Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Gordana Stipančić"'
Publikováno v:
Acta Clinica Croatica, Vol 62., Iss 3, Pp 546-550 (2023)
Alternating hypothyroidism and hyperthyroidism is a rare phenomenon, especially among pediatric patients. It is usually related to simultaneous, unbalanced presence of stimulating and blocking thyroid stimulating hormone receptor antibodies (TRAbs)
Externí odkaz:
https://doaj.org/article/a502dca504dc463f900e1d037344855b
Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 27, Iss 4, Pp 300-307 (2022)
Purpose To examine the characteristics of ambulatory blood pressure (ABP) including blood pressure variability (BPV) and its association with albuminuria in type 1 diabetic (T1D) children and to identify potential predictors of high-normal albuminuri
Externí odkaz:
https://doaj.org/article/559735fd1f9e47088ef5d023ecf216a0
Publikováno v:
JCRPE, Vol 13, Iss 2, Pp 160-169 (2021)
Objective:Characteristics of the glucose response during oral glucose tolerance test (OGTT) may reflect differences in insulin secretion and action. The aim was to examine whether timing of the glucose peak, shape of the glucose curve and their combi
Externí odkaz:
https://doaj.org/article/d7c768cd9654430bb6ee5c7ab02c0b9e
Publikováno v:
Acta Clinica Croatica, Vol 60., Iss 4., Pp 609-615 (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 (DM), which is best shown through lower glycated hemoglobin (HbA1c) levels.The aim of thi
Externí odkaz:
https://doaj.org/article/3ee671658e3248a58c2338adc7fe4a18
Publikováno v:
Acta Clinica Croatica, Vol 57., Iss 1., Pp 161-165 (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, whilst bilateral hemorrhage occurs in 10%-15% of cases. Clinical presentation shows a wide ra
Externí odkaz:
https://doaj.org/article/3e428b2757824c0790ac0b1108135358
Publikováno v:
Acta Clinica Croatica, Vol 57., Iss 4., Pp 744-754 (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 paternally inherited 15q11.2-q13 region. Hyperphagia, obesity, short stature, psychomotor retardation
Externí odkaz:
https://doaj.org/article/57493f22181a46e0b010320401faac9b
Autor:
Dubravka NEGOVETIĆ VRANIĆ, Josipa Jurković, Jesenka Jeličić, Antonija Balenović, Gordana Stipančić, Ivana Čuković-Bagić
Publikováno v:
Acta Stomatologica Croatica, Vol 50, Iss 1, Pp 72-80 (2016)
Medical emergencies that are life threatening can occur in dental practice. Complications may arise because of an underlying disease or a reaction to medication. Reactions to medications may be allergic and toxic. The most common reactions are toxic
Externí odkaz:
https://doaj.org/article/f3a63d07bfc1433a9e34d391f454225a
Autor:
Marina Pehlić, Dina Vrkić, Veselin Skrabić, Ana Jerončić, Gordana Stipančić, Anita Špehar Urojić, Igor Marjanac, Jasminka Jakšić, Zrinka Kačić, Vesna Boraska, Tatijana Zemunik
Publikováno v:
PLoS ONE, Vol 7, Iss 11, p e49133 (2012)
BACKGROUND: Common complex diseases are influenced by both genetic and environmental factors. Many genetic factors overlap between various autoimmune diseases. The aim of the present study is to determine whether four genetic variants known to be ris
Externí odkaz:
https://doaj.org/article/bf0ac2477e3a405199e73ec0511d168e
Publikováno v:
JCRPE, Vol 13, Iss 2, Pp 160-169 (2021)
Journal of Clinical Research in Pediatric Endocrinology
Journal of Clinical Research in Pediatric Endocrinology
Objective: Characteristics of the glucose response during oral glucose tolerance test (OGTT) may reflect differences in insulin secretion and action. The aim was to examine whether timing of the glucose peak, shape of the glucose curve and their comb
Autor:
Maja Oroz, Ana Vičić, Marija Požgaj Šepec, Helena Karnaš, Gordana Stipančić, Feodora Stipoljev
Objectives Approximately 90% of “XX males” are positive for SRY. However, there are isolated cases of sex reversal associated to other genes in male-determining pathway. Case presentation We describe a 1.3-old patient with 46,XX karyotype, male p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca523348981bf0585eb5922db54bb28
https://www.bib.irb.hr/1282214
https://www.bib.irb.hr/1282214