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International Journal of Molecular Sciences
|
October 14, 2022
Pathological Features in Paediatric Patients with TK2 Deficiency
Cristina Jou, Andres Nascimento, Anna Codina, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2024
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases
Berta Estévez-Arias, Leslie Matalonga, Delia Yubero, et al.
Journal of Clinical Medicine
|
January 13, 2019
Muscle Involvement in a Large Cohort of Pediatric Patients with Genetic Diagnosis of Mitochondrial Disease
Cristina Jou, Juan D Ortigoza-Escobar, Maria M O'Callaghan, et al.
European Journal of Pediatrics
|
March 14, 2023
SARS-CoV-2 transmission in teenagers and young adults in Fútbol Club Barcelona's Multidisciplinary Sports Training Academy
María Hernández-García, Quique Bassat, Victoria Fumado, et al.
Frontiers in Immunology
|
February 14, 2022
Multiplex Antibody Analysis of IgM, IgA and IgG to SARS-CoV-2 in Saliva and Serum From Infected Children and Their Close Contacts
Carlota Dobaño, Selena Alonso, Marta Vidal, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
March 12, 2021
Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 Infection Among Children in Summer Schools Applying Stringent Control Measures in Barcelona, Spain
Iolanda Jordan, Mariona Fernandez de Sevilla, Victoria Fumado, et al.
Acta Neuropathologica
|
February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
Andres Nascimento, Christine C Bruels, Sandra Donkervoort, et al.
Journal of Medical Genetics
|
May 17, 2023
Expanding the phenotypic spectrum of <i>TRAPPC11-</i>related muscular dystrophy: 25 Roma individuals carrying a founder variant
Maria Justel, Cristina Jou, Andrea Sariego-Jamardo, et al.
Brain Communications
|
October 3, 2025
Clinical and molecular characterization of SLC31A1-related developmental and epileptic encephalopathy: insights from 13 new cases
Natalia Juliá-Palacios, Gerard Muñoz-Pujol, Reza Maroofian, et al.
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of 5
Search research articles
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Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
International Journal of Molecular Sciences
|
October 14, 2022
Pathological Features in Paediatric Patients with TK2 Deficiency
Cristina Jou, Andres Nascimento, Anna Codina, et al.
European Journal of Human Genetics : EJHG
|
September 27, 2024
Phenotype-driven genomics enhance diagnosis in children with unresolved neuromuscular diseases
Berta Estévez-Arias, Leslie Matalonga, Delia Yubero, et al.
Journal of Clinical Medicine
|
January 13, 2019
Muscle Involvement in a Large Cohort of Pediatric Patients with Genetic Diagnosis of Mitochondrial Disease
Cristina Jou, Juan D Ortigoza-Escobar, Maria M O'Callaghan, et al.
European Journal of Pediatrics
|
March 14, 2023
SARS-CoV-2 transmission in teenagers and young adults in Fútbol Club Barcelona's Multidisciplinary Sports Training Academy
María Hernández-García, Quique Bassat, Victoria Fumado, et al.
Frontiers in Immunology
|
February 14, 2022
Multiplex Antibody Analysis of IgM, IgA and IgG to SARS-CoV-2 in Saliva and Serum From Infected Children and Their Close Contacts
Carlota Dobaño, Selena Alonso, Marta Vidal, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America
|
March 12, 2021
Transmission of Severe Acute Respiratory Syndrome Coronavirus 2 Infection Among Children in Summer Schools Applying Stringent Control Measures in Barcelona, Spain
Iolanda Jordan, Mariona Fernandez de Sevilla, Victoria Fumado, et al.
Acta Neuropathologica
|
February 17, 2023
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy
Andres Nascimento, Christine C Bruels, Sandra Donkervoort, et al.
Journal of Medical Genetics
|
May 17, 2023
Expanding the phenotypic spectrum of <i>TRAPPC11-</i>related muscular dystrophy: 25 Roma individuals carrying a founder variant
Maria Justel, Cristina Jou, Andrea Sariego-Jamardo, et al.
Brain Communications
|
October 3, 2025
Clinical and molecular characterization of SLC31A1-related developmental and epileptic encephalopathy: insights from 13 new cases
Natalia Juliá-Palacios, Gerard Muñoz-Pujol, Reza Maroofian, et al.
Page
of 5