ESTUDIO COOPERATIVO INTERNACIONAL DEL CRECIMIENTO
Datos básicos
- Protocolo:
- IPS-SOM-2007-02
- EUDRACT:
- NCT:
- Centro:
- HOSPITAL UNIVERSITARI I POLITÈCNIC LA FE
- Año de incio:
- 2009
- Año de finalización:
Objetivos del proyecto
Observaciones: Estado Comité: ACTIVO
Documentos
- No hay documentos
Participantes
Financiadores - Promotores
Resultados del Ensayo Clínico
NR5A1/SF-1 Collaborates with Inhibin a and the Androgen Receptor
Elzenaty, Rawda Naamneh; (...); Fluck, Christa E
Article. 10.3390/ijms251810109. 2024
A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia
Alemany, MCD; (...); Carinena, SL
Article. 10.1080/19336950.2020.1761171. 2020
A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism
Hidalgo-Santos, AD; (...); Tomas-Vila, M
Article. 10.5812/ijem.67329. 2018
Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia
Ruiz, A; (...); Clarimon, J
Article. 10.1016/j.neurobiolaging.2013.08.011. 2014
Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease.
Le Guen Y; (...); Rujescu D
Article. 10.1001/jamaneurol.2022.1166. 2022
Consensus guide on prophylactic gonadectomy in different sex development.
Guerrero-Fernandez, Julio; (...); Nistal, Manuel
Article. 10.1016/j.endien.2022.10.002. 2022
Delphi consensus on the diagnosis and treatment of patients with short stature in Spain: GROW-SENS study.
Corripio-Collado, R.; (...); Labarta-Aizpun, I, J-
Letter. 10.1007/s40618-021-01696-0. 2022
Differentiated thyroid carcinoma in a girl with resistance to thyroid hormone management with triiodothyroacetic acid.
Ramos-Prol A; (...); Merino-Torres JF
Article. 10.1515/jpem-2012-0230. 2013
Endocrinological late effects of oncologic treatment on survivors of medulloblastoma
Santos, ADH; (...); Nieto, AC
Article. 10.32641/rchped.v90i6.994. 2019
Familial hyperaldosteronism type III a novel case and review of literature.
Pons Fernández N; (...); Calvo F
Article. 10.1007/s11154-018-9481-0. 2019
Human MAMLD1 Gene Variations Seem Not Sufficient to Explain a 46,XY DSD Phenotype
Camats N; (...); Fluck CE
Article. 10.1371/journal.pone.0142831. 2015
Increased IGFBP proteolysis, IGF-I bioavailability and pappalysin levels in children with Prader-Willi syndrome.
Barrios V; (...); Argente J
Article. 10.1210/clinem/dgad754. 2023
Lack of Glibenclamide Response in a Case of Permanent Neonatal Diabetes Caused by Incomplete Inactivation of Glucokinase
Oriola, J; (...); Navas, MA
Article. 10.1007/8904_2014_383. 2015
Metyrapone as treatment in the neonatal McCune-Albright syndrome
de Mingo, Carmen; (...); Garcia-Robles, Ana
Article. 10.1515/jpem-2020-0036. 2020
Mutations in PMM2 gene in four unrelated Spanish families with polycystic kidney disease and hyperinsulinemic hypoglycemia.
Moreno Macián F; (...); Albiach Mesado V
Article. 10.1515/jpem-2020-0168. 2020
Successful Second-Line Metronomic Temozolomide in Metastatic Paraganglioma: Case Reports and Review of the Literature.
Tena, I; (...); Pacak, K
Article. 10.1177/1179554918763367. 2018
Tiroidectomia profilactica en mutacion del protooncogen RET.
Rodriguez Caraballo L; (...); Vila Carbo JJ
Abstract of Published Item. 2017
Towards an experimental proof of oligogenicity explaining a severe 46, XY DSD phenotype associated with heterozygote NR5A1/SF-1 variation
Naamneh-Elzenaty, Rawda; (...); Flueck, Christa E.
Meeting Abstract. 2024
Use of [(18)F]fluorocholine PET/CT in the detection of primary hyperparathyroidism in paediatrics: a case report.
Martínez Sánchez H; (...); Sánchez Vañó R
Case Reports. 10.1515/jpem-2023-0556. 2024