Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Multiple neurofibromatosis"'
Autor:
Syeda Ayesha, Qazi Abdul Bari Siddique, M. Vijaya Kumar, Omer Bin Ali Jabri, Mohd Naseeruddin
Publikováno v:
Annals of International medical and Dental Research. 3
Autor:
Norberto Perri Moraes, Glauco Issamu Miyahara, Marceli Moço Silva, João Paulo De Carli, Marcelo Macedo Crivelini, Soluete Oliveira da Silva, Maria Salete Sandini Linden
Publikováno v:
Currículo Lattes
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
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Autor:
Duminda Subasinghe, Neville D Perera, Chandu De Silva, Dharmabandhu N. Samarasekera, Chathuranga Tisara Keppetiyagama
Publikováno v:
BMC Surgery
Background Pelvic floor hernias pose a diagnostic and a treatment challange. Neurofibromatosis is a rare systemic disease, and urinary tract involvement is rare. Case presentation Here we report a case of a 54-year-old female with multiple neurofibro
Publikováno v:
Qatar Medical Journal. 2011
Multiple Neurofibromatosis (NF) is a disease of great interest because of the familial nature of the disease, the complexity of its morphology, the progressive character of its course and the numerous complications that may develop during its evoluti
Autor:
Lawrence Frank
Publikováno v:
Archives of dermatology and syphilology. 55(1)
The familial incidence of multiple neurofibromatosis, or von Recklinghausen's disease, has long been noted, and most authors today accept the fact that there is a hereditary transmission of the disease. Harbitz, 1 in a review of multiple neurofibroma
Publikováno v:
The Indian journal of surgery. 73(5)
Von Recklinghausen’s disease or type 1 neurofibromatosis is an autosomal dominant disease characterized by mucocutaneous neurofibromas, cafe-au-lait spots and involves many organs including gastrointestinal tract. Gastrointestinal involvement in ne
Publikováno v:
Laryngo-Rhino-Otologie. 70:154-157
A case of familial multiple neurofibromatosis with laryngeal involvement is described. The patient required surgical treatment because of rapid tumour growth associated with dyspnoea, dysphonia and dysphagia. Whereas the extensive growth prevented en
Autor:
T. R. Gopalan, Arcot Rekha
Publikováno v:
The international journal of lower extremity wounds. 5(1)
Gigantism of the lower limb can occur because of plexiform neurofibromas. This condition is seen with café au lait patches and multiple neurofibromatosis in this case of von Recklinghausen neurofibromatosis. We report our patient and review literatu
Autor:
A. Stewart, B.M.W. Bailey
Publikováno v:
British Journal of Oral and Maxillofacial Surgery. 30:56-58
A patient with multiple neurofibromatosis and a neurofibroma of the inferior alveolar nerve is described. The management is discussed with particular reference to difficult aspects of the diagnosis and treatment.
Publikováno v:
Anaesthesia. 49:453-454