Lista de obras - Anete S Grumach - Dominio Público Uruguay

A homozygous CARD9 mutation in a Brazilian patient with deep dermatophytosis

artículo científico publicado en 2015

A new CARD9 mutation (R101S) in a Brazilian patient with DEEP dermatophytosis.

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Advancing the management of primary immunodeficiency diseases in Latin America: Latin American Society for Immunodeficiencies (LASID) Initiatives.

artículo científico

Allergy to beta-lactams in pediatrics: a practical approach

artículo científico publicado en 2006

An alternative method for in vitro production of HIV-1-specific antibodies

artículo científico publicado el 1 de enero de 1991

Application of a fluorochrome-lysostaphin assay to the detection of phagocytic and bactericidal disturbances in human neutrophils and monocytes

artículo científico publicado en 1995

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

artículo científico publicado en 2014

Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice

artículo científico publicado en 2013

B cell subtypes' kinetics over a 6 monthxs period in CVID patients submitted to influenza and H1N1 immunization.

artículo científico publicado en 2015

BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies

artículo científico publicado en 2014

Brazilian guidelines for the diagnosis and treatment of hereditary angioedema

artículo científico publicado en 2011

Brazilian report on primary immunodeficiencies in children: 166 cases studied over a follow-up time of 15 years.

artículo científico publicado en 1997

Case Title: 45 year-old male with recurrent angioedema: WAO international case-based discussions

artículo científico publicado en 2014

Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics

artículo científico publicado en 2006

Chédiak-Higashi syndrome: presentation of seven cases.

artículo científico publicado en 1998

Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

artículo científico publicado en 2014

Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry

artículo científico publicado en 2015

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

artículo científico publicado en 2009

Complement and IgG subclasses in agammaglobulinemic patients

artículo científico publicado en 1995

Complement factor I deficiency in a family with recurrent infections ⬇️

artículo científico publicado el 1 de diciembre de 1997

Complement profile in neonates of different gestational ages

artículo científico publicado en 2014

Critical issues and needs in management of primary immunodeficiency diseases in Latin America.

artículo científico publicado en 2010

Deficiency of the human complement regulatory protein factor H associated with low levels of component C9.

artículo científico publicado en 2008

Deficiência de IgA: avaliação clínico-laboratorial de 60 pacientes do Instituto da Criança

scientific article published on 01 October 1998

Esophageal cancer associated with chronic mucocutaneous candidiasis. Could chronic candidiasis lead to esophageal cancer?

artículo científico publicado en 2008

Evaluation of inspiratory pressure in children with enlarged tonsils and adenoids

artículo científico publicado en 2005

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

artículo científico publicado en 2015

First report of the Hyper-IgM syndrome Registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomes

artículo científico publicado en 2014

Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencing

artículo científico publicado en 2016

Guidelines for the use of human immunoglobulin therapy in patients with primary immunodeficiencies in Latin America.

artículo científico

HLA antigens and haplotypes in IgA-deficient Brazilian paediatric patients

article

Hereditary angioedema with C1 inhibitor deficiency: experience of a new reference center

artículo científico publicado en 2015

Hereditary angioedema without deficiency of C1 inhibitor: response to therapy.

artículo científico publicado en 2015

Hereditary angioedema: quality of life in Brazilian patients

artículo científico publicado en 2013

High‐Performance Liquid Chromatography Under Partially Denaturing Conditions (dHPLC) is a Fast and Cost‐Effective Method for Screening Molecular Defects: Four Novel Mutations Found in X‐Linked Chronic Granulomatous Disease ⬇️

artículo científico publicado el 1 de agosto de 2012

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

artículo científico publicado en 2015

Hypogammaglobulinemia: a diagnosis that must not be overlooked

scientific article published on 10 October 2019

IRF8 mutations and human dendritic-cell immunodeficiency

artículo científico publicado en 2011

Icatibant, an inhibitor of bradykinin receptor 2, for hereditary angioedema attacks: prospective experimental single-cohort study

artículo científico publicado en 2014

Immunoglobulin G subclass concentrations and infections in children and adolescents with severe asthma

artículo científico publicado en 2002

Immunological Analysis in Paediatric HIV Patients at Different Stages of the Disease

article

Immunological factors in milk from Brazilian mothers delivering small-for-date term neonates

article

Improving C1 inhibitor deficiency (type 1 and type 2 hereditary angioedema) in Latin America

International consensus on hereditary and acquired angioedema

artículo científico publicado en 2012

Involvement of C4 allotypes in the pathogenesis of human diseases

artículo científico publicado en 2004

Is immunity in diabetic patients influencing the susceptibility to infections? Immunoglobulins, complement and phagocytic function in children and adolescents with type 1 diabetes mellitus

artículo científico publicado en 2005

Laboratory screening for the diagnosis of children with primary immunodeficiencies

artículo científico publicado el 1 de junio de 1991

Lymphocyte transformation assay for C neoformans antigen is not reliable for detecting cellular impairment in patients with neurocryptococcosis

artículo científico publicado en 2012

Meningococcal meningitis and complement deficiences.

