Publications by authors named "Marco Bensa"

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Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies.
Thierry Brue, Marie-Hélène Quentien, Konstantin Khetchoumian, Marco Bensa, José-Mario Capo-Chichi

BMC Med Genet· December 2014

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A case of familial hemiplegic migraine associated with a novel ATP1A2 gene mutation.
Angela De Cunto, Marco Bensa, Alessandra Tonelli

Pediatr Neurol· August 2012

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