Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
(2021).
Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature..
Cytogenet Genome Res. 159(3), 109-118.
(2019).
(2019).
(2019). Dermoscopic features of melanocytic skin lesions in Greek children and adolescents and their association with environmental factors and skin types..
J Eur Acad Dermatol Venereol. 32(12), 2142-2148.
(2018). Echolucency-based phenotype in carotid atherosclerosis disease for risk stratification of diabetes patients..
Diabetes Res Clin Pract. 143, 322-331.
(2018). Hemodialysis-related changes in phenotypical features of monocytes..
Sci Rep. 8(1), 13964.
(2018). Major Adipokines and the -420C>G Resistin Gene Polymorphism as Predictors of Acute Ischemic Stroke Severity and In-Hospital Outcome..
J Stroke Cerebrovasc Dis. 27(4), 963-970.
(2018). Mesenchymal stem cells in preclinical cancer cytotherapy: a systematic review..
Stem Cell Res Ther. 9(1), 336.
(2018). Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome..
Eur J Paediatr Neurol. 22(3), 419-426.
(2018). Splice-site mutations in VEGFC cause loss of function and Nonne-Milroy-like primary lymphedema..
Clin Genet. 94(1), 179-181.
(2018). T Cell Phenotype and T Cell Receptor Repertoire in Patients with Major Depressive Disorder..
Front Immunol. 9, 291.
(2018). Association of follicle-stimulating hormone receptor single nucleotide polymorphisms with fertility in Greek men..
J Endocrinol Invest. 40(7), 721-726.
(2017). The CpG island methylator phenotype is concordant between primary colorectal carcinoma and matched distant metastases..
Clin Epigenetics. 9, 46.
(2017). Dermoscopic features predicting the presence of mitoses in thin melanoma..
J Dermatol Sci. 86(2), 158-161.
(2017). FCGR3A-V158F polymorphism is a disease-specific pharmacogenetic marker for the treatment of psoriasis with Fc-containing TNFα inhibitors..
Pharmacogenomics J. 17(3), 237-241.
(2017). Frontotemporal dementia as the presenting phenotype of p.A53T mutation carriers in the alpha-synuclein gene..
Parkinsonism Relat Disord. 35, 82-87.
(2017). Netherton Syndrome: A Genotype-Phenotype Review..
Mol Diagn Ther. 21(2), 137-152.
(2017). A novel PLP1 mutation associated with optic nerve enlargement in two siblings with Pelizaeus-Merzbacher disease: A new MRI finding..
Brain Dev. 39(3), 271-274.
(2017). Novel quantitative pigmentation phenotyping enhances genetic association, epistasis, and prediction of human eye colour..
Sci Rep. 7, 43359.
(2017). Using CRISPR-Cas9 to Study ERK Signaling in Drosophila..
Methods Mol Biol. 1487, 353-365.
(2017). Evaluation of CpG Island Methylator Phenotype as a Biomarker in Colorectal Cancer Treated With Adjuvant Oxaliplatin..
Clin Colorectal Cancer. 15(2), 164-9.
(2016). Exome Sequencing and the Management of Neurometabolic Disorders..
N Engl J Med. 374(23), 2246-55.
(2016).
(2016).
(2016). Σελίδες
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