artículo científico publicado en 2015

Methotrexate for steroid-dependent asthmatic children and adolescents

artículo científico publicado en 1997

Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox

artículo científico publicado en 1999

Molecular characterization of patients with X-linked Hyper-IgM syndrome: description of two novel CD40L mutations.

artículo científico publicado en 2009

Mycobacterium bovis dissemination (BCG strain) among immunodeficient Brazilian infants

article

Neutrophilic dermatosis: a new skin manifestation and novel pathogenic variant in a rare autoinflammatory disease

artículo científico publicado en 2020

Neutrophils and mononuclear cells from patients with chronic granulomatous disease release nitric oxide.

artículo científico publicado en 1993

New insights in vitiligo: cellular immune response

New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema

article

Nutritional factors in milk from Brazilian mothers delivering small for gestational age neonates

article

Paracoccidioides brasiliensis Disseminated Disease in a Patient with Inherited Deficiency in the 1 Subunit of the Interleukin (IL)-12/IL-23 Receptor

artículo científico publicado en 2005

Polarized light microscopy of hair shafts aids in the differential diagnosis of Chédiak-Higashi and Griscelli-Prunieras syndromes

scientific article published on 01 August 2006

Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID Registry

scientific article published on 27 December 2006

Primary immunodeficiency diseases in Latin America: Proceedings of the Second Latin American Society for Immunodeficiencies (LASID) Advisory Board ⬇️

artículo científico publicado el 22 de febrero de 2011

Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.

artículo científico publicado en 2016

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

artículo científico publicado en 2006

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

artículo científico publicado en 2010

Severe combined immunodeficiency in Brazil: management, prognosis, and BCG-associated complications

article

Severe combined immunodeficiency: description of a clinical case

artículo científico publicado en 1995

Skipping of exon 27 in C3 gene compromises TED domain and results in complete human C3 deficiency.

artículo científico publicado en 2016

Successful Allogenic Stem Cell Transplantation in Patients with Inherited CARD9 Deficiency

artículo científico publicado en 2019

The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

artículo científico publicado en 2022

The use of reverse transcription-PCR for the diagnosis of X-linked chronic granulomatous disease.

artículo científico publicado en 2004

Therapeutic approach of hereditary angioedema

artículo científico publicado en 2004

WAO Guideline for the Management of Hereditary Angioedema

artículo científico publicado en 2012

X-linked agammaglobulinemia in nine patients: review of the literature

artículo científico publicado el 1 de julio de 1997

[Asthma - Clinical and epidemiological aspects of 237 outpatients in a specialized pediatric unit]

artículo científico publicado en 1998

[Drug hypersensitivity in AIDS patients: report of a case]

artículo científico publicado en 1997

[Hereditary angioedema: clinical and laboratory aspects of 7 cases]

artículo científico publicado en 1998

[WAO Guideline for the Management of Hereditary Angioedema]

artículo científico publicado en 2015

Lista de obras de Anete S Grumach

A homozygous CARD9 mutation in a Brazilian patient with deep dermatophytosis

A new CARD9 mutation (R101S) in a Brazilian patient with DEEP dermatophytosis.

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

Advancing the management of primary immunodeficiency diseases in Latin America: Latin American Society for Immunodeficiencies (LASID) Initiatives.

Allergy to beta-lactams in pediatrics: a practical approach

An alternative method for in vitro production of HIV-1-specific antibodies

Application of a fluorochrome-lysostaphin assay to the detection of phagocytic and bactericidal disturbances in human neutrophils and monocytes

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

Attending to warning signs of primary immunodeficiency diseases across the range of clinical practice

B cell subtypes' kinetics over a 6 monthxs period in CVID patients submitted to influenza and H1N1 immunization.

BCG vaccination in patients with severe combined immunodeficiency: complications, risks, and vaccination policies

Brazilian guidelines for the diagnosis and treatment of hereditary angioedema

Brazilian report on primary immunodeficiencies in children: 166 cases studied over a follow-up time of 15 years.

Case Title: 45 year-old male with recurrent angioedema: WAO international case-based discussions

Chronic granulomatous disease in Latin American patients: clinical spectrum and molecular genetics

Chédiak-Higashi syndrome: presentation of seven cases.

Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

Clinical and Genotypic Spectrum of Chronic Granulomatous Disease in 71 Latin American Patients: First Report from the LASID Registry

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

Complement and IgG subclasses in agammaglobulinemic patients

Complement factor I deficiency in a family with recurrent infections ⬇️

Complement profile in neonates of different gestational ages

Critical issues and needs in management of primary immunodeficiency diseases in Latin America.

