A. Thomas

发表

Characterization of a large genomic deletion in four Irish families with C7 deficiency.

C. Feighery, B. Morgan, A. Roberts, 2012, Molecular immunology.

Clinical Findings and Prevalence of the Mutation Associated with Primary Ciliary Dyskinesia in Old English Sheepdogs

M. Fredholm, C. Clercx, S. Deleuze, 2014, Journal of veterinary internal medicine.

Neoplasm-induced bleeding in inherited, heterozygous FXIII-A deficiency

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2015, Hämostaseologie.

Coagulation factor XIII deficiency

A. Biswas, J. Oldenburg, V. Ivaškevičius, 2014, Hämostaseologie.

A novel fibrinogen γ chain frameshift deletion (c.637delT) in a patient with hypodysfibrinogenemia associated with thrombosis.

A. Biswas, J. Oldenburg, A. Pavlova, 2015, Hamostaseologie.

Familial thrombophilia associated with fibrinogen paris V: Dusart syndrome.

D. Martincic, P. Baxter, R. Janco, 2000, Blood.

A Novel Mutation in a Patient with a Deficiency of the Eighth Component of Complement Associated with Recurrent Meningococcal Meningitis

B. Ferry, H. Chapel, B. Morgan, 2009, Journal of Clinical Immunology.

HLA‐D region α‐chain monoclonal antibodies: Cross‐reaction between an anti‐DP α‐chain antibody and smooth muscle

J. Bodmer, M. Wilkinson, J. Lindsay, 1988, The Journal of pathology.

The association of Peyronie's disease with HLA B7 cross-reactive antigens. A case report of identical twins.

A. Zachary, A. Thomas, M. Ziegelbaum, 1987, Cleveland Clinic journal of medicine.

Factor V Leiden, Prothrombin 20210 G → A and the MTHFR C677T Mutations in Childhood Stroke

E. Chalmers, A. Sproul, A. Thomas, 1999, Thrombosis and Haemostasis.

C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilection

A. Srivastava, M. Faruq, A. Nalini, 2020, Neurobiology of Aging.