POSTER WALK - BRAIN 3
Tracks
TIRANA
| Wednesday, October 22, 2025 |
| 8:00 AM - 9:00 AM |
Details
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
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
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)
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
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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