نتایج جستجو برای: von recklinghausen

تعداد نتایج: 96693  

Journal: :The Yale Journal of Biology and Medicine 1981
Leonard Milstone

Development of Bacterial Infections in Cancer Patients," by Michel P. Glauser and Stephen H. Zinner. The latter chapter reviews systematically the predisposing factors which result in unusual susceptibility. The specific side effects of various cytotoxic agents are discussed, but this section could be enlarged. These chapters would be illuminating to any practitioner faced with treating cancer ...

Journal: :Brazilian journal of otorhinolaryngology 2009
Vinicius Antunes Freitas Michel Cyrino Saliba Eduardo Cesar Dolabela de Moraes Gabriela Amélia Nassif de Morais Teixeira João Batista de Oliveira

Von Recklinghausen’s disease is characterized by the presence of cafe-au-lait spots, multiple neurofibromas and hamartomas. It is a dominant autosomal disease with high penetrance and variable expression, involving the head and neck in 22 to 47% of the patients. It is known as type I neurofibromatosis, in order to differentiate it from central involvement, especially that of the eight cranial n...

2016
Mohamad J. Alshikho Salem I. Noureldine Joud M. Talas Antoine Nasimian Safi Zazou Bashir Mobaed Mahmoud Nasser

BACKGROUND Pancreatic endocrine tumors (PETs) are rare and can occur as part of neurofibromatosis type 1 (NF1). Gastrinomas are functional PETs that are rarely associated with NF1. Only two cases of their occurrence have been reported in the literature. CASE REPORT A 28-year-old woman was admitted for further evaluation of epigastric soreness, heartburn, nausea, vomiting, diarrhea, and a sign...

Journal: :Internal medicine 1997
K Miyamoto

Von Recklinghausen's disease, neurofibromatosis type 1 (NF1), is a commonautosomal disorder characterized by multiple neurofibromas, cafe au lait spots, and Lisch nodules of the iris with a variable clinical expression. This disorder appears to affect all races, with a prevalence estimated to be 1 in 3,000 live births. The NF1 gene is located in 17ql 1.2. However, due to the high mutation rate ...

Journal: :Genomics 1987
S R Diehl M Boehnke R P Erickson A B Baxter M A Bruce J L Lieberman D J Platt L M Ploughman K A Seiler A M Sweet

Several recent studies indicate that the von Recklinghausen neurofibromatosis (NF1) gene is located near the centromere of chromosome 17 in some families. However, variable expressivity and a very high mutation rate suggest that defects at several different loci could result in phenotypes categorized as NF1. In order to assess this possibility and to map the NF1 gene more precisely, we have use...

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