Search Results - "Yasar, Sirin Pekcan"

Anticonvulsant hypersensitivity syndrome: clinical and laboratory features by Mansur, Ayşe Tülin, Pekcan Yaşar, Şirin, Göktay, Fatih

“…Background  Anticonvulsant hypersensitivity syndrome (AHS) is a severe adverse drug reaction with multiorgan involvement. Aromatic anticonvulsants are the most…”
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Multiple Squamous Cell Carcinoma after Vemurafenib Therapy by Sinem Çiloğlu, Alpay Duran, Şirin Yaşar Pekcan, Aslı Duran

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Leg ulcer in a patient with Rothmund–Thomson syndrome by Ciloglu, Sinem, Duran, Alpay, Pekcan, Sirin Yasar, Buyukdogan, Hasan

“…Background Rothmund–Thomson syndrome is a rare genetic condition exhibiting some dermatological, craniofacial, ophthalmological, and central nervous system…”
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DERM12345: A Large, Multisource Dermatoscopic Skin Lesion Dataset with 38 Subclasses by Yilmaz, Abdurrahim, Yasar, Sirin Pekcan, Gencoglan, Gulsum, Temelkuran, Burak

“…Skin lesion datasets provide essential information for understanding various skin conditions and developing effective diagnostic tools. They aid the artificial…”
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Generalized papular and sclerodermoid eruption: Scleromyxedema by Serdar, Zehra Aşiran, Altunay, Ilknur Kivanc, Yasar, Sirin Pekcan, Erfan, Gamze Türker, Güneş, Pembegül

“…Scleromyxedema (SM) is a rare chronic progressive and highly intractable cutaneous disease with unknown etiology, affecting both genders equally between 30 and…”
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Generalized papular and sclerodermoid eruption: scleromyxedema by Serdar, Zehra Asiran, Altunay, Ilknur Kivanc, Yasar, Sirin Pekcan, Erfan, Gamze Türker, Gunes, Pembegül

“…Scleromyxedema (SM) is a rare chronic progressive and highly intractable cutaneous disease with unknown etiology, affecting both genders equally between 30 and…”
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Tedavisiz iyileşen diffüz neonatal hemanjiomatozis by MANSUR, Ayşe Tülin, KOCAYAN, Nurhan, AKKAYA, Ayşe Deniz, YAŞAR, Şirin Pekcan, SERDAR, Zehra Aşiran

“…Diffüz neonatal hemanjiomatozis nadir görülen, deri, iç organlar ve santral sinir sisteminde doğumsal hemanjiomlarla seyreden, kötü prognozlu bir hastalıktır…”
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Konjenital trikoreksis nodoza: İki kardeş olgu sunumu by NUHOĞLU, Çağatay, YAŞAR, Şirin Pekcan, SERDAR, Zehra Aşiran, ASLAN, Canan

“…Trikoreksis nodoza en sık görülen saçın yapısal bozuklukları ndandır. Saçlar kuru, kırılgan ve mat olup, kıl şaftının yüzeyinde düzensiz yerleşimli gri-beyaz…”
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