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Brain-computer interfaces for 1-D and 2-D cursor control: designs using volitional control of the EEG spectrum or steady-state visual evoked potentials

IEEE transactions on neural systems and rehabilitation engineering, 2006-06, Vol.14 (2), p.225-229

2006

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ID 290 – Differences in sleep microstate curves among healthy sleepers and patients after stroke

Clinical neurophysiology, 2016-03, Vol.127 (3), p.e126-e126

2016

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Feature clustering of intracranial pressure time series for alarm function estimation in traumatic brain injury

Physiological measurement, 2017-11, Vol.38 (11), p.2015

2017

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ID 306 – Mirror-box training in healthy subjects and a patient with hemiparesis

Clinical neurophysiology, 2016-03, Vol.127 (3), p.e53-e53

2016

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Feature clustering of intracranial pressure time series for alarm function estimation in traumatic brain injury

Physiological measurement, 2017-10, Vol.38 (11), p.2015-2043

2017

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Multimodal neuroelectric interface development

IEEE transactions on neural systems and rehabilitation engineering, 2003-06, Vol.11 (2), p.199-203

2003

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Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update

Human mutation, 1999, Vol.13 (1), p.44-53

1999

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Neonatal hemolytic anemia due to inherited harderoporphyria : Clinical characteristics and molecular basis

Blood, 1998-02, Vol.91 (4), p.1453-1457

1998

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In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria

Journal of hepatology, 2001-04, Vol.34, p.224

Rosipal, R

2001

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Kernel PCA for Feature Extraction and De-Noising in Nonlinear Regression

Neural computing & applications, 2001-01, Vol.10 (3), p.231-243

2001

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An Expectation-Maximization Approach to Nonlinear Component Analysis

Neural computation, 2001-03, Vol.13 (3), p.505-510

2001

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Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis

Clinica chimica acta, 2006-03, Vol.365 (1), p.188-193

2006

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Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresis

Clinica chimica acta, 1999, Vol.279 (1), p.133-143

1999

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Importance of the time alignment of the sleep probabilistic curves

2017 11th International Conference on Measurement, 2017, p.27-30

2017

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Can ICA improve sleep-spindles detection?

Neural network world, 1998-01, Vol.8 (5), p.539-547

1998

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Molecular analysis of porphobilinogen (PBG) deaminase gene mutations in acute intermittent porphyria: first study in patients of Slavic origin

Scandinavian journal of clinical and laboratory investigation, 1997, Vol.57 (3), p.217-224

1997

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Spectral, complexity and interdependence measures of sleep EEG after ischemic stroke

2017 11th International Conference on Measurement, 2017, p.245-249

2017

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An in-frame insertion in exon 3 and a nonsense mutation in exon 2 of the insulin receptor gene associated with severe insulin resistance in a patient with Rabson-Mendenhall syndrome

Diabetologia, 1993-11, Vol.36 (11), p.1168-1174

1993

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In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria

Journal of hepatology, 2001-04, Vol.34, p.223-224

2001

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Protoporphyrinogen Oxidase: Complete Genomic Sequence and Polymorphisms in the Human Gene

Biochemical and biophysical research communications, 1996-09, Vol.226 (1), p.226-230

1996

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Prediction of Chaotic Time-Series with a Resource-Allocating RBF Network

Neural processing letters, 1998-06, Vol.7 (3), p.185-197

1998

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“Homozygous” variegate porfyria

Journal of hepatology, 2001-04, Vol.34, p.220-220

2001

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Congenital disorder of type Ia protein glycosylation: clinical, biochemical and molecular characteristics in 2 siblings with cerebellar hypoplasia

Časopis lékařů českých, 2003, Vol.142 (5), p.276

2003

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Analysis of the most frequent mutations in girls with Rett syndrome

Časopis lékařů českých, 2001-08, Vol.140 (15), p.473

2001

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An adaptive support vector regression filter: A signal detection application

9th International Conference on Artificial Neural Networks: ICANN '99, 1999, p.603-607

1999

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Brain-computer interfaces for 1-D and 2-D cursor control: designs using volitional control of the EEG spectrum or steady-state visual evoked potentials

ID 290 – Differences in sleep microstate curves among healthy sleepers and patients after stroke

Feature clustering of intracranial pressure time series for alarm function estimation in traumatic brain injury

ID 306 – Mirror-box training in healthy subjects and a patient with hemiparesis

Feature clustering of intracranial pressure time series for alarm function estimation in traumatic brain injury

Multimodal neuroelectric interface development

Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update

Neonatal hemolytic anemia due to inherited harderoporphyria : Clinical characteristics and molecular basis

In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria

Kernel PCA for Feature Extraction and De-Noising in Nonlinear Regression

An Expectation-Maximization Approach to Nonlinear Component Analysis

Analbuminemia in a Slovak Romany (gypsy) family: Case report and mutational analysis

Evaluation of mutation screening by heteroduplex analysis in acute intermittent porphyria: comparison with denaturing gradient gel electrophoresis

Importance of the time alignment of the sleep probabilistic curves

Can ICA improve sleep-spindles detection?

Molecular analysis of porphobilinogen (PBG) deaminase gene mutations in acute intermittent porphyria: first study in patients of Slavic origin

Spectral, complexity and interdependence measures of sleep EEG after ischemic stroke

An in-frame insertion in exon 3 and a nonsense mutation in exon 2 of the insulin receptor gene associated with severe insulin resistance in a patient with Rabson-Mendenhall syndrome

In frame deletion of glycin 390 in coproporphyrinogen oxidase gene as a cause of hereditary coproporphyria

Protoporphyrinogen Oxidase: Complete Genomic Sequence and Polymorphisms in the Human Gene

Prediction of Chaotic Time-Series with a Resource-Allocating RBF Network

“Homozygous” variegate porfyria

Congenital disorder of type Ia protein glycosylation: clinical, biochemical and molecular characteristics in 2 siblings with cerebellar hypoplasia

Analysis of the most frequent mutations in girls with Rett syndrome

An adaptive support vector regression filter: A signal detection application

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