about
Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working GroupAre complement deficiencies really rare? Overview on prevalence, clinical importance and modern diagnostic approachRecurrent infections in partial complement factor I deficiency: evaluation of three generations of a Brazilian familyBCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policiesNeutrophils and mononuclear cells from patients with chronic granulomatous disease release nitric oxide.Lymphocyte transformation assay for C neoformans antigen is not reliable for detecting cellular impairment in patients with neurocryptococcosisRevisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries.IRF8 mutations and human dendritic-cell immunodeficiency.Brazilian guidelines for the diagnosis and treatment of hereditary angioedema.Involvement of C4 allotypes in the pathogenesis of human diseases.Hereditary angioedema: quality of life in Brazilian patients.Allergy to beta-lactams in pediatrics: a practical approach.WAO Guideline for the Management of Hereditary AngioedemaCase Title: 45 year-old male with recurrent angioedema: WAO international case-based discussionsAttending to warning signs of primary immunodeficiency diseases across the range of clinical practiceCritical issues and needs in management of primary immunodeficiency diseases in Latin America.Advancing the management of primary immunodeficiency diseases in Latin America: Latin American Society for Immunodeficiencies (LASID) Initiatives.International consensus on hereditary and acquired angioedema.Guidelines for the use of human immunoglobulin therapy in patients with primary immunodeficiencies in Latin America.First report of the Hyper-IgM syndrome Registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomes.Icatibant, an inhibitor of bradykinin receptor 2, for hereditary angioedema attacks: prospective experimental single-cohort study.Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry.Skipping of exon 27 in C3 gene compromises TED domain and results in complete human C3 deficiency.Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema.A homozygous CARD9 mutation in a Brazilian patient with deep dermatophytosis.Molecular characterization of patients with X-linked Hyper-IgM syndrome: description of two novel CD40L mutations.The use of reverse transcription-PCR for the diagnosis of X-linked chronic granulomatous disease.[Therapeutic approach of hereditary angioedema].Chédiak-Higashi syndrome: presentation of seven cases.A new CARD9 mutation (R101S) in a Brazilian patient with DEEP dermatophytosis.Hereditary angioedema with C1 inhibitor deficiency: experience of a new reference center.Esophageal cancer associated with chronic mucocutaneous candidiasis. Could chronic candidiasis lead to esophageal cancer?Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics.First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor.Evaluation of inspiratory pressure in children with enlarged tonsils and adenoids.Complement profile in neonates of different gestational ages.[Severe combined immunodeficiency: description of a clinical case]Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency.Immunoglobulin G subclass concentrations and infections in children and adolescents with severe asthma.
P50
Q27009012-25AA7D7C-B2AE-47AE-BD4C-663F9E201E8CQ28244196-507D2C0E-3209-46E3-9D0F-C26F1C9EFDE6Q28291779-3DC698F2-DC27-4451-867A-2D37DB572477Q33587953-78EE8814-5699-4620-93B7-E67746745F82Q34404279-5482909D-3AA0-49F9-896E-01042A8DC278Q34461657-71082FB4-D3D6-46B0-BEEA-9062FCF3C291Q35086274-CDA87F37-2840-4623-B5A5-10AA093C8BF1Q35106002-D478B548-CF40-458B-A2DB-321501B7F50CQ35188409-664EC954-455F-49A6-880E-55F8EBC58856Q35852372-7662DA11-0576-48C7-BEBB-37D089CE71A6Q36555078-309DF380-D010-455C-B96A-58172EE3C824Q36669138-D9586EC0-1087-4A1C-A1A7-90B82AA54E7BQ36834816-D286F1A7-6B83-43BE-AE61-F08304A2CD4DQ37593155-2759BD5D-EE6A-4B0F-BBA9-1721A2E2C62DQ37595906-D9E5DD26-D346-43DC-AF6A-3BC65EE64B5DQ37822047-9522B63B-18EC-4729-97A9-2A77950167D0Q37996695-4ABA753B-C2C6-4D95-98A6-5AA16DAD00B6Q38062049-964052F3-BAE7-492B-A3F4-9B8167853170Q38075346-9B79F0BD-BD8B-470C-985D-B9C27B7CEBFAQ38928362-22749579-B191-4E8F-BE4B-AF4D6BEDF43AQ39203476-2E2D215E-61D8-48FC-9E2A-978923B37EBAQ39927203-36B8BE0F-F672-4627-8601-F69F28A96CA8Q40725842-54C52399-29DC-47EF-A59C-C75591AA0DA8Q40804538-7E85A7FB-E77E-427C-980D-035DCD83AE17Q40988824-41A7DDD5-F4AC-47D9-AB47-8DE6919126E6Q41184628-E1BF1B68-8CE1-4B89-97B9-FFBB2EDFFE34Q43498814-89E87558-4358-4FB3-A632-9E38A4956BBAQ44859797-3D9CC059-A3A9-46CB-9B04-BEE1D4B7F06DQ45119796-F67BFB5B-96E3-4458-8B6E-D98702AD63A4Q45230031-7882C76B-8C0A-4383-BC23-652DF879B766Q45910148-DA69EE1F-B0AA-4C9F-8F2B-D1BBA76D8070Q46216850-A8E75BB3-AD3D-4728-8642-1EE7A5F46025Q46362704-8DC80CF1-2C69-451D-8F7B-4397AF2643ACQ46670704-3D7F4A7D-EA6F-4816-A697-2301476B5C86Q48259111-FF3BD84D-CFB0-4647-A7D8-3839AC1A206AQ48505112-AD312FDC-5A27-4EC8-AD04-F38F044B715BQ50693765-BEF016CB-298B-4174-BD56-1CC10695936DQ51048962-02A9A043-A883-421D-93AE-5378203ECF29Q51663372-075484FD-D339-402D-B84B-3F3CB238F58FQ51709260-0140A38B-821C-4448-90AE-3D4E5515717E
P50
description
Forscher
@de
chercheur
@fr
investigador
@es
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
研究者
@zh
name
Anete S Grumach
@ast
Anete S Grumach
@en
Anete S Grumach
@es
Anete S Grumach
@nl
type
label
Anete S Grumach
@ast
Anete S Grumach
@en
Anete S Grumach
@es
Anete S Grumach
@nl
altLabel
Anete Grumach
@en
prefLabel
Anete S Grumach
@ast
Anete S Grumach
@en
Anete S Grumach
@es
Anete S Grumach
@nl
P106
P214
6151170930539091932
P2798
P31
P496
0000-0002-9803-0309
P735
P7859
viaf-6151170930539091932