Hasil Pencarian - Anil Pathare

Perbaiki Hasil
  1. 1
    IMPACT OF MANNOSE-BINDING PROTEIN GENE POLYMORPHISMS IN OMANI SICKLE CELL DISEASE PATIENTS

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

    Diterbitkan 2016-02-01
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  2. 2
    ALLOIMMUNIZATION IN PATIENTS WITH SICKLE CELL DISEASE AND THALASSAEMIA: EXPERIENCE OF SINGLE CENTRE FROM OMAN

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

    Diterbitkan 2017-02-01
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  3. 3
    COMPARISON OF METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS IN HEALTHY COMMUNITY HOSPITAL VISITORS[CA-MRSA] AND HOSPITAL STAFF [HA-MRSA]

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

    Diterbitkan 2015-10-01
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  4. 4
    INCREASED VASOOCCLUSIVE CRISIS IN “O” BLOOD GROUP SICKLE CELL DISEASE PATIENTS: ASSOCIATION WITH UNDERLYING THROMBOSPONDIN LEVELS.

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

    Diterbitkan 2017-04-01
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  5. 5
    PREVALENCE OF HEPATITIS B, HEPATITIS C AND HIV IN MULTIPLY TRANSFUSED SICKLE CELL DISEASE PATIENTS FROM OMAN

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

    Diterbitkan 2019-10-01
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  6. 6
    Transient Myeloproliferative Disorder and Down Syndrome Is there a link?

    Transient Myeloproliferative Disorder and Down Syndrome Is there a link? oleh Zenaida S. Reyes, Wafa Bashir, Anil Pathare

    Diterbitkan 2012-11-01
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  7. 7
    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 GENES

    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... oleh Said Y ALkindi, Anil Pathare, Salam Alkindi

    Diterbitkan 2015-10-01
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  8. 8
    THE USE OF HPLC AS A TOOL FOR NEONATAL CORD BLOOD SCREENING OF HAEMOGLOBINOPATHY - A VALIDATION STUDY

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

    Diterbitkan 2019-01-01
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  9. 9
    CLINICAL AND LABORATORY FEATURES OF SICKLE CELL DISEASE S/D PUNJAB: IMPACT OF HBF AND HYDROXYUREA

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

    Diterbitkan 2024-04-01
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  10. 10
    Haemostatic Parameters in Patients with Behçet’s Disease

    Haemostatic Parameters in Patients with Behçet’s Disease oleh Juma K. Alkaabi, David Gravell, Hamood Al-Haddabi, Anil Pathare

    Diterbitkan 2014-05-01
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  11. 11
    Haemostatic Parameters in Patients with Behçet’s Disease

    Haemostatic Parameters in Patients with Behçet’s Disease oleh Juma K. Alkaabi, David Gravell, Hamood Al-Haddabi, Anil Pathare

    Diterbitkan 2014-05-01
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  12. 12
    Portal Vein Thrombosis in Adult Omani Patients: A Retrospective Cohort Study

    Portal Vein Thrombosis in Adult Omani Patients: A Retrospective Cohort Study oleh Khalid Al Hashmi, Lamya Al Aamri, Sulayma Al Lamki, Anil Pathare

    Diterbitkan 2017-11-01
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  13. 13
    Complications of PORT-A-CATH® in patients with sickle cell disease

    Complications of PORT-A-CATH® in patients with sickle cell disease oleh Salam Alkindi, Samaa Matwani, Alghalia Al-Maawali, Buthaina Al-Maskari, Anil Pathare

    Diterbitkan 2012-02-01
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  14. 14
    Respiratory Viral Infections in Sickle Cell Anemia: Special Emphasis on H1N1 Co-infection

    Respiratory Viral Infections in Sickle Cell Anemia: Special Emphasis on H1N1 Co-infection oleh Salam Alkindi, Taqwa Al-Yahyai, Sameer Raniga, Mohamed Rachid Boulassel, Anil Pathare

    Diterbitkan 2020-11-01
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  15. 15
    A profile of rare bloods in Oman

    A profile of rare bloods in Oman oleh Sanmukh R Joshi, Anil Pathare, Ali Al-Marhoubi, Raya Al-Muhaidry, Thamina Ashraf

    Diterbitkan 2013-01-01
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  16. 16
    Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors : A quality initiative

    Impact of Educational Activities in Reducing Pre-Analytical Laboratory Errors : A quality initiative oleh Hamed Al-Ghaithi, Anil Pathare, Sahimah Al-Mamari, Rodrigo Villacrucis, Naglaa Fawaz, Salam Alkindi

    Diterbitkan 2017-08-01
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  17. 17
    Utility of Magnetic Resonance Imaging T2* in Diagnosing and Monitoring Severe Cardiac and Hepatic Siderosis

    Utility of Magnetic Resonance Imaging T2* in Diagnosing and Monitoring Severe Cardiac and Hepatic Siderosis oleh Shahina Daar, Moez Hassan, Vinodh Panjwani, Anil Pathare, Humoud Al-Dhuhli, Arwa Z. Al-Riyami

    Diterbitkan 2015-01-01
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  18. 18
    Utility of Magnetic Resonance Imaging T2* in Diagnosing and Monitoring Severe Cardiac and Hepatic Siderosis

    Utility of Magnetic Resonance Imaging T2* in Diagnosing and Monitoring Severe Cardiac and Hepatic Siderosis oleh Shahina Daar, Moez Hassan, Vinodh Panjwani, Anil Pathare, Humoud Al-Dhuhli, Arwa Z. Al-Riyami

    Diterbitkan 2015-02-01
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  19. 19
    Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors

    Immunophenotypic Characteristics of T-Acute Lymphoblastic Leukemia in Omani Patients: A Correlation with Demographic Factors oleh Azza Al-Mashaikhi, Zahra Al Khatri, Sahima Al Mamari, Murtadha Al Khabori, Anil Pathare, Naglaa Fawaz

    Diterbitkan 2018-01-01
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  20. 20
    Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred—PK deficiency masquerading as congenital dyserythropoietic anemia

    Novel PKLR missense mutation (A300P) causing pyruvate kinase deficiency in an Omani Kindred—PK deficiency masquerading as congenital dyserythropoietic anemia oleh Naglaa Fawaz, Ismail Beshlawi, Alauldeen Alqasim, Mathew Zachariah, Roberta Russo, Immacolata Andolfo, Antonella Gambale, Anil Pathare, Achille Iolascon

    Diterbitkan 2022-02-01
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