Mariam Kourime

An assessment of the quality of the I-DSD and the I-CAH registries - international registries for rare conditions affecting sex development

Mariam Kourime, Jillian Bryce, J. Jiang et al. · Orphanet Journal of Rare Diseases · 2017 · 42 citations · Full text

Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life

Filiz Çizmecioğlu, Jeremy Jones, Wendy F. Paterson et al. · Journal of Clinical Research in Pediatric Endocrinology · 2018 · 28 citations · Full text

Long-term outcome of thyrotoxicosis in childhood and adolescence in the west of Scotland: the case for long-term antithyroid treatment and the importance of initial counselling

Mariam Kourime, Sheena McGowan, Mabrouka Al Towati et al. · Archives of Disease in Childhood · 2017 · 26 citations · Full text

Hypogonadism in Prader–Willi syndrome from birth to adulthood: a 28-year experience in a single centre

Sakina Kherra, Wendy F. Paterson, Filiz Çizmecioğlu et al. · Endocrine Connections · 2021 · 10 citations · Full text