Hilary Longhurst

Hilary Longhurst

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Hilary Longhurst

Publications by authors named "Hilary Longhurst"

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Biological therapy in hereditary angioedema: transformation of a rare disease.

Expert Opin Biol Ther 2020 Jan 29. Epub 2020 Jan 29.

3rd Department of Internal Medicine, Semmelweis University, Kutvolgyi ut 4, H-1125, Budapest, Hungary.

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http://dx.doi.org/10.1080/14712598.2020.1724280DOI Listing
January 2020

Hereditary angioedema: an update on causes, manifestations and treatment.

Br J Hosp Med (Lond) 2019 Jul;80(7):391-398

Univ.-Prof. Dr, Department of Dermatology, University Medical Center, Johannes Gutenberg University, Mainz, Germany.

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http://dx.doi.org/10.12968/hmed.2019.80.7.391DOI Listing
July 2019

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry.

Front Immunol 2018 16;9:543. Epub 2018 Mar 16.

Center for Chronic Immunodeficiency, Medical Center - University of Freiburg, Freiburg, Germany.

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http://journal.frontiersin.org/article/10.3389/fimmu.2018.00
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http://dx.doi.org/10.3389/fimmu.2018.00543DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5863269PMC
May 2019

Long-term effects upon rituximab treatment of acquired angioedema due to C1-inhibitor deficiency.

Allergy 2019 04 18;74(4):834-840. Epub 2018 Dec 18.

Clinical Immunology and Allergy, Royal National Throat Nose and Ear Hospital, University College London Hospitals, London, UK.

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http://dx.doi.org/10.1111/all.13686DOI Listing
April 2019

Pediatricians diagnosed few patients with childhood-presented hereditary angioedema: Icatibant Outcome Survey findings.

J Allergy Clin Immunol Pract 2019 Mar 28;7(3):1078-1080. Epub 2018 Aug 28.

Department of Dermatology and Allergy, Allergie-Centrum-Charité, Charité - Universitätsmedizin Berlin, Berlin, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S22132198183052
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http://dx.doi.org/10.1016/j.jaip.2018.07.047DOI Listing
March 2019

Lanadelumab for the Prophylactic Treatment of Hereditary Angioedema with C1 Inhibitor Deficiency: A Review of Preclinical and Phase I Studies.

BioDrugs 2019 Feb;33(1):33-43

Division of Rheumatology, Allergy and Immunology, University of California, San Diego, 8899 University Center Lane, Suite 230, San Diego, CA, 92122, USA.

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http://dx.doi.org/10.1007/s40259-018-0325-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6373397PMC
February 2019

Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary Angioedema.

