Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Tulin Sayli"'
Autor:
Ahmet KAN, Tulin SAYLI
Publikováno v:
Minerva Pediatrics. 74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7a2530253bce23242707d648eeba49c
https://doi.org/10.23736/s2724-5276.20.06073-9
https://doi.org/10.23736/s2724-5276.20.06073-9
Autor:
Selen Hurmuzlu Kozler, Tulin Sayli
Publikováno v:
Current Medical Research and Opinion. 38:435-441
OBJECTIVES To determine vitamin D supplementation frequency among children aged 1 to 24 months, factors that influence adherence, and reasons for discontinuation of initiated vitamin D. METHODS This cross-sectional study was conducted using a questio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31121622489fef8bf365d542ec5db5d6
https://doi.org/10.1080/03007995.2021.2010460
https://doi.org/10.1080/03007995.2021.2010460
Publikováno v:
European Journal of Pediatrics. 175:873-876
Castleman disease (CD) is a rare poorly understood lymphoproliferative disorder. Pediatric onset CD has been reported before. However, most of them have benign unicentric pattern. Multicentric CD (MCD) is quite rare in children. Herein, we report a 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c771561a8b5ea4d4be1dd385cfea7b
https://doi.org/10.1007/s00431-015-2674-6
https://doi.org/10.1007/s00431-015-2674-6
Autor:
Fatma Karaca Kara, Cüneyt Karagöl, Tulin Sayli, Tülin Köksal, Bahar Çuhacı Çakır, Alkım Öden Akman
Immunoglobulin therapy can be used to treat a wide variety of diseases. However, intravenous immunoglobin products can cause several adverse reactions, including hemolysis. The objective of this study was to determine the extent of anemia and hemolys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdbf7c9dcdd516dd057125d2cc3efd3a
https://avesis.gazi.edu.tr/publication/details/9af4d5e8-23d3-47b5-b3dc-c640af389c48/oai
https://avesis.gazi.edu.tr/publication/details/9af4d5e8-23d3-47b5-b3dc-c640af389c48/oai
Publikováno v:
International Journal of Dermatology. 43:673-675
Langerhans' cell histiocytosis is an uncommon disorder of childhood with a wide clinical spectrum. Although liver involvement is common in the disseminated form, presentation with hepatic disfunction is unusual. We describe an 18-month-old girl who p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09df2eab1391d41c54b634fcda816e5d
https://doi.org/10.1111/j.1365-4632.2004.02160.x
https://doi.org/10.1111/j.1365-4632.2004.02160.x
Autor:
Mualla Cetin, Concetta Langella, Baris Kuskonmaz, Roberta Russo, Duygu Uçkan Çetinkaya, Fatma Gumruk, Achille Iolascon, Tülin Revide Şayli, Sule Unal, Betul Tavil
Publikováno v:
Pediatric transplantation. 18(4)
CDA are a group of inherited, rare diseases that are characterized by dyserythropoiesis and ineffective erythropoiesis associated with transfusion dependency in approximately 10% of cases. For these latter patients, the only curative treatment is HSC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb39e45f004f9793c62435e57c055a79
https://pubmed.ncbi.nlm.nih.gov/24724984
https://pubmed.ncbi.nlm.nih.gov/24724984