0
Endo-ERN Publications Database
1008 publication(s) found matching the search criteria
Executive summary of the expert consensus document from the Spanish Society of Neurosurgery and the Spanish Society of Endocrinology and Nutrition: clinical recommendations on the perioperative management of pituitary tumors
Author(s):
Araujo-Castro M, Berrocal VR, Dios E, Serramito R, Biagetti B, Bernabeu I
Affiliated Institution / ERN:
Hospital Universitari Vall d’Hebron ;
Condition / Disease:
Pituitary adenomas
Publication:
Neurocirugía (English Edition) v34.6 p292-307
Year:
2023
ORPHAcode / other:
ORPHA99408
DOI:
10.1016/j.neucie.2023.07.007
Keywords:
Acromegalia,Acromegaly,Adenoma hipofisario no funcionante,Cirugía transesfenoidal,Cushing’s disease,Diabetes insipidus,Diabetes insípida,Déficit de vasopresina,Enfermedad de cushing,Hiponatremia,Hyponatremia,Non-functioning pituitary tumor,PITNET,Pituitary tumor,SIADH,Transsphenoidal surgery,Tumor hipofisario,Vasopressin deficiency
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling
Author(s):
Schuermans N, El Chehadeh S, Hemelsoet D, Gautheron J, Vantyghem M, Nouioua S, Tazir M, Vigouroux C, Auclair M, Bogaert E, Dufour S, Okawa F, Hilbert P, Van Doninck N, Taquet M, Rosseel T, De Clercq G, Debackere E, Van Haverbeke C, Cherif FR, Urtizberea JA, Chanson J, Funalot B, Authier F, Kaya S, Terryn W, Callens S, Depypere B, Van Dorpe J, Vanlander AV, Verloo P, Coucke PJ, Poppe B, Impens F, Mizushima N, Depienne C, Jéru I, Dermaut B
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
Genetic lipodystrophy
Publication:
Nature Genetics v55.11 p1929-1940
Year:
2023
ORPHAcode / other:
ORPHA98305
Expected Basal Insulin Requirement During Continuous Subcutaneous Insulin Infusion Therapy by Age Group, Sex, and Body Mass Index, Based on 25,718 Young People with Type 1 Diabetes in the DPV Registry
Author(s):
Biester T, Eckert A, Becker M, Boettcher C, Golembowski S, Heidtmann B, Klinkert C, Müther S, Rami-Merhar B, Holl RW
Affiliated Institution / ERN:
Centre Hospitalier de Luxembourg ;
Condition / Disease:
diabetes type 1
Publication:
Diabetes Technology & Therapeutics v25.11 p774-781
Year:
2023
ORPHAcode / other:
DOI:
10.1089/dia.2023.0283
Keywords:
Automated insulin dosage,Basal rate,Continuous subcutaneous insulin infusion,Insulin pump,Type 1 diabetes
A Prospective Multicenter Study Examining the Relationship Between Thyroid Cancer Treatment Outcomes and the Presence of Autoimmune Thyroiditis
Author(s):
De Leo S, D'Elia S, Grani G, Dondi F, Bertagna F, Puxeddu E, Morelli S, Piovesan A, Nervo A, Zatelli MC, Gagliardi I, Samà MT, Aimaretti G, Crocetti U, Massa M, Deandrea M, Retta F, Pagano L, Rossi M, Solaroli E, Pezzullo L, Chiofalo MG, Pontecorvi A, Lombardi CP, Antonelli A, Patrizio A, Messuti I, Magri F, Spiazzi G, Ceresini G, Bruno R, Sparano C, Centanni M, Crescenzi A, Tallini G, Marotta V, Madeo B, Mian C, Filetti S, Durante C, Fugazzola L
Affiliated Institution / ERN:
AOU - Ferrara ; University Hospital of Padova ; AOU-Bologna ;
Condition / Disease:
Oncogenic osteomalacia
Publication:
Thyroid® v33.11 p1318-1326
Year:
2023
ORPHAcode / other:
