Suchergebnisse - "Berardo, Andres"

PubPharm (35)

1

Blockade of Rho-associated kinase prevents inhibition of axon regeneration of peripheral nerves induced by anti-ganglioside antibodies

enthalten in: Neural regeneration research | 2024

von Berardo, A. | Bacaglio, C. | Báez, B. | +3

2

Advances in Thymidine Kinase 2 Deficiency : Clinical Aspects, Translational Progress, and Emerging Therapies

enthalten in: Journal of neuromuscular diseases | 2022

von Berardo, A. | Domínguez-González, C. | Engelstad, K. | +1

3

Regulatory environment for novel therapeutic development in mitochondrial diseases

enthalten in: Journal of inherited metabolic disease | 2021

von Hirano, M. | Berardo, A. | Barca, E. | +6

4

Regulatory environment for novel therapeutic development in mitochondrial diseases

enthalten in: Journal of Inherited Metabolic Disease | 2021

von Hirano, M. | Berardo, A. | Barca, E. | +6

5

Growth Differentiation Factor 15 is a potential biomarker of therapeutic response for TK2 deficient myopathy

enthalten in: Scientific reports | 2020

von Dominguez-Gonzalez, C. | Badosa, C. | Madruga-Garrido, M. | +23

6

Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6

enthalten in: Journal of neurology | 2020

von Berardo, A. | Emmanuele, V. | Vargas, W. | +3

7

Redefining infantile-onset multisystem phenotypes of coenzyme Q10-deficiency in the next-generation sequencing era

enthalten in: Journal of translational genetics and genomics | 2020

von Berardo, A. | Quinzii, C.

8

Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6

enthalten in: Journal of neurology | 2019

von Berardo, A. | Emmanuele, V. | Vargas, W. | +3

9

Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6

enthalten in: Journal of neurology | 2019

von Berardo, A. | Emmanuele, V. | Vargas, W. | +3

10

Leber hereditary optic neuropathy plus dystonia, and transverse myelitis due to double mutations in MT-ND4 and MT-ND6

enthalten in: Journal of neurology | 2019

von Berardo, A. | Emmanuele, V. | Vargas, W. | +3