E-LIB Suche - Ergebnisse für: Delobel, Bruno

1

Missense variants in ANO4 cause sporadic encephalopathic or..:

Yang, Fang ; Begemann, Anais ; Reichhart, Nadine...
The American Journal of Human Genetics. 111 (2024) 6 - p. 1184-1205 , 2024

Link: https://doi.org/10.1016/..

2

Novel pathogenic variants in SLCO2A1 causing autosomal domi..:

Bloch, Adrien ; Couture, Guillaume ; Isidor, Bertrand...
European Journal of Medical Genetics. 66 (2023) 2 - p. 104689 , 2023

Link: https://doi.org/10.1016/..

3

Growth charts in DYRK1A syndrome:

Lanvin, Pierre‐Louis ; Goronflot, Thomas ; Isidor, Bertrand...
American Journal of Medical Genetics Part A. 194 (2023) 1 - p. 9-16 , 2023

Link: https://doi.org/10.1002/..

4

3D Operando Monitoring of Lithiation Spatial Composition in..:

Nguyen, Tuan-Tu ; Xu, Jiahui ; Su, Zeliang...
Microscopy and Microanalysis. 28 (2022) S1 - p. 194-196 , 2022

Link: https://doi.org/10.1017/..

5

Understanding the new BRD4‐related syndrome: Clinical and g..:

Jouret, Guillaume ; Heide, Solveig ; Sorlin, Arthur...
Clinical Genetics. 102 (2022) 2 - p. 117-122 , 2022

Link: https://doi.org/10.1111/..

6

1p36 deletion syndrome: Review and mapping with further cha..:

Jacquin, Clémence ; Landais, Emilie ; Poirsier, Céline...
American Journal of Medical Genetics Part A. 191 (2022) 2 - p. 445-458 , 2022

Link: https://doi.org/10.1002/..

7

Mathematical Modeling of Energy-Dense NMC Electrodes: I. De..:

Nguyen, Tuan-Tu ; Delobel, Bruno ; Berthe, Maxime...
Journal of The Electrochemical Society. 169 (2022) 4 - p. 040546 , 2022

Link: https://doi.org/10.1149/..

8

Mathematical Modeling of Energy-dense NMC Electrodes: Part ..:

Nguyen, Tuan-Tu ; Delobel, Bruno ; Demortière, Arnaud.
Journal of The Electrochemical Society. 169 (2022) 6 - p. 060510 , 2022

Link: https://doi.org/10.1149/..

9

3D Quantification of Microstructural Properties of LiNi0.5M..:

Nguyen, Tuan‐Tu ; Villanova, Julie ; Su, Zeliang...
Advanced Energy Materials. 11 (2021) 8 - p. , 2021

Link: https://doi.org/10.1002/..

10

Neurodevelopmental phenotype in 36 new patients with 8p inv..:

Vibert, Roseline ; Mignot, Cyril ; Keren, Boris...
Clinical Genetics. 101 (2021) 3 - p. 307-316 , 2021

Link: https://doi.org/10.1111/..

11

Integrative approach to interpret DYRK1A variants, leading ..:

Courraud, Jérémie ; Chater-Diehl, Eric ; Durand, Benjamin...
Genetics in Medicine. 23 (2021) 11 - p. 2150-2159 , 2021

Link: https://doi.org/10.1038/..

12

High reactivity of the nickel-rich LiNi1-x-yMnxCoyO2 layere..:

Martinez, Ana Cristina ; Grugeon, Sylvie ; Cailleu, Dominique...
Journal of Power Sources. 468 (2020) - p. 228204 , 2020

Link: https://doi.org/10.1016/..

13

Further delineation of the female phenotype with KDM5C dise..:

Carmignac, Virginie ; Nambot, Sophie ; Lehalle, Daphné...
Clinical Genetics. 98 (2020) 1 - p. 43-55 , 2020

Link: https://doi.org/10.1111/..

14

The electrode tortuosity factor: why the conventional tortu..:

Nguyen, Tuan-Tu ; Demortière, Arnaud ; Fleutot, Benoit...
npj Computational Materials. 6 (2020) 1 - p. , 2020

Link: https://doi.org/10.1038/..

15

BLOC1S5 pathogenic variants cause a new type of Hermansky–P..:

Pennamen, Perrine ; Le, Linh ; Tingaud-Sequeira, Angèle...
Genetics in Medicine. 22 (2020) 10 - p. 1613-1622 , 2020

Link: https://doi.org/10.1038/..