-
1
-
-
78049485263
-
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
-
Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2010;127:2893-2917.
-
(2010)
Int J Cancer.
, vol.127
, pp. 2893-2917
-
-
Ferlay, J.1
Shin, H.R.2
Bray, F.3
Forman, D.4
Mathers, C.5
Parkin, D.M.6
-
2
-
-
0242608613
-
The genetic basis of cancer of the kidney
-
Linehan WM, Walther MM, Zbar B. The genetic basis of cancer of the kidney. J Urol. 2003;170:2163-2172.
-
(2003)
J Urol.
, vol.170
, pp. 2163-2172
-
-
Linehan, W.M.1
Walther, M.M.2
Zbar, B.3
-
3
-
-
84868309625
-
Genetic basis of kidney cancer: Role of genomics for the development of disease-based therapeutics
-
Linehan WM. Genetic basis of kidney cancer: role of genomics for the development of disease-based therapeutics. Genome Res. 2012;22:2089-2100.
-
(2012)
Genome Res.
, vol.22
, pp. 2089-2100
-
-
Linehan, W.M.1
-
4
-
-
77952263737
-
The genetic basis of kidney cancer: A metabolic disease
-
Linehan WM, Srinivasan R, Schmidt LS. The genetic basis of kidney cancer: a metabolic disease. Nat Rev Urol. 2010;7:277-285.
-
(2010)
Nat Rev Urol.
, vol.7
, pp. 277-285
-
-
Linehan, W.M.1
Srinivasan, R.2
Schmidt, L.S.3
-
5
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F, Tory K, Gnarra JR, et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science. 1993;260:1317-1320.
-
(1993)
Science.
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.R.3
-
7
-
-
84879890360
-
Comprehensive molecular characterization of clear cell renal cell carcinoma
-
Cancer Genome Atlas Research Network
-
Cancer Genome Atlas Research Network. Comprehensive molecular characterization of clear cell renal cell carcinoma. Nature. 2013;499:43-49.
-
(2013)
Nature
, vol.499
, pp. 43-49
-
-
-
8
-
-
0028897350
-
Hereditary papillary renal cell carcinoma: Clinical studies in 10 families
-
Zbar B, Glenn GM, Lubensky IA, et al. Hereditary papillary renal cell carcinoma: clinical studies in 10 families. J Urol. 1995;153: 907-912.
-
(1995)
J Urol.
, vol.153
, pp. 907-912
-
-
Zbar, B.1
Glenn, G.M.2
Lubensky, I.A.3
-
9
-
-
17344381429
-
Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas
-
Schmidt LS, Duh FM, Chen F, et al. Germline and somatic mutations in the tyrosine kinase domain of the MET proto-oncogene in papillary renal carcinomas. Nat Genet. 1997;16:68-73.
-
(1997)
Nat Genet.
, vol.16
, pp. 68-73
-
-
Schmidt, L.S.1
Duh, F.M.2
Chen, F.3
-
10
-
-
0030799090
-
Activating mutations for the met tyrosine kinase receptor in human cancer
-
Jeffers M, Schmidt LS, Nakaigawa N, et al. Activating mutations for the met tyrosine kinase receptor in human cancer. Proc Natl Acad Sci U S A. 1997;94:11445-11450.
-
(1997)
Proc Natl Acad Sci U S A.
, vol.94
, pp. 11445-11450
-
-
Jeffers, M.1
Schmidt, L.S.2
Nakaigawa, N.3
-
11
-
-
0035400394
-
Structural basis of oncogenic activation caused by point mutations in the kinase domain of the MET proto-oncogene: Modeling studies
-
Miller M, Ginalski K, Lesyng B, Nakaigawa N, Schmidt L, Zbar B. Structural basis of oncogenic activation caused by point mutations in the kinase domain of the MET proto-oncogene: modeling studies. Proteins. 2001;44:32-43.
-
(2001)
Proteins.
, vol.44
, pp. 32-43
-
-
Miller, M.1
Ginalski, K.2
Lesyng, B.3
Nakaigawa, N.4
Schmidt, L.5
Zbar, B.6
-
12
-
-
0017760671
-
Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons
-
Birt AR, Hogg GR, Dubé WJ. Hereditary multiple fibrofolliculomas with trichodiscomas and acrochordons. Arch Dermatol. 1977;113: 1674-1677.
-
(1977)
Arch Dermatol.
