A retrospective review of 48 individuals, including 12 families, molecularly diagnosed with hereditary leiomyomatosis and renal cell cancer (HLRCC)
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[1] C. Genestie,et al. Reassessing the clinical spectrum associated with hereditary leiomyomatosis and renal cell carcinoma syndrome in French FH mutation carriers , 2017, Clinical genetics.
[2] K. Garg,et al. Immunohistochemistry for 2-Succinocysteine (2SC) and Fumarate Hydratase (FH) in Cutaneous Leiomyomas May Aid in Identification of Patients With HLRCC (Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome) , 2016, The American journal of surgical pathology.
[3] Aikseng Ooi,et al. Sustained NRF2 activation in hereditary leiomyomatosis and renal cell cancer (HLRCC) and in hereditary tyrosinemia type 1 (HT1). , 2015, Biochemical Society transactions.
[4] W. Linehan,et al. Hereditary leiomyomatosis and renal cell cancer (HLRCC): renal cancer risk, surveillance and treatment , 2014, Familial Cancer.
[5] M. Simpson,et al. Germline FH mutations presenting with pheochromocytoma. , 2014, The Journal of clinical endocrinology and metabolism.
[6] W. Linehan,et al. Hereditary leiomyomatosis and renal cell carcinoma , 2014, International journal of nephrology and renovascular disease.
[7] P. Rustin,et al. Germline mutations in FH confer predisposition to malignant pheochromocytomas and paragangliomas. , 2014, Human molecular genetics.
[8] C. Tan,et al. Potential genetic anticipation in hereditary leiomyomatosis-renal cell cancer (HLRCC) , 2014, Familial Cancer.
[9] Lars Egevad,et al. The International Society of Urological Pathology (ISUP) Vancouver Classification of Renal Neoplasia , 2013, The American journal of surgical pathology.
[10] L. Aaltonen,et al. Aberrant succination of proteins in fumarate hydratase‐deficient mice and HLRCC patients is a robust biomarker of mutation status , 2011, The Journal of pathology.
[11] H. Lehtonen,et al. Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics , 2011, Familial Cancer.
[12] L. Thomas,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 , 2011, Journal of Medical Genetics.
[13] L. Hoefsloot,et al. Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysis , 2011, Clinical genetics.
[14] C. de Bazelaire,et al. Hereditary renal cancer syndromes: an update of a systematic review. , 2010, European urology.
[15] Peter A Pinto,et al. The clinical implications of the genetics of renal cell carcinoma. , 2009, Urologic oncology.
[16] W. Linehan,et al. Association of germline mutations in the fumarate hydratase gene and uterine fibroids in women with hereditary leiomyomatosis and renal cell cancer. , 2008, Archives of dermatology.
[17] Jean-Pierre Bayley,et al. The FH mutation database: an online database of fumarate hydratase mutations involved in the MCUL (HLRCC) tumor syndrome and congenital fumarase deficiency , 2008, BMC Medical Genetics.
[18] L. Aaltonen,et al. Increased risk of cancer in patients with fumarate hydratase germline mutation , 2005, Journal of Medical Genetics.
[19] P. Choyke,et al. Novel mutations in FH and expansion of the spectrum of phenotypes expressed in families with hereditary leiomyomatosis and renal cell cancer , 2005, Journal of Medical Genetics.
[20] A. Rowan,et al. Clinical features of multiple cutaneous and uterine leiomyomatosis: an underdiagnosed tumor syndrome. , 2005, Archives of dermatology.
[21] P. Choyke,et al. Mutations in the fumarate hydratase gene cause hereditary leiomyomatosis and renal cell cancer in families in North America. , 2003, American journal of human genetics.
[22] A. Paetau,et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer , 2002, Nature Genetics.
[23] K. Nathanson,et al. Hereditary kidney cancer syndromes. , 2014, Advances in chronic kidney disease.