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Zywnosc. Nauka. Technologia. Jakosc/Food. Science Technology. Quality, ISSN 1425-6959, 2016, Volume 4, Issue 107, pp. 66 - 79
Journal Article
Archives of Metallurgy and Materials, ISSN 2300-1909, 12/2015, Volume 60, Issue 4, pp. 2625 - 2630
A paper presents a piece of information about innovate surfacing technology with micro-jet cooling. There are put down information about parameters of shaft... 
wearing | welding surfacing | micro-jet cooling | metallographic structure
Journal Article
Zywnosc. Nauka. Technologia. Jakosc/Food. Science Technology. Quality, ISSN 1425-6959, 2016, Volume 2, Issue 105, pp. 81 - 94
Journal Article
Zywnosc. Nauka. Technologia. Jakosc/Food. Science Technology. Quality, ISSN 1425-6959, 2011, Volume 18, Issue 3, pp. 98 - 108
Journal Article
Pediatria Polska, ISSN 0031-3939, 09/2011, Volume 86, Issue 6, pp. 612 - 619
Niedożywienie u chorych z (AN) może negatywnie wpłynąć na czynność wielu narządów, w tym skóry. Objawy skórne wynikają z głodzenia, wymiotów, stosowania leków... 
skin | anorexia nervosa | skóra
Journal Article
Pediatria Polska, ISSN 0031-3939, 09/2011, Volume 86, Issue 6, pp. 612 - 619
Introduction: Malnutrition in anorexia nervosa (AN) patients can negatively influence the function of many organs, including skin. Dermal symptoms result from... 
skin | anorexia nervosa
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2017, Volume 24, Issue 1, pp. 37 - 45
Background and purpose: The clinical characteristics of colony stimulating factor 1 receptor (CSF1R) related adult-onset leukoencephalopathy with axonal... 
leukoencephalopathy | pigmented orthochromatic leukodystrophy | colony stimulating factor 1 receptor | adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia | hereditary diffuse leukoencephalopathy with spheroids | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | HDLS | MRI | LEUKODYSTROPHY | INVOLVEMENT | NEUROSCIENCES | CLINICAL NEUROLOGY | FEATURES | IMPAIRMENT | PROGRESSIVE MULTIPLE-SCLEROSIS | HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY | CORPUS-CALLOSUM | PATIENT | Leukoencephalopathies - genetics | Neuroglia - pathology | Humans | Leukoencephalopathies - diagnostic imaging | Middle Aged | Male | Young Adult | Receptors, Granulocyte-Macrophage Colony-Stimulating Factor - genetics | Aged, 80 and over | Adult | Female | Pyramidal Tracts - pathology | Leukoencephalopathies - pathology | Penetrance | Sex Characteristics | Mutation - genetics | White Matter - pathology | Corpus Callosum - diagnostic imaging | Magnetic Resonance Imaging | White Matter - diagnostic imaging | Movement Disorders - physiopathology | Pyramidal Tracts - diagnostic imaging | Axons - pathology | Corpus Callosum - pathology | Movement Disorders - etiology | Adolescent | Age of Onset | Heterozygote | Aged | Tyrosine | Genetic research | Genetic aspects | Leukoencephalopathy | Kinases | Age | Mutation | Index Medicus | Original
Journal Article
European Journal of Neurology, ISSN 1351-5101, 01/2018, Volume 25, Issue 1, pp. 142 - 147
Background and purposeTo establish and validate diagnostic criteria for adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) due to... 
alanyl‐transfer | diagnostic criteria | adult‐onset leukoencephalopathy with axonal spheroids and pigmented glia | RNA | colony‐stimulating factor 1 receptor | leukoencephalopathy | pigmented orthochromatic leukodystrophy | hereditary diffuse leukoencephalopathy with spheroids | synthetase 2 | adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | colony-stimulating factor 1 receptor | alanyl-transfer RNA synthetase 2 | HDLS | LEUKODYSTROPHY | NEUROSCIENCES | CLINICAL NEUROLOGY | Leukoencephalopathies - pathology | Diagnosis, Differential | Leukoencephalopathies - genetics | Reproducibility of Results | CADASIL - pathology | Neuroglia - pathology | Humans | Middle Aged | Spheroids, Cellular - pathology | Male | Tomography, X-Ray Computed | CADASIL - genetics | Young Adult | Magnetic Resonance Imaging | Receptors, Granulocyte-Macrophage Colony-Stimulating Factor - genetics | Axons - pathology | Cognition Disorders - etiology | Leukoencephalopathies - diagnosis | Adolescent | CADASIL - diagnosis | Adult | Female | Receptor, Notch3 - genetics | Aged | Genetic aspects | Diagnosis | Ligases | Leukoencephalopathy | Analysis | Transfer RNA | Sensitivity | Macrophage colony-stimulating factor | Colony-stimulating factor | Diagnostic systems | Mutation | Criteria | Spheroids | Genetic screening | Index Medicus | Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia (ALSP) | pigmented orthochromatic leukodystrophy (POLD) | colony stimulating factor 1 receptor (CSF1R) | alanyl-transfer (t)RNA synthetase 2 (AARS2) | hereditary diffuse leukoencephalopathy with spheroids (HDLS)
Journal Article
Sleep Medicine, ISSN 1389-9457, 2012, Volume 14, Issue 8, pp. 754 - 762
Journal Article
Journal Article
Journal Article
Science Translational Medicine, ISSN 1946-6234, 07/2012, Volume 4, Issue 141, pp. 141ra90 - 141ra90
Journal Article
Journal Article