, vol.113
, pp. 1674-1677
-
-
Birt, A.R.1
Hogg, G.R.2
Dubé, W.J.3
-
13
-
-
0032718182
-
Birt-Hogg-Dubé syndrome: A novel marker of kidney neoplasia
-
Toro JR, Glenn G, Duray P, et al. Birt-Hogg-Dubé syndrome: a novel marker of kidney neoplasia. Arch Dermatol. 1999;135:1195-1202.
-
(1999)
Arch Dermatol.
, vol.135
, pp. 1195-1202
-
-
Toro, J.R.1
Glenn, G.2
Duray, P.3
-
14
-
-
0000939691
-
Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome
-
Nickerson ML, Warren MB, Toro JR, et al. Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome. Cancer Cell. 2002;2:157-164.
-
(2002)
Cancer Cell.
, vol.2
, pp. 157-164
-
-
Nickerson, M.L.1
Warren, M.B.2
Toro, J.R.3
-
15
-
-
0036122090
-
Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome
-
Zbar B, Alvord WG, Glenn GM, et al. Risk of renal and colonic neoplasms and spontaneous pneumothorax in the Birt-Hogg-Dubé syndrome. Cancer Epidemiol Biomarkers Prev. 2002;11:393-400.
-
(2002)
Cancer Epidemiol Biomarkers Prev.
, vol.11
, pp. 393-400
-
-
Zbar, B.1
Alvord, W.G.2
Glenn, G.M.3
-
17
-
-
9144249602
-
Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma
-
Vanharanta S, Buchta M, McWhinney SR, et al. Early-onset renal cell carcinoma as a novel extraparaganglial component of SDHB-associated heritable paraganglioma. Am J Hum Genet. 2004;74:153-159.
-
(2004)
Am J Hum Genet.
, vol.74
, pp. 153-159
-
-
Vanharanta, S.1
Buchta, M.2
McWhinney, S.R.3
-
18
-
-
84862701397
-
Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3
-
Malinoc A, Sullivan M, Wiech T, et al. Biallelic inactivation of the SDHC gene in renal carcinoma associated with paraganglioma syndrome type 3. Endocr Relat Cancer. 2012;19:283-290.
-
(2012)
Endocr Relat Cancer.
, vol.19
, pp. 283-290
-
-
Malinoc, A.1
Sullivan, M.2
Wiech, T.3
-
19
-
-
84869080815
-
Succinate dehydrogenase kidney cancer: An aggressive example of the Warburg effect in cancer
-
Ricketts CJ, Shuch B, Vocke CD, et al. Succinate dehydrogenase kidney cancer: an aggressive example of the Warburg effect in cancer. J Urol. 2012;188:2063-2071.
-
(2012)
J Urol.
, vol.188
, pp. 2063-2071
-
-
Ricketts, C.J.1
Shuch, B.2
Vocke, C.D.3
-
20
-
-
18544365990
-
Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer
-
Tomlinson IP, Alam NA, Rowan AJ, et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet. 2002;30:406-410.
-
(2002)
Nat Genet.
, vol.30
, pp. 406-410
-
-
Tomlinson, I.P.1
Alam, N.A.2
Rowan, A.J.3
-
21
-
-
84879875481
-
Molecular pathways: Fumarate hydratase-deficient kidney cancer-targeting the Warburg effect in cancer
-
Linehan WM, Rouault TA. Molecular pathways: fumarate hydratase-deficient kidney cancer-targeting the Warburg effect in cancer. Clin Cancer Res. 2013;19:3345-3352.
-
(2013)
Clin Cancer Res.
, vol.19
, pp. 3345-3352
-
-
Linehan, W.M.1
Rouault, T.A.2
-
23
-
-
0035853166
-
Inherited susceptibility to uterine leiomyomas and renal cell cancer
-
Launonen V, Vierimaa O, Kiuru M, et al. Inherited susceptibility to uterine leiomyomas and renal cell cancer. Proc Natl Acad Sci U S A. 2001;98:3387-3392.
-
(2001)
Proc Natl Acad Sci U S A.
, vol.98
, pp. 3387-3392
-
-
Launonen, V.1
Vierimaa, O.2
Kiuru, M.3
-
24
-
-
0037713729
-
Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America
-
Toro JR, Nickerson ML, Wei MH, et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. Am J Hum Genet. 2003;73:95-106.
-
(2003)
Am J Hum Genet.
