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Paediatria Croatica , Vol. 58 No. 4, 2014.

  • Publication date: 23.12.2014.
  • Published on HRČAK: 24.07.2015.

Table of contents

Full text

Niemann-Pickova bolest tip C: mutacije gena NPC1 i tijek bolesti (page 261-261)

Niemann-Pick disease type C: mutations of NPC1 gene and the course of disease (page 255-260)

Ljerka Cvitanović-Šojat, Maša Malenica, Kukuruzović mONIKA, Tamara Žigman, Kristina Kužnik, Ana Bielen
Original scientific paper

english pdf 78kb
Neurorazvojni ishod nakon terapijske hipotermije zbog perinatalne asfi ksije (page 269-269)

Neurodevelopmental outcome following therapeutic hypothermia for perinatal asphyxia (page 262-268)

Smail Zubčević, Suada Heljić, Raho Spahović, Ismeta Kalkan, Sabina Terzić, Mirna Sadiković
Original scientific paper

english pdf 81kb
Autoimune encefalopatije u djece: klasifi kacija, dijagnostika i liječenje (page 270-276)

croatian pdf 83kb
Autoimmune encephalopathies in children: clasifi cation, diagnosis and treatment (page 277-277)

Nina Barišić, Nina Vrsaljko, Vanja Zvonar, Goran Tešović
Review article

Kongenitalna miotonička distrofi ja – prikaz bolesnika (page 278-282)

croatian pdf 133kb
Congenital myotonic dystrophy: case report (page 282-282)

Sanja Delin, Linda Pavić, Antun Sasso, Irena Barbarić, Goran Krakar, Ida Nađ
Case report

Karakterističan fenotip u djevojčice s Rettovim sindromom i delecijom 25 bp zbog nove mutacije u 4. eksonu (.881_905del25, nm_004992.3) gena MECP2 (page 285-285)

Distinctive phenotype in a girl with Rett syndrome and a novel 25 bp deletion mutation in exon 4 (c.881_905del25, nm_004992.3) of the MECP2 gene (page 283-285)

Matej Katavić, Monika Kukuruzović, Maša Malenica, Sara Seneca, Ljerka Cvitanović-Šojat
Case report

english pdf 52kb
MASA sindrom u braće blizanaca: prikaz kliničkog praćenja kroz šesnaest godina (page 290-290)

MASA syndrome in twin brothers: case report of sixteen-year clinical follow up (page 286-290)

Matilda Kovač Šižgorić, Zlatko Sabol, Filip Sabol, Tonći Grmoja, Svjetlana Bela Klancir, Zdravka Gjergja, Ljiljana Kipke Sabol
Case report

english pdf 127kb
Identična mutacija povezana s različitim fenotipom Friedreichove ataksije (page 294-294)

Identical mutation associated with distinct clinical phenotypes of Friedreich’s ataxia: case report (page 291-294)

Maša Malenica, Monika Kukuruzović, Suzana Bitanga, Goran Krakar, Bernardica Valent, Ljerka Cvitanović-Šojat
Case report

english pdf 59kb
Cerebralna paraliza i pridružena neurorazvojna odstupanja u djece s kortikalnom disgenezom (page 295-299)

croatian pdf 607kb
Cerebral palsy and associated neurodevelopmental impairments in children with cortical dysgenesis (page 300-300)

Andrea Šimić Klarić, Zdravko Kolundžić, Želimir Šimić, Ivana Đaković, Nikola Gotovac, Vlatka Mejaški Bošnjak
Case report

Comprehensive management of severe epilepsies in small countries with limited resources (page 301-302)

Igor Mihael Ravnik, Natalija Krajnc, Mirjana Benedik Perković, David Gosar, Andrej Vranič
Short communication, Note

english pdf 40kb
Sustav zdravlja u području rane intervencije u djetinjstvu (page 303-309)

croatian pdf 129kb
Health care system in the domain of Early Childhood Intervention (page 309-309)

Tena Matijaš, Jasmina Ivšac Pavliša, Marta Ljubešić
Original scientific paper

Hipoglikemija – nuspojava terapije propranololom dojenačkih hemangioma – prikaz triju slučajeva (page 310-313)

croatian pdf 181kb
Hypoglycemia as a side eff ect of infantile hemangioma treatment with propranolol: three case reports (page 314-314)

Arnes Rešić, Zdenka Pleša Premilovac, Filip Jurić, Marko Mesić
Case report

Akutni hemoragijski edem dojenčadi (page 315-316)

croatian pdf 140kb
Acute hemorrhagic edema of infancy (page 317-317)

Zdenka Pleša Premilovac, Agneza Marija Pasini, Iva Kolaček Vacka, Nives Pustišek, Alenka Gagro
Case report

Trihotilomanija i komorbiditet u adolescenata: prikaz dvaju bolesnika (page 318-321)

croatian pdf 63kb
Trichotillomania and comorbidity in adolescents: two case reports (page 322-322)

Aleksandra Klobučar, Nenad Jakušić, Aran Tomac, Vera Folnegović Šmalc
Case report

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