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	1.	[Bronchiectasis in Recklinghausen's disease]. [electronic resource] by Kapellerová, A Hlavatá, A Boruta, P Producer: 19910620 In: Ceskoslovenska pediatrie vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Peroxisomal hereditary diseases]. [electronic resource] by Chandoga, J Tomková, M Hlavatá, A Producer: 19970821 In: Bratislavske lekarske listy vol. 98 Availability: No items available. Save to lists Add to cart (remove)
	3.	Problems of metabolic syndrome diagnostics in children. [electronic resource] by Vitariusova, E Kostalova, L Pribilincova, Z Hlavata, A Kovacs, L Producer: 20110106 In: Endocrine regulations vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	4.	Ratio of lipid parameters to coenzyme Q10 could be used as biomarker of the development of early complications of obesity in children. [electronic resource] by Gvozdjakova, A Kucharska, J Tkacov, M Singh, R B Hlavata, A Producer: 20120403 In: Bratislavske lekarske listy vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Late onset form of Pompe disease. [electronic resource] by Mattosova, S Hlavata, A Spalek, P Kotysova, L Macekova, D Chandoga, J Producer: 20151124 In: Bratislavske lekarske listy vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[Variation in manifestations of heteroplasmic mtDNA mutation 8993 T>G in two families]. [electronic resource] by Tesarová, M Hansíková, H Hlavatá, A Klement, P Houst'ková, H Houstĕk, J Zeman, J Producer: 20021118 In: Casopis lekaru ceskych vol. 141 Availability: No items available. Save to lists Add to cart (remove)
	7.	Rasopathies - dysmorphic syndromes with short stature and risk of malignancy. [electronic resource] by Cizmarova, M Kostalova, L Pribilincova, Z Lasabova, Z Hlavata, A Kovacs, L Ilencikova, D Producer: 20140311 In: Endocrine regulations vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Increased plasma levels of the high mobility group box 1 protein (HMGB1) are associated with a higher score of gastrointestinal dysfunction in individuals with autism. [electronic resource] by Babinská, K Bucová, M Ďurmanová, V Lakatošová, S Jánošíková, D Bakoš, J Hlavatá, A Ostatníková, D Producer: 20151013 In: Physiological research vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Assay design and optimization of mutant-enriched PCR based method for detection of K-ras gene mutations in pancreatic carcinoma. [electronic resource] by Ugorcáková, J Hlavatý, T Babál, P Janega, P Bukovská, G Halgasová, N Hlavatá, A Timko, J Duris, I Producer: 20070222 In: Neoplasma vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	10.	New Mutations Associated with Rasopathies in a Central European Population and Genotype-Phenotype Correlations. [electronic resource] by Čizmárová, M Hlinková, K Bertok, S Kotnik, P Duba, H C Bertalan, R Poločková, K Košťálová, Ľ Pribilincová, Z Hlavatá, A Kovács, L Ilenčíková, D Producer: 20160531 In: Annals of human genetics vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients with optic pathway glioma. [electronic resource] by Bolcekova, A Nemethova, M Zatkova, A Hlinkova, K Pozgayova, S Hlavata, A Kadasi, L Durovcikova, D Gerinec, A Husakova, K Pavlovicova, Z Holobrada, M Kovacs, L Ilencikova, D Producer: 20131114 In: Neoplasma vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II. [electronic resource] by Dvorakova, L Vlaskova, H Sarajlija, A Ramadza, D P Poupetova, H Hruba, E Hlavata, A Bzduch, V Peskova, K Storkanova, G Kecman, B Djordjevic, M Baric, I Fumic, K Barisic, I Reboun, M Kulhanek, J Zeman, J Magner, M Producer: 20170602 In: Clinical genetics vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)