Filter

Refine by collections

Refine by date

—
  • Print
  • Save

Search Results

You are looking at 11 - 20 of 60 items for :

  • "Cushing’s disease" x
Clear All
Kush Dev Singh Jarial Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Kush Dev Singh Jarial in
Google Scholar
PubMed Close
,
Anil Bhansali Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Anil Bhansali in
Google Scholar
PubMed Close
,
Vivek Gupta Department of Radio-diagnosis, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Vivek Gupta in
Google Scholar
PubMed Close
,
Paramjeet Singh Department of Radio-diagnosis, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Paramjeet Singh in
Google Scholar
PubMed Close
,
Kanchan K Mukherjee Department of Neurosurgery, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Kanchan K Mukherjee in
Google Scholar
PubMed Close
,
Akhilesh Sharma Department of Psychiatry, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Akhilesh Sharma in
Google Scholar
PubMed Close
,
Rakesh K Vashishtha Department of Histopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Rakesh K Vashishtha in
Google Scholar
PubMed Close
,
Suja P Sukumar Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Suja P Sukumar in
Google Scholar
PubMed Close
,
Naresh Sachdeva Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Naresh Sachdeva in
Google Scholar
PubMed Close
, and
Rama Walia Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, India

Search for other papers by Rama Walia in
Google Scholar
PubMed Close

% diagnostic accuracy ( 1 ). Cushing’s disease (CD) accounts for about 90–95% of the cases when there is no obvious source of ACTH hypersecretion, and this distinction is essential to decide further therapeutic strategies ( 2 , 3 , 4 , 5 ). Sellar imaging

Article Type:
Research Article
DOI:
https://doi.org/10.1530/EC-18-0046
Volume/Issue:
Volume 7: Issue 3
Open access
Amir H Zamanipoor Najafabadi Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands
Department of Medicine, Division of Endocrinology and Centre for Endocrine Tumors, Leiden University Medical Centre, Leiden, The Netherlands
Department of Neurosurgery, University Neurosurgical Centre Holland (UNCH), Leiden University Medical Centre, Haaglanden Medical Centre and Haga Teaching Hospitals, Leiden and The Hague, The Netherlands

Search for other papers by Amir H Zamanipoor Najafabadi in
Google Scholar
PubMed Close
,
Merel van der Meulen Department of Medicine, Division of Endocrinology and Centre for Endocrine Tumors, Leiden University Medical Centre, Leiden, The Netherlands

Search for other papers by Merel van der Meulen in
Google Scholar
PubMed Close
,
Ana Luisa Priego Zurita Department of Medicine, Division of Endocrinology and Centre for Endocrine Tumors, Leiden University Medical Centre, Leiden, The Netherlands

Search for other papers by Ana Luisa Priego Zurita in
Google Scholar
PubMed Close
,
S Faisal Ahmed Chair of Work Package of E-Health & ICT of Endo-ERN, Developmental Endocrinology Research Group, School of Medicine, Dentistry & Nursing, University of Glasgow and Office for Rare Conditions, Royal Hospital for Children & Queen Elizabeth University Hospital, Glasgow, UK

Search for other papers by S Faisal Ahmed in
Google Scholar
PubMed Close
,
Wouter R van Furth Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands

Search for other papers by Wouter R van Furth in
Google Scholar
PubMed Close
,
Evangelia Charmandari Pediatric Chair Main Thematic Group 6 Pituitary of Endo-ERN, Division of Endocrinology, Metabolism and Diabetes, First Department of Pediatrics, National and Kapodistrian University of Athens Medical School, ‘Aghia Sophia’ Children’s Hospital, Athens, Greece

Search for other papers by Evangelia Charmandari in
Google Scholar
PubMed Close
,
Olaf Hiort Pediatric Chair and Deputy Coordinator of Endo-ERN, Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics and Adolescent Medicine, University of Lübeck, Lübeck, Germany

