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Frequencies and phenotypic consequences of association of α‐ and β‐thalassemia alleles with sickle‐cell disease in Bahrain

International journal of laboratory hematology, 2017-02, Vol.39 (1), p.76-83

2017

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Distribution of Subtypes of Hepatitis B Surface Antigen in Western India

Vox sanguinis, 1979-01, Vol.36 (4), p.199-200

1979

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Mechanism of hemolysis of G-6-PD deficient red cells: changes in membrane lipids and polypeptides

Blut, 1982-06, Vol.44 (6), p.355-362

1982

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Genetic studies among the endogamous groups of Lohanas of North and West India

Human heredity, 1976-01, Vol.26 (4), p.298-305

1976

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Associated red cell enzyme deficiencies and their significance in a case of congenital enzymopenic methemoglobinemia

Acta haematologica, 1980-01, Vol.64 (5), p.285-288

1980

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New Laboratory Method to Detect Hepatitis-B (Australia) Antigen Based on 'Anomalous' Lactate Dehydrogenase Isoenzyme

Vox sanguinis, 1976-01, Vol.31 (1), p.70-73

1976

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Hereditary high-adenosine triphosphate syndrome: study of a new variant

Biochemical genetics, 1981-10, Vol.19 (9-10), p.1017-1022

1981

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Immunoglobulins in newborns: differential study of premature and full term infants

Journal of postgraduate medicine (Bombay), 1979-04, Vol.25 (2), p.97

1979

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Congenital agammaglobulinemia with B lymphocytes: a case report

Indian pediatrics, 1978-09, Vol.15 (9), p.777-780

1978

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Hepatitis B antigen and venereal diseases (a preliminary study)

Journal of postgraduate medicine (Bombay), 1977-10, Vol.23 (4), p.186

1977

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Quantitative levels of glucose-6-phosphate dehydrogenase, pyruvate kinase and glutathione in normal and G-6-PD deficient individuals

Indian journal of medical research (New Delhi, India : 1994), 1973-07, Vol.61 (7), p.1031

1973

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Haptoglobins in neonatal jaundice

Indian journal of medical sciences, 1975-04, Vol.29 (4-5), p.107

1975

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Acid gel reaction--a rapid and inexpensive laboratory test for the diagnosis of multiple myeloma, and its correlation with immunoglobulins

Journal of the Association of Physicians of India, 1973-08, Vol.21 (8), p.693

1973

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Possible factors involved in the methemoglobin reduction test for the G-6-PD deficiency

Indian journal of medical research (New Delhi, India : 1994), 1978-01, Vol.67, p.156

1978

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G-6-PD, PK, GSH levels and GSH stability in some haematological disorders

Indian journal of medical research (New Delhi, India : 1994), 1976-10, Vol.64 (10), p.1491

1976

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Is methemoglobin reduction test a true index of G-6-PD deficiency?

Indian journal of medical research (New Delhi, India : 1994), 1976-11, Vol.64 (11), p.1687

1976

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Role of various anticoagulants in the preservation of red cell enzymes

Indian journal of medical research (New Delhi, India : 1994), 1974-07, Vol.62 (7), p.1046

1974

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A rapid counterimmuno-electrophoretic technique for the detection of Australia antigen and alpha-fetoprotein on the same slide

Indian journal of medical research (New Delhi, India : 1994), 1973-07, Vol.61 (7), p.1036

1973

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Association of anomalous lactate dehydrogenase band with hepatitis-B (Australia) antigen--a preliminary study

Indian journal of medical research (New Delhi, India : 1994), 1975-09, Vol.63 (9), p.1363

1975

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A case of hereditary methemoglobinemia with NADH-methemoglobin reductase (diaphorase) deficiency

Indian journal of medical research (New Delhi, India : 1994), 1974-11, Vol.62 (11), p.1716

1974

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Hepatitis B antigen detection by reversed passive haemagglutination method--comparative data

Indian journal of medical research (New Delhi, India : 1994), 1977-06, Vol.65 (6), p.766

1977

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Australia antigen (HBsAg) in thallassemia children receiving multiple transfusions

Indian pediatrics, 1977-06, Vol.14 (6), p.455-459

1977

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Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Nature genetics, 2014-02, Vol.46 (2), p.107-115

2014

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Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients

British journal of cancer, 2011-06, Vol.104 (12), p.1906-1912

2011

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Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

JAMA : the journal of the American Medical Association, 2005-04, Vol.293 (16), p.1979

2005

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Frequencies and phenotypic consequences of association of α‐ and β‐thalassemia alleles with sickle‐cell disease in Bahrain

Distribution of Subtypes of Hepatitis B Surface Antigen in Western India

Mechanism of hemolysis of G-6-PD deficient red cells: changes in membrane lipids and polypeptides

Genetic studies among the endogamous groups of Lohanas of North and West India

Associated red cell enzyme deficiencies and their significance in a case of congenital enzymopenic methemoglobinemia

New Laboratory Method to Detect Hepatitis-B (Australia) Antigen Based on 'Anomalous' Lactate Dehydrogenase Isoenzyme

Hereditary high-adenosine triphosphate syndrome: study of a new variant

Immunoglobulins in newborns: differential study of premature and full term infants

Congenital agammaglobulinemia with B lymphocytes: a case report

Hepatitis B antigen and venereal diseases (a preliminary study)

Quantitative levels of glucose-6-phosphate dehydrogenase, pyruvate kinase and glutathione in normal and G-6-PD deficient individuals

Haptoglobins in neonatal jaundice

Acid gel reaction--a rapid and inexpensive laboratory test for the diagnosis of multiple myeloma, and its correlation with immunoglobulins

Possible factors involved in the methemoglobin reduction test for the G-6-PD deficiency

G-6-PD, PK, GSH levels and GSH stability in some haematological disorders

Is methemoglobin reduction test a true index of G-6-PD deficiency?

Role of various anticoagulants in the preservation of red cell enzymes

A rapid counterimmuno-electrophoretic technique for the detection of Australia antigen and alpha-fetoprotein on the same slide

Association of anomalous lactate dehydrogenase band with hepatitis-B (Australia) antigen--a preliminary study

A case of hereditary methemoglobinemia with NADH-methemoglobin reductase (diaphorase) deficiency

Hepatitis B antigen detection by reversed passive haemagglutination method--comparative data

Australia antigen (HBsAg) in thallassemia children receiving multiple transfusions

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Promoter methylation of Wnt5a is associated with microsatellite instability and BRAF V600E mutation in two large populations of colorectal cancer patients

Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type X

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