M. Lozano

High IGKC-Expressing Intratumoral Plasma Cells Predict Response to Immune Checkpoint Blockade

E. Alba, C. D. de Andrea, M. Cobo, 2022, International journal of molecular sciences.

An unusual concurrence of graft versus host disease caused by engraftment of maternal lymphocytes with DiGeorge anomaly

F. Leyva-Cobián, J. Ocejo-Vinyals, J. E. Paz-Miguel, 2000, Archives of disease in childhood.

Simultaneous multiorgan presence of human herpesvirus 8 and restricted lymphotropism of Epstein-Barr virus DNA sequences in a human immunodeficiency virus-negative immunodeficient infant.

F. Leyva-Cobián, J. Ocejo-Vinyals, J. Gómez-Román, 2001, The Journal of infectious diseases.

Mutation hotspots in the PHKA2 gene in X-linked liver glycogenosis due to phosphorylase kinase deficiency with atypical activity in blood cells (XLG2).

B. Burwinkel, I. Maire, H. Bakker, 1996, Human molecular genetics.

Frequency of microsatellite instability (MSI) in upper tract urothelial carcinoma: comparison of the Bethesda panel and the Idylla MSI assay in a consecutively collected, multi-institutional cohort

Y. Allory, I. Bièche, R. Stoehr, 2021, Journal of Clinical Pathology.

Hepatic phosphorylase b kinase deficiency with normal enzyme activity in erythrocytes and muscle

L. V. García, M. Lozano, T. Benlloch, 1994, Journal of Inherited Metabolic Disease.

Regulatory CDH4 Genetic Variants Associate With Risk to Develop Capecitabine‐Induced Hand‐Foot Syndrome

J. Benítez, R. Milne, A. González-Neira, 2020, Clinical pharmacology and therapeutics.