The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15
A Saffari, M Kellner, C Jordan, H Rosengarten, A Mo… - Brain, 2023 - academic.oup.com
In the field of hereditary spastic paraplegia (HSP), progress in molecular diagnostics needs
to be translated into robust phenotyping studies to understand genetic and phenotypic …
to be translated into robust phenotyping studies to understand genetic and phenotypic …
[HTML][HTML] Spastic paraplegia 15
Spastic Paraplegia 15 - Abstract - Europe PMC Sign in | Create an account https://orcid.org
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[HTML][HTML] Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegia
SL Hsu, YJ Lu, YS Tsai, HC Chao, JL Fuh… - Journal of the Formosan …, 2022 - Elsevier
Background/purpose Hereditary spastic paraplegia (HSP) is a heterogeneous group of
inherited neurodegenerative disorders characterized by slowly progressive lower limbs …
inherited neurodegenerative disorders characterized by slowly progressive lower limbs …
Case report: Hereditary spastic paraplegia with a novel homozygous mutation in ZFYVE26
Z Lai, X Liu, Y Song, H Zhou, L Zeng - Frontiers in Neurology, 2023 - frontiersin.org
Hereditary spastic paraplegia (HSP) is a group of neurodegenerative diseases with genetic
and clinical heterogeneity characterized by spasticity and weakness of the lower limbs. It …
and clinical heterogeneity characterized by spasticity and weakness of the lower limbs. It …
A SPAST gene-related hereditary spastic paraplegia type 4 family: Identification by a novel mutation
L Zhang, X He - 2022 - researchsquare.com
Objective: The aim of this study was to confirm the disease causing of a family with
hereditary spastic paraplegia. Methods: Detailed clinical characterization analysis was …
hereditary spastic paraplegia. Methods: Detailed clinical characterization analysis was …
[HTML][HTML] Spastic Paraplegia 15 Synonyms: Hereditary Spastic Paraplegia Type 15, HSP-ZFYVE26, SPG15, ZFYVE26-Related Hereditary Spastic Paraplegia
Spastic paraplegia 15 (SPG15), typically an early-onset complex hereditary spastic
paraplegia, is characterized by progressive spasticity that begins in the lower extremities …
paraplegia, is characterized by progressive spasticity that begins in the lower extremities …
[PDF][PDF] Analysis of genome-wide mutation profile and establishment of risk signature for prognosis of bladder cancer
Y Zhao, R Ma, F Liu, L Zhang, X Lv, P Su, Y Fan… - 2020 - scholar.archive.org
Background: Emerging studies have shown that a variety of gene mutations occur in
development and progression of cancer and highly mutation genes could play oncogenic or …
development and progression of cancer and highly mutation genes could play oncogenic or …