Directional coupling of oligodendrocyte connexin‐47 and astrocyte connexin‐43 gap junctions by Fasciani, Ilaria, Pluta, Paula, González‐Nieto, Daniel, Martínez‐Montero, Paloma, Molano, Jesús, Paíno, Carlos L., Millet, Oscar, Barrio, Luis C.

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Regulation of connexin hemichannel activity by membrane potential and the extracellular calcium in health and disease by Fasciani, Ilaria, Temperán, Ana, Pérez-Atencio, Leonel F., Escudero, Adela, Martínez-Montero, Paloma, Molano, Jesús, Gómez-Hernández, Juan M., Paino, Carlos L., González-Nieto, Daniel, Barrio, Luis C.

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Myotonia congenita: mutation spectrum of CLCN1 in Spanish patients by Palma Milla, Carmen, Prior De Castro, Carmen, Gómez-González, Clara, Martínez-Montero, Paloma, I. Pascual Pascual, Samuel, Molano Mateos, Jesús

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Fast skeletal myofibers of mdx mouse, model of Duchenne muscular dystrophy, express connexin hemichannels that lead to apoptosis by Cea, Luis A., Puebla, Carlos, Cisterna, Bruno A., Escamilla, Rosalba, Vargas, Aníbal A., Frank, Marina, Martínez-Montero, Paloma, Prior, Carmen, Molano, Jesús, Esteban-Rodríguez, Isabel, Pascual, Ignacio, Gallano, Pía, Lorenzo, Gustavo, Pian, Héctor, Barrio, Luis C., Willecke, Klaus, Sáez, Juan C.

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A SCN4A mutation causing paramyotonia congenita by Palma, Carmen, Prior, Carmen, Gómez-González, Clara, Rodríguez-Antolin, Carlos, Martínez-Montero, Paloma, Pérez de Ayala, Lucía, Pascual, Samuel I., Molano Mateos, Jesús

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A novel PLP1 deletion causing classic Pelizaeus-Merzbacher disease by Prior, Carmen, Muñoz-Calero, Maria, Gómez-Gonzalez, Clara, Martinez-Montero, Paloma, Barrio, Luis, Poo, Pilar, Martorell, Loreto, Molano, Jesus

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A novel PLP1 deletion causing classic Pelizaeus-Merzbacher disease by Prior, Carmen, Muñoz-Calero, Maria, Gómez-Gonzalez, Clara, Martinez-Montero, Paloma, Barrio, Luis, Poo, Pilar, Martorell, Loreto, Molano, Jesus

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