A. Camacho Salas

Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy

J. J. Padilla, A. N. Osorio, M. Madruga Garrido, 2019, Neurología (English Edition).

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.

M. Gómez Gallego, I. Jericó, J. Díaz-Manera, 2020, Neurologia.

Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies

M. D. de Castro, P. Sánchez-Pintos, M. Couce, 2022, Journal of clinical medicine.

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease

M. Gómez Gallego, I. Jericó, J. Díaz-Manera, 2019, Neurología (English Edition).

Consensus on the diagnosis, treatment and follow-up of patients with Duchenne muscular dystrophy.

M. Madruga Garrido, A. Nascimento Osorio, J. Medina Cantillo, 2018, Neurologia.

[TSC2/PKD1 contiguous gene deletion syndrome].

A. Camacho Salas, C. Moreno, R. S. L. Heras, 2013, Anales de pediatria.

[TSC2/PKD1 contiguous gene deletion syndrome].

A. Camacho Salas, C. Vidales Moreno, R. Simón de la Heras, 2013, Anales de pediatria.