| P2093 | author name string | David E Deas | |
| | Howard T McDonnell | |
| | Scott A Mackey | |
| P2860 | cites work | Follow up of patients with chronic granulomatous disease diagnosed since 1990 | Q24681802 |
| | Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder | Q28138040 |
| | Clinical, molecular, and cell biological aspects of Chediak-Higashi syndrome | Q33755016 |
| | Management of Kostmann syndrome in the G-CSF era. | Q33962053 |
| | Review of systemic lupus erythematosus | Q34247865 |
| | Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review | Q34344755 |
| | Oral manifestations of congenital neutropenia or Kostmann syndrome. | Q34425947 |
| | Clinical manifestation of myeloperoxidase deficiency | Q34474652 |
| | Characterization of matrix metalloproteinase (MMP-8 and -9) activities in the saliva and in gingival crevicular fluid of children with Down's syndrome | Q36826552 |
| | Neutrophil function disorders | Q39685236 |
| | Periodontal Disease Among Children with Down's Syndrome and Their Siblings | Q39785373 |
| | The Chediak-Higashi syndrome. Report of a case and review of the literature | Q39911652 |
| | Neutrophil defects as risk factors for periodontal diseases | Q40681123 |
| | An Association Between Crohn's Disease, Periodontal Disease and Enhanced Neutrophil Function | Q40968673 |
| | 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 | Q40999514 |
| | Neutropenia: when and when not to treat | Q41241607 |
| | Periodontal diseases: pathogenesis | Q41444984 |
| | Agranulocytosis. Dental case report | Q43428661 |
| | Prepubertal periodontitis affecting the deciduous and permanent dentition in a patient with cyclic neutropenia. A case report and discussion | Q43725546 |
| | Recombinant human interferon-gamma in patients with chronic granulomatous disease —European follow up study | Q44518637 |
| | Prepubertal periodontitis associated with chronic granulomatous disease | Q62658352 |
| | The granulocytopenic patient: another consideration for antimicrobial prophylaxis | Q67918775 |
| | Periodontal manifestations of the heritable Mac-1, LFA-1, deficiency syndrome. Clinical, histopathologic and molecular characteristics | Q68163119 |
| | Chronic neutropenia during childhood. A 13-year experience in a single institution | Q68196810 |
| | Defective Neutrophil Chemotaxis and Cellular Immunity in a Child with Recurrent Infections | Q69248052 |
| | Phagocytic cells in periodontal defense. Periodontal status of patients with chronic granulomatous disease of childhood | Q69847182 |
| | Abnormal lymphocyte profiles and leukotriene B4 status in a patient with Crohn's disease and severe periodontitis | Q69849053 |
| | Chédiak-Higashi syndrome. Neurologic appearance | Q70611104 |
| | The Chediak-Higashi-Steinbrinck syndrome. Presentation of three cases with features resembling spinocerebellar degeneration | Q70702292 |
| | The importance of regular dental treatment in patients with cyclic neutropenia. Follow-up of 2 cases | Q71262477 |
| | Familial benign chronic neutropenia associated with periodontal disease. A case report | Q71976705 |
| | An analysis of peripheral blood and salivary polymorphonuclear leukocyte function, circulating immune complex levels and oral status in patients with inflammatory bowel disease | Q72037917 |
| | Prolonged pure granulocytopenia in children | Q72610856 |
| | The Papillon-Lefèvre syndrome: Neutrophil dysfunction with severe periodontal disease | Q72812165 |
| | Chronic granulomatous disease | Q73023702 |
| | Chronic granulomatous disease in Japan: incidence and natural history. The Study Group of Phagocyte Disorders of Japan | Q73103253 |
| | 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 | Q73678536 |
| | Chédiak-Higashi syndrome: hematopoietic chimerism corrects genetic defect | Q74497916 |
| | FAMILIAL BENIGN CHRONIC NEUTROPENIA | Q77129986 |
| | Oral aspects of mongolism. I. Periodontal disease in mongolism | Q78822961 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | periodontitis | Q520127 |
| P304 | page(s) | 82-104 | |
| P577 | publication date | 2003-01-01 | |
| P1433 | published in | Periodontology 2000 | Q15724648 |
| P1476 | title | Systemic disease and periodontitis: manifestations of neutrophil dysfunction | |
| P478 | volume | 32 | |