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ArticlesPeer ReviewedFull Text
Genetic spectrum of neonatal diabetes
Author / Creator:Kocova, M
Publisher:Poland: Sciendo
Journal title:Balkan journal of medical genetics, 2021-03, Vol.23 (2), p.5-15
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ArticlesPeer ReviewedFull Text
Trends in childhood type 1 diabetes incidence in Europe during 1989–2008: evidence of non-uniformity over time in rates of increase
Author / Creator:Patterson, C. C. ; Gyürüs, E. ; Rosenbauer, J. ; Cinek, O. ; Neu, A. ; Schober, E. ; Parslow, R. C. ; Joner, G. ; Svensson, J. ; Castell, C. ; Bingley, P. J. ; Schoenle, E. ; Jarosz-Chobot, P. ; Urbonaité, B. ; Rothe, U. ; Krzisnik, C. ; Ionescu-Tirgoviste, C. ; Weets, I. ; Kocova, M. ; Stipancic, G. ; Samardzic, M. ; de Beaufort, C. E. ; Green, A ; Dahlquist, G. G. ; Soltész, G.
Publisher:Berlin/Heidelberg: Springer-Verlag
Journal title:Diabetologia, 2012-08, Vol.55 (8), p.2142-2147
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Newsletter articlesFull Text
Diabetes; Studies from University Children's Hospital Yield New Information about Diabetes
Publisher:Atlanta: NewsRx
Journal title:Obesity, Fitness & Wellness Week, 2012, p.2762
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Newsletter articlesFull Text
Diabetes; Research Conducted at University Children's Hospital Has Provided New Information about Diabetes
Publisher:Atlanta: NewsRx
Journal title:Obesity, Fitness & Wellness Week, 2012, p.1706
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ArticlesPeer ReviewedFull Text
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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ArticlesPeer ReviewedFull Text
High Incidence of Congenital Hypothyroidism in One Region of the Republic of Macedonia
Author / Creator:Anastasovska, V. ; R., Koviloska ; M., Kocova
Publisher:Poland: De Gruyter Open
Journal title:Balkan journal of medical genetics, 2014-06, Vol.17 (1), p.31-35
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ArticlesPeer ReviewedFull Text
Clinical variability in two Macedonian families with Arterial tortuosity syndrome
Author / Creator:Kocova, M ; Kacarska, R ; Kuzevska-Maneva, K ; Prijic, S ; Lazareska, M ; Dordoni, C ; Ritelli, M ; Colombi, M
Publisher:Macedonia: Sciendo
Journal title:Balkan journal of medical genetics, 2018-10, Vol.21 (1), p.47-52
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ArticlesPeer ReviewedFull Text
The fibre orientation influence in cementitious composite against extreme load resistance
Author / Creator:Lovichova, R ; Fornusek, J ; Mara, M ; Kocova, M ; Rihova, Z
Publisher:Bristol: IOP Publishing
Journal title:IOP conference series. Materials Science and Engineering, 2018-02, Vol.307 (1), p.12069
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ArticlesPeer ReviewedFull Text
Phenotypic variations in wolf-hirschhorn syndrome
Author / Creator:Sukarova-Angelovska, E ; Kocova, M ; Sabolich, V ; Palcevska, S ; Angelkova, N
Publisher:Poland: Macedonian Science of Sciences and Arts
Journal title:Balkan journal of medical genetics, 2014-06, Vol.17 (1), p.23-30
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ArticlesPeer ReviewedFull Text
Phenotypic Variations in Wolfhirschhorn Syndrome
Author / Creator:E, Sukarova-Angelovska ; M, Kocova ; V, Sabolich ; S, Palcevska ; N, Angelkova
Publisher:Sofia: De Gruyter Open
Journal title:Balkan journal of medical genetics, 2014-06, Vol.17 (1), p.23-30
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ArticlesPeer ReviewedFull Text
The Many Faces of Oral-Facial-Digital Syndrome
Author / Creator:Sukarova-Angelovska, E ; Angelkova, N ; Palcevska-Kocevska, S ; Kocova, M
Publisher:Poland: Versita
Journal title:Balkan journal of medical genetics, 2012-01, Vol.15 (1), p.37-44
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ArticlesPeer ReviewedFull Text
Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia
Author / Creator:Anastasovska, V ; Kocova, M
Publisher:Sofia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2010-01, Vol.13 (2), p.27-33
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ArticlesPeer ReviewedFull Text
A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia
Author / Creator:Anastasovska, V ; Kocova, E ; Kocova, M
Publisher:Sofia: Versita
Journal title:Balkan journal of medical genetics, 2010-01, Vol.13 (1), p.17-21
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ArticlesPeer ReviewedFull Text
Systemic chimerism in human female recipients of male livers
Author / Creator:Starzl, T.E ; Ramos, H ; Zeevi, A ; Ricordi, C ; Ildstad, S ; Murase, N ; Demetris, A.J ; Trucco, M ; Rudert, W.A ; Kocova, M
Publisher:London: Elsevier Ltd
Journal title:The Lancet (British edition), 1992-10, Vol.340 (8824), p.876-877
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ArticlesPeer ReviewedFull Text
Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy
Author / Creator:Anastasovska, V ; Kocova, M
Publisher:Sofia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2007-01, Vol.10 (2), p.23-28
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ArticlesPeer ReviewedFull Text
Analysis of the SRY Gene in Turner Syndrome Patients from the Republic of Macedonia
Author / Creator:Papazovska-Cherepnalkovski, A ; Koceva, S ; Kocova, M
Publisher:Sofia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2008-01, Vol.11 (2), p.31-37
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ArticlesPeer ReviewedFull Text
Autoimmune thyroiditis and vitiligo in a child with minimal change nephrotic syndrome
Author / Creator:KUZMANOVSKA, Dafina B ; SHAHPAZOVA, Emilija M ; KOCOVA, Mirjana J ; GRUEVSKA, Stevka J ; PETRUSHEVSKA, Gordana
Publisher:Heidelberg: Springer
Journal title:Pediatric nephrology (Berlin, West), 2001-12, Vol.16 (12), p.1137-1138
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ArticlesPeer ReviewedFull Text
Organochloride Pesticides in Macedonian Girls With Premature Sexual Development
Author / Creator:Krstevska-Konstantinova, M ; Kocova, M ; Charlier, C ; Bourguignon, J
Publisher:Sofia: De Gruyter Poland
Journal title:Balkan journal of medical genetics, 2007-04, Vol.10 (1), p.43-48
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ArticlesPeer ReviewedFull Text
Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA
Author / Creator:Kocova, M. ; Siegel, S.F. ; Trucco, M. ; Siegel, S.F. ; Lee, P.A. ; Wenger, S.L.
Publisher:London: Elsevier Ltd
Journal title:The Lancet (British edition), 1993-07, Vol.342 (8864), p.140-143
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ArticlesPeer ReviewedFull Text
Naturally occurring amino acid substitutions at Arg1174 in the human insulin receptor result in differential effects on receptor biosynthesis and hybrid formation, leading to discordant clinical pheno...
Author / Creator:RAU, H ; KOCOVA, M ; O'RAHILLY, S ; WHITEHEAD, J. P
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2000-07, Vol.49 (7), p.1264-1268
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Showing 1 to 20 of 33 results

