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:
ESTUDIO OBSERVACIONAL INTERNACIONAL

Objetivos del proyecto

Observaciones: Estado Comité: ACTIVO

Documentos

  • No hay documentos

Participantes

Grupos

Financiadores - Promotores

IPSEN PHARMA S.A.U.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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

  • Open Access.

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


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