Clinical Immunology Review Series: An approach to the patient with angio-oedema

Por Grigoriadou, S, Longhurst, H J
Publicado em 2009

Pancreatitis associated with hydroxyurea in combination with didanosine

Por Longhurst, H J, Pinching, A J
Publicado em 2001

C1-inhibitor concentrate home therapy for hereditary angioedema: a viable, effective treatment option

Por Longhurst, H J, Carr, S, Khair, K
Publicado em 2007

Serological Markers (Anti-Saccharomyces cerevisiae Mannan Antibodies and Antineutrophil Cytoplasmic Antibodies) in Inflammatory Bowel Disease: Diagnostic Utility and Phenotypic Cor...

Por Buckland, M. S., Mylonaki, M., Rampton, D., Longhurst, H. J.
Publicado em 2005

An evaluation of tests used for the diagnosis and monitoring of C1 inhibitor deficiency: normal serum C4 does not exclude hereditary angio-oedema

Por Tarzi, M D, Hickey, A, Förster, T, Mohammadi, M, Longhurst, H J
Publicado em 2007

Clinical Immunology Review Series: An approach to the management of pulmonary disease in primary antibody deficiency

Por Tarzi, M D, Grigoriadou, S, Carr, S B, Kuitert, L M, Longhurst, H J
Publicado em 2009

Changes in B cell immunophenotype in common variable immunodeficiency: cause or effect – is bronchiectasis indicative of undiagnosed immunodeficiency?

Por Bright, P, Grigoriadou, S, Kamperidis, P, Buckland, M, Hickey, A, Longhurst, H J
Publicado em 2013

Immune deficiency: changing spectrum of pathogens

Por Duraisingham, S S, Manson, A, Grigoriadou, S, Buckland, M, Tong, C Y W, Longhurst, H J
Publicado no Clin Exp Immunol (2015)

Mullins’ syndrome: a new gammopathy-related autoinflammatory syndrome resistant to anakinra

Por Longhurst, H.J., Yong, P.F.K., Manson, A.L., Cavenagh, J.D., Grigoriadou, S., Buckland, M.S.
Publicado no QJM (2015)

Anti-D immunoglobulin treatment for thrombocytopenia associated with primary antibody deficiency

Por Longhurst, H J, O'Grady, C, Evans, G, De Lord, C, Hughes, A, Cavenagh, J, Helbert, M R
Publicado em 2002

Comparing acquired angioedema with hereditary angioedema (types I/II): findings from the Icatibant Outcome Survey

Por Longhurst, H. J., Zanichelli, A., Caballero, T., Bouillet, L., Aberer, W., Maurer, M., Fain, O., Fabien, V., Andresen, I.
Publicado no Clin Exp Immunol (2017)

A simple method for the detection of Chlamydia trachomatis infections in general practice

Por Longhurst, H.J., Flower, N., Thomas, B.J., Munday, P.E., Elder, A., Constantinidou, M., Wilton, J., Taylor-Robinson, D.
Publicado em 1987

In pursuit of excellence: an integrated care pathway for C(1) inhibitor deficiency

Por Manson, A L, Price, A, Dempster, J, Clinton-Tarestad, P, Greening, C, Enti, R, Hill, S, Grigoriadou, S, Buckland, M S, Longhurst, H J
Publicado em 2013

C1 inhibitor deficiency: 2014 United Kingdom consensus document

Por Longhurst, H J, Tarzi, M D, Ashworth, F, Bethune, C, Cale, C, Dempster, J, Gompels, M, Jolles, S, Seneviratne, S, Symons, C, Price, A, Edgar, D
Publicado no Clin Exp Immunol (2015)

C1 inhibitor deficiency: consensus document

Por Gompels, M M, Lock, R J, Abinun, M, Bethune, C A, Davies, G, Grattan, C, Fay, A C, Longhurst, H J, Morrison, L, Price, A, Price, M, Watters, D
Publicado em 2005

Phase II study results of a replacement therapy for hereditary angioedema with subcutaneous C1‐inhibitor concentrate

Por Zuraw, B. L., Cicardi, M., Longhurst, H. J., Bernstein, J. A., Li, H. H., Magerl, M., Martinez‐Saguer, I., Rehman, S. M. M., Staubach, P., Feuersenger, H., Parasrampuria, R., Sidhu, J., Edelman, J., Craig, T.
Publicado no Allergy (2015)

Measurement of Typhi Vi antibodies can be used to assess adaptive immunity in patients with immunodeficiency

Por Evans, C., Bateman, E., Steven, R., Ponsford, M., Cullinane, A., Shenton, C., Duthie, G., Conlon, C., Jolles, S., Huissoon, A. P., Longhurst, H. J., Rahman, T., Scott, C., Wallis, G., Harding, S., Parker, A. R., Ferry, B. L.
Publicado no Clin Exp Immunol (2018)

The United Kingdom Primary Immune Deficiency (UKPID) registry 2012 to 2017

Por Shillitoe, B., Bangs, C., Guzman, D., Gennery, A. R., Longhurst, H. J., Slatter, M., Edgar, D. M., Thomas, M., Worth, A., Huissoon, A., Arkwright, P. D., Jolles, S., Bourne, H., Alachkar, H., Savic, S., Kumararatne, D. S., Patel, S., Baxendale, H., Noorani, S., Yong, P. F. K., Waruiru, C., Pavaladurai, V., Kelleher, P., Herriot, R., Bernatonienne, J., Bhole, M., Steele, C., Hayman, G., Richter, A., Gompels, M., Chopra, C., Garcez, T., Buckland, M.
Publicado no Clin Exp Immunol (2018)

The Icatibant Outcome Survey: experience of hereditary angioedema management from six European countries

Por Caballero, T., Aberer, W., Longhurst, H.J., Maurer, M., Zanichelli, A., Perrin, A., Bouillet, L., Andresen, I., Arcoleo, F., Bova, M., Cicardi, M., Cillari, E., Montinaro, V., Marone, G., Blanchard Delauny, C., Boccon‐Gibod, I., Coppere, B., Dzviga, C., Fain, O., Goichot, B., Gompel, A., Guez, S., Jeandel, P.Y., Kanny, G., Launay, D., Maillard, H., Martin, L., Masseau, A., Ollivier, Y., Magerl, M., Baeza, M.L., Cabañas, R., Guilarte, M., Hernández, D., Hernando de Larramendi, C., Lleonart, R., Lobera, T., Marqués, L., Bangs, C., Buckland, M., Grigoriadou, S., Helbert, M., Lorenzo, L.
Publicado no J Eur Acad Dermatol Venereol (2017)

The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008–2012

Por Edgar, J D M, Buckland, M, Guzman, D, Conlon, N P, Knerr, V, Bangs, C, Reiser, V, Panahloo, Z, Workman, S, Slatter, M, Gennery, A R, Davies, E G, Allwood, Z, Arkwright, P D, Helbert, M, Longhurst, H J, Grigoriadou, S, Devlin, L A, Huissoon, A, Krishna, M T, Hackett, S, Kumararatne, D S, Condliffe, A M, Baxendale, H, Henderson, K, Bethune, C, Symons, C, Wood, P, Ford, K, Patel, S, Jain, R, Jolles, S, El-Shanawany, T, Alachkar, H, Herwadkar, A, Sargur, R, Shrimpton, A, Hayman, G, Abuzakouk, M, Spickett, G, Darroch, C J, Paulus, S, Marshall, S E, McDermott, E M, Heath, P T, Herriot, R, Noorani, S, Turner, M, Khan, S, Grimbacher, B
Publicado em 2014