Search Results - "Mashon, Ranjeet"

Hb Rush (HBB: c.304G>C): A Rare Variant Hemoglobin Mimicking the Hb S (HBB: c.20A>T) Variant on High Performance Liquid Chromatography by Mashon, Ranjeet S., Das, Reena, Dhawan, Radhika, Kakkar, Naveen, Dhar, Tapasya

“…High performance liquid chromatography (HPLC) is a useful and rapid tool in the evaluation of hemoglobin (Hb) disorders that include thalassemia and various…”
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Coinheritance of Hb D-Punjab and β-Thalassemia: Diagnosis and Implications in Prenatal Diagnosis by Das, Sheila, Mashon, Ranjeet S.

“…Abstract Hb D-Punjab (HBB: c.364G>C) is an abnormal hemoglobin (Hb) associated with genetic risk in association with Hb S (HBB: c.20A>T). In addition,…”
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Discriminant indices for thalassemia screening: Need for a higher sensitivity by Mashon, Ranjeet, Kakkar, Naveen

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Low Dose Hydroxyurea is Effective in Reducing the Incidence of Painful Crisis and Frequency of Blood Transfusion in Sickle Cell Anemia Patients from Eastern India by Patel, Dilip K., Mashon, Ranjeet S., Patel, Siris, Das, Bhabani S., Purohit, Prasanta, Bishwal, Subasa C.

“…There are several questions pertaining to dosage, duration and potential long-term toxicity of hydroxyurea (HU) therapy. Use of HU is extremely limited in…”
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Effect of Assorted Globin Haplotypes and α-Thalassemia on the Clinical Heterogeneity of Hb S-β-Thalassemia by Dash, Preetinanda M., Sahu, Praveen K., Patel, Siris, Mashon, Ranjeet S., Kharat, Kiran R., Mukherjee, Malay B.

“…Hemoglobinopathies and thalassemias are the most commonly encountered monogenic disorders of blood in humans, posing a major genetic and public health problem…”
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Elevated HbF Labelled as LA1C/cHb1 on BioRad D10 HPLC: Missed Diagnosis of Homozygous Beta Thalassemia by Vaswani, Shruti, Mashon, Ranjeet Singh, Kakkar, Naveen

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Clinico-Hematological Profile of Hb Q India: An Uncommon Hemoglobin Variant by Harrison, Aradhana, Mashon, Ranjeet Singh, Kakkar, Naveen, Das, Sheila

“…Inherited hemoglobin disorders include thalassemias and structural variants like HbS, HbE, and HbD, Hb Lepore, HbD-Iran, Hb-H disease and HbQ India. HbQ India…”
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Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family by Patel, Dilip K., Patel, Siris, Mashon, Ranjeet S., Dash, Preetinanda M., Mukherjee, Malay B.

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Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India by Mashon, Ranjeet, Nair, Sona, Sawant, Pratibha, Colah, Roshan, Ghosh, Kanjaksha, Das, Sheila

“…Structural hemoglobin (Hb) variants are mainly due to point mutations in the globin genes resulting in single amino acid substitutions. Until date, about 200…”
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β-Globin Gene Haplotypes Linked with the Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA] Mutation in Eastern India by Patel, Dilip K., Mashon, Ranjeet S., Patel, Siris, Dash, Preetinanda M., Das, Bhabani S.

“…Hb D-Punjab [β121(GH4)Glu→Gln] is prevalent in the northern states of the Indian subcontinent. Due to inadequate data from Asian countries, the origin and…”
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Demographic profile and real world data of persons with hemophilia in a resource constrained setup by John, M, Tanuja, Tanuja, Mathew, Amrith, Philip, Chepsy, Singh, Jasprit, Dinakaran, Mullai, Vandhiyadevan, G, Mathangi, Santhosh, Singh, Suvir, Mashon, Ranjeet, Kakkar, Naveen

“…Background: Hemophilia is underdiagnosed in India, and there is lack of state specific data on the extent and morbidity. This article provides the real world…”
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Experience of Antenatal Thalassemia Screening and Prenatal Diagnosis from a Tertiary Care Teaching Hospital in Punjab by Mashon, Ranjeet Singh, Mandrelle, Kavita, Kakkar, Naveen

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Influence of Sickle Cell Gene on the Allelic Diversity at the msp-1 locus of Plasmodium falciparum in Adult Patients with Severe Malaria by Patel, Dilip Kumar, Mashon, Ranjeet Singh, Purohit, Prasanta, Meher, Satyabrata, Dehury, Snehadhini, Marndi, Chhatray, Das, Kishalaya, Kullu, Bipin Kishore, Patel, Siris, Das, Padmalaya

“…Although several studies have supported that sickle cell trait (HbAS) protects against falciparum malaria, the exact mechanism by which sickle gene confers…”
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The effect of hydroxyurea on compound heterozygotes for sickle cell-hemoglobin D-Punjab-A single centre experience in eastern India by Patel, Siris, Purohit, Prasanta, Mashon, Ranjeet Singh, Dehury, Snehadhini, Meher, Satyabrata, Sahoo, Sulia, Dash, Subhransu Sekhar, Das, Kishalaya, Das, Padmalaya, Patel, Dilip Kumar

“…Background Although hydroxyurea is the only effective agent for the treatment of sickle cell disease, published experience with this drug is limited to…”
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Higher fetal hemoglobin concentration in patients with sickle cell disease in eastern India reduces frequency of painful crisis by Mashon, Ranjeet Singh, Dash, Preetinanda Manaswini, Khalkho, Janet, Dash, Laxmikanta, Mohanty, Pradeep Kumar, Patel, Siris, Mohanty, Ramesh Chandra, Das, Bhabani Shankar, Das, Upendra Kumar, Das, Prasanta Kumar, Patel, Dilip Kumar

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Cost Effectiveness of Hematopoietic Stem Cell Transplantation Compared with Transfusion Chelation for Treatment of Thalassemia Major by John, M. Joseph, Jyani, Gaurav, Jindal, Aikaj, Mashon, Ranjeet Singh, Mathew, Amrith, Kakkar, Shruti, Bahuguna, Pankaj, Prinja, Shankar

“…•HSCT for thalassemia is a long-term value-for-money intervention in a developing country.•The clinical and economic benefits of HSCT far outweigh TC.•The ICER…”
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Clinical and Molecular Characterization of βS and Gγ(Aγδβ)0-Thalassemia in Eastern India by Patel, Dilip Kumar, Patel, Madhumita, Mashon, Ranjeet Singh, Patel, Siris, Dash, Preetinanda Manaswini, Das, Bhabani Shankar

“…Fetal hemoglobin (Hb F) is the most studied modifier of sickle cell disease. Coinheritance of high Hb F determinants such as δβ-thalassemia (δβ-thal) and…”
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Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India by Patel, Dilip Kumar, Patel, Madhumita, Mashon, Ranjeet Singh, Patel, Siris, Dash, Preetinanda Manaswini, Das, Bhabani Shankar

“…Fetal hemoglobin (Hb F) is the most studied modifier of sickle cell disease. Coinheritance of high Hb F determinants such as δβ-thalassemia (δβ-thal) and…”
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Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India by Mashon, Ranjeet Singh, Nair, Sona, Sawant, Pratibha, Colah, Roshan B, Ghosh, Kanjaksha, Das, Sheila

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Diverse phenotypic expression of sickle cell hemoglobin C disease in an Indian family by Patel, Dilip K, Patel, Siris, Mashon, Ranjeet S, Dash, Preetinanda M, Mukherjee, Malay B

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