Search Results - "Grumach AS"

Current challenges and future opportunities in patient‐focused management of hereditary angioedema: A narrative review.

Authors: Grumach, Anete S. Gadir, Noga Kessel, Aharon et al.

Source: Clinical & Translational Allergy. May2023, Vol. 13 Issue 5, p1-29. 29p.

Impact of asthma control on quality of life in an outpatient setting in Brazil.

Authors: Lourenco, Cristina Bassi Martins, Franco Fiss, Elie et al.

Source: Journal of Asthma. Apr2023, Vol. 60 Issue 4, p794-801. 8p.

Subjects: Asthma, Quality control, Asthmatics, Quality of life, Wheeze, Disease management, Cough

Geographic Terms: Brazil, São Paulo (Brazil)

Complement Profile in Neonates of Different Gestational Ages.

Authors: Grumach, A. S. Ceccon, M. E. Rutz, R. et al.

Source: Scandinavian Journal of Immunology. Apr2014, Vol. 79 Issue 4, p276-281. 6p.

Complement 4 phenotypes and genotypes in Brazilian patients with classical 21-hydroxylase deficiency.

Authors: Guerra-Junior, G. Grumach, A. Sevciovic de Lemos-Marini, S. H. Valente et al.

Source: Clinical & Experimental Immunology. Feb2009, Vol. 155 Issue 2, p182-188. 7p. 1 Black and White Photograph, 1 Diagram, 1 Chart.

Recurrent infections in partial complement factor I deficiency: evaluation of three generations of a Brazilian family.

Authors: Grumach, A. S. Leitão, M. F. Arruk, V. G. et al.

Source: Clinical & Experimental Immunology. Feb2006, Vol. 143 Issue 2, p297-304. 8p. 1 Diagram, 4 Charts.

New medications to mitigate attacks of hereditary angioedema: does one size fit all?

Authors: Reshef, Avner Grumach, Anete S

Source: Lancet. Feb2023, Vol. 401 Issue 10375, p413-415. 3p.

An International Delphi Study on Barriers to On‐Demand Treatment of Hereditary Angioedema Attacks.

Authors: Banerji, Aleena Aygören‐Pürsün, Emel Bara, Noemi‐Anna et al.

Source: Clinical & Translational Allergy. Mar2026, Vol. 16 Issue 3, p1-12. 12p.

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An ABC of the Warning Signs of Hereditary Angioedema.

Authors: Grumach, anete Sevciovic Ferraroni, Natasha Olivares, Maria Margarita et al.

Source: International Archives of Allergy & Immunology. Oct2017, Vol. 174 Issue 1, p1-6. 6p.

Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema.

Authors: Grumach, A. S. Stieber, C. Veronez, C. L. et al.

Source: Allergy. Jan2016, Vol. 71 Issue 1, p119-123. 5p. 1 Diagram, 1 Chart.

A Homozygous CARD9 Mutation in a Brazilian Patient with Deep Dermatophytosis.

Authors: Grumach, Anete Queiroz-Telles, Flavio Migaud, Mélanie et al.

Source: Journal of Clinical Immunology. Jul2015, Vol. 35 Issue 5, p486-490. 5p.

Are complement deficiencies really rare? Overview on prevalence, clinical importance and modern diagnostic approach.

Authors: Grumach, Anete Sevciovic Kirschfink, Michael

Source: Molecular Immunology. Oct2014, Vol. 61 Issue 2, p110-117. 8p.

Attending to Warning Signs of Primary Immunodeficiency Diseases Across the Range of Clinical Practice.

Authors: Costa-Carvalho, Beatriz Grumach, Anete Franco, José et al.

Source: Journal of Clinical Immunology. Jan2014, Vol. 34 Issue 1, p10-22. 13p.

Hereditary angioedema: first report of the Brazilian registry and challenges.

Authors: Grumach, A.S. Valle, S.O.R. Toledo, E. et al.

Source: Journal of the European Academy of Dermatology & Venereology. Mar2013, Vol. 27 Issue 3, pe338-e344. 7p.

Adenotonsillectomy improves the strength of respiratory muscles in children with upper airway obstruction

Authors: Banzatto, Melissa Guerato Pires Grumach, Anete S. Mello, João F. et al.

Source: International Journal of Pediatric Otorhinolaryngology. Aug2010, Vol. 74 Issue 8, p860-863. 4p.

Paracoccidioides brasiliensis Disseminated Disease in a Patient with Inherited Deficiency in the β1 Subunit of the Interleukin (IL)--12/IL-23 Receptor.

Authors: de Moraes-vasconcelos, Dewton Grumach, Anete S. Yamaguti, Augusto et al.

Source: Clinical Infectious Diseases. 8/15/2005, Vol. 41 Issue 4, pe31-e37. 7p.

Completion of the Icatibant Outcome Survey and What We Learned.

Authors: Bouillet, Laurence Aberer, Werner Caballero, Teresa et al.

Source: Clinical & Experimental Allergy. Jul2026, Vol. 56 Issue 7, p784-787. 4p.

Human Plasma‐Derived C1 Inhibitor for Short‐Term Prophylaxis in Hereditary Angioedema With Normal C1 Inhibitor.

Authors: de Melo Maricondi, Paula Christina Cavallini Minafra, Fernanda Gontijo Angulski, Luis Felipe Ramos Berbel et al.

Source: Clinical & Experimental Allergy. May2026, Vol. 56 Issue 5, p565-568. 4p.

First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor.

Authors: Stieber, C. Grumach, A.S. Cordeiro, E. et al.

Source: British Journal of Dermatology. Oct2015, Vol. 173 Issue 4, p1102-1104. 3p.

Targeting Complex Cutaneous Viral Infections in Search of Inborn Errors of Immunity.

Authors: DO CARMO, Ana Paula BATLLE, Amanda R. Lobao FRAGNAN, Nyla T. Melo et al.

Source: Acta Dermato-Venereologica. 2025, Vol. 105, p1-7. 7p.