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Endo-ERN Publications Database
895 publication(s) found matching the search criteria
Growth response of syndromic versus non-syndromic children born small for gestational age (SGA) to growth hormone therapy: a Belgian study
Author(s):
Becker M, Thomas M, Brachet C, Heinrichs C, Dotremont H, De Schepper J, Lysy P, Beckers D
Affiliated Institution / ERN:
Centre Hospitalier de Luxembourg ;
Condition / Disease:
growth hormone deficiency (GHD)
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA631; ORPHA101957
DOI:
10.3389/fendo.2023.1112938
Keywords:
adult height,children,growth,growth hormone,short for gestational age,short stature,syndromic
Psychological Care for Children and Adolescents with Diabetes and Patient Outcomes: Results from the International Pediatric Registry SWEET
Author(s):
Chobot A, Eckert AJ, Biester T, Corathers S, Covinhas A, de Beaufort C, Imane Z, Kim J, Malatynska A, Moravej H, Pokhrel S, Skinner T, Study Group S
Affiliated Institution / ERN:
Centre Hospitalier de Luxembourg ;
Condition / Disease:
diabetes type 1
Publication:
Pediatric Diabetes v2023 p1-9
Year:
2023
ORPHAcode / other:
[18F]FDG Uptake and Expression of Immunohistochemical Markers Related to Glycolysis, Hypoxia, and Proliferation in Indeterminate Thyroid Nodules
Author(s):
de Koster EJ, van Engen-van Grunsven ACH, Bussink J, Frielink C, de Geus-Oei L, Kusters B, Peters H, Oyen WJG, Vriens D, Netea-Maier RT, Smit JWA, de Wilt JHW, Booij J, Fliers E, Klooker TK, van Dam EWCM, Dreijerink KMA, Raijmakers PGHM, Kam BLR, Peeters RP, Verzijlbergen JF, van Aken MO, Jager PL, Mijnhout GS, van den Hout WB, Arias AMP, Morreau J, Snel M, Dijkhorst-Oei L, de Klerk JMH, Havekes B, Mitea DC, Vöö S, Brouwer CB, van Dam PS, Sivro F, te Beek ET, Jebbink MCW, Bleumink GS, Schelfhout VJR, Keijsers RGM, Wakelkamp IMMJ, Brouwers AH, Links TP, de Keizer B, van Leeuwaarde RS, Bonenkamp JJ, Donders ART, Fütterer JJ
Affiliated Institution / ERN:
University Medical Center Utrecht ;
Condition / Disease:
Follicular thyroid carcinoma
Publication:
Molecular Imaging and Biology v25.3 p483-494
Year:
2023
ORPHAcode / other:
ORPHA146
DOI:
10.1007/s11307-022-01776-4
Keywords:
Glucose Metabolism,Glycolysis,Immunohistochemistry,Thyroid Nodule,[18F]FDG-PET/CT
Gene expression signature predicts rate of type 1 diabetes progression
Author(s):
Suomi T, Starskaia I, Kalim UU, Rasool O, Jaakkola MK, Grönroos T, Välikangas T, Brorsson C, Mazzoni G, Bruggraber S, Overbergh L, Dunger D, Peakman M, Chmura P, Brunak S, Schulte AM, Mathieu C, Knip M, Lahesmaa R, Elo LL, Mathieu C, Gillard P, Casteels K, Overbergh L, Dunger D, Wallace C, Evans M, Thankamony A, Hendriks E, Bruggraber S, Marcoveccchio L, Peakman M, Tree T, Morgan NG, Richardson S, Todd JA, Wicker L, Mander A, Dayan C, Alhadj Ali M, Pieber T, Eizirik DL, Cnop M, Brunak S, Pociot F, Johannesen J, Rossing P, Quigley CL, Mallone R, Scharfmann R, Boitard C, Knip