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Author/Creator Gerou, Spyros

1. Cerebral folate deficiency in two siblings caused by biallelic variants including a novel mutation of FOLR1 gene: Intrafamilial heterogeneity following early treatment and the role of ketogenic diet. Issue 1 (4th June 2021)

Authors:
Papadopoulou, Maria T.; Dalpa, Efterpi; Portokalas, Michalis; Katsanika, Irene; Tirothoulaki, Katerina; Spilioti, Martha; Gerou, Spyros; Plecko, Barbara; Evangeliou, Athanasios E.
Journal:
JIMD reports
Issue:
Volume 60:Issue 1(2021)
Page Start:
3
Record Type:
Journal Article
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2. Syncope without prodromes is associated with excessive plasma release of adenosine at the time of syncope during head-up tilt table test. (15th September 2022)

Authors:
Fragakis, Nikolaos; Antoniadis, Antonios P.; Sotiriadou, Melani; Virgiliou, Christina; Ballauri, Iris; Gika, Helen G.; Bougiouklis, Dimitrios; Gerou, Spyros; Lazaridis, Charalampos; Vergopoulos, Stavros; Bakogiannis, Constantinos; Giannopoulos, Georgios; Theodoridis, Georgios A.; Papadopoulos, Ch...
Journal:
International journal of cardiology
Issue:
Volume 363(2022)
Page Start:
43
Record Type:
Journal Article
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3. Total IgE, eosinophils, and interleukins 16, 17A, and 23 correlations in severe bullous pemphigoid and treatment implications. Issue 6 (25th July 2020)

Authors:
Delli, Florentina Silvia; Sotiriou, Elena; Lazaridou, Elizabeth; Apalla, Zoe; Lallas, Aimilios; Vakirlis, Efstratios; Gerou, Spyros; Bougioukas, Konstantinos; Ioannides, Demetrios
Journal:
Dermatologic therapy
Issue:
Volume 33:Issue 6(2020)
Page Start:
n/a
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