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zahraniční

Witsø E, Tapia G, Cinek O, Pociot FM, Stene LC, Rønningen KS: Polymorphisms in the innate immune IFIH1 gene, frequency of enterovirus in monthly fecal samples during infancy, and islet autoimmunity. PLoS One (2011), 6 (11): e27781.


Konopac M, Dusatkova P, Cinek O: SNPman: a program for genotype calling using run data from TaqMan allelic discrimination.Bioinformatics (2011), 27 (16): 2306-2308.


Hradsky O, Dusatkova P, Lenicek M, Bronsky J, Duricova D, Nevoral J, Vitek L, Lukas M, Cinek O: Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn’s disease in the Czech population. Inflammatory Bowel Diseases (2011), 17 (7): 1523-1529.


Gonsorcikova L, Vaxillaire M, Pruhova S, Dechaume A, Dusatkova P, Cinek O, Pedersen O, Froguel P, Hansen T, Lebl J: Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generations. Pediatric Diabetes (2011), 12 (3): 266-269.


Dusatkova P, Pruhova S, Sumnik Z, Kolouskova S, Obermannova B, Cinek O, Lebl J: HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes. J Pediatr Endocrinol Metab (2011), 24: 187-189.


Cardwell CR, Stene LC, Joner G, Bulsara MK, Cinek O, Rosenbauer J, Ludvigsson J, Svensson J, Goldacre MJ, Waldhoer T, Jarosz-Chobot P, Gimeno SG, Chuang LM, Roberts CL, Parslow RC, Wadsworth EJ, Chetwynd A, Brigis G, Urbonaite B, Sipetic S, Schober E, De: Birth order and childhood type 1 diabetes risk: a pooled analysis of 31 observational studies. International Journal of Epidemiology (2011), 40 (2): 363-374.


Soucek O, Lebl J, Snajderova M, Kolouskova S, Rocek M, Hlavka Z, Cinek O, Rittweger J, Sumnik Z: Bone geometry and volumetric bone mineral density in girls with Turner syndrome of different pubertal stages. Clinical Endocrinology (2011), 74 (4): 445-452.


Tapia G, Cinek O, Rasmussen T, Grinde B, Stene LC, Rønningen KS: Longitudinal study of parechovirus infection in infancy and risk of repeated positivity for multiple islet autoantibodies: the MIDIA study. Pediatric Diabetes (2011), 12 (1): 58-62.


Obermannova B, Pfaeffle R, Zygmunt-Gorska A, Starzyk J, Verkauskiene R, Smetanina N, Bezlepkina O, Peterkova V, Frisch H, Cinek O, Child CJ, Blum WF, Lebl J: Mutations and Pituitary Morphology in a Series of 82 Patients with PROP1 Gene Defects.Hormone Research in Paediatrics (2011), 76 (5): 348-354.


Cinek O: Epidemiology of childhood type 1 diabetes mellitus: lessons from Central and Eastern European data. Hormone Research in Paediatrics (2011), 76: 52-56.


Tapia G, Cinek O, Rasmussen T, Witsø E, Grinde B, Stene LC, Rønningen KS: Human enterovirus RNA in monthly fecal samples and islet autoimmunity in Norwegian children with high genetic risk for type 1 diabetes: the MIDIA study. Diabetes Care(2011), 34 (1): 151-155.


Pruhova S, Dusatkova P, Sumnik Z, Kolouskova S, Pedersen O, Hansen T, Cinek O, Lebl J: Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations.Pediatric Diabetes (2010), 11 (8): 529-535.


Dusatkova P, Vesela K, Pruhova S, Lebl J, Cinek O: Lack of PAX4 mutations in 53 Czech MODYX families. Diabetic Medicine(2010), 27 (12): 1459-1460.


Hradsky O, Dusatkova P, Lenicek M, Bronsky J, Nevoral J, Vitek L, Lukas M, Zeniskova I, Cinek O: The CTLA4 variants may interact with the IL23R- and NOD2-conferred risk in development of Crohn’s disease. BMC Medical Genetics (2010), 11: 91.


Boesgaard TW, Pruhova S, Andersson EA, Cinek O, Obermannova B, Lauenborg J, Damm P, Bergholdt R, Pociot F, Pisinger C, Barbetti F, Lebl J, Pedersen O, Hansen T.: Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY). BMC Med Genet (2010), 11: 42.