M, Otonkoski T, Veijola R, Lahesmaa R, Oresic M, Toppari J, Danne T, Ziegler AG, Achenbach P, Rodriguez-Calvo T, Solimena M, Bonifacio EE, Speier S, Holl R, Dotta F, Chiarelli F, Marchetti P, Bosi E, Cianfarani S, Ciampalini P, De Beaufort C, Dahl-Jørgensen K, Skrivarhaug T, Joner G, Krogvold L, Jarosz-Chobot P, Battelino T, Thorens B, Gotthardt M, Roep BO, Nikolic T, Zaldumbide A, Lernmark A, Lundgren M, Costacalde G, Strube T, Schulte AM, Nitsche A, Peakman M, Vela J, Von Herrath M, Wesley J, Napolitano-Rosen A, Thomas M, Schloot N, Goldfine A, Waldron-Lynch F, Kompa J, Vedala A, Hartmann N, Nicolas G, van Rampelbergh J, Bovy N, Dutta S, Soderberg J, Ahmed S, Martin F, Latres E, Agiostratidou G, Koralova A, Willemsen R, Smith A, Anand B, Datta V, Puthi V, Zac-Varghese S, Dias R, Sundaram P, Vaidya B, Patterson C, Owen K, Dayan C, Piel B, Heller S, Randell T, Gazis T, Reismen EB, Carel J, Riveline J, Gautier J, Andreelli F, Travert F, Cosson E, Penfornis A, Petit C, Feve B, Lucidarme N, Cosson E, Beressi J, Ajzenman C, Radu A, Greteau-Hamoumou S, Bibal C, Meissner T, Heidtmann B, Toni S, Rami-Merhar B, Eeckhout B, Peene B, Vantongerloo N, Maes T, Gommers L
Affiliated Institution / ERN:
Centre Hospitalier de Luxembourg ; Meyer Children’s Hospital Florence ; Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
diabetes type 1
Publication:
eBioMedicine v92 p104625
Year:
2023
ORPHAcode / other:
DOI:
10.1016/j.ebiom.2023.104625
Keywords:
Autoantibodies,Gene expression signature,Predictive model,RNA-seq,Type 1 diabetes
Clinical course of autoimmune thyroid diseases in women with prolactinomas: Results from a prospective study in a single tertiary centre
Author(s):
Elenkova A, Racheva P, Kirilov G, Zacharieva S
Affiliated Institution / ERN:
USHATE “ACAD IVAN Penchev” ;
Condition / Disease:
Prolactinoma
Publication:
Endocrinología, Diabetes y Nutrición (English ed.) v70 p27-34
Year:
2023
ORPHAcode / other:
ORPHA2965
DOI:
10.1016/j.endien.2023.05.008
Keywords:
Autoimmune thyroiditis,Hipertiroidismo,Hipotiroidismo,Hyperthyroidism,Hypothyroidism,Prolactin,Prolactina,Prolactinoma,Tiroiditis autoinmune
Who is sensitising whom? A participatory interview guide development as an awareness tool within a health care research project
Author(s):
Kalender U, Wiegmann S, Ernst M, Ihme L, Neumann U, Stöckigt B
Affiliated Institution / ERN:
Charité Universitätsmedizin Berlin ;
Condition / Disease:
Publication:
Heliyon v9.6 pe16778
Year:
2023
ORPHAcode / other:
Proposal of early CT morphological criteria for response of liver metastases to systemic treatments in gastroenteropancreatic neuroendocrine tumors: Alternatives to RECIST
Author(s):
de Mestier L, Resche‐Rigon M, Dromain C, Lamarca A, La Salvia A, de Baker L, Fehrenbach U, Pusceddu S, Colao A, Borbath I, de Haas R, Rinzivillo M, Zerbi A, Funicelli L, de Herder WW, Selberherr A, Wagner AD, Manoharan P, De Cima A, Lybaert W, Jann H, Prinzi N, Faggiano A, Annet L, Walenkamp A, Panzuto F, Pedicini V, Pitoni MG, Siebenhuener A, Mayerhoefer ME, Ruszniewski P, Vullierme M
