The non-surgical management of a patient with Kostmann syndrome-associated periodontitis: a case report
Author:
Publisher
Nihon University School of Dentistry
Subject
General Dentistry
Link
https://www.jstage.jst.go.jp/article/josnusd/56/4/56_315/_pdf
Reference10 articles.
1. 1. Kostman R (1975) Infantile genetic agranulocytosis: a review with presentation of ten new cases. Acta Paediatr Scand 64, 362-368.
2. 2. Melin M, Entesarian M, Carlsson G, Garwicz D, Klein C, Fadeel B et al. (2007) Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern Sweden. Biochem Biophys Res Commun 353, 571-575.
3. 3. Carlsson G, Fasth A (2001) Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original “Kostmann family” and a review. Acta Paediatr 90, 757-764.
4. 4. Dale DC, Bonilla MA, Davis MW, Nakanishi AM, Hammond WP, Kurtzberg J et al. (1993) A randomized controlled phase III trial of recombinant human granulocyte colony-stimulating factor (filgrastim) for treatment of severe chronic neutropenia. Blood 81, 2496-2502.
5. 5. Defraia E, Marinelli A (2001) Oral manifestations of congenital neutropenia or Kostmann syndrome. J Clin Pediatr Dent 26, 99-102.
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