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Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review

Audrey Benyamine 1 Fanny Bernard-Guervilly Céline Tummino Nicolas Macagno 2 Laurent Daniel 3 Sophie Valleix 4 Brigitte Granel 5, 1
1 VRCM - Vascular research center of Marseille
2 CRO2 - Centre de Recherches en Oncologie biologique et Oncopharmacologie
3 LMT - Laboratoire de Mécanique et Technologie
4 Laboratoire de Biochimie et Génétique Moléculaire
5 Hôpital Nord [CHU - APHM]
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https://hal-amu.archives-ouvertes.fr/hal-01792229
Contributor : Françoise Dignat-George <>
Submitted on : Thursday, May 24, 2018 - 11:27:09 AM
Last modification on : Monday, July 5, 2021 - 9:50:59 AM

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CNRS | ENS-CACHAN | UNIV-AMU | UNIV-PARIS5 | USPC | LMT | SORBONNE-UNIVERSITE | SU-SCIENCES | UNIV-PARIS | ENS-PARIS-SACLAY | GS-ENGINEERING

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Audrey Benyamine, Fanny Bernard-Guervilly, Céline Tummino, Nicolas Macagno, Laurent Daniel, et al.. Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review. 2017, pp.2623 - 2628. ⟨10.1007/s10067-017-3839-7⟩. ⟨hal-01792229⟩

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