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Distribution of alpha thalassaemia gene variants in diverse ethnic populations in malaysia: data from the institute for medical research

International journal of molecular sciences, 2013-09, Vol.14 (9), p.18599-18614

2013

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Molecular characterization of α- and β-thalassaemia among Malay patients

International journal of molecular sciences, 2014-05, Vol.15 (5), p.8835-8845

2014

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Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis

BMC research notes, 2020-02, Vol.13 (1), p.65-65, Article 65

2020

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A Novel Single Gene Deletion (−αMAL3.5) Giving Rise to Silent α Thalassemia Carrier Removing the Entire HBA2 Gene Observed in Two Chinese Patients with Hb H Disease: Case Report of Two Probands

Thalassemia reports, 2015-07, Vol.5 (1), p.4675

2015

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Inhibition of ricin A-chain (RTA) catalytic activity by a viral genome-linked protein (VPg)

Biochimica et biophysica acta. Proteins and proteomics, 2019-06, Vol.1867 (6), p.645-653

2019

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Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review

Pediatric blood & cancer, 2022-09, Vol.69 (9), p.e29629-n/a

2022

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Educational development and reformation in Malaysia: past, present and future

Journal of educational administration, 1998-01, Vol.36 (5), p.462-475

Haji Ahmad, Rahimah

1998

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Transfusion Dependent Homozygous α-Thalassemia in Patients Associated with Hypospadias in Three Survivors

Journal of blood disorders & transfusion, 2015, Vol.6 (1)

Rahimah Ahmad, Syahzuwan Hassan

2015

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Compound Heterozygous -30 (T>C) and Cd 41/42 (-TTCT) Leading to β-Thalassemia Major in a Malay Autistic Patient

Journal of blood disorders & transfusion, 2015, Vol.6 (1)

Rahimah Ahmad, Syahzuwan Hassan

2015

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A nonsense mutation in exon 8 of the APC gene (Arg283Ter) causes clinically variable FAP in a Malaysian Chinese family

Cancer science, 2003-08, Vol.94 (8), p.725-728

2003

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Abstract 476: A human scFv as a tool to understand the biogenesis of a subset of oncogenic microRNAs

Cancer research (Chicago, Ill.), 2018-07, Vol.78 (13_Supplement), p.476-476

2018

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Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Annals of human genetics, 2017-09, Vol.81 (5), p.205-212

2017

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Abstract 2609: Columbia University’s Center for Cancer Systems Therapeutics (CaST) 2017 Scholars Program: A synergistic partnership with students from Brooklyn College, CUNY

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.2609-2609

2017

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Coinheritance of Southeast Asian ovalocytosis and the β-thalassemia trait in a Malay family

Asian biomedicine, 2017-01, Vol.9 (5), p.691-695

2017

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Molecular Characterisation of [alpha]- and [beta]-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Annals of human genetics, 2017-09, Vol.81 (5), p.205

2017

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Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction

The Malaysian journal of medical sciences, 2013-01, Vol.20 (1), p.13-20

2013

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First Two Cases of Fungal Infections Associated with Multi-drug Resistant Yeast, Fereydounia khargensis

Mycopathologia (1975), 2016-08, Vol.181 (7-8), p.531-537

2016

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Scholarship of engagement: Knowledge transfer program for developmental instructional supervision

Leading Change in Teacher Education, 2019, p.195-209

1, 2019

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A Conceptual Study on Green Management Practices in Banking Industry

Global business and management research, 2022-12, Vol.14 (4S), p.298-306

2022

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Molecular Characterization of [alpha]- and [beta]-Thalassaemia among Malay Patients

International journal of molecular sciences, 2014-05, Vol.15 (5), p.8835

2014

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Distribution of alpha thalassaemia in 16 year old Malaysian Students in Penang, Melaka and Sabah

Medical journal of Malaysia, 2012-12, Vol.67 (6), p.565-570

2012

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Reprogramming of peripheral blood from Malaysian beta thalassaemia patients to induced pluripotent stem cell

Frontiers in bioengineering and biotechnology, 2016, Vol.4

2016

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Detection of [Beta]-globin Gene Mutations Among [Beta]-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction

The Malaysian journal of medical sciences, 2013-01, Vol.20 (1), p.13

2013

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Haemoglobin sickle d punjab: - a case report

Medical journal of Malaysia, 2014-02, Vol.69 (1), p.42-43

2014

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Distribution of alpha thalassaemia gene variants in diverse ethnic populations in malaysia: data from the institute for medical research

Molecular characterization of α- and β-thalassaemia among Malay patients

Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis

A Novel Single Gene Deletion (−αMAL3.5) Giving Rise to Silent α Thalassemia Carrier Removing the Entire HBA2 Gene Observed in Two Chinese Patients with Hb H Disease: Case Report of Two Probands

Inhibition of ricin A-chain (RTA) catalytic activity by a viral genome-linked protein (VPg)

Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review

Educational development and reformation in Malaysia: past, present and future

Transfusion Dependent Homozygous α-Thalassemia in Patients Associated with Hypospadias in Three Survivors

Compound Heterozygous -30 (T>C) and Cd 41/42 (-TTCT) Leading to β-Thalassemia Major in a Malay Autistic Patient

A nonsense mutation in exon 8 of the APC gene (Arg283Ter) causes clinically variable FAP in a Malaysian Chinese family

Abstract 476: A human scFv as a tool to understand the biogenesis of a subset of oncogenic microRNAs

Molecular Characterisation of α‐ and β‐Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Abstract 2609: Columbia University’s Center for Cancer Systems Therapeutics (CaST) 2017 Scholars Program: A synergistic partnership with students from Brooklyn College, CUNY

Coinheritance of Southeast Asian ovalocytosis and the β-thalassemia trait in a Malay family

Molecular Characterisation of [alpha]- and [beta]-Thalassaemia among Indigenous Senoi Orang Asli Communities in Peninsular Malaysia

Detection of β-globin Gene Mutations Among β-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction

First Two Cases of Fungal Infections Associated with Multi-drug Resistant Yeast, Fereydounia khargensis

Scholarship of engagement: Knowledge transfer program for developmental instructional supervision

A Conceptual Study on Green Management Practices in Banking Industry

Molecular Characterization of [alpha]- and [beta]-Thalassaemia among Malay Patients

Distribution of alpha thalassaemia in 16 year old Malaysian Students in Penang, Melaka and Sabah

Reprogramming of peripheral blood from Malaysian beta thalassaemia patients to induced pluripotent stem cell

Detection of [Beta]-globin Gene Mutations Among [Beta]-thalassaemia Carriers and Patients in Malaysia: Application of Multiplex Amplification Refractory Mutation System-Polymerase Chain Reaction

Haemoglobin sickle d punjab: - a case report

Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia

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