[VEXAS gene variants explain previously unrecognized clinical syndrome].

Rasch, Mads Nyhuus Bendix; Szabados, Fruzsina; Jensen, Jens Magnus Bernth; Nielsen, Kirstine Overgaard; Hauge, Ellen-Margrethe; Troldborg, Anne

Rasch, Mads Nyhuus Bendix; Szabados, Fruzsina; Jensen, Jens Magnus Bernth; Nielsen, Kirstine Overgaard; Hauge, Ellen-Margrethe; Troldborg, Anne.

Affiliation

Rasch MNB; Led- og Bindevævssygdomme, Aarhus Universitetshospital.
Szabados F; Reumatologisk Afdeling, Regionshospitalet Nordjylland, Hjørring.
Jensen JMB; Blodbank og Immunologi, Aarhus Universitetshospital.
Nielsen KO; Blodbank og Immunologi, Aarhus Universitetshospital.
Hauge EM; Led- og Bindevævssygdomme, Aarhus Universitetshospital.
Troldborg A; Institut for Klinisk Medicin, Health, Aarhus Universitet.

Ugeskr Laeger ; 184(40)2022 10 03.

Article in Da | MEDLINE | ID: mdl-36205150

Subject(s)

Anemia, Macrocytic; Anemia; Anemia/etiology; Anemia/genetics; Anemia, Macrocytic/etiology; Diagnosis, Differential; Humans; Inflammation/complications; Male; Syndrome

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Anemia / Anemia, Macrocytic Type of study: Diagnostic_studies / Etiology_studies Limits: Humans / Male Language: Da Journal: Ugeskr Laeger Year: 2022 Document type: Article Country of publication: Denmark

Search on Google

Add to My VHL

XML

PubMed Links