Endo-ERN Publications Database
940 publication(s) found matching the search criteria
How to design a registry for undiagnosed patients in the framework of rare disease diagnosis: suggestions on software, data set and coding system
Author(s):
Berger A, Rustemeier A, Göbel J, Kadioglu D, Britz V, Schubert K, Mohnike K, Storf H, Wagner TOF
Affiliated Institution / ERN:
São João University Hospital(CHUSJ) ;
Condition / Disease:
Rare endocrine conditions
Publication:
Orphanet Journal of Rare Diseases v16.1
Year:
2021
ORPHAcode / other:
ORPHA97978
Technical aspects of paediatric robotic pancreatic enucleation based on a case of an insulinoma
Author(s):
Schulte am Esch J, Krüger M, Barthlen W, Förster C, Mohnike K, Empting S, Benhidjeb T, Vossschulte H
Affiliated Institution / ERN:
Universitätsklinikum Magdeburg ;
Condition / Disease:
Insulinoma
Publication:
The International Journal of Medical Robotics and Computer Assisted Surgery v17.6
Year:
2021
ORPHAcode / other:
ORPHA97279
DOI:
10.1002/rcs.2317
Keywords:
abdominal,augmented reality,computer-assisted surgery,digestive system,gastrointestinal,general surgery,hepato-pancreato-biliary,imaged guided surgery,insulinoma,minimal invasive surgery,paediatric surgery,pancreas,pancreatectomy,pancreatic,preoperative planning,resection,robotic visceral surgery,ultrasound
Patients’ priorities and expectations on an EU registry for rare bone and mineral conditions
Author(s):
Javaid MK, Mordenti M, Boarini M, Sangiorgi L, Westerheim I, Alves I, Skarberg RT, Appelman-Dijkstra NM, Grasemann C
Affiliated Institution / ERN:
Leiden University Medical Center ; Katholisches Klinikum Bochum ;
Condition / Disease:
Rare mineral conditions
Publication:
Orphanet Journal of Rare Diseases v16.1
Year:
2021
ORPHAcode / other:
ORPHA68415
DOI:
10.1186/s13023-021-02069-9
Keywords:
Natural History,Osteogenesis imperfecta,Rare bone and mineral conditions,Rare disease registries,Survey
Hypoparathyroidism and pseudohypoparathyroidism in pregnancy: an Italian retrospective observational study
Author(s):
Marcucci G, Altieri P, Benvenga S, Bondanelli M, Camozzi V, Cetani F, Cianferotti L, Duradoni M, Fossi C, degli Uberti E, Famà F, Mantovani G, Marcocci C, Masi L, Pagotto U, Palermo A, Parri S, Ruggeri RM, Zatelli MC, Brandi ML
Affiliated Institution / ERN:
University Hospital Florence ; AOU polyclinic "G.Martino" of Messina ; AOU - Ferrara ; University Hospital of Padova ; AOU Pisan ; Foundation IRCCS CA'Granda Ospedale Maggiore polyclinic - Milan ;
Condition / Disease:
Hypoparathyroidism and pseudohypoparathyroidism
Publication:
Orphanet Journal of Rare Diseases v16.1
Year:
2021
ORPHAcode / other:
ORPHA181405, ORPHA97593
DOI:
10.1186/s13023-021-02053-3
Keywords:
Breastfeeding,Calcitriol,Calcium carbonate,Hypocalcemia,Hypoparathyroidism,Miscarriages,Pregnancy,Preterm birth,Pseudohypoparathyroidism,Treatment
Loss of KDM1A in GIP-dependent primary bilateral macronodular adrenal hyperplasia with Cushing’s syndrome: a multicentre, retrospective, cohort study
Author(s):
Chasseloup F, Bourdeau I, Tabarin A, Regazzo D, Dumontet C, Ladurelle N, Tosca L, Amazit L, Proust A, Scharfmann R, Mignot T, Fiore F, Tsagarakis S, Vassiliadi D, Maiter D, Young J, Lecoq A, Deméocq V, Salenave S, Lefebvre H, Cloix L, Emy P, Dessailloud R, Vezzosi D, Scaroni C, Barbot M, de Herder W, Pattou F, Tétreault M, Corbeil G, Dupeux M, Lambert B, Tachdjian G, Guiochon-Mantel A, Beau I, Chanson P, Viengchareun S, Lacroix A, Bouligand J, Kamenický P
