E-LIB Suche - Ergebnisse für: Spinazzola, A

1

DMD – ANIMAL MODELS:

Lambert, M. ; Zhang, Y. ; Spinazzola, J....
Neuromuscular Disorders. 31 (2021) - p. S78 , 2021

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

2

PRE-CLINICAL DEVELOPMENTS IN NEUROMUSCULAR DISORDERS:

Zhang, Y. ; Lambert, M. ; Widrick, J....
Neuromuscular Disorders. 31 (2021) - p. S161 , 2021

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

3

The mitochondrial type IB topoisomerase drives mitochondria..:

Baechler, S. A. ; Factor, V. M. ; Dalla Rosa, I....
Nature Communications. 10 (2019) 1 - p. , 2019

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

4

Mitochondrial ribosomal protein S25 (MRPS25) mutations impa..:

Bugiardini, E. ; Mitchell, A. ; Dalla Rosa, I....
Neuromuscular Disorders. 28 (2018) - p. S30-S31 , 2018

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

5

Mitochondrial nucleoid interacting proteins support mitocho..:

He, J. ; Cooper, H. M. ; Reyes, A....
Nucleic Acids Research. 40 (2012) 13 - p. 6109-6121 , 2012

Link: https://doi.org/10.1093/..

6

Mitochondrial DNA mutations and depletion in pediatric medi..:

Spinazzola, A.
Seminars in Fetal and Neonatal Medicine. 16 (2011) 4 - p. 190-196 , 2011

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

7

EFNS guidelines for the molecular diagnosis of neurogenetic..:

Burgunder, J.‐M. ; Schöls, L. ; Baets, J....
European Journal of Neurology. 18 (2011) 2 - p. 207-217 , 2011

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

8

EFNS guidelines on the molecular diagnosis of channelopathi..:

Burgunder, J‐M. ; Finsterer, J. ; Szolnoki, Z....
European Journal of Neurology. 17 (2010) 5 - p. 641-648 , 2010

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

9

EFNS guidelines on the molecular diagnosis of ataxias and s..:

Gasser, T. ; Finsterer, J. ; Baets, J....
European Journal of Neurology. 17 (2010) 2 - p. 179-188 , 2010

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

10

EFNS guidelines on the molecular diagnosis of mitochondrial..:

Finsterer, J. ; Harbo, H. F. ; Baets, J....
European Journal of Neurology. 16 (2009) 12 - p. 1255-1264 , 2009

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

11

Collated mutations in mitochondrial DNA (mtDNA) depletion s..:

Poulton, J. ; Hirano, M. ; Spinazzola, A....
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792 (2009) 12 - p. 1109-1112 , 2009

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

12

Disorders from perturbations of nuclear‐mitochondrial inter..:

Spinazzola, A. ; Zeviani, M.
Journal of Internal Medicine. 265 (2009) 2 - p. 174-192 , 2009

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

13

T.P.4.04 Automated drug screening with contractile muscle t..:

Vandenburgh, H. ; Shansky, J. ; Benesch-Lee, F....
Neuromuscular Disorders. 19 (2009) 8-9 - p. 614 , 2009

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

14

EFNS guidelines on the molecular diagnosis of neurogenetic ..:

Harbo, H. F. ; Finsterer, J. ; Baets, J....
European Journal of Neurology. 16 (2009) 7 - p. 777-785 , 2009

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

15

Clinical and molecular features of mitochondrial DNA deplet..:

Spinazzola, A. ; Invernizzi, F. ; Carrara, F....
Journal of Inherited Metabolic Disease. 32 (2008) 2 - p. 143-158 , 2008

Link: https://doi.org/10.1007/..