ORPH352540
Pituitary macroadenomas in childhood and adolescence: a clinical analysis of 7 patients
Author(s):
Aguilar-Riera C, Clemente M, González-Llorens N, Mogas E, Campos-Martorell A, Fàbregas A, Biagetti B, Vázquez E, Yeste D
Affiliated Institution / ERN:
Hospital Universitari Vall d’Hebron ;
Condition / Disease:
pituitary adenoma
Publication:
Clinical Diabetes and Endocrinology v9.1
Year:
2023
ORPHAcode / other:
ORPHA99408
DOI:
10.1186/s40842-023-00153-6
Keywords:
Adolescent,Cabergoline,Child,Genetic analysis,Macroadenoma,Transsphenoidal
XLH Matters 2022: Insights and recommendations to improve outcomes for people living with X-linked hypophosphataemia (XLH)
Author(s):
Seefried L, Alzahrani A, Arango Sancho P, Bacchetta J, Crowley R, Emma F, Gibbins J, Grandone A, Javaid MK, Mindler G, Raimann A, Rothenbuhler A, Tucker I, Zeitlin L, Linglart A
Affiliated Institution / ERN:
Hôpital Bicêtre ; AOU University of Campania "Luigi Vanvitelli", Naples ;
Condition / Disease:
XLH
Publication:
Orphanet Journal of Rare Diseases v18.S2
Year:
2023
ORPHAcode / other:
ORPHA89936
Perinatally diagnosed congenital craniopharyngiomas in the KRANIOPHARYNGEOM trials
Author(s):
Beckhaus J, Boekhoff S, Scheinemann K, Schilling FH, Fleischhack G, Binder G, Bison B, Pietsch T, Friedrich C, Müller HL
Affiliated Institution / ERN:
Universitätsklinikum Tübingen ;
Condition / Disease:
craniopharyngioma
Publication:
Endocrine Connections v12.12
Year:
2023
ORPHAcode / other:
ORPHA54595
DOI:
10.1530/ec-23-0294
Keywords:
congenital,craniopharyngioma,irradiation,neurosurgery,quality of life
Perinatal asphyxia and hypothermic treatment from the endocrine perspective
Author(s):
Improda N, Capalbo D, Poloniato A, Garbetta G, Dituri F, Penta L, Aversa T, Sessa L, Vierucci F, Cozzolino M, Vigone MC, Tronconi GM, del Pistoia M, Lucaccioni L, Tuli G, Munarin J, Tessaris D, de Sanctis L, Salerno M
Affiliated Institution / ERN:
San Raffaele hospital - Milan ;
Condition / Disease:
Perinatal asphyxia and hypothermic treatment
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
DOI:
10.3389/fendo.2023.1249700
Keywords:
electrolytes disturbances,endocrine sequelae,glucose abnormalities,hypothermic treatment,perinatal asphyxia,stress adaptations
Editorial: Thyroid nodules and tumors in childhood
Author(s):
de Sanctis L, Wasniewska M, Vigone MC
Affiliated Institution / ERN:
San Raffaele hospital - Milan ;
Condition / Disease:
Thyroid cancer
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA146
DOI:
10.3389/fendo.2023.1303749
Keywords:
ACR-TIRADS,EU-TIRADS,FNAB,del22q11 syndrome,phosphatase and tensin homolog deleted on chromosome 10 (PTEN),thyroid cancer,thyroid nodules,thyroiditis
Neonatal and Early Infancy Features of Patients With Inactivating PTH/PTHrP Signaling Disorders/Pseudohypoparathyroidism
Author(s):
Del Sindaco G, Berkenou J, Pagnano A, Rothenbuhler A, Arosio M, Mantovani G, Linglart A
Affiliated Institution / ERN:
Hôpital Bicêtre ; Foundation IRCCS CA'Granda Ospedale Maggiore polyclinic - Milan ;
Condition / Disease:
Inactivating PTH,PTHrP Signaling Disorders,Pseudohypoparathyroidism
Publication:
