Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Senjie Du"'
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Charcot-Marie-Tooth disease (CMT) is a group of single-gene hereditary diseases of peripheral nerve with high clinical variability and genetic heterogeneity. The typical clinical manifestations include progressive muscle weakness
Externí odkaz:
https://doaj.org/article/7fc473ee92e543898fa219242b0dfb4c
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background The Raynaud-Claes type of X-linked syndromic mental retardation (MRXSRC) is a very rare condition, by intellectual disability ranged from borderline to profound, impaired language development, brain abnormalities, facial dysmorphi
Externí odkaz:
https://doaj.org/article/3af77ba6c366490ba77318f002dc3fb8
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundSpastic paraplegia type 54 (SPG54) is a rare inherited autosomal recessive disorder, and a complex hereditary spastic paraplegia (HSP) caused by mutations in the phospholipase DDHD2 gene. SPG54 is characterized by early onset of spastic par
Externí odkaz:
https://doaj.org/article/a0c4eaf526a7402e84544edb647cc8eb
Autor:
Dalin Fu, Weisheng Lin, Fen Lu, Senjie Du, Min Zhu, Xiaoke Zhao, Jian Tang, Chuan Chen, Xiaoli Chui, Shanmei Tang, Kai Wang, Chuanchun Yang, Bei Han
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Interstitial deletions of chromosome band 10q11-q22 was a genomic disorder distinguished by developmental delay, congenital cleft palate and muscular hypotonia. The phenotypes involved were heterogeneous, hinge on the variable bre
Externí odkaz:
https://doaj.org/article/dad7b4dbdff94bdca5fc5603724feb5b
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
BMC Pediatrics
BMC Pediatrics
Background The Raynaud-Claes type of X-linked syndromic mental retardation (MRXSRC) is a very rare condition, by intellectual disability ranged from borderline to profound, impaired language development, brain abnormalities, facial dysmorphisms and s
Publikováno v:
Journal of Cancer
Objective: Previous studies have demonstrated that circular RNAs (circRNAs) play vital roles in pathological process of various diseases, including tumors. This study aimed at exploring the role and mechanism of circRNA RNA ZNF609 (circ-ZNF609) in th
Autor:
Chuanchun Yang, Fen Lu, Xiaoke Zhao, Kai Wang, Chuan Chen, Senjie Du, Weisheng Lin, Min Zhu, Jian Tang, Shanmei Tang, Xiaoli Chui, Dalin Fu, Bei Han
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-5 (2021)
BMC Pediatrics
BMC Pediatrics
Background Interstitial deletions of chromosome band 10q11-q22 was a genomic disorder distinguished by developmental delay, congenital cleft palate and muscular hypotonia. The phenotypes involved were heterogeneous, hinge on the variable breakpoints
Publikováno v:
Neuro Oncol
Neuro-oncology, vol 22, iss Suppl 2
Neuro-Oncology, vol 22, iss Supplement_2
Neuro-oncology, vol 22, iss Suppl 2
Neuro-Oncology, vol 22, iss Supplement_2
BACKGROUNDS Glioblastoma (GBM) is an aggressive infiltrative brain tumor, and has an extremely poor prognosis despite the use of multiple treatment modalities, including surgery, radiation, and chemotherapy. Meanwhile, mitochondrial changes represent
Publikováno v:
American Journal of Physical Medicine & Rehabilitation. 94:169-179
Objective The aim of this study was to use the Face, Legs, Activity, Cry, Consolability Scale; salivary cortisol levels; and withdrawal reflex thresholds to assess pain, stress, and pain sensitivity in young children with cerebral palsy during early
Publikováno v:
American Journal of Physical Medicine & Rehabilitation. 92:905-911
The aim of this study was to compare the effectiveness of treatment with hinged ankle-foot orthoses (AFOs) during the day vs. during both the day and the night in young ambulant children with spastic diplegia.In this prospective randomized controlled