E-LIB Suche - Ergebnisse für: Bonis, Ana Coral Barreda

1

Achondroplasia: Update on diagnosis, follow-up and treatmen:

Leiva-Gea, Antonio ; Martos Lirio, María F. ; Barreda Bonis, Ana Coral...
Anales de Pediatría (English Edition). 97 (2022) 6 - p. 423.e1-423.e11 , 2022

Link: https://doi.org/10.1016/..

2

Acondroplasia: actualización en diagnóstico, seguimiento y ..:

Leiva-Gea, Antonio ; Martos Lirio, María F. ; Barreda Bonis, Ana Coral...
Anales de Pediatría. 97 (2022) 6 - p. 423-423.e10 , 2022

Link: https://doi.org/10.1016/..

3

Achondroplasia: Update on diagnosis, follow-up and treatmen:

Leiva-Gea, Antonio ; Lirio, Maria F. Martos ; Bonis, Ana Coral Barreda...
1695-4033. , 2022

Link: http://hdl.handle.net/10..

4

Transition of patients with metabolic bone disease from pae..:

Casado, Enrique ; Gómez-Alonso, Carlos ; Pintos-Morell, Guillem...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

5

Multiple SLC26A2 mutations occurring in a three-generationa..:

Barreda-Bonis, Ana Coral ; Barraza-García, Jimena ; Parrón, Manuel...
European Journal of Medical Genetics. 61 (2018) 1 - p. 24-28 , 2018

Link: https://doi.org/10.1016/..

6

Familial glucocorticoid deficiency due to compound heterozy..:

Aza-Carmona, Miriam ; Barreda-Bonis, Ana Coral ; Guerrero-Fernández, Julio...
Journal of Pediatric Endocrinology and Metabolism. 24 (2011) 5-6 - p. , 2011

Link: https://doi.org/10.1515/..

7

Transition of patients with metabolic bone disease from pae..:

Casado, Enrique ; Gomez Alonso, Carlos ; Bou, Rosa...
Orphanet Journal of Rare Diseases;18. , 2023

Link: https://hdl.handle.net/1..

8

Acondroplasia: actualización en diagnóstico, seguimiento y ..:

Antonio Leiva Gea ; María F. Martos Lirio ; Ana Coral Barreda Bonis...
http://www.sciencedirect.com/science/article/pii/S1695403322002284. , 2022

Link: https://doi.org/10.1016/..

9

Achondroplasia: Update on diagnosis, follow-up and treatmen..:

Leiva-Gea, Antonio ; Martos Lirio, María Fuensanta ; Barreda Bonis, Ana Coral...
Anales de Pediatría (English Edition);97(6). , 2022

Link: https://hdl.handle.net/1..

10

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic g..:

Leiter, Sarah M ; Parker, Victoria E R ; Welters, Alena...
European Journal of Endocrinology. 177 (2017) 2 - p. 175-186 , 2017

Link: https://doi.org/10.1530/..

11

Transition of patients with metabolic bone disease from pae..:

Enrique Casado ; Carlos Gómez-Alonso ; Guillem Pintos-Morell...
https://doi.org/10.1186/s13023-023-02856-6. , 2023

Link: https://doi.org/10.1186/..

12

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic g..:

Leiter, Sarah M ; Parker, Victoria E R ; Welters, Alena...
https://eprints.soton.ac.uk/428808/1/hypoinsulinaemic_hypoketotic_pik3.pdf. , 2017

Link: https://eprints.soton.ac..

13

Hypoinsulinaemic, hypoketotic hypoglycaemia due to mosaic g..:

Leiter, Sarah M ; Parker, Victoria ER ; Welters, Alena...
https://www.repository.cam.ac.uk/handle/1810/266663. , 2017

Link: https://www.repository.c..

14

Heterozygous aggrecan variants are associated with short st..:

Sentchordi‐Montané, Lucía ; Aza‐Carmona, Miriam ; Benito‐Sanz, Sara...
Clinical Endocrinology. 88 (2018) 6 - p. 820-829 , 2018

Link: https://doi.org/10.1111/..

15

Central Hypothyroidism and Novel Clinical Phenotypes in Hem..:

García, Marta ; Barreda-Bonis, Ana C ; Jiménez, Paula...
Journal of the Endocrine Society. 3 (2018) 1 - p. 119-128 , 2018

Link: https://doi.org/10.1210/..