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Genetics of Gland- in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia

Frontiers in endocrinology (Lausanne), 2020-07, Vol.11, p.413

2020

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A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia

Endocrine, 2021-07, Vol.73 (1), p.196-202

2021

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Collodion phenotype remains a challenge for neonatologists: A rare case of self‐healing collodion baby

Clinical case reports, 2022-07, Vol.10 (7), p.e6158-n/a

2022

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Improved feeding tolerance and growth linked to gut microbial diversity in very‐low‐birthweight infants fed with mother's own milk vs donor milk

Acta Paediatrica, 2020-02, Vol.109 (2), p.424-425

Zdraveska, Nikolina

2020

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Thyroid function and dysfunction in preterm infants—Challenges in evaluation, diagnosis and therapy

Clinical endocrinology (Oxford), 2021-10, Vol.95 (4), p.556-570

2021

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Multiple vital signs analysis algorithm detects systemic inflammatory response in premature infants with late‐onset sepsis and necrotising enterocolitis

Acta Paediatrica, 2019-08, Vol.108 (8), p.1548-1548

Zdraveska, Nikolina

2019

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Neonatal lupus erythematosus—a rare syndrome of transient autoimmunity

Clinical case reports, 2022-06, Vol.10 (6), p.e6004-n/a

2022

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Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism

Endocrine Connections, 2018-02, Vol.7 (2), p.278-285

2018

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First Macedonian child with tyrosinemia type 1 successfully treated with nitisinone and report of a novel mutation in the FAH gene

Srpski arhiv za celokupno lekarstvo, 2017, Vol.145 (9-10), p.530-533

2017

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Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood

SAGE open medical case reports, 2016-01, Vol.4, p.2050313X16683623

2016

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Coagulopathy as initial manifestation of concomitant celiac disease and cystic fibrosis: a case report

Journal of medical case reports, 2011-03, Vol.5 (1), p.116-116, Article 116

2011

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PP‐16 WEAK ACID REFLUX A TRIGGER FOR RECURRENT RESPIRATORY DISEASES IN CHILDREN

Journal of pediatric gastroenterology and nutrition, 2015-10, Vol.61 (4), p.527-527

2015

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Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism

Journal of Pediatric Endocrinology and Metabolism, 2016-07, Vol.29 (7), p.795

2016

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A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia

Endocrine, 2021-07, Vol.73 (1), p.196-202

2021

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Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years

The Turkish journal of pediatrics, 2023-03, Vol.65 (2), p.227-234

2023

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Diagnostic approach in children with unusual symptoms of acquired hypothyroidism. When to look for pituitary hyperplasia?

Journal of Pediatric Endocrinology and Metabolism, 2016-03, Vol.29 (3), p.297

2016

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Indications for gastrointestinal endoscopy in children

Zdravniški vestnik (Ljubljana, Slovenia : 1992), 2013-10, Vol.82

2013

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Epilepsy presenting only with severe abdominal pain

Journal of pediatric neurosciences, 2010-07, Vol.5 (2), p.169-170

2010

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Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes

Journal of Pediatric Endocrinology and Metabolism, 2011-10, Vol.24 (9-10), p.815-818

2011

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Vesicoureteral Reflux Detected with (99m)Tc-DTPA Renal Scintigraphy during Evaluation of Renal Function

Open access Macedonian journal of medical sciences, 2016-03, Vol.4 (1), p.135

2016

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Evaluation of Neonatal Hemolytic Jaundice: Clinical and Laboratory Parameters

Open access Macedonian journal of medical sciences, 2015-12, Vol.3 (4), p.694-698

2015

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Vesicoureteral Reflux Detected with 99mTc-DTPA Renal Scintigraphy during Evaluation of Renal Function

Open access Macedonian journal of medical sciences, 2015-12, Vol.4 (1), p.135-138

2015

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PP-241. Congenital adrenal hyperplasia: An endocrine disorder with neonatal onset — Case report

Early human development, 2010-11, Vol.86, p.S113-S113

2010

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UNUSUAL PRESENTATION OF BECKWITH-WIEDEMANN SYNDROME IN AN INFANT

Academic Medical Journal, 2023, Vol.3 (3), p.79-81

2023

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Genetics of Gland- in-situ or Hypoplastic Congenital Hypothyroidism in Macedonia

A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia

Collodion phenotype remains a challenge for neonatologists: A rare case of self‐healing collodion baby

Improved feeding tolerance and growth linked to gut microbial diversity in very‐low‐birthweight infants fed with mother's own milk vs donor milk

Thyroid function and dysfunction in preterm infants—Challenges in evaluation, diagnosis and therapy

Multiple vital signs analysis algorithm detects systemic inflammatory response in premature infants with late‐onset sepsis and necrotising enterocolitis

Neonatal lupus erythematosus—a rare syndrome of transient autoimmunity

Diagnostic re-evaluation of congenital hypothyroidism in Macedonia: predictors for transient or permanent hypothyroidism

First Macedonian child with tyrosinemia type 1 successfully treated with nitisinone and report of a novel mutation in the FAH gene

Submental thyroid ectopy might cause subclinical hypothyroidism in early childhood

Coagulopathy as initial manifestation of concomitant celiac disease and cystic fibrosis: a case report

PP‐16 WEAK ACID REFLUX A TRIGGER FOR RECURRENT RESPIRATORY DISEASES IN CHILDREN

Frequency of thyroid status monitoring in the first year of life and predictors for more frequent monitoring in infants with congenital hypothyroidism

A novel 9 bp deletion (c.1271_1279delGTGCCCGCG) in exon 10 of CYP21A2 gene causing severe congenital adrenal hyperplasia

Prevalence of congenital hypothyroidism in North Macedonia: data from a newborn screening program conducted for twenty years

Prevalence of Functional Gastrointestinal Disorders in Children and Adolescents in the Mediterranean Region of Europe

Diagnostic approach in children with unusual symptoms of acquired hypothyroidism. When to look for pituitary hyperplasia?

Indications for gastrointestinal endoscopy in children

Epilepsy presenting only with severe abdominal pain

Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetes

Vesicoureteral Reflux Detected with (99m)Tc-DTPA Renal Scintigraphy during Evaluation of Renal Function

Evaluation of Neonatal Hemolytic Jaundice: Clinical and Laboratory Parameters

Vesicoureteral Reflux Detected with 99mTc-DTPA Renal Scintigraphy during Evaluation of Renal Function

PP-241. Congenital adrenal hyperplasia: An endocrine disorder with neonatal onset — Case report

UNUSUAL PRESENTATION OF BECKWITH-WIEDEMANN SYNDROME IN AN INFANT

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