versus open posterior adrenalectomy: a case-control study of 100 patients. Surgery 122:1132-1136
-
(1997)
Surgery
, vol.122
, pp. 1132-1136
-
-
Thompson, G.B.1
Grant, C.S.2
Van Heerden, J.A.3
-
87
-
-
0020568781
-
Unilateral versus bilateral adrenalectomy in multiple endocrine neoplasia IIA
-
Tibblin S, Dymling JF, Ingemansson S, et al (1983) Unilateral versus bilateral adrenalectomy in multiple endocrine neoplasia IIA. World J Surg 7:201-208
-
(1983)
World J Surg
, vol.7
, pp. 201-208
-
-
Tibblin, S.1
Dymling, J.F.2
Ingemansson, S.3
-
88
-
-
0021604045
-
Surgical management of the adrenal glands in the multiple endocrine neoplasia type II syndrome
-
van Heerden J.A., Sizemore GW, Carney J.A., et al (1984) Surgical management of the adrenal glands in the multiple endocrine neoplasia type II syndrome. World J Surg 8:612-621
-
(1984)
World J Surg
, vol.8
, pp. 612-621
-
-
Van Heerden, J.A.1
Sizemore, G.W.2
Carney, J.A.3
-
89
-
-
0022335261
-
Bilateral subtotal adrenal resection for bilateral pheochromocytomas in multiple endocrine neoplasia, type IIa: A case report
-
van Heerden J.A., Sizemore GW, Carney J.A., et al (1985) Bilateral subtotal adrenal resection for bilateral pheochromocytomas in multiple endocrine neoplasia, type IIa: a case report. Surgery 98:363-365
-
(1985)
Surgery
, vol.98
, pp. 363-365
-
-
Van Heerden, J.A.1
Sizemore, G.W.2
Carney, J.A.3
-
90
-
-
0027985697
-
High frequency of germline p53 mutations in childhood adrenocortical cancer
-
Wagner J, Portwine C, Rabin K., et al (1994) High frequency of germline p53 mutations in childhood adrenocortical cancer. J Natl Cancer Inst 86:1707-1710
-
(1994)
J Natl Cancer Inst
, vol.86
, pp. 1707-1710
-
-
Wagner, J.1
Portwine, C.2
Rabin, K.3
-
91
-
-
0032825694
-
Von recklinghausen's disease and pheochromocytomas
-
Walther MM, Herring J, Enquist E., et al (1999) Von Recklinghausen's disease and pheochromocytomas. J Urol 162:1582-1586
-
(1999)
J Urol
, vol.162
, pp. 1582-1586
-
-
Walther, M.M.1
Herring, J.2
Enquist, E.3
-
92
-
-
6544234532
-
Clinical and genetic characterization of pheochromocytoma in von hippel-lindau families: Comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma
-
Walther MM, Reiter R, Keiser H.R., et al (1999) Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma. J Urol 162:659-664
-
(1999)
J Urol
, vol.162
, pp. 659-664
-
-
Walther, M.M.1
Reiter, R.2
Keiser, H.R.3
-
93
-
-
0033935327
-
Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma
-
Walther MM, Herring J, Choyke P.L., et al (2000) Laparoscopic partial adrenalectomy in patients with hereditary forms of pheochromocytoma. J Urol 164:14-17
-
(2000)
J Urol
, vol.164
, pp. 14-17
-
-
Walther, M.M.1
Herring, J.2
Choyke, P.L.3
-
94
-
-
33745819042
-
Von hippel-lindau disease and von recklinghausen's disease
-
Doherty GM, Skogseid B (eds) Lip-pincott Williams & Wilkins, Philadelphia
-
Walther MM, Linehan WM, Libutti S.K. (2001) von Hippel-Lindau disease and von Recklinghausen's disease. In: Doherty GM, Skogseid B (eds) Surgical endocrinology. Lip-pincott Williams & Wilkins, Philadelphia, pp 581-591
-
(2001)
Surgical Endocrinology
, pp. 581-591
-
-
Walther, M.M.1
Linehan, W.M.2
Libutti, S.K.3
-
95
-
-
0037024513
-
New therapeutic and surgical approaches for sporadic and hereditary pheochromocy-toma
-
Walther MM (2002) New therapeutic and surgical approaches for sporadic and hereditary pheochromocy-toma. Ann N Y Acad Sci 970:41-53
-
(2002)
Ann N y Acad Sci
, vol.970
, pp. 41-53
-
-
Walther, M.M.1
-
96
-
-
0031947929
-
Subtotal adrenalectomy by the posterior retroperitoneoscopic approach
-
Walz MK, Peitgen K, Saller B., et al (1998) Subtotal adrenalectomy by the posterior retroperitoneoscopic approach. World J Surg 22:621-627
-
(1998)
World J Surg
, vol.22
, pp. 621-627
-
-
Walz, M.K.1
Peitgen, K.2
Saller, B.3
-
97
-
-
0022896381
-
The association of neurofibromatosis, pheochromocytoma, and somatostatinrich duodenal carcinoid tumor
-
Wheeler MH, Curley IR, Williams E.D. (1986) The association of neurofibromatosis, pheochromocytoma, and somatostatinrich duodenal carcinoid tumor. Surgery 100: 1163-1169
-
(1986)
Surgery
, vol.100
, pp. 1163-1169
-
-
Wheeler, M.H.1
Curley, I.R.2
Williams, E.D.3
-
98
-
-
76549164702
-
Complex malformatif familial avec hernie ombilicale et macroglossie-Un syndrome nouveau?
-
Wiedemann HR (1964) Complex malformatif familial avec hernie ombilicale et macroglossie-un syndrome nouveau? J Genet Hum 13:223-232
-
(1964)
J Genet Hum
, vol.13
, pp. 223-232
-
-
Wiedemann, H.R.1
|