Initiating Pancreatic Neuroendocrine Tumor (pNET) Screening in Young MEN1 Patients

Autor: Olaf M. Dekkers, Gerlof D. Valk, Wouter T Zandee, M. R. Vriens, Wouter W. de Herder, Bas Havekes, Mirthe J Klein Haneveld, Annenienke C van de Ven, Peter H. Bisschop, Carolina R.C. Pieterman, Madeleine L. Drent, Annemarie A Verrijn Stuart, Mark J C van Treijen, Rachel S van Leeuwaarde

Publikováno v: Journal of Clinical Endocrinology and Metabolism, 106, 3515-3525
Journal of Clinical Endocrinology and Metabolism, 106(12), 3515-3525. Endocrine Society
Journal of Clinical Endocrinology and Metabolism, 106(12), 3515-3525. ENDOCRINE SOC
Journal of Clinical Endocrinology and Metabolism, 106(12), 3515-3525. The Endocrine Society
Journal of Clinical Endocrinology & Metabolism, 106(12), 3515-3525. Oxford University Press
Journal of Clinical Endocrinology and Metabolism, 106, 12, pp. 3515-3525
Journal of clinical endocrinology and metabolism, 106(12), 3515-3525. The Endocrine Society
Klein Haneveld, M J, van Treijen, M J C, Pieterman, C R C, Dekkers, O M, van de Ven, A, de Herder, W W, Zandee, W T, Drent, M L, Bisschop, P H, Havekes, B, Vriens, M R, Verrijn Stuart, A A, Valk, G D & van Leeuwaarde, R S 2021, ' Initiating Pancreatic Neuroendocrine Tumor (pNET) Screening in Young MEN1 Patients : Results from the DutchMEN Study Group ', Journal of Clinical Endocrinology and Metabolism, vol. 106, no. 12, pp. 3515-3525 . https://doi.org/10.1210/clinem/dgab569

ContextNonfunctioning pancreatic neuroendocrine tumors (NF-pNETs) are highly prevalent and constitute an important cause of mortality in patients with multiple endocrine neoplasia type 1 (MEN1). Still, the optimal age to initiate screening for pNETs

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2ce36b25c25d31e1a499d42dbc31157
https://doi.org/10.1210/clinem/dgab569

Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children

Autor: Fabrizio Drago, Carlo Dionisi-Vici, Corrado Di Mambro, Valentina Lodato, Enrico Bertini, Giovanni Parlapiano, Rachele Adorisio, Diego Martinelli, Anwar Baban

Publikováno v: Biomolecules, Vol 11, Iss 1578, p 1578 (2021)
Biomolecules

Neuromuscular disorders (NMDs) are highly heterogenous from both an etiological and clinical point of view. Their signs and symptoms are often multisystemic, with frequent cardiac involvement. In fact, childhood onset forms can predispose a person to

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f45ae9e0ebf2ce3d6f1f2ccc9b3aeb87
https://www.mdpi.com/2218-273X/11/11/1578

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.