Sol Balsells

发表

Chromosome Microarray Analysis for the Investigation of Deletions in Pediatric Movement Disorders: A Systematic Review of the Literature

L. Soliani, Cristina Hernando-Davalillo, J. Ortigoza-Escobar, 2023, Movement disorders clinical practice.

Full-Length SMN Transcript in Extracellular Vesicles as Biomarker in Individuals with Spinal Muscular Atrophy Type 2 Treated with Nusinersen

C. Ortez, D. Alcolea, C. Jiménez-Mallebrera, 2023, Journal of neuromuscular diseases.

Coexistence of junctional epidermolysis bullosa, autosomal recessive deafness type 57, and Angelman syndrome: A case report

J. Armstrong, L. Martorell, M. Serrano, 2023, Clinical case reports.

Factors involved in changes in the levator ani during pregnancy

D. Parés, Laura Altimira Queral, Eva Martínez Franco, 2023, International Urogynecology Journal.