Results 111 to 120 of about 2,921 (283)
Cytologic and Histologic Findings of Extrapleural Solitary Fibrous Tumor: Report of Two Cases
Diagnostic Cytopathology, Volume 54, Issue 2, Page E46-E53, February 2026.ABSTRACT Solitary fibrous tumors (SFT) are a rare neoplasm of mesenchymal origin. SFT was previously described primarily in the pleura and meninges; however, extrapleural and extra‐meningeal SFT have been reported in almost every anatomic site and account for up to 40% of cases.
Michael Tyler +4 more
wiley +1 more source
Holocentric Chromosomes of <i>Luzula elegans</i> Are Characterized by a Longitudinal Centromere Groove, Chromosome Bending, and a Terminal Nucleolus Organizer Region [PDF]
, 2011 Stefan Heckmann +7 more
openalex +1 more source
Molecular alterations in high‐grade neuroendocrine tumors of the small intestine
The Journal of Pathology, Volume 268, Issue 2, Page 215-226, February 2026.Abstract High‐grade neuroendocrine tumors of the small intestine are separated into two groups: well‐differentiated neuroendocrine tumors (NETs, high‐grade) and poorly differentiated neuroendocrine carcinomas (NECs). They represent very rare entities, with few molecular data available, and are very challenging to treat.
Agathe Hercent +9 more
wiley +1 more source
Prolonged survival in a young Dobermann with adrenal neuroblastoma
Veterinary Record Case Reports, Volume 14, Issue 1, February 2026.Abstract A 1‐year‐old Dobermann presented with recurrent episodes of acute diarrhoea and weight loss starting at 5 months of age. An adrenal mass was identified via ultrasound and computed tomography, leading to adrenalectomy. A diagnosis of adrenal neuroblastoma was obtained through histopathology and immunohistochemistry.
Nataliia Ignatenko +8 more
wiley +1 more source
Andrology, Volume 14, Issue 2, Page 398-410, February 2026.Abstract Background WFS1 spectrum disorder, also known as Wolfram syndrome (WS) is an ultra‐rare (<1:500,000; ORPHA: 3463) monogenic (OMIM #222300) progressive neuroendocrine and neurodegenerative disorder, characterised by early‐onset insulin‐dependent diabetes, optic atrophy, central diabetes insipidus and sensi‐neuronal deafness.
Julia Rohayem +6 more
wiley +1 more source
Acta Physiologica, Volume 242, Issue 2, February 2026.ABSTRACT Aim Identifying interactors in sensorimotor processing and neurotransmission remains a current challenge for understanding neural information processing and brain function. Methods To evaluate the role of p11 in sensorimotor processing and excitatory synaptic neurotransmission, neuron‐specific lentivirus‐directed p11 silencing, small ...
Esther Vilches‐Herrando +7 more
wiley +1 more source
Journal of Cutaneous Pathology, Volume 53, Issue 2, Page 153-157, February 2026.ABSTRACT Melanoma arising in blue nevus (MBN) is a rare, aggressive malignancy that can develop from a preexisting blue nevus or resemble a cellular blue nevus without a clear precursor. We present a diagnostically challenging case of MBN on the foot of a 13‐year‐old female, with two sentinel lymph nodes (SLNs) showing heavily pigmented cells within ...
Kathie Velez +6 more
wiley +1 more source
European Journal of Haematology, Volume 116, Issue 2, Page 116-128, February 2026.ABSTRACT Primary cutaneous B‐cell lymphomas (CBCL) represent a clinically and biologically heterogeneous group of extranodal non‐Hodgkin lymphomas confined to the skin at the time of diagnosis. They account for approximately 25% of all primary cutaneous lymphomas and are subclassified into distinct entities according to the World Health Organization ...
A. Bernardelli +5 more
wiley +1 more source