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System of fuzzy relation equations with inf - → composition: Complete set of solutions

Fuzzy sets and systems, 2008-09, Vol.159 (17), p.2256-2271

2008

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Arithmetic Fuzzy Models

IEEE transactions on fuzzy systems, 2010-12, Vol.18 (6), p.1058-1069

2010

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Age Dependent Progression of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Due to Heterozygous Mutations in COMP Gene

Prague medical report, 2020, Vol.121 (3), p.153-162

2020

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Novel phenotype of COASY deficiency is characterized by fatal neonatal hepathopathy with severe hypoglycaemia, hyperammonaemia and lactic acidosis

Biochimica et biophysica acta. Bioenergetics, 2024-09, Vol.1865

2024

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Integration of Innovative Methods into the Teaching of Literature in Lower-Secondary Schools

The new educational review, 2023, Vol.73 (3), p.175-186

2023

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Integration of Innovative Methods into the Teaching of Literature in Lower-Secondary Schools

The new educational review, 2023 (73), p.175-186

2023

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Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency

BMC genomics, 2008-01, Vol.9 (1), p.38-38, Article 38

2008

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System of fuzzy relation equations with - composition: Complete set of solutions

Fuzzy sets and systems, 2008-09, Vol.159 (17), p.2256-2271

2008

Volltextzugriff (PDF)

Novel phenotype associated with OPA1 mutations?

Mitochondrion, 2012-09, Vol.12 (5), p.559

2012

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Primary AA Amyloidosis due to a chr11:18287683 T>C (hg19) Mutation in the SAA1 Promoter Linked to the Amyloidogenic SAA1.1 Haplotype: PO1335

Journal of the American Society of Nephrology, 2021-10, Vol.32 (10S), p.427-427

2021

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The influence of pore size on colonization of poly(l-lactide-glycolide) scaffolds with human osteoblast-like MG 63 cells in vitro

Journal of materials science. Materials in medicine, 2008, Vol.19 (1), p.425-435

2008

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Nanocomposite Ti/hydrocarbon plasma polymer films from reactive magnetron sputtering as growth support for osteoblast-like and endothelial cells

Journal of Biomedical Materials Research Part B, 2009-03, Vol.88A (4), p.952-966

2009

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System of fuzzy relation equations with sup- composition in semi-linear spaces: minimal solutions

2007 IEEE International Fuzzy Systems Conference, 2007, p.1-6

2007

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TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Nature genetics, 2008, Vol.40 (11), p.1290-1292

2008

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Tau Protein in Biological Fluids and Its Clinical Value

Chemické listy, 2024-03, Vol.118 (3), p.138-145

2024

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System of fuzzy relation equations with inf - → composition: Complete set of solutions

Arithmetic Fuzzy Models

Age Dependent Progression of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Due to Heterozygous Mutations in COMP Gene

Novel phenotype of COASY deficiency is characterized by fatal neonatal hepathopathy with severe hypoglycaemia, hyperammonaemia and lactic acidosis

Integration of Innovative Methods into the Teaching of Literature in Lower-Secondary Schools

Integration of Innovative Methods into the Teaching of Literature in Lower-Secondary Schools

Development of a human mitochondrial oligonucleotide microarray (h-MitoArray) and gene expression analysis of fibroblast cell lines from 13 patients with isolated F1Fo ATP synthase deficiency

System of fuzzy relation equations with - composition: Complete set of solutions

Novel phenotype associated with OPA1 mutations?

Primary AA Amyloidosis due to a chr11:18287683 T>C (hg19) Mutation in the SAA1 Promoter Linked to the Amyloidogenic SAA1.1 Haplotype: PO1335

The influence of pore size on colonization of poly(l-lactide-glycolide) scaffolds with human osteoblast-like MG 63 cells in vitro

Nanocomposite Ti/hydrocarbon plasma polymer films from reactive magnetron sputtering as growth support for osteoblast-like and endothelial cells

System of fuzzy relation equations with sup- composition in semi-linear spaces: minimal solutions

Development of a human mitochondrial oligonucleotide microarray and gene expression analysis of fibroblast cell lines from 13 patients with isolated F.sub.1 F.sub.o ATP synthase deficiency

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Tau Protein in Biological Fluids and Its Clinical Value

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