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humans (104) 104
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Pediatric Drugs, ISSN 1174-5878, 4/2018, Volume 20, Issue 2, pp. 135 - 151
Journal Article
Paediatric drugs, 04/2018, Volume 20, Issue 2, p. 135
Hereditary angioedema with C1-inhibitor deficiency (C1-INH-HAE) is a form of bradykinin-mediated angioedema. It is a rare disorder with an onset during... 
Journal Article
Expert Opinion on Pharmacotherapy, ISSN 1465-6566, 04/2013, Volume 14, Issue 5, pp. 571 - 586
Introduction: Bradykinin-mediated angioedema is characterized by subcutaneous and/or submucosal edema formation without wheals and pruritus. It is linked to... 
treatment | attenuated androgens | recombinant human C1-inhibitor concentrate | antifibrinolytics | plasma derived C1-inhibitor concentrate | bradykinin-mediated angioedema | bradykinin B2 receptor antagonist | kallikrein inhibitor | Kallikrein inhibitor | Antifibrinolytics | Attenuated androgens | Recombinant human C1-inhibitor concentrate | Treatment | Bradykinin B2 receptor antagonist | Bradykinin-mediated angioedema | Plasma derived C1-inhibitor concentrate | ACUTE ATTACKS | HEREDITARY ANGIONEUROTIC-EDEMA | SHORT-TERM PROPHYLAXIS | ACQUIRED C1-INHIBITOR DEFICIENCY | RECEPTOR ANTAGONIST | TRANEXAMIC ACID | C1 INHIBITOR DEFICIENCY | FACTOR-XII GENE | PHARMACOLOGY & PHARMACY | FRESH-FROZEN PLASMA | ESTERASE INHIBITOR | Recombinant Proteins - therapeutic use | Antifibrinolytic Agents - therapeutic use | Complement C1 Inhibitor Protein - therapeutic use | Bradykinin - metabolism | Hereditary Angioedema Types I and II - physiopathology | Humans | Hereditary Angioedema Type III - metabolism | Capillary Permeability - drug effects | Hereditary Angioedema Types I and II - metabolism | Treatment Outcome | Bradykinin - antagonists & inhibitors | Receptors, Bradykinin - metabolism | Signal Transduction - drug effects | Bradykinin Receptor Antagonists | Hereditary Angioedema Types I and II - drug therapy | Hereditary Angioedema Type III - drug therapy | Androgens - therapeutic use | Hereditary Angioedema Types I and II - diagnosis
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 02/2019, Volume 143, Issue 2, pp. AB48 - AB48
Journal Article
Pediatrics, ISSN 0031-4005, 02/2016, Volume 137, Issue 2, pp. 1 - 1
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare genetic disease that causes recurrent swelling attacks that may affect various body... 
Journal Article
Pediatrics, ISSN 0031-4005, 02/2016, Volume 137, Issue 2, p. 1
  Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare genetic disease that causes recurrent swelling attacks that may affect various... 
Babies | Pediatrics | Edema | Tissue | Genetic disorders | Blood vessels
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2012, Volume 129, Issue 2, pp. 308 - 320
Background There are a limited number of publications on the management of gynecologic/obstetric events in female patients with hereditary angioedema caused by... 
Allergy and Immunology | genetic counseling | delivery | hereditary angioedema | treatment | Angioedema | fertility | pregnancy | breast cancer | C1 inhibitor deficiency | contraception | UPPER AIRWAY-OBSTRUCTION | HUMAN C1-INHIBITOR CONCENTRATE | IMMUNOLOGY | HORMONE REPLACEMENT THERAPY | ANGIONEUROTIC-EDEMA | FACTOR-XII | PREIMPLANTATION GENETIC DIAGNOSIS | RECOMBINANT HUMAN C1-INHIBITOR | ALLERGY | LONG-TERM TREATMENT | FRESH-FROZEN PLASMA | ESTERASE INHIBITOR | Menstruation | Hereditary Angioedema Types I and II - complications | Lactation | Chemoprevention | Humans | Menopause | Prenatal Diagnosis | Infant | Complement C1 Inhibitor Protein | Contraception | Genital Diseases, Female - complications | Genetic Counseling | Hereditary Angioedema Types I and II - genetics | Pregnancy | Breast Neoplasms - complications | Complement C1 Inactivator Proteins - deficiency | Pregnancy Complications, Cardiovascular - drug therapy | Delivery, Obstetric | Hereditary Angioedema Types I and II - drug therapy | Female | Hereditary Angioedema Types I and II - diagnosis | Pregnancy Complications, Cardiovascular - diagnosis | Infant, Newborn | Women | Medroxyprogesterone | Angioneurotic edema | Universities and colleges | Health aspects | Plasma | Androgens | Task forces | Womens health | Amino acids | FDA approval | Family medical history | Drug dosages | Obstetrics
Journal Article
Expert Review of Clinical Pharmacology, ISSN 1751-2433, 06/2016, Volume 9, Issue 6, pp. 779 - 788
Journal Article
Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9875, pp. 1404 - 1404
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 02/2018, Volume 141, Issue 2, pp. AB49 - AB49
Time from the onset of the attack to dosing with rhC1-INH correlated with time to the nadir of worsening (R=0.1929, p<0.0001), to the beginning of improvement... 
ALLERGY | IMMUNOLOGY | Inhibitors | Patient satisfaction | Angioedema | Recombinant
Journal Article
Pediatrics, ISSN 0031-4005, 02/2016, Volume 137, Issue 2, pp. e20152411 - e20152411
Hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE) is a rare genetic disease that causes recurrent swelling attacks that may affect various body... 
C1 INHIBITOR | DIAGNOSIS | ATTACKS | PEDIATRICS | PRODROMAL SYMPTOMS | EDEMA | Erythema - etiology | Female | Hereditary Angioedema Types I and II - diagnosis | Hereditary Angioedema Types I and II - complications | Humans | Infant, Newborn | Infants (Newborn) | Complications and side effects | Angioneurotic edema | Care and treatment | Erythema | Health aspects
Journal Article
World Allergy Organization Journal, ISSN 1939-4551, 2012, Volume 5, Issue 12, pp. 182 - 199
: Hereditary Angioedema (HAE) is a rare disease and for this reason proper diagnosis and appropriate therapy are often unknown or not available for physicians... 
Therapy | Hereditary Angioedema | Medications | Diagnosis | Management | HAE | Guidelines | International | Angioneurotic edema | Care and treatment | Health care industry | Evidence-based medicine
Journal Article