Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review - Aix-Marseille Université Access content directly
Other Publications Clinical Rheumatology Year : 2017

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

Domains

Life Sciences [q-bio]

Françoise DIGNAT-GEORGE  : Connect in order to contact the contributor

https://hal-amu.archives-ouvertes.fr/hal-01792229

Submitted on : Thursday, May 24, 2018-11:27:09 AM

Last modification on : Friday, March 24, 2023-2:53:07 PM

Not file

Dates and versions

hal-01792229 , version 1 (24-05-2018)

Identifiers

Cite

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⟩

Export

BibTeX TEI Dublin Core DC Terms EndNote Datacite

Collections

CNRS UNIV-AMU ENS-CACHAN LMT USPC UNIV-PARIS-SACLAY SORBONNE-UNIVERSITE SU-SCIENCES ENS-PARIS-SACLAY GS-ENGINEERING LMPS
34 View
0 Download

Altmetric

Share

Gmail Facebook Twitter LinkedIn More