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Showing results (51-60 of 60) with videos related to

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Biochemical and Biophysical Research Communications|December 26, 2006
Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern SwedenM Melin, M Entesarian, G Carlsson, et al.
Pediatric Blood & Cancer|November 13, 2010
Hematopoietic stem cell transplantation in severe congenital neutropeniaG Carlsson, J Winiarski, P Ljungman, et al.
Journal of Internal Medicine|June 3, 2008
Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutationsG Carlsson, I van't Hooft, M Melin, et al.
Pediatric Blood & Cancer|July 28, 2005
Risk factors for diabetes insipidus in langerhans cell histiocytosisN Grois, U Pötschger, H Prosch, et al.
Science (New York, N.Y.)|December 3, 1999
Perforin gene defects in familial hemophagocytic lymphohistiocytosisS E Stepp, R Dufourcq-Lagelouse, F Le Deist, et al.
Journal of Medical Genetics|November 13, 2007
Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosisE Rudd, Y T Bryceson, C Zheng, et al.
Nature Genetics|August 1, 1997
Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 MbP Gustavsson, T N Willing, A van Haeringen, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutationsA Trizzino, U zur Stadt, I Ueda, et al.
Medical and Pediatric Oncology|September 1, 1997
Contemporary classification of histiocytic disorders. The WHO Committee On Histiocytic/Reticulum Cell Proliferations. Reclassification Working Group of the Histiocyte SocietyB E Favara, A C Feller, M Pauli, et al.
Blood|March 9, 1999
Effective control of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis with immunochemotherapy. Histiocyte SocietyS Imashuku, S Hibi, T Ohara, et al.
Pageof 6

Showing results (51-60 of 60) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 60 results.
Biochemical and Biophysical Research Communications|December 26, 2006
Assignment of the gene locus for severe congenital neutropenia to chromosome 1q22 in the original Kostmann family from Northern SwedenM Melin, M Entesarian, G Carlsson, et al.
Pediatric Blood & Cancer|November 13, 2010
Hematopoietic stem cell transplantation in severe congenital neutropeniaG Carlsson, J Winiarski, P Ljungman, et al.
Journal of Internal Medicine|June 3, 2008
Central nervous system involvement in severe congenital neutropenia: neurological and neuropsychological abnormalities associated with specific HAX1 mutationsG Carlsson, I van't Hooft, M Melin, et al.
Pediatric Blood & Cancer|July 28, 2005
Risk factors for diabetes insipidus in langerhans cell histiocytosisN Grois, U Pötschger, H Prosch, et al.
Science (New York, N.Y.)|December 3, 1999
Perforin gene defects in familial hemophagocytic lymphohistiocytosisS E Stepp, R Dufourcq-Lagelouse, F Le Deist, et al.
Journal of Medical Genetics|November 13, 2007
Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosisE Rudd, Y T Bryceson, C Zheng, et al.
Nature Genetics|August 1, 1997
Diamond-Blackfan anaemia: genetic homogeneity for a gene on chromosome 19q13 restricted to 1.8 MbP Gustavsson, T N Willing, A van Haeringen, et al.
Journal of Medical Genetics|September 18, 2007
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutationsA Trizzino, U zur Stadt, I Ueda, et al.
Medical and Pediatric Oncology|September 1, 1997
Contemporary classification of histiocytic disorders. The WHO Committee On Histiocytic/Reticulum Cell Proliferations. Reclassification Working Group of the Histiocyte SocietyB E Favara, A C Feller, M Pauli, et al.
Blood|March 9, 1999
Effective control of Epstein-Barr virus-related hemophagocytic lymphohistiocytosis with immunochemotherapy. Histiocyte SocietyS Imashuku, S Hibi, T Ohara, et al.
Pageof 6