Hadija Trojer

London, ENG, United Kingdom

Last Updated: 09/26/2026

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Found 8 publications

British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literature.

British kindred with dominant FMF associated with high incidence of AA amyloidosis caused by novel MEFV variant, and a review of the literature.

Journal: Rheumatology (Oxford, England)

Published: June 04, 2019

Analysis of the TTR gene in the investigation of amyloidosis: A 25-year single UK center experience.

Analysis of the TTR gene in the investigation of amyloidosis: A 25-year single UK center experience.

Journal: Human mutation

Published: August 03, 2018

Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome.

Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome.

Journal: Blood

Published: October 11, 2017

Late-Onset Cryopyrin-Associated Periodic Syndromes Caused by Somatic NLRP3 Mosaicism-UK Single Center Experience.

Late-Onset Cryopyrin-Associated Periodic Syndromes Caused by Somatic NLRP3 Mosaicism-UK Single Center Experience.

Journal: Frontiers in immunology

Published: July 21, 2017

Adult-onset tumour necrosis factor receptor-associated periodic syndrome presenting as transfusion-dependent refractory haemophagocytosis.

Adult-onset tumour necrosis factor receptor-associated periodic syndrome presenting as transfusion-dependent refractory haemophagocytosis.

Journal: Rheumatology (Oxford, England)

Published: March 25, 2017

Brief Report: Association of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome With Gonosomal Mosaicism of a Novel 24-Nucleotide TNFRSF1A Deletion.

Brief Report: Association of Tumor Necrosis Factor Receptor-Associated Periodic Syndrome With Gonosomal Mosaicism of a Novel 24-Nucleotide TNFRSF1A Deletion.

Journal: Arthritis & rheumatology (Hoboken, N.J.)

Published: June 17, 2015

Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration.

Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration.

Journal: Rheumatology (Oxford, England)

Published: May 29, 2015

Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.

Clinical characteristics in subjects with NLRP3 V198M diagnosed at a single UK center and a review of the literature.

Journal: Arthritis research & therapy

Published: July 20, 2012

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Last Updated: 09/26/2026