, vol.73
, pp. 95-106
-
-
Toro, J.R.1
Nickerson, M.L.2
Wei, M.H.3
-
25
-
-
30744457565
-
Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer
-
Wei MH, Toure O, Glenn GM, et al. Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer. J Med Genet. 2006;43:18-27.
-
(2006)
J Med Genet.
, vol.43
, pp. 18-27
-
-
Wei, M.H.1
Toure, O.2
Glenn, G.M.3
-
26
-
-
78650024234
-
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis
-
Smit DL, Mensenkamp AR, Badeloe S, et al. Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis. Clin Genet. 2011;79:49-59.
-
(2011)
Clin Genet.
, vol.79
, pp. 49-59
-
-
Smit, D.L.1
Mensenkamp, A.R.2
Badeloe, S.3
-
27
-
-
58049204264
-
Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer
-
Stewart L, Glenn GM, Stratton P, et al. Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer. Arch Dermatol. 2008;144:1584-1592.
-
(2008)
Arch Dermatol.
, vol.144
, pp. 1584-1592
-
-
Stewart, L.1
Glenn, G.M.2
Stratton, P.3
-
28
-
-
13444309137
-
Clinical features of multiple cutaneous and uterine leiomyomatosis: An underdiagnosed tumor syndrome
-
Alam NA, Barclay E, Rowan AJ, et al. Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndrome. Arch Dermatol. 2005;141:199-206.
-
(2005)
Arch Dermatol.
, vol.141
, pp. 199-206
-
-
Alam, N.A.1
Barclay, E.2
Rowan, A.J.3
-
29
-
-
0141956454
-
Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomata
-
Martinez-Mir A, Glaser B, Chuang GS, et al. Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomata. J Invest Dermatol. 2003;121:741-744.
-
(2003)
J Invest Dermatol.
, vol.121
, pp. 741-744
-
-
Martinez-Mir, A.1
Glaser, B.2
Chuang, G.S.3
-
30
-
-
84871619844
-
Morphologic and molecular characteristics of uterine leiomyomas in hereditary leiomyomatosis and renal cancer (HLRCC) syndrome
-
Sanz-Ortega J, Vocke C, Stratton P, Linehan WM, Merino MJ. Morphologic and molecular characteristics of uterine leiomyomas in hereditary leiomyomatosis and renal cancer (HLRCC) syndrome. Am J Surg Pathol. 2013;37:74-80.
-
(2013)
Am J Surg Pathol.
, vol.37
, pp. 74-80
-
-
Sanz-Ortega, J.1
Vocke, C.2
Stratton, P.3
Linehan, W.M.4
Merino, M.J.5
-
31
-
-
1542469716
-
Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors
-
Lehtonen R, Kiuru M, Vanharanta S, et al. Biallelic inactivation of fumarate hydratase (FH) occurs in nonsyndromic uterine leiomyomas but is rare in other tumors. Am J Pathol. 2004;164:17-22.
-
(2004)
Am J Pathol.
, vol.164
, pp. 17-22
-
-
Lehtonen, R.1
Kiuru, M.2
Vanharanta, S.3
-
32
-
-
34248336258
-
Hereditary leiomyomatosis and renal cell cancer: A syndrome associated with an aggressive form of inherited renal cancer
-
Grubb RL 3rd, Franks ME, Toro J, et al. Hereditary leiomyomatosis and renal cell cancer: a syndrome associated with an aggressive form of inherited renal cancer. J Urol. 2007;177:2074-2080.
-
(2007)
J Urol.
, vol.177
, pp. 2074-2080
-
-
Grubb III, R.L.1
Franks, M.E.2
Toro, J.3
-
33
-
-
79953703400
-
Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma
-
Gardie B, Remenieras A, Kattygnarath D, et al. Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma. J Med Genet. 2011;48:226-234.
-
(2011)
J Med Genet.
, vol.48
, pp. 226-234
-
-
Gardie, B.1
Remenieras, A.2
Kattygnarath, D.3
-
34
-
-
34748836454
-
The morphologic spectrum of kidney tumors in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome
-
Merino MJ, Torres-Cabala C, Pinto PA, Linehan WM. The morphologic spectrum of kidney tumors in hereditary leiomyomatosis and renal cell carcinoma (HLRCC) syndrome. Am J Surg Pathol. 2007;31:1578-1585.
-
(2007)
Am J Surg Pathol.
