L. Pirra

Genetic characterization of Limb Girdle Muscular Dystrophies and Pompe Disease in a large Argentine serie

R. Reisin, C. Marchesoni, M. Schiava, 2022, Neurology Perspectives.

SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome.

R. Finkel, P. Bauer, M. Baudis, 2013, Brain : a journal of neurology.

The difficult path to diagnosis of the patient with spinal muscular atrophy.

A. Jáuregui, L. Pirra, A. Dubrovsky, 2022, Archivos argentinos de pediatria.

Integrated DNA, cDNA, and protein studies in Becker muscular dystrophy show high exception to the reading frame rule

E. Hoffman, A. Kesari, E. Gordon, 2008, Human mutation.

Intraneural perineuriomas: diagnostic value of magnetic resonance neurography

S. Monges, A. Taratuto, M. Socolovsky, 2018, Journal of the peripheral nervous system : JPNS.

C.P.4.11 Ragged red fibres finding in muscle biopsy of dynamin 2-related centronuclear myopathy

N. Romero, M. Bitoun, A. Taratuto, 2007, Neuromuscular Disorders.

Time distribution of epileptic seizures during video-EEG monitoring. Implications for health insurance systems in developing countries

A. Rabinowicz, R. Leiguarda, L. Pirra, 1997, Seizure.