The Journal of Clinical Endocrinology & Metabolism v108.11 p2961-2969
Year:
2023
ORPHAcode / other:
ORPHA97593
DOI:
10.1210/clinem/dgad236
Keywords:
ectopic ossifications,infancy,neonatal complications,newborns,pseudohypoparathyroidism
Impact of Newborn Screening on Adult Height in Patients With Congenital Adrenal Hyperplasia (CAH)
Author(s):
Hoyer-Kuhn H, Eckert AJ, Binder G, Bonfig W, Dübbers A, Riedl S, Woelfle J, Dörr HG, Holl RW
Affiliated Institution / ERN:
Universitätsklinikum Tübingen ; Klinikum Wels Grieskirchen ;
Condition / Disease:
Congenital Adrenal Hyperplasia
Publication:
The Journal of Clinical Endocrinology & Metabolism v108.11 pe1199-e1204
Year:
2023
ORPHAcode / other:
ORPHA418
DOI:
10.1210/clinem/dgad307
Keywords:
CYP21A2,congenital adrenal hyperplasia,near adult height,newborn screening
Comorbidities in mild autonomous cortisol secretion and the effect of treatment: systematic review and meta-analysis
Author(s):
Pelsma ICM, Fassnacht M, Tsagarakis S, Terzolo M, Tabarin A, Sahdev A, Newell-Price J, Marina L, Lorenz K, Bancos I, Arlt W, Dekkers OM
Affiliated Institution / ERN:
Evangelismos General Hospital ;
Condition / Disease:
Cushing syndrome
Publication:
European Journal of Endocrinology v189.4 pS88-S101
Year:
2023
ORPHAcode / other:
ORPHA647758; ORPHA189427; ORPHA314749;
DOI:
10.1093/ejendo/lvad134
Keywords:
adrenal adenoma,comorbidities,cortisol,mild autonomous cortisol secretion,systematic review
Hormonal control during infancy and testicular adrenal rest tumor development in males with congenital adrenal hyperplasia: a retrospective multicenter cohort study
Author(s):
Schröder MAM, Neacşu M, Adriaansen BPH, Sweep FCGJ, Ahmed SF, Ali SR, Bachega TASS, Baronio F, Birkebæk NH, de Bruin C, Bonfig W, Bryce J, Clemente M, Cools M, Elsedfy H, Globa E, Guran T, Güven A, Amr NH, Janus D, Taube NL, Markosyan R, Miranda M, PoyrazoÄlu Å, Rees A, Salerno M, Stancampiano MR, Vieites A, de Vries L, Yavas Abali Z, Span PN, Claahsen-van der Grinten HL
Affiliated Institution / ERN:
Klinikum Wels Grieskirchen ; Aarhus University Hospital ; AOU Federico II - Naples ; Radboud University Medical Centre Nijmegen ; AOU-Bologna ;
Condition / Disease:
Congenital adrenal hyperplasia
Publication:
European Journal of Endocrinology v189.4 p460-468
Year:
2023
ORPHAcode / other:
ORPHA418
DOI:
10.1093/ejendo/lvad143
Keywords:
congenital adrenal hyperplasia,diagnosis,early childhood,testicular adrenal rest tumors
Therapeutic Management and Long-Term Outcome of Hyperthyroidism in Patients with Antithyroid-Induced Agranulocytosis: A Retrospective, Multicenter Study
Author(s):
García Gómez C, Navarro E, Alcázar V, López-Guzmán A, Arrieta F, Anda E, Biagetti B, Guerrero-Pérez F, Villabona C, de Assín Valverde AR, Lamas C, Lecumberri B, Rosado Sierra JA, Sastre J, Díez JJ, Iglesias P
Affiliated Institution / ERN:
Hospital Universitari Vall d’Hebron ;
Condition / Disease:
Antithyroid-Induced Agranulocytosis, Hyperthyroidism
Publication:
Journal of Clinical Medicine v12.20 p6556
Year:
2023
ORPHAcode / other:
DOI:
10.3390/jcm12206556
Keywords:
antithyroid drug-induced agranulocytosis (AIA),carbimazole (CBZ),methimazole (MMI),propylthiouracil (PTU)
