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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

Neurology, 2011-08, Vol.77 (6), p.540-548

2011

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An evaluation of noise reduction algorithms for particle-based fluid simulations in multi-scale applications

Journal of computational physics, 2016-11, Vol.325, p.380-394

2016

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A novel coupling of noise reduction algorithms for particle flow simulations

Journal of computational physics, 2016-09, Vol.321, p.169-190

2016

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Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy

Human molecular genetics, 2013-08, Vol.22 (15), p.2975-2983

2013

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Experimental Studies in Deep Hole Drilling of Ti-6Al-4V with Twist Drills

Production at the Leading Edge of Technology, p.219-227

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S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC GENE

HemaSphere, 2022-06, Vol.6, p.175-176

2022

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High-throughput microscopy profiling of LDLR variants

Atherosclerosis, 2020-12, Vol.315, p.e97-e97

2020

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4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder

Clinical neurophysiology, 2013-07, Vol.124 (7), p.e10-e10

2013

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G.P.237

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.888-888

2014

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Genetic spectrum of hereditary neuropathies with onset in the first year of life

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2664-2676

2011

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PP09.9 – 2907: Is it easy to recognize HINT1 neuropathy

European journal of paediatric neurology, 2015-05, Vol.19, p.S67-S67

2015

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Gene-gene interactions at GWAS loci modulate lipid plasma levels and cellular uptake of low-density lipoprotein

Atherosclerosis, 2020-12, Vol.315, p.e191-e191

2020

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Functional Genomics In A Cohort Of Fh Mutation Negative Patients

Atherosclerosis, 2019-08, Vol.287, p.e93-e93

2019

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The importance to track variants in a genes causing recessive disorders within the family: A FH/Sitosterolemia clinical case

Atherosclerosis, 2018-08, Vol.275, p.e80-e80

2018

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Improving familial dyslipidaemia diagnosis

Atherosclerosis, 2018-08, Vol.275, p.e99-e99

2018

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G.P.237: Autosomal-dominant spinal muscular atrophy due to mutations in BICD2 gene in Bulgarian patients

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.888-888

2014

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Efficient Adaptive Stochastic Collocation Strategies for Advection–Diffusion Problems with Uncertain Inputs

Journal of scientific computing, 2023-09, Vol.96 (3), p.64, Article 64

2023

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Remdesivir Reduces Mortality in Hemato-Oncology Patients with COVID-19

Journal of inflammation research, 2022-01, Vol.15, p.4907-4920

2022

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Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies

Brain (London, England : 1878), 2010-06, Vol.133 (6), p.1798-1809

2010

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Enabling UQ for Complex Modelling Workflows

Computational Science – ICCS 2019, p.269-281

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Different Approaches for Silver Nanoparticle Sterilization for Administration to Cell Culture

Nano biomedicine and engineering, 2023-06, Vol.15 (3), p.253-261

2023

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118 Characterisation of tumorspheres cultured from circulating epithelial tumor cells (CETCs) in pancreatic cancer patients

European journal of cancer (1990), 2015-09, Vol.51, p.S6-S6

2015

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165 PDL-1 is highly expressed on circulating epithelial tumor cells (CETCs) and could be a crucial factor in the inhibition of immune response to CETCs during metastasis formation

European journal of cancer (1990), 2015-09, Vol.51, p.S18-S19

2015

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318: Chemosensitivity differs between CETCs and spheroids grown from the CETCs in cancer patients with solid tumors

European journal of cancer (1990), 2014-07, Vol.50, p.S76-S76

2014

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317: Analysis of HER2 amplification and IGF-IR expression in CETCs and its possible association with resistance to trastuzumab in HER2 positive breast cancers

European journal of cancer (1990), 2014-07, Vol.50, p.S76-S76

2014

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Dominant GDAP1 mutations cause predominantly mild CMT phenotypes

An evaluation of noise reduction algorithms for particle-based fluid simulations in multi-scale applications

A novel coupling of noise reduction algorithms for particle flow simulations

Deficiency of the E3 ubiquitin ligase TRIM2 in early-onset axonal neuropathy

Experimental Studies in Deep Hole Drilling of Ti-6Al-4V with Twist Drills

S274: A NOVEL SUBTYPE OF ANEMIA CAUSED BY MUTATIONS IN TFRC GENE

High-throughput microscopy profiling of LDLR variants

4. Neurophysiologic and clinical characteristic of neuromyotonia in new hereditary neuromuscular disorder

G.P.237

Genetic spectrum of hereditary neuropathies with onset in the first year of life

PP09.9 – 2907: Is it easy to recognize HINT1 neuropathy

Gene-gene interactions at GWAS loci modulate lipid plasma levels and cellular uptake of low-density lipoprotein

Functional Genomics In A Cohort Of Fh Mutation Negative Patients

The importance to track variants in a genes causing recessive disorders within the family: A FH/Sitosterolemia clinical case

Improving familial dyslipidaemia diagnosis

G.P.237: Autosomal-dominant spinal muscular atrophy due to mutations in BICD2 gene in Bulgarian patients

Efficient Adaptive Stochastic Collocation Strategies for Advection–Diffusion Problems with Uncertain Inputs

Remdesivir Reduces Mortality in Hemato-Oncology Patients with COVID-19

Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies

Enabling UQ for Complex Modelling Workflows

Different Approaches for Silver Nanoparticle Sterilization for Administration to Cell Culture

118 Characterisation of tumorspheres cultured from circulating epithelial tumor cells (CETCs) in pancreatic cancer patients

165 PDL-1 is highly expressed on circulating epithelial tumor cells (CETCs) and could be a crucial factor in the inhibition of immune response to CETCs during metastasis formation

318: Chemosensitivity differs between CETCs and spheroids grown from the CETCs in cancer patients with solid tumors

317: Analysis of HER2 amplification and IGF-IR expression in CETCs and its possible association with resistance to trastuzumab in HER2 positive breast cancers

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