Zobrazeno 1 - 10
of 173
pro vyhledávání: '"Pangalos C"'
Background. Although several studies in various countries have indicated that the presence of the E4 allele of the apolipoprotein-E (APOE) gene is a risk factor for ischemic cerebrovascular disease, the strength of this association still remains a ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::36d0652ce43c7e5afa9ca9bd98657957
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086618
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3086618
Objective: The aim of this study was to examine whether resistin is present in second trimester amniotic fluid from trisomy 21 (also known as Down’s syndrome) pregnancies and whether its concentration differs compared with euploid pregnancies. Meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::fa96d55b5d7317dba88b58ba86be9f73
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3159283
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3159283
Objective. We investigated whether the concentration of the glycoprotein fetuin A is altered in the second trimester amniotic fluid of trisomy 21 pregnancies compared with euploid pregnancies. Methods. 25 pregnancies with an extra chromosome 21 were
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::4c3b653a710344c695e8296efb1f7229
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3002979
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3002979
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an important cause of hereditary stroke. Mutations in the Notch3 gene are clearly causally linked to this progressive vascular disorder. Cerebral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::8044aa59d441a39ba0939dc4b78c3c1a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3097729
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3097729
Tetrasomy 8 is an extremely rare chromosome abnormality, one that has been reported in only a few cases with myeloid malignancies. The majority of reported cases consist of acute myelogenous leukemias (AML) of monocytic lineage. In slightly more than
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::3d482640c5a440c451bea1fd6fadde7f
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3095511
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3095511
Transferrin receptor (TfR, CD71) is an integral membrane glycoprotein that mediates cellular uptake of iron. In most tissues, TfR expression is correlated positively with proliferation and regulated at the post-transcriptional level. The available da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f567f52688225168bd3a0c010bcaf27a
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3080751
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3080751
Acute promyelocytic leukemia was diagnosed in a 48-year-old man; the karyotype was normal, whereas reverse transcriptase polymerase chain reaction (RT-PCR) analysis identified PML/RAR alpha chimeric transcripts of the bcr3 type. Rather unexpectedly,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::f978fc971fa8786ee2aa9d8bbd11faa3
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3052926
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3052926
Cytogenetic analysis was performed in 60 patients with primary myelodysplastic syndromes-diagnosed, treated, and followed in our department. In 41 cases, the presence of the NRAS mutation was also evaluated. The aim of this study was to evaluate the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::698f680a9374046526509f0730b4b0e6
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3051824
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3051824
Cytogenetic analysis of bone marrow cells from a patient with myelodysplastic syndrome associated with eosinophilia showed a complex translocation with a 46,XY,t(2;18;2)(p23;q11;q32) karyotype The patient has refractory anemia (RA) according to the F
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::cd1fb3a46362f9eec62578f36294907c
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049392
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049392
Partial trisomy 17q22-qter is a rare but well-recognized clinical entity, We present a case of partial trisomy for the long arm of chromosome 17, which was detected in a female infant with severe psychomotor and somatic retardation, Stargardt disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::51ff9503401164b3be643781cdf0c43b
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049298
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3049298