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4.
J Eur Acad Dermatol Venereol ; 29(5): 899-903, 2015 May.
Article in English | MEDLINE | ID: mdl-25201089

ABSTRACT

BACKGROUND: Epidermolysis bullosa (EB) is a rare and so far incurable genetic disease, affecting mainly the skin and mucosal membranes, manifesting with blisters triggered by minor mechanical trauma. Since only few epidemiological data on EB are available, we established a Registry for EB and implemented molecular diagnostic methods. OBJECTIVE: We present epidemiologic data from the EB Registry and genotype-phenotype correlations. METHODS: In 2006, a registry of patients with EB was initiated in the Department of Dermatology of the University of Medicine, as well as molecular diagnostic tools. The patients were diagnosed on clinical bases, and whenever possible, immunofluorescence mapping and molecular analysis were performed. RESULTS: 89 EB patients were enrolled in the study from 2006 to 2012: 58 patients with dystrophic EB (DEB), 20 with EB simplex, one patient was diagnosed with Kindler syndrome; in 10 patients, the type of EB could not be determined. DISCUSSION AND CONCLUSION: We have estimated, the total number of EB patients in Romania and we have estimated the incidence and the prevalence of EB. We have also managed to approximate the distribution of EB types in Romania. Moreover, we performed a phenotypic and genotypic characterization in some of the patients included in the EB register.


Subject(s)
Epidermolysis Bullosa Dystrophica/epidemiology , Epidermolysis Bullosa Simplex/epidemiology , Adolescent , Adult , Blister/epidemiology , Child , Child, Preschool , Collagen Type VII/genetics , Epidermolysis Bullosa/epidemiology , Epidermolysis Bullosa Dystrophica/genetics , Epidermolysis Bullosa Simplex/genetics , Exons , Female , Genotype , Humans , Infant , Infant, Newborn , Male , Middle Aged , Periodontal Diseases/epidemiology , Phenotype , Photosensitivity Disorders/epidemiology , Prevalence , Registries , Romania/epidemiology , Young Adult
5.
Genes Brain Behav ; 11(4): 398-403, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22348680

ABSTRACT

This study investigated whether somatic markers mediate the effect of serotonin transporter genotype on Iowa Gambling Task (IGT) performance. Participants (N = 135) were genotyped for the insertion/deletion and single-nucleotide (rs25531) polymorphisms in the promoter region of the serotonin transporter gene (5-HTTLPR). The results of mediation analyses indicated that skin conductance responses that anticipated IGT card selections partially (i.e. 42% of the total effect) mediated the effect of genotype on IGT performance. In comparison with high-functioning 5-HTTLPR genotypes, the low-functioning genotypes were associated with higher total IGT scores. This suggests that the higher synaptic availability of serotonin, associated with the low-functioning 5-HTTLPR genotypes, may confer differential susceptibility to decision making under risk, and that almost half of this effect is explained by facilitated somatic markers during IGT.


Subject(s)
Decision Making/physiology , Polymorphism, Single Nucleotide , Promoter Regions, Genetic , Serotonin Plasma Membrane Transport Proteins/genetics , Adolescent , Adult , Female , Gambling , Genotype , Humans , Male , Neuropsychological Tests
6.
Phys Rev Lett ; 95(13): 137402, 2005 Sep 23.
Article in English | MEDLINE | ID: mdl-16197177

ABSTRACT

Femtosecond electron and spin dynamics of the Gd(0001) surface are investigated by time-resolved photoemission and second harmonic generation. Upon optical excitation the spin polarization of the surface state is reduced by half while its exchange splitting remains nearly unchanged. Electron-magnon interaction is proposed to facilitate electron-spin-flip scattering among spin-mixed surface and bulk states, which provides a mechanism for ultrafast demagnetization.

15.
Genève; Organisation mondiale de la Santé; 1958. (WHO/Mal/206).
in English, French | WHO IRIS | ID: who-64586
16.
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