Zobrazeno 1 - 10
of 59
pro vyhledávání: '"ŞİRİN, Aydan"'
Autor:
Aksu, Bağdagül, Yıldırım, Zeynep Yürük, Yılmaz, Alev, Pehlivanoğlu, Cemile, Türkkan, Özde, Al, Aslı Derya Kardelen, Bilge, Ilmay, Şirin, Aydan, Emre, Sevinç
Publikováno v:
Osmangazi Journal of Medicine / Osmangazi Tip Dergisi; 2023, Vol. 45 Issue 5, p747-754, 8p
Akademický článek
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Autor:
Bilge, Ilmay1, Şirin, Aydan1, Emre, Sevinç1, Ağaçhan, Bedia2, Ispi, Turgay2, Õktem, Faruk3 oktemfaruk@hotmail.com
Publikováno v:
Pediatric Nephrology. Apr2004, Vol. 19 Issue 4, p384-389. 6p. 3 Charts.
Autor:
Kara, Bülent, Alpay, Harika, Nayır, Ahmet, Devecioğlu, Ömer, Emre, Sevinç, Şirin, Aydan, Tanman, Faik
Publikováno v:
Volume: 27, Issue: 3
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Cystinosis is an otosomal recessive inherited lysosomal disease in which the primary defect causes an abnormal accumulation of cystine in various tissues Cystine is deposited in the bone marrow lymph nodes conjunctiva rectal mucosa and kidney The cys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::7b17ff5111e845cdd3aa467a41254ecf
https://dergipark.org.tr/tr/pub/tpedar/issue/13259/160050
https://dergipark.org.tr/tr/pub/tpedar/issue/13259/160050
Autor:
Ünüvar, Ayşegül, Nayır, Ahmet, Alpay, Harika, Uysal, Veli, Emre, Sevinç, Şirin, Aydan, Tanman, Faik, Çubukçu, Olcay
Publikováno v:
Volume: 28, Issue: 1
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Oxalosis in an inherited disease characterized by growth retardation recurrent urolithiasis nephrocalcinosis renal failure and deposition of oxalates in the tissues Type I is the most common from seen in early childhood on the other hand in type II L
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::6631259b7a0d9c70bfdde0379827474b
https://dergipark.org.tr/tr/pub/tpedar/issue/13258/160038
https://dergipark.org.tr/tr/pub/tpedar/issue/13258/160038
Autor:
KIYAK, Aysel, NAYIR, Ahmet, BİLGE, İlmay, ŞİRİN, Aydan, EMRE, Sevinç, KADIOĞLU, Alev, TANMAN, Faik
Publikováno v:
Volume: 29, Issue: 3
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Three boys and two girls aged five to nine months with bilateral medullary nephrocalcinosis hypercalcemia and hypercalciuria due to vitamin D intoxication were reported This clinical presentation had developed in three patients on normal doses of vit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::d5fe72e00c9e6092f1e53657e3c2239b
https://dergipark.org.tr/tr/pub/tpedar/issue/13252/159966
https://dergipark.org.tr/tr/pub/tpedar/issue/13252/159966
Autor:
UZPAK, Hasan, NAYIR, Ahmet, ALPAY, Harika, KILIÇASLAN, İşın, SAVAŞAN, Süreyya, EMRE, Sevinç, ŞİRİN, Aydan, TANMAN, Faik
Publikováno v:
Volume: 30, Issue: 1
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Imerslund Grâsbeck syndrome is a rarely seen autosomal recessive syndrome characterized by megaloblastic anemia and proteinuria This syndrome occurs due to the absorption defect of vitamin B12 and intrinsic factor complex in the terminal ileum Prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::4d1d9070525c7565318d3fe753983fc6
https://dergipark.org.tr/tr/pub/tpedar/issue/13250/159948
https://dergipark.org.tr/tr/pub/tpedar/issue/13250/159948
Autor:
Baş, Firdevs, Alpay, Harika, Nayır, Ahmet, Emre, Sevinç, Şirin, Aydan, Kadıoğlu, Alev, Tanman, Faik
Publikováno v:
Volume: 29, Issue: 2
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Horseshoe kidney is the most common fusion anomaly of the kidney and can be associated with certain syndromes While 2 3 of the cases may be asymptomatic throughout life 1 3 of may be merged with hydronephrosis calculus formation recurrent urinary tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::a9b2827d753e823a07cf3c629a9b74d5
https://dergipark.org.tr/tr/pub/tpedar/issue/13253/159980
https://dergipark.org.tr/tr/pub/tpedar/issue/13253/159980
Publikováno v:
Volume: 29, Issue: 3
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Mesoblastik nephroma is a renal tumor that is also named as fetal renal hamartoma neonatal mesangimal hamartoma or leiomyomatose hamartoma The physical examination of neonates and infants reveal mostly an abdominal palpable mass In addition hematuria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::2a20ecd59fad7654c4e3ead48fe86e60
https://dergipark.org.tr/tr/pub/tpedar/issue/13252/159968
https://dergipark.org.tr/tr/pub/tpedar/issue/13252/159968
Publikováno v:
Volume: 29, Issue: 4
Türk Pediatri Arşivi
Türk Pediatri Arşivi
Neurofibromatosis is a multisystemic and autosomal dominant inherited disorder in which vascular anomalies may lead to secondary hypertension Renal artery stenosis is the most common cause of hypertension in such patients A 10 year old male patient w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=tubitakulakb::20e66a8def9e4f3c6f025b791df6e4a7
https://dergipark.org.tr/tr/pub/tpedar/issue/13251/159950
https://dergipark.org.tr/tr/pub/tpedar/issue/13251/159950