Brief Report: AA Amyloidosis Complicating the Hereditary Periodic Fever Syndromes
Lane, Thirusha, Loeffler, Jutta M., Rowczenio, Dorota M., Gilbertson, Janet A., Bybee, Alison, Russell, Tonia L., Gillmore, Julian D., Wechalekar, Ashutosh D., Hawkins, Philip N., Lachmann, Helen J.
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.04.2013)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.04.2013)
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Journal Article
Misdiagnosis of Hereditary Amyloidosis as AL (Primary) Amyloidosis
Lachmann, Helen J, Booth, Susanne E, Booth, David R, Bybee, Alison, Gilbertson, Janet A, Gillmore, Julian D, Pepys, Mark B, Hawkins, Philip N
Published in The New England journal of medicine (06.06.2002)
Published in The New England journal of medicine (06.06.2002)
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A Review of 1000 Molecular Investigations of Rare Inherited Anaemia and Related Conditions with the Red Cell Gene Panel
Mayhew, Rachel, Smith, Frances, Steedman, Laura, Parkin, Nicholas, Moldes Beiro, Eva, Rushton, Peter, Bybee, Alison, Brawand, David, Marsh, Judith, Kulasekararaj, Austin G., Ghandi, Shreyans, Mansour, Sahar, Mufti, Ghulam, Pagliuca, Antonio, Chakravorty, Subarna, Rees, David C, Clark, Barnaby
Published in Blood (29.11.2018)
Published in Blood (29.11.2018)
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Journal Article
Clinical characteristics and SAP scintigraphic findings in 10 patients with AGel amyloidosis
Rowczenio, Dorota, Tennent, Glenys A., Gilbertson, Janet, Lachmann, Helen J., Hutt, David F., Bybee, Alison, Hawkins, Philip N., Gillmore, Julian D.
Published in Amyloid (01.12.2014)
Published in Amyloid (01.12.2014)
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Journal Article
Autoimmunity and glomerulonephritis in mice with targeted deletion of the serum amyloid P component gene: SAP deficiency or strain combination?
Gillmore, Julian D., Hutchinson, Winston L., Herbert, Jeff, Bybee, Alison, Mitchell, Daniel A., Hasserjian, Robert P., Yamamura, Ken‐Ichi, Suzuki, Misao, Sabin, Caroline A., Pepys, Mark B.
Published in Immunology (01.06.2004)
Published in Immunology (01.06.2004)
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Journal Article
Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aα chain gene
Kang, Hee Gyung, Bybee, Alison, Ha, Il Soo, Park, Moon Soo, Gilbertson, Janet A., Cheong, Hae Il, Choi, Yong, Hawkins, Philip N.
Published in Kidney international (01.11.2005)
Published in Kidney international (01.11.2005)
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Journal Article
Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen A[alpha] chain gene
Kang, Hee Gyung, Bybee, Alison, Ha, Il Soo, Park, Moon Soo, Gilbertson, Janet A, HAE IL CHEONG, Choi, Yong, Hawkins, Philip N
Published in Kidney international (01.11.2005)
Published in Kidney international (01.11.2005)
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Journal Article
GENETIC DISORDERS - DEVELOPMENT: Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen A alpha chain gene
Gyung Kang, Hee, Bybee, Alison, Soo Ha, Il, Park, Moon Soo, Gilbertson, Janet A, Cheong, Hae Il, Choi, Yong, Hawkins, Philip N
Published in Kidney international (01.11.2005)
Published in Kidney international (01.11.2005)
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Journal Article
Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene
Kang, Hee Gyung, Bybee, Alison, Ha, Il Soo, Park, Moon Soo, Gilbertson, Janet A, Cheong, Hae Il, Choi, Yong, Hawkins, Philip N
Published in Kidney international (01.11.2005)
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Published in Kidney international (01.11.2005)
Journal Article
MHC typing in variant Creutzfeldt-Jakob disease
Pepys, Mark B, Bybee, Alison, Booth, David R, Bishop, Matthew T, Will, Robert G, Little, Ann-Margaret, Prokupek, Bedrich, Madrigal, J Alejandro
