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Advances in Therapy|November 10, 2021
Treatment of Idiopathic Pulmonary Fibrosis with Capsule or Tablet Formulations of Pirfenidone in the Real-Life French RaDiCo-ILD CohortVincent Cottin, Sonia Guéguen, Hilario Nunes, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|April 6, 2017
Specific Polysaccharide Antibody Deficiency Revealed by Severe Bacterial Infections in Adulthood: A Report on 11 CasesBenjamin Lopez, Anne Boucher, Mathilde Bahuaud, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 13, 2024
Epidemiological and clinicopathological characteristics of vascular-limited renal AL amyloidosisNoémie Senot, Jean Baptiste Gibier, Marion Rabant, et al.
European Journal of Haematology|September 1, 2022
Ibrutinib as a treatment of hematologic autoimmune disorders in patients with indolent B-cell lymphomaAdrien Daniel, David Ghez, Camille Ravaiau, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 10, 2014
Impact of initial FDG-PET/CT and serum-free light chain on transformation of conventionally defined solitary plasmacytoma to multiple myelomaGuillemette Fouquet, Stéphanie Guidez, Charles Herbaux, et al.
Respiratory Research|April 27, 2018
Rituximab for auto-immune alveolar proteinosis, a real life cohort studyBerenice Soyez, Raphael Borie, Cedric Menard, et al.
Respiratory Medicine and Research|April 23, 2026
Design of PROGRESSION-IPF: A pragmatic, open-label, randomized trial of patients with progressive disease in idiopathic pulmonary fibrosisVincent Cottin, Bruno Crestani, Carole Planès, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|January 24, 2015
Severe hematologic complications after lung transplantation in patients with telomerase complex mutationsRaphael Borie, Caroline Kannengiesser, Sandrine Hirschi, et al.
British Journal of Haematology|August 28, 2014
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndromeStéphanie Poulain, Eileen M Boyle, Christophe Roumier, et al.
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