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Hemoglobin Shimonoseki HBA1:c.164A > G Illustrating the Continuing Utility of the Sickling Test and the Challenges in Antenatal Genetic Counselling

Indian journal of hematology & blood transfusion, 2024-01, Vol.40 (1), p.166-168

2024

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CE-HPLC Derived P2 and P3-Peaks in Health and in Hb D-Punjab and HbE States

Indian journal of hematology & blood transfusion, 2021-07, Vol.37 (3), p.503-504

2021

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A Screening Approach for Inherited Erythrocytosis due to the VHL:c.598C > T Mutation (Chuvash Polycythemia)

Indian journal of hematology & blood transfusion, 2024-04, Vol.40 (2), p.346-350

2024

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Hb Brugg [HBA1:c.63C>A]: Report of an Ultra-Rare Variant Hemoglobin and Its Co-inheritance with Hb D-Punjab

Indian journal of hematology & blood transfusion, 2021-04, Vol.37 (2), p.326-328

2021

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Fever as an independent prognostic factor in traumatic brain injury

Romanian neurosurgery, 2020-09, Vol.34 (3), p.424-426

2020

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A high frequency of Gilbert syndrome (UGT1A128/28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia

Annals of hematology, 2020-09, Vol.99 (9), p.2019-2026

2020

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Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis

Indian journal of hematology & blood transfusion, 2021-10, Vol.37 (4), p.689-691

2021

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Short Research Communication Anti-Spike Antibody Response to COVISHIELD™ (SII-ChAdOx1 nCoV-19) Vaccine in Patients with B-Cell and Plasma Cell Malignancies and Hematopoietic Cell Transplantation Recipients

Indian journal of hematology & blood transfusion, 2022-10, Vol.38 (4), p.745-749

2022

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Laparoscopic cholecystectomy in a 2 year old male child with choleilithiasis and recurrent Right hypochondrial pain: Case Report and Review of Literature

International journal of surgery case reports, 2016-01, Vol.26, p.142-145

2016

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EVALUATION OF TESTICULAR LESIONS, SCROTAL SWELLINGS BY HIGH RESOLUTION ULTRASONOGRAPHY AND COLOUR DOPPLER AND ITS CORRELATION WITH SURGICAL MANAGEMENT

Journal of evolution of medical and dental sciences, 2015-12, Vol.4 (104), p.16960-16964

2015

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Laparoscopic common bile duct exploration versus ERCP/stenting and cholecystectomy: Is a single staged procedure better?

International Journal of Hepatobiliary and Pancreatic Diseases(IJHPD), 2016-06, Vol.6 (1), p.57-63

2016

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Ultra-rare Hb Regina (HBB:c.289C>G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosis

Journal of clinical pathology, 2022-11, Vol.75 (11), p.791-792

2022

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A 37-Year-Old Man With Bronchial Asthma and Unexplained Hypoxemia

Chest, 2021-12, Vol.160 (6), p.e633-e638

2021

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Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall

Journal of clinical pathology, 2024-04, Vol.77 (4), p.257-258

2024

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β‐thalassemia intermedia mimicking β‐thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases

International journal of laboratory hematology, 2023-08, Vol.45 (4), p.609-612

2023

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Hemoglobin Andrew‐Minneapolis‐Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β‐thalassemia trait: A diagnostic and management conundrum

International journal of laboratory hematology, 2022-08, Vol.44 (4), p.e164-e167

2022

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First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β-thalassemia

International journal of laboratory hematology, 2023-12, Vol.45 (6), p.999-1002

2023

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Hemoglobin Beth Israel [HBB:c.308A>G (p.Asn103Ser)]: an ultra-rare, low oxygen-affinity, non-methemoglobinemic hemoglobin diagnosed on targeted resequencing as cause of dominantly inherited benign cyanosis

Annals of hematology, 2022-12, Vol.101 (12), p.2799-2801

2022

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De novo haemoglobin sabine masquerading as double heterozygosity for HbQ-India and β-thalassemia trait: first report from South Asia

Journal of clinical pathology, 2020-04, Vol.73 (4), p.236-238

2020

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Hematological and genetic profiles of persons with co‐inherited heterozygous β‐thalassemia and supernumerary α‐globin genes

