Search Results - "Dănescu, S."

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  1. 1
    Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosa

    Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosa by Dănescu, S., Has, C., Senila, S., Ungureanu, L., Cosgarea, R.

    “…Background Epidermolysis bullosa (EB) is a rare and so far incurable genetic disease, affecting mainly the skin and mucosal membranes, manifesting with…”
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  2. 2
    Correlation between disease severity and quality of life in patients with epidermolysis bullosa

    Correlation between disease severity and quality of life in patients with epidermolysis bullosa by Dănescu, S., Sălăvăstru, C., Sendrea, A., Tiplica, S., Baican, A., Ungureanu, L., Senila, S., Morariu, S., Ignat, S., Vesa, S., Cosgarea, R.

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  3. 3
    Compound heterozygosity for dominant and recessive DSG1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting)

    Compound heterozygosity for dominant and recessive DSG1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting) by Dănescu, S., Leppert, J., Cosgarea, R., Zurac, S., Pop, S., Baican, A., Has, C.

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  4. 4
    Low Vitamin K Status in Patients with Psoriasis Vulgaris: A Pilot Study

    Low Vitamin K Status in Patients with Psoriasis Vulgaris: A Pilot Study by Gheorghe, Simona R, Ilyés, Tamás, Filip, Gabriela A, Dănescu, Ana S, Timiș, Teodora L, Orăsan, Meda, Stamate, Irina, Crăciun, Alexandra M, Silaghi, Ciprian N

    Published in Biomedicines (26-05-2024)
    “…Psoriasis vulgaris (PV) is a disease characterized by skin manifestations and systemic inflammation. There are no published studies to date on vitamin K status…”
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  5. 5
    Patient compliance: the main drawback in the dermoscopic follow-up of melanocytic lesions

    Patient compliance: the main drawback in the dermoscopic follow-up of melanocytic lesions by Ungureanu, L., Senilă, S., Dănescu, S., Vesa, S.C., Cosgarea, R.

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  6. 6
    Compound heterozygosity for dominant and recessive DSG 1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting)

    Compound heterozygosity for dominant and recessive DSG 1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting) by Dănescu, S., Leppert, J., Cosgarea, R., Zurac, S., Pop, S., Baican, A., Has, C.

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  7. 7
    Incontinentia pigmenti in a newborn with a novel nonsense mutation in the NEMO gene

    Incontinentia pigmenti in a newborn with a novel nonsense mutation in the NEMO gene by Has, C., Danescu, S., Volz, A., Nöh, F., Technau, K., Bruckner-Tuderman, L.

    Published in British journal of dermatology (1951) (01-02-2007)
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  8. 8
    Compound heterozygosity for dominant and recessive DSG1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting)

    Compound heterozygosity for dominant and recessive DSG1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting) by Dănescu, S, Leppert, J, Cosgarea, R, Zurac, S, Pop, S, Baican, A, Has, C

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