Showing 81 - 100 results of 165 for search 'Széll Márta', query time: 0.06s Refine Results
  1. 81
    JAK2 V617F, MPL, and CALR Mutations in Essential Thrombocythaemia and Major Thrombotic Complications A Single-Institute Retrospective Analysis /
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  2. 82
    Analysis of psoriasis-relevant gene expression and exon usage alterations after silencing of SR-rich splicing regulators
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  3. 83
    Electrochemotherapy for non-melanoma skin cancer in a child with xeroderma pigmentosum
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  4. 84
    Splicing factors differentially expressed in psoriasis alter mRNA maturation of disease-associated EDA+ fibronectin.
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  5. 85
    Re-analysis of the Hungarian amyotrophic lateral sclerosis population and evaluation of novel ALS genetic risk variants.
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  6. 86
    Multidisciplinary Approach for Mapping Genetic Variants in Naevoid Basal Cell Carcinoma Syndrome. Newly Identified Patched 1 Mutations in Half-Sisters
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  7. 87
    A tünetmentes állapot fenntartásáért felelős szerkezeti és immunológiai aspektusok azonosítása a pikkelysömörös nem léziós bőrben
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  8. 88
    Constitutive Photomorphogenic Protein is involved in the UVB-induced cellular response of human keratinocytes
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  9. 89
    In vitro dedifferentiation of melanocytes from adult epidermis
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  10. 90
    Polymorphisms of the IL23R gene are associated with psoriasis but not with immunoglobulin A nephropathy in a Hungarian population
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  11. 91
    Somatic mosaicism of the PIK3CA gene identified in a Hungarian girl with macrodactyly and syndactyly
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  12. 92
    Could basement membrane alterations, resembling micro-wounds at the dermo-epidermal junction in psoriatic non-lesional skin, make the skin susceptible to lesion formation?
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  13. 93
    A novel missense mutation of the CYLD gene identified in a Hungarian family with Brooke-Spiegler syndrome
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  14. 94
    Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases
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  15. 95
    Regulatory Networks Contributing to Psoriasis Susceptibility
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  16. 96
    Nemaline Myopathy Type 2 (NEM2) Two Novel Mutations in the Nebulin (NEB) Gene /
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  17. 97
    Simultaneous adeno- and squamous cell carcinoma with different phenotypic profiles in a rat model of chronic gastroesophageal reflux
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  18. 98
    Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient
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  19. 99
    Bőrbetegségek immunpatogenezisének és genetikájának vizsgálata
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  20. 100
    Magától gyógyuló kollodium bébi
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