Marie-Laure Armand

ORCID: 0009-0007-3210-6757
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About
Contact & Profiles
Research Areas
  • Neurofibromatosis and Schwannoma Cases
  • Soft tissue tumors and treatment
  • Soft tissue tumor case studies
  • Vascular Malformations and Hemangiomas
  • Dupuytren's Contracture and Treatments
  • Myasthenia Gravis and Thymoma

Assistance Publique – Hôpitaux de Paris
2022-2023

Hôpitaux Universitaires Henri-Mondor
2023

Neurofibromatosis Type 1 (NF1) is a common genetic neurocutaneous disease, with an autosomal dominant inheritance mode. Quality of life has been shown impaired in NF1, due to severe complications, cosmetic features, and uncertainty about the disorder. This study sought develop self-administered questionnaire French assess burden NF1 (BoN), then translate linguistically cross-culturally validate it into American English, standardized methodology applied, as outlined report. Based on several...

10.1186/s13023-019-1067-8 article EN cc-by Orphanet Journal of Rare Diseases 2019-05-03

Cutaneous neurofibromas (cNF), present in 95% of individuals with neurofibromatosis 1 (NF1), are considered as one the greatest medical burden because physical disfigurement. No specific score evaluates their impact on quality life (QoL).To develop a assessing cNF-related QoL.Through multidisciplinary workshop including 10 patients, 3 expert-in-NF1 physicians, health care workers (nurses and psychologist) methodologist, French version Skindex-16 was modified by adding items. The new...

10.1111/jdv.18140 article EN Journal of the European Academy of Dermatology and Venereology 2022-04-12
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