SPSD more often had hypertonia (60% vs. 24%, p < 0.001), hyperreflexia (71% vs. 43%, p = 0.001), and lumbar hyperlordosis (
…Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2015 | 1 |
2020 | 1 |
2023 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
Page 1
Stiff person spectrum disorder diagnosis, misdiagnosis, and suggested diagnostic criteria.
Ann Clin Transl Neurol. 2023 Jul;10(7):1083-1094. doi: 10.1002/acn3.51791. Epub 2023 May 22.
Ann Clin Transl Neurol. 2023.
PMID: 37212351
Free PMC article.
SPSD more often had hypertonia (60% vs. 24%, p < 0.001), hyperreflexia (71% vs. 43%, p = 0.001), and lumbar hyperlordosis (67% vs. 9%, p < 0.001) and less likely functional neurologic signs (6% vs. 33%, p = 0.001). ...
A narrative review on spinal deformities in people with cerebral palsy: Measurement, norm values, incidence, risk factors and treatment.
Britz E, Langerak NG, Lamberts RP.
Britz E, et al.
S Afr Med J. 2020 Jul 29;110(8):767-776. doi: 10.7196/SAMJ.2020.v110i8.14472.
S Afr Med J. 2020.
PMID: 32880305
Review.
There is especially a worry about the increase of scoliosis, thoracic hyperkyphosis, lumbar hyperlordosis, spondylolysis and spondylolisthesis incidence, though supporting literature is lacking. ...
There is especially a worry about the increase of scoliosis, thoracic hyperkyphosis, lumbar hyperlordosis, spondylolysis and s …
Item in Clipboard
Height outcome of short children with hypochondroplasia after recombinant human growth hormone treatment: a meta-analysis.
Massart F, Miccoli M, Baggiani A, Bertelloni S.
Massart F, et al.
Pharmacogenomics. 2015 Nov;16(17):1965-73. doi: 10.2217/pgs.15.129. Epub 2015 Nov 10.
Pharmacogenomics. 2015.
PMID: 26555758
Hypochondroplasia (HCH) is a genetic skeletal dysplasia, characterized by rhizomelic short height (Ht) with facial dysmorphology and lumbar hyperlordosis. Albeit there are concerns that HCH children may not achieve optimal long-term outcome in response to recombinan …
Hypochondroplasia (HCH) is a genetic skeletal dysplasia, characterized by rhizomelic short height (Ht) with facial dysmorphology and lumb …
Item in Clipboard
Cite
Cite