| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Access to patient oriented information—a baseline Endo-ERN survey among patients with rare endocrine disorders
|
Iotova, Violeta
|
|
|
71 |
3 |
p. 542-548
|
artikel
|
| 2 |
Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity
|
Dassie, Francesca
|
|
|
71 |
3 |
p. 618-625
|
artikel
|
| 3 |
Assessing the health-related management of people with differences of sex development
|
Jürgensen, Martina
|
|
|
71 |
3 |
p. 675-680
|
artikel
|
| 4 |
Clinical management of patients with genetic obesity during COVID-19 pandemic: position paper of the ESE Growth & Genetic Obesity COVID-19 Study Group and Rare Endo-ERN main thematic group on Growth and Obesity
|
De Groot, Cornelis Jan
|
|
|
71 |
3 |
p. 653-662
|
artikel
|
| 5 |
Collaboration for rare diabetes: understanding new treatment options for Wolfram syndrome
|
Reschke, Felix
|
|
|
71 |
3 |
p. 626-633
|
artikel
|
| 6 |
Correction to: Patient’s view on better care
|
Kristensen, Jette
|
|
|
71 |
3 |
p. 708
|
artikel
|
| 7 |
CPMS–improving patient care in Europe via virtual case discussions
|
Mönig, Isabel
|
|
|
71 |
3 |
p. 549-554
|
artikel
|
| 8 |
ENDO-ERN expert opinion on the differential diagnosis of pubertal delay
|
Persani, Luca
|
|
|
71 |
3 |
p. 681-688
|
artikel
|
| 9 |
EndoERN patient survey on their perception of health care experience and of unmet needs for rare endocrine diseases
|
Webb, Susan M.
|
|
|
71 |
3 |
p. 569-577
|
artikel
|
| 10 |
Hypercalcemia during pregnancy: management and outcomes for mother and child
|
Appelman-Dijkstra, Natasha M.
|
|
|
71 |
3 |
p. 604-610
|
artikel
|
| 11 |
Introduction to Endo-ERN–scope and mission
|
Pereira, Alberto M.
|
|
|
71 |
3 |
p. 537-538
|
artikel
|
| 12 |
Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes
|
Butz, Henriett
|
|
|
71 |
3 |
p. 641-652
|
artikel
|
| 13 |
Monocarboxylate transporter 8 deficiency: update on clinical characteristics and treatment
|
van Geest, Ferdy S.
|
|
|
71 |
3 |
p. 689-695
|
artikel
|
| 14 |
New genetics in congenital hypothyroidism
|
Stoupa, Athanasia
|
|
|
71 |
3 |
p. 696-705
|
artikel
|
| 15 |
Patients’ perception on the quality of care for multiple endocrine neoplasia disorders in Europe: an online survey from a patient support group
|
Drewitz, Karl Philipp
|
|
|
71 |
3 |
p. 634-640
|
artikel
|
| 16 |
Patient’s view on better care
|
Kristensen, Jette
|
|
|
71 |
3 |
p. 706-707
|
artikel
|
| 17 |
Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research
|
de Graaf, Johan P.
|
|
|
71 |
3 |
p. 561-568
|
artikel
|
| 18 |
Perspectives of the European Society of Endocrinology (ESE) and the European Society of Paediatric Endocrinology (ESPE) on rare endocrine disease
|
Reincke, Martin
|
|
|
71 |
3 |
p. 539-541
|
artikel
|
| 19 |
Rare diseases caused by abnormal calcium sensing and signalling
|
Tőke, Judit
|
|
|
71 |
3 |
p. 611-617
|
artikel
|
| 20 |
Rare endocrine disease: Still a long and a winding road
|
Filetti, Sebastiano
|
|
|
71 |
3 |
p. 535-536
|
artikel
|
| 21 |
Serum insulin-like factor 3 quantification by LC–MS/MS in male patients with hypogonadotropic hypogonadism and Klinefelter syndrome
|
Johannsen, Trine Holm
|
|
|
71 |
3 |
p. 578-585
|
artikel
|
| 22 |
Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model
|
Ali, S. R.
|
|
|
71 |
3 |
p. 555-560
|
artikel
|
| 23 |
The clinical aspects of pituitary tumour genetics
|
Dénes, Judit
|
|
|
71 |
3 |
p. 663-674
|
artikel
|
| 24 |
Therapy options for adrenal insufficiency and recommendations for the management of adrenal crisis
|
Nowotny, Hanna
|
|
|
71 |
3 |
p. 586-594
|
artikel
|
| 25 |
Update on primary bilateral macronodular adrenal hyperplasia (PBMAH)
|
Bouys, Lucas
|
|
|
71 |
3 |
p. 595-603
|
artikel
|
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