Works matching Infantile agranulocytosis

Results: 14

Kostmann syndrome or infantile genetic agranulocytosis, part two: understanding the underlying genetic defects in severe congenital neutropenia.

Published in:

Acta Paediatrica, 2007, v. 96, n. 6, p. 813, doi. 10.1111/j.1651-2227.2007.00274.x

By:

Carlsson, Göran;
Melin, Malin;
Dahl, Niklas;
Ramme, Kim Göransdotter;
Nordenskjöld, Magnus;
Palmblad, Jan;
Henter, Jan-Inge;
Fadeel, Bengt

Publication type:

Article

Spatial Distribution of the Gene for Infantile Genetic Agranulocytosis.

Published in:

Human Heredity, 1984, v. 34, n. 6, p. 358, doi. 10.1159/000153496

By:

Iselius, L.;
Gustavson, K.H.

Publication type:

Article

Kostmann syndrome or infantile genetic agranulocytosis, part one: celebrating 50 years of clinical and basic research on severe congenital neutropenia.

Published in:

2006

By:

Carlsson, Göran;
Andersson, Mats;
Pütsep, Katrin;
Garwicz, Daniel;
Nordenskjöld, Magnus;
Henter, Jan-Inge;
Palmblad, Jan;
Fadeel, Bengt;
Carlsson, Göran;
Pütsep, Katrin;
Nordenskjöld, Magnus

Publication type:

journal article

Kostmann disease--infantile genetic agranulocytosis: historical views and new aspects.

Published in:

Acta Paediatrica, 2002, v. 91, n. 12, p. 1279

By:

Zetterström, Rolf

Publication type:

Article

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

Published in:

Acta Paediatrica, 2001, v. 90, n. 7, p. 757, doi. 10.1111/j.1651-2227.2001.tb02801.x

By:

Carlsson, G;
Fasth, A

Publication type:

Article

Can infantile hereditary agranulocytosis be diagnosed prenatally?

Published in:

Prenatal Diagnosis, 1983, v. 3, n. 2, p. 157, doi. 10.1002/pd.1970030215

By:

Cividalli, Gabriel;
Yarkoni, Shaul;
Dar, Hanna;
Kohn, Gertrude

Publication type:

Article

INFANTILE GENETIC AGRANULOCYTOSIS.

Published in:

Acta Paediatrica, 1975, v. 64, n. 2, p. 362, doi. 10.1111/j.1651-2227.1975.tb03847.x

By:

KOSTMANN, ROLF

Publication type:

Article

INFANTILE GENETIC AGRANULOCYTOSIS ASSOCIATED WITH CHANGES IN SERUM VITAMIN B<sub>12</sub> BINDING PROTEINS.

Published in:

Acta Paediatrica, 1972, v. 61, n. 5, p. 526, doi. 10.1111/j.1651-2227.1972.tb15939.x

By:

BEARD, M. E. J.;
NEWMARK, P.;
SMITH, M. E.;
FRANKLIN, A. W.

Publication type:

Article

Genetic Aspects of Infantile Agranulocytosis.

Published in:

Acta Paediatrica, 1956, v. 45, n. S105, p. 64, doi. 10.1111/j.1651-2227.1956.tb05363.x

By:

BÖÖK, JAN A.;
KOSTMANN, ROLF

Publication type:

Article

Infantile Genetic Agranulocytosis (Agranulocytosis infantilis hereditaria) A New Recessive Lethal Disease in Man.

Published in:

Acta Paediatrica, 1956, v. 45, n. 3, p. 309, doi. 10.1111/j.1651-2227.1956.tb06875.x

By:

KOSTMANN, ROLF

Publication type:

Article

Eponym. Kostmann disease.

Published in:

2010

By:

Aytekin, Caner;
Germeshausen, Manuela;
Tuygun, Nilden;
Tanir, Gonul;
Dogu, Figen;
Ikinciogullari, Aydan

Publication type:

journal article

Kostmann disease and other forms of severe congenital neutropenia.

Published in:

Acta Paediatrica, 2021, v. 110, n. 11, p. 2912, doi. 10.1111/apa.16005

By:

Fadeel, Bengt;
Garwicz, Daniel;
Carlsson, Göran;
Sandstedt, Bengt;
Nordenskjöld, Magnus

Publication type:

Article

Measuring parent proxy-reported quality of life of 11 rare diseases in children in Zhejiang, China.

Published in:

2020

By:

Gao, Qisheng;
Wang, Shanshan;
Ren, Jianping;
Wen, Xin

Publication type:

journal article

Nigella sativa and Saudi Honey Diminish Infections and Improve the Survival in a Kostmann's Syndrome Patient: Case Report.

Published in:

Journal of Applied Hematology, 2017, v. 8, n. 3, p. 119, doi. 10.4103/joah.joah_37_17

By:

Al Jaouni, Soad K.;
Halawa, Taher;
Hussein, Abear;
Al Najjar, Salwa;
Almuhayawi, Mohammad S.;
Harakeh, Steve

Publication type:

Article