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Martin O. Savage

Researcher at Queen Mary University of London

Publications -  69
Citations -  6229

Martin O. Savage is an academic researcher from Queen Mary University of London. The author has contributed to research in topics: Short stature & Cushing's disease. The author has an hindex of 26, co-authored 69 publications receiving 5422 citations. Previous affiliations of Martin O. Savage include University of London & University of Leicester.

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The diagnosis of Cushing's syndrome: an Endocrine Society Clinical Practice Guideline.

TL;DR: Developing clinical practice guidelines for the diagnosis of Cushing's syndrome in patients with multiple and progressive features compatible with the syndrome, particularly those with a high discriminatory value, and patients with adrenal incidentaloma is recommended.
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Treatment of Cushing's Syndrome: An Endocrine Society Clinical Practice Guideline.

TL;DR: Treatment of Cushing's syndrome is essential to reduce mortality and associated comorbidities and the choice of second-line treatments, including medication, bilateral adrenalectomy, and radiation therapy, must be individualized to each patient.
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Consensus guidelines for the diagnosis and treatment of growth hormone (GH) deficiency in childhood and adolescence: Summary statement of the GH research society

Kenneth M. Attie, +43 more
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European Society for Paediatric Endocrinology/Lawson Wilkins Pediatric Endocrine Society consensus statement on diabetic ketoacidosis in children and adolescents.

TL;DR: The Consensus statement was developed with close partnership between the ESPE and LWPES and the International Society for Pediatric and Adolescent Diabetes, all 3 organizations being represented by members who participated in the writing process.
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Evidence for a continuum of genetic, phenotypic, and biochemical abnormalities in children with growth hormone insensitivity.

TL;DR: An overall view of genotype and phenotype relationships is presented, together with an updated approach to the assessment of the patient with GHI, focusing on investigation of the GH-IGF-I axis and relevant molecular studies contributing to this diagnosis.