138 research outputs found
Diagnosis and treatment of viral diseases in recipients of allogeneic hematopoietic stem cell transplantation
A key step towards setting a benchmark for tackling transplant‐associated thrombotic microangiopathy
Mémoire présenté par la chambre d'agriculture à M. le gouverneur de l'île de la Réunion, au sujet du régime du travail établi dans la colonie et des modifications que l'on veut y apporter. [Signé : Alph. Sicre de Fontbrune (1er décembre 1877).]
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Management of suspected monogenic lung fibrosis in a specialised centre
At least 10% of patients with interstitial lung disease present monogenic lung fibrosis suspected on familial aggregation of pulmonary fibrosis, specific syndromes or early age of diagnosis. Approximately 25% of families have an identified mutation in genes mostly involved in telomere homeostasis, and more rarely in surfactant homeostasis. Beyond pathophysiological knowledge, detection of these mutations has practical consequence for patients. For instance, mutations involved in telomere homeostasis are associated with haematological complications after lung transplantation and may require adapted immunosuppression. Moreover, relatives may benefit from a clinical and genetic evaluation that should be specifically managed. The field of genetics of pulmonary fibrosis has made great progress in the last 10 years, raising specific problems that should be addressed by a specialised team
Viral Respiratory Infections Diagnosed by Multiplex PCR after Allogeneic Hematopoietic Stem Cell Transplantation: Long-Term Incidence and Outcome
P824: HEMATOLOGIC FEATURES IN 102 FRENCH PATIENTS DIAGNOSED WITH GERMLINE MUTATIONS OF TELOMERES RELATED GENES AGED 15 YEARS OLD OR MORE
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