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ArticlesPeer ReviewedFull Text
Delineation of Partial Chromosomal Abnormalities in Early Pregnancy Losses
Author / Creator:Bozhinovski, Gj ; Terzikj, M ; Kubelka-Sabit, K ; Plaseska-Karanfilska, D
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2024-12, Vol.27 (2), p.23-32
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ANXA5 and VEGFA Gene Variants in Women with Early Pregnancy Losses from North Macedonia
Author / Creator:Terzikj, M ; Bozhinovski, Gj ; Branoski, A ; Dimkovska, M ; Kubelka-Sabit, K ; Plaseska-Karanfilska, D
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2024-06, Vol.27 (1), p.5-14
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Chromosomal Abnormalities in Early Pregnancy Losses: A Study of 900 Samples
Author / Creator:Bozhinovski, Gj ; Terzikj, M ; Kubelka-Sabit, K ; Jasar, Dz ; Lazarevski, S ; Livrinova, V ; Plaseska-Karanfilska, D
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2023-12, Vol.26 (2), p.11-20
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Two Brothers from Macedonia with Gitelman Syndrome
Author / Creator:Janchevska, A ; Tasic, V ; Jordanova, O ; Gucev, Z ; Jenkins, L ; Jovanovska, N ; Plaseska-Karanfilska, D ; Ashton, E ; Bockenhauer, D
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2023-07, Vol.26 (1), p.69-74
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Proteomic analysis of seminal plasma in men with different spermatogenic impairment
Author / Creator:Davalieva, K. ; Kiprijanovska, S. ; Noveski, P. ; Plaseski, T. ; Kocevska, B. ; Broussard, C. ; Plaseska-Karanfilska, D.
Publisher:Germany: Blackwell Publishing Ltd
Journal title:Andrologia, 2012-08, Vol.44 (4), p.256-264
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Cystic fibrosis mutation spectrum in north macedonia: A step toward personalized therapy
Author / Creator:Terzic, M ; Jakimovska, M ; Fustik, S ; Jakovska, T ; Sukarova-Stefanovska, E ; Plaseska-Karanfilska, D
Publisher:Sofia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2019-08, Vol.22 (1), p.35-40
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Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis
Author / Creator:Kocova, M ; Plaseska-Karanfilska, D ; Noveski, P ; Kuzmanovska, M
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2019-12, Vol.22 (2), p.69-76
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Two years of newborn screening for cystic fibrosis in North Macedonia: First experience
Author / Creator:Fustik, S ; Anastasovska, V ; Plaseska-Karanfilska, D ; Stamatova, A ; Spirevska, L ; Pesevska, M ; Terzikj, M ; Vujovic, M
Publisher:Sofia: Sciendo
Journal title:Balkan journal of medical genetics, 2021-07, Vol.24 (1), p.41-46
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de novo TINF2 C.845G>A: Pathogenic Variant in Patient with Dyskeratosis Congenita
Author / Creator:Kocheva, SA ; Gjorgjievska, M ; Martinova, K ; Antevska-Trajkova, Z ; Jovanovska, A ; Plaseska-Karanfilska, D
Publisher:Sofia: Sciendo
Journal title:Balkan journal of medical genetics, 2021-11, Vol.24 (2), p.89-93
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Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature
Author / Creator:Tasic, V ; Mitrotti, A ; Riepe, FG ; Kulle, AE ; Laban, N ; Polenakovic, M ; Plaseska-Karanfilska, D ; Sanna-Cherchi, S ; Kostovski, M ; Gucev, Z
Publisher:Poland: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2019-08, Vol.22 (1), p.81-88
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Characteristic diagnostic clues of metatropic dysplasia: The lumbothoracic humpback with dumbbell appearance of the long bones
Author / Creator:Gucev, Z ; Kalcev, G ; Laban, N ; Bozinovski, Z ; Popovski, N ; Saveski, A ; Daskalov, B ; Plaseska-Karanfilska, D ; Tasic, V
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2018-12, Vol.21 (2), p.35-38
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ArticlesPeer ReviewedFull Text
Molecular and immunohistochemical characteristics of complete hydatidiform moles
Author / Creator:Kubelka-Sabit, KB ; Prodanova, I ; Jasar, D ; Bozinovski, G ; Filipovski, V ; Drakulevski, S ; Plaseska-Karanfilska, D
Publisher:Macedonia: De Gruyter
Journal title:Balkan journal of medical genetics, 2017-06, Vol.20 (1), p.27-34
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A Homozygous Deletion of the DPY19L2 Gene is a Cause of Globozoospermia in Men From the Republic of Macedonia
Author / Creator:Noveski, P ; Madjunkova, S ; Maleva, I ; Sotiroska, V ; Petanovski, Z ; Plaseska-Karanfilska, D
Publisher:Macedonia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2013-06, Vol.16 (1), p.73-76
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Study of Three Single Nucleotide Polymorphisms in the Slc6a14 Gene in Association with Male Infertility
Author / Creator:Noveski, P. ; Mircevska, M. ; Plaseski, T. ; Peterlin, B. ; Plaseska-Karanfilska, D.
Publisher:Poland: De Gruyter Open
Journal title:Balkan journal of medical genetics, 2014-12, Vol.17 (2), p.61-66
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CYP2D6 Allele Distribution in Macedonians, Albanians and Romanies in The Republic of Macedonia
Author / Creator:Kuzmanovska, M ; Dimishkovska, M ; Maleva Kostovska, I ; Noveski, P ; Sukarova Stefanovska, E ; Plaseska-Karanfilska, Dijana
Publisher:Sofia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2015-12, Vol.18 (2), p.49
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Genetics of non Syndromic Hearing Loss in the Republic of Macedonia
Author / Creator:Sukarova Stefanovska, Emilija ; Plaseska Karanfilska, D ; Cakar, M ; Filipce, I
Publisher:Macedonia: Versita
Journal title:Balkan journal of medical genetics, 2012-12, Vol.15 (Supplement), p.57-59
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Human Seminal Plasma Proteome Study: a Search for Male Infertility Biomarkers
Author / Creator:Davalieva, Katarina ; Kiprijanovska, S ; Noveski, P ; Plaseska-Karanfilska, D ; Plaseski, T ; Kocevska, B
Publisher:Macedonia: Versita
Journal title:Balkan journal of medical genetics, 2012-12, Vol.15 (Supplement), p.35-38
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Androgen Insensitivity Syndrome DUE to Non-Coding Variation in the Androgen Receptor Gene: Review of the Literature and Case Report of a Patient with Mosaic c.-547C>T Variant
Author / Creator:Noveski, P ; Plaseski, T ; Dimitrovska, M ; Plaseska-Karanfilska, D
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2023-07, Vol.26 (1), p.51-56
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Cag Repeat Number in the Androgen Receptor Gene and Prostate Cancer
Author / Creator:Madjunkova, S ; Eftimov, A ; Georgiev, V ; Petrovski, D ; Dimovski, A ; Plaseska-Karanfilska, D
Publisher:Macedonia: Versita
Journal title:Balkan journal of medical genetics, 2012-01, Vol.15 (1), p.31-36
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Five Novel Mutations in Cystinuria Genes SLC3A1 and SLC7A9
Author / Creator:Popovska-Jankovic, K ; Tasic, V ; Bogdanovic, R ; Miljkovic, P ; Baskin, E ; Efremov, G ; Plaseska-Karanfilska, D
Publisher:Sofia: Versita
Journal title:Balkan journal of medical genetics, 2009-01, Vol.12 (1), p.15-20
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Showing 1 to 20 of 37 results

