Zobrazeno 1 - 10
of 43
pro vyhledávání: '"HSCT, hematopoietic stem cell therapy"'
Autor:
Motomichi Kosuga, Kumiko Yanagi, Yasuyuki Fukuhara, Torayuki Okuyama, Narutoshi Yamazaki, Ai Miura, Takanori Yamagata, Tadashi Kaname, Hitoshi Sakuraba, Tetsumin So
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100692-(2020)
Molecular Genetics and Metabolism Reports, Vol 25, Iss, Pp 100692-(2020)
We previously showed that the genotype-phenotype correlation in MPS II is well-conserved in Japan (Kosuga et al., 2016). Almost all of our patients with attenuated MPS II have missense variants, which is expected to result in residual activity of idu
Autor:
Kenji E. Orii, Shunji Tomatsu, Robert W. Mason, Yasuyuki Suzuki, Tadao Orii, Hiromasa Yabe, Shunichi Kato, Akemi Tanaka, Pravin Patel, Tsutomu Shimada, Toshiyuki Fukao
Publikováno v:
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 184-196 (2014)
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 184-196 (2014)
Patients with Hunter syndrome (mucopolysaccharidosis II) present with skeletal dysplasia including short stature as well as CNS and visceral organ involvement. A previous study on Hunter syndrome indicated an impact on brain and heart involvement aft
Autor:
Tsutomu Shimada, Shunji Tomatsu, Eriko Yasuda, Kenji E. Orii, Yasuyuki Suzuki, Miho Maeda, Pravin Patel, Tadao Orii
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 5-18 (2014)
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports
Children with mucopolysaccharidosis II (MPS II), also known as Hunter syndrome, an X-linked disorder, suffer from a multisystem dysfunction caused by the accumulation of glycosaminoglycans. However, there has been no systemic report on the growth of
Publikováno v:
EBioMedicine, Vol 16, Iss C, Pp 41-50 (2017)
EBioMedicine
EBioMedicine
Although multiple sclerosis (MS) is considered to be a CD4, Th17-mediated autoimmune disease, supportive evidence is perhaps circumstantial, often based on animal studies, and is questioned by the perceived failure of CD4-depleting antibodies to cont
Autor:
Hosseini, Mohammad-Salar, Sanaie, Sarvin, Mahmoodpoor, Ata, Jabbari Beyrami, Saba, Jabbari Beyrami, Hossein, Fattahi, Shirin, Jahanshahlou, Farid, Zarei, Mahdi, Rahimi Mamaghani, Alireza, Kuchaki Rafsanjani, Mahshid
Publikováno v:
European Journal of Medical Research; 11/30/2024, Vol. 29 Issue 1, p1-18, 18p
Autor:
Toskov, Vasil, Cseh, Annamaria, Claviez, Alexander, Drexler, Beatrice, Rotari, Natalia, Schwarz-Furlan, Stephan, Braun, Matthias, Bader, Peter, Lang, Peter, Beier, Rita, Erdlenbruch, Bernhard, Führer, Monika, Erlacher, Miriam, Niemeyer, Charlotte M., Strahm, Brigitte, Yoshimi, Ayami
Publikováno v:
Journal of Pediatric Hematology/Oncology; Jul2024, Vol. 46 Issue 5, pe354-e359, 6p
Autor:
Bruce, Iain A.1 (AUTHOR), Ezgü, Fatih S.2 (AUTHOR), Kampmann, Christoph3 (AUTHOR), Kenis, Vladimir4 (AUTHOR), Mackenzie, William5 (AUTHOR), Stevens, Bob6 (AUTHOR), Walker, Robert7 (AUTHOR), Hendriksz, Christian8 (AUTHOR) chris@fymcamedical.co.uk
Publikováno v:
Orphanet Journal of Rare Diseases. 3/2/2022, Vol. 17 Issue 1, p1-18. 18p.
Autor:
Younan, Romy G.1 (AUTHOR) younaromy@gmail.com, Raad, Roy A.2 (AUTHOR), Sawan, Bassem Y.3 (AUTHOR), Said, Rabih1 (AUTHOR)
Publikováno v:
Allergy, Asthma & Clinical Immunology. 10/26/2021, Vol. 17 Issue 1, p1-5. 5p.
Autor:
Singh, Sunita1 (AUTHOR) drsunitasingh28@gmail.com, Varshney, Abhimanyu1 (AUTHOR), Borkar, Nitin1 (AUTHOR), Jindal, Atul2 (AUTHOR), Padhi, Phalguni3 (AUTHOR), Ahmed, Intezar4 (AUTHOR), Srivastava, Niraj5 (AUTHOR)
Publikováno v:
Indian Journal of Surgery. 2020, Vol. 82 Issue 6, p1219-1228. 10p.
Publikováno v:
Turkish Journal of Gastroenterology; Aug2023, Vol. 34 Issue 8, p782-794, 13p