[Hereditary renal tumors: More common than expected?].

[1]  M. Abdel-Rahman,et al.  Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases , 2016, Clinical genetics.

[2]  A. Sangoi,et al.  Eosinophilic, Solid, and Cystic Renal Cell Carcinoma: Clinicopathologic Study of 16 Unique, Sporadic Neoplasms Occurring in Women , 2016, The American journal of surgical pathology.

[3]  P. Humphrey,et al.  Hereditary Renal Cell Carcinoma Syndromes: Clinical, Pathologic, and Genetic Features , 2015, The American journal of surgical pathology.

[4]  D. Solomon,et al.  Morphology and Immunohistochemistry for 2SC and FH Aid in Detection of Fumarate Hydratase Gene Aberrations in Uterine Leiomyomas From Young Patients , 2015, The American journal of surgical pathology.

[5]  Douglas E. V. Pires,et al.  Germline Mutations in the CDKN2B Tumor Suppressor Gene Predispose to Renal Cell Carcinoma. , 2015, Cancer discovery.

[6]  B. Dickson,et al.  Familial pheochromocytoma and renal cell carcinoma syndrome: TMEM127 as a novel candidate gene for the association , 2015, Virchows Archiv.

[7]  A. Sangoi,et al.  Tuberous Sclerosis–associated Renal Cell Carcinoma: A Clinicopathologic Study of 57 Separate Carcinomas in 18 Patients , 2014, The American journal of surgical pathology.

[8]  R. Hammer,et al.  Bap1 is essential for kidney function and cooperates with Vhl in renal tumorigenesis , 2014, Proceedings of the National Academy of Sciences.

[9]  R. Nussbaum,et al.  Renal Cell Carcinoma in Tuberous Sclerosis Complex , 2014, The American journal of surgical pathology.

[10]  M. Berger,et al.  Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome–associated Renal Cancer: Recognition of the Syndrome by Pathologic Features and the Utility of Detecting Aberrant Succination by Immunohistochemistry , 2014, The American journal of surgical pathology.

[11]  L. Strong,et al.  Expanding the clinical phenotype of hereditary BAP1 cancer predisposition syndrome, reporting three new cases , 2014, Genes, chromosomes & cancer.

[12]  W. Linehan,et al.  Germline PTEN mutation Cowden syndrome: an underappreciated form of hereditary kidney cancer. , 2013, The Journal of urology.

[13]  A. Vortmeyer,et al.  Renal cancer in von Hippel–Lindau disease and related syndromes , 2013, Nature Reviews Nephrology.

[14]  J. McKenney,et al.  Hereditary Syndromes With Associated Renal Neoplasia: A Practical Guide to Histologic Recognition in Renal Tumor Resection Specimens , 2013, Advances in anatomic pathology.

[15]  N. Grishin,et al.  A Novel Germline Mutation in BAP1 Predisposes to Familial Clear-Cell Renal Cell Carcinoma , 2013, Molecular Cancer Research.

[16]  S. Richard,et al.  Von Hippel-Lindau: how a rare disease illuminates cancer biology. , 2013, Seminars in cancer biology.

[17]  Ming Zhou,et al.  Papillary renal cell carcinoma is associated with PTEN hamartoma tumor syndrome. , 2012, Urology.

[18]  V. Reuter,et al.  Morphologic Features of Uterine Leiomyomas Associated With Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome: A Case Report , 2011, The American journal of surgical pathology.

[19]  H. Lehtonen,et al.  Hereditary leiomyomatosis and renal cell cancer: update on clinical and molecular characteristics , 2011, Familial Cancer.

[20]  H. Moch Cystic Renal Tumors: New Entities and Novel Concepts , 2010, Advances in anatomic pathology.

[21]  S. Richard,et al.  Birt-Hogg-Dubé syndrome: diagnosis and management. , 2009, The Lancet. Oncology.

[22]  Charis Eng,et al.  Germline mutations and variants in the succinate dehydrogenase genes in Cowden and Cowden-like syndromes. , 2008, American journal of human genetics.

[23]  H. Moch,et al.  Sporadic human renal tumors display frequent allelic imbalances and novel mutations of the HRPT2 gene , 2007, Oncogene.

[24]  J. Carpten,et al.  Somatic and germ-line mutations of the HRPT2 gene in sporadic parathyroid carcinoma. , 2003, The New England journal of medicine.

[25]  M. Coppes,et al.  Recent advances in Wilms tumor genetics , 2002, Current opinion in pediatrics.

[26]  A. Jochemsen,et al.  WT1 proteins: functions in growth and differentiation. , 2001, Gene.

[27]  P. Choyke,et al.  Familial renal oncocytoma: clinicopathological study of 5 families. , 1998, The Journal of urology.

[28]  C. Larsson,et al.  Autosomal dominant primary hyperparathyroidism and jaw tumor syndrome associated with renal hamartomas and cystic kidney disease: linkage to 1q21-q32 and loss of the wild type allele in renal hamartomas. , 1996, The Journal of clinical endocrinology and metabolism.

[29]  Jonathan I. Epstein,et al.  WHO Classification of of Tumours of the Urinary System and Male Genital Organs , 2016 .

[30]  R. Lonser,et al.  von Hippel-Lindau disease , 2003, The Lancet.

[31]  Fahed Abdullah Salem SIU Scholar: Dr. Fahed Abdullah Salem Baaboud. , 2012 .