Gender-related differences in patients with carcinoid syndrome: new insights from an Italian multicenter cohort study
Author(s):
Ruggeri RM, Altieri B, Razzore P, Retta F, Sperti E, Scotto G, Brizzi MP, Zumstein L, Pia A, Lania A, Lavezzi E, Nappo G, Laffi A, Albertelli M, Boschetti M, Hasballa I, Veresani A, Prinzi N, Pusceddu S, Oldani S, Nichetti F, Modica R, Minotta R, Liccardi A, Cannavale G, Grossrubatscher EM, Tarsitano MG, Zamponi V, Zatelli MC, Zanata I, Mazzilli R, Appetecchia M, Davì MV, Guarnotta V, Giannetta E, La Salvia A, Fanciulli G, Malandrino P, Isidori AM, Colao A, Faggiano A
Affiliated Institution / ERN:
AOU Federico II - Naples ; AOU polyclinic "G.Martino" of Messina ; IRCCS Ospedale Policlinico San Martino – Genova ; AOU Policlinico Umberto I - Rome ; AOU - Ferrara ;
Condition / Disease:
Hereditary pheochromocytoma-paraganglioma
Publication:
Journal of Endocrinological Investigation v47.4 p959-971
Year:
2023
ORPHAcode / other:
ORPHA29072
DOI:
10.1007/s40618-023-02213-1
Keywords:
Carcinoid syndrome,Gender,Gender medicine,Neuroendocrine neoplasm,Neuroendocrine tumors,Prognosis,Sex
Long-term efficacy and safety of subcutaneous pasireotide alone or in combination with cabergoline in Cushing’s disease
Author(s):
Feelders RA, Fleseriu M, Kadioglu P, Bex M, González-Devia D, Boguszewski CL, Yavuz DG, Patino H, Pedroncelli AM, Maamari R, Chattopadhyay A, Biller BMK, Pivonello R
Affiliated Institution / ERN:
AOU Federico II - Naples ;
Condition / Disease:
Cushing's disease
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA96253
DOI:
10.3389/fendo.2023.1165681
Keywords:
Cushing’s disease,cabergoline,hypercortisolism,pasireotide,somatostatin
The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion
Author(s):
Murphy R, Colclough K, Pollin TI, Ikle JM, Svalastoga P, Maloney KA, Saint-Martin C, Molnes J, Tobias DK, Merino J, Ahmad A, Aiken C, Benham JL, Bodhini D, Clark AL, Colclough K, Corcoy R, Cromer SJ, Duan D, Felton JL, Francis EC, Gillard P, Gingras V, Gaillard R, Haider E, Hughes A, Ikle JM, Jacobsen LM, Kahkoska AR, Kettunen JLT, Kreienkamp RJ, Lim L, Männistö JME, Massey R, Mclennan N, Miller RG, Morieri ML, Most J, Naylor RN, Ozkan B, Patel KA, Pilla SJ, Prystupa K, Raghaven S, Rooney MR, Schön M, Semnani-Azad Z, Sevilla-Gonzalez M, Takele WW, Tam CH, Thuesen ACB, Tosur M, Wallace AS, Wang CC, Wong JJ, Yamamoto JM, Young K, Amouyal C, Andersen MK, Bonham MP, Chen M, Cheng F, Chikowore T, Chivers SC, Clemmensen C, Dabelea D, Dawed AY, Deutsch AJ, Dickens LT, DiMeglio LA, Dudenhöffer-Pfeifer M, Evans-Molina C, Fernández-Balsells MM, Fitipaldi H, Fitzpatrick SL, Gitelman SE, Goodarzi MO, Grieger JA, Guasch-Ferré M, Habibi N, Hansen T, Huang C, Harris-Kawano A, Ismail HM, Hoag B, Johnson RK, Jones AG, Koivula RW, Leong A, Leung GKW, Libman IM, Liu K, Long SA, Lowe WL, Morton RW, Motala AA, Onengut-Gumuscu S, Pankow JS, Pathirana M, Pazmino S, Perez D, Petrie JR, Powe CE, Quinteros A, Jain R, Ray D, Ried-Larsen M, Saeed Z, Santhakumar V, Kanbour S, Sarkar S, Monaco GSF, Scholtens DM, Selvin E, Sheu WH, Speake C, Stanislawski