Search Results - Anil Pathare

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  1. 1

    IMPACT OF MANNOSE-BINDING PROTEIN GENE POLYMORPHISMS IN OMANI SICKLE CELL DISEASE PATIENTS by Mathew Zachariah, Anil Pathare

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  2. 2

    ALLOIMMUNIZATION IN PATIENTS WITH SICKLE CELL DISEASE AND THALASSAEMIA: EXPERIENCE OF SINGLE CENTRE FROM OMAN by Anil Pathare, Salam Alkindi

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  3. 3

    COMPARISON OF METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS IN HEALTHY COMMUNITY HOSPITAL VISITORS[CA-MRSA] AND HOSPITAL STAFF [HA-MRSA] by Nirmal A Pathare, Anil Pathare

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  4. 4

    INCREASED VASOOCCLUSIVE CRISIS IN “O” BLOOD GROUP SICKLE CELL DISEASE PATIENTS: ASSOCIATION WITH UNDERLYING THROMBOSPONDIN LEVELS. by M. Al Huneini, Anil Pathare

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  5. 5

    PREVALENCE OF HEPATITIS B, HEPATITIS C AND HIV IN MULTIPLY TRANSFUSED SICKLE CELL DISEASE PATIENTS FROM OMAN by Anil Pathare, Salam Alkindi, prof.

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  6. 6

    SERUM TOTAL BILIRUBIN, NOT CHOLELITHIASIS, IS INFLUENCED BY UGT1A1 POLYMORPHISM, ALPHA THALASSEMIA AND S GENOTYPE: FIRST REPORT ON COMPARISON BETWEEN ARAB-INDIAN AND AFRICAN S GE... by Said Y ALkindi, Anil Pathare, Salam Alkindi

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  7. 7

    THE USE OF HPLC AS A TOOL FOR NEONATAL CORD BLOOD SCREENING OF HAEMOGLOBINOPATHY - A VALIDATION STUDY by A. Al-Madhani, Anil Pathare, Salam Alkindi

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  8. 8

    CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA by r. Salam Al-Kindi, Isra Al-Busaidi, Anil Pathare

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  9. 9

    Clinical, laboratory and ultrastructural findings in patients with storage pool disease: A case series by Anil Pathare, Kawthar Said Hamed Al Adawi, Kawther Al Adawi, Badriya Al Balushi, Karima Al Falahi, Yasser Wali

    Published in Pediatric Hematology Oncology Journal (2023-12-01)
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  10. 10

    CORRELATION OF TRANSIENT ELASTOGRAPHY WITH LIVER IRON CONCENTRATION, AND SERUM FERRITIN LEVELS IN PATIENTS WITH TRANSFUSION-DEPENDENT THALASSEMIA MAJOR PATIENTS FROM OMAN by Hammad Khan, Vinodh Panjwani, Sara Al Rahbi, Abubakr Eltigani, Rizwan Qureshi, Khaleeq Unnisa, Najmus Sehar, Alok Mittal, Anil Pathare

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  11. 11

    Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes by Salam Alkindi, Shoaib Al Zadjali, Mohamed Al Rawahi, Hamoud Al Haddabi, Shahina Daar, Refaat Abdullah Elsadek, Bahaa Eldeen Diab Sherkawy, Anil Pathare

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