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Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?

Balkan journal of medical genetics, 2023-12, Vol.26 (2), p.51-58

2023

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Transient hyperinsulinemia may be responsible from electrolyte abnormalities of refeeding syndrome seen in very low birth weight infants with intrauterine growth-restriction

Journal of perinatology, 2014-03, Vol.34 (3), p.247-247

2014

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Assessment of novel biomarkers: sTREM-1, pentraxin-3 and pro-adrenomedullin in the early diagnosis of neonatal early onset sepsis

Journal of neonatal-perinatal medicine, 2020, Vol.13 (1), p.47

2020

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Outcome of Surgery for Toxic Goitres in Maiduguri: A Single Teaching Hospital's Perspective

The Journal of surgical research, 2012, Vol.172 (2), p.188-188

2012

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190 Predicting The Efficacy of Oral Sucrose in Reducing Pain During Ophtalmological Examination for Retinopathy of Prematurity: A Prospective Randomised Study

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A55-A55

2012

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1358 Effect of Mode of Delivery on Mortality and Morbidity in Very Low Birth Weight Neonates with Respiratory Distress Syndrome

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A387-A387

2012

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1081 Levels of Serum N-Terminal Pro-Brain Natriuretic Peptide, Cystatin C, and Urinary B2 Microglobulin in Newborns with Hypoxic Ischemic Encephalopathy

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A310-A310

2012

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1180 The Predictive Values of Mean Platelet Volume (MPV) in the Diagnosis of Neonatal Sepsis

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A338-A338

2012

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1634 The Effects of Synbiotic use on Morbidity and Mortality in Premature Infants: A Prospective Randomized Controlled Trial

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A462-A462

2012

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1678 Treatment of Infantile Colic with Lactobacillus Reuteri and the Relationship with Postpartum Depression: A Randomized Controlled Trial Study

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A474-A475

2012

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1699 Distribution of Congenital Malformation in a Neonatal Intensive Care Unit in Turkey

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A480-A480

2012

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1633 The Effects of Synbiotics on Morbidity and Mortality in Newborns with Cyanotic Congenital Heart Disease: A Prospective Randomized Controlled Trial

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A462-A462

2012

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1122 The Effect of Heparin Infusion on Development of ThrombosİS Secondary to Cardiac Catheterization

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A322-A322

2012

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1146 Perfusion Index Variability and N-Terminal Pro-Brain Natriuretic Peptide Levels Before and After Cardiac Interventions in Congenital Heart Disease

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A328-A329

2012

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1039 Determination of the Perfusion Index Reference Values and Variation in Clinically and Hemodinamically Stable Newborns During the Early Neonatal Period

Archives of disease in childhood, 2012-10, Vol.97 (Suppl 2), p.A298-A298

2012

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AXILLARY ARTERY THROMBOSIS IN A NEWBORN HOMOZYGOUS FOR METHYLENETETRAHYDROFOLATE REDUCTASE (A1298C) MUTATION AND HETEROZYGOUS FOR FACTOR V LEIDEN (G506A) MUTATION

Genetic counseling, 2016, Vol.27 (1), p.87

2016

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Recent findings on pertussis epidemiology in Turkey

European journal of clinical microbiology & infectious diseases, 2008-05, Vol.27 (5), p.335-341

2008

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Rapid control of an outbreak of Pseudomonas putida in a tertiary neonatal intensive care unit

The Journal of hospital infection, 2010-12, Vol.76 (4), p.361-362

2010

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Treacher Collins syndrome with multiple congenital heart defects after paroxetine exposure: case report

Genetic counseling, 2014, Vol.25 (1), p.7

2014

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A case of congenital warfarin syndrome due to maternal drug administration during the pregnancy

Genetic counseling, 2011-01, Vol.22 (2), p.221

2011

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Lower extremity amputation in a preterm infant due to MTHFR homozygosity

Genetic counseling, 2014-01, Vol.25 (2), p.245

2014

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A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal period

Genetic counseling, 2013, Vol.24 (2), p.141

2013

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Sonographic findings in premature infants with necrotising enterocolitis

Archives of disease in childhood. Fetal and neonatal edition, 2009-05, Vol.94 (3), p.F232-F233

2009

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Calcified thrombosis of the inferior vena cava extending to renal veins in a newborn with homozygous MTHFR a1298c mutation

Genetic counseling, 2012-01, Vol.23 (4), p.523

2012

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A case of fetal carbamazepine syndrome with right hemihypoplasia of the entire body

Genetic counseling, 2012, Vol.23 (1), p.19

2012

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Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?

Transient hyperinsulinemia may be responsible from electrolyte abnormalities of refeeding syndrome seen in very low birth weight infants with intrauterine growth-restriction

Assessment of novel biomarkers: sTREM-1, pentraxin-3 and pro-adrenomedullin in the early diagnosis of neonatal early onset sepsis

Outcome of Surgery for Toxic Goitres in Maiduguri: A Single Teaching Hospital's Perspective

190 Predicting The Efficacy of Oral Sucrose in Reducing Pain During Ophtalmological Examination for Retinopathy of Prematurity: A Prospective Randomised Study

1358 Effect of Mode of Delivery on Mortality and Morbidity in Very Low Birth Weight Neonates with Respiratory Distress Syndrome

1081 Levels of Serum N-Terminal Pro-Brain Natriuretic Peptide, Cystatin C, and Urinary B2 Microglobulin in Newborns with Hypoxic Ischemic Encephalopathy

1180 The Predictive Values of Mean Platelet Volume (MPV) in the Diagnosis of Neonatal Sepsis

1634 The Effects of Synbiotic use on Morbidity and Mortality in Premature Infants: A Prospective Randomized Controlled Trial

1678 Treatment of Infantile Colic with Lactobacillus Reuteri and the Relationship with Postpartum Depression: A Randomized Controlled Trial Study

1699 Distribution of Congenital Malformation in a Neonatal Intensive Care Unit in Turkey

1633 The Effects of Synbiotics on Morbidity and Mortality in Newborns with Cyanotic Congenital Heart Disease: A Prospective Randomized Controlled Trial

1122 The Effect of Heparin Infusion on Development of ThrombosİS Secondary to Cardiac Catheterization

1146 Perfusion Index Variability and N-Terminal Pro-Brain Natriuretic Peptide Levels Before and After Cardiac Interventions in Congenital Heart Disease

1039 Determination of the Perfusion Index Reference Values and Variation in Clinically and Hemodinamically Stable Newborns During the Early Neonatal Period

AXILLARY ARTERY THROMBOSIS IN A NEWBORN HOMOZYGOUS FOR METHYLENETETRAHYDROFOLATE REDUCTASE (A1298C) MUTATION AND HETEROZYGOUS FOR FACTOR V LEIDEN (G506A) MUTATION

Recent findings on pertussis epidemiology in Turkey

Rapid control of an outbreak of Pseudomonas putida in a tertiary neonatal intensive care unit

Treacher Collins syndrome with multiple congenital heart defects after paroxetine exposure: case report

A case of congenital warfarin syndrome due to maternal drug administration during the pregnancy

Lower extremity amputation in a preterm infant due to MTHFR homozygosity

A novel mutation of laminin β-2 gene in Pierson syndrome manifested with nephrotic syndrome in the early neonatal period

Sonographic findings in premature infants with necrotising enterocolitis

Calcified thrombosis of the inferior vena cava extending to renal veins in a newborn with homozygous MTHFR a1298c mutation

A case of fetal carbamazepine syndrome with right hemihypoplasia of the entire body

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