Results 241 to 250 of about 5,424,670 (342)

Autoantibodies as Precision Tools in Connective Tissue Diseases: From Epiphenomenon to Endophenotype. [PDF]

Antibodies (Basel)
Soyfoo M, Sarrand J.
europepmc   +1 more source

Soft Tissue Sarcoma, Version 2.2018, NCCN Clinical Practice Guidelines in Oncology.

The Journal of the National Comprehensive Cancer Network, 2016
M. von Mehren, R. Randall, R. Benjamin, Sarah G. Boles, M. Bui, K. Ganjoo, S. George, R. Gonzalez, M. Heslin, J. Kane, V. Keedy, Edward Kim, H. Koon, J. Mayerson, M. McCarter, Sean V. McGarry, C. Meyer, Z. Morris, R. O'Donnell, A. Pappo, I. Paz, I. Petersen, J. Pfeifer, R. Riedel, B. Ruo, S. Schuetze, W. Tap, J. Wayne, Mary Anne Bergman, Jillian L. Scavone   +29 more
semanticscholar   +1 more source

SPG4 and Dementia: Expanding the Clinical Spectrum

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza, Arun Meyyazhagan, Eliseo Picchi, Gustavo Ribas, Ingrid Faber, Ryosuke Miyamoto, Preethi Basavaraju, Paolo Eusebi, Haripriya Kuchi Bhotla, Mario Stasi, Fabrizio Gaudiello, Francesco Patti, Filippo Maria Santorelli, Marcondes Cavalcante França Jr, José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Hélio Afonso Ghizoni Teive, Peter Henry St George‐Hyslop, Toshitaka Kawarai, Antonio Orlacchio   +19 more
wiley   +1 more source

Human connective tissue - 3D datasets to characterise the material properties. [PDF]

Sci Data
Stark H, Sartori J.
europepmc   +1 more source

High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders.

Journal of Allergy and Clinical Immunology, 2013
J. Abonia, T. Wen, E. Stucke, Tommie M. Grotjan, M. Griffith, Katherine A. Kemme, M. Collins, P. Putnam, J. Franciosi, Karl von Tiehl, Brad T. Tinkle, K. Marsolo, Lisa J. Martin, Stephanie M. Ware, M. Rothenberg   +14 more
semanticscholar   +1 more source

The Role of Calcitonin Gene‐Related Peptide in High‐Altitude Headache: A Prospective Field Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective High‐altitude headache (HAH) is a common neurological condition associated with rapid ascent to high altitude. The pathophysiological mechanisms underlying HAH remain incompletely understood. Calcitonin gene‐related peptide (CGRP), a neuropeptide implicated in migraine pathophysiology, may play a key role in the pathophysiology of ...
Roman Schniepp, Ludwig Karrasch, Helena Breitenstein, Andreas Straube, Katharina Kamm   +4 more
wiley   +1 more source

Multidimensional regulation of estrogen signaling in pelvic floor connective tissue homeostasis and remodeling. [PDF]

Front Immunol
Wang L, Geng M, Wei L, Wang S, Wang W, Liu X.   +5 more
europepmc   +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

Cardiovascular Functioning Features in Individuals with Connective Tissue Dysplasia Engaged in Sports for the Disabled. [PDF]

Sports (Basel)
Vinokurova K, Zakharova A, Zinovieva Y, Epifanov A, Galdobina A, Sharkova E, Blyakhman F.   +6 more
europepmc   +1 more source

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu, Xin Duan, Fatemeh Peymani, Jia Wang, Chengjia Bao, Chaolong Xu, Ying Zou, Zixuan Zhang, Yunxi Zhang, Tongyue Li, Martin Pavlov, Junling Wang, Minhan Song, Tianyu Song, Xiaodi Han, Mingxi Sun, Danmin Shen, Ruoyu Duan, Huafang Jiang, Manting Xu, Holger Prokisch, Fang Fang   +21 more
wiley   +1 more source