N Engl J Med 2018 07;379(4):352-362

From the Division of Hematology, Oncology, and Hemostaseology, Department of Children and Adolescents, Angioedema Center, University Hospital Frankfurt (E.A.-P.), and the Fraunhofer Institute for Molecular Biology and Applied Ecology, Translational Medicine and Pharmacology (J. Graff), Frankfurt, the Department of Dermatology and Allergy, Charité-Universitätsmedizin Berlin, Berlin (M. Magerl, M. Maurer), and the Department of Otorhinolaryngology and Head and Neck Surgery, Ulm University Medical Center, Ulm (J. Greve) - all in Germany; the Department of Dermatology and Allergy Center, Odense University Hospital, Odense, Denmark (A.B.); Public Health Institution University Clinic of Dermatology, School of Medicine, University Sts. Cyril and Methodius, Skopje, Macedonia (V.G.-P.); the Department of Clinical Immunology, University Hospital Zurich, Zurich, Switzerland (U.C.S.); Assistance Publique-Hôpitaux de Paris Hôpital Saint Antoine, Sorbonne Université, Paris (O.F.), and the Department of Dermatology, Université de Montpellier, Montpellier (A.D.-T.) - both in France; the Allergy and Immunology West Midlands, Birmingham Heartlands Hospital, Birmingham (A.H.), Barts Health NHS Trust-Royal London Hospital, London (H.J.L.), the National Institute for Health Research Southampton Clinical Research Facility, Southampton (W.R.), and the North Bristol NHS Trust, Southmead Hospital, Bristol (M. Gompels) - all in the United Kingdom; the Department of Dermatology, Medical University of Vienna, Vienna (T.K.), and the Department of Dermatology and Venereology, Medical University of Graz, Graz (W.A.) - both in Austria; the Hungarian Angioedema Reference Center, 3rd Department of Internal Medicine, Semmelweis University, Budapest, Hungary (H.F.); the Allergology Unit, Department of Internal Medicine, Hospital Universitario Bellvitge de L'Hospitalet de Llobregat (R.L.) and Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute (M. Guilarte), Barcelona, Hospital General Universitario Gregorio Marañón, Biomedical Research Network on Rare Diseases (Centro de Investigación Biomédica en Red de Enfermedades Raras)-Unit 761, Institute for Health Research, Gregorio Marañon, Madrid (M.L.B.), and Hospital Universitario Virgen del Rocío, Seville (T.G.-Q.) - all in Spain; the Division of Allergy and Clinical Immunology, University of Salerno, Salerno (M.T.), the Department of Medicine, University of Padua, Padua (M. Cancian), and Azienda Socio Sanitaria Territoriale Fatebenefratelli Sacco-Università degli Studi di Milano, Milan (A.Z., M. Cicardi) - all in Italy; the Department of Clinical Immunology and Allergy, Royal Adelaide Hospital, Adelaide, SA (W.B.S.), and Campbelltown Hospital, Immunology and Allergy, Western Sydney University, Sydney (C.K.) - both in Australia; and BioCryst Pharmaceuticals (S.D., M. Cornpropst, D.C., P.C., W.S.) and PharStat (L.F.) - both in Durham, NC.

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http://dx.doi.org/10.1056/NEJMoa1716995DOI Listing
July 2018

Cladribine treatment of multiple sclerosis is associated with depletion of memory B cells.

J Neurol 2018 May 17;265(5):1199-1209. Epub 2018 Mar 17.

Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, 4 Newark Street, London, E1 2AT, UK.

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http://dx.doi.org/10.1007/s00415-018-8830-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937883PMC
May 2018

Optimum Use of Acute Treatments for Hereditary Angioedema: Evidence-Based Expert Consensus.

Authors:
Hilary Longhurst

Front Med (Lausanne) 2017 12;4:245. Epub 2018 Mar 12.

Honorary Consultant Immunologist, Department of Clinical Biochemistry and Immunology, Addenbrooke's Hospital, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.

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http://dx.doi.org/10.3389/fmed.2017.00245DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5857575PMC
March 2018

A novel de novo activating mutation in STAT3 identified in a patient with common variable immunodeficiency (CVID).

Clin Immunol 2018 02 24;187:132-136. Epub 2017 Nov 24.

Institute of Biomedical and Clinical Science, University of Exeter, Exeter, UK.

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http://dx.doi.org/10.1016/j.clim.2017.11.007DOI Listing
February 2018

Kidney Transplantation in a Patient Lacking Cytosolic Phospholipase A Proves Renal Origins of Urinary PGI-M and TX-M.

Circ Res 2018 02 3;122(4):555-559. Epub 2018 Jan 3.

From the National Heart and Lung Institute, Imperial College London, United Kingdom (J.A.M., N.S.K., D.M.R.); Blizard Institute, Queen Mary University of London, United Kingdom (R.B.K., W.E.W., M.V.C., M.M.Y., T.D.W.); National Institute for Environmental Health Sciences, Research Triangle, NC (M.L.E., D.C.Z.); Department of Nephrology (W.E.W., M.M.Y.) and Immunology Department (H.L.), Barts Health NHS Trust, London, United Kingdom; and Departments of Pharmacology and Medicine, Vanderbilt University, Nashville, TN (G.L.M.).

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http://dx.doi.org/10.1161/CIRCRESAHA.117.312144DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5816977PMC
February 2018

Prophylactic Therapy for Hereditary Angioedema.

Immunol Allergy Clin North Am 2017 08;37(3):557-570

Department of Immunology, Barts Health NHS Trust, Pathology and Pharmacy Building, 80 Newark Street, London E1 2HS, UK.

