Volume 71, Issue 3

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Volume 71, Issue 3

March 2021

Special Issue: Rare Endocrine Disease

Issue Editors:

ALBERTO M. PEREIRA,
Olaf Hiort

25 articles in this issue

Rare endocrine disease: Still a long and a winding road
Sebastiano Filetti
Editorial 23 February 2021 Pages: 535 - 536
Introduction to Endo-ERN–scope and mission
Alberto M. Pereira
Olaf Hiort
Viewpoint Open access 15 January 2021 Pages: 537 - 538
Perspectives of the European Society of Endocrinology (ESE) and the European Society of Paediatric Endocrinology (ESPE) on rare endocrine disease
Martin Reincke
Anita Hokken-Koelega
Review Open access 19 March 2021 Pages: 539 - 541
Access to patient oriented information—a baseline Endo-ERN survey among patients with rare endocrine disorders
Violeta Iotova
Camilla Schalin-Jäntti
Olaf Hiort
Original Article Open access 18 February 2021 Pages: 542 - 548
CPMS–improving patient care in Europe via virtual case discussions
Isabel Mönig
Danielle Steenvoorden
Alberto M. Pereira
Review Open access 02 February 2021 Pages: 549 - 554
Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model
S. R. Ali
J. Bryce
S. F. Ahmed
Review Open access 29 January 2021 Pages: 555 - 560
Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research
Johan P. de Graaf
Friso de Vries
on behalf of Research and Science Work Package of Endo-ERN
Original Article Open access 03 February 2021 Pages: 561 - 568
EndoERN patient survey on their perception of health care experience and of unmet needs for rare endocrine diseases
Susan M. Webb
Jette Kristensen
Anna Nordenström
Original Article 05 February 2021 Pages: 569 - 577
Serum insulin-like factor 3 quantification by LC–MS/MS in male patients with hypogonadotropic hypogonadism and Klinefelter syndrome
Trine Holm Johannsen
Marie Lindhardt Ljubicic
Anders Juul
Original Article 22 January 2021 Pages: 578 - 585
Therapy options for adrenal insufficiency and recommendations for the management of adrenal crisis
Hanna Nowotny
S. Faisal Ahmed
On Behalf of Endo ERN (MTG1)
Mini Review Open access 04 March 2021 Pages: 586 - 594
Update on primary bilateral macronodular adrenal hyperplasia (PBMAH)
Lucas Bouys
Iacopo Chiodini
Jérôme Bertherat
Review 15 February 2021 Pages: 595 - 603
Hypercalcemia during pregnancy: management and outcomes for mother and child
Natasha M. Appelman-Dijkstra
Diana- Alexandra Ertl
Elizabeth M. Winter
Clinical Management of Endocrine Diseases Open access 05 February 2021 Pages: 604 - 610
Rare diseases caused by abnormal calcium sensing and signalling
Judit Tőke
Gábor Czirják
Miklós Tóth
Review Open access 02 February 2021 Pages: 611 - 617
Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity
Francesca Dassie
Francesca Favaretto
Pietro Maffei
Review 10 February 2021 Pages: 618 - 625
Collaboration for rare diabetes: understanding new treatment options for Wolfram syndrome
Felix Reschke
Julia Rohayem
Thomas Danne
Mini Review 01 February 2021 Pages: 626 - 633
Patients’ perception on the quality of care for multiple endocrine neoplasia disorders in Europe: an online survey from a patient support group
Karl Philipp Drewitz
Jo Grey
Ludwig Schaaf
Original Article 03 February 2021 Pages: 634 - 640
Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes
Henriett Butz
Jo Blair
Attila Patócs
Mini Review Open access 11 February 2021 Pages: 641 - 652
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
Cornelis Jan De Groot
Christine Poitou Bernert
E. L. T. Van Den Akker
Review Open access 29 January 2021 Pages: 653 - 662
The clinical aspects of pituitary tumour genetics
Judit Dénes
Márta Korbonits
Review Open access 04 February 2021 Pages: 663 - 674
Assessing the health-related management of people with differences of sex development
Martina Jürgensen
Marion Rapp
Olaf Hiort
Mini Review Open access 30 January 2021 Pages: 675 - 680
ENDO-ERN expert opinion on the differential diagnosis of pubertal delay
Luca Persani
Marco Bonomi
Anders Juul
Clinical Management of Endocrine Diseases Open access 29 January 2021 Pages: 681 - 688
Monocarboxylate transporter 8 deficiency: update on clinical characteristics and treatment
Ferdy S. van Geest
Stefan Groeneweg
W. Edward Visser
Review Open access 01 March 2021 Pages: 689 - 695
New genetics in congenital hypothyroidism
Athanasia Stoupa
Dulanjalee Kariyawasam
Aurore Carré
Review 01 March 2021 Pages: 696 - 705
Patient’s view on better care
Jette Kristensen
Manuela Brösamle
Bas van den Berg
Letter to the Editor Open access 24 February 2021 Pages: 706 - 707
Correction to: Patient’s view on better care
Jette Kristensen
Manuela Brösamle
Bas van den Berg
Correction 17 March 2021 Pages: 708 - 708

Volume 71, Issue 3

Rare endocrine disease: Still a long and a winding road

Introduction to Endo-ERN–scope and mission

Perspectives of the European Society of Endocrinology (ESE) and the European Society of Paediatric Endocrinology (ESPE) on rare endocrine disease

Access to patient oriented information—a baseline Endo-ERN survey among patients with rare endocrine disorders

CPMS–improving patient care in Europe via virtual case discussions

Supporting international networks through platforms for standardised data collection—the European Registries for Rare Endocrine Conditions (EuRRECa) model

Patients with rare endocrine conditions have corresponding views on unmet needs in clinical research

EndoERN patient survey on their perception of health care experience and of unmet needs for rare endocrine diseases

Serum insulin-like factor 3 quantification by LC–MS/MS in male patients with hypogonadotropic hypogonadism and Klinefelter syndrome

Therapy options for adrenal insufficiency and recommendations for the management of adrenal crisis

Update on primary bilateral macronodular adrenal hyperplasia (PBMAH)

Hypercalcemia during pregnancy: management and outcomes for mother and child

Rare diseases caused by abnormal calcium sensing and signalling

Alström syndrome: an ultra-rare monogenic disorder as a model for insulin resistance, type 2 diabetes mellitus and obesity

Collaboration for rare diabetes: understanding new treatment options for Wolfram syndrome

Patients’ perception on the quality of care for multiple endocrine neoplasia disorders in Europe: an online survey from a patient support group

Molecular genetic testing strategies used in diagnostic flow for hereditary endocrine tumour syndromes

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

The clinical aspects of pituitary tumour genetics

Assessing the health-related management of people with differences of sex development

ENDO-ERN expert opinion on the differential diagnosis of pubertal delay

Monocarboxylate transporter 8 deficiency: update on clinical characteristics and treatment

New genetics in congenital hypothyroidism

Patient’s view on better care

Correction to: Patient’s view on better care

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