Hereditary amyloid neuropathy by transthyretin Val107 mutation in a patient of African origin
Julien Cassereau(Centre National de la Recherche Scientifique), Guillaume Nicolas(Centre Hospitalier Universitaire d'Angers), Christian Lavigne(Université d'Angers), Franck Devière(Centre Hospitalier Universitaire d'Angers), Frédéric Dubas(Centre Hospitalier Universitaire d'Angers), A. Ghali(Laboratoires d'Anjou (France)), Christophe Verny(Centre Hospitalier Universitaire d'Angers), Franck Letournel(Université d'Angers)
Cited by 7
Related Papers
Systemic and immune manifestations in myelodysplasia: A multicenter retrospective study
|Arthritis Care & Research|2011|97
The relevance of pacing strategies in managing symptoms of post-COVID-19 syndrome
|Journal of Translational Medicine|2023|71
Persistent elevation of plasma vitamin B12 is strongly associated with solid cancer
|Scientific Reports|2021|54
Elevated blood lactate in resting conditions correlate with post-exertional malaise severity in patients with Myalgic encephalomyelitis/Chronic fatigue syndrome
|Scientific Reports|2019|37
Unstimulated whole saliva flow for diagnosis of primary Sjögren’s syndrome: time to revisit the threshold?
|Arthritis Research & Therapy|2020|33