Affiliated Institution / ERN:
Hôpital Bicêtre ; Evangelismos General Hospital ; Assistance Publique-Hôpitaux de Paris, Hôpital Cochin ; Hospices Civils de Lyon ; University Hospital of Padova ; Erasmus MC: University Medical Center Rotterdam ; CHU de Toulouse ; University Hospitals Saint-Luc ;
Condition / Disease:
Cushing syndrome due to bilateral macronodular adrenocortical disease
Publication:
The Lancet Diabetes & Endocrinology v9.12 p813-824
Year:
2021
ORPHAcode / other:
ORPHA189427
Ultrasound criteria (EU-TIRADS) to identify thyroid nodule malignancy risk in adolescents. Correlation with cyto-histological findings
Author(s):
Yeste Fernández D, Vega Amenabar E, Coma Muñoz A, Arciniegas Vallejo L, Clemente León M, Planes-Conangla M, Iglesias Felip C, Sábado Álvarez C, Guillén Burrieza G, Campos-Martorell A
Affiliated Institution / ERN:
Hospital Universitari Vall d’Hebron ;
Condition / Disease:
Follicular thyroid carcinoma
Publication:
Endocrinología, Diabetes y Nutrición (English ed.) v68.10 p728-734
Year:
2021
ORPHAcode / other:
ORPHA146
DOI:
10.1016/j.endien.2020.11.006
Keywords:
Adolescencia,Adolescent,Bethesda classification,Citología,Clasificación Bethesda,Cytology,Cáncer de tiroides,EU-TIRADS,Ecografía de tiroides,FNAB,Nódulos tiroideos,PAAF,Thyroid cancer,Thyroid nodule,Thyroid ultrasound
Paradoxical low severity of COVID-19 in Prader-Willi syndrome: data from a French survey on 647 patients
Author(s):
Coupaye M, Laurier V, Benvegnu G, Poitou C, Faucher P, Mosbah H, Diene G, Pinto G, Briceño LG, Merrien C, Toyos AC, Montastier E, Tauber M, Mourre F
Affiliated Institution / ERN:
CHU de Toulouse ; Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
Prader-Willi syndrome
Publication:
Orphanet Journal of Rare Diseases v16.1
Year:
2021
ORPHAcode / other:
ORPHA739
DOI:
10.1186/s13023-021-01949-4
Keywords:
COVID-19,Obesity,Oxytocin,Prader-Willi syndrome,SARS-CoV-2
Safe and persistent growth-promoting effects of vosoritide in children with achondroplasia: 2-year results from an open-label, phase 3 extension study
Author(s):
Savarirayan R, Tofts L, Irving M, Wilcox WR, Bacino CA, Hoover-Fong J, Font RU, Harmatz P, Rutsch F, Bober MB, Polgreen LE, Ginebreda I, Mohnike K, Charrow J, Hoernschemeyer D, Ozono K, Alanay Y, Arundel P, Kotani Y, Yasui N, White KK, Saal HM, Leiva-Gea A, Luna-González F, Mochizuki H, Basel D, Porco DM, Jayaram K, Fisheleva E, Huntsman-Labed A, Day JR
Affiliated Institution / ERN:
ERN BOND ;
Condition / Disease:
Achondroplasia
Publication:
Genetics in Medicine v23.12 p2443-2447
Year:
2021
ORPHAcode / other:
ORPHA15
Use of Salivary Iodine Concentrations to Estimate the Iodine Status of Adults in Clinical Practice
Author(s):
Dekker BL, Touw DJ, van der Horst-Schrivers ANA, Vos MJ, Links TP, Dijck-Brouwer DJ, Muller Kobold AC
Affiliated Institution / ERN:
University Medical Center Groningen ; Maastricht University Medical Center+ ;
Condition / Disease:
Iodine status
Publication:
The Journal of Nutrition v151.12 p3671-3677
Year:
2021
ORPHAcode / other:
DOI:
10.1093/jn/nxab303
Keywords:
iodine intake,salivary iodine,salivary protein,salivary urea,urinary iodine
Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases
Author(s):
