Search Results - "Patel, Ashwin P."
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1
Use of Daratumumab in Patients With Previously Treated Multiple Myeloma
Published in Journal of clinical oncology (10-05-2023)Get full text
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"Selection of statistical tests influences the interpretation of a study outcome" a comment on "Giriraja KV, Bhatnagar SK, Tomlinson L, Sancilio F. An open-label, multicenter, phase 2 study of a food enriched with docosahexaenoic acid in adults with sickle cell disease. Prostaglandins Leukot Essent Fatty Acids. 2023 Jun; 193:102574. Doi: 10.1016/j.plefa.2023.102574. Epub 2023 Apr 7. PMID: 37121179"
Published in Prostaglandins, leukotrienes and essential fatty acids (01-12-2023)“…Parametric tests such as t-tests require a normal distribution of data. However, the determination of normal distribution may not be conclusive while dealing…”
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Letter to the Editor concerning “Age- and sex-related changes in facet orientation and tropism in lower lumbar spine: an MRI study of 600 patients” by Degulmadi D, et al. (Eur Spine J [2019] 28:961–966, https://doi.org/10.1007/s00586-019-05953-y)
Published in European spine journal (01-06-2020)Get full text
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Concerns With Statistical Analysis of 2016 CDC Opioid Guideline and Sickle Cell Outcomes
Published in JAMA internal medicine (01-09-2024)Get more information
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5
Dapsone for immune thrombocytopenic purpura in children and adults
Published in Platelets (Edinburgh) (01-01-2015)“…Abstract Dapsone is one of the second line treatments of immune thrombocytopenic purpura (ITP). Dapsone is cheap and has response rates comparable to other…”
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Validation of the breathmobile case identification survey for asthma screening in children with sickle cell disease
Published in The Journal of asthma (03-06-2021)“…Background: Asthma is a chronic airway disorder with variable/recurring symptoms, airflow obstruction, bronchial hyperresponsiveness, and an inflammation. The…”
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A polygenic score for acute vaso-occlusive pain in pediatric sickle cell disease
Published in Blood advances (27-07-2021)“…Individuals with monogenic disorders can experience variable phenotypes that are influenced by genetic variation. To investigate this in sickle cell disease…”
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β-Thalassemia Mutations in Western India: Outcome of Prenatal Diagnosis in a Hemoglobinopathies Project
Published in Hemoglobin (01-10-2014)“…Abstract Prenatal diagnosis (PND) is one of the most cost effective preventive methods, but it is available only in the large cities of India. Therefore, we…”
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Long term survival in aggressive NK-cell leukemia
Published in Indian pediatrics (01-09-2010)“…Aggressive natural killer cell leukemia (ANKL) is a rare type of leukemia. It is rapidly progressing and the outcome is poor, with short survival. There is…”
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Idiopathic autoimmune thrombocytopenia and neutropenia in siblings
Published in European journal of haematology (01-08-2002)“…: Familial incidences of autoimmune disorders involving red cells, white cells and platelets are rare. Two cases of autoimmune neutropenia and thrombocytopenia…”
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Red Cell Rheology and Blood Viscosity in Pediatric Individuals Having Received Allogenic Hematopoietic Stem Cell Transplantation or Ex Vivo Autologous Gene Therapy for Sickle Cell Disease
Published in Blood (02-11-2023)“…Background: Allogenic hematopoietic stem cell transplantation (HCT) and ex vivo autologous gene therapies (GT) are potentially curative treatments for sickle…”
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Impact of Vaso-Occlusive Crises on the Transcriptomes of Patients with Sickle Cell Disease
Published in Blood (02-11-2023)“…Introduction: Sickle cell disease (SCD) is an inherited, multisystem blood disorder that affects millions of people worldwide and is particularly common among…”
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Increase in Fetal Hemoglobin Levels in Pediatric Patients with Sickle Cell Disease after Vitamin D Replacement
Published in Blood (05-11-2020)“…Background: High fetal hemoglobin (HbF) levels reduce mortality and morbidity in sickle cell disease (SCD). Results from a prior clinical trial to assess…”
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An analysis of 8 cases of factor X deficiency
Published in Indian journal of hematology & blood transfusion (01-03-2008)“…Background Factor X deficiency is a rare coagulation defect. There are occasional reports of factor X deficiency from India. Difficulty in accurate diagnosis…”
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An analysis of 30 cases of myelodysplastic syndrome
Published in Indian journal of pathology & microbiology (01-04-2009)“…Myelodysplastic syndrome (MDS) is a clonal disorder of pluripotential stem cells of the bone marrow. The purpose of the study was to obtain epidemiological…”
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Rheological Characteristics of Elderly Individuals with Sickle Cell Disease Compared with an Adult Sickle Cell Population
Published in Blood (02-11-2023)“…Introduction: Individuals with sickle cell disease (SCD) have a shorter life expectancy (median age 43 years in the US) compared with the general population…”
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Evaluation of the Impact of a Naturally Occurring Beta Hemoglobin Variant, Hb G-Makassar, on Mature Red Blood Cell Function and Pathology in a Sickle Cell Disease Mouse Model
Published in Blood (02-11-2023)“…Background: Gene based therapy may provide a cure for individuals with sickle cell disease (SCD); base editing is a novel strategy with the ability to directly…”
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Radchip: A Laminin-Lined Red Blood Cell (RBC) Adhesion Device for Functional Characterization and Clinical Evaluation of Sickle RBCs at Steady-State
Published in Blood (02-11-2023)“…Sickle cell disease (SCD) is a genetic disorder caused by a point mutation in the beta-globin gene producing an abnormal hemoglobin (HbS) which, under…”
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Evaluation of GBT021601 As a Therapeutic Agent to Restore Bone Marrow Health and Effective Erythropoiesis in a Sickle Mouse Model
Published in Blood (02-11-2023)“…Introduction: Hypoxia-mediated damage resulting from vaso-occlusion in sickle cell disease (SCD) leads to abnormal angiogenesis, such as occurs with moyamoya…”
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Comparison of Devices That Measure Sickle Red Cell Deformability
Published in Blood (02-11-2023)“…Background With the emergence of novel pharmacologic and gene-based therapies, identifying the rheological and biophysical RBC abnormalities of sickle cell…”
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