Results 51 to 60 of about 298,096 (289)

Compartment-specific antigen expression.

, 2016
Compartment-specific expression (peritubular (A), glomerular (B), perivascular(C)) of MHCII-HLA-DR positive cells in renal allograft biopsies dependent on histopathological grading. # p < 0.05 vs. normal histology. D: Representative slide of a CD68-MHCII-
Felix Bourier (2827478), Bettina Jung (2827469), Simone Wurm (2827484), Miriam C. Banas (2827475), Petra Rümmele (165164), Louisa Kühne (2827481), Bernhard Banas (2827472), Tobias Bergler (2827487)   +7 more
core   +1 more source

Chronobiology of Cancer: How Aging Fuels Oncogenesis at the Molecular Level

Aging and Cancer, EarlyView.
This graphical abstract illustrates the key biological pathways linking aging with cancer development and progression. In the upper left, cumulative exposure to ultraviolet radiation, toxins, and reactive oxygen species (ROS) causes DNA damage and genomic instability, whereas age‐related decline in repair mechanisms, such as ATM/ATR, BER, and NER ...
Anu Singh, Aroonima Misra, Sufian Zaheer
wiley   +1 more source

Survival following traumatic thoracic compartment syndrome managed with VV-ECMO

Trauma Case Reports, 2019
Whilst post-traumatic respiratory failure is the most common indication for use of VV-ECMO in trauma patients, its use in traumatic thoracic compartment syndrome is not yet well described.
Timothy Amos, Meei Yeung, Julian Gooi, Mark Fitzgerald   +3 more
doaj   +1 more source

Compartment-specific cellular proliferation.

, 2016
Compartment-specific expression (peritubular (A), glomerular (B), perivascular (C)) of Ki67 positive cells in renal allograft biopsies dependent on histopathological grading.
Felix Bourier (2827478), Bettina Jung (2827469), Simone Wurm (2827484), Miriam C. Banas (2827475), Petra Rümmele (165164), Louisa Kühne (2827481), Bernhard Banas (2827472), Tobias Bergler (2827487)   +7 more
core   +1 more source

Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone, Freddy Chafota, Miguel E. Rentería, Randi J. Hagerman, Ellery Santos, Anna Atkinson, Nicholas G. Martin, Elsdon Storey, Danuta Z. Loesch   +8 more
wiley   +1 more source

[18F]Fluorodeprenyl‐D2 PET as a Tool to Monitor Disease Activity in GAD65‐Ab Autoimmune Encephalitis

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To evaluate [18F]fluorodeprenyl‐D2 ([18F]F‐DED) positron‐emission tomography (PET) imaging as a biomarker of disease activity in autoimmune encephalitis (AIE) associated with glutamic acid decarboxylase 65 (GAD65) antibodies. Methods [18F]F‐DED PET was performed in 25 GAD65‐AIE patients and 8 controls using dynamic (0–60 min) and ...
Julia S. Dorneich, Jonathan A. Gernert, Hanna Zimmermann, Lisa Tagnin, Marianthi Zeinaki, Laura Sanzo, Letizia Vogler, Elisabeth Kaufmann, Justina Dargvainiene, Frank Leypoldt, Gérard N. Bischof, Robert Perneczky, Boris‐Stephan Rauchmann, Simon Lindner, Günter U. Höglinger, Rudolf A. Werner, Martin Kerschensteiner, Tania Kümpfel, Matthias Brendel, Franziska S. Thaler   +19 more
wiley   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

Compartment-specific macrophages expression.

, 2016
Compartment-specific expression (peritubular (A), glomerular (B), perivascular (C)) of CD68 positive macrophages in renal allograft biopsies dependent on histological grading. # p < 0.05 vs. normal histology; * p < 0.05 vs TCMR without arteritis. D: CD68
Felix Bourier (2827478), Bettina Jung (2827469), Simone Wurm (2827484), Miriam C. Banas (2827475), Petra Rümmele (165164), Louisa Kühne (2827481), Bernhard Banas (2827472), Tobias Bergler (2827487)   +7 more
core   +1 more source

Sertraline Treatment Can Mimic Niemann‐Pick Type C Biomarker Profile: A Diagnostic Pitfall

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Oxysterols (cholestane‐3β,5α,6β‐triol and 7‐ketocholesterol) and N‐palmitoyl‐O‐phosphocholineserine (PPCS) are sensitive biomarkers for Niemann‐Pick disease type C (NPC) screening. However, false‐positive results occur, with a biomarker profile suggestive of NPC despite the absence of pathogenic variants in genes involved in NPC or ...
Maria Makrygianni, Cecile Pagan, Antony Citterio‐Quentin, Isabelle Rouvet, Giulia Dingeo, Cyril Hanin, Claudine Laurent‐Levinson, Samia Pichard, Bénédicte Héron, Clément Gourguechon, Daniele Mandia, Jerome Guitton, Carole Lacout, Nicolas Schleinitz, Florient Potier, Olivier Flabeau, Elsa Besse‐Pinot, Foudil Lamari, Magali Pettazzoni, Yann Nadjar   +19 more
wiley   +1 more source

When Time Is Not on Your Side: Delayed Recognition of Hand Compartment Syndrome After a Fracture

Case Reports in Orthopedics
Compartment syndrome of the forearm is a well-described clinical entity, but only a few case reports on hand compartment syndromes have been reported due to its rarity.
Edmund M. Bediako, Geraldine K. Mould, Eadbert Nortey, Abigail Mills-Annoh, Priscilla Kyei-Baffour, Ama Ekem, Jemima C. A. Clarke, Eugene F. E. K. Apaloo, Susan Quartey-Papafio, Kwame Ekremet   +9 more
doaj   +1 more source