Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Şit UÇAR"'
Publikováno v:
Balkan Medical Journal, Vol 31, Iss 4, Pp 349-351 (2014)
Background: Hamartoma of the larynx is a very rare lesion, and the number of reported cases is limited. Signs and symptoms include stridor, changes in voice, eating and respiratory complaints. Stridor is a sign of upper airway obstruction. Patients p
Externí odkaz:
https://doaj.org/article/61926645993b4bf5aa933195841eaf48
Autor:
Gürses Şahin, Şit Uçar, Basak Adakli, Gülseren (Evirgen) Şahin, Binnaz Celik, Pelin Zorlu, Ozlem Ozgur
Publikováno v:
Turkish Thoracic Journal/Türk Toraks Dergisi. 15:122-127
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19d62213825ce4d4faede89182bde58e
https://doi.org/10.5152/ttd.2014.4117
https://doi.org/10.5152/ttd.2014.4117
Publikováno v:
The Journal of Pediatric Research. 1:104-107
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0fcba778667e5ef649ba92af96773b3
https://doi.org/10.4274/jpr.91300
https://doi.org/10.4274/jpr.91300
Publikováno v:
Turkiye Klinikleri Journal of Medical Sciences. 34:385-395
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18e5a3c19fabc7f333d17b5251666225
https://doi.org/10.5336/medsci.2014-39647
https://doi.org/10.5336/medsci.2014-39647
Autor:
Esma Altinel Acoglu, Pelin Zorlu, Gülseren (Evirgen) Şahin, Nilgün Çaylan, Gürses Şahin, Şit Uçar
Publikováno v:
Türk Pediatri Arşivi. 48:251-254
Primary polydipsia is a clinical status with excessive fluid consumption without any physiological need A seventeen month old male infant with severe malnutrition and developmental retardation was found to have polyuria and polydipsia in the follow u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::860fbbd99a7424c31d67729909d65013
https://doi.org/10.4274/tpa.695
https://doi.org/10.4274/tpa.695
Publikováno v:
Balkan Medical Journal, Vol 31, Iss 4, Pp 349-351 (2014)
Volume: 31, Issue: 4 349-351
Balkan Medical Journal
Volume: 31, Issue: 4 349-351
Balkan Medical Journal
Background: Hamartoma of the larynx is a very rare lesion, and the number of reported cases is limited. Signs and symptoms include stridor, changes in voice, eating and respiratory complaints. Stridor is a sign of upper airway obstruction. Patients p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29e78b23fadfa603b1c759bc0bc5b9c8
http://balkanmedicaljournal.org/text.php?lang=en&id=275
http://balkanmedicaljournal.org/text.php?lang=en&id=275
Publikováno v:
Pediatric Hematology and Oncology. 26:461-466
Congenital syphilis is a rare, serious disease that continues to be a major health-care problem. The infected neonate may be asymptomatic or multiple-organ system involvement may occur. Anemia and thrombocytopenia are common hematological findings. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f07df7a646a5c0f05a85f193ac0400f
https://doi.org/10.3109/08880010903091897
https://doi.org/10.3109/08880010903091897
Publikováno v:
Volume: 9, Issue: 4 274-277
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Akçaağaç şurubu idrar hastalığı, valin, lösin, izolosin ve onların ilgili ketoasitlerinin vücut sıvılarında yüksek miktarda birikmesinin neden olduğu, nadir görülen, dallı zincirli aminoasitlerin katabolizma bozukluğudur. Toksik me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29941577df0458b200c8cf79d1243313
https://dergipark.org.tr/tr/pub/tchd/issue/44333/547844
https://dergipark.org.tr/tr/pub/tchd/issue/44333/547844
Publikováno v:
Archives of Disease in Childhood. 99:A303.1-A303
Background and aims Hemophagocytic lymphohistiocytosis (HLH) is a rare, life threatening disorder characterizedby uncontrolled activation of T-helper 1 lymphocytes and macrophages and overproductionof inflammatory cytokines. Visceral leishmaniasis (V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe1a0396984620ebd6a117755eb13ab6
https://doi.org/10.1136/archdischild-2014-307384.833
https://doi.org/10.1136/archdischild-2014-307384.833
Publikováno v:
Volume: 27, Issue: 1 54-57
Marmara Medical Journal
Marmara Medical Journal
Niemann-Pick disease is an autosomal recessively inherited group of congenital lipidoses in which sphingolipids accumulate in certain tissues, especially reticuloendothelial cells. The clinical phenotype is extremely variable, ranging from an acute n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a808c541915a8c8f2533b739ccede277
https://doi.org/10.5472/mmj.2013.02845.2
https://doi.org/10.5472/mmj.2013.02845.2