Visualitza per autor "Domínguez-Gonzalez, C."
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Collaborative model for diagnosis and treatment of very rare diseases: experience in Spain with thymidine kinase 2 deficiency
Domínguez-Gonzalez, C.; Madruga‑Garrido, Marcos; Hirano, Michio; Martí, Itxaso; Martín, Miguel A.; Munell Casadesus, Francina; Martí Seves, Ramón (BMC, 2021-10-02) -
Identification of Potential Muscle Biomarkers in McArdle Disease: Insights from Muscle Proteome Analysis
Garcia-Consuegra Galiana, Ines; Asensio-Peña, Sara; Garrido Moraga, Rocio; Pinós Figueras, Tomàs; Domínguez-Gonzalez, C.; Santalla Hernández, Alfredo (MDPI, 2022-04-22) -
Late-onset thymidine kinase 2 deficiency: a review of 18 cases
Domínguez-Gonzalez, C.; Hernández-Laín, Aurelio; Rivas, Eloy; Hernández-Voth, Ana; Sayas Catalán, Javier; Fernández-Torrón, Roberto; García Arumí, Elena (BMC, 2019-05-06) -
Survey on the management of Pompe disease in routine clinical practice in Spain
Domínguez-Gonzalez, C.; Díaz Marín, Carmen; Juntas Morales, Raul; Nascimiento‑Osorio, Andrés; Rivera‑Gallego, Alberto; Díaz-Manera, Jordi (BMC, 2022-11-05)