New mutation in the CPOX gene associated with hereditary coproporphyria by Motos Garcia, J.A, Garcia Lax, N, Martinez Navarro, M.L, Garcia Medina, A.M, Sanz Monllor, A, Palao Rico, M, Sanchez Ortuño, I, Iniesta Valera, J.A, Rodriguez Garcia, J.M, Marin Marin, J, Salmeron Ato, M.P, Diaz Ortuño, A

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Gradenigo's syndrome: A case report by Palao Rico, M., Motos Garcia, J.A., Garcia Lax, N., Pellicer Espinosa, I., Marin Marin, J.

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Ischemic optic neuropathies: A case series study by Motos Garcia, J.A., Palao Rico, M., Pellicer Espinosa, I., Garcia Lax, N., Marin Marin, J.

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Paresthesias: A case series study by Motos Garcia, J.A., Garcia Lax, N., Palao Rico, M., Pellicer Espinosa, I., Martinez Navarro, M.L.

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X-linked-adrenoleukodistrophy with a new mutation in the ABCD1 gene by García Lax, N, Marín Marín, J, Sánchez Ayaso, P.A, García Medina, A.M, Sánchez Ortuño, I, Sanz Monllor, A, Motos García, J.A, Palao Rico, M, Salmerón Ato, M.P, Martínez Navarro, M.L, Iniesta Valera, J.A, Díaz Ortuño, A

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Neuropatía aislada del sexto nervio craneal. Una manifestación inusual de preeclampsia by Baidez Guerrero, A.E., García Lax, N., Hernández Clares, R., Martín Fernández, J.J.

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Comparison of Tissue Molecular Biomarker Testing Turnaround Times and Concordance Between Standard of Care and the Biocartis Idylla Platform in Patients With Colorectal Cancer by Tsongalis, Gregory J, Al Turkmani, M Rabie, Suriawinata, Michael, Babcock, Michael J, Mitchell, Kristi, Ding, Yi, Scicchitano, Lisa, Tira, Adrian, Buckingham, Lela, Atkinson, Sara, Lax, Amy, Aisner, Dara L, Davies, Kurtis D, Wood, Holly N, O’Neill, Stacey S, Levine, Edward A, Sequeira, Judy, Harada, Shuko, DeFrank, Gina, Paluri, Ravikumar, Tan, Bradford A, Colabella, Heather, Snead, Christopher, Cruz-Correa, Marcia, Ramirez, Virginia, Rojas, Arnaldo, Huang, Huiya, Mackinnon, Alexander C, Garcia, Fernando U, Cavone, Sharon M, Elfahal, Mutasim, Abel, Gyorgy, Vasef, Mohammad A, Judd, Andrew, Linder, Mark W, Alkhateeb, Khaled, Skinner, William L, Boccia, Ralph, Patel, Kashyap

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Diagnosis and management of isolated serous tubal intraepithelial carcinoma: A qualitative focus group study by Negri, Serena, Fisch, Charlotte, Hullu, Joanne A., Bommel, Majke, Simons, Michiel, Bogaerts, Joep, Apperloo, Mirjam J.A., Baiocchi, Glauco, Bakker, Janine L., Bart, Joost, Beekhuizen, Heleen J., Bernardini, Marcus Q., Boere, Ingrid, Bulten, Johan, Chen, Lee‐may, Chrzan, Alicja, Dørum, Anne, Ewing‐Graham, Patricia C., Ferrero, Annamaria, Flöter Rådestad, Angelique, Fruscio, Robert, Gaarenstroom, Katja N., Garcia, Christine, Harter, Philipp, Hoogstad‐van Evert, Janneke S., Iaco, Pierandrea, Klooster, Astrid, Kooreman, Loes F.S., Jacobsen, Michelle, Kruse, Arnold‐Jan, Kwon, Janice S., Lawson, Barrett C., Lax, Sigurd F., Lonkhuijzen, Luc R.C.W., Lu, Karen H., Manchanda, Ranjit, Marchetti, Claudia, McCluggage, W. Glenn, McNally, Orla M., Mourits, Marian J.E., Nicum, Shibani, Norquist, Barbara M., Perrone, Anna Myriam, Piek, Jurgen M.J., Polastro, Laura, Polee, Marco B., Rabban, Joseph T., Reesink, Nathalie, Reyes Oliver Pérez, Maria, Roes, Eva‐Maria, Rychlik, Agnieszka, Shih, Ie‐Ming, Soong, T. Rinda, Speiser, Paul, Stone, Rebecca L., Tamussino, Karl, Tognon, Germana, Tuninetti, Valentina, Valabrega, Giorgio, Vos, M. Caroline, Welz, Julia, Zizioli, Valentina, Hermens, Rosella P. M. G., Steenbeek, Miranda P.

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Changes in chronobiological function related to retina degeneration P23H line 1 transgenic rats by PINILLA, I, LAX, P, FUENTES, L, FERNANDEZ‐SANCHEZ, L, ESQUIVA, GEMA, PEREZ‐GARCIA, D, RAMIRO, P, SANCHEZ‐CANO, A, SEGURA, F, CUENCA, N

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