نتایج جستجو برای: loghman
تعداد نتایج: 246 فیلتر نتایج به سال:
Background: Skull base chordoma is a rare tumor with slow and progressive growth. Significance of this tumor is it’s difficult to access location in skull base. This is the reason for various proposed techniques for resection of the tumor. Endoscopic endonasal technique is a minimally invasive approach that gives surgeons opportunity of total resection of tumor and low morbidity. Total resectio...
Background: Retroperitoneal Abscess (RA) is a rare and often insidious disease, i.e., difficult to diagnose. RA could originate from different retroperitoneal or intra-abdominal organs. The disease manifests various clinical symptoms usually treated with combination of antibiotics therapeutic interventions. Methods: Data total 25 patients who were admitted Loghman Hospital in Tehran City, Iran ...
Basal cell carsinoma is the most frequent skin tumor of the white people & radiotherapy is one of it’s known etiology. To determine the correlation of histopathologic type of basal cell carcinoma with previous history of radiotherapy. Evaluation of retrospective inpatient & outpatient histopathologic & clinical files in Department of dermatology Loghman Hospital Tehran (between 1987 &n...
SUMMARY From April L 989 to March 1989 !here were 13 patients with small intestinal volvulus 23%, or all palients operated for small intestinal obstruction.All were male, age between 6 to 75, without any history of abdominal operation. Mortality was 38, 5% and morbidity included, intraabdominal abscesses, recurrent obstruction and wound infection were observed. Being the 3rd cause of intestin...
steoporosis is a common disease in which the bones become prone to fracture as a result of loss of bone mineral density (BMD). The estrogen receptor (ER) gene is a candidate gene for osteoporosis. This study assesses the relation between estrogen receptor-α gene polymorphism and osteoporosis in a population of Iranian women. Materials & Methods: In the present study, we investigated 200 preand/...
Vitamin D resistant rickets with alopecia is a rather rare heritable disease probably caused by a different variety of metabolic disorder of this vitamin. Disturbances of protoplasmic and unclear receptors for vitamin D metabolites in bones and intestinal cells have been proposed as basic mechanism; Alopecia is attributed to hypersensitivity to vitamin D; very much like what usually appears in ...
We inspected on about 110 patients of spinal tumors in the neurosurgical department of Loghman-eHakim Medical Center. According with our inspectation, we have considered the factors such as age, sex, pathology, clinical signs, radiology, kind of operation and…. cases were up to 16 years ( 15 % ) and the 17 others were adult. 62 (56%) were male and 38 (44%) were female. The most privalent ...
Camptomelic dwarfism or dysplas1a is a rare syndrome in which· short stature is associated with angulation and bowing of the lower limb Long bones, hypoplasia of the facial bones and scapula and various other skeletal and respiratory and nervous system. A 9 day old girl with this syndrome was admitted in our peiatric Department, Loghman Hospital medical center because of Dwarfism and hypotonia....
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