Tapia G, Cinek O, Rasmussen T, Grinde B, Rønningen KS.: No Ljungan virus RNA in stool samples from the norwegian environmental triggers of type 1 diabetes (MIDIA) cohort study. Diabetes Care (2010), 33 (5): 1069-71.


Drevinek P, Vosahlikova S, Dedeckova K, Cinek O, Mahenthiralingam E.: Direct culture-independent Strain typing of Burkholderia cepacia complex in sputum samples from patients with cystic fibrosis. J Clin Microbiol (2010), 48 (5): 1888-91.


Cardwell CR, Stene LC, Joner G, Davis EA, Cinek O, Rosenbauer J, Ludvigsson J, Castell C, Svensson J, Goldacre MJ, Waldhoer T, Polanska J, Gimeno SG, Chuang LM, Parslow RC, Wadsworth EJ, Chetwynd A, Pozzilli P, Brigis G, Urbonaite B, Sipetić S, Schober E,: Birthweight and the risk of childhood-onset type 1 diabetes: a meta-analysis of observational studies using individual patient data. Diabetologia (2010), 53 (4): 641-51.


Mahenthiralingam E, Marchbank A, Drevinek P, Garaiova I, Plummer S.: Use of colony-based bacterial strain typing for tracking the fate of Lactobacillus strains during human consumption. BMC Microbiol (2009), 9: 251.


Witsø E, Cinek O, Aldrin M, Grinde B, Rasmussen T, Wetlesen T, Rønningen KS.: Predictors of sub-clinical enterovirus infections in infants: a prospective cohort study. Int J Epidemiol (2010), 39 (2): 459-68.


Drevinek P, Baldwin A, Lindenburg L, Joshi LT, Marchbank A, Vosahlikova S, Dowson CG, Mahenthiralingam E.: Oxidative stress of Burkholderia cenocepacia induces insertion sequence-mediated genomic rearrangements that interfere with macrorestriction-based genotyping. J Clin Microbiol (2010), 48 (1): 34-40.


Cardwell CR, Stene LC, Joner G, Bulsara MK, Cinek O, Rosenbauer J, Ludvigsson J, Jané M, Svensson J, Goldacre MJ, Waldhoer T, Jarosz-Chobot P, Gimeno SG, Chuang LM, Parslow RC, Wadsworth EJ, Chetwynd A, Pozzilli P, Brigis G, Urbonaite B, Sipetic S, Schobe: Maternal age at birth and childhood type 1 diabetes: a pooled analysis of 30 observational studies. Diabetes (2010), 59 (2): 486-94.


Rasmussen T, Stene LC, Samuelsen SO, Cinek O, Wetlesen T, Torjesen PA, Rønningen KS.: Maternal BMI before pregnancy, maternal weight gain during pregnancy, and risk of persistent positivity for multiple diabetes-associated autoantibodies in children with the high-risk HLA genotype: the MIDIA study. Diabetes Care (2009), 32 (10): 1904-6.


Dusatkova P, Hradsky O, Lenicek M, Bronsky J, Nevoral J, Kotalova R, Bajerova K, Vitek L, Lukas M, Cinek O.: Association of IL23R p.381Gln and ATG16L1 p.197Ala with Crohn disease in the Czech population. J Pediatr Gastroenterol Nutr (2009), 49 (4): 405-10.


Malina M, Cinek O, Janda J, Seeman T.: Partial remission with cyclosporine A in a patient with nephrotic syndrome due to NPHS2 mutation. Pediatr Nephrol (2009), 24 (10): 2051-3.


Hubacek P, Virgili A, Ward KN, Pohlreich D, Keslova P, Goldova B, Markova M, Zajac M, Cinek O, Nacheva EP, Sedlacek P, Cetkovsky P.: HHV-6 DNA throughout the tissues of two stem cell transplant patients with chromosomally integrated HHV-6 and fatal CMV pneumonitis. Br J Haematol (2009), 145 (3): 394-8.


Balascaková M, Holubová A, Skalická V, Zemková D, Kracmar P, Gonsorcíkova L, Camajová J, Piskácková T, Lebl J, Drevínek P, Gregor V, Vávrová V, Votava F, Macek M Jr.: Pilot newborn screening project for cystic fibrosis in the Czech Republic: defining role of the delay in its symptomatic diagnosis and influence of ultrasound-based prenatal diagnosis on the incidence of the disease. J Cyst Fibros (2009), 8 (3): 224-7.


