Miguel Reyes‐Múgica

Assessment and classification of sex cord‐stromal tumours of the testis: recommendations from the testicular sex cord‐stromal tumour (<scp>TESST</scp>) group, an Expert Panel of the Genitourinary Pathology Society (<scp>GUPS</scp>) and International Society of Urological Pathology (<scp>ISUP</scp>)

Germ cell tumors in children

WHO Classification of Tumours: evolution of a global resource in the molecular era

Congenital melanocytic neoplasms: clinical, histopathological and recent molecular developments

Observer Variation in the Diagnosis of Testicular Sex Cord-Stromal Tumors by a Genitourinary Pathology Society and International Society of Urological Pathology Panel: Paving the Way for a New Classification

Data set for reporting paediatric renal tumours: recommendations from the international collaboration on cancer reporting (<scp>ICCR</scp>)

Data set for reporting of peripheral neuroblastic tumours: recommendations from the international collaboration on cancer reporting (<scp>ICCR</scp>)

Pathology reporting of hepatoblastoma resections: recommendations from the international collaboration on cancer reporting

Editorial: Challenges and novelties in pediatric pathology

Schwannian and Perineuriomatous Differentiation in a Series of Giant Congenital Melanocytic Nevi

Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes

Pediatric BCOR-Altered Tumors From Soft Tissue/Kidney Display Specific DNA Methylation Profiles

Melanoma in infants, caused by a gene fusion involving the anaplastic lymphoma kinase (<scp>ALK)</scp>

Addressing the diagnostic and therapeutic dilemmas of ovarian immature teratoma: Report from a clinicopathologic consensus conference

A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era

Guidelines for synoptic reporting of surgery and pathology in Hirschsprung disease

Host conditioning and rejection monitoring in hepatocyte transplantation in humans

Identification of intestinal ion transport defects in microvillus inclusion disease

ARMC4 Mutations Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry