scholarly article | Q13442814 |
P356 | DOI | 10.1016/J.JACI.2010.07.037 |
P698 | PubMed publication ID | 20864152 |
P50 | author | Margarita López-Trascasa | Q54422019 |
Christian Drouet | Q57082941 | ||
P2093 | author name string | Alberto López-Lera | |
Sofía Garrido | |||
Bertrand Favier | |||
Rocío Mena de la Cruz | |||
P433 | issue | 6 | |
P921 | main subject | homozygosity | Q114049690 |
P304 | page(s) | 1307-10.e3 | |
P577 | publication date | 2010-12-01 | |
P1433 | published in | The Journal of Allergy and Clinical Immunology | Q7743550 |
P1476 | title | A new case of homozygous C1-inhibitor deficiency suggests a role for Arg378 in the control of kinin pathway activation | |
P478 | volume | 126 |
Q37833773 | Advances in basic and clinical immunology in 2010. |
Q38817627 | Angioedema Phenotypes: Disease Expression and Classification. |
Q33969976 | Expression of the SERPING1 gene is not regulated by promoter hypermethylation in peripheral blood mononuclear cells from patients with hereditary angioedema due to C1-inhibitor deficiency. |
Q41072058 | Fatal laryngeal angioedema: a case report and a workup of angioedema in a forensic setting |
Q38818135 | Genetics of Hereditary Angioedema Revisited |
Q64107494 | Identification and Mapping of a 2,009-bp DNA Deletion in of a Hereditary Angioedema Patient |
Q48223638 | Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight |
Q38025607 | Long-term prophylaxis in hereditary angio-oedema: a systematic review. |
Q62273446 | Pathophysiology of Hereditary Angioedema |
Q34805433 | Pediatric hereditary angioedema |
Q90090895 | SERPING1 mutation update: Mutation spectrum and C1 Inhibitor phenotypes |
Search more.