Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Safak Güçer"'
Autor:
Şule Ünal, İlhan Tezcan, Safak Güçer, Meryem Seda Boyraz, Deniz Cağdas, Duygu Uçkan Çetinkaya
Publikováno v:
Turkish Journal of Hematology, Vol 32, Iss 4, Pp 378-379 (2015)
Externí odkaz:
https://doaj.org/article/e6ab6190039844d79d7d51b2d7ec3157
Publikováno v:
The Turkish journal of pediatrics. 53(3)
Condyloma acuminatum (CA), which is a large cauliflower-like tumor, has been linked to human papilloma virus (HPV) types associated with skin warts. It is an uncommon condition in children, and there is no consensus regarding the optimal treatment. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5b04a0c77e5a309c86881898508f2fdf
https://pubmed.ncbi.nlm.nih.gov/21980819
https://pubmed.ncbi.nlm.nih.gov/21980819
Publikováno v:
The Turkish journal of pediatrics. 53(1)
Epidermoid cysts are slowly growing tumors arising from invagination of the epidermis into the dermis traumatically or spontaneously. This implantation in the clitoris is most commonly induced by female genital mutilation. The reported cases with spo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5eca3fc572669ce1914157d7acf0f5c1
https://pubmed.ncbi.nlm.nih.gov/21534352
https://pubmed.ncbi.nlm.nih.gov/21534352
Autor:
Fatma Semsa, Altugan, Seza, Ozen, Nuray, Aktay-Ayaz, Safak, Güçer, Rezan, Topaloğlu, Ali, Düzova, Fatih, Ozaltin, Nesrin, Beşbaş
Publikováno v:
The Turkish journal of pediatrics. 51(6)
The prognosis of Henoch-Schönlein purpura (HSP) nephritis is more severe than originally thought, with a significant portion progressing to deterioration of renal function in adulthood. Proteinuria adversely affects the outcome. The aim of this stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fef7e559982f3c6a08d583d40cc86f8a
https://pubmed.ncbi.nlm.nih.gov/20196388
https://pubmed.ncbi.nlm.nih.gov/20196388
Autor:
Ercan, Sivasli, Ozlem, Tekşam, Mithat, Haliloğlu, Safak, Güçer, Diclehan, Orhan, Aytemiz, Gürgey, Gülsevin, Tekinalp
Publikováno v:
The Turkish journal of pediatrics. 51(5)
Placental chorioangioma and thrombosis of an umbilical vein varix are rare etiologic factors of non-immune hydrops fetalis. Herein, we report a patient who had hydrops fetalis associated with placental chorioangioma and thrombosis of an umbilical vei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7af4278513ed1cc2e3eef6214e16a0a6
https://pubmed.ncbi.nlm.nih.gov/21428207
https://pubmed.ncbi.nlm.nih.gov/21428207
Autor:
Erkan, Demirkaya, Hasan Fatih, Cakmakli, Safak, Güçer, Nuray, Aktay-Ayaz, Aytemiz, Gürgey, Seza, Ozen
Publikováno v:
The Turkish journal of pediatrics. 51(4)
We present a 12-year-old girl with systemic lupus erythematosus and associated antiphospholipid syndrome who developed an unusual manifestation of purpura fulminans in an accelerated fashion. The patient improved after prompt treatment with anticoagu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::115654c27c0a13d45371c71801233651
https://pubmed.ncbi.nlm.nih.gov/19950848
https://pubmed.ncbi.nlm.nih.gov/19950848
Publikováno v:
The Turkish journal of pediatrics. 50(6)
Trisomy 13 is a very rare and lethal autosomal chromosomal malformation syndrome. Its incidence is 1/12,000 births. In this paper, we present a new trisomy 13 case associated with unusual and undescribed findings. This patient was the first child of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f077368840f7ec7260dc0fe799ea3082
https://pubmed.ncbi.nlm.nih.gov/19227428
https://pubmed.ncbi.nlm.nih.gov/19227428
Publikováno v:
The Turkish journal of pediatrics. 49(4)
We report a five-month-old boy who was referred to the hospital with a presumptive diagnosis of hydrocele of the cord. Ultrasonography revealed a cystic mass within the left testis. A complete removal of the cystic mass was done. Histopathological di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::836671d9e6a38bd6d176b2950cf725bd
https://pubmed.ncbi.nlm.nih.gov/18246753
https://pubmed.ncbi.nlm.nih.gov/18246753
Publikováno v:
European journal of dermatology : EJD. 17(4)
Multiple endocrine neoplasia (MEN) type 2B syndrome is an autosomal dominantly inherited endocrine disorder with rare skin manifestations. We report the case of a 19-year-old Turkish girl who presented with skin-colored flat papules scattered all ove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4375b1a41f5cd27a802a2f723f710528
https://pubmed.ncbi.nlm.nih.gov/17540634
https://pubmed.ncbi.nlm.nih.gov/17540634
Autor:
Süheyla, Ozkutlu, Canan, Ayabakan, Tevfik, Karagöz, Lütfü, Onderoğlu, Ozgür, Deren, Melda, Cağlar, Safak, Güçer
Publikováno v:
The Turkish journal of pediatrics. 47(3)
The increased experience in interpretation of fetal echocardiographic images may change the accuracy of fetal echocardiography in diagnosing fetal heart defects. We thus decided to evaluate the specificity and the sensitivity of our fetal echocardiog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ad7dd640e7fff6aa13fcfaa793c0b928
https://pubmed.ncbi.nlm.nih.gov/16250307
https://pubmed.ncbi.nlm.nih.gov/16250307