Cargando…
Haploinsufficiency of CSF-1R and clinicopathologic characterization in patients with HDLS
OBJECTIVE: To clarify the genetic, clinicopathologic, and neuroimaging characteristics of patients with hereditary diffuse leukoencephalopathy with spheroids (HDLS) with the colony stimulating factor 1 receptor (CSF-1R) mutation. METHODS: We performed molecular genetic analysis of CSF-1R in patients...
Autores principales: | Konno, Takuya, Tada, Masayoshi, Tada, Mari, Koyama, Akihide, Nozaki, Hiroaki, Harigaya, Yasuo, Nishimiya, Jin, Matsunaga, Akiko, Yoshikura, Nobuaki, Ishihara, Kenji, Arakawa, Musashi, Isami, Aiko, Okazaki, Kenichi, Yokoo, Hideaki, Itoh, Kyoko, Yoneda, Makoto, Kawamura, Mitsuru, Inuzuka, Takashi, Takahashi, Hitoshi, Nishizawa, Masatoyo, Onodera, Osamu, Kakita, Akiyoshi, Ikeuchi, Takeshi |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3937843/ https://www.ncbi.nlm.nih.gov/pubmed/24336230 http://dx.doi.org/10.1212/WNL.0000000000000046 |
Ejemplares similares
-
Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes
por: Takeuchi, Ryoko, et al.
Publicado: (2016) -
Increased cytoplasmic TARDBP mRNA in affected spinal motor neurons in ALS caused by abnormal autoregulation of TDP-43
por: Koyama, Akihide, et al.
Publicado: (2016) -
Novel CHP1 mutation in autosomal-recessive cerebellar ataxia: autopsy features of two siblings
por: Saito, Rie, et al.
Publicado: (2020) -
Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends
por: Takahashi, Tetsuya, et al.
Publicado: (2007) -
HDLs extract lipophilic drugs from cells
por: Zheng, Adi, et al.
Publicado: (2022)