Search Results - "Jernej BRECELJ"
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Partial enteral nutrition induces clinical and endoscopic remission in active pediatric Crohn’s disease: results of a prospective cohort study
Published in European journal of pediatrics (01-03-2020)“…The aim of this study was to evaluate rates of clinical remission, endoscopic remission, and mucosal healing after a 6-week treatment period with partial…”
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2
Non-Alcoholic Fatty Liver Disease in Children
Published in Medicina (Kaunas, Lithuania) (16-07-2021)“…Background and Objectives: The prevalence of pediatric non-alcoholic fatty liver disease is increasing. A lot of new data are published regularly. Materials…”
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PREPOZNAVA IN ZDRAVLJENJE BOLNIKOV Z MOTNJAMI SINTEZE ŽOLČNIH KISLIN
Published in Slovenska pediatrija (01-11-2022)“…Motnje sinteze žolčnih kislin so skupina redkih dednih pre-snovnih bolezni, ki se kažejo s holestazo, odpovedjo ali cirozo jeter ter občasno s steatorejo…”
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4
Role of endoscopic ultrasound-guided fine needle aspiration biopsies in diagnosing pancreatic neoplasms in the paediatric population: experience from a tertiary center and review of the literature
Published in Radiology and oncology (01-03-2024)“…Endoscopic ultrasound-guided fine needle aspiration biopsy (EUS FNAB) is a well established diagnostic method in adult patients, but is rarely used in the…”
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5
Success and safety of high infliximab trough levels in inflammatory bowel disease
Published in Scandinavian journal of gastroenterology (03-08-2018)“…Objective: A prospective trial suggests target infliximab trough levels of 3-7 μg/mL, yet data on additional therapeutic benefits and safety of higher trough…”
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Clinical and genetic characteristics of a patient with phosphoribosyl pyrophosphate synthetase 1 deficiency and a systematic literature review
Published in Molecular genetics and metabolism reports (01-09-2023)“…Phosphoribosylpyrophosphate synthetase 1 (PRSI) is an enzyme involved in nucleotide metabolism. Pathogenic variants in the PRPS1 are rare and PRS-I deficiency…”
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7
Clinical and genetic characteristics of two patients with tyrosinemia type 1 in Slovenia – A novel fumarylacetoacetate hydrolase (FAH) intronic disease-causing variant
Published in Molecular genetics and metabolism reports (01-03-2022)“…Tyrosinemia type 1 (HT1) is an inborn error of tyrosine catabolism that leads to severe liver, kidney, and neurological dysfunction. Newborn screening (NBS)…”
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Dual Role of PTPN22 but Not NLRP3 Inflammasome Polymorphisms in Type 1 Diabetes and Celiac Disease in Children
Published in Frontiers in pediatrics (12-03-2019)“…Genetic polymorphisms in genes coding for inflammasome components and have been associated with autoinflammatory and autoimmune diseases. On the other hand…”
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9
NEALKOHOLNI STEATOHEPATITIS PRI OTROKU − PRAKTIČNI PRISTOP S PREDSTAVITVIJO PRIMERA
Published in Slovenska pediatrija (01-10-2021)“…Nealkoholna maščobna spremenjenost jeter pri otrocih je kronična bolezen jeter, ki nastane zaradi kopičenja maščob v jetrih. Tesno je povezana z debelostjo in…”
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10
CISTIČNA HIDATIDNA BOLEZEN PRI OTROKU: PRIKAZ PRIMERA
Published in Slovenska pediatrija (01-12-2020)“…Cistična ehinokokoza ali hidatidna bolezen je široko endemična parazitoza, ki jo povzroča okužba z jajčeci trakulje Echinococcus granulosus. Kaže se lahko z…”
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11
Pregled in ocena kazalcev bolezni otrok in mladostnikov s cistično fibrozo v Sloveniji
Published in Zdravniški vestnik (Ljubljana, Slovenia : 1992) (01-08-2023)“…Izhodišča: Cistična fibroza (CF) je najpogostejša kronična avtosomno recesivno dedna bolezen belcev. Kaže se s prizadetostjo številnih organov, zato se bolniki…”
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12
RECOGNITION AND TREATMENT OF PATIENTS WITH BILE ACID SYNTHESIS DISORDERS
Published in Slovenska pediatrija (01-11-2022)“…Bile acids synthesis disorders are a group of rare inherited metabolic diseases that present with cholestasis, liver failure or cirrhosis and are sometimes…”
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13
Effects of formula supplementation in breast-fed infants with failure to thrive
Published in Pediatrics international (01-06-2009)“…Background: The aim of the present study was to assess whether formula supplementation of infants with failure to thrive can improve underweight without…”
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14
RECOGNITION AND TREATMENT OF PATIENTS WITH BILE ACID SYNTHESIS DISORDERS
Published in Slovenska pediatrija (2022)“…Abstract only…”
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15
Severe dermatitis with anemia and edema in an infant
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16
Comparison of liquid chromatography with tandem mass spectrometry and ion-exchange chromatography by post-column ninhydrin derivatization for amino acid monitoring
Published in Clinica chimica acta (01-08-2019)“…Precise quantification of amino acids (AAs) is mandatory for successful diagnosis and monitoring of patients with metabolic diseases. We compared ion-exchange…”
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CYSTIC HYDATID DISEASE IN A CHILD: CASE REPORT
Published in Slovenska pediatrija (01-12-2020)“…Cystic echinococcosis or hydatid disease is a widely endemic parasitosis caused by infection with eggs of the Echinococcus granulosus tapeworm. The symptoms…”
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Sedation and analgesia for gastrointestinal endoscopy in children
Published in Zdravniški vestnik (Ljubljana, Slovenia : 1992) (01-10-2013)“…Different sedation or anesthesia protocols are available to enable gastrointestinal endoscopic examinations in children. None is optimal. Sedation is organized…”
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Morphological and Functional Assessment of Oesophageal Mucosa Integrity in Children With Cystic Fibrosis
Published in Journal of pediatric gastroenterology and nutrition (01-05-2016)“…ABSTRACT Objectives: The aim of the study was to investigate morphological and functional characteristics of oesophageal epithelial barrier in children with…”
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Severe acute hepatitis and acute liver failure of unknown origin in children: a questionnaire-based study within 34 paediatric liver centres in 22 European countries and Israel, April 2022
Published in Euro surveillance : bulletin européen sur les maladies transmissibles (12-05-2022)“…To detect potential concern about severe acute hepatitis in children, we conducted a survey among 50 ERN RARE-LIVER centres. By 26 April 2022, 34 centres,…”
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