Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Petroula, Gerasimou"'
Autor:
Petroula Gerasimou, Laura Koumas, Andri Miltiadous, Ioannis Kyprianou, Jianxiang Chi, Rafaella Gavrielidou, Elena Socratous, Loizos Loizou, Eleni Papachristodoulou, Evagelia Karaoli, Anastasios Loizos, Violetta Anastasiadou, Paul Costeas
Publikováno v:
Human Pathology: Case Reports, Vol 22, Iss , Pp 200442- (2020)
The DNA ligase IV syndrome is a rare hereditary disorder associated with impaired DNA double-strand break repair mechanisms, associated with combined immunodeficiency. We investigated a 12-year old patient with obvious syndromic features, severe micr
Externí odkaz:
https://doaj.org/article/96a0a6aed7b345c8810f87aa72f44033
Autor:
Thomas McKerrell, Naomi Park, Jianxiang Chi, Grace Collord, Thaidy Moreno, Hannes Ponstingl, Joao Dias, Petroula Gerasimou, Kiki Melanthiou, Chrystalla Prokopiou, Marios Antoniades, Ignacio Varela, Paul A. Costeas, George S. Vassiliou
Publikováno v:
Blood Advances, Vol 1, Iss 14, Pp 968-971 (2017)
Externí odkaz:
https://doaj.org/article/0d26922650744b6497528cb1f2bdb2a0
Autor:
Elena Panayiotou, Eleni Fella, Savanna Andreou, Revekka Papacharalambous, Petroula Gerasimou, Paul Costeas, Stella Angeli, Ioanna Kousiappa, Savvas Papacostas, Theodoros Kyriakides
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0225417 (2019)
According to the amyloid hypothesis of Alzheimer's disease (AD) the deposition of prefibrillar and fibrillar Aβ peptide sets off the pathogenic cascades of neuroinflammation and neurodegeneration that lead to synaptic and neuronal loss resulting in
Externí odkaz:
https://doaj.org/article/83d887e5f100465fb4158a2ae951ef5f
Autor:
Maamoun Adra, Hayato Nakanishi, Eleni Papachristodoulou, Evangelia Karaoli, Petroula Gerasimou, Antri Miltiadous, Katerina Nicolaou, Loizos Loizou, Nicos Skordis
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Autor:
Petroula Gerasimou, Vicky Nicolaidou, Nicos Skordis, Michalis Picolos, Demetrios Monos, Paul A Costeas
Publikováno v:
PLoS ONE, Vol 13, Iss 3, p e0193684 (2018)
The contribution of specific HLA Class II alleles in type 1 diabetes is determined by polymorphic amino acid epitopes that direct antigen binding therefore, along with conventional allele frequency analysis, epitope analysis can provide important ins
Externí odkaz:
https://doaj.org/article/22d903e40694491882b1c9167d023f43
Akademický článek
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Autor:
Andri, Miltiadous, Philippos, Demetriou, Maria, Kyriakou, Petroula, Gerasimou, George, Herodotou, Agathi, Elpidoforou, Yiannos, Kyprianou, Maria, Iacovou, Jianxiang, Chi, Paul, Costeas, George A, Tanteles
Publikováno v:
Cold Spring Harbor molecular case studies. 8(3)
Poland syndrome is a rare developmental disorder characterized by unilateral, complete or partial, absence of the pectoralis major (and often minor) muscle, accompanied with ipsilateral hand malformations. To date, no clear genetic cause has been ass
Autor:
Fella, Eleni, Papacharalambous, Revekka, Kynigopoulos, Demos, Ioannou, Maria, Derua, Rita, Christodoulou, Christiana, Stylianou, Myrto, Karaiskos, Christos, Kagiava, Alexia, Petroula, Gerasimou, Pierides, Chryso, Kyriakou, Maria, Koumas, Laura, Costeas, Paul, Panayiotou, Elena
Publikováno v:
Frontiers in Immunology; 8/26/2022, Vol. 13, p1-14, 14p
Autor:
Chrystalla Prokopiou, George S. Vassiliou, Thaidy Moreno, Hannes Ponstingl, João M. L. Dias, Naomi Park, Thomas McKerrell, Grace Collord, Ignacio Varela, Marios Antoniades, Paul Costeas, Jianxiang Chi, Kiki Melanthiou, Petroula Gerasimou
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Blood Adv. 2017 Jun 12;1(14):968-971
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
instname
Blood Adv. 2017 Jun 12;1(14):968-971
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
McKerrell, Thomas et al.
The JAK2 V617F mutation is the most common somatic mutation in the classical myeloproliferative neoplasms (MPNs), present in >95% of cases of polycythemia vera (PV) and ~50% of essential thrombocythemia (ET) and myelofib
The JAK2 V617F mutation is the most common somatic mutation in the classical myeloproliferative neoplasms (MPNs), present in >95% of cases of polycythemia vera (PV) and ~50% of essential thrombocythemia (ET) and myelofib
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2475a59bd311b779bd2aa5461d90913a