Deficiency of the human complement regulatory protein factor H associated with low levels of component C9.

Deficiência de IgA: avaliação clínico-laboratorial de 60 pacientes do Instituto da Criança

Esophageal cancer associated with chronic mucocutaneous candidiasis. Could chronic candidiasis lead to esophageal cancer?

Evaluation of inspiratory pressure in children with enlarged tonsils and adenoids

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

First report of the Hyper-IgM syndrome Registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomes

Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencing

Guidelines for the use of human immunoglobulin therapy in patients with primary immunodeficiencies in Latin America.

HLA antigens and haplotypes in IgA-deficient Brazilian paediatric patients

Hereditary angioedema with C1 inhibitor deficiency: experience of a new reference center

Hereditary angioedema without deficiency of C1 inhibitor: response to therapy.

Hereditary angioedema: quality of life in Brazilian patients

High‐Performance Liquid Chromatography Under Partially Denaturing Conditions (dHPLC) is a Fast and Cost‐Effective Method for Screening Molecular Defects: Four Novel Mutations Found in X‐Linked Chronic Granulomatous Disease ⬇️

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

Hypogammaglobulinemia: a diagnosis that must not be overlooked

IRF8 mutations and human dendritic-cell immunodeficiency

Icatibant, an inhibitor of bradykinin receptor 2, for hereditary angioedema attacks: prospective experimental single-cohort study

Immunoglobulin G subclass concentrations and infections in children and adolescents with severe asthma

Immunological Analysis in Paediatric HIV Patients at Different Stages of the Disease

Immunological factors in milk from Brazilian mothers delivering small-for-date term neonates

Improving C1 inhibitor deficiency (type 1 and type 2 hereditary angioedema) in Latin America

International consensus on hereditary and acquired angioedema

Involvement of C4 allotypes in the pathogenesis of human diseases

Is immunity in diabetic patients influencing the susceptibility to infections? Immunoglobulins, complement and phagocytic function in children and adolescents with type 1 diabetes mellitus

Laboratory screening for the diagnosis of children with primary immunodeficiencies

Lymphocyte transformation assay for C neoformans antigen is not reliable for detecting cellular impairment in patients with neurocryptococcosis

Meningococcal meningitis and complement deficiences.

Methotrexate for steroid-dependent asthmatic children and adolescents

Molecular analysis of chronic granulomatous disease caused by defects in gp91-phox

Molecular characterization of patients with X-linked Hyper-IgM syndrome: description of two novel CD40L mutations.

Mycobacterium bovis dissemination (BCG strain) among immunodeficient Brazilian infants

Neutrophilic dermatosis: a new skin manifestation and novel pathogenic variant in a rare autoinflammatory disease

Neutrophils and mononuclear cells from patients with chronic granulomatous disease release nitric oxide.

New insights in vitiligo: cellular immune response

New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema

Nutritional factors in milk from Brazilian mothers delivering small for gestational age neonates

Paracoccidioides brasiliensis Disseminated Disease in a Patient with Inherited Deficiency in the 1 Subunit of the Interleukin (IL)-12/IL-23 Receptor

Polarized light microscopy of hair shafts aids in the differential diagnosis of Chédiak-Higashi and Griscelli-Prunieras syndromes

Primary Immunodeficiency Diseases in Latin America: The Second Report of the LAGID Registry

Primary immunodeficiency diseases in Latin America: Proceedings of the Second Latin American Society for Immunodeficiencies (LASID) Advisory Board ⬇️

Psychometric Field Study of Hereditary Angioedema Quality of Life Questionnaire for Adults: HAE-QoL.

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

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

Severe combined immunodeficiency in Brazil: management, prognosis, and BCG-associated complications

Severe combined immunodeficiency: description of a clinical case

Skipping of exon 27 in C3 gene compromises TED domain and results in complete human C3 deficiency.

Successful Allogenic Stem Cell Transplantation in Patients with Inherited CARD9 Deficiency

The international WAO/EAACI guideline for the management of hereditary angioedema—The 2021 revision and update

The use of reverse transcription-PCR for the diagnosis of X-linked chronic granulomatous disease.

Therapeutic approach of hereditary angioedema

WAO Guideline for the Management of Hereditary Angioedema

X-linked agammaglobulinemia in nine patients: review of the literature

[Asthma - Clinical and epidemiological aspects of 237 outpatients in a specialized pediatric unit]

[Drug hypersensitivity in AIDS patients: report of a case]

[Hereditary angioedema: clinical and laboratory aspects of 7 cases]

[WAO Guideline for the Management of Hereditary Angioedema]