Hubacek P, Muzikova K, Hrdlickova A, Cinek O, Hyncicova K, Hrstkova H, Sedlacek P, Stary J.: Prevalence of HHV-6 integrated chromosomally among children treated for acute lymphoblastic or myeloid leukemia in the Czech Republic. J Med Virol (2009), 81 (2): 258-63.


Hubacek P, Keslova P, Formankova R, Pochop P, Cinek O, Zajac M, Lochmanova J, Stary J, Sedlacek P.: Cytomegalovirus encephalitis/retinitis in allogeneic haematopoietic stem cell transplant recipient treated successfully with combination of cidofovir and foscarnet. Pediatr Transplant (2009), 13 (7): 919-22.


Drevinek P, Holden MT, Ge Z, Jones AM, Ketchell I, Gill RT, Mahenthiralingam E: Gene expression changes linked to antimicrobial resistance, oxidative stress, iron depletion and retained motility are observed when Burkholderia cenocepacia grows in cystic fibrosis sputum. BMC Infect Dis (2008), 8: 121.


Drevinek P, Baldwin A, Dowson CG, Mahenthiralingam E: Diversity of the parB and repA genes of the Burkholderia cepacia complex and their utility for rapid identification of Burkholderia cenocepacia. BMC Microbiol (2008), 8: 44.


Baldwin A, Mahenthiralingam E, Drevinek P, Pope C, Waine DJ, Henry DA, Speert DP, Carter P, Vandamme P, LiPuma JJ, Dowson CG: Elucidating global epidemiology of Burkholderia multivorans in cases of cystic fibrosis by multilocus sequence typing. J Clin Microbiol (2008), 46 (1): 290-5.


Coenye T, Drevinek P, Mahenthiralingam E, Shah SA, Gill RT, Vandamme P,Ussery DW: Identification of putative noncoding RNA genes in the Burkholderia cenocepacia J2315 genome. FEMS Microbiol Lett (2007), 276 (1): 83-92.


B. Obermannova, K. Banghova, Z. Sumník, H. M. Dvorakova, J. Betka, F. Fencl, S. Kolouskova, O. Cinek, J. Lebl: Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. Eur J Pediatr (2008), 168 (5): 569-573.


G. Tapia, O. Cinek, E. Witsø, M. Kulich, T. Rasmussen, B. Grinde, K. S. Rønningen: Longitudinal observation of parechovirus in stool samples from Norwegian infants. Journal of Medical Virology (2008), 80 (10): 569-573.


O. Hradsky, M. Lenicek, P. Dusatkova, J. Bronsky, J. Nevoral, V. Valtrova, R. Kotalova, P. Szitanyi, R. Petro, V. Starzykova, M. Bortlik, L. Vitek, M. Lukas, O. Cinek: Variants of CARD15, TNFA and PTPN22 and susceptibility to Crohn’s disease in the Czech population: high frequency of the CARD15 1007fs. Tissue Antigens (2008), 71 (6): 538-547.


K. Banghova, O. Cinek, E. Al Taji, J. Zapletalova, R. Vidura, J. Lebl: Thyroidectomy in a patient with dyshromonogenetic goitre – a case of Pendred syndrome confirmed by finding mutations in the PDS/SLC26A4 gene. J Pediatr Endocrinol Metab (2008), 167 (7): 777-783.


C.R. Cardwell, L.C. Stene, G. Joner, O Cinek, J. Svensson, M.J. Goldacre, R.C. Parslow, P. Pozzilli, G. Brigis, D. Stoyanov, B. Urbonaite, S. Sipetic, E. Schober, C. Ionescu-Tirgoviste, G. Devoti, C.E. de Beaufort, C.C. Patterson: Caesarean section is associated with an increased risk of childhood onset type 1 diabetes mellitus: A meta-analysis of observational studies.Diabetologia (2008), 51: 726-735.


L. Gonsorčíková, Š. Průhová, O. Cinek, J. Ek, T. Pelikánová, T. Jørgensen, H. Eiberg, O. Pedersen, T. Hansen, J. Lebl: Autosomal inheritance of diabetes in two families characterised by obesity and a novel H241Q mutation in NEUROD1. Pediatric Diabetes (2008), 9 (4/2): 367-372.


