Hasil Pencarian - Aaron Chapla

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  1. 1
    Molecular diagnosis of maturity onset diabetes of the young in India

    Molecular diagnosis of maturity onset diabetes of the young in India oleh Veena V Nair, Aaron Chapla, Nishanth Arulappan, Nihal Thomas

    Diterbitkan 2013-01-01
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  2. 2
    Congenital Adrenal Hyperplasia – A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India

    Congenital Adrenal Hyperplasia – A Comprehensive Review of Genetic Studies on 21-Hydroxylase Deficiency from India oleh Lavanya Ravichandran, Hesarghatta S. Asha, Sarah Mathai, Nihal Thomas, Aaron Chapla

    Diterbitkan 2024-04-01
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  3. 3
    Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal Hyperplasia

    Allele-specific and multiplex PCR based tools for cost-effective and comprehensive genetic testing in Congenital Adrenal Hyperplasia oleh Lavanya Ravichandran, Deny Varghese, Parthiban R, Asha H. S, Sophy Korula, Nihal Thomas, Aaron Chapla

    Diterbitkan 2022-01-01
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  4. 4
    Parallel Multi-Gene Panel Testing for Diagnosis of Idiopathic Hypogonadotropic Hypogonadism/Kallmann Syndrome

    Parallel Multi-Gene Panel Testing for Diagnosis of Idiopathic Hypogonadotropic Hypogonadism/Kallmann Syndrome oleh Manickavasagam Senthilraja, Aaron Chapla, Felix K. Jebasingh, Dukhabhandhu Naik, Thomas V. Paul, Nihal Thomas

    Diterbitkan 2019-01-01
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  5. 5
    CFTR mutations and phenotypic correlations in people with cystic fibrosis: a retrospective study from a single centre in south IndiaResearch in context

    CFTR mutations and phenotypic correlations in people with cystic fibrosis: a retrospective study from a single centre in south IndiaResearch in context oleh Sneha D. Varkki, Rekha Aaron, Aaron Chapla, Sumita Danda, Priyanka Medhi, N. Jansi Rani, Grace R. Paul

    Diterbitkan 2024-08-01
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  6. 6
    Genetic heterogeneity and challenges in the management of permanent neonatal diabetes mellitus: A single-centre study from South India

    Genetic heterogeneity and challenges in the management of permanent neonatal diabetes mellitus: A single-centre study from South India oleh Sophy Korula, Lavanya Ravichandran, Praveen G Paul, Jabasteen Johnson, Aaron Chapla, Sridhar Santhanam, Anna Simon, Sarah Mathai

    Diterbitkan 2022-01-01
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  7. 7
    P227: High carrier frequency of CYP21A2 hotspot mutations in Southern India: Underscoring the need for genetic testing in congenital adrenal hyperplasia

    P227: High carrier frequency of CYP21A2 hotspot mutations in Southern India: Underscoring the need for genetic testing in congenital adrenal hyperplasia oleh Lavanya Ravichandran, Shriti Paul, ReKha A, Asha HS, Sarah Mathai, Anna Simon, Sumitha Danda, Nihal Thomas, Aaron Chapla

    Diterbitkan 2024-01-01
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  8. 8
    Genetic predisposition and high exposure to colistin in the early treatment period as independent risk factors for colistin‐induced nephrotoxicity

    Genetic predisposition and high exposure to colistin in the early treatment period as independent risk factors for colistin‐induced nephrotoxicity oleh Sumith K. Mathew, Aaron Chapla, Padmanaban Venkatesan, Vishnu Eriyat, Blessed Winston Aruldhas, Ratna Prabha, Michael N. Neely, Shoma V. Rao, Subramani Kandasamy, Binu Susan Mathew

    Diterbitkan 2024-03-01
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  9. 9
    Next-Generation Sequencing-Based Genetic Testing For Familial Partial Lipodystrophy

    Next-Generation Sequencing-Based Genetic Testing For Familial Partial Lipodystrophy oleh Hesarghatta Shyamasunder Asha, MBBS, MD, DNB (Endo), Aaron Chapla, MSc, Shrinath Shetty, MBBS, MD, Nihal Thomas, MBBS, MD, MNAMS, DNB (Endo), FRACP (Endo), FRCP (Edin), FRCP (Glasg)

    Diterbitkan 2015-01-01
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  10. 10
    Diabetes Mellitus With Renal and Müllerian Anomalies

    Diabetes Mellitus With Renal and Müllerian Anomalies oleh Khushboo Agarwal, MBBS, MD, Aaron Chapla, MSC, PhD, Anuradha Chandramohan, MBBS, MD, Chandra J. Singh, MS, MCh, DNB, Nihal Thomas, MBBS, MD, DNB, PhD, Felix K. Jebasingh, MBBS, MD, DM, DNB

    Diterbitkan 2022-01-01
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  11. 11
    Comprehensive Maturity Onset Diabetes of the Young (MODY) Gene Screening in Pregnant Women with Diabetes in India.

    Comprehensive Maturity Onset Diabetes of the Young (MODY) Gene Screening in Pregnant Women with Diabetes in India. oleh Mahesh Doddabelavangala Mruthyunjaya, Aaron Chapla, Asha Hesarghatta Shyamasunder, Deny Varghese, Manika Varshney, Johan Paul, Mercy Inbakumari, Flory Christina, Ron Thomas Varghese, Kurien Anil Kuruvilla, Thomas V Paul, Ruby Jose, Annie Regi, Jessie Lionel, L Jeyaseelan, Jiji Mathew, Nihal Thomas

    Diterbitkan 2017-01-01
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  12. 12
    The H Syndrome: Molecular Diagnosis Using Next-Generation Sequencing

    The H Syndrome: Molecular Diagnosis Using Next-Generation Sequencing oleh Mahesh Doddabelavangala Mruthyunjaya, MBBS, MD, DM, Aaron Chapla, MSc, PhD, Sahana Shetty, MBBS, MD, Asha Hesarghatta Shyamasunder, MBBS, DNB, DNB, Lydia Mathew, MBBS, MD, Renu George, MBBS, MD, Thomas Vizhalil Paul, MBBS, MD, DNB, PhD, Nihal Thomas, MBBS, MD, MNAMS, DNB, FRACP, FRCP, FRCP

    Diterbitkan 2016-01-01
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