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https://linkinghub.elsevier.com/retrieve/pii/S08898561173004
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http://dx.doi.org/10.1016/j.iac.2017.04.003DOI Listing
August 2017

Prevention of Hereditary Angioedema Attacks with a Subcutaneous C1 Inhibitor.

N Engl J Med 2017 03;376(12):1131-1140

From Barts Health NHS Trust (H.L.) and St. John's Institute of Dermatology, Guy's Hospital (C.G.), London, and the Clinical Investigation and Research Unit, Royal Sussex County Hospital, Brighton (M.T.) - all in the United Kingdom; Ospedale Luigi Sacco-U.O. Medicina Generale, Milan (M.C.), and the Department of Internal Medicine, University of Catania, Catania (S.N.) - both in Italy; Department of Medicine and Pediatrics, Penn State Hershey Allergy, Asthma, and Immunology, Hershey (T. Craig), and CSL Behring, King of Prussia (D.B.-K., J.E., D.P.) - both in Pennsylvania; the Department of Dermatology, Johannes Gutenberg University Mainz, Mainz (K.B.), and CSL Behring, Marburg (H. Feuersenger, J.-P.L., T.M., I.P.) - both in Germany; Baker Allergy, Asthma and Dermatology Research Center, Portland, OR (J. Baker); Institute for Asthma and Allergy, Chevy Chase, MD (H.H.L.); Allergy and Immunology Unit, Chaim Sheba Medical Center, Tel Hashomer (A.R.), and Allergy and Immunology Unit, Tel Aviv Sourasky Medical Center, Tel Aviv (S.K.) - both in Israel; Clinical Research Center of Alabama, Birmingham (J. Bonner, J.A.); Department of Internal Medicine, Allergy Section Cincinnati, University of Cincinnati College of Medicine, Cincinnati (J.A.B.), and Toledo Institute of Clinical Research, Toledo (S.M.R.) - both in Ohio; Allergy Asthma Research Associates Research Center, Dallas (W.R.L.); Hungarian Angioedema Center, Third Department of Internal Medicine, Semmelweis University, Budapest (H. Farkas); the Department of Medicine, Immunology, and Allergy, Campbelltown Hospital, Campbelltown, NSW, Australia (C.H.K.); the Department of Clinical Immunology and Allergy, St. Michael's Hospital, Toronto (G.L.S.), Centre de Recherche Appliqué en Allergie de Québec, Quebec, QC (J.H.), McMaster University, Hamilton, ON (P.K.K.), Ottawa Allergy Research and University of Ottawa Medical School, Ottawa (W.Y.), and University of Alberta Hospital, Edmonton (B.R.) - all in Canada; Allergy and Asthma Clinical Research, Walnut Creek (J.J.), University of California, San Diego School of Medicine, La Jolla (M.R., B.L.Z.), and 705 W. La Veta Ave., Suite 101, Orange (D.S.L.) - all in California; Medical Research of Arizona, Scottsdale (M.E.M.); Hospital General Universitario Gregorio Marañón and Biomedical Research Network on Rare Diseases-U761, Institute for Health Research, Gregorio Marañón (M.L.B.), and the Allergy Department, Hospital La Paz Institute for Health Research, Biomedical Research Network on Rare Diseases (T. Caballero), Madrid, the Allergy Department, IIS Hospital Universitario La Fe, Valencia (M.D.H.), and Hospital Universitario Vall d'Hebron, Barcelona (M.G.) - all in Spain; Asthma and Allergy Association, Colorado Springs, CO (R.N.); Department of Internal Medicine, Virginia Commonwealth University, Richmond (L.B.S.); Spitalul Clinic Municipal, Cluj-Napoca, Romania (I.C.); Vital Prospects Clinical Research Institute, Tulsa, OK (I.H.); Institute of Clinical Immunology and Allergology, University Hospital, Hradec Kralove, Czech Republic (P.K.); Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital, Boston (A.B.); and Marycliff Allergy Specialists, Spokane, WA (R.G.G.).

