Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Judy R. Pipo"'
Autor:
Marissa B. Lukban, Aida M. Salonga, Judy R. Pipo-Deveza, Benilda C. Sanchez-Gan, Catherine Lynne T. Silao, Annabell Chua
Publikováno v:
Acta Medica Philippina. 56
Background. Subacute sclerosing panencephalitis (SSPE) is a fatal neurodegenerative disease caused by prolonged persistent infection of the central nervous system with a measles virus mutant. Though various treatment modalities have been tried, there
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1489d977058131a73a44e6f6ebd8dd27
https://doi.org/10.47895/amp.v56i9.5341
https://doi.org/10.47895/amp.v56i9.5341
Analysis of MxA, IL-4, and IRF-1 Genes in Filipino Patients with Subacute Sclerosing Panencephalitis
Autor:
Aida M. Salonga, Megumi Takemoto, Koichi Kusuhara, Judy R. Pipo-Deveza, Toshiro Hara, Marissa B. Lukban, B. C. Sanchez, Catherine Lynn T. Silao, Ryutaro Kira, Hiroyuki Torisu
Publikováno v:
Neuropediatrics. 37:222-228
BACKGROUND: Subacute sclerosing panencephalitis (SSPE) is a chronic and debilitating disease of the central nervous system caused by a latent measles virus infection. Three candidate genes, MxA, IL-4, and IRF-1 genes were shown to be associated with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd9713fd9153f4ccf99dea93e9e7ae8b
https://doi.org/10.1055/s-2006-924724
https://doi.org/10.1055/s-2006-924724
Autor:
Catherine Lynn T. Silao, Ryutaro Kira, Masafumi Sanefuji, Koichi Kusuhara, Yoshito Ishizaki, Marissa B. Lukban, Toshiro Hara, Yasunari Sakai, Judy R. Pipo-Deveza, Benilda C. Sanchez, Aida M. Salonga, Kenji Ihara, Hiroyuki Torisu, Naoko Yukaya
Publikováno v:
Human genetics. 127(4)
Although the exact pathogenesis of subacute sclerosing panencephalitis (SSPE) remains to be determined, our previous data suggested a genetic contribution to the host susceptibility to SSPE. During chronic viral infection, virus-specific cytotoxic T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cc9f233459f5b995be36a4226502a0a
https://pubmed.ncbi.nlm.nih.gov/20066438
https://pubmed.ncbi.nlm.nih.gov/20066438
Autor:
Toshiyuki Yamamoto, Norio Sakuragawa, Frank Martiniuk, Akira Oka, Eiji Nanba, Haruaki Ninomiya, Jian-Hua Feng, Yuki Ohsaki, Judy R. Pipo, Seiichi Tsujino, Kousaku Ohno
Publikováno v:
Pediatric neurology. 29(4)
Glycogen storage disease type II (Pompe disease) is inherited by autosomal recessive transmission and caused by a deficiency of acid alpha-glucosidase (GAA), resulting in impaired degradation and lysosomal accumulation of glycogen. The GAA gene, resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e673f2b797f75de40a44f80d0411e77b
https://pubmed.ncbi.nlm.nih.gov/14643388
https://pubmed.ncbi.nlm.nih.gov/14643388
Autor:
Toshiyuki Yamamoto, Hiromasa Takeda, Haruaki Ninomiya, Kousaku Ohno, Jian-Hua Feng, Judy R. Pipo, Eiji Nanba
Publikováno v:
Braindevelopment. 24(4)
Tuberous sclerosis complex (TSC) is a neurocutaneous syndrome characterized by development of unusual tumor-like growths. Involvement of the brain is associated with the most problematic clinical manifestations of TSC, including intellectual retardat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a3249db383baeb4e50b6def4f1b1f2b
https://pubmed.ncbi.nlm.nih.gov/12015165
https://pubmed.ncbi.nlm.nih.gov/12015165
Publikováno v:
Braindevelopment. 23(1)
Forced normalization (FN) is a well known phenomenon of acute psychosis accompanying seizure control. An 11-year-old boy with intractable myoclonic epilepsy and severe psychomotor delay experienced FN during medication of ethosuximide. Although his m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db8e4a260878ba8fdd59af6576440aa5
https://pubmed.ncbi.nlm.nih.gov/11226734
https://pubmed.ncbi.nlm.nih.gov/11226734
Autor:
Kenzo Takeshita, Toshiyuki Yamamoto, Kousaku Ohno, Haruaki Ninomiya, Hiromasa Takeda, Judy R. Pipo, Shinji Maegawa, Eiji Nanba
Publikováno v:
Human Mutation. 16:375-375
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92c8723c3f5197e34ed3d501f2193727
https://doi.org/10.1002/1098-1004(200010)16:4<375::aid-humu18>3.0.co
https://doi.org/10.1002/1098-1004(200010)16:4<375::aid-humu18>3.0.co