Публикации
2014
D.T. Babikyan, S. Midyan, A. Hovhannisyan, H. Mkrtchyan, K. Männik, A. Gasparyan, A. Kurg, T. F. Sarkisian. De novo single exon deletion of AUTS2 in a patient with profound intellectual disability. European Journal of Human Genetics. Vol 18, (Supl 1), (Abstract PO3,011), p.105, 2014.
2013
H. Mkrtchyan, A. Hovhannisyan, A. Gasparyan, L. Nazaryan, S. Midyan, N. Tommerup. Proximal monosomy of 13q due to 6;13 translocation. European Journal of Human Genetics. Vol 21, (Abstractor P13.86), p. 352, 2013.
2012
D. Babikyan, H. Mkrtchyan, S. Midyan, M. Noukas, K. Mannik, A. Hovhannesyan, A.Gasparyan, T. Liehr, A. Kurg, T. F. Sarkisian. Molecular cytogenetic characterization of a family with 3p deletion and 3p duplication cases. European Journal of Human Genetics. Vol 20, (Abstract P02.009), p. 52, 2012.
2012
S. Midyan, A. Hovhannisyan, A. Gasparyan, E. Klein, T. Liehr, H. Mkrtchyan. Trisomy 8pl 1.23 as a result of a dicentric chromosome 8. European Journal of Human Genetics. Vol20, (Abstract P03.052), p. 114, 2012.
2012
H. Mkrtchyan, S. Midyan, A. Gasparyan, T. Liehr, A. Hovhannisyan . A new case with de novo proximal duplication of 10q11.2q21.3 European Journal of Human Genetics. Vol 20, (Abstract P03.055), p. 115, 2012.
2012
A. Hovhanissyan, S. Midyan, A. Gasparyan, T. Liehr, H. Mkrtchyan. A de novo interstitial duplication 14q32.11-q32.32. European Journal of Human Genetics. Vol 20. (Abstract P03.057), p. 115, 2012.
2011
D. Babikyan, S. Midyan, K. Mannik, S. Parkel, A. Hovhannisyan, H. Mkrtchyan, A. Gasparyan, A. Kurg, T. Sarkisian. Use of SNP-Array in a cohort of Armenian children with mental retardation. European Journal of Human Genetics. Vol 19 (Supl 2). (Abstract P03.027), p. 136. 2011
2011
D. Babikyan, S. Midyan, K. Mannik, S. Parkel, A. Hovhannisyan, H.Mkrtchyan, A. Gasparyan, A. Kurg, T. Sarkisian. Use of SNP-Array in a cohort of Armenian children with mental retardation. European Journal of Human Genetics. Vol 19 (Supl 2), (Abstract P02, 92). 2011
2011
D. Babikyan, S. Midyan, K. Mannik, S. Parkel, A. Hovhannisyan, H. Mkrtchyan, A. Gasparyan. A. Kurg, T. Sarkisian; Use of DNA-chips for diagnostics of mental retardation of Armenian children. Armenian Medical Congress, 2011, Yerevan
2010
S. Midyan, D. Babikyan, A. Hovhannisyan, H. Mkrtchyan, K. Mannik, A. Gasparyan, V. Galkina, A. Kurg, T. Sarkisian. Duplication 14q22.3-q24.2 in a mentally retarded patient with clinical resemblance to BOR-BOS and OAVS. 21-th European Meeting on Dysmorphology, Le Bischenberg, 2010, France.
2004
Gasparyan A.V. Tumor necrosis factor - α (TNF-α) in serum of patients with focal infiltrative tuberculosis before and after the intensive phase of short course chemotherapy Proceedings of the graduate students of Yerevan State Medical University, 2004 Issue -2 station, 46-50
2004
Gasparyan A.V. Interleukin - 1 (IL-1β) in serum of patients with focal infiltrative tuberculosis before and after application of the program DOTS. WW Proceedings of the graduate students of the Yerevan State Medical University, 2004 Issue -2 station, 50-55
2003
Gasparyan A.V., Sagradyan Z.M. Value of immunological studies in evaluating the effectiveness of treatment of ТВ patients on DOTS strategy. Armenia First International Medical Conference Materials Collection June 1-3. 2003. p. 79.
2003
Gasparyan A.V. The contents of cytokines in the blood of patients with pulmonary tuberculosis in the application of short course chemotherapy Biologically active substances in organisms integrative operations and the norm adaptation syndrome during the formation of a collection of articles, Yerevan 2003. Page 67
2003
Safaryan M.D., Gasparyan A.V. The content of interleukin, interferon, tumor necrosis factor with pulmonary tuberculosis in the application of short courses of chemotherapy. - Medical Science of Armenia XLIII N April 2003 Art. 82-84
2003
Gasparyan A.V. Production of tumor necrosis factor in the application of short course chemotherapy in patients with primary pulmonary tuberculosis. Modern rehabilitation medicine materials st international conference. 23-25 September. Yerevan. 2003 Art. 97
A. Hakobyan, K. Hovhannesyan, A. Gasparyan, T.Sargsyan. Perspectives of healthcare and well-being of children with duchenne muscular dystrophy in Armenia.
G. Shahsuvaryan, A. Gasparyan, A. Hovhannesyan, S. Midyan T. Sargsyan. Molecular-cytogenetic diagnosis of microdeletion 22q11.2 associated syndromes
