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ACS Nano|May 23, 2018
Compression-Induced Modification of Boron Nitride Layers: A Conductive Two-Dimensional BN CompoundAna P M Barboza, Matheus J S Matos, Helio Chacham, et al.
Journal of Inherited Metabolic Disease|August 18, 2009
Glyceryl triacetate for Canavan disease: a low-dose trial in infants and evaluation of a higher dose for toxicity in the tremor rat modelC N Madhavarao, P Arun, Y Anikster, et al.
American Journal of Medical Genetics. Part A|August 26, 2021
Deep intronic variant in the ARSB gene as the genetic cause for Maroteaux-Lamy syndrome (MPS VI)Dina Marek-Yagel, Aviva Eliyahu, Alvit Veber, et al.
Clinical Genetics|March 12, 2020
B4GALT1-congenital disorders of glycosylation: Expansion of the phenotypic and molecular spectrum and review of the literatureOrna Staretz-Chacham, Iris Noyman, Ohad Wormser, et al.
Pediatric Nephrology (Berlin, Germany)|April 20, 2019
Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in childrenAsaf Vivante, Orna Staretz Chacham, Shirlee Shril, et al.
Journal of Inherited Metabolic Disease|November 15, 2015
Primary and maternal 3-methylcrotonyl-CoA carboxylase deficiency: insights from the Israel newborn screening programJonathan Rips, Shlomo Almashanu, Hanna Mandel, et al.
Journal of Inherited Metabolic Disease|July 23, 2024
The natural history of dihydrolipoamide dehydrogenase deficiency in IsraelBen Pode-Shakked, Yuval E Landau, Nava Shaul Lotan, et al.
Physical Review Letters|July 23, 2008
Deformation induced semiconductor-metal transition in single wall carbon nanotubes probed by electric force microscopyA P M Barboza, A P Gomes, B S Archanjo, et al.
ACS Omega|March 31, 2022
Aerosol-Printed MoS<sub>2</sub> Ink as a High Sensitivity Humidity SensorNeuma M Pereira, Natália P Rezende, Thiago H R Cunha, et al.
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