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http://dx.doi.org/10.1056/NEJMoa1613627DOI Listing
March 2017

How Not to Be Misled by Disorders Mimicking Angioedema: A Review of Pseudoangioedema.

Int Arch Allergy Immunol 2016 22;169(3):163-70. Epub 2016 Apr 22.

Department of Otorhinolaryngology, Head and Neck Surgery, University Hospital of Sjaelland, Koege, Denmark.

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http://dx.doi.org/10.1159/000445835DOI Listing
February 2017

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study.

J Allergy Clin Immunol 2017 02 16;139(2):597-606.e4. Epub 2016 Jul 16.

Department of Paediatric Immunology, Newcastle upon Tyne hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom; Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, United Kingdom.

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http://dx.doi.org/10.1016/j.jaci.2016.06.021DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292996PMC
February 2017

Kallikrein Inhibition for Hereditary Angioedema.

N Engl J Med 2017 02;376(8):788-789

From the Barts Health NHS Trust, London.

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http://dx.doi.org/10.1056/NEJMe1611929DOI Listing
February 2017

The Humanistic, Societal, and Pharmaco-economic Burden of Angioedema.

Clin Rev Allergy Immunol 2016 Oct;51(2):230-9

HAE Centre Denmark, Department of Dermatology and Allergy Centre, Odense University Hospital, 5000, Odense C, Denmark.

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http://link.springer.com/10.1007/s12016-016-8575-2
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http://dx.doi.org/10.1007/s12016-016-8575-2DOI Listing
October 2016

Misdiagnosis trends in patients with hereditary angioedema from the real-world clinical setting.

Ann Allergy Asthma Immunol 2016 10;117(4):394-398

Allergy Department, Hospital La Paz Institute for Health Research, Biomedical Research Network on Rare Diseases (CIBERER, U754), Madrid, Spain.

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http://dx.doi.org/10.1016/j.anai.2016.08.014DOI Listing
October 2016

Prophylaxis of hereditary angioedema attacks: A randomized trial of oral plasma kallikrein inhibition with avoralstat.

J Allergy Clin Immunol 2016 09 11;138(3):934-936.e5. Epub 2016 May 11.

Department of Dermatology and Allergy, Allergie-Centrum-Charité, Charité - Universitätsmedizin Berlin, Berlin, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00916749163027
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http://dx.doi.org/10.1016/j.jaci.2016.03.043DOI Listing
September 2016

Optimizing hereditary angioedema management through tailored treatment approaches.

Expert Rev Clin Immunol 2016 23;12(1):19-31. Epub 2015 Oct 23.

a Department of Immunology, Barts Health NHS Trust , London , UK.

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http://dx.doi.org/10.1586/1744666X.2016.1100963DOI Listing
August 2016

The Icatibant Outcome Survey: treatment of laryngeal angioedema attacks.

Eur J Emerg Med 2016 Jun;23(3):224-7

aDepartment of Immunology, Barts Health NHS TrustbDepartment of Dermatology and Venereology, Medical University of Graz, Graz, AustriacInternal Medicine Department, National Reference Centre for Angioedema, Grenoble University Hospital, Grenoble, FrancedAllergy Department, Hospital La Paz Institute for Health Research (IdiPaz), Biomedical Research Network on Rare Diseases (CIBERER, U754), Madrid, SpaineDepartment of Dermatology and Allergy, Allergie-Centrum-Charité, Charité - Universitätsmedizin Berlin, Berlin, GermanyfShire, Zug, SwitzerlandgDepartment of Biomedical and Clinical Sciences, University of Milan, Luigi Sacco Hospital, Milan, Italy.

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http://dx.doi.org/10.1097/MEJ.0000000000000292DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892758PMC
June 2016

Human Platelets Utilize Cycloxygenase-1 to Generate Dioxolane A3, a Neutrophil-activating Eicosanoid.

J Biol Chem 2016 Jun 22;291(26):13448-64. Epub 2016 Apr 22.