Affiliated Institution / ERN:
AOU Federico II - Naples ;
Condition / Disease:
neuroendocrine tumors
Publication:
Journal of Neuroendocrinology v35.6
Year:
2023
ORPHAcode / other:
ORPHA100092
DOI:
10.1111/jne.13311
Keywords:
computed tomography,neuroendocrine tumors,response evaluation,systemic treatments
Intermittent Use of Continuous Glucose Monitoring: A New Paradigm in Treatment of Type 2 Diabetes
Author(s):
Banshi Saboo, Ranjit Unnikrishnan, Jothydev Kesavadev, Mangesh Tiwaskar, Leszek Czupryniak, Manoj Chawla, Pratik Choudhary, Tadej Battelino, Sanjay Agarwal, Thomas Danne, Viswanathan Mohan
Affiliated Institution / ERN:
University Medical Centre Ljubljana ; Hannoversche Kinderheilanstalt ;
Condition / Disease:
diabetes type 2
Publication:
J Assoc Physicians India 71(6):11-12
Year:
2023
ORPHAcode / other:
The pathogenic p.Gln319Ter variant is not causing congenital adrenal hyperplasia when inherited in one of the duplicated CYP21A2 genes
Author(s):
Fanis P, Skordis N, Toumba M, Picolos M, Tanteles GA, Neocleous V, Phylactou LA
Affiliated Institution / ERN:
Cyprus Institute of Neurology and Genetics ;
Condition / Disease:
Congenital Adrenal Hyperplasia
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA418
DOI:
10.3389/fendo.2023.1156616
Keywords:
21-hyrdroxylase deficiency,CAH,CYP21A2,RCCX,gene duplications
Plasma-free metanephrines, nerve growth factor, and renalase significance in patients with PCOS
Author(s):
Robeva R, Elenkova A, Kirilov G, Zacharieva S
Affiliated Institution / ERN:
USHATE “ACAD IVAN Penchev” ;
Condition / Disease:
PCOS
Publication:
Endocrine v81.3 p602-612
Year:
2023
ORPHAcode / other:
DOI:
10.1007/s12020-023-03404-9
Keywords:
Nerve growth factor (NGF),Normetanephrine,Polycystic ovarian syndrome (PCOS),Renalase,Sympathetic noradrenergic activity
Current Treatments for Patients with Genetic Obesity
Author(s):
Faccioli N, Poitou C, Clément K, Dubern B
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
Genetic non-syndromic obesity, leptin/melanocortin pathway
Publication:
Journal of Clinical Research in Pediatric Endocrinology v15.2 p108-119
Year:
2023
ORPHAcode / other:
ORPHA77828
DOI:
10.4274/jcrpe.galenos.2023.2023-3-2
Keywords:
Genetic obesity,syndromic obesity,personalized medicine,setmelanotide
Prolyl Endopeptidase-like Deficiency Associated with Growth Hormone Deficiency
Author(s):
Sayol-Torres L, Valenzuela MI, Tomasini R, Fernández-Alvarez P, Clemente M, Yeste D
Affiliated Institution / ERN:
Hospital Universitari Vall d’Hebron ;
Condition / Disease:
Non-acquired pituitary hormone deficiency
Publication:
Journal of Clinical Research in Pediatric Endocrinology v15.2 p205-209
Year:
2023
ORPHAcode / other:
ORPHA95488
DOI:
10.4274/jcrpe.galenos.2021.2021.0128
Keywords:
Prolyl endopeptidase-like,genetics,growth hormone deficiency
What is the role of CHCHD2 in adrenal tumourigenesis?
