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Raquel Montero

Showing results (51-60 of 55) with videos related to

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Journal of Clinical Medicine|January 13, 2019
Muscle Involvement in a Large Cohort of Pediatric Patients with Genetic Diagnosis of Mitochondrial DiseaseCristina Jou, Juan D Ortigoza-Escobar, Maria M O'Callaghan, et al.
Stem Cells (Dayton, Ohio)|May 5, 2017
Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q<sub>10</sub> DeficiencyDamià Romero-Moya, Carlos Santos-Ocaña, Julio Castaño, et al.
Orphanet Journal of Rare Diseases|December 31, 2015
Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disordersLinda Cassis, Elisenda Cortès-Saladelafont, Marta Molero-Luis, et al.
Journal of Inherited Metabolic Disease|July 25, 2019
Clinical presentation and proteomic signature of patients with TANGO2 mutationsNadja Mingirulli, Angela Pyle, Denisa Hathazi, et al.
Mitochondrion|July 5, 2016
Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disordersDelia Yubero, Raquel Montero, Miguel A Martín, et al.
Pageof 6

Showing results (51-60 of 55) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 55 results.
Journal of Clinical Medicine|January 13, 2019
Muscle Involvement in a Large Cohort of Pediatric Patients with Genetic Diagnosis of Mitochondrial DiseaseCristina Jou, Juan D Ortigoza-Escobar, Maria M O'Callaghan, et al.
Stem Cells (Dayton, Ohio)|May 5, 2017
Genetic Rescue of Mitochondrial and Skeletal Muscle Impairment in an Induced Pluripotent Stem Cells Model of Coenzyme Q<sub>10</sub> DeficiencyDamià Romero-Moya, Carlos Santos-Ocaña, Julio Castaño, et al.
Orphanet Journal of Rare Diseases|December 31, 2015
Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disordersLinda Cassis, Elisenda Cortès-Saladelafont, Marta Molero-Luis, et al.
Journal of Inherited Metabolic Disease|July 25, 2019
Clinical presentation and proteomic signature of patients with TANGO2 mutationsNadja Mingirulli, Angela Pyle, Denisa Hathazi, et al.
Mitochondrion|July 5, 2016
Secondary coenzyme Q10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disordersDelia Yubero, Raquel Montero, Miguel A Martín, et al.
Pageof 6