von Hippel-Lindau disease affecting 43 members of a single kindred.
about
Genotype-phenotype correlation in von Hippel-Lindau disease with retinal angiomatosisVHL c.505 T>C mutation confers a high age related penetrance but no increased overall mortalityBiological and clinical impact of hemangioblastoma-associated peritumoral cysts in von Hippel-Lindau disease.Prospective natural history study of central nervous system hemangioblastomas in von Hippel-Lindau diseaseLong-term outcome after resection of brainstem hemangioblastomas in von Hippel-Lindau disease.Developmentally arrested structures preceding cerebellar tumors in von Hippel-Lindau diseaseCentral nervous system lesions in von Hippel-Lindau syndromePresymptomatic diagnosis of von Hippel-Lindau disease with flanking DNA markers.Detailed genetic mapping of the von Hippel-Lindau disease tumour suppressor gene.Von Hippel-Lindau disease: a genetic study.Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinomaMutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.Detection of germline mutations in the von Hippel-Lindau disease gene by the primer specified restriction map modification methodA genetic register for von Hippel-Lindau diseaseOcular manifestations of von Hippel-Lindau disease: clinical and genetic investigations.Estrogen inhibits renal cell carcinoma cell progression through estrogen receptor-β activation.A von Hippel-Lindau disease-associated microcystic adenoma of the ethmoid sinus: case report.The impact of molecular genetic analysis of the VHL gene in patients with haemangioblastomas of the central nervous system.Multiple neuroendocrine tumors of the pancreas in von Hippel-Lindau disease patients: histopathological and molecular genetic analysisAllelic deletion and mutation of the von Hippel-Lindau (VHL) tumor suppressor gene in pancreatic microcystic adenomas.Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients.Histopathology and molecular genetics of multiple cysts and microcystic (serous) adenomas of the pancreas in von Hippel-Lindau patients.Germ-line mutations in the von Hippel-Lindau tumor-suppressor gene are similar to somatic von Hippel-Lindau aberrations in sporadic renal cell carcinoma.Ocular clusterin expression in von Hippel-Lindau diseaseSpinal cord hemangioblastomas in von hippel-lindau disease: management of asymptomatic and symptomatic tumors.Neurologic manifestations of von Hippel-Lindau diseaseLongitudinal analysis of retinal hemangioblastomatosis and visual function in ocular von Hippel-Lindau diseaseA novel mutation in the von hippel-lindau tumor suppressor gene identified in a patient presenting with gestational diabetes mellitus.Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of Von Hippel Lindau disease.Long-term follow-up clinical courses of cerebellar hemangioblastoma in von hippel-lindau disease : two case reports and a literature review.Familial renal cell carcinoma: clinical and molecular genetic aspects.Management of uncommon disorders in pregnancy: Von Hippel-Lindau disease, Gitelman syndrome, and Nutcracker syndrome.Management Strategies and Outcomes for VHL-related Craniospinal Hemangioblastomas.Von Hippel-Lindau disease.Von Hippel-Lindau Disease.
P2860
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P2860
von Hippel-Lindau disease affecting 43 members of a single kindred.
description
1989 nî lūn-bûn
@nan
1989年の論文
@ja
1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
@zh-cn
name
von Hippel-Lindau disease affecting 43 members of a single kindred.
@en
type
label
von Hippel-Lindau disease affecting 43 members of a single kindred.
@en
prefLabel
von Hippel-Lindau disease affecting 43 members of a single kindred.
@en
P2093
P1433
P1476
von Hippel-Lindau disease affecting 43 members of a single kindred.
@en
P2093
P407
P577
1989-01-01T00:00:00Z