Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nikoletta Smyrni"'
Autor:
Styliani-Aggeliki Sintila, Marina Boziki, Christos Bakirtzis, Thomai Stardeli, Nikoletta Smyrni, Ioannis Nikolaidis, Dimitrios Parissis, Theodora Afrantou, Theodore Karapanayiotides, Ioanna Koutroulou, Virginia Giantzi, Paschalis Theotokis, Evangelia Kesidou, Georgia Xiromerisiou, Efthimios Dardiotis, Panagiotis Ioannidis, Nikolaos Grigoriadis
Publikováno v:
Medicina, Vol 59, Iss 2, p 266 (2023)
Background and Objectives: Rare diseases (RDs) are life-threatening or chronically impairing conditions that affect about 6% of the world’s population. RDs are often called ‘orphan’ diseases, since people suffering from them attract little supp
Externí odkaz:
https://doaj.org/article/9257866a752d4e268b3a17be28d8176d
Autor:
Nikoletta Smyrni, Maria Koutsaki, Marianna Petra, Eirini Nikaina, Maria Gontika, Helen Strataki, Fotini Davora, Helen Bouza, George Damianos, Helen Skouteli, Sotiria Mastroyianni, Zoi Dalivigka, Argyris Dinopoulos, Margarita Tzaki, Antigone Papavasiliou
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: While most studies on the association of preterm birth and cerebral palsy (CP) have focused on very preterm infants, lately, attention has been paid to moderately preterm [32 to
Externí odkaz:
https://doaj.org/article/85652371508b47a194a57bc02c074621
Autor:
Eleni Konstantinopoulou, Nikolaos Grigoriadis, Theodora Afrantou, Dimitrios Parissis, Thomai Stardeli, Nikoletta Smyrni, Panagiotis Ioannidis, Panagiotis Stoiloudis
Publikováno v:
Neurological Sciences. 42:3431-3433
Hereditary diffuse leukoencephalopathy with spheroids (HDLS) is an adult onset leukodystrophy, causally related to mutations in the colony-stimulating factor 1 receptor (CSF1R) gene. We report the unique case of a Greek HDLS patient, demonstrating an
Autor:
Marianna Petra, Eirini Nikaina, Helen Bouza, Maria Gontika, Fotini Davora, Zoi Dalivigka, Argyris Dinopoulos, Helen Strataki, Helen N. Skouteli, Margarita Tzaki, Maria Koutsaki, Antigone Papavasiliou, George Damianos, Sotiria Mastroyianni, Nikoletta Smyrni
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Frontiers in Neurology
Background:While most studies on the association of preterm birth and cerebral palsy (CP) have focused on very preterm infants, lately, attention has been paid to moderately preterm [32 to Methods:In order to report on the outcomes of a cohort of mod
Publikováno v:
Clinical Neurology and Neurosurgery. 208:106895
Hyperargininemia is an autosomal recessive disorder caused by a defect in the arginase I enzyme. We present a case of a 20-year-old male with severe spastic gait, intellectual disability and seizures. Metabolic tests revealed high levels of arginine
Autor:
Evgenia Verigou, Polixeni Lampropoulou, Panagiotis Zikos, Argiris Symeonidis, Ioannis Starakis, Nikoletta Smyrni, Georgia Kolliopoulou, Elena E. Solomou, Marina Karakantza, George Sakellaropoulos
Publikováno v:
Cardiovascular & Hematological Disorders-Drug Targets. 15:148-161
Background: Myelodysplastic Syndromes (MDS) are a group of clonal hematopoietic stem cell disorders with significant heterogeneity in their clinical presentation and the prognosis of the patients. Several attempts have been made to incorporate flow c
Autor:
G. Damianos, Helen Bouza, E. Strataki, M. Gontika, Irene Nikaina, S. Mastrogianni, M. Tzaki, H. Skouteli, Nikoletta Smyrni, Marianna Petra, A. Dinopoulos, Antigoni Papavasiliou
Publikováno v:
European Journal of Paediatric Neurology. 21:e70