Background: Severe congenital neutropenia (SCN), also known as Kostmann syndrome, was originally reported as an autosomal recessive disease of neutrophil production. The disease is characterized by a maturation arrest of neutrophil precursors at the promyelocytic stage of differentiation and by extremely low levels of mature neutrophils in peripheral blood
Background, aims: Congenital neutropenia is one condition that may predispose for destructive period...
Severe congenital neutropenia (SCN) is a rare primary immunodeficiency. Different genes are found to...
We have analysed a family with nine congenital neutropenia patients in four generations, several of ...
Background: Severe congenital neutropenia (SCN), also known as Kostmann syndrome, was originally rep...
Severe congenital neutropenia (SCN) comprises a heterogenous group of disorders characterized by a c...
Kostmann syndrome or severe congenital neutropenia (SCN) is a rare disease, usually diagnosed during...
Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemi...
Severe congenital neutropenia (SCN), Kostmann syndrome is a heterogenous disorder of myelopoiesis ch...
Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental di...
Patients with severe congenital neutropenia (SCN) often develop periodontitis despite standard medic...
Severe congenital neutropenia (SCN), often referred to as Kostmann syndrome, is a rare immune defici...
SEVERE PERIODONTITIS IN A PATIENT WITH INFANTILE genetic agranulocytosis (Kostmann syndrome) is pres...
PubMed ID: 17315808The purpose of this report is to describe dental findings and treatment of an 11-...
Severe congenital neutropenia (SCN) is a rare primary immunodefi ciency disease that is characterize...
Congenital neutropenia with autosomal recessive inheritance was first described by the Swedish paedi...
Background, aims: Congenital neutropenia is one condition that may predispose for destructive period...
Severe congenital neutropenia (SCN) is a rare primary immunodeficiency. Different genes are found to...
We have analysed a family with nine congenital neutropenia patients in four generations, several of ...
Background: Severe congenital neutropenia (SCN), also known as Kostmann syndrome, was originally rep...
Severe congenital neutropenia (SCN) comprises a heterogenous group of disorders characterized by a c...
Kostmann syndrome or severe congenital neutropenia (SCN) is a rare disease, usually diagnosed during...
Neutrophil elastase and granulocyte colony-stimulating factor receptor mutation analyses and leukemi...
Severe congenital neutropenia (SCN), Kostmann syndrome is a heterogenous disorder of myelopoiesis ch...
Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental di...
Patients with severe congenital neutropenia (SCN) often develop periodontitis despite standard medic...
Severe congenital neutropenia (SCN), often referred to as Kostmann syndrome, is a rare immune defici...
SEVERE PERIODONTITIS IN A PATIENT WITH INFANTILE genetic agranulocytosis (Kostmann syndrome) is pres...
PubMed ID: 17315808The purpose of this report is to describe dental findings and treatment of an 11-...
Severe congenital neutropenia (SCN) is a rare primary immunodefi ciency disease that is characterize...
Congenital neutropenia with autosomal recessive inheritance was first described by the Swedish paedi...
Background, aims: Congenital neutropenia is one condition that may predispose for destructive period...
Severe congenital neutropenia (SCN) is a rare primary immunodeficiency. Different genes are found to...
We have analysed a family with nine congenital neutropenia patients in four generations, several of ...