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Showing 10 out of a total of 16 results for collection: Dermatology - Faculty Publications. (0.008 seconds)

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Asymptomatic solitary nodule over the right hand

Marrouche N.; Kurban M.; Salman S.; Kibbi A.-G.; Abbas O. (HOBOKEN, 2012)
Late evolution of giant verruciform xanthoma in the setting of child syndrome

Kurban M.; Abbas O.; Ghosn S.; Kibbi A.-G. (MALDEN, 2010)
Expanding the histologic spectrum of angina bullosa hemorrhagica: Report of one case

Kurban M.; Kibbi A.-G.; Ghosn S. (PHILADELPHIA, 2007)
A Homozygous Frameshift Mutation in the HOXC13 Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family

Farooq M.; Kurban M.; Fujimoto A.; Fujikawa H.; Abbas O.; Nemer G.; Saliba J.; Sleiman R.; Tofaili M.; Kibbi A.-G.; Ito M.; Shimomura Y. (HOBOKEN, 2013)
Clinicopathological study of 81 cases of localized and systemic scleroderma

Succaria F.; Kurban M.; Kibbi A.-G.; Abbas O. (HOBOKEN, 2013)
A novel mutation in the PLCD1 gene, which leads to an aberrant splicing event, underlies autosomal recessive leuconychia

Farooq M.; Kurban M.; Abbas O.; Obeidat O.; Fujikawa H.; Kibbi A.-G.; Fujimoto A.; Shimomura Y. (HOBOKEN, 2012)
Fibroblast-activation protein: Valuable marker of cutaneous epithelial malignancy

El Khoury J.; Kurban M.; Kibbi A.-G.; Abbas O. (Springer Verlag; NEW YORK, 2014)
Evidence for a founder mutation in the cathepsin C gene in three families with papillon-lefèvre syndrome

Kurban M.; Wajid M.; Shimomura Y.; Bahhady R.; Kibbi A.-G.; Christiano A.M. (BASEL, 2009)
Nonsense mutation in the ALOX12B gene leads to autosomal recessive congenital ichthyosis in a Lebanese family

Kurban M.; Shimomura Y.; Bahhady R.; Ghosn S.; Kibbi A.-G.; Christiano A.M. (MALDEN, 2010)
Plasmacytoid dendritic cell involvement in the host response against keratoacanthoma

Abbas O.; Hussein L.; Kurban M.; Kibbi A.-G. (Mosby Inc.; NEW YORK, 2014)

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