Author(s):
Karapanagioti A, Nasiri-Ansari N, Moustogiannis A, Trigas GC, Zografos G, Aggeli C, Kyriakopoulos G, Choreftaki T, Philippou A, Kaltsas G, Kassi E, Angelousi A
Affiliated Institution / ERN:
General Hospital of Athens “LAIKO” ;
Condition / Disease:
Adrenocortical carcinoma
Publication:
Endocrine v81.2 p357-367
Year:
2023
ORPHAcode / other:
ORPHA1501
DOI:
10.1007/s12020-023-03393-9
Keywords:
Adrenal adenomas,Adrenocortical carcinoma,Apoptosis,BAX,BCL2,CHCHD2
Quality of life in children and adolescents with growth hormone deficiency and their caregivers: an Italian survey
Author(s):
Maghnie M, Orso M, Polistena B, Cappa M, Pozzobon G, d’Angela D, Patti G, Spandonaro F, Granato S, Di Virgilio R, La Torre D, Salerno M
Affiliated Institution / ERN:
San Raffaele hospital - Milan ;
Condition / Disease:
growth hormone deficiency
Publication:
Journal of Endocrinological Investigation v46.12 p2513-2523
Year:
2023
ORPHAcode / other:
ORPHA631; ORPHA101957;
DOI:
10.1007/s40618-023-02106-3
Keywords:
Children,Growth hormone deficiency,Italy,Quality of life,Survey
Child and adolescent obesity
Author(s):
Lister NB, Baur LA, Felix JF, Hill AJ, Marcus C, Reinehr T, Summerbell C, Wabitsch M
Affiliated Institution / ERN:
Ulm University Medical Center ;
Condition / Disease:
Child and adolescent obesity
Publication:
Nature Reviews Disease Primers v9.1
Year:
2023
ORPHAcode / other:
ORPHA77828
Novel Insulin-Like Growth Factor 1 Gene Mutation: Broadening of the Phenotype and Implications for Insulin Resistance
Author(s):
Giacomozzi C, Martin A, Fernández MC, Gutiérrez M, Iascone M, Domené HM, Dominici FP, Bergadá I, Cangiano B, Persani L, Pennisi PA
Affiliated Institution / ERN:
AOU-Bologna ;
Condition / Disease:
growth hormone deficiency (GHD)
Publication:
The Journal of Clinical Endocrinology & Metabolism v108.6 p1355-1369
Year:
2023
ORPHAcode / other:
ORPHA101957; ORPHA95488
DOI:
10.1210/clinem/dgac738
Keywords:
IGF1 mutation,IGF1 primary insufficiency,impaired glucose tolerance,insulin resistance,short stature
Bilateral inferior petrosal sinus sampling with human CRH stimulation in ACTH-dependent Cushing’s syndrome: results from a retrospective multicenter study
Author(s):
Detomas M, Ritzel K, Nasi-Kordhishti I, Schernthaner-Reiter MH, Losa M, Tröger V, Altieri B, Kroiss M, Kickuth R, Fassnacht M, Micko A, Honegger J, Reincke M, Deutschbein T
Affiliated Institution / ERN:
University Hospital Würzburg ;
Condition / Disease:
Cushing Syndrome
Publication:
European Journal of Endocrinology v188.5 p448-456
Year:
2023
ORPHAcode / other:
ORPHA647758; ORPHA189427; ORPHA314749;
DOI:
10.1093/ejendo/lvad050
Keywords:
Catheter,Cushing’s disease,IPSS,ectopic,petrosal sinus,pituitary,prolactin
Individuals with numerical and structural variations of sex chromosomes: interdisciplinary management with focus on fertility potential
Author(s):
Juul A, Gravholt CH, De Vos M, Koledova E, Cools M
Affiliated Institution / ERN:
Aarhus University Hospital ;
Condition / Disease:
DSD
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA325546
DOI:
10.3389/fendo.2023.1160884
Keywords:
DSD,Klinefelter syndrome,NSVSC,Turner syndrome,sex chromosomes
Characterization of lymphocyte profiles in children with syndromic obesity
Author(s):
Dieme A, André S, Lapillonne H, Tounian P, Clément K, Dubern B
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
Syndromic Genetic Obesity
Publication:
Archives de Pédiatrie v30.4 p212-218
Year:
2023
ORPHAcode / other:
ORPHA240371
DOI:
10.1016/j.arcped.2023.02.009
Keywords:
Adipose tissue,Childhood obesity,Immunology,Inflammation
Immune checkpoint inhibitor-related thyroid dysfunction