Sedlacek P, Formankova R, Mejstrikova E, Keslova P, Hubacek P, Dobrovolna M, Vrana M, Kupkova L, Pittrova H, Stary J.: Allogeneic stem cell transplantation in children with leukemia using human leukocyte antigen-mismatched unrelated donors.Pediatr Transplant (2008), 12 (1): 24-31.


Hubacek P, Sedlacek P, Keslova P, Formankova R, Stary J, Kulich M, Cinek O.: Incidence of HHV7 in donors and recipients of allogeneic hematopoietic stem cell transplantation. Pediatr Blood Cancer (2008), 50 (4): 935.


Hubacek P, Maalouf J, Zajickova M, Kouba M, Cinek O, Hyncicova K, Fales I, Cetkovsky P.: Failure of multiple antivirals to affect high HHV-6 DNAaemia resulting from viral chromosomal integration in case of severe aplastic anaemia.. Haematologica (2007), 92 (10): e98-e100.


Hubacek P, Hyncicova K, Muzikova K, Cinek O, Zajac M, Sedlacek P.: Disappearance of pre-existing high HHV-6 DNA load in blood after allogeneic SCT. Bone Marrow Transplant (2007), 40 (8): 805-806.


K. Banghova, E. Al Taji, O. Cinek, D. Novotna, R. Pourova, J. Zapletalova, O. Hnikova, J. Lebl: Pendred syndrome among patients with congenital hypothyroidism detected by neonatal screening: identification of two novel PDS/SLC26A4 mutations.Eur J Pediatr (2008), 167 (7): 777-783.


A. Janda, P. Sedlacek, E. Mejstrikova, K. Zdrahalova, O. Hrusak, T. Kalina, Z. Sieglova, H. Zizkova, R. Formankova, P. Keslova, P. Hubacek, A. Sediva, J. Bartunkova, K. Dlask, J. Stary: Unrelated partially matched lymphocyte infusions in a patient with complete DiGeorge/CHARGE syndrome.. Pediatr Transplant. (2007), 11 (4): 441-447. (.pdf)


L. C. Stene, E. Witsø, P. A. Torjesen, T. Rasmussen, P. Magnus, O. Cinek, T. Wetlesen, K. S. Rønningen: Islet autoantibody development during follow-up of high-risk children from the general Norwegian population from three months of age: Design and early results from the MIDIA study.. Journal of Autoimmunity (2007), 29 (1): 44-51.


Z. Sumnik, S. Kolouskova, J. K. H. Wales, V. Komarek, O. Cinek: Sulfonylurea treatment does not improve psychomotor development in children with KCNJ11 mutations causing permanent neonatal diabetes mellitus accompanied by developmental delay and epilepsy (DEND syndrome). Diabetic Medicine (2007), 24 (10): 1176-1178.


S. Vosahlikova, P. Drevinek, O. Cinek, P. Pohunek, M. Maixnerova, P. Urbaskova, T. J. K. van den Reijden, L. Dijkshoorn, A. Nemec: High phenotypic diversity of Pseudomonas aeruginosa strains isolated from patients with cystic fibrosis in the Czech Republic. Research in Microbiology (2007), 158 (4): 324-329.


O. Cinek, O. Hradsky, G. Ahmedov, A. Slavcev, S. Kolouskova, M. Kulich, Z. Sumnik: No independent role of the -1123 G>C and +2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations. Dia Res Clin Pr (2007), 76 (2): 297-303.


P. Sedlacek, R. Formankova, P. Keslova, L. Sramkova, P. Hubacek, L. Krol, M. Kulich, J. Stary: Low mortality of children undergoing hematopoietic stem cell transplantation from 7 to 8/10 human leukocyte antigen allele-matched unrelated donors with the use of antithymocyte globulin. Bone Marrow Transplant. (2006), 38 (11): 745-750. (.pdf)


DIAMOND project group: K. Bessaoud, G Boudraa, M.M. de Ropolo et al. (O. Cinek): Incidence and trends of childhood Type 1 diabetes worldwide 1990-1999. Diabetic Medicine (2006), 23 (8): 857-866.


E. Witso, G. Palacios, K. S. Rønningen, O. Cinek, D. Janowitz, M. Rewers, W. Lipkin: Asymptomatic circulation of EV71 in Norway. Virus Research (2007), 123 (1): 19-29.


