Resultados da busca - Ramelli, Gian Paolo

Blake’s pouch cyst in children: Atypical clinical presentation por Bontognali, Martina, Poretti, Andrea, Guzman, Raphael, Huisman, Thierry AGM, Ramelli, Gian Paolo

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Sleep‐Related Disorders in Children with Attention‐Deficit Hyperactivity Disorder: Preliminary Results of a Full Sleep Assessment Study por Miano, Silvia, Esposito, Maria, Foderaro, Giuseppe, Ramelli, Gian Paolo, Pezzoli, Valdo, Manconi, Mauro

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Regional differences in symptomatic fever management among paediatricians in Switzerland: the results of a cross-sectional Web-based survey por Lava, Sebastiano A G, Simonetti, Giacomo D, Ferrarini, Alessandra, Ramelli, Gian Paolo, Bianchetti, Mario G

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Sleep Power Topography in Children with Attention Deficit Hyperactivity Disorder (ADHD) por Castelnovo, Anna, Lividini, Althea, Bernardi, Giulio, Pezzoli, Valdo, Foderaro, Giuseppe, Ramelli, Gian Paolo, Manconi, Mauro, Miano, Silvia

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Metabolic disturbances and renal stone promotion on treatment with topiramate: a systematic review por Dell'Orto, Valentina G, Belotti, Eva A, Goeggel-Simonetti, Barbara, Simonetti, Giacomo D, Ramelli, Gian Paolo, Bianchetti, Mario G, Lava, Sebastiano A G

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Fingolimod in children with Rett syndrome: the FINGORETT study por Naegelin, Yvonne, Kuhle, Jens, Schädelin, Sabine, Datta, Alexandre N., Magon, Stefano, Amann, Michael, Barro, Christian, Ramelli, Gian Paolo, Heesom, Kate, Barde, Yves-Alain, Weber, Peter, Kappos, Ludwig

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Clinical data for paediatric research: the Swiss approach: Proceedings of the National Symposium in Bern, Switzerland, Dec 5-6, 2019 por Rakic, Milenko, Jaboyedoff, Manon, Bachmann, Sara, Berger, Christoph, Diezi, Manuel, do Canto, Philipp, Forrest, Christopher B., Frey, Urs, Fuchs, Oliver, Gervaix, Alain, Gluecksberg, Amalia Stefani, Grotzer, Michael, Heininger, Ulrich, Kahlert, Christian R., Kaiser, Daniela, Kopp, Matthias V., Lauener, Roger, Neuhaus, Thomas J., Paioni, Paolo, Posfay-Barbe, Klara, Ramelli, Gian Paolo, Simeoni, Umberto, Simonetti, Giacomo, Sokollik, Christiane, Spycher, Ben D., Kuehni, Claudia E.

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Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy por O’Donnell-Luria, Anne H., Pais, Lynn S., Faundes, Víctor, Wood, Jordan C., Sveden, Abigail, Luria, Victor, Abou Jamra, Rami, Accogli, Andrea, Amburgey, Kimberly, Anderlid, Britt Marie, Azzarello-Burri, Silvia, Basinger, Alice A., Bianchini, Claudia, Bird, Lynne M., Buchert, Rebecca, Carre, Wilfrid, Ceulemans, Sophia, Charles, Perrine, Cox, Helen, Culliton, Lisa, Currò, Aurora, Demurger, Florence, Dowling, James J., Duban-Bedu, Benedicte, Dubourg, Christèle, Eiset, Saga Elise, Escobar, Luis F., Ferrarini, Alessandra, Haack, Tobias B., Hashim, Mona, Heide, Solveig, Helbig, Katherine L., Helbig, Ingo, Heredia, Raul, Héron, Delphine, Isidor, Bertrand, Jonasson, Amy R., Joset, Pascal, Keren, Boris, Kok, Fernando, Kroes, Hester Y., Lavillaureix, Alinoë, Lu, Xin, Maas, Saskia M., Maegawa, Gustavo H.B., Marcelis, Carlo L.M., Mark, Paul R., Masruha, Marcelo R., McLaughlin, Heather M., McWalter, Kirsty, Melchinger, Esther U., Mercimek-Andrews, Saadet, Nava, Caroline, Pendziwiat, Manuela, Person, Richard, Ramelli, Gian Paolo, Ramos, Luiza L.P., Rauch, Anita, Reavey, Caitlin, Renieri, Alessandra, Rieß, Angelika, Sanchez-Valle, Amarilis, Sattar, Shifteh, Saunders, Carol, Schwarz, Niklas, Smol, Thomas, Srour, Myriam, Steindl, Katharina, Syrbe, Steffen, Taylor, Jenny C., Telegrafi, Aida, Thiffault, Isabelle, Trauner, Doris A., van der Linden, Helio, van Koningsbruggen, Silvana, Villard, Laurent, Vogel, Ida, Vogt, Julie, Weber, Yvonne G., Wentzensen, Ingrid M., Widjaja, Elysa, Zak, Jaroslav, Baxter, Samantha, Banka, Siddharth, Rodan, Lance H.

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