Merih Berberoğlu

Human and mouse<i>TPIT</i>gene mutations cause early onset pituitary ACTH deficiency

Anne-Marie Pulichino, Sophie Vallette-Kasic, Catherine Couture et al. · Genes & Development · 2003 · 216 citations · Full text

Medicine, Endocrinology, Genetics +14

Phenotypical, Biological, and Molecular Heterogeneity of 5α-Reductase Deficiency: An Extensive International Experience of 55 Patients

Laurent Maı̈moun, Pascal Philibert, B. Cammas et al. · The Journal of Clinical Endocrinology & Metabolism · 2010 · 213 citations

Medicine, Endocrinology, Genetics +17

Severe Growth Hormone Insensitivity Resulting from Total Absence of Signal Transducer and Activator of Transcription 5b

Vivian Hwa, Brian M. Little, Pelin Adıyaman et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 150 citations · Full text

Medicine, Endocrinology, Endocrine Genetics +11

Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by<i>TPIT</i>Gene Mutations

Sophie Vallette-Kasic, Thierry Brue, Anne-Marie Pulichino et al. · The Journal of Clinical Endocrinology & Metabolism · 2005 · 126 citations · Full text

Medicine, Endocrinology, Genetics +17

Adherence to Growth Hormone Therapy: Results of a Multicenter Study

Banu Küçükemre Aydın, Zehra Aycan, Zeynep Şıklar et al. · Endocrine Practice · 2013 · 87 citations

Pharmacy, Endocrinology, Pharmacotherapy +11