E. Witso, G. Palacios, O. Cinek, L.C. Stene, B. Grinde, D. Janowicz, W.I. Lipkin, K.S. Ronningen: High prevalence of human enterovirus A infections in natural circulation of human enteroviruses. J Clin Microbiol (2006), 44 (11): 4095-4100.


Z. Sumnik*, O. Cinek* (* the first two authors contributed equally to the work), N. Bratanic, O. Kordonouri, M. Kulich, B. Roszai, A. Arato, J. Lebl, G. Soltesz, T. Danne, T. Battelino, E. Schober: The risk of celiac disease in children with type 1 diabetes is modified by positivity for HLA-DQB1*02-DQA1*05 and TNF-alpha -308A. Diabetes Care (2006), 29 (4): 858-863.


Z. Sumnik, O. Cinek, N. Bratanic, J. Lebl, B. Rozsai, C. Limbert, M. Paskova, E. Schober: Thyroid autoimmunity in children with coexisting type 1 diabetes mellitus and celiac disease: a multicenter study. Journal of Pediatric Endocrinology and Metabolism (2006), 19: 517-522.


G. Ahmedov, L. Ahmedova, P. Sedlakova, O. Cinek: Genetic association of type 1 diabetes in an Azerbaijanian population: the HLA-DQ, -DRB1*04, the insulin gene and CTLA4. Pediatric Diabetes (2006), 7: 88-93.


H. Malcova, Z. Sumnik, P. Drevinek, J. Venhacova, J. Lebl, O. Cinek: Absence of breast-feeding is associated with risk of type 1 diabetes: a case-control study in a population with rapidly increasing incidence. Eur J Pediatr (2006), 165 (2): 114-119.


EC Claas, MW Schilham, CS de Brouwer, P Hubacek, M Echavarria, AC Lankester, MJ van Tol, AC Kroes: Internally controlled real-time PCR monitoring of adenovirus DNA load in serum or plasma of transplant recipients. J Clin Microbiol (2005), 43 (4): 1738-1744. (.pdf)


P. Drevinek, S. Vosahlikova, O. Cinek, V. Vavrova, J. Bartosova, P. Pohunek, E. Mahenthiralingham: Widespread clone of Burkholderia cenocepacia in Czech patients with cystic fibrosis. J Med Microbiol (2005), 54 (7): 655-659. (.pdf)


K. Stechova, S. Kolouskova, Z. Sumnik, O. Cinek, M. Kverka, M. Karlsson Faresjő, D. Chudoba, E. Dovolilova, M. Pechova, Z. Vrabelova, K. Bohmova, L. Janecek, F. Saudek, J. Vavrinec: Anti-GAD65 reactive peripheral blood mononuclear cells in the pathogenesis of cystic fibrosis related diabetes mellitus. Autoimmunity (2005), 38 (4): 319-323.


O. Cinek, E. Witsř, S. Jeansson, T. Rasmussen, P. Drevinek, T. Wetlesen, J. Vavrinec, B. Grinde, K.S. Rřnningen: Longitudinal observation of enterovirus and adenovirus in stool samples from Norwegian infants with the highest genetic risk of type 1 diabetes. J Clin Virol (2006), 35 (1): 33-40.


Z. Sumnik, S. Kolouskova, H. Malcova, J. Vavrinec, J. Venhacova, J. Lebl, O. Cinek: High prevalence of coeliac disease in siblings of children with type 1 diabetes. Eur J Pediatr (2005), 164 (1): 9-12. (.pdf)


O. Cinek, P. Vavřincová, I. Striz, P. Dřevínek, P. Sedláková, J. Vavřinec, A. Slavčev: Association of single nucleotide polymorphisms within cytokine genes with juvenile idiopathic arthritis in the Czech population. Journal of Rheumatology(2004), 31: 1206-1210. (.pdf)


Z. Sumnik, P. Drevinek, V. Lanska, H. Malcova, J. Vavrinec, O. Cinek: Higher maternal age at delivery, and lower birth orders are associated with increased risk of childhood type 1 diabetes mellitus. Exp Clin Endocrinol Diabetes (2004), 112: 294-297.(.pdf)


K. Stechova, D. Bartaskova, M. Mrstinova, M. Cerny, M. Snajderova, O. Cinek, Z. Sumnik, J. Vavrinec: Pregnancy in a woman suffering from type 1 diabetes associated with Addison’s disease and Hashimoto’s thyroiditis. Exp Clin Endocrinol Metab(2004), 112: 333-337. (.pdf)


