Resultados da busca - Girish Meenakshi

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  1. 1
    ST Elevation Acute Myocardial Infarction (STEMI) in a Child with Multisystem Inflammatory Syndrome

    ST Elevation Acute Myocardial Infarction (STEMI) in a Child with Multisystem Inflammatory Syndrome por Choudhary, Abhijit, Jain, Shikha, Khemka, Nishu, Chauhan, Urmila, Bang, Akash, Girish, Meenakshi, Makode, Sagar

    Publicado em 2022
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  2. 2
    The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India

    The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India por Shabrish, Snehal, Kelkar, Madhura, Yadav, Reetika Malik, Bargir, Umair Ahmed, Gupta, Maya, Dalvi, Aparna, Aluri, Jahnavi, Kulkarni, Manasi, Shinde, Shweta, Sawant-Desai, Sneha, Kambli, Priyanka, Hule, Gouri, Setia, Priyanka, Jodhawat, Neha, Gaikwad, Pallavi, Dhawale, Amruta, Nambiar, Nayana, Gowri, Vijaya, Pandrowala, Ambreen, Taur, Prasad, Raj, Revathi, Uppuluri, Ramya, Sharma, Ratna, Kini, Pranoti, Sivasankaran, Meena, Munirathnam, Deenadayalan, Vedam, Ramprasad, Vignesh, Pandiarajan, Banday, Aaqib, Rawat, Amit, Aggarwal, Amita, Poddar, Ujjal, Girish, Meenakshi, Chaudhary, Abhijit, Sampagar, Abhilasha, Jayaraman, Dharani, Chaudhary, Narendra, Shah, Nitin, Jijina, Farah, Chandrakla, S., Kanakia, Swati, Arora, Brijesh, Sen, Santanu, Lokeshwar, Madhukar, Desai, Mukesh, Madkaikar, Manisha

    Publicado em 2021
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  3. 3
    The genetic basis of DOORS syndrome: an exome-sequencing study

    The genetic basis of DOORS syndrome: an exome-sequencing study por Philippe M. Campeau, Dalia Kasperavičiūtė, James T. Lu, Lindsay C. Burrage, Choel Kim, Mutsuki Hori, Berkley R. Powell, Fiona Stewart, Têmis Maria Félix, Jenneke van den Ende, Marzena Wiśniewska, Hülya Kayserili, Patrick Rump, Sheela Nampoothiri, Salim Aftimos, Antje Mey, Lal D V Nair, Michael L. Begleiter, Isabelle De Bie, Girish Meenakshi, Mitzi L. Murray, Gabriela M. Repetto, Mahin Golabi, Edward Blair, Alison Male, Fabienne Giuliano, Ariana Kariminejad, William G. Newman, Sanjeev S. Bhaskar, Jonathan E. Dickerson, Bronwyn Kerr, Siddharth Banka, Jacques C. Giltay, Dagmar Wieczorek, Anna Tostevin, Joanna Wiszniewska, Sau Wai Cheung, Raoul C. M. Hennekam, Richard A. Gibbs, Brendan Lee, Sanjay M. Sisodiya

    Publicado em 2013
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  4. 4
    <i>TBC1D24</i> genotype–phenotype correlation

    <i>TBC1D24</i> genotype–phenotype correlation por Simona Balestrini, Mathieu Milh, Claudia Castiglioni, Kevin Lüthy, Mattéa J. Finelli, Patrik Verstreken, Aaron L. Cardon, Barbara Gnidovec Stražišar, J. Lloyd Holder, Gaëtan Lesca, Maria Margherita Mancardi, Anne Lise Poulat, Gabriela M. Repetto, Siddharth Banka, Leonilda Bilo, Laura E. Birkeland, Friedrich Bosch, Knut Brockmann, J. Helen Cross, Diane Doummar, Têmis Maria Félix, Fabienne Giuliano, Mutsuki Hori, Irina Hüning, Hulia Kayserili, Usha Kini, Melissa Lees, Girish Meenakshi, Leena Mewasingh, Alistair T. Pagnamenta, Silvio Peluso, Antje Mey, Gregory M. Rice, Jill A. Rosenfeld, Jenny C. Taylor, Matthew M. Troester, Christine M. Stanley, Dorothée Ville, Magdalena Walkiewicz, Antonio Falace, Anna Fassio, Johannes R. Lemke, Saskia Biskup, Jessica Tardif, Norbert Fonya Ajeawung, Aslıhan Tolun, Mark Corbett, Jozef Gécz, Zaid Afawi, Katherine B. Howell, Karen Oliver, Samuel F. Berkovic, Ingrid E. Scheffer, De Falco Fa, Peter L. Oliver, Pasquale Striano, Federico Zara, Philippe M. Campeau, Sanjay M. Sisodiya

    Publicado em 2016
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