Results 101 to 110 of about 2,895 (221)

Correction of osteopetrosis in the neonate oc/oc murine model after lentiviral vector gene therapy and non-genotoxic conditioning

Frontiers in Endocrinology
IntroductionAutosomal recessive osteopetrosis (ARO) is a rare genetic disease, characterized by increased bone density due to defective osteoclast function.
Sara Penna, Alessandra Zecchillo, Alessandra Zecchillo, Martina Di Verniere, Elena Fontana, Elena Fontana, Valeria Iannello, Valeria Iannello, Eleonora Palagano, Eleonora Palagano, Stefano Mantero, Stefano Mantero, Andrea Cappelleri, Andrea Cappelleri, Elena Rizzoli, Elena Rizzoli, Ludovica Santi, Laura Crisafulli, Laura Crisafulli, Marta Filibian, Antonella Forlino, Luca Basso-Ricci, Serena Scala, Eugenio Scanziani, Eugenio Scanziani, Thorsten Schinke, Francesca Ficara, Francesca Ficara, Cristina Sobacchi, Cristina Sobacchi, Anna Villa, Anna Villa, Valentina Capo, Valentina Capo   +33 more
doaj   +1 more source

Heterotopic bone formation with extramedullary haematopoiesis in a thyroid nodule. [PDF]

BMJ Case Rep, 2023
García J, Alvarez M, Moreno D, Acosta B.   +3 more
europepmc   +1 more source

Interactions between megakaryocytes and tumour cells in the bone marrow vascular stem cell niche promote tumour growth and metastasis

, 2010
Specialized bone marrow microenvironments (vascular and osteoblastic 'niches') regulate normal haematopoietic stem/progenitor cells. Recently, the vascular niche has also been implicated as an area for preferential engraftment of malignant cells.
Psaila, Bethan, Psaila, Bethan
core   +1 more source

Frequent NPM1 mutation, monoblastic/monocytic origin and prognostic significance of organ and system involvement in myeloid sarcoma: a multicenter study

The Journal of Pathology: Clinical Research, Volume 12, Issue 2, March 2026.
Abstract Myeloid sarcoma (MS) is a tumorous extramedullary proliferation of blast or blast equivalent cells (e.g., promonocytes or promyelocytes). The most frequent cutaneous presentation is often referred to as leukemia cutis (LC). These lesions, especially without the clinical context of a known bone marrow disease, pose a differential diagnostic ...
Alex Jenei, Béla Kajtár, Tamás László, Hazem A Juratli, Livia Vida, Ágota Szepesi, Réka Mózes, Botond Timár, Jörg Halter, Stefan Dirnhofer, Alexandar Tzankov   +10 more
wiley   +1 more source

A Multicenter Survival Analysis of Adults Type B‐Acute Lymphoblastic Leukemia in Ecuador. A Retrospective Study of the Real World

Cancer Medicine, Volume 15, Issue 3, March 2026.
Analysis of adults type b‐acute lymphoblastic leukemia in ecuador. This demonstrates inferior response and survival outcomes for b‐all in Ecuador and can serve as a reference to Latin America countries due to geographic, racial and socioeconomic similarities.
Brenner Sabando, Jairo Quinonez, Andrés Orquera, Danilo Navarrete, Jhoanna Ramírez, Lorena Sanchez, Teodoro Chisesi, Jorge Oliveros, María A. Pacheco, María C. Trujillo, Carlos Plaza, Rafael Lochamin, D. Jimmy Martin   +12 more
wiley   +1 more source

Paraspinal extramedullary haematopoiesis: a rare radiological diagnosis. [PDF]

BMJ Case Rep, 2022
Carter S, Spanger M, Koshy M, Weinberg L.   +3 more
europepmc   +1 more source

A Novel Modified Bu/Vp16/cy/Flu/Ara‐C Conditioning Regimen Enhances Outcomes for High‐Risk Acute Lymphoblastic Leukemia Patients Undergoing Allogeneic Hematopoietic Stem Cell Transplantation

Cancer Medicine, Volume 15, Issue 3, March 2026.
ABSTRACT Purpose Allogeneic hematopoietic stem cell transplantation (allo‐HSCT) effectively treats high‐risk acute lymphoblastic leukemia (ALL), yet challenges persist due to post‐transplant relapse and conditioning regimen toxicities. The determination of an appropriate preconditioning regimen is critical to improving patient outcomes.
Xiaoyan Zhao, Yifan Yao, Yan Sun, Ziwei Xu, Aiguo Liu, Xin Dong, Huafang Wang   +6 more
wiley   +1 more source

Non‐Syndromic Paucity of Interlobular Bile Ducts (NSPIBD) Presenting as Neonatal Cholestasis in an Infant With Down Syndrome: A Case Report

Clinical Case Reports, Volume 14, Issue 3, March 2026.
ABSTRACT Non‐syndromic paucity of interlobular bile ducts (NSPIBD) is a rare cause of neonatal cholestasis, often presenting with clinical features similar to extrahepatic biliary atresia. This report presents a case of NSPIBD in an infant with Down syndrome who exhibited jaundice and pale stools.
Pui Ling Thong, Nurfirdaus Musa, Nurul Husna Mohd Dani, Zurina Zainuddin   +3 more
wiley   +1 more source

Extramedullary haematopoiesis presenting as an adnexal mass in a patient with β-thalassaemia. [PDF]

BMJ Case Rep, 2022
Filippi V, Reina H, Monod C, Manegold-Brauer G.   +3 more
europepmc   +1 more source

Radiological conference. Paget's disease [PDF]

, 1998
published_or_final_versio
Ching, ASC, Peh, WCG
core