Zobrazeno 1 - 10
of 91
pro vyhledávání: '"V M, Riccardi"'
Autor:
V. M. Riccardi
Publikováno v:
Archives of Dermatology. 129:577-581
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f85ac621a179b72b29ba58d7648db978
https://doi.org/10.1001/archderm.129.5.577
https://doi.org/10.1001/archderm.129.5.577
Autor:
G. E. Farmer, Kevin M. Anderson, Anil G. Menon, Richard N. Freiman, Jeng-Shin Lee, Jean M. Whaley, Fugen Li, David W. Yandell, Richard Y. Chung, V M Riccardi
Publikováno v:
Proceedings of the National Academy of Sciences. 87:5435-5439
von Recklinghausen neurofibromatosis (NF1) is a common hereditary disorder characterized by neural crest-derived tumors, particularly benign neurofibromas whose malignant transformation to neurofibrosarcomas can be fatal. The NF1 gene has been mapped
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c18d3d2e6616adb4f668f77f8b11e8c0
https://doi.org/10.1073/pnas.87.14.5435
https://doi.org/10.1073/pnas.87.14.5435
Autor:
V M, Riccardi
Publikováno v:
Clinical genetics. 58(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8668350454cbd086a3122440c28b16d8
https://pubmed.ncbi.nlm.nih.gov/11140831
https://pubmed.ncbi.nlm.nih.gov/11140831
Autor:
G E, Airewele, A J, Sigurdson, K J, Wiley, B E, Frieden, L W, Caldarera, V M, Riccardi, R A, Lewis, M M, Chintagumpala, J L, Ater, S E, Plon, M L, Bondy
Publikováno v:
Genetic epidemiology. 20(1)
The risk of malignancies among persons with neurofibromatosis 1 (NF1) is higher than in the general population, but the excess risk has not been precisely estimated. The effects of gender and inheritance pattern on cancer risk are unclear. Therefore,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8c755bfcf7bacba748449884f24e8864
https://pubmed.ncbi.nlm.nih.gov/11119298
https://pubmed.ncbi.nlm.nih.gov/11119298
Publikováno v:
Genetic epidemiology. 19(4)
Neurofibromatosis 1 (NF1), an autosomal dominant disease, exhibits extreme clinical variability. This variability greatly increases the burden for affected families and impairs our ability to understand the pathogenesis of NF1. Recognition of heterog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d311621fb5135416492ef4f8a9a4debc
https://pubmed.ncbi.nlm.nih.gov/11108651
https://pubmed.ncbi.nlm.nih.gov/11108651
Publikováno v:
American journal of medical genetics. 93(5)
One of the most clinically aggressive cancers associated with neurofibromatosis 1 (NF1) is the malignant peripheral nerve sheath tumor (MPNST). To determine the incidence and relative risk (RR) of MPNSTs in individuals with NF1, 1,475 individuals wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4a9a11f406582078273999bb6c78173c
https://pubmed.ncbi.nlm.nih.gov/10951462
https://pubmed.ncbi.nlm.nih.gov/10951462
Autor:
V M, Riccardi
Publikováno v:
Teratology. 62(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c52f4f870b377fa676824bcf95e9f3bc
https://pubmed.ncbi.nlm.nih.gov/10861625
https://pubmed.ncbi.nlm.nih.gov/10861625
Autor:
V M, Riccardi
Publikováno v:
Administrative radiology journal : AR. 17(11)
If there is any one thing that is missing in today's health care delivery system, it is consumerism. This will be remedied as more and more Americans start taking direct responsibility for how their health care dollars are spent. Hand in hand with su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f00a922544422a8455f7f63d53c17291
https://pubmed.ncbi.nlm.nih.gov/10345001
https://pubmed.ncbi.nlm.nih.gov/10345001
Publikováno v:
Journal of the American Academy of Dermatology. 37(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1d14c0d392e85a679f60b26e97d946bf
https://pubmed.ncbi.nlm.nih.gov/9344204
https://pubmed.ncbi.nlm.nih.gov/9344204
Publikováno v:
Genetic epidemiology. 14(5)
Sporadic neurofibromatosis 1 (NF1) occurs in the absence of a family history of the disease and usually results from a new mutation in the germ cell of one of the parents, most commonly the father. Older paternal age may increase the risk for a new g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0b3c402048bbc52436b4fccbcd54ae1d
https://pubmed.ncbi.nlm.nih.gov/9358268
https://pubmed.ncbi.nlm.nih.gov/9358268