ISSN 1662-4009 (online)

ey0017.13-5 | Advocacy, History and Society | ESPEYB17

13.5. Branding of subjects affected with genetic syndromes of severe short stature in developing countries

J Guevara-Aguirre , C Guevara , A Guevara , AA Gavilanes

To read the full abstract: BMJ Case Rep 2020;13:e231737. doi: 10.1136/bcr-2019-231737• The authors report 2 cases of severe short stature, Laron Syndrome and Cornelia-Delange-like syndrome, followed in Ecuador, a country with limited resources.• They highlight the tendency of a society to discuss children with severe short stature with derogatory terms to automatically assume tha...

ey0017.14-6 | (1) | ESPEYB17

14.6. How frequently are articles in predatory open access journals cited

B-C Bjork , S Kanto-Karvonen , JT Harviainen

To read the full abstract: Publications 2020;8:17Predatory journals, sometimes called write-only publishing or deceptive publishing, follow an exploitive academic publishing business model that involves charging publication fees to authors without checking articles for quality and legitimacy and without providing the other editorial and publishing services that legitimate academic journals provide, whether open access or not. Their numbers keep ...

ey0016.8-12 | New Genes | ESPEYB16

8.12. Targeted next-generation sequencing detects rare genetic events in pheochromocytoma and paraganglioma

L Ben Aim , P Pigny , LJ Castro-Vega , A Buffet , L Amar , J Bertherat , D Drui , I Guilhem , E Baudin , C Lussey-Lepoutre , C Corsini , G Chabrier , C Briet , L Faivre , C Cardot-Bauters , J Favier , AP Gimenez-Roqueplo , N Burnichon

To read the full abstract: J Med Genet. 2019 Mar 15. pii: jmedgenet-2018-105714. [Epub ahead of print].Paragangliomas and pheochromocytomas (PPGL) are rare neuroendocrine tumours that can arise either from the adrenal medulla (pheochromocytomas, PCC) or from extra-adrenal paraganglia (paragangliomas, PGL). PPGLs are considered to be the most heritable of human tumours with at least...

ey0016.11-7 | Tracking, Programming, and Epigenetics | ESPEYB16

11.7. Transgenerational epigenetic mechanisms in adipose tissue development

S Lecoutre , P Petrus , M Ryden , C Breton

To read the full abstract: Trends Endocrinol Metab. 2018; 29(10):675–685This paper comprehensively reviews current knowledge on epigenetic mechanisms in adipose tissue that may account for transgenerational dysregulation of adipocyte formation and adipose tissue function.There is increasing evidence that adult-onset disorders, including obesity, may derive fro...

ey0016.12-8 | Metabolic Syndrome | ESPEYB16

12.8. Carbotoxicity-noxious effects of carbohydrates

G Kroemer , C Lopez-Otin , F Madeo , R de Cabo

Cell 2018;175:605–614.DOI: 10.1016/j.cell.2018.07.044.http://www.ncbi.nlm.nih.gov/pubmed/30340032Summary: Epidemiological, clinical intervention trials and experimental evidence indicate the negative impact of excessive carbohydrate uptake. This review details the history of carbohydrate consumption and mechanisms of ca...

ey0015.1-11 | Reviews | ESPEYB15

1.11 Central hypothyroidism - a neglected thyroid disorder

P Beck-Peccoz , G Rodari , C Giavoli , A Lania

To read the full abstract: Nat Rev Endocrinol 2017;13:588-598Central hypothyroidism has received much interest in recent years, partly due to the discovery of new causal gene mutations. This is a comprehensive review on several aspects of central hypothyroidism. It discusses prevalence, and its variation between different countries; pitfalls in diagnosis, including assay interference; concurrent...

ey0015.3-8 | Congenital hypothyroidism | ESPEYB15

3.8 Are lower TSH cutoffs in neonatal screening for congenital hypothyroidism warranted?

S Lain , C Trumpff , SD Grosse , A Olivieri , G Van Vliet

To read the full abstract: Eur J Endocrinol 2017;177:D1-D12Newborn screening (NBS) is an invaluable tool for identification of CH; however almost 70% of newborns worldwide do not benefit from NBS at all. In countries with NBS, lowering of TSH cut-offs over the years led to major controversy on the optimal TSH screening cut-off. In this very interesting debate paper, arguments are presented f...

ey0015.6-9 | New hope | ESPEYB15

6.9 Fertility Preservation for Transgender Adolescents

D Chen , L Simons , EK Johnson , BA Lockart , C Finlayson

To read the full abstract: J Adolesc Health. 2017 Jul;61(1):120-123Recent developments in assisted reproduction technologies (ART) have changed the scene for fertility wishes in a number of disorders, including GD. Fertility preservation is now routinely offered to postpubertal adolescent and adult GD patients at increasing numbers of medical centers. For biological boys, this is a non...

ey0015.6-17 | Psychological aspects | ESPEYB15

6.17 Methodological Issues for Psychological Evaluation across the Lifespan of Individuals with a Difference/Disorder of Sex Development

F D'Alberton , S Vissani , C Ferracuti , V Pasterski

To read the full abstract: Sex Dev. 2018;12(1-3):123-134There is a paucity of psychological follow-up studies in DSD patients. This is especially problematic since differences in sex development often affect the individual in fundamental ways that are related to their self-perception and social experiences. In this paper, the authors explain, in an illustrative way, the different strategies that can ...

ey0015.12-2 | New Paradigm | ESPEYB15

12.2 Childhood BMI and Adult Type 2 Diabetes, Coronary Artery Diseases, Chronic Kidney Disease, and Cardiometabolic Traits: A Mendelian Randomization Analysis

T Geng , CE Smith , C Li , T Huang

To read the full abstract: Diabetes Care 2018;41:1089-1096These findings show that a 1-SD increase in childhood BMI was associated with a 47–83% increased relative risk of T2DM and a 28% increased relative risk of CAD in adult life, yet childhood BMI was not associated with adult chronic kidney disease. This is the first study to examine the causal relationship between childhood BMI and cardio-...