Portal de investigación
ESTUDIO RETROSPECTIVO SOBRE LA INFLUENCIA DE LA EDAD DE INICIO DEL TRATAMIENTO CON GH EN LA GANANCIA DE TALLA EN NIÑOS NACIDOS PEG.
Datos básicos
- Código:
- PFI-SOM-2011-01
- Protocolo:
- PFI-SOM-2011-01
- EUDRACT:
- NCT:
- Centro:
- HOSPITAL UNIVERSITARI I POLITÈCNIC LA FE
- Dotación:
- Año de incio:
- 2012
- Año de finalización:
- 2013
Objetivos del proyecto
Observaciones: Estado Comité: FINALIZADO
Documentos
- No hay documentos
Participantes
Financiadores - Promotores
Resultados del Ensayo Clínico
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
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
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
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