Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Meltem, Akcaboy"'
Autor:
Melahat Melek Oguz, Esma Altinel Acoglu, Fatma Zehra Oztek Celebi, Emine Polat, Husniye Yucel, Sanliay Sahin, Meltem Akcaboy, Saliha Senel
Publikováno v:
Iranian Journal of Public Health.
The Article Abstract is not available.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc15cab01c3e79b53ee071b0fad4ce9a
https://doi.org/10.18502/ijph.v52i2.11900
https://doi.org/10.18502/ijph.v52i2.11900
Publikováno v:
Turkish archives of pediatrics. 57(3)
Breastfeeding is the principal feeding source in the first years of life. Its targeted rates are not achieved properly, globally. Multifactorial reasons have been reported, but the effect of the facilities in the hospitals including lactation consult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fcdec594e2122ed6042aa02b2652240d
https://pubmed.ncbi.nlm.nih.gov/35781231
https://pubmed.ncbi.nlm.nih.gov/35781231
Autor:
Mehmet Bülbül, Saliha Senel, Mehmet Fatih Akif Özdemir, Harun Terin, Meltem Akcaboy, Rukiye Demet
Publikováno v:
Zeitschrift für Rheumatologie. 81:339-341
Involuntary movement disorders are rare in childhood. Hyperkinetic movement disorders including chorea stand as the leading cause. Although Sydenham chorea is the major diagnosis in most children and adolescents, appropriate differential diagnosis is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de17ad08b6c11db6bf448c9fc248597c
https://doi.org/10.1007/s00393-021-01070-8
https://doi.org/10.1007/s00393-021-01070-8
Autor:
Saliha Senel, Meltem Akcaboy, Şenay Savaş Erdeve, Ülkühan Öztoprak, Gülin Karacan Küçükali, Husniye Yucel, Serdar Ceylaner, Çiğdem Seher Kasapkara, Çiğdem Genç Sel
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 114-118 (2021)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Hypomagnesemia is a rare cause of seizures in childhood but should be kept in mind in recurrent and intractable seizures and hypocalcemia in communities where consanguineous marriages are common. Familial hypomagnesemia with secondary hypocalcemia is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3abd45600c0455bf334cc6ccf3fc6c15
https://doi.org/10.4274/jcrpe.galenos.2020.2020.0004
https://doi.org/10.4274/jcrpe.galenos.2020.2020.0004
Autor:
Ali Fettah, Fatma Zehra Öztek Çelebi, Tamer Yoldaş, Meltem Akcaboy, Sule Yesil, Gönül Tanır, Saliha Senel
Publikováno v:
Paediatrics and International Child Health. 40:207-210
Chlamydophila pneumoniae, a common cause of respiratory tract infections, rarely leads to serious conditions. A 13-year-old boy with serologically confirmed C. pneumoniae infection presented with p...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a25717d35f081fba62970c0a0b561f3d
https://doi.org/10.1080/20469047.2020.1728163
https://doi.org/10.1080/20469047.2020.1728163
Autor:
Fatma Yazılıtaş, Saliha Senel, Fatma Zehra Öztek Çelebi, Meltem Akcaboy, Eyup Sari, Ozlem Akisoglu
Publikováno v:
Volume: 16, Issue: 2 138-143
Türkiye Çocuk Hastalıkları Dergisi
Türkiye Çocuk Hastalıkları Dergisi
Objective: Increased antibiotic resistance is a significant problem associated with higher morbidity, mortality, and costs in managing urinary tract infections (UTI). This study aims to analyze the antimicrobial resistance profile of uropathogens iso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dd5880d5d2a7b945ad028697c74120f
https://dergipark.org.tr/tr/pub/tchd/issue/68821/1071855
https://dergipark.org.tr/tr/pub/tchd/issue/68821/1071855
Autor:
Shenzhao Lu, Rebecca Hernan, Paul C. Marcogliese, Yan Huang, Tracy S. Gertler, Meltem Akcaboy, Shiyong Liu, Hyung-lok Chung, Xueyang Pan, Xiaoqin Sun, Melahat Melek Oguz, Ulkühan Oztoprak, Jeroen H.F. de Baaij, Jelena Ivanisevic, Erin McGinnis, Maria J. Guillen Sacoto, Wendy K. Chung, Hugo J. Bellen
Publikováno v:
American Journal of Human Genetics, 109, 571-586
Am J Hum Genet
American Journal of Human Genetics, 109, 4, pp. 571-586
Am J Hum Genet
American Journal of Human Genetics, 109, 4, pp. 571-586
TIAM Rac1-associated GEF 1 (TIAM1) regulates RAC1 signaling pathways that affect the control of neuronal morphogenesis and neurite outgrowth by modulating the actin cytoskeletal network. To date, TIAM1 has not been associated with a Mendelian disorde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c807b03d07ea87952f02aa162ee4ccc5
http://hdl.handle.net/2066/250181
http://hdl.handle.net/2066/250181
Autor:
Emine Polat, Fatma Zehra Öztek Çelebi, Melahat Melek Oguz, Saliha Senel, Husniye Yucel, Esma Altinel Acoglu, Gürses Şahin, Hilal Unsal, Meltem Akcaboy, Eyup Sari
Publikováno v:
Pediatric Hematology and Oncology. 36:1-16
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening syndrome of excessive immune activation. Secondary HLH syndrome develops as a complication of infection, drugs, rheumatologic conditions, or malignancy. The main objectives of this work w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ca5f6e1d14f3c5498a7b6bbdeac4ebc
https://doi.org/10.1080/08880018.2019.1572253
https://doi.org/10.1080/08880018.2019.1572253
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 1 (2014)
Background: Human species does not synthesize vitamin B12. In developing countries, vitamin B12 deficiency in infants due to maternal diet without adequate protein of animal origin has some characteristic clinical and laboratory features. We report o
Externí odkaz:
https://doaj.org/article/faa8a9a54309409ab76c5b43e3aaac74