M. Matejkova-Behanova, M. Vankova, M. Hill, P. Kucera, O. Cinek, M. Andel, B. Bendlova: Polymorphism of INS VNTR is associated with glutamic acid decarboxylase antibodies and postprandial C-peptide in Patients with Diabetes Onset after 35 Years of Age. Physiol Res (2004), 53 (2): 187-190. (.pdf)


O. Cinek, Z. Šumník, J. Vavřinec: Continuing increase in incidence of childhood-onset Type 1 diabetes in the Czech Republic over 1990-2001. Eur J Pediatr (2003), 162 (6): 428-429. (.pdf)


P. Dřevínek, O. Cinek, J. Melter, L. Lanšádl, Y. Návesňáková, V. Vávrová: Genomovar distribution of Burkholderia cepacia complex significantly differs between Czech and Slovak patients with cystic fibrosis. J Med Microbiol (2003), 52: 603-604.(.pdf)


O. Cinek, P. Dřevínek, Z. Šumník, B. Bendlová, P. Sedláková, S. Koloušková, M. Šnajderová, J. Vavřinec: NEUROD polymorphism Ala45Thr is associated with Type 1 diabetes mellitus in Czech children.. Dia Res Clin Pract (2003), 60 (1): 49-56. (.pdf)


Z. Šumník, P. Dřevínek, M. Šnajderová, S. Koloušková, P. Sedláková, M. Pechová, J. Vavřinec, O. Cinek: HLA-DQ polymorphisms modify the risk of thyroid autoimmunity in children with Type 1 diabetes. J Pediatr Endocr Met (2003), 16 (6): 851-858. (.pdf)


P. Dřevínek, H. Hrbáčková, O. Cinek, J. Bartošová, O. Nyč, A. Nemec, P. Pohunek: Direct PCR detection of Burkholderia cepacia complex and identification of its genomovars using sputum as source of DNA. J Clin Microbiol (2002), 9: 3485-3488. (.pdf)


I. Hromadnikova, B. Houbova, D. Hridelova, S. Voslarova, P. Calda, K. Nekolarova, J. Kofer, D. Stejskal, J. Doucha, O. Cinek, J. Vavrinec: Quantitative analysis of DNA levels in maternal plasma in normal and Down syndrome pregnancies. BMC Pregnancy Childbirth (2002), 2 (1): 4.


M. Vankova, J. Vrbikova, M. Hill, O. Cinek, B. Bendlova: Association of Insulin Gene VNTR Polymorphism with Polycystic Ovary Syndrome. Ann NY Acad Sci (2002), 967: 558-565.


O. Cinek, P. Dřevínek, Z. Šumník, B. Bendlová, S. Koloušková, M. Šnajderová, J. Vavřinec: The CTLA4 +49 A/G dimorphism is not associated with Type 1 diabetes in Czech children.. Eur J Immunogenet (2002), 29 (3): 219-222. (.pdf)


O. Cinek, S. Koloušková, M. Šnajderová, Z. Šumník, P. Sedláková, P. Dřevínek, J. Vavřinec, K.S. Rønningen: HLA class II genetic association of Type I diabetes mellitus in Czech children. Pediatric Diabetes (2001), 2 (3): 98-102. (.pdf)


Z Šumník, S Koloušková, O Cinek, R Kotalová, J Vavřinec, M Šnajderová: HLA – DQA1*05-DQB1*0201 positivity predisposes to coeliac disease in Czech diabetic children. Acta Paediatr (2000), 89 (12): 1426-30. (.pdf)


O. Cinek, E. Wilkinson, R. H. Tullis, L. Paltiel, O. D. Saugstad, P. Magnus, K. S. Ronningen: Screening for the IDDM high risk genotype. A rapid microtitre plate method using serum as source of DNA. Tissue Antigens (2000), 56 (4): 344-349. (.pdf)


O. Cinek, V. Lánská, S. Koloušková, Z. Šumník, M. Šnajderová, K.S. Ronningen, J. Vavřinec: Type 1 diabetes mellitus in Czech children diagnosed in 1990-1997: a significant increase in incidence, and male predominance in the age group 0-4. Diabet Med(2000), 17: 64-69. (.pdf)