Torthaí cuardaigh - Ved Bhushan Arya

  • 1 - 9 toradh as 9 á dtaispeáint
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  1. 1
    The molecular mechanisms, diagnosis and management of congenital hyperinsulinism

    The molecular mechanisms, diagnosis and management of congenital hyperinsulinism de réir Khalid Hussain, Senthil Senniappan, VedBhushan Arya

    Foilsithe / Cruthaithe 2013
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  2. 2
    Hyperinsulinaemic Hypoglycaemia: Genetic Mechanisms, Diagnosis and Management

    Hyperinsulinaemic Hypoglycaemia: Genetic Mechanisms, Diagnosis and Management de réir Zainaba Mohamed, Ved Bhushan Arya, Khalid Hussain

    Foilsithe / Cruthaithe 2012
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  3. 3
    Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism

    Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism de réir Ritika R. Kapoor, Sarah E. Flanagan, Ved Bhushan Arya, Julian Hamilton‐Shield, Sian Ellard, Khalid Hussain

    Foilsithe / Cruthaithe 2013
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  4. 4
    Long-Term Follow-Up of Children With Congenital Hyperinsulinism on Octreotide Therapy

    Long-Term Follow-Up of Children With Congenital Hyperinsulinism on Octreotide Therapy de réir Hüseyin Demirbilek, Pratik Shah, Ved Bhushan Arya, Louise Hinchey, Sarah E. Flanagan, Sian Ellard, Khalid Hussain

    Foilsithe / Cruthaithe 2014
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  5. 5
    Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism

    Pancreatic Endocrine and Exocrine Function in Children following Near-Total Pancreatectomy for Diffuse Congenital Hyperinsulinism de réir Ved Bhushan Arya, Senthil Senniappan, Hüseyin Demirbilek, Syeda Tabassum Alam, Sarah E. Flanagan, Sian Ellard, Khalid Hussain

    Foilsithe / Cruthaithe 2014
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  6. 6
    Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age

    Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age de réir Ved Bhushan Arya, Sarah E. Flanagan, Anitha Kumaran, Julian Hamilton‐Shield, Sian Ellard, Khalid Hussain, Ritika R. Kapoor

    Foilsithe / Cruthaithe 2013
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  7. 7
    Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations

    Clinical and histological heterogeneity of congenital hyperinsulinism due to paternally inherited heterozygous ABCC8/KCNJ11 mutations de réir Ved Bhushan Arya, María Güemes, Azizun Nessa, Syeda Tabassum Alam, Pratik Shah, Clare Gilbert, Senthil Senniappan, Sarah E. Flanagan, Sian Ellard, Khalid Hussain

    Foilsithe / Cruthaithe 2014
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  8. 8
    Sirolimus Therapy in Infants with Severe Hyperinsulinemic Hypoglycemia

    Sirolimus Therapy in Infants with Severe Hyperinsulinemic Hypoglycemia de réir Senthil Senniappan, Sanda Alexandrescu, Nina Tatevian, Pratik Shah, Ved Bhushan Arya, Sarah E. Flanagan, Sian Ellard, Dyanne Rampling, Michael Ashworth, Robert Brown, Khalid Hussain

    Foilsithe / Cruthaithe 2014
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  9. 9
    Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations

    Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations de réir Hüseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Özbek, Jayne Houghton, Rıza Taner Baran, Melek Akar, S. Tekeş, Heybet Tüzün, Deborah Mackay, Sarah E. Flanagan, Andrew T. Hattersley, Sian Ellard, Khalid Hussain

    Foilsithe / Cruthaithe 2015
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