نتایج جستجو برای: hereditary bleeding disease
تعداد نتایج: 1589001 فیلتر نتایج به سال:
The development of capsule endoscopy (CE) in 2001 has given gastroenterologists the opportunity to investigate the small bowel in a non-invasive way. CE is most commonly performed for obscure gastrointestinal bleeding, but other indications include diagnosis or follow-up of Crohn's disease, suspicion of a small bowel tumor, diagnosis and surveillance of hereditary polyposis syndromes, Nonsteroi...
The pathophysiology of (deep) endometriosis is still unclear. As originally suggested by Cullen, change the definition "deeper than 5 mm" to "adenomyosis externa." With the discovery of the old European literature on uterine bleeding in 5%-10% of the neonates and histologic evidence that the bleeding represents decidual shedding, it is postulated/hypothesized that endometrial stem/progenitor ce...
Hereditary haemorrhagic telangiectasis associated with hepatic artery aneurysm has only once been recorded in the literature (Graham, Eiseman, and Pryor, 1964). This case is reported because the concurrence of these conditions, together with gastric and duodenal ulcers, serves to illustrate difficulties in the management of a patient with a bleeding diathesis who has four possible causes of gas...
Primary hyperoxaluria type 1 is an autosomal recessive hereditary glyoxylate metabolism disorder characterized by excessive production of oxalate, caused by the deficiency of liver specific peroxisomal enzyme: alanineglyoxylate aminotransferase. For patients with end-stage renal disease, combined liver and kidney transplantation was needed. This report describes one patient, with a diagnosis of...
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