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Journal of the American Academy of Dermatology, ISSN 0190-9622, 02/2016, Volume 74, Issue 2, pp. 231 - 231
There are a significant number of diseases and treatment considerations of considerable importance relating to the skin and renal systems. This emphasizes the... 
genetic | nephrology | dermatology | autoimmune | genodermatoses | inflammatory | nephrocutaneous | Uterine Neoplasms - therapy | Skin Diseases - genetics | Tuberous Sclerosis - complications | Beckwith-Wiedemann Syndrome - therapy | Fabry Disease - genetics | Humans | Genetic Diseases, Inborn - genetics | von Hippel-Lindau Disease - complications | Genetic Diseases, Inborn - therapy | Beckwith-Wiedemann Syndrome - genetics | Kidney Diseases - genetics | Nail-Patella Syndrome - therapy | Neurofibromatosis 1 - therapy | Neoplastic Syndromes, Hereditary | Beckwith-Wiedemann Syndrome - complications | Leiomyomatosis - complications | Leiomyomatosis - therapy | Birt-Hogg-Dube Syndrome - complications | Turner Syndrome - complications | Turner Syndrome - therapy | Neurofibromatosis 1 - genetics | Uterine Neoplasms - genetics | von Hippel-Lindau Disease - therapy | Hamartoma Syndrome, Multiple - genetics | Skin Neoplasms - therapy | Nail-Patella Syndrome - genetics | Fabry Disease - complications | von Hippel-Lindau Disease - genetics | Hamartoma Syndrome, Multiple - complications | Birt-Hogg-Dube Syndrome - genetics | Tuberous Sclerosis - genetics | Tuberous Sclerosis - therapy | Skin Neoplasms - complications | Birt-Hogg-Dube Syndrome - therapy | Hamartoma Syndrome, Multiple - therapy | Skin Neoplasms - genetics | Neurofibromatosis 1 - complications | Uterine Neoplasms - complications | Nail-Patella Syndrome - complications | Turner Syndrome - genetics | Fabry Disease - therapy | Mutation | Leiomyomatosis - genetics
Journal Article
Nature Reviews Cancer, ISSN 1474-175X, 03/2003, Volume 3, Issue 3, pp. 193 - 202
Mitochondrial defects have been associated with neurological disorders, as well as cancers. Two ubiquitously expressed mitochondrial enzymes - succinate... 
RESPIRATORY-CHAIN | GERM-LINE MUTATIONS | ONCOLOGY | LEIGH-SYNDROME | C-OXIDASE DEFICIENCY | HEREDITARY PARAGANGLIOMA | SACCHAROMYCES-CEREVISIAE | RENAL-CELL CANCER | DNA MUTATIONS | RET PROTOONCOGENE | COMPLEX-I DEFICIENCY | Mitochondria - enzymology | Protein Subunits | Kidney Neoplasms - genetics | Humans | Mitochondrial Encephalomyopathies - enzymology | Carcinoma, Renal Cell - genetics | Pheochromocytoma - enzymology | Apoptosis - genetics | Oxidoreductases - physiology | Fumarate Hydratase - deficiency | Electron Transport Complex II | Multienzyme Complexes - deficiency | Carcinoma, Renal Cell - enzymology | Neoplastic Syndromes, Hereditary - genetics | Oxidoreductases - deficiency | Paraganglioma - enzymology | Free Radicals | Neovascularization, Physiologic - genetics | Oxidoreductases - genetics | Paraganglioma - genetics | Fumarate Hydratase - physiology | Mitochondrial Encephalomyopathies - genetics | Multienzyme Complexes - genetics | Fumarate Hydratase - genetics | Forecasting | Succinate Dehydrogenase - deficiency | Homozygote | Neovascularization, Physiologic - physiology | Citric Acid Cycle - genetics | Succinate Dehydrogenase - genetics | Energy Metabolism | Kidney Neoplasms - enzymology | Multienzyme Complexes - physiology | Neoplastic Syndromes, Hereditary - enzymology | Heterozygote | Pheochromocytoma - genetics | Apoptosis - physiology | Mutation | Succinate Dehydrogenase - physiology | Leiomyomatosis - enzymology | Leiomyomatosis - genetics | Enzymes | Mitochondria | Gene mutations | Physiological aspects | Genetic aspects | Research | Health aspects | Cancer
Journal Article
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e76 - e82
Journal Article
European Journal of Radiology, ISSN 0720-048X, 04/2018, Volume 101, pp. 8 - 16
It is estimated that up to 8% of currently diagnosed renal cancers are part of a hereditary syndrome. The radiologist may be the first person to associate a... 
