Search Results - "Çizmecioglu, Filiz Mine"

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  1. 1

    Educational Needs of Adolescents Regarding Normal Puberty and Menstrual Patterns by İşgüven, Pınar, Yörük, Göze, Çizmecioğlu, Filiz Mine

    “…The study aimed to determine the level of knowledge and the sources of information about normal puberty and menstrual patterns in Turkish schoolgirls from…”
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    Journal Article
  2. 2

    Spondyloenchondrodysplasia: a rare cause of short stature by Yeşiltepe-Mutlu, Gül, Ozsu, Elif, Cizmecioğlu, Filiz Mine, Alanay, Yasemin, Hatun, Sükrü

    Published in Turkish journal of pediatrics (01-07-2011)
    “…Skeletal dysplasias (osteochondrodysplasias) are a group of diseases that must be included in the differential diagnosis of disproportionate short stature…”
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    Girls with Premature Thelarche Younger than 3 Years of Age May Have Stimulated Luteinizing Hormone Greater than 10 IU/L by Seymen Karabulut, Gülcan, Atar, Müge, Çizmecioğlu Jones, Filiz Mine, Hatun, Şükrü

    “…Premature thelarche (PT) is defined as isolated breast development in girls before eight years of age. Gonadotropin-releasing hormone (GnRH) stimulation test…”
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  4. 4

    Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life by Çizmecioğlu, Filiz Mine, Jones, Jeremy Huw, Paterson, Wendy Forsyth, Kherra, Sakina, Kourime, Mariam, McGowan, Ruth, Shaikh, M. Guftar, Donaldson, Malcolm

    “…Early diagnosis is of proven benefit in Prader-Willi syndrome (PWS). We therefore examined key perinatal features to aid early recognition. Data were collected…”
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    Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 38,935 Infants by Güran, Tülay, Tezel, Başak, Gürbüz, Fatih, Selver Eklioğlu, Beray, Hatipoğlu, Nihal, Kara, Cengiz, Şimşek, Enver, Çizmecioğlu, Filiz Mine, Ozon, Alev, Baş, Firdevs, Aydın, Murat, Darendeliler, Feyza

    “…Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting…”
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    A case of adrenal insufficiency during multisystem inflammatory syndrome in children by Kilci, Fatih, Yetimakman, Ayşe Filiz, Jones, Jeremy Huw, Çizmecioğlu, Filiz Mine

    Published in Clinical Pediatric Endocrinology (01-01-2022)
    “…Multisystem inflammatory syndrome in children (MIS-C) is a disease related to coronavirus disease 2019 (COVID-19). Although the effects of COVID-19 on many…”
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  8. 8

    Successful Management of Severe Hypercalcemia with Zoledronic Acid: A Report of Two Pediatric Cases by Kilci, Fatih, Jones, Jeremy Huw, Çizmecioğlu-Jones, Filiz Mine

    “…Severe hypercalcemia associated with vitamin D intoxication or malignancy in children is a rare and life-threatening condition. There is little published…”
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  9. 9

    Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre by Kherra, Sakina, Forsyth Paterson, Wendy, Cizmecioglu, Filiz Mine, Jones, Jeremy Huw, Kourime, Mariam, Elsedfy, Heba Hassan, Tawfik, Sameh, Kyriakou, Andreas, Shaikh, Mohamad Guftar, Donaldson, Malcolm David Cairns

    Published in Endocrine Connections (01-09-2021)
    “…Background Hypogonadism is a key feature of Prader–Willi syndrome (PWS) but clear strategies for hormone replacement are lacking. Objective To evaluate the…”
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    Vitamin D deficiency in children and adolescents with type 1 diabetes by Mutlu, Ajda, Mutlu, Gül Yeşiltepe, Özsu, Elif, Çizmecioğlu, Filiz Mine, Hatun, Şükrü

