Search Results - "Stipancić, Gordana"

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    ALTERNATING HYPOTHYROIDISM AND HYPERTHYROIDISM IN AN ADOLESCENT BOY - DO WE ALWAYS UNDERSTAND WHAT DRIVES THE SWITCH? by La Grasta Sabolić, Lavinia, Požgaj Šepec, Marija, Stipančić, Gordana

    Published in Acta clinica Croatica (Tisak) (01-01-2023)
    “…Alternating hypothyroidism and hyperthyroidism is a rare phenomenon, especially among pediatric patients. It is usually related to simultaneous, unbalanced…”
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    Is there a characteristic pattern of ambulatory blood pressure profile in type 1 diabetic children and adolescents? by Morić, Bernardica Valent, Šamija, Ivan, Sabolić, Lavinia La Grasta, Stipančić, Gordana

    “…To examine the characteristics of ambulatory blood pressure (ABP) including blood pressure variability (BPV) and its association with albuminuria in type 1…”
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    Continuous Glucose Monitoring and Type 1 Diabetes Mellitus Control in Child, Adolescent and Young Adult Population – Arguments for Its Use and Effects by Rubelj, Karla

    Published in Acta clinica Croatica (Tisak) (01-12-2021)
    “…Sensors for continuous glucose monitoring (CGM) in intercellular fluid are used as a contemporary method to achieve better control in type 1 diabetes mellitus…”
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    Does Urinary Tract Ultrasound Have Its Place in the Treatment of Early Neonatal Jaundice? Neonatal Bilateral Adrenal Hemorrhage: Case Report by Trutin, Ivana, Valent Morić, Bernardica, Borošak, Jesenka, Stipančić, Gordana

    Published in Acta clinica Croatica (Tisak) (01-03-2018)
    “…Adrenal hemorrhage is a rare clinical entity in the neonatal period, with an incidence of 1.7-2.1/1000 births. It is more often diagnosed on the right side,…”
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    EFFECT OF GROWTH HORMONE THERAPY IN CHILDREN WITH PRADER-WILLI SYNDROME - OUR FIRST EXPERIENCES by Stipancic, Gordana, Sepec, Marija Pozgaj, La Grasta Sabolic, Lavinia

    Published in Acta clinica Croatica (Tisak) (01-12-2018)
    “…- Prader-Willi syndrome (PWS) is the most common cause of morbid obesity in childhood. It is the consequence of the lack of expression of genes on the…”
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    Turner Syndrome: for successful treatment it is necessary to diagnose it early by Oletić, Lea, Šepec, Marija P, Sabolić, Lavinia L, Stipančić, Gordana

    Published in Minerva endocrinology (01-03-2021)
    “…Turner Syndrome (TS) is a chromosomal disorder with short stature as the most common feature. The aim of this paper was to show the characteristics of TS…”
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    Croatia Needs a Gender Incongruence Diagnosis for Prepubertal Children by Jokić-Begić, Nataša, Altabas, Velimir, Antičević, Vesna, Arbanas, Goran, Begić, Dražen, Budi, Srećko, Dumić, Miroslav, Grubić, Marina, Grujić, Jasenka, Jakušić, Nenad, Stipančić, Gordana, Šarić, Davorka, Žegura, Iva

    Published in Archives of sexual behavior (01-11-2017)
    “…A commentary on "The proposed ICD-11 gender incongruence of childhood diagnosis: A World Professional Association for Transgender Health Membership Survey" by…”
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    IL12RB2 gene is associated with the age of type 1 diabetes onset in Croatian family Trios by Pehlić, Marina, Vrkić, Dina, Skrabić, Veselin, Jerončić, Ana, Stipančić, Gordana, Urojić, Anita Špehar, Marjanac, Igor, Jakšić, Jasminka, Kačić, Zrinka, Boraska, Vesna, Zemunik, Tatijana