, vol.31
, pp. 1578-1585
-
-
Merino, M.J.1
Torres-Cabala, C.2
Pinto, P.A.3
Linehan, W.M.4
-
35
-
-
12444259659
-
Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency
-
Alam NA, Rowan AJ, Wortham NC, et al. Genetic and functional analyses of FH mutations in multiple cutaneous and uterine leiomyomatosis, hereditary leiomyomatosis and renal cancer, and fumarate hydratase deficiency. Hum Mol Genet. 2003;12:1241-1252.
-
(2003)
Hum Mol Genet.
, vol.12
, pp. 1241-1252
-
-
Alam, N.A.1
Rowan, A.J.2
Wortham, N.C.3
-
36
-
-
84872137300
-
Adrenal nodular hyperplasia in hereditary leiomyomatosis and renal cell cancer
-
Shuch B, Ricketts CJ, Vocke CD, et al. Adrenal nodular hyperplasia in hereditary leiomyomatosis and renal cell cancer. J Urol. 2013;189: 430-435.
-
(2013)
J Urol.
, vol.189
, pp. 430-435
-
-
Shuch, B.1
Ricketts, C.J.2
Vocke, C.D.3
-
37
-
-
77954978039
-
Hereditary leiomyomatosis and renal cell carcinoma: Very early diagnosis of renal cancer in a paediatric patient
-
Alrashdi I, Levine S, Paterson J, et al. Hereditary leiomyomatosis and renal cell carcinoma: very early diagnosis of renal cancer in a paediatric patient. Fam Cancer. 2010;9:239-243.
-
(2010)
Fam Cancer.
, vol.9
, pp. 239-243
-
-
Alrashdi, I.1
Levine, S.2
Paterson, J.3
-
38
-
-
42449137948
-
The FH mutation database: An online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency
-
Bayley JP, Launonen V, Tomlinson IP. The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency. BMC Med Genet. 2008;9:20.
-
(2008)
BMC Med Genet.
, vol.9
, pp. 20
-
-
Bayley, J.P.1
Launonen, V.2
Tomlinson, I.P.3
-
39
-
-
22944469759
-
Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer
-
Alam NA, Olpin S, Leigh IM. Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer. Br J Dermatol. 2005;153:11-17.
-
(2005)
Br J Dermatol.
, vol.153
, pp. 11-17
-
-
Alam, N.A.1
Olpin, S.2
Leigh, I.M.3
-
40
-
-
24944506461
-
Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata
-
Chuang GS, Martinez-Mir A, Geyer A, et al. Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata. J Am Acad Dermatol. 2005;52:410-416.
-
(2005)
J Am Acad Dermatol.
, vol.52
, pp. 410-416
-
-
Chuang, G.S.1
Martinez-Mir, A.2
Geyer, A.3
-
41
-
-
13244279482
-
Familial multiple cutaneous and uterine leiomyomas associated with papillary renal cell cancer
-
Chan I, Wong T, Martinez-Mir A, Christiano AM, McGrath JA. Familial multiple cutaneous and uterine leiomyomas associated with papillary renal cell cancer. Clin Exp Dermatol. 2005;30:75-78.
-
(2005)
Clin Exp Dermatol.
, vol.30
, pp. 75-78
-
-
Chan, I.1
Wong, T.2
Martinez-Mir, A.3
Christiano, A.M.4
McGrath, J.A.5
-
42
-
-
37849000143
-
Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC)
-
Heinritz W, Paasch U, Sticherling M, et al. Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC). Ann Hum Genet. 2008;72:35-40.
-
(2008)
Ann Hum Genet.
, vol.72
, pp. 35-40
-
-
Heinritz, W.1
Paasch, U.2
Sticherling, M.3
-
43
-
-
33749249394
-
Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer
-
Pithukpakorn M, Wei MH, Toure O, et al. Fumarate hydratase enzyme activity in lymphoblastoid cells and fibroblasts of individuals in families with hereditary leiomyomatosis and renal cell cancer. J Med Genet. 2006;43:755-762.
-
(2006)
J Med Genet.
, vol.43
, pp. 755-762
-
-
Pithukpakorn, M.1
Wei, M.H.2
Toure, O.3
-
44
-
-
23644448721
-
HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: Novel role of fumarate in regulation of HIF stability
-
Isaacs JS, Jung YJ, Mole DR, et al. HIF overexpression correlates with biallelic loss of fumarate hydratase in renal cancer: novel role of fumarate in regulation of HIF stability. Cancer Cell. 2005;8:143-153.
-
(2005)
Cancer Cell.
