Search Results - "Danarti, R"

Modified Non-Cultured Cell Spray Induced Epithelization in LAMB3 Mutation Epidermolysis Bullosa by Widhiati, Suci, Dewi, Shinta Trilaksmi, Yefta, Danarti, Retno, Soebono, Hardyanto, Irmawati, Yulia Eka, Puspitasari, Monika, Trisnowati, Niken, Wibawa, Tri, Purnomosari, Dewajani, Wirohadidjojo, Yohanes Widodo

“…Autologous non-cultured cell (ANCC) spray has been used to treat burns, chronic wounds, and vitiligo, but its use in junctional epidermolysis bullosa (JEB) has…”
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Mutational spectrum of NSDHL in CHILD syndrome by Bornholdt, D, König, A, Happle, R, Leveleki, L, Bittar, M, Danarti, R, Vahlquist, A, Tilgen, W, Reinhold, U, Poiares Baptista, A, Grosshans, É, Vabres, P, Niiyama, S, Sasaoka, K, Tanaka, T, Meiss, A L, Treadwell, P A, Lambert, D, Camacho, F, Grzeschik, K-H

“…[...]their case had all the clinical features of X linked dominant chondrodysplasia punctata but none of the morphological criteria of CHILD syndrome. 1, 22…”
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Becker's nevus syndrome revisited by Danarti, Retno, König, Arne, Salhi, Aïcha, Bittar, Mario, Happle, Rudolf

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Linear atrophoderma of Moulin: postulation of mosaicism for a predisposing gene by Danarti, Retno, Bittar, Mario, Happle, Rudolf, König, Arne

“…Hyperpigmented atrophoderma arranged in a pattern following the lines of Blaschko and appearing during childhood or adolescence on the trunk or the limbs is a…”
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Paradominant inheritance of twin spotting: phacomatosis pigmentovascularis as a further possible example by Danarti, Retno, Happle, Rudolf

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Large congenital melanocytic nevi may reflect paradominant inheritance implying allelic loss by DANARTI, Retno, KÖNIG, Arne, HAPPLE, Rudolf

“…Large congenital melanocytic nevi have so far always been considered to occur sporadically, and until now little has been written about a possible role of…”
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Paradominant inheritance may explain familial occurrence of Cutis marmorata telangiectatica congenita by Danarti, R, Happle, R, König, A

“…Cutis marmorata telangiectatica congenita (CMTC) is a rare congenital vascular anomaly that virtually always occurs sporadically and in a patchy, quadrant,…”
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Late-onset familial onychodystrophy heralding incontinentia pigmenti by Bittar, Mario, Danarti, Retno, König, Arne, Gal, Andreas, Happle, Rudolf

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