European journal of haematology, 2023-05, Vol.110 (5), p.510-517

2023

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HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches

Pediatric blood & cancer, 2020-04, Vol.67 (4), p.e28161-n/a

2020

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Misdiagnosis of double heterozygous εGγ(Aγδβ)0-thalassemia/β++ thalassemia as homozygous β-thalassemia: A pitfall for molecular diagnostic laboratories

Blood cells, molecules, & diseases, 2020-03, Vol.81, p.102394-102394, Article 102394

2020

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HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases

Annals of hematology, 2017-07, Vol.96 (7), p.1227-1229

2017

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Genetic basis of unexplained erythrocytosis in Indian patients

European journal of haematology, 2019-08, Vol.103 (2), p.124-130

2019

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A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1

Cancer genetics, 2022-01, Vol.260-261, p.53-56

2022

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Hemoglobin Shimonoseki HBA1:c.164A > G Illustrating the Continuing Utility of the Sickling Test and the Challenges in Antenatal Genetic Counselling

CE-HPLC Derived P2 and P3-Peaks in Health and in Hb D-Punjab and HbE States

A Screening Approach for Inherited Erythrocytosis due to the VHL:c.598C > T Mutation (Chuvash Polycythemia)

Hb Brugg [HBA1:c.63C>A]: Report of an Ultra-Rare Variant Hemoglobin and Its Co-inheritance with Hb D-Punjab

Fever as an independent prognostic factor in traumatic brain injury

A high frequency of Gilbert syndrome (UGT1A128/28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemia

Extreme Genotype/Phenotype Heterogeneity of Double Heterozygous Sickle β-Thalassemia in a Family: Implications in Antenatal Diagnosis

Short Research Communication Anti-Spike Antibody Response to COVISHIELD™ (SII-ChAdOx1 nCoV-19) Vaccine in Patients with B-Cell and Plasma Cell Malignancies and Hematopoietic Cell Transplantation Recipients

Laparoscopic cholecystectomy in a 2 year old male child with choleilithiasis and recurrent Right hypochondrial pain: Case Report and Review of Literature

EVALUATION OF TESTICULAR LESIONS, SCROTAL SWELLINGS BY HIGH RESOLUTION ULTRASONOGRAPHY AND COLOUR DOPPLER AND ITS CORRELATION WITH SURGICAL MANAGEMENT

Laparoscopic common bile duct exploration versus ERCP/stenting and cholecystectomy: Is a single staged procedure better?

Ultra-rare Hb Regina (HBB:c.289C>G) with coinherited β-thalassaemia trait: solving the puzzle for extreme erythrocytosis

A 37-Year-Old Man With Bronchial Asthma and Unexplained Hypoxemia

Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall

β‐thalassemia intermedia mimicking β‐thalassemia trait: The importance of family studies and HBB genotyping in phenotypically ambiguous cases

Hemoglobin Andrew‐Minneapolis‐Bijnor HBB:c.[413T>C;435G>C] in a complex genotype with β‐thalassemia trait: A diagnostic and management conundrum

First reported co-occurrence of "GATA1-mutated X-linked thrombocytopenia with thalassemia (XLTT)" with heterozygous β-thalassemia

Hemoglobin Beth Israel [HBB:c.308A>G (p.Asn103Ser)]: an ultra-rare, low oxygen-affinity, non-methemoglobinemic hemoglobin diagnosed on targeted resequencing as cause of dominantly inherited benign cyanosis

De novo haemoglobin sabine masquerading as double heterozygosity for HbQ-India and β-thalassemia trait: first report from South Asia

Hematological and genetic profiles of persons with co‐inherited heterozygous β‐thalassemia and supernumerary α‐globin genes

HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches

Misdiagnosis of double heterozygous εGγ(Aγδβ)0-thalassemia/β++ thalassemia as homozygous β-thalassemia: A pitfall for molecular diagnostic laboratories

HbQ-India (HBA1:c.193G>C): hematological profiles and unique CE-HPLC findings of potential diagnostic utility in 65 cases

Genetic basis of unexplained erythrocytosis in Indian patients

A novel ATRX splice variant causing acquired HbH disease in myelodysplastic syndrome with excess blasts-1

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