Brief Report: AA Amyloidosis Complicating the Hereditary Periodic Fever Syndromes von 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.

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Misdiagnosis of Hereditary Amyloidosis as AL (Primary) Amyloidosis von Lachmann, Helen J, Booth, Susanne E, Booth, David R, Bybee, Alison, Gilbertson, Janet A, Gillmore, Julian D, Pepys, Mark B, Hawkins, Philip N

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A Review of 1000 Molecular Investigations of Rare Inherited Anaemia and Related Conditions with the Red Cell Gene Panel von 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

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Autoimmunity and glomerulonephritis in mice with targeted deletion of the serum amyloid P component gene: SAP deficiency or strain combination? von 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.

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Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aα chain gene von Kang, Hee Gyung, Bybee, Alison, Ha, Il Soo, Park, Moon Soo, Gilbertson, Janet A., Cheong, Hae Il, Choi, Yong, Hawkins, Philip N.

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GENETIC DISORDERS - DEVELOPMENT: Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen A alpha chain gene von Gyung Kang, Hee, Bybee, Alison, Soo Ha, Il, Park, Moon Soo, Gilbertson, Janet A, Cheong, Hae Il, Choi, Yong, Hawkins, Philip N

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Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen Aalpha chain gene von Kang, Hee Gyung, Bybee, Alison, Ha, Il Soo, Park, Moon Soo, Gilbertson, Janet A, Cheong, Hae Il, Choi, Yong, Hawkins, Philip N

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Hereditary amyloidosis in early childhood associated with a novel insertion-deletion (indel) in the fibrinogen A[alpha] chain gene von Kang, Hee Gyung, Bybee, Alison, Ha, Il Soo, Park, Moon Soo, Gilbertson, Janet A, HAE IL CHEONG, Choi, Yong, Hawkins, Philip N

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MHC typing in variant Creutzfeldt-Jakob disease von Pepys, Mark B, Bybee, Alison, Booth, David R, Bishop, Matthew T, Will, Robert G, Little, Ann-Margaret, Prokupek, Bedrich, Madrigal, J Alejandro

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AA amyloidosis complicating the hereditary periodic fever syndromes von 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

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Familial amyloidotic polyneuropathy with severe renal involvement in association with transthyretin Gly47Glu in Dutch, British and American-Finnish families von Haagsma, Elizabeth B, Hawkins, Philip N, Benson, Merrill D, Lachmann, Helen J, Bybee, Alison, Hazenberg, Bouke PC

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MHC typing in variant Creutzfeldt-Jakob disease. Commentary von PEPYS, Mark B, BYBEE, Alison, BOOTH, David R, BISHOP, Matthew T, WILL, Robert G, LITTLE, Ann-Margaret, PROKUPEK, Bedrich, MADRIGAL, J. Alejandro, PARTANEN, Jukka

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Phenotype, Genotype, and Sustained Response to Anakinra in 22 Patients With Autoinflammatory Disease Associated With CIAS-1/NALP3 Mutations von 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

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Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis von 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.

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Heterogeneity among patients with tumor necrosis factor receptor–associated periodic syndrome phenotypes von 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.

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Response to anakinra in a de novo case of neonatal‐onset multisystem inflammatory disease von Hawkins, Philip N., Bybee, Alison, Aganna, Ebun, McDermott, Michael F.

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Differentiation-linked changes in tyrosine phosphorylation, functional activity, and gene expression downstream from the granulocyte-macrophage colony-stimulating factor receptor von ROBERTS, P. J, ASIM KHWAJA, LIE, A. K. W, BYBEE, A, KWEE YONG, THOMAS, N. S. B, LINCH, D. C

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Interferon-alpha treatment of Daudi cells down-regulates the octamer binding transcription/DNA replication factors Oct-1 and Oct-2 von Dent, C.L., Lillycrop, K.A., Bybee, A., Latchman, D.S., Thomas, N.S.

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AA amyloidosis complicating hyperimmunoglobulinemia D with periodic fever syndrome: A report of two cases von Lachmann, Helen J., Goodman, Hugh J. B., Andrews, Peter A., Gallagher, Hugh, Marsh, James, Breuer, Stephan, Rowczenio, Dorota M., Bybee, Alison, Hawkins, Philip N.

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Studies on the hyperplastic responsiveness of binucleated rat hepatocytes von Styles, J.A., Bybee, Alison, Pritchard, N.R., Kelly, M.D.

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