Kallali W, Messiaen C, Saïdi R, Lessim S, Viaud M, Dulon J, Nedelcu M, Samara D, Houang M, Donadille B, Courtillot C, de Filippo G, Carel J, Christin-Maitre S, Touraine P, Netchine I, Polak M, Léger J
Affiliated Institution / ERN:
Hospital Universitario Cruces ;
Condition / Disease:
Congenital endocrine conditions
Publication:
Orphanet Journal of Rare Diseases v16.1
Year:
2021
ORPHAcode / other:
ORPHA631, ORPHA238666, ORPHA2614, ORPHA562, ORPHA99429, ORPHA1772
The first European consensus on principles of management for achondroplasia
Author(s):
Cormier-Daire V, AlSayed M, Ben-Omran T, de Sousa SB, Boero S, Fredwall SO, Guillen-Navarro E, Irving M, Lampe C, Maghnie M, Mortier G, Peijin Z, Mohnike K
Affiliated Institution / ERN:
IRCCS Istituto Giannina Gaslini, Genova ; UZ Antwerpen ; Universitätsklinikum Magdeburg ; ERN BOND ;
Condition / Disease:
Achondroplasia
Publication:
Orphanet Journal of Rare Diseases v16.1
Year:
2021
ORPHAcode / other:
ORPHA15
DOI:
10.1186/s13023-021-01971-6
Keywords:
Achondroplasia,European Achondroplasia Forum,Guiding principles
Paediatric Cushing’s disease: Epidemiology, pathogenesis, clinical management and outcome
Author(s):
Ferrigno R, Hasenmajer V, Caiulo S, Minnetti M, Mazzotta P, Storr HL, Isidori AM, Grossman AB, De Martino MC, Savage MO
Affiliated Institution / ERN:
AOU Federico II - Naples ;
Condition / Disease:
Cushing disease
Publication:
Reviews in Endocrine and Metabolic Disorders v22.4 p817-835
Year:
2021
ORPHAcode / other:
ORPHA96253
Oral octreotide capsules for the treatment of acromegaly: comparison of 2 phase 3 trial results
Author(s):
Labadzhyan A, Nachtigall LB, Fleseriu M, Gordon MB, Molitch M, Kennedy L, Samson SL, Greenman Y, Biermasz N, Bolanowski M, Haviv A, Ludlam W, Patou G, Strasburger CJ
Affiliated Institution / ERN:
Leiden University Medical Center ; Charité Universitätsmedizin Berlin ;
Condition / Disease:
Acromegaly
Publication:
Pituitary v24.6 p943-953
Year:
2021
ORPHAcode / other:
ORPHA963
DOI:
10.1007/s11102-021-01163-2
Keywords:
Acromegaly,Growth hormone,IGF-I,Oral octreotide,Somatostatin analogs,Somatostatin receptor ligands
Long-term male fertility after treatment with radioactive iodine for differentiated thyroid carcinoma
Author(s):
Nies M, Arts EGJM, van Velsen EFS, Burgerhof JGM, Muller Kobold AC, Corssmit EPM, Netea-Maier RT, Peeters RP, van der Horst-Schrivers ANA, Cantineau AEP, Links TP
Affiliated Institution / ERN:
University Hospital Essen ; Universitätsklinikum Schleswig-Holstein ; Universitätsklinikum Tübingen ; Sestre milosrdnice University Hospital Center ; Ulm University Medical Center ;
Condition / Disease:
Differentiated Thyroid Carcinoma
Publication:
European Journal of Endocrinology v185.6 p775-782
Year:
2021
ORPHAcode / other:
ORPHA142
Novel presentation of the c.1856A > G (p.Asp619Gly) TSHR gene-activating variant: relapsing hyperthyroidism in three subsequent generations manifesting in early childhood and an in vitro functional study
Author(s):
Bezdicka M, Kleiblova P, Soucek J, Borecka M, El-Lababidi E, Smrz D, Rataj M, Sumnik Z, Malikova J, Soucek O
Affiliated Institution / ERN:
Motol and Homolka University Hospital ; General University Hospital in Prague ;
Condition / Disease:
Familial hyperthyroidism due to mutations in TSH receptor
Publication:
Hormones v20.4 p803-812
Year:
2021
ORPHAcode / other:
ORPHA424
DOI:
10.1007/s42000-021-00299-x
Keywords:
