Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Su M. Lwin"'
Autor:
Farzin Farzaneh, Anna E. Martinez, Magdalena Martinez-Queipo, Havinder Hara, Wei Wang, Adrian J. Thrasher, Alya Abdul-Wahab, Jemima E. Mellerio, Alex Virasami, Su M. Lwin, Waseem Qasim, John A. McGrath, Farhatullah Syed, Dale Moulding, Neil J. Sebire, John I. Harper, Wei Li Di, Tendai Kadiyirire, Anastasia Petrova, Catina Bernadis, M. Zamiri, Dyanne Rampling
Publikováno v:
Human gene therapy. 30(9)
Netherton syndrome (NS) is a rare autosomal recessive skin disorder caused by mutations in SPINK5. It is a debilitating condition with notable mortality in the early years of life. There is no cura...
Autor:
Emanuele de Rinaldis, Dusko Ilic, Magdalena Martinez-Queipo, Sabrina Zeddies, Alka Saxena, Ineke Slaper-Cortenbach, Sophia Aristodemou, Lu Liu, Su M. Lwin, James R. McMillan, Anna E. Martinez, Chrysanthi Ainali, John A. McGrath, Kasper Westinga, Gabriela Petrof, Alyson Guy, Marcel P. H. van den Broek, Rashida Pramanik, Francesco Dazzi, Venu Pullabhatla, Rosamund Nuamah, Linda Ozoemena, Salma Ayis, John B. Mee, Sonia Serrano, Clarisse Maurin, Jemima E. Mellerio, Ellie Rashidghamat, Alexandros Onoufriadis, Tendai Kadiyirire
Publikováno v:
Journal of the American Academy of Dermatology. 83(2)
Background Recessive dystrophic epidermolysis bullosa (RDEB) is a hereditary blistering disorder due to a lack of type VII collagen. At present, treatment is mainly supportive. Objectives To determine whether intravenous allogeneic bone marrow–deri