MA, Steenackers N, Steck AK, Stefan N, Støy J, Taylor R, Tye SC, Ukke GG, Urazbayeva M, Van der Schueren B, Vatier C, Wentworth JM, Hannah W, White SL, Yu G, Zhang Y, Zhou SJ, Beltrand J, Polak M, de Franco E, Flanagan SE, Maloney KA, McGovern A, Nakabuye M, Njølstad PR, Pomares-Millan H, Provenzano M, Zhang C, Zhu Y, Auh S, de Souza R, Fawcett AJ, Gruber C, Mekonnen EG, Mixter E, Sherifali D, Eckel RH, Nolan JJ, Philipson LH, Brown RJ, Billings LK, Boyle K, Costacou T, Dennis JM, Florez JC, Gloyn AL, Gomez MF, Gottlieb PA, Greeley SAW, Griffin K, Hattersley AT, Hirsch IB, Hivert M, Hood KK, Josefson JL, Kwak SH, Laffel LM, Lim SS, Loos RJF, Ma RCW, Mathieu C, Mathioudakis N, Meigs JB, Misra S, Mohan V, Murphy R, Oram R, Owen KR, Ozanne SE, Pearson ER, Perng W, Pollin TI, Pop-Busui R, Pratley RE, Redman LM, Redondo MJ, Reynolds RM, Semple RK, Sherr JL, Sims EK, Sweeting A, Tuomi T, Udler MS, Vesco KK, Vilsbøll T, Wagner R, Rich SS, Franks PW, Misra S, Aukrust I, de Franco E, Flanagan SE, Njølstad PR, Billings LK, Owen KR, Gloyn AL
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
monogenic diabetes
Publication:
Communications Medicine v3.1
Year:
2023
ORPHAcode / other:
ORPHA552
The highly and perpetually upregulated thyroglobulin gene is a hallmark of functional thyrocytes
Author(s):
Ullrich S, Leidescher S, Feodorova Y, Thanisch K, Fini J, Kaspers B, Weber F, Markova B, Führer D, Romitti M, Krebs S, Blum H, Leonhardt H, Costagliola S, Heuer H, Solovei I
Affiliated Institution / ERN:
University Hospital Essen ;
Condition / Disease:
thyroglobulin gene
Publication:
Frontiers in Cell and Developmental Biology v11
Year:
2023
ORPHAcode / other:
DOI:
10.3389/fcell.2023.1265407
Keywords:
gene upregulation,thyroglobulin gene,thyroid hormones,transcription,transcription loop
Application of calcium-to-phosphorus (Ca/P) ratio in the diagnosis of pseudohypoparathyroidism: another piece in the puzzle of diagnosis of Ca-P metabolism disorders
Author(s):
De Vincentis S, Del Sindaco G, Pagnano A, Brigante G, Moretti A, Zirilli L, Rochira V, Simoni M, Mantovani G, Madeo B
Affiliated Institution / ERN:
Foundation IRCCS CA'Granda Ospedale Maggiore polyclinic - Milan ;
Condition / Disease:
Inactivating PTH/PTHrP Signaling Disorders/Pseudohypoparathyroidism
Publication:
Frontiers in Endocrinology v14
Year:
2023
ORPHAcode / other:
ORPHA97593
DOI:
10.3389/fendo.2023.1268704
Keywords:
hyperphosphatemia,hypocalcemia,hypoparathyroidism,mineral disorders,parathyroid dysfunctions
Subcentimetric papillary thyroid carcinoma with extensive lymph node and brain metastasis: case report and review of literature
Author(s):
Amado A, Teixeira E, Canberk S, Macedo S, Castro B, Pereira H, Varanda J, Graça S, Tavares A, Soares C, Oliveira MJ, Oliveira M, Soares P, Sobrinho Simões M, Póvoa AA
Affiliated Institution / ERN:
São João University Hospital(CHUSJ) ;
Condition / Disease:
papillary thyroid carcinoma
Publication:
Endocrinology, Diabetes & Metabolism Case Reports v2023.4
Year:
2023
ORPHAcode / other:
ORPHA146
Endocortical Trabecularization in Acromegaly: The Cause for the Paradoxically Increased Vertebral Fracture Risk?