, vol.8
, pp. 143-153
-
-
Isaacs, J.S.1
Jung, Y.J.2
Mole, D.R.3
-
45
-
-
26444570010
-
Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations
-
Pollard PJ, Briere JJ, Alam NA, B et al. Accumulation of Krebs cycle intermediates and over-expression of HIF1α in tumours which result from germline FH and SDH mutations. Hum Mol Genet. 2005;14: 2231-2239.
-
(2005)
Hum Mol Genet.
, vol.14
, pp. 2231-2239
-
-
Pollard, P.J.1
Briere, J.J.2
Alam, N.A.B.3
-
46
-
-
33646875238
-
S-(2-succinyl)cysteine: A novel chemical modification of tissue proteins by a Krebs cycle intermediate
-
Alderson NL, Wang Y, Blatnik M, et al. S-(2-succinyl)cysteine: a novel chemical modification of tissue proteins by a Krebs cycle intermediate. Arch Biochem Biophys. 2006;450:1-8.
-
(2006)
Arch Biochem Biophys.
, vol.450
, pp. 1-8
-
-
Alderson, N.L.1
Wang, Y.2
Blatnik, M.3
-
47
-
-
79960916285
-
Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status
-
Bardella C, El-Bahrawy M, Frizzell N, et al. Aberrant succination of proteins in fumarate hydratase-deficient mice and HLRCC patients is a robust biomarker of mutation status. J Pathol. 2011;225:4-11.
-
(2011)
J Pathol.
, vol.225
, pp. 4-11
-
-
Bardella, C.1
El-Bahrawy, M.2
Frizzell, N.3
-
48
-
-
84878785993
-
The Keap1-Nrf2 pathway: Mechanisms of activation and dysregulation in cancer
-
Kansanen E, Kuosmanen SM, Leinonen H, Levonen AL. The Keap1-Nrf2 pathway: mechanisms of activation and dysregulation in cancer. Redox Biol. 2013;1:45-49.
-
(2013)
Redox Biol.
, vol.1
, pp. 45-49
-
-
Kansanen, E.1
Kuosmanen, S.M.2
Leinonen, H.3
Levonen, A.L.4
-
49
-
-
80054767730
-
Renal cyst formation in Fh1-deficient mice is independent of the Hif/Phd pathway: Roles for fumarate in KEAP1 succination and Nrf2 signaling
-
Adam J, Hatipoglu E, O'Flaherty L, et al. Renal cyst formation in Fh1-deficient mice is independent of the Hif/Phd pathway: roles for fumarate in KEAP1 succination and Nrf2 signaling. Cancer Cell. 2011;20:524-537.
-
(2011)
Cancer Cell.
, vol.20
, pp. 524-537
-
-
Adam, J.1
Hatipoglu, E.2
O'Flaherty, L.3
-
50
-
-
80054772589
-
An antioxidant response phenotype shared between hereditary and sporadic type 2 papillary renal cell carcinoma
-
Ooi A, Wong JC, Petillo D, et al. An antioxidant response phenotype shared between hereditary and sporadic type 2 papillary renal cell carcinoma. Cancer Cell. 2011;20:511-523.
-
(2011)
Cancer Cell.
, vol.20
, pp. 511-523
-
-
Ooi, A.1
Wong, J.C.2
Petillo, D.3
-
53
-
-
28844473140
-
Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's syndrome)
-
Ritzmann S, Hanneken S, Neumann NJ, Ruzicka T, Kruse R. Type 2 segmental manifestation of cutaneous leiomyomatosis in four unrelated women with additional uterine leiomyomas (Reed's syndrome). Dermatology. 2006;212:84-87.
-
(2006)
Dermatology.
, vol.212
, pp. 84-87
-
-
Ritzmann, S.1
Hanneken, S.2
Neumann, N.J.3
Ruzicka, T.4
Kruse, R.5
-
54
-
-
33749137315
-
Multiple painful cutaneous nodules and renal mass
-
Rothman A, Glenn GM, Choyke L, Srinivasan R, Linehan WM, Cowen EW. Multiple painful cutaneous nodules and renal mass. J Am Acad Dermatol. 2006;55:683-686.
-
(2006)
J Am Acad Dermatol.
, vol.55
, pp. 683-686
-
-
Rothman, A.1
Glenn, G.M.2
Choyke, L.3
Srinivasan, R.4
Linehan, W.M.5
Cowen, E.W.6
|