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Orphanet Journal of Rare Diseases|June 25, 2020
Raising rare disease awareness using red flags, role play simulation and patient educators: results of a novel educational workshop on Raynaud phenomenon and systemic sclerosisS Sanges, M-M Farhat, M Assaraf, et al.
Sleep Medicine|December 4, 2018
Prothrombotic state in children with obstructive sleep apneaAntonia Barceló, Daniel Morell-Garcia, Pilar Sanchís, et al.
European Journal of Clinical Investigation|November 6, 2025
Long-term effectiveness and safety outcomes in adults with Fabry disease treated with agalsidase alfa: 20 years of data from the Fabry Outcome SurveyDerralynn A Hughes, Guillem Pintos-Morell, Christoph Kampmann, et al.
The Journal of Infection|December 17, 2017
Usefulness of midregional pro-adrenomedullin as a marker of organ damage and predictor of mortality in patients with sepsisEnrique Bernal-Morell, Eva García-Villalba, Maria Del Carmen Vera, et al.
World Neurosurgery|June 21, 2021
Perioperative Complications in Endoscopic Endonasal versus Transcranial Resections of Adult CraniopharyngiomasVaidya Govindarajan, Evan M Luther, Alexis A Morell, et al.
Archivos De Bronconeumologia|June 5, 2021
Polysomnographic Characteristics of Snoring Children: A Familial Study of Obstructive Sleep Apnea SyndromeDaniel Morell-Garcia, José Antonio Peña-Zarza, Pilar Sanchís, et al.
La Revue De Medecine Interne|June 7, 2024
[HYPNOSTRESS study: Interest of medical hypnosis in the evaluation of perceived stress and the experience of hospitalization in an internal medicine department]L Chikhoune, S Morell Dubois, E Ledoult, et al.
Journal of Neuro-Oncology|February 22, 2022
Same-day discharge after brain tumor resection: a prospective pilot studyFrederic A Vallejo, Daniel G Eichberg, Alexis A Morell, et al.
Journal of Immunology (Baltimore, Md. : 1950)|August 7, 2013
Paradoxical effect of cortistatin treatment and its deficiency on experimental autoimmune encephalomyelitisLuciana Souza-Moreira, Maria Morell, Virginia Delgado-Maroto, et al.
American Journal of Human Genetics|February 23, 2010
Targeted capture and next-generation sequencing identifies C9orf75, encoding taperin, as the mutated gene in nonsyndromic deafness DFNB79Atteeq Ur Rehman, Robert J Morell, Inna A Belyantseva, et al.
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