Search for other papers by Olaf Hiort in
Google Scholar
PubMed Close
,
Alberto M Pereira Adult Chair and Coordinator of Endo-ERN, Department of Endocrinology and Metabolism, Amsterdam University Medical Center, Amsterdam, The Netherlands

Search for other papers by Alberto M Pereira in
Google Scholar
PubMed Close
,
Mehul Dattani London Centre for Pediatric Endocrinology and Diabetes at Great Ormond Street Children's Hospital and University College London Hospitals, London, UK

Search for other papers by Mehul Dattani in
Google Scholar
PubMed Close
,
Diana Vitali SOD ITALIA (Italian Organization for Septo Optic Dysplasia and other Neuroendocrine Disorders), European Patient Advocacy Group, Rome, Italy

Search for other papers by Diana Vitali in
Google Scholar
PubMed Close
,
Johan P de Graaf Dutch Pituitary Foundation, European Patient Advocacy Group, Nijkerk, The Netherlands

Search for other papers by Johan P de Graaf in
Google Scholar
PubMed Close
, and
Nienke R Biermasz Adult Chair Main Thematic Group 6 Pituitary of Endo-ERN, Department of Medicine, Division of Endocrinology and Centre for Endocrine Tumors, Leiden University Medical Centre, Leiden, The Netherlands

Search for other papers by Nienke R Biermasz in
Google Scholar
PubMed Close

. Pituitary adenomas comprise non-hormone-producing adenomas and adenomas producing an excess of growth hormone (acromegaly), adrenocorticotropic hormone (Cushing’s disease), prolactin (prolactinoma), thyrotropin hormone (TSH-producing adenoma), and

Article Type:
Review Article
Collections:
Pituitary and Hypothalamus
DOI:
https://doi.org/10.1530/EC-22-0349
Volume/Issue:
Volume 12: Issue 1
Open access
Nidan Qiao Department of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China
Neuroendocrine Unit, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA

Search for other papers by Nidan Qiao in
Google Scholar
PubMed Close

pituitary neoplasms, acromegaly, Cushing’s disease, craniopharyngioma and growth hormone deficiency. More than half of the studies were published in the recent 2 years. Table 2 Summary of studies on sellar region disease using machine learning methods

Article Type:
Research Article
DOI:
https://doi.org/10.1530/EC-19-0156
Volume/Issue:
Volume 8: Issue 7
Open access
Ida Staby Department of Medical Endocrinology and Metabolism, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Search for other papers by Ida Staby in
Google Scholar
PubMed Close
,
Jesper Krogh Department of Medical Endocrinology and Metabolism, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Search for other papers by Jesper Krogh in
Google Scholar
PubMed Close
,
Marianne Klose Department of Medical Endocrinology and Metabolism, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Search for other papers by Marianne Klose in
Google Scholar
PubMed Close
,
Jonas Baekdal Department of Medical Endocrinology and Metabolism, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Search for other papers by Jonas Baekdal in
Google Scholar
PubMed Close
,
Ulla Feldt-Rasmussen Department of Medical Endocrinology and Metabolism, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Department of Clinical Medicine, Faculty of Health and Clinical Sciences, Copenhagen University, Copenhagen, Denmark

Search for other papers by Ulla Feldt-Rasmussen in
Google Scholar
PubMed Close
,
Lars Poulsgaard Department of Neurosurgery, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Search for other papers by Lars Poulsgaard in
Google Scholar
PubMed Close
,
Jacob Bertram Springborg Department of Neurosurgery, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark

Search for other papers by Jacob Bertram Springborg in
Google Scholar
PubMed Close
, and
Mikkel Andreassen Department of Medical Endocrinology and Metabolism, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Department of Clinical Medicine, Faculty of Health and Clinical Sciences, Copenhagen University, Copenhagen, Denmark

Search for other papers by Mikkel Andreassen in
Google Scholar
PubMed Close

/oligomenorrhoea for premenopausal women. A diagnosis of Cushing’s disease or acromegaly was established according to the standard criteria. We did not report on GH deficiency or anti-diuretic hormone insufficiency because only a few patients were examined with GH