Activating TSHR pathogenic variant,Case report,Familial non-autoimmune hyperthyroidism,Functional study,Radioiodine ablative treatment,Repeated thyroid surgery
A recessive variant in TFAM causes mtDNA depletion associated with primary ovarian insufficiency, seizures, intellectual disability and hearing loss
Author(s):
Ullah F, Rauf W, Khan K, Khan S, Bell KM, de Oliveira VC, Tariq M, Bakhshalizadeh S, Touraine P, Katsanis N, Sinclair A, He S, Tucker EJ, Baig SM, Davis EE
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
Rare disorder with hypergonadotropic hypogonadism
Publication:
Human Genetics v140.12 p1733-1751
Year:
2021
ORPHAcode / other:
ORPHA181441
Sunitinib-Induced Hypothyroidism and Survival in Pancreatic Neuroendocrine Tumors
Author(s):
Mathew A, Führer D, Lahner H
Affiliated Institution / ERN:
ERN BOND ; University Hospital Essen ;
Condition / Disease:
Neuroendocrine tumours
Publication:
Hormone and Metabolic Research v53.12 p794-800
Year:
2021
ORPHAcode / other:
Sex Bias in Differentiated Thyroid Cancer
Author(s):
Suteau V, Munier M, Briet C, Rodien P
Affiliated Institution / ERN:
CHU d'Angers ;
Condition / Disease:
Follicular thyroid carcinoma
Publication:
International Journal of Molecular Sciences v22.23 p12992
Year:
2021
ORPHAcode / other:
ORPHA146
DOI:
10.3390/ijms222312992
Keywords:
estrogens,oncogenes,reactive oxygen species (ROS),sex bias,thyroid cancer
Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia
Author(s):
Katkevica A, Kreile M, Grinfelde I, Taurina G, Micule I, Dzivite-Krisane I, Smite-Laguna A, Malniece I
Affiliated Institution / ERN:
Condition / Disease:
Publication:
Case Reports in Medicine v2021 p1-5
Year:
2021
ORPHAcode / other:
The Quality Evaluation of Rare Disease Registries—An Assessment of the Essential Features of a Disease Registry
Author(s):
Ali SR, Bryce J, Kodra Y, Taruscio D, Persani L, Ahmed SF
Affiliated Institution / ERN:
IRCCS Auxologico Italian Institute - Milan ; Leiden University Medical Center ;
Condition / Disease:
Rare disease registries
Publication:
International Journal of Environmental Research and Public Health v18.22 p11968
Year:
2021
ORPHAcode / other:
ORPHA97978
Pheochromocytoma Resection in a Patient With Chronic Thromboembolic Pulmonary Hypertension and Thrombocytopenia
Author(s):
Stombaugh DK, Thomas C, Dalton A, Chaney MA, Nunnally ME, Berends AM, Kerstens MN
Affiliated Institution / ERN:
University Medical Center Groningen ;
Condition / Disease:
Phaeochromocytoma
Publication:
Journal of Cardiothoracic and Vascular Anesthesia v35.11 p3423-3433
Year:
2021
ORPHAcode / other:
ORPHA573163
DOI:
10.1053/j.jvca.2021.03.034
Keywords:
Pheochromocytoma,chronic thromboembolic pulmonary hypertension,right ventricular dysfunction
Persistent Postthyroidectomy Hypoparathyroidism in the Netherlands
Author(s):
Lončar I, Noltes ME, Dickhoff C, Engelsman AF, Schepers A, Vriens MR, Bouvy ND, Kruijff S, van Ginhoven TM
Affiliated Institution / ERN:
Universitätsklinikum Schleswig-Holstein ; University Hospital Essen ; Universitätsklinikum Tübingen ; University Hospital Florence ; Ulm University Medical Center ;
Condition / Disease:
Hypoparathyroidism
Publication:
JAMA Otolaryngology–Head & Neck Surgery v147.11 p959
Year:
2021
ORPHAcode / other:
Seventy eight children born small for gestational age without catch-up growth treated with growth hormone from the prepubertal stage until adult height age. An evaluation of puberty and changes in the metabolic profile
