Search Results - Špehar Uroić, Anita

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  1. 1
    Distinct association patterns of chemokine profile and cardiometabolic status in children and adolescents with type 1 diabetes and obesity

    Distinct association patterns of chemokine profile and cardiometabolic status in children and adolescents with type 1 diabetes and obesity by Špehar Uroić, Anita, Filipović, Maša, Šućur, Alan, Kelava, Tomislav, Kovačić, Nataša, Grčević, Danka

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  2. 2
    Role of Parents in Body Mass Reduction in Children with Obesity-Adherence and Success of 1-Year Participation in an Intervention Program

    Role of Parents in Body Mass Reduction in Children with Obesity-Adherence and Success of 1-Year Participation in an Intervention Program by Rahelić, Valentina, Głąbska, Dominika, Guzek, Dominika, Pavić, Eva, Rumora Samarin, Ivana, Bogdanić, Ana, Špehar Uroić, Anita, Rojnić Putarek, Nataša, Krnić, Nevena

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  3. 3
    Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott–Rallison syndrome

    Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott–Rallison syndrome by Špehar Uroić, Anita, Mulliqi Kotori, Vjosa, Rojnić Putarek, Nataša, Kušec, Vesna, Dumić, Miroslav

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  4. 4
    208 Use of GLP-1 analog in a patient with prader-willi syndrome

    208 Use of GLP-1 analog in a patient with prader-willi syndrome by Duje, Braovac, Nevena, Krnić, Katja, Dumić Kubat, Anita, Špehar Uroić, Igor, Marjanac, Jurica, Vuković

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  5. 5
    209 Are kindey malformations possible feature of men2b syndrome? – report of a patient with men2b, type 1 diabetes, situs viscerum inversus and kidney malformations

    209 Are kindey malformations possible feature of men2b syndrome? – report of a patient with men2b, type 1 diabetes, situs viscerum inversus and kidney malformations by Mrkic, Lucija Kolega, Uroić, Anita Špehar, Putarek, Nataša Rojnić, Sertić, Jadranka, Krnić, Nevena

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  6. 6
    222 Van Wyk-grumbach syndrome – a rare manifestation of untreated primary hypothyroidism

    222 Van Wyk-grumbach syndrome – a rare manifestation of untreated primary hypothyroidism by Vinković, Maja, Krnić, Nevena, Uroić, Anita Špehar, Kušec, Vesna, Braovac, Duje, Kubat, Katja Dumić

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  7. 7
    Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation

    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
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  8. 8
    Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant

    Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant by Grubic, Zorana, Rojnic Putarek, Natasa, Maskalan, Marija, Zunec, Renata, Stingl Jankovic, Katarina, Burek Kamenaric, Marija, Knezevic-Cuca, Jadranka, Spehar Uroic, Anita, Dumic, Miroslav

    Published in Gene
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  9. 9
    Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia—Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation

    Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia—Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation by Spehar Uroic, Anita, Milenkovic, Dragan, De Franco, Elisa, Bilic, Ernest, Rojnic Putarek, Natasa, Krnic, Nevena

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  10. 10
    Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population

    Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population by Boraska, Vesna, Torlak, Vesela, Škrabić, Veselin, Kačić, Zrinka, Jakšić, Jasminka, Stipančić, Gordana, Špehar Uroić, Anita, Markotić, Anita, Zemunik, Tatijana

    Published in Clinical biochemistry
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  11. 11
    Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia-Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation

    Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia-Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation by Spehar Uroic, Anita, Milenkovic, Dragan, De Franco, Elisa, Bilic, Ernest, Rojnic Putarek, Natasa, Krnic, Nevena

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