    Published in PloS one (13-11-2012)
    “…Common complex diseases are influenced by both genetic and environmental factors. Many genetic factors overlap between various autoimmune diseases. The aim of…”
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    Medical Emergencies in Pediatric Dentistry by Vranić, Dubravka Negovetić, Jurković, Josipa, Jeličić, Jesenka, Balenović, Antonija, Stipančić, Gordana, Čuković-Bagić, Ivana

    Published in Acta stomatologica croatica (01-03-2016)
    “…Medical emergencies that are life threatening can occur in dental practice. Complications may arise because of an underlying disease or a reaction to…”
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    Regional differences in incidence and clinical presentation of type 1 diabetes in children aged under 15 years in Croatia by Stipancić, Gordana, La Grasta Sabolić, Lavinia, Pozgaj Sepec, Marija, Radica, Ana, Skrabić, Veselin, Severinski, Srećko, Kujundzić Tiljak, Mirjana

    Published in Croatian medical journal (01-04-2012)
    “…To determine regional differences in the incidence, incidence trends, and clinical presentation of type 1 diabetes in children under the age of 15 years in…”
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    Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation by Boraska, Vesna, Torlak, Vesela, Skrabić, Veselin, Kacić, Zrinka, Jaksić, Jasminka, Stipancić, Gordana, Uroić, Anita Spehar, Markotić, Anita, Zemunik, Tatijana

    Published in Clinical biochemistry (01-06-2009)
    “…Type 1 diabetes mellitus (T1DM) is an autoimmune disease characterized by destruction of pancreatic beta cells. Gangliosides are thought to be a target of a…”
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    Screening of patients at risk for 22q11 deletion by Barisić, Ingeborg, Morozin Pohovski, Leona, Petković, Iskra, Cvetko, Zeljko, Stipancić, Gordana, Bagatin, Marijo

    Published in Collegium antropologicum (01-03-2008)
    “…The aim of this study was to determine whether deletion 22q11.2 studies should become apart of a standardized diagnostic workup for selected groups of at risk…”
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    Missense mutation W86R in exon 3 of the lipoprotein lipase gene in a boy with chylomicronemia by Pašalić, Daria, Jurčić, Zvonko, Stipančić, Gordana, Ferenčak, Goran, Leren, Trond P., Djurovic, Srdjan, Stavljenić-Rukavina, Ana

    Published in Clinica chimica acta (01-05-2004)
    “…Background: Familial LPL deficiency is a rare inborn error of metabolism caused by mutational change within the LPL gene, which leads to massive…”
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    Growth disorders in children with type 1 diabetes mellitus by Stipancić, Gordana, La Grasta Sabolić, Lavinia, Jurcić, Zvonimir

    Published in Collegium antropologicum (01-06-2006)
    “…The aim of the research was to analyze anthropometric variables in children with type 1 diabetes mellitus (DM) in relation with the stage of pubertal…”
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    216 Discrepancy between clinical presentation and sex streroid hormone values in a prepubertal girl by Sabolić, Lavinia La Grasta, Šepec, Marija Požgaj, Zec, Ivana, Mandić, Dario, Stipančić, Gordana

    Published in Archives of disease in childhood (11-10-2021)
    “…BackgroundLaboratory evaluation is crucial for accurate assessment of patients with endocrine disorders. When clinical picture is in obvious contradiction with…”
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    Trisomy 21 Is a Cause of Permanent Neonatal Diabetes That Is Autoimmune but Not HLA Associated by Johnson, Matthew B, De Franco, Elisa, Greeley, Siri Atma W, Letourneau, Lisa R, Gillespie, Kathleen M, Wakeling, Matthew N, Ellard, Sian, Flanagan, Sarah E, Patel, Kashyap A, Hattersley, Andrew T

    Published in Diabetes (New York, N.Y.) (01-07-2019)
    “…Identifying new causes of permanent neonatal diabetes (PNDM) (diagnosis <6 months) provides important insights into β-cell biology. Patients with Down syndrome…”
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