Article Type:
Research Article
DOI:
https://doi.org/10.1530/EC-21-0155
Volume/Issue:
Volume 10: Issue 7
Open access
Rachel Forfar Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Rachel Forfar in
Google Scholar
PubMed Close
,
Mashal Hussain Centre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, UK

Search for other papers by Mashal Hussain in
Google Scholar
PubMed Close
,
Puneet Khurana Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Puneet Khurana in
Google Scholar
PubMed Close
,
Jennifer Cook Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Jennifer Cook in
Google Scholar
PubMed Close
,
Steve Lewis Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Steve Lewis in
Google Scholar
PubMed Close
,
Dillon Popat Centre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, UK

Search for other papers by Dillon Popat in
Google Scholar
PubMed Close
,
David Jackson Centre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, UK

Search for other papers by David Jackson in
Google Scholar
PubMed Close
,
Ed McIver Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Ed McIver in
Google Scholar
PubMed Close
,
Jeff Jerman Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Jeff Jerman in
Google Scholar
PubMed Close
,
Debra Taylor Centre for Therapeutics Discovery, LifeArc, Accelerator Building, Open Innovation Campus, Stevenage, UK

Search for other papers by Debra Taylor in
Google Scholar
PubMed Close
,
Adrian JL Clark Centre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, UK

Search for other papers by Adrian JL Clark in
Google Scholar
PubMed Close
, and
Li F Chan Centre for Endocrinology, William Harvey Research Institute, Queen Mary University of London, London, UK

Search for other papers by Li F Chan in
Google Scholar
PubMed Close

excess ( 6 ). Conditions include Cushing’s disease where pituitary adenoma removal is unsuccessful, ectopic ACTH syndrome from tumours such as small cell lung cancers, and congenital adrenal hyperplasia (CAH) where ACTH drives excess androgen production

Article Type:
Research Article
Collections:
Adrenal
DOI:
https://doi.org/10.1530/EC-22-0338
Volume/Issue:
Volume 11: Issue 12
Open access
Solène Castellnou Service d’Endocrinologie, Centre de Référence des Maladies Rares de l’Hypophyse HYPO, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France
Université Lyon 1, Villeurbanne, France

Search for other papers by Solène Castellnou in
Google Scholar
PubMed Close
,
Alexandre Vasiljevic Université Lyon 1, Villeurbanne, France
Centre de Biologie et Pathologie Est, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France
INSERM U1052, CNRS, UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France

Search for other papers by Alexandre Vasiljevic in
Google Scholar
PubMed Close
,
Véronique Lapras Service de Radiologie, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre-Bénite, France

Search for other papers by Véronique Lapras in
Google Scholar
PubMed Close
,
Véronique Raverot Laboratoire d’Hormonologie, Centre de Biologie et Pathologie Est, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France

Search for other papers by Véronique Raverot in
Google Scholar
PubMed Close
,
Eudeline Alix Département de Cytogénétique, Centre de Biologie et Pathologie Est, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France

Search for other papers by Eudeline Alix in
Google Scholar
PubMed Close
,
Françoise Borson-Chazot Service d’Endocrinologie, Centre de Référence des Maladies Rares de l’Hypophyse HYPO, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France
Université Lyon 1, Villeurbanne, France

Search for other papers by Françoise Borson-Chazot in
Google Scholar
PubMed Close
,
Emmanuel Jouanneau Université Lyon 1, Villeurbanne, France
INSERM U1052, CNRS, UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France
Service de Neurochirurgie, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France

Search for other papers by Emmanuel Jouanneau in
Google Scholar
PubMed Close
,
Gérald Raverot Service d’Endocrinologie, Centre de Référence des Maladies Rares de l’Hypophyse HYPO, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France
Université Lyon 1, Villeurbanne, France
INSERM U1052, CNRS, UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France