Author(s):
Campos-Martorell A, Fernández-Cancio M, Clemente León M, Mogas Viñals E, Fàbregas Martori A, Carrascosa Lezcano A, Yeste Fernández D
Affiliated Institution / ERN:
Hospital Universitari Vall d’Hebron ;
Condition / Disease:
Small for gestational age
Publication:
Endocrinología, Diabetes y Nutrición (English ed.) v68.9 p612-620
Year:
2021
ORPHAcode / other:
DOI:
10.1016/j.endien.2021.11.024
Keywords:
Adult height,Growth hormone,Hormona de crecimiento,Pequeño para la edad gestacional,Pubertad,Pubertal maturity group,Puberty,Small for gestational age,Talla adulta
Defective Levothyroxine Response in a Patient with Dyshormonogenic Congenital Hypothyroidism Caused by a Concurrent Pathogenic Variant in Thyroid Hormone Receptor-β
Author(s):
Lauffer P, Bikker H, Garrelfs MR, Hillebrand JJ, de Sonnaville MC, Zwaveling-Soonawala N, van Trotsenburg AP
Affiliated Institution / ERN:
Amsterdam UMC ;
Condition / Disease:
Congenital hypothyroidism
Publication:
Thyroid v31.11 p1757-1762
Year:
2021
ORPHAcode / other:
ORPHA442
DOI:
10.1089/thy.2021.0204
Keywords:
congenital hypothyroidism,resistance to thyroid hormone,sodium-iodide symporter,thyroid hormone receptor-β
Effectiveness of a closed‐loop control system and a virtual educational camp for children and adolescents with type 1 diabetes: A prospective, multicentre, real‐life study
Author(s):
Cherubini V, Rabbone I, Berioli MG, Giorda S, Lo Presti D, Maltoni G, Mameli C, Marigliano M, Marino M, Minuto N, Mozzillo E, Piccinno E, Predieri B, Ripoli C, Schiaffini R, Rigamonti A, Salzano G, Tinti D, Toni S, Zanfardino A, Scaramuzza AE, Gesuita R, Tiberi V, Savastio S, Pigniatiello C, Trada M, Zucchini S, Redaelli FC, Maffeis C, Bassi M, Rosanio FM, Delvecchio M, Buzzi P, Ricciardi MR, Carducci C, Bonfanti R, Lombardo F, Piccini B, Iafusco D, Calandretti M, Daga FA
Affiliated Institution / ERN:
AO City of Health and Science - Turin ; AOU-Bologna ; AOUI Verona ; IRCCS Istituto Giannina Gaslini, Genova ; AOU Federico II - Naples ; San Raffaele hospital - Milan ; AOU polyclinic "G.Martino" of Messina ; Meyer Children’s Hospital Florence ; AOU University of Campania "Luigi Vanvitelli", Naples ;
Condition / Disease:
Type 1 Diabetes Mellitus
Publication:
Diabetes, Obesity and Metabolism v23.11 p2484-2491
Year:
2021
ORPHAcode / other:
5A10
DOI:
10.1111/dom.14491
Keywords:
CSII,continuous glucose monitoring,glycaemic control,insulin pump therapy,observational study,type 1 diabetes
Adrenalectomy for incidental and symptomatic phaeochromocytoma: retrospective multicentre study based on the Eurocrine® database
Author(s):
Hallin Thompson L, Makay Ã, Brunaud L, Raffaelli M, Bergenfelz A, Musholt T, Palazzo F, Almquist M, Barczynski M, Clerici T, Vriens M, Raffaelli M, Makay Ã, Munos Pérez N, Hansen MH, Brunaud L, Van Slycke S, Riss P, Iacobone M, Nordenström E
Affiliated Institution / ERN:
University Medical Center Mainz ; University Medical Center Utrecht ; San Raffaele hospital - Milan ; University Hospital of Padova ;
Condition / Disease:
Phaeochromocytoma
Publication:
British Journal of Surgery v108.10 p1199-1206
Year:
2021
ORPHAcode / other:
ORPHA573163
DOI:
10.1093/bjs/znab199
Keywords:
pheochromocytoma, hypertension, catecholamines, adrenal, ectomyperioperative carepreoperative caresurgical procedures, operativeneoplasms
