(Q35130973)

6 August 2017

title

Systemic disease and periodontitis: manifestations of neutrophil dysfunction (English)

1 reference

6 August 2017

0 references

David E Deas

1

1 reference

6 August 2017

Scott A Mackey

series ordinal

2

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6 August 2017

Howard T McDonnell

series ordinal

3

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6 August 2017

language of work or name

1 reference

1 January 2003

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6 August 2017

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6 August 2017

volume

32

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6 August 2017

page(s)

82-104

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Neutrophil function disorders

6 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Follow up of patients with chronic granulomatous disease diagnosed since 1990

21 January 2018

1 reference

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Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Agranulocytosis. Dental case report

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

21 January 2018

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Characterization of matrix metalloproteinase (MMP-8 and -9) activities in the saliva and in gingival crevicular fluid of children with Down's syndrome

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

The Chediak-Higashi syndrome. Report of a case and review of the literature

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Neutrophil defects as risk factors for periodontal diseases

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Clinical, molecular, and cell biological aspects of Chediak-Higashi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

An Association Between Crohn's Disease, Periodontal Disease and Enhanced Neutrophil Function

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Clinical manifestation of myeloperoxidase deficiency

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Review of systemic lupus erythematosus

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Periodontal diseases: pathogenesis

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Periodontal Disease Among Children with Down's Syndrome and Their Siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Prepubertal periodontitis affecting the deciduous and permanent dentition in a patient with cyclic neutropenia. A case report and discussion

21 January 2018

1 reference

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Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Neutropenia: when and when not to treat

21 January 2018

1 reference

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Recombinant human interferon-gamma in patients with chronic granulomatous disease —European follow up study

21 January 2018

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Management of Kostmann syndrome in the G-CSF era.

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Prepubertal periodontitis associated with chronic granulomatous disease

21 January 2018

1 reference

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Defective Neutrophil Chemotaxis and Cellular Immunity in a Child with Recurrent Infections

21 January 2018

1 reference

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CD8+, CD57+ T cells from healthy elderly subjects suppress neutrophil development in vitro: implications for the neutropenia of Felty's and large granular lymphocyte syndromes

21 January 2018

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Oral aspects of mongolism. I. Periodontal disease in mongolism

21 January 2018

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Phagocytic cells in periodontal defense. Periodontal status of patients with chronic granulomatous disease of childhood

21 January 2018

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FAMILIAL BENIGN CHRONIC NEUTROPENIA

21 January 2018

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Familial benign chronic neutropenia associated with periodontal disease. A case report

21 January 2018

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Oral manifestations of congenital neutropenia or Kostmann syndrome.

21 January 2018

1 reference

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Abnormal lymphocyte profiles and leukotriene B4 status in a patient with Crohn's disease and severe periodontitis

21 January 2018

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Chronic granulomatous disease

21 January 2018

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Chronic granulomatous disease in Japan: incidence and natural history. The Study Group of Phagocyte Disorders of Japan

21 January 2018

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Chronic neutropenia during childhood. A 13-year experience in a single institution

21 January 2018

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An analysis of peripheral blood and salivary polymorphonuclear leukocyte function, circulating immune complex levels and oral status in patients with inflammatory bowel disease

21 January 2018

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The granulocytopenic patient: another consideration for antimicrobial prophylaxis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

The importance of regular dental treatment in patients with cyclic neutropenia. Follow-up of 2 cases

21 January 2018

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https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Chédiak-Higashi syndrome. Neurologic appearance

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Prolonged pure granulocytopenia in children

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

The Chediak-Higashi-Steinbrinck syndrome. Presentation of three cases with features resembling spinocerebellar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Chédiak-Higashi syndrome: hematopoietic chimerism corrects genetic defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

The Papillon-Lefèvre syndrome: Neutrophil dysfunction with severe periodontal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

Periodontal manifestations of the heritable Mac-1, LFA-1, deficiency syndrome. Clinical, histopathologic and molecular characteristics

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0906-6713.2003.03207.X

10.1046/J.0906-6713.2003.03207.X

21 January 2018

Identifiers

DOI

1 reference

6 August 2017

1 reference