Author(s):
Heck A, Godang K, Lekva T, Markussen KN, De Vincentis S, Ueland T, Bollerslev J
Affiliated Institution / ERN:
AOU - Modena ; Oslo University Hospital ;
Condition / Disease:
Acromegaly
Publication:
JBMR Plus v7.10
Year:
2023
ORPHAcode / other:
ORPHA963
Testosterone Restores Body Composition, Bone Mass, and Bone Strength Following Early Puberty Suppression in a Mouse Model Mimicking the Clinical Strategy in Trans Boys
Author(s):
Dubois V, Ciancia S, Doms S, El Kharraz S, Sommers V, Kim NR, David K, Van Dijck J, Valle-Tenney R, Maes C, Antonio L, Decallonne B, Carmeliet G, Claessens F, Cools M, Vanderschueren D
Affiliated Institution / ERN:
UZ Leuven ;
Condition / Disease:
Gender dysphoria
Publication:
Journal of Bone and Mineral Research v38.10 p1497-1508
Year:
2023
ORPHAcode / other:
HA61
Giant prolactinomas, a detailed analysis of 196 adult cases
Author(s):
Lisa B, Arno V, Christophe DB, Heyning Paul Vd, Carlien DH
Affiliated Institution / ERN:
UZ Antwerpen ;
Condition / Disease:
Prolactinoma
Publication:
Pituitary v26.5 p529-537
Year:
2023
ORPHAcode / other:
ORPHA2965
DOI:
10.1007/s11102-023-01337-0
Keywords:
Dopamine agonists,Giant prolactinoma,Hyperprolactinemia,Prolactin,Prolactinoma
Pilot study to define criteria for Pituitary Tumors Centers of Excellence (PTCOE): results of an audit of leading international centers
Author(s):
Giustina A, Uygur MM, Frara S, Barkan A, Biermasz NR, Chanson P, Freda P, Gadelha M, Kaiser UB, Lamberts S, Laws E, Nachtigall LB, Popovic V, Reincke M, Strasburger C, van der Lely AJ, Wass JAH, Melmed S, Casanueva FF
Affiliated Institution / ERN:
Charité Universitätsmedizin Berlin ;
Condition / Disease:
Pituitary adenoma
Publication:
Pituitary v26.5 p583-596
Year:
2023
ORPHAcode / other:
ORPHA99408
DOI:
10.1007/s11102-023-01345-0
Keywords:
Acromegaly,Centers of Excellence,Criteria,Cushing’s disease,Medical treatment,Neurosurgery,Pituitary tumors,Prolactinoma
Characterisation and clinical outcomes in children and adolescents with diabetes according to newly defined subgroups: a cohort study from the DPV registry
Author(s):
Warncke K, Eckert A, Bonifacio E, Achenbach P, Kordonouri O, Meissner T, Ohlenschläger U, Bonfig W, Ziegler A, Holl RW
Affiliated Institution / ERN:
Klinikum Wels Grieskirchen ;
Condition / Disease:
diabetes type 1
Publication:
eClinicalMedicine v64 p102208
Year:
2023
ORPHAcode / other:
DOI:
10.1016/j.eclinm.2023.102208
Keywords:
Children,Complications,Diabetes,Personalised medicine,Subgroups
Giant prolactinomas, a detailed analysis of 196 adult cases
Author(s):
Billion L, Verleye A, Block CD, Heyning PVd, Herdt CD
Affiliated Institution / ERN:
UZ Antwerpen ;
Condition / Disease:
Prolactinoma
Publication:
Pituitary v26.5 p529-537
Year:
2023
ORPHAcode / other:
ORPHA2965
DOI:
10.1007/s11102-023-01337-0
Keywords:
Dopamine agonists,Giant prolactinoma,Hyperprolactinemia,Prolactin,Prolactinoma
Adjuvant mitotane versus surveillance in low-grade, localised adrenocortical carcinoma (ADIUVO): an international, multicentre, open-label, randomised, phase 3 trial and observational study
Author(s):
Terzolo M, Fassnacht M, Perotti P, Libé R, Kastelan D, Lacroix A, Arlt W, Haak HR, Loli P, Decoudier B, Lasolle H, Quinkler M, Haissaguerre M, Chabre O, Caron P, Stigliano A, Giordano R, Zatelli MC, Bancos I, Fragoso MCBV, Canu L, Luconi M, Puglisi S, Basile V, Reimondo G, Kroiss M, Megerle F, Hahner S, Kimpel O, Dusek T, Nölting S, Bourdeau I, Chortis V, Ettaieb MH, Cosentini D, Grisanti S, Baudin E, Berchialla P, Bovis F, Sormani MP, Bruzzi P, Beuschlein F, Bertherat J, Berruti A
