All Stories

  1. A Unique Genotype of Pseudohypoaldosteronism Type 1b in a Highly Consanguineous Population

    Article • Journal of the Endocrine Society, May 2021, Endocrine Society

    Aisha Al senani

  2. Use of ambulatory glucose monitoring and analysis of ambulatory glucose profile in clinical practice for diabetes management; a position statement of the Arab Society of Paediatric Endocrinology and diabetes

    Article • Diabetes Research and Clinical Practice, March 2021, Elsevier

    Aisha Al senani

  3. Demographic Features and Etiology of Congenital Hypothyroidism at the National Diabetes and Endocrine Center in Oman from 2004 to 2016

    Article • Oman Medical Journal, September 2020, Oman Medical Journal

    Aisha Al senani

  4. Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia

    Article • F1000Research, December 2019, Faculty of 1000, Ltd.

    Aisha Al senani

  5. Clinical characteristics and phenotype-genotype review of 25 Omani children with congenital hyperinsulinism in infancy. A one-decade single-center experience

    Article • Saudi Medical Journal, July 2019, Saudi Medical Journal

    Aisha Al senani

  6. Genetic mutations associated with neonatal diabetes mellitus in Omani patients

    Article • Journal of Pediatric Endocrinology and Metabolism, January 2018, De Gruyter

    Aisha Al senani

  7. Erratum. Recessively Inherited LRBA Mutations Cause Autoimmunity Presenting as Neonatal Diabetes. Diabetes 2017;66:2316–2322

    Article • Diabetes, January 2018, American Diabetes Association

    Aisha Al senani

  8. Agammaglobulinaemia despite terminal B-cell differentiation in a patient with a novel LRBA mutation

    Article • Clinical & Translational Immunology, May 2017, Wiley

    Aisha Al senani

  9. Recessively InheritedLRBAMutations Cause Autoimmunity Presenting as Neonatal Diabetes

    Article • Diabetes, May 2017, American Diabetes Association

    Aisha Al senani

  10. A novel mutation inHSD11B2causes apparent mineralocorticoid excess in an Omani kindred

    Article • Annals of the New York Academy of Sciences, July 2016, Wiley

    Aisha Al senani

  11. i am the main auther in this case report

    Article • Oman Medical Journal, March 2015, Oman Medical Journal

    Aisha Al senani

  12. Pulmonary hemorrhage in a case of CD25 deficiency

    Article • LymphoSign Journal, September 2014, LymphoSign Journal Limited Partnership

    Aisha Al senani

  13. Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined byTMEM38Bmutation

    Article • Journal of Medical Genetics, October 2012, BMJ

    Aisha Al senani

  14. A novel leprechaunism mutation, Cys807Arg, in an Arab infant: a rare cause of hypoglycaemia

    Article • Paediatrics and International Child Health, August 2012, Taylor & Francis

    Aisha Al senani

  15. i am coauther in this research

    Article • Pediatric Diabetes, September 2010, Wiley

    Aisha Al senani