Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Marija P. ŠEPEC"'
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
Autor:
Matea Crnković Ćuk, Ana Kovačević, Orjena Žaja, Marija Požgaj Šepec, Goran Roić, Bernardica Valent Morić, Ivana Trutin
Publikováno v:
Acta Clinica Croatica, Vol 61., Iss 4, Pp 717-721 (2022)
We present a case of transient form of type 1 pseudohypoaldosteronism (S-PHA) in a 1.5-month-old male infant who presented with lethargy, failure to thrive, severe hyponatremia (Na=118 mmol/L), hypochloremia (Cl=93 mmol/L) and fever due to urinary
Externí odkaz:
https://doaj.org/article/97dd2556a9794008b6ba05412b85e9b0
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 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
Publikováno v:
Minerva endocrinology. 46(1)
ACKGROUND: 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 patients treated at our Clinic, with an emphasis on their age at diagnosis and the ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f7f302fe2c2b12bb204a1ea95e37981
https://pubmed.ncbi.nlm.nih.gov/32623843
https://pubmed.ncbi.nlm.nih.gov/32623843