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  1. ... sensation in limbs clinical diagnosis: no tests required Von Hippel-Lindau syndrome History Exam 1st investigation Other investigations imbalance; ... sensation in limbs clinical diagnosis: no tests required Von Hippel-Lindau syndrome History Exam 1st investigation Other investigations imbalance; ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  2. ... sclerosis may present with ungual angiofibromas. vision loss (von Hippel Lindau) Patients with the hereditary syndrome von Hippel Lindau may present with vision loss and retinal angiomatosis ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  3. ... 2A and 2B is the RET proto-oncogene. Von Hippel-Lindau (VHL) disease In those with VHL disease, lifetime risk is 10% to 20%. [23] Maher ER. Von Hippel-Lindau disease. Curr Mol Med. 2004 Dec;4(8): ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  4. ... 2A and 2B is the RET proto-oncogene. Von Hippel-Lindau (VHL) disease In those with VHL disease, lifetime risk is 10% to 20%. [23] Maher ER. Von Hippel-Lindau disease. Curr Mol Med. 2004 Dec;4(8): ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  5. ... cysts, and renal cell carcinomas. Tuberous sclerosis complex von Hippel-Lindau syndrome(VHL) SIGNS / SYMPTOMS INVESTIGATIONS SIGNS / SYMPTOMS Renal ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  6. ... Risk factors include multiple endocrine neoplasia type 2, Von Hippel-Lindau syndrome, and neurofibromatosis type 1. ◊ Diagnosed by increased ... such as multiple endocrine neoplasia type 2 or Von Hippel-Lindau syndrome. [ 1] [ 2] [ 3] [ 4] The tumour was ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  7. ... rates are variable. This is especially true of von Hippel Lindau (VHL) syndrome, which is associated with the clear ... known syndromes with identified gene mutations (e.g., von Hippel Lindau, tuberous sclerosis, constitutional chromosome 3 translocation, hereditary papillary ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  8. ... Risk factors include multiple endocrine neoplasia type 2, Von Hippel-Lindau syndrome, and neurofibromatosis type 1. Diagnosed by increased ... such as multiple endocrine neoplasia type 2 or Von Hippel-Lindau syndrome. [1] Lenders JW, Eisenhofer G, Manelli M, ...
    Source: BMJ Best Practice, BMJ Best Practice
    Information Type: Oppslagsverk, Oppslagsverk
  9. ... rates are variable. This is especially true of von Hippel Lindau (VHL) syndrome, which is associated with the clear ... et al. Clinical features and natural history of von Hippel-Lindau disease. Q J Med. 1990;77:1151-1163. ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
  10. ... reveal history of causative hereditary syndromes (e.g., von Hippel Lindau, hereditary papillary RCC, Birt-Hogg-Dube, hereditary leiomyomatous ... angiofibromas/ungual fibromas (tuberous sclerosis); and retinal angiomatosis (von Hippel Lindau). Physical examination should also include an assessment of ...
    Source: BMJ Best Practice
    Information Type: Oppslagsverk
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