Zobrazeno 1 - 10
of 153
pro vyhledávání: '"rapp-hodgkin syndrome"'
Autor:
Liu, Ning1, Niu, Shu1, Cao, Xiao-Rui1, ChENg, Jia-Qi1, Gao, Shu-Yuan1, Yu, Xiu-Ju1, Wang, Hai-Dong1, Dong, Chang-ShENg1, He, Xiao-Yan1 sxndhxy@163.com
Publikováno v:
Molecular Medicine Reports. Mar2018, Vol. 17 Issue 3, p4688-4694. 7p. 1 Color Photograph, 6 Graphs.
Autor:
Nikolay N. Murashkin, Alexander I. Materikin, Roman V. Epishev, Maria A. Leonova, Leonid A. Opryatin, Dmitri V. Fedorov, Roman A. Ivanov, Alena A. Savelova, Oksana R. Katunina, Kirill A. Kulikov, Anastasiya U. Ufimtseva
Publikováno v:
Вопросы современной педиатрии, Vol 22, Iss 5, Pp 450-457 (2023)
Background. Rapp-Hodgkin syndrome is a rare genetic disease from the ectodermal dysplasia group. It manifests with damage of ectodermal structures — layer of embrional tissue that provides the development of many organs and tissues in the body, suc
Externí odkaz:
https://doaj.org/article/61973a6001704cbd81c711cba0495ce1
Autor:
Arif, Tasleem1 dr_tasleem_arif@yahoo.com, Adil, Mohammad1, Amin, Syed Suhail1, Dorjay, Konchok1
Publikováno v:
Indian Journal of Paediatric Dermatology. Jan-Mar2018, Vol. 19 Issue 1, p84-86. 3p.
Autor:
Fusco, Francesca1 (AUTHOR), Pescatore, Alessandra1 (AUTHOR), Conte, Matilde Immacolata1 (AUTHOR), Mirabelli, Peppino2 (AUTHOR), Paciolla, Mariateresa1,3 (AUTHOR), Esposito, Elio1 (AUTHOR), Lioi, Maria Brigida3 (AUTHOR), Ursini, Matilde Valeria1,2 (AUTHOR) matildevaleria.ursini@igb.cnr.it
Publikováno v:
International Reviews of Immunology. 2015, Vol. 34 Issue 6, p445-459. 15p.
Publikováno v:
Indian Dermatology Online Journal. Sep/Oct2016, Vol. 7 Issue 5, p393-395. 3p.
Publikováno v:
Anaesthesia Reports; Jan-Jun2023, Vol. 11 Issue 1, p1-4, 4p
Autor:
Lam, Ching-Wan
Publikováno v:
Journal of Laboratory Medicine; Dec2021, Vol. 45 Issue 6, p259-266, 8p
Autor:
Yosuke Harazono, Kei-ichi Morita, Erina Tonouchi, Eri Anzai, Namiaki Takahara, Tomohiro Kohmoto, Issei Imoto, Tetsuya Yoda
Publikováno v:
Advances in Oral and Maxillofacial Surgery, Vol 5, Iss , Pp 100253- (2022)
The transcription factor tumour protein 63, encoded by the TP63 gene, is a regulator of epidermal development. Heterozygous mutations in TP63 cause a variety of human ectodermal dysplasia disorders, including ankyloblepharon-ectodermal defects-cleft
Externí odkaz:
https://doaj.org/article/202363e211234e5797f81ff133603ee7
Autor:
Chaudhary, A.K.1, Mohapatra, R.2, Nagarajaram, H.A.2, Ranganath, P.3,4, Dalal, A.3, Dutta, A.5, Danda, S.5, Girisha, K.M.6, Bashyam, M.D.1 bashyam@cdfd.org.in
Publikováno v:
Journal of the European Academy of Dermatology & Venereology. Jan2017, Vol. 31 Issue 1, pe17-e20. 4p.
Publikováno v:
International Journal of Paediatric Dentistry; Sep2021 Supplement S2, Vol. 31, p428-444, 17p