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of 5 171
pro vyhledávání: ''
Autor:
Jose Marquez, Zayd Al Rawi, Elizabeth C. Bryda, Daniel J. Davis, Mona O. Garro-Kacher, Caley E. Smith, Christian L. Lorson, Catherine L Smith, Nicole L. Nichols, Amy N Keilholz, Jiude Mao, Eric Villalón, Sara M. Ricardez Hernandez, Toni I. Morcos, Monique A. Lorson
Publikováno v:
Hum Mol Genet
Spinal muscular atrophy with respiratory distress type I (SMARD1) is a neurodegenerative disease defined by respiratory distress, muscle atrophy and sensory and autonomic nervous system defects. SMARD1 is a result of mutations within the IGHMBP2 gene
Histologic Analysis of Urethral Stricture in 9 Patients Following Dorsal Vaginal Graft Urethroplasty
Publikováno v:
American Journal of Clinical Pathology. 157:742-747
Objective To present the pathologic analysis of female urethral strictures obtained during reconstructive urethroplasty. Methods Nine separate female urethral tissue specimens were obtained during dorsal vaginal graft urethroplasty by a single surgeo
Autor:
Fausto J. Rodriguez, Roxana Rivera, Jonathan Levi, Avi Z. Rosenberg, Nicholas R. Mahoney, Pouya Jamshidi, Charles G. Eberhart, Maria J Suarez
Publikováno v:
Am J Clin Pathol
Objectives Ocular amyloidoma is a rare disorder characterized by deposition of insoluble proteinaceous fibrils in the extracellular space of the ocular adnexa. This study details the clinicopathologic features and proteomic characteristics of periocu
Publikováno v:
Clinical and Experimental Dermatology. 47:216-219
Non-Langerhans cell histiocytosis is a collective term encompassing a vast group of benign proliferative disorders of histiocytes, macrophages and dendritic cells that do not meet the criteria of Langerhans cell histiocytosis. We describe a case of j
Autor:
Azim Pothiawala, Leomar Y. Ballester, Meenakshi B. Bhattacharjee, Cole T. Lewis, Antonio Dono, Nitin Tandon
Publikováno v:
J Neuropathol Exp Neurol
Meningioangiomatosis (MA) is a rare process at the intersection of cerebral developmental and neoplastic disorders that often results in epilepsy. We evaluated molecular alterations in MA to characterize its biology and pathogenesis. We searched a co
Publikováno v:
American Journal of Clinical Pathology. 157:202-211
Objectives In this retrospective study, we report a series of benign lymph nodes showing small populations of normal B-cell precursors characterized by flow cytometry and immunohistochemistry. Methods Ten cases identified during clinical flow cytomet
Publikováno v:
American Journal of Clinical Pathology. 157:171-179
Objectives Monoclonal immunoglobulins (M-proteins) that migrate in the β region on serum protein electrophoresis (SPEP) are often cloaked by this region’s normal constituents. The present study interrogates the utility of using both quantitative a
Autor:
Kristina L. Hunker, Yu Wang, James C. Stanley, Min-Lee Yang, Isabelle Birt, Ingrid L. Bergin, Dawn M. Coleman, Santhi K. Ganesh, Jun Li
Publikováno v:
Hum Mol Genet
The etiology of renal artery stenosis (RAS) and abdominal aortic coarctation (AAC) causing the midaortic syndrome (MAS), often resulting in renovascular hypertension (RVH), remains ill-defined. Neurofibromatosis type 1 (NF-1) is frequently observed i
Autor:
Olivia Foley, Shuk On Annie Leung, Annacarolina da Silva, David Chapel, Marisa R. Nucci, Michael G. Muto, Susana M. Campos
Publikováno v:
Oncologist
Endometrial cancer is the most common gynecologic cancer in the U.S., but metastasis to the brain is rare, and diagnosis can be challenging. Traditional tools for determining if a tumor is a primary or metastatic lesion include pan-imaging, histopath
Publikováno v:
American Journal of Clinical Pathology. 156:871-885
Objectives Follicular hyperplasias (FHs) with light chain–restricted (LCR) plasmacytoid/plasma cells (PCs) within germinal centers (GCs) based on immunohistochemistry (IHC)/in situ hybridization (ISH) can potentially lead to diagnostic error. This