Search for other papers by Gérald Raverot in
Google Scholar
PubMed Close
, and
Hélène Lasolle Service d’Endocrinologie, Centre de Référence des Maladies Rares de l’Hypophyse HYPO, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France
Université Lyon 1, Villeurbanne, France
INSERM U1052, CNRS, UMR5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France

Search for other papers by Hélène Lasolle in
Google Scholar
PubMed Close

Introduction Cushing’s disease is a rare disorder defined as chronic hypercortisolism due to a corticotropin-secreting pituitary tumor (corticotroph tumor) ( 1 ). Chronic cortisol excess is responsible for multisystem morbidity, contributing

Article Type:
Research Article
DOI:
https://doi.org/10.1530/EC-20-0035
Volume/Issue:
Volume 9: Issue 3
Open access
Ramjan Sanas Mohamed Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Ramjan Sanas Mohamed in
Google Scholar
PubMed Close
,
Biyaser Abuelgasim Imperial College School of Medicine, Department of Biochemistry, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Biyaser Abuelgasim in
Google Scholar
PubMed Close
,
Sally Barker Imperial College School of Medicine, Department of Biochemistry, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Sally Barker in
Google Scholar
PubMed Close
,
Hemanth Prabhudev Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Hemanth Prabhudev in
Google Scholar
PubMed Close
,
Niamh M Martin Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK

Search for other papers by Niamh M Martin in
Google Scholar
PubMed Close
,
Karim Meeran Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK

Search for other papers by Karim Meeran in
Google Scholar
PubMed Close
,
Emma L Williams Department of Biochemistry, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Emma L Williams in
Google Scholar
PubMed Close
,
Sarah Darch Department of Biochemistry, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Sarah Darch in
Google Scholar
PubMed Close
,
Whitlock Matthew Department of Biochemistry, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Whitlock Matthew in
Google Scholar
PubMed Close
,
Tricia Tan Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK
Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK

Search for other papers by Tricia Tan in
Google Scholar
PubMed Close
, and
Florian Wernig Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK

Search for other papers by Florian Wernig in
Google Scholar
PubMed Close

suspected to have cyclical CS, subclinical CS, pseudo-CS due to disrupted circadian rhythm or patients who were known non-compliant with the collection protocol were excluded from the study. The diagnosis of pituitary Cushing’s disease (CD) was confirmed by

Article Type:
Research Article
Collections:
Adrenal
DOI:
https://doi.org/10.1530/EC-22-0050
Volume/Issue:
Volume 11: Issue 7
Open access
Benedetta Zampetti Department of Endocrinology, Ospedale Niguarda, Milano, Italy

Search for other papers by Benedetta Zampetti in
Google Scholar
PubMed Close
,
Erika Grossrubatscher Department of Endocrinology, Ospedale Niguarda, Milano, Italy

Search for other papers by Erika Grossrubatscher in
Google Scholar
PubMed Close
,
Paolo Dalino Ciaramella Department of Endocrinology, Ospedale Niguarda, Milano, Italy

Search for other papers by Paolo Dalino Ciaramella in
Google Scholar
PubMed Close
,
Edoardo Boccardi Department of Neuroradiology, Ospedale Niguarda, Milano, Italy

Search for other papers by Edoardo Boccardi in
Google Scholar
PubMed Close
, and
Paola Loli Department of Endocrinology, Ospedale Niguarda, Milano, Italy

Search for other papers by Paola Loli in
Google Scholar
PubMed Close

use of more stringent criteria to define responsiveness to the diagnostic tests increases the ability to differentiate Cushing’s disease (CD) from EAS, but invariably leads to reduced diagnostic sensitivity ( 12 ). On the other hand, dynamic gadolinium

Article Type:
Review Article
DOI:
https://doi.org/10.1530/EC-16-0029
Volume/Issue:
Volume 5: Issue 4
Open access
Elena Valassi Endocrinology Department, Germans Trias i Pujol Hospital and Research Institute, Badalona, Barcelona, Spain
IRCCS, Istituto Auxologico Italiano, Milan, Italy
Department of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy

