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[A family of infantile genetic agranulocytosis].
1976
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Associated MeSH Terms
Cite
UI
MeSH Term
Description
Entries
D007223
Infant
A child between 1 and 23 months of age.
Infants
D005260
Female
Females
D006801
Humans
Members of the species Homo sapiens.
Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000380
Agranulocytosis
A decrease in the number of GRANULOCYTES; (BASOPHILS; EOSINOPHILS; and NEUTROPHILS).
Granulocytopenia,Agranulocytoses,Granulocytopenias
Related Publications
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
INFANTILE GENETIC AGRANULOCYTOSIS.
April 1965, Pediatrics,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Infantile genetic agranulocytosis; agranulocytosis infantilis hereditaria.
February 1956, Acta paediatrica. Supplementum,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
[Infantile genetic agranulocytosis (Kostmann syndrome)].
May 1983, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Infantile genetic agranulocytosis in three siblings.
March 1981, Medical journal of Osaka University,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Infantile genetic agranulocytosis (Kostmann type). A case report.
September 1995, Journal of periodontology,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Optic neuropathy, chloramphenicol, and infantile genetic agranulocytosis.
July 1973, Investigative ophthalmology,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Infantile genetic agranulocytosis, morbus Kostmann: presentation of six cases from the original "Kostmann family" and a review.
July 2001, Acta paediatrica (Oslo, Norway : 1992),
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Spatial distribution of the gene for infantile genetic agranulocytosis.
January 1984, Human heredity,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
Infantile genetic agranulocytosis. A review with presentation of ten new cases.
March 1975, Acta paediatrica Scandinavica,
T Ninomiya, and F Sakamoto, and T Yukita, and M Miyao, and Y Uyama
[Diagnostic-therapeutic trial in infantile genetic agranulocytosis with leucorecruitin].
October 1982, Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde,
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