Search Results - "Janchevska, Aleksandra"
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IGF1R Gene Alterations in Children Born Small for Gestitional Age (SGA)
Published in Open access Macedonian journal of medical sciences (25-11-2018)“…Small for gestational age (SGA)-born children are a heterogeneous group with few genetic causes reported. Genetic alterations in the IGF1 receptor (IGF1R) are…”
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GP297 Evaluation of an early biochemistry marker of renal injury in obese children
Published in Archives of disease in childhood (01-06-2019)“…BackgroundThe obesity is the most prevalent nutrition-related disorder in children and becomes a major health issue worldwide. An increased risk of renal…”
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P429 Gitelman Syndrome – Report of the first pediatric patient from Macedonia
Published in Archives of disease in childhood (01-06-2019)“…Background and aimsGitelman syndrome (GS) is a rare renal channelopathy with an autosomal recessive type of inheritance, caused by homozygous or compound…”
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IGF1R Gene Alterations in Small for Gestational Age (SGA) Children
Published in Open access Macedonian journal of medical sciences (20-05-2018)“…Small for gestational age children (SGA) is born on term with BW and or BL of -2.0 standard deviation score (SDS). SGA children have an increased risk of being…”
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Congenital Anomalies of the Kidney and Urinary Tract in Children Born Small for Gestational Age
Published in Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki) (01-03-2017)“…Congenital anomalies of the kidney and urinary tract (CAKUT) represent several types of malformations with occurrence of 1 in about 500 live births. Small for…”
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Chronic kidney disease - pediatric risk factors
Published in Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki) (01-01-2016)“…The knowledge about the progression of chronic kidney disease is an important issue for every pediatric nephrologist and pediatrician in order to implement…”
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Tricho-rhino-phalangeal syndrome in a 13-year-old girl with chronic renal failure and severe growth retardation
Published in Renal failure (01-05-2014)“…The tricho-rhino-phalangeal syndrome type III (TRPS III) is a rare autosomal dominantly inherited condition. The main clinical features are sparse and…”
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Peripheral Insulin Edema and Pericardial Effusion in a 12-Year-Old Newly Diagnosed Girl with Type 1 Diabetes
Published in Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki) (01-07-2023)“…: Insulin induced edema (IIE) is a rare condition, usually found in newly diagnosed diabetes patients, either after insulin treatment initiation or after dose…”
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