Focal Thyroid Incidentalomas on 18F-FDG PET/CT: A Systematic Review and Meta-Analysis on Prevalence, Risk of Malignancy and Inconclusive Fine Needle Aspiration
Author(s):
de Leijer JF, Metman MJH, van der Hoorn A, Brouwers AH, Kruijff S, van Hemel BM, Links TP, Westerlaan HE
Affiliated Institution / ERN:
University Hospital Essen ;
Condition / Disease:
Thyroid carcinoma
Publication:
Frontiers in Endocrinology v12
Year:
2021
ORPHAcode / other:
ORPHA100088
DOI:
10.3389/fendo.2021.723394
Keywords:
FDG (18F-fluorodeoxyglucose)-PET/CT,incidentaloma,thyroid,thyroid cancer,thyroid nodule
Consensus on diagnosis and management of Cushing’s disease: a guideline update
Author(s):
Maria Fleseriu, Richard Auchus, Irina Bancos, Anat Ben-Shlomo, Jerome Bertherat, Nienke R Biermasz, Cesar L Boguszewski, Marcello D Bronstein, Michael Buchfelder, John D Carmichael, Felipe F Casanueva, Frederic Castinetti, Philippe Chanson, James Findling, Mônica Gadelha, Eliza B Geer, Andrea Giustina, Ashley Grossman, Mark Gurnell, Ken Ho, Adriana G Ioachimescu, Ursula B Kaiser, Niki Karavitaki, Laurence Katznelson, Daniel F Kelly, André Lacroix, Ann McCormack, Shlomo Melmed, Mark Molitch, Pietro Mortini, John Newell-Price, Lynnette Nieman, Alberto M Pereira, Stephan Petersenn, Rosario Pivonello, Hershel Raff, Martin Reincke, Roberto Salvatori, Carla Scaroni, Ilan Shimon, Constantine A Stratakis, Brooke Swearingen, Antoine Tabarin, Yutaka Takahashi, Marily Theodoropoulou, Stylianos Tsagarakis, Elena Valassi, Elena V Varlamov, Greisa Vila, John Wass, Susan M Webb, Maria C Zatelli, Beverly M K Bill
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Cochin ; Leiden University Medical Center ; Assistance Publique-Hôpitaux de Marseille ; Hôpital Bicêtre ; San Raffaele hospital - Milan ; University Hospital Essen ; AOU Federico II - Naples ; Klinikum der Universität München ; University Hospital of Padova ; Evangelismos General Hospital ; Hospital de la Santa Creu i Sant Pau ; AOU - Ferrara ;
Condition / Disease:
Cushing's disease
Publication:
The Lancet Diabetes & Endocrinology
Year:
2021
ORPHAcode / other:
ORPHA96253
Opposite Incidence Trends for Differentiated and Medullary Thyroid Cancer in Young Dutch Patients over a 30-Year Time Span
Author(s):
Lebbink C, van den Broek M, Kwast A, Derikx J, Dierselhuis M, Kruijff S, Links T, van Trotsenburg A, Valk G, Vriens M, Verrijn Stuart A, van Santen H, Karim-Kos H
Affiliated Institution / ERN:
University Hospital Florence ; University Hospital Essen ;
Condition / Disease:
Differentiated and medullary thyroid carcinoma
Publication:
Cancers v13.20 p5104
Year:
2021
ORPHAcode / other:
ORPHA146, ORPHA1332
DOI:
10.3390/cancers13205104
Keywords:
adolescents,children,epidemiology,incidence,survival,thyroid cancer,young adults
Cost-Utility of Acromegaly Pharmacological Treatments in a French Context
Author(s):
Brue T, Chanson P, Rodien P, Delemer B, Drui D, Marié L, Juban L, Salvi L, Henocque R, Raverot G
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Marseille ; Hôpital Bicêtre ; CHU d'Angers ; Assistance Publique-Hôpitaux de Paris, Hôpital Cochin ; Hospices Civils de Lyon ;
Condition / Disease:
Acromegaly
Publication:
Frontiers in Endocrinology v12
Year:
2021
ORPHAcode / other:
ORPHA963
DOI:
10.3389/fendo.2021.745843
Keywords:
QALY,acromegaly,cost-utility,growth hormone,insulin-like growth factor-1,pasireotide,pegvisomant,somatostatin