Search for other papers by Elena Valassi in
Google Scholar
PubMed Close
,
Iacopo Chiodini IRCCS, Istituto Auxologico Italiano, Milan, Italy
Department of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy

Search for other papers by Iacopo Chiodini in
Google Scholar
PubMed Close
,
Richard A Feelders Division of Endocrinology, Erasmus Medical Centre, Rotterdam, Netherlands

Search for other papers by Richard A Feelders in
Google Scholar
PubMed Close
,
Cornelie D Andela Division of Endocrinology and Centre for Endocrine Tumours, Leiden University Medical Centre, Leiden, Netherlands

Search for other papers by Cornelie D Andela in
Google Scholar
PubMed Close
,
Margueritta Abou-Hanna HRA Pharma Rare Diseases, Châtillon, France

Search for other papers by Margueritta Abou-Hanna in
Google Scholar
PubMed Close
,
Sarah Idres HRA Pharma Rare Diseases, Châtillon, France

Search for other papers by Sarah Idres in
Google Scholar
PubMed Close
, and
Antoine Tabarin Department of Endocrinology and INSERM U862 University and CHU of Bordeaux, Pessac, France

Search for other papers by Antoine Tabarin in
Google Scholar
PubMed Close

386 913 – 927 . ( https://doi.org/10.1016/S0140-6736(1461375-1 ) 4 Pivonello R De Martino MC De Leo M Simeoli C Colao A . Cushing’s disease: the burden of illness . Endocrine 2017 56 10 – 18 . ( https://doi.org/10.1007/s12020

Article Type:
Research Article
Collections:
Adrenal
DOI:
https://doi.org/10.1530/EC-22-0027
Volume/Issue:
Volume 11: Issue 7
Open access
Paula Bruna Araujo Department of Internal Medicine and Endocrine Unit, Medical School and Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil
Diagnósticos da América SA, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Paula Bruna Araujo in
Google Scholar
PubMed Close
,
Leandro Kasuki Department of Internal Medicine and Endocrine Unit, Medical School and Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil
Neuroendocrinology Unit, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil
Endocrinology Unit, Hospital Federal de Bonsucesso, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Leandro Kasuki in
Google Scholar
PubMed Close
,
Carlos Henrique de Azeredo Lima Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Carlos Henrique de Azeredo Lima in
Google Scholar
PubMed Close
,
Liana Ogino Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Liana Ogino in
Google Scholar
PubMed Close
,
Aline H S Camacho Neuropathology Laboratory Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil
National Cancer Institute, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Aline H S Camacho in
Google Scholar
PubMed Close
,
Leila Chimelli Neuropathology Laboratory Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Leila Chimelli in
Google Scholar
PubMed Close
,
Márta Korbonits Centre for Endocrinology, William Harvey Research Institute, Barts and The London School of Medicine, Queen Mary University of London, Charterhouse Square, London, UK

Search for other papers by Márta Korbonits in
Google Scholar
PubMed Close
, and
Monica R Gadelha Department of Internal Medicine and Endocrine Unit, Medical School and Hospital Universitário Clementino Fraga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil
Molecular Genetics Laboratory, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil
Neuroendocrinology Unit, Instituto Estadual do Cérebro Paulo Niemeyer, Rio de Janeiro, Rio de Janeiro, Brazil

Search for other papers by Monica R Gadelha in
Google Scholar
PubMed Close

with micro or macroadenomas diagnosed until 18 years of age were included. Of these patients, 74 (56%) had acromegaly or gigantism, 38 (28.8%) had prolactinoma, 10 (7.6%) had non-functioning pituitary adenoma (NFPA) and 10 (7.6%) had Cushing’s disease

Article Type:
Research Article
DOI:
https://doi.org/10.1530/EC-17-0237
Volume/Issue:
Volume 6: Issue 8
Open access