Search Results - Bahl, Shailini

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  1. 1
    Long term tapering versus standard prednisolone treatment for first episode of childhood nephrotic syndrome: phase III randomised controlled trial and economic evaluation

    Long term tapering versus standard prednisolone treatment for first episode of childhood nephrotic syndrome: phase III randomised controlled trial and economic evaluation by Webb, Nicholas J A, Woolley, Rebecca L, Lambe, Tosin, Frew, Emma, Brettell, Elizabeth A, Barsoum, Emma N, Trompeter, Richard S, Cummins, Carole, Deeks, Jonathan J, Wheatley, Keith, Ives, Natalie J

    Published in BMJ (Online)
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  2. 2
    Activating Mutations of the G-protein Subunit α 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2

    Activating Mutations of the G-protein Subunit α 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2 by Gorvin, Caroline M, Stokes, Victoria J, Boon, Hannah, Cranston, Treena, Glück, Anna K, Bahl, Shailini, Homfray, Tessa, Aung, Theingi, Shine, Brian, Lines, Kate E, Hannan, Fadil M, Thakker, Rajesh V

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  3. 3
    Activating Mutations of the G-protein Subunit [alpha] 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2

    Activating Mutations of the G-protein Subunit [alpha] 11 Interdomain Interface Cause Autosomal Dominant Hypocalcemia Type 2 by Gorvin, Caroline M, Stokes, Victoria J, Boon, Hannah, Cranston, Treena, K. Gluck, Anna, Bahl, Shailini, Homfray, Tessa, Aung, Theingi, Shine, Brian, Lines, Kate E, Hannan, Fadil M

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  4. 4
    Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism

    Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hyp... by Bowl, Michael R., Mirczuk, Samantha M., Grigorieva, Irina V., Piret, Sian E., Cranston, Treena, Southam, Lorraine, Allgrove, Jeremy, Bahl, Shailini, Brain, Caroline, Loughlin, John, Mughal, Zulf, Ryan, Fiona, Shaw, Nick, Thakker, Yogini V., Tiosano, Dov, Nesbit, M. Andrew, Thakker, Rajesh V.

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  5. 5
    Activating mutations of the G-protein subunit α11 interdomain interface cause autosomal dominant hypocalcemia type 2

    Activating mutations of the G-protein subunit α11 interdomain interface cause autosomal dominant hypocalcemia type 2 by Gorvin, Caroline M, Stokes, Victoria J, Boon, Hannah, Cranston, Treena, Glück, Anna K, Bahl, Shailini, Homfray, Tessa, Aung, Theingi, Shine, Brian, Lines, Kate E, Hannan, Fadil M, Thakker, Rajesh V

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