POSTER WALK - BRAIN 3
Tracks
SKOPJE
| Wednesday, October 22, 2025 |
| 8:00 AM - 9:00 AM |
Details
Skopje Room
Chairs: Sylke Steggerda, Jeroen Dudink
45
Umbilical cord management strategies and risk of intraventricular hemorrhage in preterm neonates – a systematic review and meta-analysis
Ilari Kuitunen
592
The Role of Neonatal Factors in SLC6A4 Gene Expression in Preterm Infants
Stanislava Voloshyn
600
Early diagnosis of hyperphosphatemic familial tumoral calcinosis in a neonate
Tania Siachanidou
653
Isochromosome X Turner Syndrome: Early Detection based on Dental Abnormalities. A case study.
Vasiliki Psaromiligkou
553
A Rare Association: Maple Syrup Urine Disease (MSUD) in a Newborn with Transposition of the Great Arteries (TGA)
İsmail Çağrı AÇIKGÖZ
350
NEONATAL-ONSET EPILEPTIC ENCEPHALOPATHY WITH KCNQ2 MUTATION IN A TERM INFANT: A CASE REPORT
Antigone Pavlaki
134
A rare cause of abdominal massive ascites in newborns: Galactosemia
Umit Ayse Tandircioglu
453
Rare Diseases Diagnosis – a Challenge in Low Resource Settings
Maria Livia Ognean
373
A Case of Molybdenum Cofactor Deficiency Presenting with Feeding Difficulty in the Neonatal Period
Aslı Melekoğlu
39
A case of Neonatal Congenital Myasthenic Syndrome
Abdullah Anees Khan
314
Unveiling The Missing Eye How Imaging Reveals The Secret Of Bilateral Anophthalmia In A Level Two Neonatal Unit
Nazakat Merchant
638
Evaluation of Preterm Infants with Retinopathy of Prematurity: A Clinical Study
Ayşen Sumru Kavurt
Chairs: Sylke Steggerda, Jeroen Dudink
45
Umbilical cord management strategies and risk of intraventricular hemorrhage in preterm neonates – a systematic review and meta-analysis
Ilari Kuitunen
592
The Role of Neonatal Factors in SLC6A4 Gene Expression in Preterm Infants
Stanislava Voloshyn
600
Early diagnosis of hyperphosphatemic familial tumoral calcinosis in a neonate
Tania Siachanidou
653
Isochromosome X Turner Syndrome: Early Detection based on Dental Abnormalities. A case study.
Vasiliki Psaromiligkou
553
A Rare Association: Maple Syrup Urine Disease (MSUD) in a Newborn with Transposition of the Great Arteries (TGA)
İsmail Çağrı AÇIKGÖZ
350
NEONATAL-ONSET EPILEPTIC ENCEPHALOPATHY WITH KCNQ2 MUTATION IN A TERM INFANT: A CASE REPORT
Antigone Pavlaki
134
A rare cause of abdominal massive ascites in newborns: Galactosemia
Umit Ayse Tandircioglu
453
Rare Diseases Diagnosis – a Challenge in Low Resource Settings
Maria Livia Ognean
373
A Case of Molybdenum Cofactor Deficiency Presenting with Feeding Difficulty in the Neonatal Period
Aslı Melekoğlu
39
A case of Neonatal Congenital Myasthenic Syndrome
Abdullah Anees Khan
314
Unveiling The Missing Eye How Imaging Reveals The Secret Of Bilateral Anophthalmia In A Level Two Neonatal Unit
Nazakat Merchant
638
Evaluation of Preterm Infants with Retinopathy of Prematurity: A Clinical Study
Ayşen Sumru Kavurt
Speaker
Dr. İsmail Çağrı AÇIKGÖZ
Physician
University of Health Sciences, Ankara Bilkent Ci̇ty Hospital
A Rare Association: Maple Syrup Urine Disease (MSUD) in a Newborn with Transposition of the Great Arteries (TGA)
Prof. Ayşen Sumru Kavurt
Doctor
Ankara Etlik City Hospital
Evaluation of Preterm Infants with Retinopathy of Prematurity: A Clinical Study
Dr. Abdullah Anees Khan
Doctor
St Peters Hospital
A case of Neonatal Congenital Myasthenic Syndrome
Dr. Ilari Kuitunen
Doctor
Kuopio University Hospital
Umbilical cord management strategies and risk of intraventricular hemorrhage in preterm neonates – a systematic review and meta-analysis
Dr. Aslı Melekoğlu
Doctor
Turgut Ozal University Medical Faculty
A Case of Molybdenum Cofactor Deficiency Presenting with Feeding Difficulty in the Neonatal Period
Dr. Nazakat Merchant
Physician
West Hertfordshire Teaching Hospitals NHS Trust
Unveiling The Missing Eye How Imaging Reveals The Secret Of Bilateral Anophthalmia In A Level Two Neonatal Unit
Prof. Maria Livia Ognean
Physician
Lucian Blaga University Sibiu
Rare Diseases Diagnosis – a Challenge in Low Resource Settings
Dr. Antigone Pavlaki
Physician
Hippokrateion General Hospital Thessaloniki
NEONATAL-ONSET EPILEPTIC ENCEPHALOPATHY WITH KCNQ2 MUTATION IN A TERM INFANT: A CASE REPORT
Dr. Vasiliki Psaromiligkou
Resident
Asklepieio General Hospital
Isochromosome X Turner Syndrome: Early Detection based on Dental Abnormalities. A case study.
Prof. Tania Siachanidou
Doctor
Aghia Sofia Children's Hospital
Early diagnosis of hyperphosphatemic familial tumoral calcinosis in a neonate
Dr. Umit Ayse Tandircioglu
Doctor
Kirikkale University
A rare cause of abdominal massive ascites in newborns: Galactosemia
Dr. Stanislava Voloshyn
Physician
Ternopil Regional Children's Clinical Hospital
The Role of Neonatal Factors in SLC6A4 Gene Expression in Preterm Infants
The Organising Secretariat
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