Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Withholding transfusion therapy in children with sickle cell disease with abnormal transcranial doppler and normal magnetic resonance angiography: a retrospective analysis
Haematologica. 2024 Mar 7. doi: 10.3324/haematol.2023.284506. Online ahead of print.ABSTRACTNot available.PMID:38450542 | DOI:10.3324/haematol.2023.284506 (Source: Haematologica)
Source: Haematologica - March 7, 2024 Category: Hematology Authors: Lydian A De Ligt Karin Fijnvandraat Bart J Biemond Harriet Heijboer Source Type: research
Clinical features and prognosis of chronic natural killer cell lymphoproliferative disorders
CONCLUSION: Most patients with CLPD-NK have inert progression and a good prognosis, whereas some patients have a poor prognosis after progressing to ANKL and combined with hemophagocytic syndrome. Abnormal NK cells invading the center suggest a high possibility of ANKL development, and immunosuppressants and hormones are effective treatments for this disease.PMID:38319083 | DOI:10.1080/16078454.2024.2307817 (Source: Hematology)
Source: Hematology - February 6, 2024 Category: Hematology Authors: Dong-Lin Liu Yan-Jie Wang Si-Yu Qian Shan-Shan Ma Meng-Jie Ding Meng Dong Jie-Ming Zhang Ming-Zhi Zhang Qing-Jiang Chen Xu-Dong Zhang Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
First investigation of RH gene polymorphism in patients with sickle cell disease and associated blood donors in Cameroon, Central Africa
DISCUSSION: Beyond the comprehensive report of the nature and distribution of RH variant alleles in a subset of Cameroonian patients treated by transfusion therapy, this work highlights the need for an extensive review of current practice, including routine serologic typing procedures, preferably in the near future.PMID:38315540 | DOI:10.2450/BloodTransfus.660 (Source: Blood Transfusion)
Source: Blood Transfusion - February 5, 2024 Category: Hematology Authors: Jeanne Manga Messina Mbeti Caroline B énech Fran çoise Ngo Sack Estelle Wete Hortense Ngegni Pangetha Simon No ël Ateba Jules Tchatchueng Alexandre Njan Nloga Yann Fichou Source Type: research
