Suchergebnisse - "Castillejo, Adela"

PubPharm (74)

1

Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome

enthalten in: Orphanet journal of rare diseases | 2024

von Sánchez-Heras, A. | Dámaso, E. | Castillejo, A. | +17

2

Genetic and clinical characterization of a novel FH founder mutation in families with hereditary leiomyomatosis and renal cell cancer syndrome

enthalten in: Orphanet journal of rare diseases | 2024

von Sánchez-Heras, A. | Dámaso, E. | Castillejo, A. | +17

3

Lynch-like Syndrome : Potential Mechanisms and Management

enthalten in: Cancers | 2022

von Martínez-Roca, A. | Giner-Calabuig, M. | Murcia, O. | +4

4

Co-occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

enthalten in: Cancer communications (London, England) | 2021

von Ferrer-Avargues, R. | Castillejo, M. | Dámaso, E. | +8

5

Metagenomic analysis of formalin-fixed paraffin-embedded tumor and normal mucosa reveals differences in the microbiome of colorectal cancer patients

enthalten in: Scientific reports | 2021

von Debesa-Tur, G. | Pérez-Brocal, V. | Ruiz-Ruiz, S. | +4

6

Co‐occurrence of germline pathogenic variants for different hereditary cancer syndromes in patients with Lynch syndrome

enthalten in: Cancer Communications | 2021

von Ferrer‐Avargues, R. | Castillejo, M. | Dámaso, E. | +8

7

Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome in Spain : Clinical and Genetic Characterization

enthalten in: Cancers | 2020

von Sánchez-Heras, A. | Castillejo, A. | García-Díaz, J. | +22

8

Risk of Cancer in Family Members of Patients with Lynch-Like Syndrome

enthalten in: Cancers | 2020

von Picó, M. | Sánchez-Heras, A. | Castillejo, A. | +27

9

Clinical and Pathological Characterization of Lynch-Like Syndrome

enthalten in: Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association | 2020

von Picó, M. | Castillejo, A. | Murcia, �. | +30

CommentIn: Clin Gastroenterol Hepatol. 2020 Feb;18(2):294-296. - PMID 31408703

10

Implementation of massive sequencing in the genetic diagnosis of hereditary cancer syndromes : diagnostic performance in the Hereditary Cancer Programme of the Valencia Community (FamCan-NGS)

enthalten in: Hereditary cancer in clinical practice | 2019

von Ramírez-Calvo, M. | García-Casado, Z. | Fernández-Serra, A. | +14

1
2
3
4
5
6
7
8
Nächster »
[8]