1. AB0828 Comparing Synovial Fluids and Inflammatory Markers during Acute Pseudogout in Patients with and without Known Inflammatory Arthropathy. (10th June 2014) Authors: Alhaddad, B.; Ballou, S.; Aponte, J. Journal: Annals of the rheumatic diseases Issue: Volume 73:Supplement 2(2014) Page Start: 1077 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. SAT0305 Interstitial Lung Disease (ILD) in Patients with Anti-Jo-1 Syndrome (AJS): A Descriptive Analysis. (10th June 2014) Authors: Alhaddad, B.; O'Rourke, C.; Alalwani, M.; Zraik, B.; Yadav, R.; Chatterjee, S. Journal: Annals of the rheumatic diseases Issue: Volume 73:Supplement 2(2014) Page Start: 703 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. AB0240 The Effect of Anti Estrogen Therapy (AET) on Rheumatoid Arthritis. (9th June 2015) Authors: Alhaddad, B.; Ballou, S.; Chen, J. Journal: Annals of the rheumatic diseases Issue: Volume 74(2015)Supplement 2 Page Start: 971 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Expanding the phenotype of DNAJC3 mutations: A case with hypothyroidism additionally to diabetes mellitus and multisystemic neurodegeneration. Issue 5 (21st September 2017) Authors: Bublitz, S.K.; Alhaddad, B.; Synofzik, M.; Kuhl, V.; Lindner, A.; Freiberg, C.; Schmidt, H.; Strom, T.M.; Haack, T.B.; Deschauer, M. Journal: Clinical genetics Issue: Volume 92:Issue 5(2017) Page Start: 561 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Extension of the phenotype of biallelic loss‐of‐function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I. Issue 2 (8th November 2017) Authors: Braunisch, M.C.; Gallwitz, H.; Abicht, A.; Diebold, I.; Holinski‐Feder, E.; Van Maldergem, L.; Lammens, M.; Kovács‐Nagy, R.; Alhaddad, B.; Strom, T.M.; Meitinger, T.; Senderek, J.; Rudnik‐Schöneborn, S.; Haack, T.B. Journal: Clinical genetics Issue: Volume 93:Issue 2(2018) Page Start: 255 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations. (June 2017) Authors: Wagner, A.; Alhaddad, B.; Ahting, U.; Prokisch, H.; Rodenburg, R.; Mayatepek, E.; Haack, T.; Distelmaier, F. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e128 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