Jacopo Ferro

Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.

Journal: medRxiv : the preprint server for health sciences

Published: July 30, 2026

Double immunohistochemistry to detect transglutaminase 2-IgA deposits in celiac children: a multicentre study.

Journal: Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver

Published: February 27, 2026

Unmasking Celiac Disease Through Chronic Urticaria: Case Report and Scoping Review.

Journal: Nutrients

Published: December 09, 2025

Severe Vanishing Bile Duct Syndrome after Allogeneic Hematopoietic Stem Cell Transplantation in Pediatric Patients.

Journal: Transplantation and cellular therapy

Published: November 16, 2025

Efficacy of combined JAK1/2 inhibition and cyclosporine in paediatric-onset Still's disease with lung involvement: a case report.

Journal: Pediatric rheumatology online journal

Published: November 08, 2025

Subcutaneous Pediatric Nasal Glial Heterotopia.

Journal: Turkish archives of pediatrics

Published: April 16, 2025

Efficacy of High-Dose Intravenous Anakinra in Pediatric TAFRO Syndrome: Report of Two Cases and Literature Review.

Journal: Pediatric blood & cancer

Published: January 30, 2025

Histologic alterations are common in Monogenic Disease patients with 'healthy' endoscopy: Results from a GIPAD-GIPPI multicenter study.

Journal: Human pathology

Published: December 24, 2024

SARS-CoV-2 Vaccination Coverage in Italian Children with Celiac Disease.

Journal: Journal of clinical medicine

Published: August 15, 2024

Clinicopathologic Features of Primary Immunodeficiency Monogenic Disease-related Very Early Onset Inflammatory Bowel Disease: Focus on Gastrointestinal Histologic Features in IFIH1 Mutations.

Journal: Advances in anatomic pathology

Published: August 14, 2024

Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.

Human GPR174 deficiency drives polyclonal lymphoproliferative disease via defects in T cell function.

Double immunohistochemistry to detect transglutaminase 2-IgA deposits in celiac children: a multicentre study.

Double immunohistochemistry to detect transglutaminase 2-IgA deposits in celiac children: a multicentre study.

Unmasking Celiac Disease Through Chronic Urticaria: Case Report and Scoping Review.

Unmasking Celiac Disease Through Chronic Urticaria: Case Report and Scoping Review.

Severe Vanishing Bile Duct Syndrome after Allogeneic Hematopoietic Stem Cell Transplantation in Pediatric Patients.

Severe Vanishing Bile Duct Syndrome after Allogeneic Hematopoietic Stem Cell Transplantation in Pediatric Patients.

Efficacy of combined JAK1/2 inhibition and cyclosporine in paediatric-onset Still's disease with lung involvement: a case report.

Efficacy of combined JAK1/2 inhibition and cyclosporine in paediatric-onset Still's disease with lung involvement: a case report.

Subcutaneous Pediatric Nasal Glial Heterotopia.

Subcutaneous Pediatric Nasal Glial Heterotopia.

Efficacy of High-Dose Intravenous Anakinra in Pediatric TAFRO Syndrome: Report of Two Cases and Literature Review.

Efficacy of High-Dose Intravenous Anakinra in Pediatric TAFRO Syndrome: Report of Two Cases and Literature Review.

Histologic alterations are common in Monogenic Disease patients with 'healthy' endoscopy: Results from a GIPAD-GIPPI multicenter study.

Histologic alterations are common in Monogenic Disease patients with 'healthy' endoscopy: Results from a GIPAD-GIPPI multicenter study.

SARS-CoV-2 Vaccination Coverage in Italian Children with Celiac Disease.

SARS-CoV-2 Vaccination Coverage in Italian Children with Celiac Disease.

Clinicopathologic Features of Primary Immunodeficiency Monogenic Disease-related Very Early Onset Inflammatory Bowel Disease: Focus on Gastrointestinal Histologic Features in IFIH1 Mutations.

Clinicopathologic Features of Primary Immunodeficiency Monogenic Disease-related Very Early Onset Inflammatory Bowel Disease: Focus on Gastrointestinal Histologic Features in IFIH1 Mutations.

Early Onset of Wilson's Disease and Possible Role of Disease-Modifying Genes: A Case Report and Literature Review.

Early Onset of Wilson's Disease and Possible Role of Disease-Modifying Genes: A Case Report and Literature Review.

Nerve Sheath Myxoma in Pregnancy: A Case Report.

Nerve Sheath Myxoma in Pregnancy: A Case Report.