From the Systems Immunity Research Institute and Division of Infection and Immunity, School of Medicine, Cardiff University, Cardiff CF14 4XN, United Kingdom,

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http://dx.doi.org/10.1074/jbc.M115.700609DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919433PMC
June 2016

Inherited human group IVA cytosolic phospholipase A2 deficiency abolishes platelet, endothelial, and leucocyte eicosanoid generation.

FASEB J 2015 Nov 16;29(11):4568-78. Epub 2015 Jul 16.

*National Heart and Lung Institute, Imperial College London, London, United Kingdom; William Harvey Research Institute, Queen Mary University of London, London, United Kingdom; National Institutes of Health, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA; Department of Comparative Biomedical Sciences, Royal Veterinary College, London, United Kingdom; Department of Pharmacology and Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA; and Immunology Department, Barts Health and the London National Health Service Trust, London, United Kingdom

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http://www.fasebj.org/content/early/2015/07/16/fj.15-275065.
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http://www.fasebj.org/cgi/doi/10.1096/fj.15-275065
Publisher Site
http://dx.doi.org/10.1096/fj.15-275065DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4608906PMC
November 2015

Development and content validity testing of a patient-reported outcomes questionnaire for the assessment of hereditary angioedema in observational studies.

Health Qual Life Outcomes 2015 Jul 1;13:92. Epub 2015 Jul 1.

Department of Medicine, Division of Rheumatology, Allergy and Immunology, UC San Diego School of Medicine, San Diego, CA, USA.

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http://dx.doi.org/10.1186/s12955-015-0292-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487558PMC
July 2015

Treatment of hereditary angioedema with icatibant: efficacy in clinical trials versus effectiveness in the real-world setting.

Allergy Asthma Proc 2014 Sep-Oct;35(5):377-81. Epub 2014 Aug 6.

Department of Dermatology and Allergy, Allergie-Centrum-Charité, Charité-Universitätsmedizin Berlin, Berlin, Germany.

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http://dx.doi.org/10.2500/aap.2014.35.3780DOI Listing
June 2015

Longitudinally extensive transverse myelitis: a rare association with common variable immunodeficiency.

Pract Neurol 2015 Feb 21;15(1):49-52. Epub 2014 Oct 21.

Homerton University Hospital NHS Trust, National Hospital of Neurology and Neurosurgery, UCH, London, UK.

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http://dx.doi.org/10.1136/practneurol-2014-000953DOI Listing
February 2015

Secondary antibody deficiency.

Expert Rev Clin Immunol 2014 May 31;10(5):583-91. Epub 2014 Mar 31.

Immunology Department, Royal London Hospital, Barts Health NHS Trust, London, UK.

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http://dx.doi.org/10.1586/1744666X.2014.902314DOI Listing
May 2014

Acquired C1 inhibitor deficiency: should we monitor for associated antibody deficiency?

Ann Allergy Asthma Immunol 2014 Mar;112(3):265-7

Department of Immunopathology, Barts Health NHS Trust, Royal London Hospital, London, England. Electronic address:

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http://dx.doi.org/10.1016/j.anai.2013.12.024DOI Listing
March 2014

Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α.

Gut 2014 Jan 25;63(1):96-104. Epub 2012 Dec 25.

Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, , London, UK.

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http://dx.doi.org/10.1136/gutjnl-2012-303581DOI Listing
January 2014

Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe.

Allergy Asthma Clin Immunol 2013 Aug 12;9(1):29. Epub 2013 Aug 12.

Department of Clinical Science "Luigi Sacco", University of Milan, Milan, Italy.

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http://dx.doi.org/10.1186/1710-1492-9-29DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751114PMC
August 2013

Recurrent mycobacterial infections in a patient with IL-12 deficiency.

BMJ Case Rep 2009 1;2009. Epub 2009 Dec 1.

Barts and the London NHS Trust, Immunology, 214, 80 Newark St, London E1 2ES, UK.

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http://dx.doi.org/10.1136/bcr.11.2008.1278DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3028165PMC
October 2012

Many faces of angioedema: focus on the diagnosis and management of abdominal manifestations of hereditary angioedema.

