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Metabolic syndrome: definitions and controversies
It is suggested that diagnosis, prevention and treatment in children and adolescents should better focus on established risk factors rather than the diagnosis of MetS, because of its alarmingly increasing prevalence.
Gastroenteropancreatic neuroendocrine tumours.
ENETS Consensus Guidelines Update for the Management of Patients with Functional Pancreatic Neuroendocrine Tumors and Non-Functional Pancreatic Neuroendocrine Tumors
The ENETS Consensus Guidelines Update for the Management of Patients with Functional Pancreatic Neuroendocrine Tumors and Non-Functional Pancreatics with Functional and non-functional tumours is published.
The diagnosis and medical management of advanced neuroendocrine tumors.
Assessment of specific or general tumor markers offers high sensitivity in establishing the diagnosis and can also have prognostic significance, and therapy with radionuclides may be used for tumors exhibiting uptake to a diagnostic scan, either after surgery to eradicate microscopic residual disease or later if conventional treatment or biotherapy fails.
Management of adult patients with Langerhans cell histiocytosis: recommendations from an expert panel on behalf of Euro-Histio-Net
The first recommendations for management of adult patients with LCH, a number of experts in this field cooperated to develop, were developed according to the clinical relevance focusing on diagnostic work up, therapy, and follow up.
ENETS Consensus Guidelines for the Management of Patients with Digestive Neuroendocrine Neoplasms: Functional Pancreatic Endocrine Tumor Syndromes
The two most common functional p-NETs (gastrinomas, insulinomas) are considered separately, whereas the other well-described and possible rarefunctional p- NETs are considered together as a group called rare functional rFTs (RFTs).
Polycystic ovary syndrome: the spectrum of the disorder in 1741 patients.
Describing data from the largest reported series of women with PCOS enables the development of a management-orientated approach to the syndrome.
The ectopic adrenocorticotropin syndrome: clinical features, diagnosis, management, and long-term follow-up.
A variety of tests and imaging studies are necessary for the correct diagnosis of the EAS, but up to 20% of cases present a covert or occult EAS syndrome, and these cases require a prolonged follow-up, review, and repetition of diagnostic tests and scans.
ENETS Consensus Guidelines for the Standards of Care in Neuroendocrine Tumors: Radiological Examinations
The ENETS Consensus Guidelines for the Standards of Care in Neuroendocrine Tumors : Radiological Examinations show clear trends in acceptable levels of care for these patients and provide a roadmap for future generations to follow.
Clinical review: Diagnosis and management of pituitary carcinomas.
- G. Kaltsas, P. Nomikos, G. Kontogeorgos, M. Buchfelder, A. Grossman
- MedicineThe Journal of clinical endocrinology and…
It is believed there will be any real prospect of long-term survival until the development and use of therapies targeted at specific molecular abnormalities are targeted, including various attempts at medical therapy.