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Maria Chrysoulaki
Maria Chrysoulaki
Medicine
Pediatrics
ROHHAD Syndrome
Gastroenterology
Gene polymorphism
6
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Epidemiology, clinical course, and genetic analysis of pheochromocytomas/paragangliomas: A single centre tertiary care experience over 16 years from crete-greece
2021
Maria Chrysoulaki
Florentia Fostira
Vasiliki Daraki
Grigoria Betsi
Maria Sfakiotaki
Maria Mytilinaiou
Katerina Bouki
Konstantinos Stathias
Konstantinos Spanakis
Tsakalomatis Panagiotis-Nikolaos
Syntzanaki Eleni-Konstantina
Kalliopi Kontolaimaki
Rodanthi Vamvoukaki
Konstantinos Nastos
Paraskevi Xekouki
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Graves disease and concurrent immune thrombocytopenia in a patient with albinism following alemtuzumab treatment for multiple sclerosis: a rare case report
2021
Vasiliki Daraki
Syntzanaki Eleni-Konstantina
Vasileios Mastorodemos
Kalliopi Kontolaimaki
Maria Mytilinaiou
Maria Chrysoulaki
Maria Sfakiotaki
Grigoria Betsi
Paraskevi Xekouki
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Rohhad Syndrome: Report of 2 Rare Cases From Crete-Greece
2019
Pinelopi Smyrnaki
Maria Chrysoulaki
Vasiliki Daraki
Grigoria Betsi
Maria Sfakiotaki
Paraskevi Floroskoufi
Katerina Bouki
Diamandis Kofteridis
Christina Kanaka-Gantenbein
Paraskevi Xekouki
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Rohhad Syndrome: Report of 2 Rare Cases From Crete-Greece
2019
Pinelopi Smyrnaki
Maria Chrysoulaki
Vasiliki Daraki
Grigoria Betsi
Maria Sfakiotaki
Paraskevi Floroskoufi
Katerina Bouki
Diamandis Kofteridis
Christina Kanaka-Gantenbein
Paraskevi Xekouki
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Multiple pathologic fractures as the presenting manifestation of Cushing's syndrome in patients with vitamin D receptor FokI gene polymorphism
2017
Vasiliki Daraki
Paraskevi Floroskoufi
Theodoros Liarigkovinos
Maria Chrysoulaki
Vasilios Tsamadias
Emmanuel Economou
Stathis Papavasiliou
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