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Journal Articles

Newborn Haemoglobinopathy Carrier Screening: Towards Comprehensive and Improved Patient Care of Sickle Cell Disease in Oman, a Cost Effective Analysis.

Salam Alkindi, MD, Anil Pathare, MD, Ali Al Madhani, MD, Shoaib Al Zadjali, M.Sc, S. Muralitharan, Ph.D, Hamood Al Haddabi, M.Sc, Qamariya Al Abri, M.Sc, David Gravell, M.Sc, Shahina Daar, MD, J. David Dennison, MD, R. Krishnamoorthy, Ph.D

Blood (2007) 110 (11): 5155.

https://doi.org/10.1182/blood.V110.11.5155.5155

Published: 2007

Journal Articles

Predictive Value of Red Cell Indices and High Performance Liquid Chromatography in the Diagnosis of Haemoglobinopathies: Interim Results of the National Neonatal Cord Blood Screening Programme.

Anil Pathare, Salam AlKindi, Ali AlMadhani, Shoaib AlZadjali, Hamood AlHaddabi, Qamariya AlAbri, S. Muralitharan, J. David Dennison, R. Krishnamoorthy

Blood (2006) 108 (11): 3352.

https://doi.org/10.1182/blood.V108.11.3352.3352

Published: 2006

Journal Articles

Permanent Alopecia in Children Following Busulfan Based Conditioning Is Associated with Glutathione M1 Null Genotype.

J. David Dennison, S. Muralitharan, Melanie Tauro, Shoaib Zadjali, Salam Al Kindi, Maria Lourdes Macalalad, Anil Pathare, Krishnaratnam Kannan, Aqueela Taqi Al Lawatia, R. Krishnamoorthy, Shyam Sunder Ganguly

Blood (2005) 106 (11): 2740.

https://doi.org/10.1182/blood.V106.11.2740.2740

Published: 2005

Journal Articles

Suboptimal Busulphan Exposure Is Associated with Mixed Hematopoietic Chimerism, a Risk Factor for Rejection in Bone Marrow Transplantation for Homozygous beta Thalassemia.

J. David Dennison, MD, Shoaib Al Zadjali, Melanie Tauro, Salam Al Kindi, MD, S. Muralitharan, Krishnaratnam Kanan, MD, Shahina Daar, MD, Anil Pathare, MD, Marie-Helene Quernin, Evelyne Jacqz-Aigrain, MD, R. Krishnamoorthy, MD, Shyam Sundar Ganguly, MD

Blood (2004) 104 (11): 1149.

https://doi.org/10.1182/blood.V104.11.1149.1149

Published: 2004

Journal Articles

A single tube multiplex PCR method to detect the common alpha + thalassemia alleles

R.V. Shaji, A. Srivastava, M. Chandy, R. Krishnamoorthy

Blood (2000) 95 (5): 1879.

https://doi.org/10.1182/blood.V95.5.1879

Published: 2000

Journal Articles

Milder Clinical Course of Sickle Cell Disease in Patients With α Thalassemia in the Indian Subcontinent

M.B. Mukherjee, R.B. Colah, K. Ghosh, D. Mohanty, R. Krishnamoorthy

Blood (1997) 89 (2): 732.

https://doi.org/10.1182/blood.V89.2.732a

Published: 1997

Journal Articles

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]

T Merghoub, M Maier-Redelsperger, D Labie, B Perichon, N Feingold, SP Dibenedetto, G Schiliro, P Samperi, r Ducrocq, J Elion, R Krishnamoorthy

Blood (1996) 87 (6): 2607.

https://doi.org/10.1182/blood.V87.6.2607.bloodjournal8762607

Published: 1996

Journal Articles

Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island [letter]

N Kotea, S Baligadoo, S Surran, R Ramasawmy, CY Lu, R Ducrocq, D Labie, R Krishnamoorthy, R Nagel

Blood (1995) 86 (1): 407–408.

https://doi.org/10.1182/blood.V86.1.407.bloodjournal861407

Published: 1995

Journal Articles

DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation

J Elion, PE Berg, C Lapoumeroulie, G Trabuchet, M Mittelman, R Krishnamoorthy, AN Schechter, D Labie

Blood (1992) 79 (3): 787–792.

https://doi.org/10.1182/blood.V79.3.787.787

Published: 1992

Journal Articles

The enhancer-like sequence 3′ to the A gamma gene is polymorphic in human populations

EE Bouhassira, R Krishnamoorthy, A Ragusa, C Driscoll, D Labie, RL Nagel

Blood (1989) 73 (4): 1050–1053.

https://doi.org/10.1182/blood.V73.4.1050.1050

Published: 1989

Journal Articles

The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level

RL Nagel, SK Rao, O Dunda-Belkhodja, MM Connolly, ME Fabry, A Georges, R Krishnamoorthy, D Labie

Blood (1987) 69 (4): 1026–1030.

https://doi.org/10.1182/blood.V69.4.1026.1026

Published: 1987

NARROW

Newborn Haemoglobinopathy Carrier Screening: Towards Comprehensive and Improved Patient Care of Sickle Cell Disease in Oman, a Cost Effective Analysis.

Predictive Value of Red Cell Indices and High Performance Liquid Chromatography in the Diagnosis of Haemoglobinopathies: Interim Results of the National Neonatal Cord Blood Screening Programme.

Permanent Alopecia in Children Following Busulfan Based Conditioning Is Associated with Glutathione M1 Null Genotype.

Suboptimal Busulphan Exposure Is Associated with Mixed Hematopoietic Chimerism, a Risk Factor for Rejection in Bone Marrow Transplantation for Homozygous beta Thalassemia.

A single tube multiplex PCR method to detect the common alpha + thalassemia alleles

Milder Clinical Course of Sickle Cell Disease in Patients With α Thalassemia in the Indian Subcontinent

Variation of fetal hemoglobin and F-cell number with the LCR-HS2 polymorphism in nonanemic individuals [letter]

Bicentric origin of sickle hemoglobin among the inhabitants of Mauritius Island [letter]

DNA sequence variation in a negative control region 5' to the beta- globin gene correlates with the phenotypic expression of the beta s mutation

The enhancer-like sequence 3′ to the A gamma gene is polymorphic in human populations

The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level

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American Society of Hematology

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American Society of Hematology

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