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Genetic spectrum of neonatal diabetes

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Trends in childhood type 1 diabetes incidence in Europe during 1989–2008: evidence of non-uniformity over time in rates of increase

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Diabetes; Studies from University Children's Hospital Yield New Information about Diabetes

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Diabetes; Research Conducted at University Children's Hospital Has Provided New Information about Diabetes

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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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High Incidence of Congenital Hypothyroidism in One Region of the Republic of Macedonia

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Clinical variability in two Macedonian families with Arterial tortuosity syndrome

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The fibre orientation influence in cementitious composite against extreme load resistance

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Phenotypic variations in wolf-hirschhorn syndrome

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Phenotypic Variations in Wolfhirschhorn Syndrome

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The Many Faces of Oral-Facial-Digital Syndrome

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Intron 2 Splice Mutation at CYP21 Gene in Patients with Congenital Adrenal Hyperplasia in the Republic of Macedonia

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A p.P30L Mutation at the CYP21A2 Gene in Macedonian Patients with Nonclassical Congenital Adrenal Hyperplasia

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Systemic chimerism in human female recipients of male livers

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Molecular Analysis of a Family With Congenital Adrenal Hyperplasia - Genotype/Phenotype Discrepancy

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Analysis of the SRY Gene in Turner Syndrome Patients from the Republic of Macedonia

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Autoimmune thyroiditis and vitiligo in a child with minimal change nephrotic syndrome

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Organochloride Pesticides in Macedonian Girls With Premature Sexual Development

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Detection of Y chromosome sequences in Turner's syndrome by Southern blot analysis of amplified DNA

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Naturally occurring amino acid substitutions at Arg1174 in the human insulin receptor result in differential effects on receptor biosynthesis and hybrid formation, leading to discordant clinical pheno...

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