    “…To investigate the frequency and effects of vitamin D deficiency in children with type 1 diabetes (T1D) in a region which is known to have a high rate of…”
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    HADH Mutation is a Rare Cause of Hyperinsulinaemic Hypoglycaemia by Özsu, Elif, Mutlu, Gül Yesiltepe, Çizmecioglu, Filiz Mine, Hatun, Sükrü

    “…Introduction Hydroxyacyl CoA dehydrogenase is coded by HADH gene. Mutations in this gene are a rare cause of recessively inherited hyperinsulinaemic…”
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  13. 13

    Can HbA1c and one-hour glucose concentration in standard OGTT be used for evaluation of glucose homeostasis in childhood? by Yeşiltepe Mutlu, Gül, Özsu, Elif, Çizmecioğlu, Filiz Mine, Hatun, Şükrü

    “…To investigate whether glycosylated hemoglobin (HbA1c) and 1-hour glucose level in oral glucose tolerance test (OGTT) are useful parameters for evaluation of…”
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    Congenital hypothyroidism screening program in Turkey: a local evaluation by Kusdal, Yusuf, Yesiltepe-Mutlu, Gü, Özsu, Elif, Çizmecioglu, Filiz Mine, Hatun, Sükrü

    Published in Turkish journal of pediatrics (01-11-2012)
    “…It was aimed to evaluate the national congenital hypothyroidism program in terms of thyroid-stimulating hormone (TSH) cut-off level, frequency of cases that…”
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    No relationship between vitamin D status and insulin resistance in a group of high school students by Erdönmez, Dilek, Hatun, Sükrü, Çizmecioğlu, Filiz Mine, Keser, Alev

    “…To investigate the effects of vitamin D deficiency on both insulin resistance and risk of metabolic syndrome in children. The study group consisted of 301…”
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    Nutritional status of students in Kocaeli, Turkey: A population-based study by Etiler, Nilay, Cizmecioglu, Filiz Mine, Hatun, Sukru, Hamzaoglu, Onur

    Published in Pediatrics international (01-04-2011)
    “…Background:  The aim of this study was to determine the nutritional status of students in Kocaeli, Turkey. Methods:  This cross‐sectional study was carried out…”
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    Audit of microalbumin excretion in children with type I diabetes by Cizmecioğlu, Filiz Mine, Noyes, Kathryn, Bath, Louise, Kelnar, Chris

    “…To investigate prevalence, persistence and clinical correlates of increased microalbumin excretion in random urine samples collected in a paediatric diabetes…”
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    A case of adrenal insufficiency during multisystem inflammatory syndrome in children by Fatih Kilci, Ayse Filiz Yetimakman, Jeremy Huw Jones, Filiz Mine Cizmecioglu

    Published in Clinical Pediatric Endocrinology (01-07-2022)
    “…[Highlights] ●To the best of our knowledge, this is the first reported pediatric case with adrenal insufficiency due to MIS-C. ●The…”
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    Measured parental height in Turner syndrome—a valuable but underused diagnostic tool by Ouarezki, Yasmine, Cizmecioglu, Filiz Mine, Mansour, Chourouk, Jones, Jeremy Huw, Gault, Emma Jane, Mason, Avril, Donaldson, Malcolm D. C.

    Published in European journal of pediatrics (01-02-2018)
    “…Early diagnosis of Turner syndrome (TS) is necessary to facilitate appropriate management, including growth promotion. Not all girls with TS have overt short…”
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    Outcomes of Endoscopic Transsphenoidal Approach for More Aggressive Pediatric Pituitary Adenomas: Early- and Late-Term Results from a Single Center Experience by Caklili, Melih, Yilmaz, Eren, Duman Ozturk, Seda, Uzuner, Ayse, Yildirim, Pinar, Cizmecioglu Jones, Filiz Mine, Tas, Abdurrahim, Cabuk, Burak, Anik, Ihsan, Ceylan, Savas

    Published in World neurosurgery (01-08-2023)
    “…Pediatric pituitary adenomas are rare lesions and account for approximately 3% of all supratentorial tumors in children. There is a paucity of reports on…”
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