Browsing by Author Kochova, Mirjana


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Target setting in intensive insulin management is associated with metabolic control: the Hvidoere childhood diabetes study group centre differences study 2005Swift, P G F; Skinner, T C; de Beaufort, C E; Cameron, F J; Aman, J; Aanstoot, H-J; Castaño, L; Chiarelli, F; Daneman, D; Danne, T; Dorchy, H; Hoey, H; Kaprio, E A; Kaufman, F; Kocova, M ; Mortensen, H B; Njølstad, P R; Phillip, M; Robertson, K J; Schoenle, E J; Urakami, T; Vanelli, M; Ackermann, R W; Skovlund, S EJun-2010Article
Targeted sequencing of dyshormonogenesis-associated genes in Macedonian cases with congenital hypothyroidism and gland-in-situ reveals a low mutation frequencyZdraveska, Nikolina ; Kocova, Mirjana ; Nicholas, Adeline K; Anastasovska, Violeta ; Schoenmakers, Nadia2-Nov-2018Proceeding article
Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomesSkinner, Timothy C; Lange, Karin S; Hoey, Hilary; Mortensen, Henrik B; Aanstoot, Henk-Jan; Castaňo, Luis; Skovlund, Soren; Swift, Peter Gf; Cameron, Fergus J; Dorchy, Harry R; Palmert, Mark R; Kaprio, Eero; Robert, Jean-Jacques; Danne, Thomas; Neu, Andreas; Shalitin, Shlomit; Chiarelli, Francesco; Chiari, Giovanni; Urakami, Tatsuhiko; Njølstad, Pål R; Jarosz-Chobot, Premyslawa K; Roche, Edna F; Castro-Correia, Cintia G; Kocova, Mirjana ; Åman, Jan; Schönle, Eugen; Barrett, Timothy G; Fisher, Lynda; de Beaufort, Carine E2018Article
Testicular adrenal rest tumors in boys with 21-hydroxylase deficiency, timely diagnosis and follow-upMirjana Kocova ; Vesna Janevska ; Violeta Anastasovska Apr-2018Article
Therapeutic challenges in a patient with the simple virilizing (SV) form of congenital adrenal hyperplasia (CAH) due to the P30L/I172N genotypeMaja Tankoska; Violeta Anastasovska ; Marina Krstevska-Konstantinova ; Michel Naydenov; Mirjana Kocova 27-May-2019Article
Thyroid dysfunction in children with trisomy 21: when subclinical hypothyroidism should be treated?Sukarova Angelovska, E ; Kocova, M ; Zorcec, T 2015Proceeding article
Thyroid function and dysfunction in preterm infants-Challenges in evaluation, diagnosis and therapyZdraveska, Nikolina ; Kochova, Mirjana Oct-2021Article
Thyroid peroxidase (TPO) mutations in Macedonian patients with congenital hypothyroidismZdraveska, Nikolina ; Anastasovska, Violeta ; Schoenmakers, Nadia; Nicholas, K. Adeline; Kochova, Mirjana 6-Jun-2020Proceeding article
Transient congenital hypothyroidism in preterm and full-term infantsZdraveska, Nikolina ; Anastasovska, Violeta ; Kochova, Mirjana 9-Jun-2019Proceeding article
Translocation 4;11 acute leukemia: three case reports and review of the literatureKocova, M ; Kowalczyk, J R; Sandberg, A A1-Mar-1985Article
Translocation between chromosomes 1 and 9 in childhood acute lymphoblastic leukemiaOhyashiki, K; Kocova, M ; Ohyashiki, J H; Ryan, D H; Rowe, J M; Sandberg, A A1-Mar-1986Article
Trends and cyclical variation in the incidence of childhood type 1 diabetes in 26 European centres in the 25 year period 1989-2013: a multicentre prospective registration studyPatterson, Christopher C; Harjutsalo, Valma; Rosenbauer, Joachim; Neu, Andreas; Cinek, Ondrej; Skrivarhaug, Torild; Rami-Merhar, Birgit; Soltesz, Gyula; Svensson, Jannet; Parslow, Roger C; Castell, Conxa; Schoenle, Eugen J; Bingley, Polly J; Dahlquist, Gisela; Jarosz-Chobot, Przemysława K; Marčiulionytė, Dalė; Roche, Edna F; Rothe, Ulrike; Bratina, Natasa; Ionescu-Tirgoviste, Constantin; Weets, Ilse; Kocova, Mirjana ; Cherubini, Valentino; Rojnic Putarek, Natasa; deBeaufort, Carine E; Samardzic, Mira; Green, Anders2019Article
Trends in childhood type 1 diabetes incidence in Europe during 1989-2008: evidence of non-uniformity over time in rates of increasePatterson, 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, GAug-2012Article
The unique combination of dermatological and ocular phenotypes in Alström syndrome: severe presentation, early onset and two novel ALMS1 mutationsM. Kocova ; E. Sukarova-Angelovska ; R. Kacarska ; P. Maffei; G. Milan; J.D. MarshallApr-2011Article
Unique concurrent appearance of two rare conditions in a young girl: central precocious puberty due to hypothalamic hamartoma and uncommon type of diabetesMirjana Kocova ; Nikolina Zdraveska ; Elena Sukarova-Angelovska 2011Article
Variation within the PPARG gene is associated with residual beta-cell function and glycemic control in children and adolescents during the first year of clinical type 1 diabetesPörksen, Sven; Nielsen, Lotte B; Mortensen, Henrik B; Danne, Thomas; Kocova, Mirjana ; Castaño, Luis; Pociot, Flemming; Hougaard, Philip; Ekstrøm, Claus T; Gammeltoft, Steen; Knip, Mikael; Hansen, Lars28-Jul-2008Article
Variations in incidence of congenital hypothyroidism in association with changes of cutoff valuePesevska, Milica; Anastasovska, Violeta ; Taseva, Elizabeta; Zdraveska, Nikolina ; Gurzanova-Durnev, Liljana; Kochova, Mirjana 3-Oct-2018Proceeding article
Weight, height and puberty in a cohort of Macedonian girlsMarina Krstevska-Konstantinova ; Aleksandra Jancevska; Mirjana Kocova ; Zoran Gucev 2009Article
Xenotransplantation of hematopoietic cells resistant to HIV as a potential treatment for patients with AIDSRicordi, C; Tzakis, A G; Rybka, W B; Fontes, P; Ball, E D; Trucco, M; Kocova, M ; Triulzi, D; McMichael, J; Doyle, HJun-1994Article
Y Chromosomal Sequences Identified in Gonadal Tissue of Two 45,X Patients with Turner SyndromeKocova, Mirjana ; Witchel, Selma Feldman; Nalesnik, Michael; Lee, Peter A.; Dickman, Paul S.; MacGillivray, Margaret H.; Reiter, Edward O.; Trucco, Giuliana; Trucco, Massimo1995Article