E-LIB Suche - Ergebnisse für: González, Diana Vanesa

1

Encefalopatía epiléptica infantil en un paciente colombiano..:

Paredes, Angela Camila ; González, Diana Vanesa ; Espinosa, Eugenia
Shbarou R, Mikati MA. The Expanding Clinical Spectrum of Genetic Pediatric Epileptic Encephalopathies. Semin Pediatr Neurol. 2016;23(2):134-142. doi:10.1016/j.spen.2016.06.002. , 2022

Link: https://doi.org/10.31260..

2

Lifetime impact of achondroplasia study in Europe (LIAISE):..:

Maghnie, Mohamad ; Semler, Oliver ; Guillen-Navarro, Encarna...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023

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

3

Health-related quality of life (HRQoL) in achondroplasia: f..:

Maghnie, Mohamad ; Semler, Oliver ; Guillen-Navarro, Encarna...
Molecular Genetics and Metabolism. 132 (2021) - p. S127-S128 , 2021

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

4

Lifetime impact of achondroplasia in Europe (LIAISE): findi..:

Maghnie, Mohamad ; Semler, Oliver ; Guillen-Navarro, Encarna...
Molecular Genetics and Metabolism. 132 (2021) - p. S65-S66 , 2021

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

5

Encefalopatía epiléptica infantil en un paciente colombiano..:

Angela Camila Paredes ; Diana Vanesa González ; Eugenia Espinosa
https://revistas.fucsalud.edu.co/index.php/repertorio/article/view/966. , 2020

Link: https://doi.org/10.31260..

6

Oncoguía de apoyo integral en mieloma múltiple 2023:

Espinoza Zamora, José Ramiro ; Zapata Canto, Nidia Paulina ; Lozano Zavaleta, Valentín...
Latin american journal of clinical sciences and medical technology. 6 (2024) 1 - p. 64-74 , 2024

Link: https://doi.org/10.34141..

7

Oncoguía de mieloma múltiple 2023:

Espinoza Zamora, José Ramiro ; Zapata Canto, Nidia Paulina ; Lozano Zavaleta, Valentín...
Latin american journal of clinical sciences and medical technology. 5 (2023) 1 - p. 170-183 , 2023

Link: https://doi.org/10.34141..

8

Biological macromolecules as nutraceuticals:

, In: Biological Macromolecules,

Carbajal-Valenzuela, Ireri Alejandra ; Apolonio–Hernandez, Nuvia Marina ; Gutierrez-Chavez, Diana Vanesa... - p. 97-138 , 2022

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

9

List of contributors:

, In: Biological Macromolecules,

Abo Dena, Ahmed S. ; Acquah, Caleb ; Ahmed, Tanvir... - p. xiii-xvii , 2022

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

10

Genotype and phenotype in patients with Noonan syndrome and..:

Kouz, Karim ; Lissewski, Christina ; Spranger, Stephanie...
Genetics in Medicine. 18 (2016) 12 - p. 1226-1234 , 2016

Link: https://doi.org/10.1038/..

11

Exome sequencing unravels unexpected differential diagnoses..:

Bramswig, Nuria C. ; Lüdecke, Hermann-Josef ; Alanay, Yasemin...
Human Genetics. 134 (2015) 6 - p. 553-568 , 2015

Link: https://doi.org/10.1007/..

12

X-linked intellectual disability type Nascimento is a clini..:

Czeschik, Johanna Christina ; Bauer, Peter ; Buiting, Karin...
Orphanet Journal of Rare Diseases. 8 (2013) 1 - p. , 2013

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

13

Red "Universidad, género, docencia e igualdad":

Rodríguez-Jaume, María-José ; Contreras-Llave, Natalia ; De-Juan-Vigaray, María D...
http://hdl.handle.net/10045/85067. , 2018

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

14

Red "Universidad, género, docencia e igualdad":

Rodríguez-Jaume, María-José ; Provencio Garrigós, Herminia ; Albaladejo-Blázquez, Natalia...
http://hdl.handle.net/10045/72112. , 2017

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

15

Lifetime impact of achondroplasia study in Europe (LIAISE):..:

Maghnie, Mohamad ; Semler, Oliver ; Guillen-Navarro, Encarna...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10015810/. , 2023

Link: http://www.ncbi.nlm.nih...