Published in The Lancet (British edition) (08.02.2003)
Published in The Lancet (British edition) (08.02.2003)
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Journal Article
AA amyloidosis complicating the hereditary periodic fever syndromes
Lane, Thirusha, Loeffler, Jutta M, Rowczenio, Dorota M, Gilbertson, Janet A, Bybee, Alison, Russell, Tonia L, Gillmore, Julian D, Wechalekar, Ashutosh D, Hawkins, Philip N, Lachmann, Helen J
Published in Arthritis and rheumatism (01.04.2013)
Published in Arthritis and rheumatism (01.04.2013)
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Journal Article
MHC typing in variant Creutzfeldt-Jakob disease. Commentary
PEPYS, Mark B, BYBEE, Alison, BOOTH, David R, BISHOP, Matthew T, WILL, Robert G, LITTLE, Ann-Margaret, PROKUPEK, Bedrich, MADRIGAL, J. Alejandro, PARTANEN, Jukka
Published in The Lancet (British edition) (2003)
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Published in The Lancet (British edition) (2003)
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Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families
Haagsma, Elizabeth B, Hawkins, Philip N, Benson, Merrill D, Lachmann, Helen J, Bybee, Alison, Hazenberg, Bouke PC
Published in Amyloid (01.03.2004)
Published in Amyloid (01.03.2004)
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Proto-oncogenic properties of the DP family of proteins
Jooss, K, Lam, E W, Bybee, A, Girling, R, Müller, R, La Thangue, N B
Published in Oncogene (20.04.1995)
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Published in Oncogene (20.04.1995)
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Phenotype, genotype, and sustained response to anakinra in 22 patients with autoinflammatory disease associated with CIAS-1/NALP3 mutations
Leslie, Kieron S, Lachmann, Helen J, Bruning, Elizabeth, McGrath, John A, Bybee, Alison, Gallimore, J Ruth, Roberts, Philip F, Woo, Patricia, Grattan, Clive E, Hawkins, Philip N
Published in Archives of dermatology (1960) (01.12.2006)
Published in Archives of dermatology (1960) (01.12.2006)
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Journal Article
Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis
Aganna, Ebun, Martinon, Fabio, Hawkins, Philip N., Ross, John B., Swan, Daniel C., Booth, David R., Lachmann, Helen J., Gaudet, Roxanne, Woo, Patricia, Feighery, Conleth, Cotter, Finbarr E., Thome, Margot, Hitman, Graham A., Tschopp, Jürg, McDermott, Michael F.
Published in Arthritis and rheumatism (01.09.2002)
Published in Arthritis and rheumatism (01.09.2002)
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Heterogeneity among patients with tumor necrosis factor receptor–associated periodic syndrome phenotypes
Aganna, Ebun, Hammond, Linda, Hawkins, Philip N., Aldea, Anna, McKee, Shane A., van Amstel, Hans Kristian Ploos, Mischung, Claudia, Kusuhara, Koichi, Saulsbury, Frank T., Lachmann, Helen J., Bybee, Alison, McDermott, Elizabeth M., La Regina, Micaela, Arostegui, Juan I., Campistol, Josep M., Worthington, Sharron, High, Kevin P., Molloy, Michael G., Baker, Nicholas, Bidwell, Jeff L., Castañer, José L., Whiteford, Margo L., Janssens‐Korpola, P. L., Manna, Raffaele, Powell, Richard J., Woo, Patricia, Solis, Pilar, Minden, Kirsten, Frenkel, Joost, Yagüe, Jordi, Mirakian, Rita M., Hitman, Graham A., McDermott, Michael F.
Published in Arthritis and rheumatism (01.09.2003)
Published in Arthritis and rheumatism (01.09.2003)
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Journal Article
Response to anakinra in a de novo case of neonatal‐onset multisystem inflammatory disease
Hawkins, Philip N., Bybee, Alison, Aganna, Ebun, McDermott, Michael F.
Published in Arthritis and rheumatism (01.08.2004)
Published in Arthritis and rheumatism (01.08.2004)
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