Search Results - "Pytel, Peter"

Papillary tumor of the pineal region: analysis of DNA methylation profiles and clinical outcomes in 76 cases.

Authors: Wu, Zhichao Dazelle, Karen Abdullaev, Zied et al.

Source: Acta Neuropathologica Communications. 7/16/2024, Vol. 12 Issue 1, p1-7. 7p.

Correction: Predominant expression of Alzheimer's disease-associated BIN1 in mature oligodendrocytes and localization to white matter tracts.

Authors: De Rossi, Pierre Buggia-Prévot, Virginie Clayton, Benjamin L. L. et al.

Source: Molecular Neurodegeneration. 10/2/2023, Vol. 18 Issue 1, p1-1. 1p.

Low-grade NTRK-rearranged spindle cell neoplasm presenting as a colonic polyp and managed by polypectomy: a rare case report and literature review.

Authors: Evaristo, Gertruda Setia, Namrata Wang, Peng et al.

Source: Diagnostic Pathology. 10/14/2025, Vol. 20 Issue 1, p1-7. 7p.

A mouse model of stereotactic radiosurgery-induced neuroinflammation and blood-brain barrier compromise.

Authors: Alcazar-Felix, Roberto J. Cheng, Lin Srinath, Abhinav et al.

Source: Acta Neuropathologica Communications. 9/24/2025, Vol. 13 Issue 1, p1-14. 14p.

Systemic transthyretin amyloidosis in a patient with bent spine syndrome.

Authors: Rezania, Kourosh Pytel, Peter Smit, Laurel J. et al.

Source: Amyloid. Jun2013, Vol. 20 Issue 2, p131-134. 4p.

Radiological and pathological features of orbital cranial fasciitis.

Authors: Ginat, Daniel Thomas Pytel, Peter Horowitz, Peleg M.

Source: Orbit. Oct2020, Vol. 39 Issue 5, p390-390. 1p.

Cervicomedullary compression as the main manifestation of wild-type transthyretin amyloidosis.

Authors: Rezania, Kourosh Pytel, Peter Highsmith, W. Edward et al.

Source: Amyloid. 2017, Vol. 24 Issue 2, p133-134. 2p.

Update on Diagnostic Practice.

Authors: Pytel, Peter Lukas, Rimas V.

Source: Archives of Pathology & Laboratory Medicine. Jul2009, Vol. 133 Issue 7, p1062-1077. 16p. 28 Color Photographs, 3 Black and White Photographs.

Atomic-level differences between brain parenchymal- and cerebrovascular-seeded Aβ fibrils.

Authors: Scherpelz, Kathryn P. Wang, Songlin Pytel, Peter et al.

Source: Scientific Reports. 1/8/2021, Vol. 11 Issue 1, p1-14. 14p.

Capture of magnetic carriers within large arteries using external magnetic fields.

Authors: Chen, Haitao Kaminski, Michael D. Pytel, Peter et al.

Source: Journal of Drug Targeting. May2008, Vol. 16 Issue 4, p262-268. 7p. 1 Color Photograph, 4 Diagrams, 1 Chart, 2 Graphs.

Animal models of antimuscle-specific kinase myasthenia.

Authors: Richman, David P. Nishi, Kayoko Ferns, Michael J. et al.

Source: Annals of the New York Academy of Sciences; Dec2012, Vol. 1274 Issue 1, p140-147, 8p, 1 Color Photograph, 1 Chart

Histological Analysis of Early Osteolysis in Total Ankle Arthroplasty.

Authors: Schipper, Oliver N. Haddad, Steven L. Pytel, Peter et al.

Source: Foot & Ankle International. Apr2017, Vol. 38 Issue 4, p351-359.

TDP-43 proteinopathy in Theiler’s murine encephalomyelitis virus infection.

Authors: Masaki, Katsuhisa Sonobe, Yoshifumi Ghadge, Ghanashyam et al.

Source: PLoS Pathogens. 2/11/2019, Vol. 15 Issue 2, p1-20. 20p.

Presynaptic congenital myasthenic syndrome with altered synaptic vesicle homeostasis linked to compound heterozygous sequence variants in RPH3A.

Authors: Maselli, Ricardo A. Vázquez, Jessica Schrumpf, Leah et al.

Source: Molecular Genetics & Genomic Medicine. May2018, Vol. 6 Issue 3, p434-440. 7p.

A presynaptic congenital myasthenic syndrome attributed to a homozygous sequence variant in LAMA5.

Authors: Maselli, Ricardo A. Arredondo, Juan Vázquez, Jessica et al.

Source: Annals of the New York Academy of Sciences. Feb2018, Vol. 1413 Issue 1, p119-125. 7p. 4 Diagrams, 1 Graph.

High prevalence of Mi TF staining in undifferentiated pleomorphic sarcoma: caution in the use of melanocytic markers in sarcoma.

Authors: Choy, Bonnie Hyjek, Elizabeth Montag, Anthony G et al.

Source: Histopathology. Apr2017, Vol. 70 Issue 5, p734-745. 12p. 3 Color Photographs, 1 Diagram, 4 Charts.

Predominant expression of Alzheimer's disease-associated BIN1 in mature oligodendrocytes and localization to white matter tracts.

Authors: De Rossi, Pierre Buggia-Prévot, Virginie Clayton, Benjamin L. L. et al.

Source: Molecular Neurodegeneration. 8/3/2016, Vol. 11, p1-21. 21p. 3 Diagrams, 2 Charts, 6 Graphs.

Eps 15 Homology Domain (EHD)-1 Remodels Transverse Tubules in Skeletal Muscle.

Authors: Demonbreun, Alexis R. Swanson, Kaitlin E. Rossi, Ann E. et al.

Source: PLoS ONE. 9/1/2015, Vol. 10 Issue 9, p1-17. 17p.

Altered Chromosomal Positioning, Compaction, and Gene Expression with a Lamin A/C Gene Mutation.

Authors: Mewborn, Stephanie K. Puckelwartz, Megan J. Abuisneineh, Fida et al.

Source: PLoS ONE. 2010, Vol. 5 Issue 12, p1-13. 13p.

Two Children With Macrocephaly, Developmental Delay, and PTEN Mutation.

Authors: Schwab, Joel G. Pena, Loren Waggoner, Darrel et al.

Source: Clinical Pediatrics. Jan2009, Vol. 48 Issue 1, p89-92. 4p.

Subject Terms: *Developmental delay, *Child development, Genetic disorders in children, Juvenile diseases, Genetic testing, Genetic disorder diagnosis, Pediatrics, Chromosome abnormalities, Genetic mutation