Affiliated Institution / ERN:
AO City of Health and Science - Turin ;
Condition / Disease:
Adrenocortical carcinomas
Publication:
The Lancet Diabetes & Endocrinology v11.10 p720-730
Year:
2023
ORPHAcode / other:
ORPHA1501
Recent data on iodine intake in Croatian schoolchildren: results of 2014–2019 survey
Author(s):
Filipan D, Vidranski V, Bosak Butković M, Blažeković I, Romić M, Mihaljević I, Bogović Crnčić T, Kusić Z, Šamija I, Fröbe A, Jukić T
Affiliated Institution / ERN:
Sestre milosrdnice University Hospital Center ;
Condition / Disease:
Thyroid volume iodine intake hypothyroidism
Publication:
European Journal of Clinical Nutrition v77.10 p959-965
Year:
2023
ORPHAcode / other:
Unravelling leptin variants: advancing precision medicine in obesity
Author(s):
Dubern B, Clément K
Affiliated Institution / ERN:
Assistance Publique-Hôpitaux de Paris, Hôpital Pitié-Salpétrière ;
Condition / Disease:
obesity associated with defect in leptin/melanocortin pathway
Publication:
Nature Reviews Endocrinology v19.10 p562-563
Year:
2023
ORPHAcode / other:
ORPHA77828
Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine
Author(s):
Tobias DK, Merino J, Ahmad A, Aiken C, Benham JL, Bodhini D, Clark AL, Colclough K, Corcoy R, Cromer SJ, Duan D, Felton JL, Francis EC, Gillard P, Gingras V, Gaillard R, Haider E, Hughes A, Ikle JM, Jacobsen LM, Kahkoska AR, Kettunen JLT, Kreienkamp RJ, Lim L, Männistö JME, Massey R, Mclennan N, Miller RG, Morieri ML, Most J, Naylor RN, Ozkan B, Patel KA, Pilla SJ, Prystupa K, Raghavan S, Rooney MR, Schön M, Semnani-Azad Z, Sevilla-Gonzalez M, Svalastoga P, Takele WW, Tam CH, Thuesen ACB, Tosur M, Wallace AS, Wang CC, Wong JJ, Yamamoto JM, Young K, Amouyal C, Andersen MK, Bonham MP, Chen M, Cheng F, Chikowore T, Chivers SC, Clemmensen C, Dabelea D, Dawed AY, Deutsch AJ, Dickens LT, DiMeglio LA, Dudenhöffer-Pfeifer M, Evans-Molina C, Fernández-Balsells MM, Fitipaldi H, Fitzpatrick SL, Gitelman SE, Goodarzi MO, Grieger JA, Guasch-Ferré M, Habibi N, Hansen T, Huang C, Harris-Kawano A, Ismail HM, Hoag B, Johnson RK, Jones AG, Koivula RW, Leong A, Leung GKW, Libman IM, Liu K, Long SA, Lowe WL, Morton RW, Motala AA, Onengut-Gumuscu S, Pankow JS, Pathirana M, Pazmino S, Perez D, Petrie JR, Powe CE, Quinteros A, Jain R, Ray D, Ried-Larsen M, Saeed Z, Santhakumar V, Kanbour S, Sarkar S, Monaco GSF, Scholtens DM, Selvin E, Sheu WH, Speake C, Stanislawski MA, Steenackers N, Steck AK, Stefan N, Støy J, Taylor R, Tye SC, Ukke GG, Urazbayeva M, Van der Schueren B, Vatier C, Wentworth JM, Hannah W, White SL, Yu G, Zhang Y, Zhou SJ, Beltrand J, Polak M, Aukrust I, de Franco E, Flanagan SE, Maloney KA, McGovern A, Molnes J, Nakabuye M, Njølstad PR, Pomares-Millan H, Provenzano M, Saint-Martin C, Zhang C, Zhu Y, Auh S, de Souza R, Fawcett AJ, Gruber C, Mekonnen EG, Mixter E, Sherifali D, Eckel RH, Nolan JJ, Philipson LH, Brown RJ, Billings LK, Boyle K, Costacou T, Dennis JM, Florez JC, Gloyn AL, Gomez MF, Gottlieb PA, Greeley SAW, Griffin K, Hattersley AT, Hirsch IB, Hivert M, Hood KK, Josefson JL, Kwak SH, Laffel LM, Lim SS, Loos RJF, Ma RCW, Mathieu C, Mathioudakis N, Meigs JB, Misra S, Mohan V, Murphy R, Oram R, Owen KR, Ozanne SE, Pearson ER, Perng W, Pollin TI, Pop-Busui R, Pratley RE, Redman LM, Redondo MJ, Reynolds RM, Semple RK, Sherr JL, Sims EK, Sweeting A, Tuomi T, Udler MS, Vesco KK, Vilsbøll T, Wagner R, Rich SS, Franks PW
Affiliated Institution / ERN:
Aarhus University Hospital ;
Condition / Disease:
Precision diabetes medicine
Publication:
Nature Medicine v29.10 p2438-2457
Year:
2023
ORPHAcode / other:
ORPHA552
