نتایج جستجو برای: multiple hereditary

تعداد نتایج: 831640  

2017
Hans-Ulrich Voelter Hans-Peter Schlake Paul Eling Helmut Hildebrandt

2013
Ehud Lavi Cris S. Constantinescu Scott S. Zamvil Stephen M Anderton Michael K. Racke Richard M. Ransohoff

A Omidvar Borna M Maleki V Mashayekhi Y Nahidi Z Javidi

Hereditary benign telangiectasia is an uncommon idiopathic skin disorder characterized by generalized telangiectases and angiomatous lesions of the skin. The diagnosis should be suspected in patients with such cutaneous lesions, positive family history, no associated bleeding problems, and no mucosal involvement. We present six cases of hereditary benign telangiectasia in three generations of o...

Journal: :iranian journal of radiation research 0
c. yavas konya training and research hospital, department of radiation oncology konya, turkey p. karabagli selcuk university, department of pathology konya, turkey g. yavas selcuk university, department of radiation oncology konya, turkey h. acar selcuk university, department of medical genetics konya, turkey o. ata selcuk university, department of medical oncology konya, turkey

multiple primary tumors in a single patient are relatively rare when four or more distinct lesions are considered. herein, we report a case of woman with four different primary tumors: meningioma, renal angiomyolipoma, spinal ependymoma and high-grade soft tissue sarcoma. there was no family history and hereditary syndrome. the genetic analysis was completely normal. to best of our knowledge, t...

Journal: :Journal of neurology, neurosurgery, and psychiatry 2001
C Liu

The association between Leber’s hereditary optic neuropathy and multiple sclerosis has encouraged the search for susceptibility genes in multiple sclerosis. This symbiotic relation is reversed in the paper by Inglese et al (this issue, pp 444–449) in which magnetic resonance (MR) techniques originally developed for studying multiple sclerosis were applied to patients with Leber’s hereditary opt...

C. Yavas, G. Yavas, H. Acar, O. Ata, P. Karabagli,

Multiple primary tumors in a single patient are relatively rare when four or more distinct lesions are considered. Herein, we report a case of woman with four different primary tumors: meningioma, renal angiomyolipoma, spinal ependymoma and high-grade soft tissue sarcoma. There was no family history and hereditary syndrome. The genetic analysis was completely normal. To best of our knowledge, t...

A seven year-old boy with several painless masses on the ribs and shoulder was referred to our hospital. The masses were so prominent that they prevented the child’s sleep. Since the patient had been ridiculed by his friends due to the rib prominences, he had refused to attend school. After clinical and radiological evaluations, the masses were diagnosed as hereditary multiple exostoses of the ...

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