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Delineation of Partial Chromosomal Abnormalities in Early Pregnancy Losses

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ANXA5 and VEGFA Gene Variants in Women with Early Pregnancy Losses from North Macedonia

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Chromosomal Abnormalities in Early Pregnancy Losses: A Study of 900 Samples

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Two Brothers from Macedonia with Gitelman Syndrome

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Proteomic analysis of seminal plasma in men with different spermatogenic impairment

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Cystic fibrosis mutation spectrum in north macedonia: A step toward personalized therapy

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Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis

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Two years of newborn screening for cystic fibrosis in North Macedonia: First experience

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de novo TINF2 C.845G>A: Pathogenic Variant in Patient with Dyskeratosis Congenita

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Duplication of the SOX3 gene in an sry-negative 46,XX male with associated congenital anomalies of kidneys and the urinary tract: Case report and review of the literature

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Characteristic diagnostic clues of metatropic dysplasia: The lumbothoracic humpback with dumbbell appearance of the long bones

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Molecular and immunohistochemical characteristics of complete hydatidiform moles

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A Homozygous Deletion of the DPY19L2 Gene is a Cause of Globozoospermia in Men From the Republic of Macedonia

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Study of Three Single Nucleotide Polymorphisms in the Slc6a14 Gene in Association with Male Infertility

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CYP2D6 Allele Distribution in Macedonians, Albanians and Romanies in The Republic of Macedonia

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Genetics of non Syndromic Hearing Loss in the Republic of Macedonia

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Human Seminal Plasma Proteome Study: a Search for Male Infertility Biomarkers

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Androgen Insensitivity Syndrome DUE to Non-Coding Variation in the Androgen Receptor Gene: Review of the Literature and Case Report of a Patient with Mosaic c.-547C>T Variant

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Cag Repeat Number in the Androgen Receptor Gene and Prostate Cancer

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Five Novel Mutations in Cystinuria Genes SLC3A1 and SLC7A9

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