Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Fatma İssi"'
1
Akademický článek
Frequency of Congenital Sucrase-Isomaltase Deficiency by Whole Exome Sequencing: Is It Really Rare?
Autor: Fatma İssi Irlayıcı, Halil Özbaş, Hakan Salman, Mustafa Akçam
Publikováno v: Journal of Pediatric Research, Vol 11, Iss 4, Pp 225-231 (2024)
Aim: Congenital sucrase-isomaltase deficiency (CSID) is an autosomal recessive disease with a mutation in the sucrase-isomaltase (SI) gene and disaccharide maldigestion. With limited data, the estimated incidence of this disease is 57.59/10⁶ births
Externí odkaz: https://doaj.org/article/6e2b6c94578943f6889fe0b19d5d6785
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2
Akademický článek
Congenital Sucrase–Isomaltase Deficiency: Same Mutation with Different Clinical Presentations
Autor: Fatma İssi İrlayıcı, Burcu Güven, Murat Çakır
Publikováno v: The Turkish Journal of Gastroenterology, Vol 35, Iss 4, Pp 343-349 (2024)
Background/Aims: Congenital sucrase–isomaltase deficiency is an autosomal recessive inherited disaccharidase deficiency characterized by chronic osmotic diarrhea. In this study, the genotype–phenotype relationships of close relatives of an index
Externí odkaz: https://doaj.org/article/50249017e1f14a4a9e46bda3269a4873
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3
Akademický článek
Impact of Fecal Calprotectin Measurement for Inflammatory Bowel Disease in Children with Alarm Symptoms
Autor: Burcu Güven, Fatma İssi, Elif Sağ, Kurtuluş Buruk, Murat Çakır
Publikováno v: Journal of Pediatric Research, Vol 9, Iss 2, Pp 126-131 (2022)
Aim:The differentiation of inflammatory bowel diseases (IBD) from other gastrointestinal diseases in pediatric patients is highly important and the definitive diagnosis of IBD is established by endoscopic examination. The use of non-invasive methods
Externí odkaz: https://doaj.org/article/9ec3c795f07f4b4cb5b8106cb10b4083
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4
Akademický článek
Early onset congenital diarrheas; single center experience
Autor: Murat Cakir, Elif Sag, Burcu Guven, Ulas Emre Akbulut, Fatma Issi, Alper Han Cebi, Thomas Müller, Denise Aldrian, Andreas R. Janecke
Publikováno v: Pediatrics and Neonatology, Vol 62, Iss 6, Pp 612-619 (2021)
Background: Congenital diarrheal disorders (CDDs) are a rare group of enteropathies that typically present in the early few months of life and pose a diagnostic challenge. We aimed to analyze the clinical findings and outcome of infants with CDDs and
Externí odkaz: https://doaj.org/article/4f1f67007e0342319775497790907672
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5
Akademický článek
Frequency of Congenital Sucrase-Isomaltase Deficiency by Whole Exome Sequencing: Is It Really Rare?
Autor: Irlayıcı, Fatma İssi (AUTHOR), Özbaş, Halil (AUTHOR), Salman, Hakan (AUTHOR), Akçam, Mustafa (AUTHOR)
Publikováno v: Journal of Pediatric Research. Dec2024, Vol. 11 Issue 4, p1-7. 7p.
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6
Akademický článek
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8
Akademický článek
Congenital Sucrase-Isomaltase Deficiency: Same Mutation with Different Clinical Presentations.
Autor: Irlayıcı, Fatma İssi, Güven, Burcu, Çakır, Murat
Publikováno v: Turkish Journal of Gastroenterology; Apr2024, Vol. 35 Issue 4, p343-349, 7p
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9
Evaluation of Liver Elasticity Using pSWE and 2D-SWE Techniques in Healthy Children
Autor: Hüseyin AYDIN, Fatma İSSİ
Publikováno v: SDÜ Tıp Fakültesi Dergisi.
Objective: Shear wave elastography (SWE) is a new ultrasonography technique that can non-invasively evaluate liver stiffness. The efficacy of SWE in adults has been demonstrated by numerous studies, but there are few SWE studies of pediatric groups.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2ac82a0b9ff90ae51b7e9905893e4411
https://doi.org/10.17343/sdutfd.1252498
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Plný text Recenzováno Digitální knihovna AV ČR
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