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Journal of Burn Care & Research : Official Publication of the American Burn Association|October 22, 2020
Missed Diagnosis of Epilepsy-Associated Scald Burns: Two Cases Initially Diagnosed as Bullous DermatosisLaura Giraud-Kerleroux, Chloé Charpentier, Charlotte Bernigaud, et al.
The British Journal of Dermatology|August 7, 2019
Health-related quality of life and long-term sequelae in survivors of epidermal necrolysis: an observational study of 57 patientsS Ingen-Housz-Oro, A Alves, A Colin, et al.
Neuro-Oncology|January 14, 2014
mTORC1 inhibition delays growth of neurofibromatosis type 2 schwannomaMarco Giovannini, Nicolas-Xavier Bonne, Jeremie Vitte, et al.
The British Journal of Dermatology|August 10, 2019
Incidence of and mortality from epidermal necrolysis (Stevens-Johnson syndrome/toxic epidermal necrolysis) in France during 2003-16: a four-source capture-recapture estimateG Chaby, C Maldini, C Haddad, et al.
European Journal of Cancer (Oxford, England : 1990)|December 16, 1998
Radiosurgery without whole brain radiotherapy in melanoma brain metastases. Club de Cancérologie CutanéeJ J Grob, J Regis, R Laurans, et al.
Plos One|March 18, 2016
Metabolic Tumour Burden Measured by 18F-FDG PET/CT Predicts Malignant Transformation in Patients with Neurofibromatosis Type-1Axel Van Der Gucht, Ouidad Zehou, Soraya Djelbani-Ahmed, et al.
European Journal of Human Genetics : EJHG|July 31, 2014
Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?Eric Pasmant, Béatrice Parfait, Armelle Luscan, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 14, 2021
Face transplantation: A longitudinal histological study focusing on chronic active and mucosal rejection in a series with long-term follow-upAnissa Moktefi, Mikael Hivelin, Philippe Grimbert, et al.
The Journal of Molecular Diagnostics : JMD|September 22, 2009
Detection and characterization of NF1 microdeletions by custom high resolution array CGHEric Pasmant, Audrey Sabbagh, Julien Masliah-Planchon, et al.
Human Mutation|September 12, 2000
NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1E Girodon-Boulandet, J Pantel, C Cazeneuve, et al.
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