Blood Pressure Monitoring – the Von Recklinghausen Oscillotonometer
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چکیده
منابع مشابه
Von recklinghausen disease: one patient – various problems
von Recklinghausen disease (vRD), more widely known as neurofibromatosis type 1, belongs to a group of genetic disorders and it is considered to be the most common genodermatosis. The disease has an autosomal dominant pattern of inheritance that involves mutations within the NF1 gene located on chromosome 17 in locus q11.2. The product of the NF1 gene is neurofibromin and the protein is well kn...
متن کاملLinkage analysis of neurofibromatosis (von Recklinghausen disease).
Linkage analysis of 28 genetic markers was undertaken in 108 subjects from 11 families with well-documented, classic, peripheral neurofibromatosis. Fifty-four persons were affected in one four-generation family, seven three-generation families, and three two-generation families. Lod scores were calculated using the standard LIPED programme for 49 combinations of theta male and theta female from...
متن کاملType 1 neurofibromatosis (von Recklinghausen disease).
Type 1 neurofibromatosis (NF1), or von Recklinghausen disease, is a genetic disorder that is well known for its clinical features. Effective treatment modalities for NF1 have not yet been established. The advent of new treatment options for NF1 such as topical vitamin D3 analogues, lovastatin, rapamycin (or sirolimus), and imatinib mesylate has added new dimensions that require further invest...
متن کاملPsychological aspects of von Recklinghausen neurofibromatosis (NF1)
Neurofibromatosis is a devasting autosomal dominant disease which is extremely variable in its symptomatology, intensity, and progression. There have been numerous reports published about the physical aspects of neurofibromatosis, while psychological issues have been given little attention so far. The present article presents a review of the current knowledge concerning psychological aspects of...
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ژورنال
عنوان ژورنال: Anaesthesia and Intensive Care
سال: 2009
ISSN: 0310-057X,1448-0271
DOI: 10.1177/0310057x0903700223