Author(s):
Illouz F, Briet C, Rodien P
Affiliated Institution / ERN:
CHU d'Angers ;
Condition / Disease:
Immune checkpoint inhibitor-related thyroid dysfunction
Publication:
Annales d'Endocrinologie v84.3 p346-350
Year:
2023
ORPHAcode / other:
DOI:
10.1016/j.ando.2023.03.005
Keywords:
Dysfonction thyroïdienne,Hypothyroidism,Hypothyroïdie,Immune checkpoint inhibitors,Inhibiteurs des points de contrôle immunitaire,Thyroid dysfunction,Thyroiditis,Thyrotoxicose,Thyrotoxicosis,Thyroïdite
Novel therapeutics in rare genetic obesities: A narrative review
Author(s):
Dubern B, Faccioli N, Poitou C, Clément K
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
obesity associated with defect in leptin/melanocortin pathway
Publication:
Pharmacological Research v191 p106763
Year:
2023
ORPHAcode / other:
ORPHA77828
DOI:
10.1016/j.phrs.2023.106763
Keywords:
Childhood obesity,Genetics,Hypothalamus,Melanocortins,Monogenic obesity
Epidemiology and diagnostic trends of congenital adrenal hyperplasia in Denmark: a retrospective, population-based study
Author(s):
Berglund A, Ornstrup MJ, Lind-Holst M, Dunø M, Bækvad-Hansen M, Juul A, Borch L, Jørgensen N, Rasmussen ÃK, Andersen M, Main KM, Hansen D, Gravholt CH
Affiliated Institution / ERN:
Aarhus University Hospital ;
Condition / Disease:
Congenital Adrenal Hyperplasia
Publication:
The Lancet Regional Health - Europe v28 p100598
Year:
2023
ORPHAcode / other:
ORPHA418
DOI:
10.1016/j.lanepe.2023.100598
Keywords:
Congenital adrenal hyperplasia,Diagnosis age,Epidemiology,Incidence,Prevalence
Adipose tissue function and insulin sensitivity in syndromic obesity of Bardet-Biedl syndrome
Author(s):
Baig S, Wanninayake S, Foggensteiner L, Elhassan YS, Manolopoulos K, Ali S, Lassen PB, Clément K, Steeds RP, Tomlinson JW, Geberhiwot T
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
BBS
Publication:
International Journal of Obesity v47.5 p382-390
Year:
2023
ORPHAcode / other:
ORPHA110
João Raposo: moving beyond recommendations and guidelines
Author(s):
Burki T
Affiliated Institution / ERN:
APDP – Diabetes Portugal ;
Condition / Disease:
diabetes and behaviour
Publication:
The Lancet Diabetes & Endocrinology v11.5 p313
Year:
2023
ORPHAcode / other:
Clinical consensus guideline on the management of phaeochromocytoma and paraganglioma in patients harbouring germline SDHD pathogenic variants
Author(s):
Taïeb D, Wanna GB, Ahmad M, Lussey-Lepoutre C, Perrier ND, Nölting S, Amar L, Timmers HJLM, Schwam ZG, Estrera AL, Lim M, Pollom EL, Vitzthum L, Bourdeau I, Casey RT, Castinetti F, Clifton-Bligh R, Corssmit EPM, de Krijger RR, Del Rivero J, Eisenhofer G, Ghayee HK, Gimenez-Roqueplo A, Grossman A, Imperiale A, Jansen JC, Jha A, Kerstens MN, Kunst HPM, Liu JK, Maher ER, Marchioni D, Mercado-Asis LB, Mete O, Naruse M, Nilubol N, Pandit-Taskar N, Sebag F, Tanabe A, Widimsky J, Meuter L, Lenders JWM, Pacak K
Affiliated Institution / ERN:
University Medical Center Groningen ;
Condition / Disease:
Phaeochromocytoma and paraganglioma
Publication:
The Lancet Diabetes & Endocrinology v11.5 p345-361
Year:
2023
ORPHAcode / other:
ORPHA276621
Integrated safety and efficacy analysis of dasiglucagon for the treatment of severe hypoglycaemia in individuals with type 1 diabetes
Author(s):
Heller S, Battelino T, Bailey TS, Pieber TR, Hövelmann U, Plum‐Mörschel L, Melgaard AE, Aronson R, DiMeglio LA, Johansen T, Danne T
Affiliated Institution / ERN:
University Medical Centre Ljubljana ;
Condition / Disease:
Diabetes mellitus
Publication:
Diabetes, Obesity and Metabolism v25.5 p1351-1360
Year:
2023
ORPHAcode / other:
Transition for adolescents with a rare disease: results of a nationwide German project
Author(s):
Grasemann C, Höppner J, Burgard P, Schündeln MM, Matar N, Müller G, Krude H, Berner R, Lee-Kirsch MA, Hauck F, Wainwright K, Baumgarten S, Atinga J, Bauer JJ, Manka E, Körholz J, Kiewert C, Heinen A, Kretschmer T, Kurth T, Mittnacht J, Schramm C, Klein C, Graessner H, Hiort O, Muntau AC, Grüters A, Hoffmann GF, Choukair D
Affiliated Institution / ERN:
Charité Universitätsmedizin Berlin ;
Condition / Disease:
transition of care, rare diseases
Publication:
Orphanet Journal of Rare Diseases v18.1
Year:
2023
ORPHAcode / other:
DOI:
10.1186/s13023-023-02698-2
Keywords:
Adolescent health,Empowerment,Health literacy,Pathway,Rare disease,Transition
Increase of jump performance during GH treatment in short children born SGA
Author(s):
Schweizer R, Martin DD, Binder G
Affiliated Institution / ERN:
Universitätsklinikum Tübingen ;
Condition / Disease:
growth hormone deficiency (GHD)
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA631; ORPHA101957
DOI:
10.3389/fendo.2023.1122287
Keywords:
children,growth hormone treatment (GH),jumping mechanography,muscle function,muscle power,peak jump force,small for gestation age (SGA)
Unusual causes of hyperthyrotropinemia and differential diagnosis of primary hypothyroidism: a revised diagnostic flowchart
Author(s):
Campi I, Dell’Acqua M, Stellaria Grassi E, Cristina Vigone M, Persani L
Affiliated Institution / ERN:
San Raffaele hospital - Milan ;
Condition / Disease:
Resistance to thyroid hormone
Publication:
European Thyroid Journal v12.4
Year:
2023
ORPHAcode / other:
ORPHA596426
DOI:
10.1530/etj-23-0012
Keywords:
TSH,assay artifacts,consumptive hypothyroidism,deiodinases,hypothyroidism,macro-TSH,malabsorption,resistance to TSH
Cushing’s syndrome in the elderly: data from the European Registry on Cushing’s syndrome
Author(s):
Amodru V, Ferriere A, Tabarin A, Castinetti F, Tsagarakis S, Toth M, Feelders RA, Webb SM, Reincke M, Netea-Maier R, Kastelan D, Elenkova A, Maiter D, Ragnarsson O, Santos A, Valassi E, Amaral C, Ambrogio A, Aranda G, Arosio M, Balomenaki M, Berr-Kirmair C, Bertherat J, Bolanowski M, Bollerslev J, Cardoso H, Carvalho D, Cavagnini F, Ceccato P, Chabre O, Chanson P, Christ E, Demtröder Zentrum fur Endokrinologie F, Denes J, Deutschbein T, Dimopoulou C, Dreval A, Droste M, Duarte JS, Dusek T, Ertürk E, Evang JA, Fajardo C, Fazel J, Feelders RA, Fica S, García-Centeno R, Ghigo E, Goth M, Godlewska M, Greenman Y, Halperin I, Hanzu FA, Hermus A, Johannsson G, Hubina E, Januszewska A, Kamenicky P, Kasperlik-Zaluska A, Kirchner J, Kastelan D, Komerdus I, Kraljevic I, Krsek M, Kruszynska A, Lamas C, Lambrescu I, Lang S, Luger A, Maiter D, Marpole N, Martin S, Martinie M, Martins Oliveira MJ, Moros O, Netea-Maier R, Newell-Price J, Orbetzova M, Paiva I, Pecori Giraldi F, Percovich JC, Pereira AM, Pfeifer M, Pickel J, Pirags V, Ragnarsson O, Reghina AD, Reincke M, Riesgo P, Roberts M, Roerink S, Roig O, Rowan C, Rudenko P, Salvador J, Santos A, Scaroni C, Sigurjonsdottir HA, Skoric Polovina T, Smith R, Stachowska B, Stalla G, Strasburger C, Tabarin A, Terzolo M, Tőke J, Tóth M, Touraine P, Trainer PJ, Tsagarakis S, Valassi E, Vila G, Vinay S, Wagenmakers M, Werner S, Young J, Zdunowski P, Zopf K, Zopp S, Zosin I
Affiliated Institution / ERN:
University Hospitals Saint-Luc ; Semmelweis University ; Hospital de la Santa Creu i Sant Pau ; Evangelismos General Hospital ;
Condition / Disease:
Cushing's syndrome
Publication:
European Journal of Endocrinology v188.4 p395-406
Year:
2023
ORPHAcode / other:
ORPHA96253; ORPHA647758; ORPHA189427; ORPHA314749;
