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作者:Şeniz Ergin , Elif Kazancı ...
来源:[J].Pediatrics & Neonatology(IF 0.932), 2015, Vol.56 (4), pp.271-274
摘要:Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biphenotypic or mixed phenotype ac...
作者:Şeniz Ergin , Elif Kazancı ...
来源:[J].Pediatrics and Neonatology(IF 0.932), 2015, Vol.56 (4), pp.271-274
摘要:Congenital leukemia is a rare disease. The majority of cases of this disease are acute myelogenous leukemia (AML). Congenital acute lymphoblastic leukemia (ALL) is rare and most often is of B cell lineage. Rarely, some cases have been designated biphenotypic or mixed phenotype ac...
作者:Şeniz Ergin , Neşe Demirkan ...
来源:[J].Turkderm(IF 0.12), 2008, Vol.42 (4), pp.137
摘要:Familial lichen amyloidosis which is also referred to familial primary cutaneous amyloidosis is a rare clinical variant of cutaneous amyloidosis. Lichen amyloidosis is characterized by persistent, pruritic, small brown papules often located on anterior surfaces of legs which show...
作者:... Muzaffer Kahyaoğlu , Nida Kaçar , Şeniz Ergin
来源:[J].Turkderm(IF 0.12), 2012, Vol.46 (2), pp.67-72
摘要:Background and Design: Most patients with dermatological complaints first present to their general practitioners. In the present study, we aimed to investigate the experiences of primary care physicians on dermatological diseases and their opinions of undergraduate education...
作者:Şeniz Ergin , Nergül Çördük
来源:[J].The Indian Journal of Pediatrics(IF 0.715), 2011, Vol.78 (11), pp.1424-1426
摘要:Abstract(#br)Pseudohypoparathyroidism (PHP) is a heterogenous group of disorders characterized by hypocalcemia with hyperphosphatemia, increased serum concentration of parathyroid hormone (PTH), and insensitivity to the biological activity of PTH. Calcinosis cutis, the cutan...
作者:Şeniz Ergin , M. Levent Taşlı ...
来源:[J].Turk Dermatoloji Dergisi, 2015, Vol.9 (4), pp.195-197
摘要:Pseudoxanthoma elasticum (PXE) is a multisystemic, metabolic and autosomal recessive inherited disorder affecting especially elastic fibers of skin, retina and blood vessels. The prevalence varies from 1:25,000 to 1:100,000. The average age of onset is 13.5 years. Yellowish papul...
作者:Şeniz Ergin , Paula Molés‐Poveda ...
来源:[J].Journal of Cutaneous Pathology(IF 1.766), 2015, Vol.42 (12), pp.937-943
摘要:Consumption of the epidermis associated with effacement of the rete ridge pattern has been cited as a useful criterion in the diagnosis of melanoma, but the significance of consumption in the absence of rete ridge effacement is unknown. We evaluated 701 melanocytic neoplasms...
作者:Şeniz Ergin , Pınar Başak , Aliye Sari
来源:[J].Journal of the European Academy of Dermatology and Venereology(IF 2.694), 2000, Vol.14 (1), pp.47-49
摘要:Abstract(#br)Milia en plaque is a rarely reported entity which is usually appearing in the auricular region. We describe a well‐defined, U‐shaped milia en plaque arizing in the infraorbital area, and emphasize that it should be considered in the differential diagnosis of xan...

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