A new tool for the paediatric HIV research: general data from the Cohort of the Spanish Paediatric HIV Network (CoRISpe)

Por de Jose, Ma Isabel, Jiménez de Ory, Santiago, Espiau, Maria, Fortuny, Claudia, Navarro, Ma Luisa, Soler-Palacín, Pere, Muñoz-Fernandez, Ma Angeles
Publicado em 2013

Complement factor I deficiency: a not so rare immune defect. Characterization of new mutations and the first large gene deletion

Por Alba-Domínguez, María, López-Lera, Alberto, Garrido, Sofía, Nozal, Pilar, González-Granado, Ignacio, Melero, Josefa, Soler-Palacín, Pere, Cámara, Carmen, López-Trascasa, Margarita
Publicado em 2012

Clinical Experience With an L-Proline–Stabilized 10 % Intravenous Immunoglobulin (Privigen®): Real-Life Effectiveness and Tolerability

Por Dorsey, Morna J., Ho, Viet, Mabudian, Mohsen, Soler-Palacín, Pere, Domínguez-Pinilla, Nerea, Rishi, Radha, Rishi, Rahul, Wong, Duane, Rojavin, Mikhail, Hubsch, Alphonse, Berger, Melvin
Publicado em 2014

Off-label use of rilpivirine in combination with emtricitabine and tenofovir in HIV-1-infected pediatric patients: A multicenter study

Por Falcon-Neyra, Lola, Palladino, Claudia, Navarro Gómez, María Luisa, Soler-Palacín, Pere, González-Tomé, María Isabel, De Ory, Santiago J., Frick, Marie Antoinette, Fortuny, Clàudia, Noguera-Julian, Antoni, Moreno, Elena Bermúdez, Santos, Juan Luis, Olbrich, Peter, López-Cortés, Luis F., Briz, Verónica, Neth, Olaf
Publicado no Medicine (Baltimore) (2016)

Primary immunodeficiency associated with chromosomal aberration – an ESID survey

Por Schatorjé, Ellen, van der Flier, Michiel, Seppänen, Mikko, Browning, Michael, Morsheimer, Megan, Henriet, Stefanie, Neves, João Farela, Vinh, Donald Cuong, Alsina, Laia, Grumach, Anete, Soler-Palacin, Pere, Boyce, Thomas, Celmeli, Fatih, Goudouris, Ekaterini, Hayman, Grant, Herriot, Richard, Förster-Waldl, Elisabeth, Seidel, Markus, Simons, Annet, de Vries, Esther
Publicado no Orphanet J Rare Dis (2016)

AP1S3 Mutations Cause Skin Autoinflammation by Disrupting Keratinocyte Autophagy and Up-Regulating IL-36 Production

Por Mahil, Satveer K., Twelves, Sophie, Farkas, Katalin, Setta-Kaffetzi, Niovi, Burden, A. David, Gach, Joanna E., Irvine, Alan D., Képíró, László, Mockenhaupt, Maja, Oon, Hazel H., Pinner, Jason, Ranki, Annamari, Seyger, Marieke M.B., Soler-Palacin, Pere, Storan, Eoin R., Tan, Eugene S., Valeyrie-Allanore, Laurence, Young, Helen S., Trembath, Richard C., Choon, Siew-Eng, Szell, Marta, Bata-Csorgo, Zsuzsanna, Smith, Catherine H., Di Meglio, Paola, Barker, Jonathan N., Capon, Francesca
Publicado no J Invest Dermatol (2016)

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency

Por Lee, Yu Nee, Frugoni, Francesco, Dobbs, Kerry, Walter, Jolan E., Giliani, Silvia, Gennery, Andrew R., Al-Herz, Waleed, Haddad, Elie, LeDeist, Francoise, Bleesing, Jack H., Henderson, Lauren A., Pai, Sung-Yun, Nelson, Robert P., El-Ghoneimy, Dalia H., El-Feky, Reem A., Reda, Shereen M., Hossny, Elham, Soler-Palacin, Pere, Fuleihan, Ramsay L., Patel, Niraj C., Massaad, Michel J., Geha, Raif S., Puck, Jennifer M., Palma, Paolo, Cancrini, Caterina, Chen, Karin, Vihinen, Mauno, Alt, Frederick W., Notarangelo, Luigi D.
Publicado em 2013

The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis

Por Bode, Sebastian FN, Ammann, Sandra, Al-Herz, Waleed, Bataneant, Mihaela, Dvorak, Christopher C, Gehring, Stephan, Gennery, Andrew, Gilmour, Kimberly C, Gonzalez-Granado, Luis I, Groß-Wieltsch, Ute, Ifversen, Marianne, Lingman-Framme, Jenny, Matthes-Martin, Susanne, Mesters, Rolf, Meyts, Isabelle, van Montfrans, Joris M, Schmid, Jana Pachlopnik, Pai, Sung-Yun, Soler-Palacin, Pere, Schuermann, Uta, Schuster, Volker, Seidel, Markus G., Speckmann, Carsten, Stepensky, Polina, Sykora, Karl-Walter, Tesi, Bianca, Vraetz, Thomas, Waruiru, Catherine, Bryceson, Yenan T., Moshous, Despina, Lehmberg, Kai, Jordan, Michael B, Ehl, Stephan
Publicado no Haematologica (2015)