Eur J Gastroenterol Hepatol 2012 Apr;24(4):353-61

Department of Gastroenterology, Hepatology, and Gastrointestinal Endoscopy, Watson Clinic LLP, Lakeland, Florida 33805, USA.

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http://dx.doi.org/10.1097/MEG.0b013e3283517998DOI Listing
April 2012

Diagnosis and treatment of hereditary angio-oedema attacks.

Br J Hosp Med (Lond) 2012 Mar;73(3):148-54

Department of Immunopathology, Barts and The London NHS Trust, London E1 2ES.

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http://dx.doi.org/10.12968/hmed.2012.73.3.148DOI Listing
March 2012

Hereditary angio-oedema.

Lancet 2012 Feb;379(9814):474-81

Department of Immunology, Barts and The London National Health Service Trust, Whitechapel, London, UK.

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http://dx.doi.org/10.1016/S0140-6736(11)60935-5DOI Listing
February 2012

New Frontiers in Subcutaneous Immunoglobulin Treatment.

Biol Ther 2011 14;1. Epub 2011 Dec 14.

CSL Behring LLC, King of Prussia, PA USA ; Case Western Reserve University, Cleveland, OH USA.

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http://dx.doi.org/10.1007/s13554-011-0009-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3873072PMC
December 2011

Management of acute attacks of hereditary angioedema: potential role of icatibant.

Vasc Health Risk Manag 2010 Sep 7;6:795-802. Epub 2010 Sep 7.

Department of Immunology, Barts and The London NHS Trust, London, UK.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2941790PMC
http://dx.doi.org/10.2147/vhrm.s4332DOI Listing
September 2010

Disease expression in women with hereditary angioedema.

Am J Obstet Gynecol 2008 Nov 13;199(5):484.e1-4. Epub 2008 Jun 13.

Department of Internal Medicine, Grenoble University Hospital, Grenoble, France.

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http://dx.doi.org/10.1016/j.ajog.2008.04.034DOI Listing
November 2008

Rhucin, a recombinant C1 inhibitor for the treatment of hereditary angioedema and cerebral ischemia.

Authors:
Hilary Longhurst

Curr Opin Investig Drugs 2008 Mar;9(3):310-23

Barts and The London NHS Trust, Department of Immunology, 80 Newark Street, London E1 2ES, UK.

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March 2008

Secondary systemic lupus erythematosus: an analysis of 4 cases of uncontrolled hereditary angioedema.

Clin Immunol 2007 Apr 13;123(1):14-7. Epub 2006 Nov 13.

Path Links Immunology, Scunthorpe General Hospital, Scunthorpe, North Lincolnshire, UK.

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http://dx.doi.org/10.1016/j.clim.2006.09.015DOI Listing
April 2007

Hereditary angioedema: causes, manifestations and treatment.

Br J Hosp Med (Lond) 2006 Dec;67(12):654-7

Department of Immunology, Barts and The London NHS Trust, London E1 2ES.

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http://dx.doi.org/10.12968/hmed.2006.67.12.22439DOI Listing
December 2006

Sporadic case of warts, hypogammaglobulinemia, immunodeficiency, and myelokathexis syndrome.

J Allergy Clin Immunol 2005 Nov 10;116(5):1101-5. Epub 2005 Oct 10.

Department of Immunology, St Bartholomew's Hospital, West Smithfield, London, EC1A 7BE, United Kingdom.

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http://dx.doi.org/10.1016/j.jaci.2005.08.040DOI Listing
November 2005

Osteomyelitis complicating pyomyositis in HIV disease.

Int J STD AIDS 2004 Sep;15(9):632-4

Department of Immunology, Imperial College, Hammersmith Campus, 10th Floor, Commonwealth Building, Du Cane Road, London W12 0NN, UK.

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http://dx.doi.org/10.1258/0956462041724226DOI Listing
September 2004

Non-myeloablative bone marrow transplantation in an adult with Wiskott-Aldrich syndrome.

Br J Haematol 2002 Feb;116(2):497-9

Department of Immunopathology, St Bartholomew's Hospital, London, UK.

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http://dx.doi.org/10.1046/j.1365-2141.2002.03269.xDOI Listing
February 2002