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Clinical Endocrinology|June 23, 2021
Children with multiple endocrine neoplasia type 2B: Not tall and marfanoid, but short with normal body proportionsMedard F M van den Broek, Hanneke M van Santen, Gerlof D Valk, et al.
European Journal of Medical Genetics|April 23, 2013
Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 casesMartin Poot, Annemarie A Verrijn Stuart, Emma van Daalen, et al.
Journal of the Endocrine Society|January 21, 2022
Is There a Role for Biomarkers in Surveillance of Pancreatic Neuroendocrine Neoplasms in Von Hippel-Lindau Disease?Myrthe R Naber, Saya Ahmad, Annemarie A Verrijn Stuart, et al.
American Journal of Medical Genetics. Part A|June 25, 2016
Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletionIris M de Lange, Annemarie A Verrijn Stuart, Rob B van der Luijt, et al.
European Journal of Medical Genetics|October 13, 2007
Proportional growth failure and oculocutaneous albinism in a girl with a 6.87 Mb deletion of region 15q26.2-->qterMartin Poot, Marc J Eleveld, Ruben van 't Slot, et al.
Frontiers in Endocrinology|January 11, 2020
Clinical Relevance of Genetic Analysis in Patients With Pituitary Adenomas: A Systematic ReviewMedard F M van den Broek, Bernadette P M van Nesselrooij, Annemarie A Verrijn Stuart, et al.
Pediatric Blood & Cancer|January 6, 2026
Psychosocial Outcomes in Patients With Endocrine Tumor Syndromes: A Systematic ReviewDaniël Zwerus, Floortje Strobbe, Annemarie A Verrijn Stuart, et al.
Plos One|January 12, 2016
Serum Cytokines as Biomarkers in Islet Cell Transplantation for Type 1 DiabetesCornelis R van der Torren, Annemarie A Verrijn Stuart, DaHae Lee, et al.
Hormone Research in Paediatrics|March 28, 2023
The Effects of 5 Years of Growth Hormone Treatment on Growth and Body Composition in Patients with Temple SyndromeAlicia F Juriaans, Demi J Trueba-Timmermans, Gerthe F Kerkhof, et al.
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