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Showing page 1 of results 1 - 5 of about 5 pages

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The Molecular Causes of Congenital Hypothyroidism: The Scottish experience | ESPE2016
Mariam Kourime; Jeremy Jones; Aisha Ansari; Therese Bradley; Avril Mason; Guftar Shaikh
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p890.htm
Published: 2016-08-19

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Recognition of the Fetal and Perinatal Features of the Prader-Willi Syndrome is Required to Avoid Delay in Diagnosis | ESPE2016
Filiz Mine Cizmecioglu; Jeremy Huw Jones; Wendy Forsyth Paterson; Sakina Kherra; Mariam Kourime; M Guftar Shaikh; Malcolm Donald
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p559.htm
Published: 2016-08-19

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A New International Registry Highlights the Differences in Practice for Reaching a Diagnosis of CAH - On Behalf of the I-CAH/I-DSD Registry User Group | ESPE2016
Mariam Kourime; Jillian Bryce; Jipu Jiang; Nayananjani Karunasena; Tulay Guran; Sabine Elisabeth Hannema; Martine Cools; Der Gri
http://abstracts.eurospe.org/hrp/0086/hrp0086p1-p356.htm
Published: 2016-08-19

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Outcome of Thyrotoxicosis in Childhood and Adolescence in a Geographically Define Area; a 24-Year Experience | ESPE2015
Mariam Kourime; Sheena McGowan; Mabrouka Al-Towati; Faisal Ahmed; Graham Stewart; Scott Williamson; Ian Hunter; Malcolm Donaldso
http://abstracts.eurospe.org/hrp/0084/hrp0084p3-1180.htm
Published: 2015-08-26

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Gonadal Function in the Prader-Willi Syndrome from Infancy to Adulthood | ESPE2015
Sakina Kherra; Mariam Kourime; Heba El-Sedfy; Wendy Paterson; M Guftar Shaikh; Malcolm Donaldson
http://abstracts.eurospe.org/hrp/0084/hrp0084p2-438.htm
Published: 2015-08-26

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