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

Audrey Benyamine; Fanny Bernard-Guervilly; Céline Tummino; Nicolas Macagno; Laurent Daniel; Sophie Valleix; Brigitte Granel

doi:10.1007/s10067-017-3839-7

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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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Life Sciences [q-bio]

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https://hal-amu.archives-ouvertes.fr/hal-01792229
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Submitted on : Thursday, May 24, 2018 - 11:27:09 AM
Last modification on : Thursday, April 14, 2022 - 4:49:39 PM

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

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

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