Tuberous sclerosis | von Hippel-Lindau Disease | Genetic predisposition to disease | Renal cell carcinoma | Neoplasms | Hereditary leiomyomatosis and renal cell cancer | GERMLINE MUTATION | MANAGEMENT | HIPPEL-LINDAU-DISEASE | CELL CARCINOMA | TUBEROUS SCLEROSIS COMPLEX | ANGIOMYOLIPOMA | HOGG-DUBE-SYNDROME | LEIOMYOMATOSIS | VISIBLE FAT | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | KIDNEY CANCER | Kidney Neoplasms - genetics | Birt-Hogg-Dube Syndrome - diagnostic imaging | Uterine Neoplasms - diagnostic imaging | Humans | Carcinoma, Renal Cell - genetics | Tomography, X-Ray Computed | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnostic imaging | Neoplastic Syndromes, Hereditary - diagnostic imaging | Neoplastic Syndromes, Hereditary - genetics | Uterine Neoplasms - genetics | Skin Neoplasms - diagnostic imaging | Genetic Predisposition to Disease - genetics | Tuberous Sclerosis - diagnostic imaging | Carcinoma, Renal Cell - diagnostic imaging | Early Detection of Cancer | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | von Hippel-Lindau Disease - genetics | Mutation - genetics | Birt-Hogg-Dube Syndrome - genetics | Tuberous Sclerosis - genetics | Magnetic Resonance Imaging | Kidney Neoplasms - diagnostic imaging | Skin Neoplasms - genetics | von Hippel-Lindau Disease - diagnostic imaging | Leiomyomatosis - genetics | Leiomyomatosis - diagnostic imaging
Journal Article
Cancer, ISSN 0008-543X, 07/2017, Volume 123, Issue 13, pp. 2452 - 2458
BACKGROUND Patients with hereditary leiomyomatosis and renal cell carcinoma (HLRCC) resulting from fumarate hydratase (FH) mutations may present with skin,... 
hereditary leiomyomatosis and renal cell carcinoma (HLRCC) | renal cell carcinoma | pathology | histology | fumarate hydratase | genetic testing | diagnosis | FH | CLASSIFICATION | CANCER | TUMORS | FEATURES | ONCOLOGY | FAMILIES | HLRCC SYNDROME | MUTATIONS | SPECTRUM | UTERINE LEIOMYOMAS | Kidney Neoplasms - genetics | Neoplastic Syndromes, Hereditary - pathology | Genetic Testing | Uterine Neoplasms - pathology | Humans | Middle Aged | Carcinoma, Renal Cell - genetics | Male | Leiomyoma - pathology | Urinary Bladder Neoplasms - genetics | Leiomyomatosis - pathology | Urinary Bladder Neoplasms - pathology | Adult | Female | Neoplastic Syndromes, Hereditary - genetics | Retrospective Studies | Skin Neoplasms - pathology | Uterine Neoplasms - genetics | Carcinoma, Renal Cell - pathology | Fumarate Hydratase - genetics | Skin Neoplasms - genetics | Kidney Neoplasms - pathology | Mutation | Leiomyomatosis - genetics | Neoplasm Staging | Leiomyoma - genetics | Cohort Studies | Pathology | Cancer patients | Usage | Care and treatment | Genetic aspects | Carcinoma, Renal cell | Health aspects | Evaluation | Test procedures | Health risks | Bladder | Event-related potentials | Medical screening | Patients | Genetic screening | Metastases | Fumarate hydratase | Uterus | Urinary bladder | Kidney cancer | Skin | Diagnostic systems | Age | Clear cell-type renal cell carcinoma | Tumors | Cancer | Kidney transplantation
Journal Article