Found: 8
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Rare cases of congenital arthrogryposis multiplex caused by novel recurrent CHRNG mutations.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 4, p. 213, doi. 10.1038/jhg.2015.2
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- Publication type:
- Article
GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.
- Published in:
- 2017
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- Publication type:
- journal article
Battery-free, wireless soft sensors for continuous multi-site measurements of pressure and temperature from patients at risk for pressure injuries.
- Published in:
- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-25324-w
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- Publication type:
- Article
Author Correction: Battery-free, wireless soft sensors for continuous multi-site measurements of pressure and temperature from patients at risk for pressure injuries.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Wireless, multimodal sensors for continuous measurement of pressure, temperature, and hydration of patients in wheelchair.
- Published in:
- NPJ Flexible Electronics, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41528-023-00238-3
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- Publication type:
- Article
An early seizure variant type of a male Rett syndrome patient with a MECP2 p.Arg133His missense mutation.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 3, p. N.PAG, doi. 10.1002/mgg3.532
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- Publication type:
- Article
Battery‐Free, Wireless, Ionic Liquid Sensor Arrays to Monitor Pressure and Temperature of Patients in Bed and Wheelchair.
- Published in:
- Small, 2023, v. 19, n. 9, p. 1, doi. 10.1002/smll.202205048
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- Publication type:
- Article
Battery‐Free, Wireless, Ionic Liquid Sensor Arrays to Monitor Pressure and Temperature of Patients in Bed and Wheelchair.
- Published in:
- Small, 2023, v. 19, n. 9, p. 1, doi. 10.1002/smll.202205048
- By:
- Publication type:
- Article