Results 171 to 180 of about 244,589 (288)

Effects of Audio-Guided Imagery on Raynaud Phenomenon in Connective Tissue Disease. [PDF]

ACR Open Rheumatol
Padilla C, Katikineni V, Park Y, Freno L, Laffoon M, Reichbaum L, Lafyatis R, Domsic R.   +7 more
europepmc   +1 more source

Identifying Differences in Risk Factors for Depression and Anxiety in Pediatric Chronic Disease: A Matched Cross-Sectional Study of Youth with Lupus/Mixed Connective Tissue Disease and Their Peers with Diabetes

, 2015
Andrea Knight, Pamela F. Weiss, Knashawn H. Morales, Marsha Gerdes, Melissa Andrews Rearson, Michelle Vickery, Ron Keren   +6 more
openalex   +1 more source

Effectiveness and Safety of Nusinersen and Risdiplam in Spinal Muscular Atrophy: A Systematic Review

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Spinal Muscular Atrophy (SMA) is a rare genetic disorder marked by progressive muscle weakness and mobility loss. It has a profound physical, emotional and social impact on patients and caregivers, requiring comprehensive medical and supportive care.
Amin Mehrabian, Peter Auguste, Amy Grove, Anna Brown, Janette Parr, Mubarak Patel, Furqan Butt, Jeremiah Donoghue, Mehdi Yousefi, Jo Parsons   +9 more
wiley   +1 more source

THU0635 Pregnancy outcomes in mixed connective tissue disease: results from a multicentre cohort study [PDF]

, 2018
Massimo Radin, Karen Schreiber, M J Cuadrado, Irene Cecchi, Asakura Laura, Franco Franceschini, Teresa Caleiro, E. Gibbone, M. Khamashta, Jill P. Buyon, Peter Izmirly, M. Aguirre Zamorano, Dario Roccatello, Luca Marozio, Savino Sciascia   +14 more
openalex   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron, Nicholas E. Clifton, Daniel Cabezas de la Fuente, Peter Holmans, Nicholas J. Bray, Kathryn J. Peall   +5 more
wiley   +1 more source

Pulmonary Complications in Connective Tissue Disease-Associated Interstitial Lung Disease. [PDF]

Clin Respir J
Lewandowska AA, Waśniowska D, Rybacki C, Graczyk M, Duszyńska O, Mirus-Arabik H, Gaczkowska A, Kołodziej M.   +7 more
europepmc   +1 more source

An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco, Caterina Motta, Enrica Marchionni, Maria Rosaria D'Apice, Carlangelo Carrese, Giuseppe Novelli, Alessandro Martorana, Chiara Giuseppina Bonomi   +7 more
wiley   +1 more source

Rituximab in Connective Tissue Disease-Associated Interstitial Lung Disease: From Immunopathogenesis to Therapeutic Implications. [PDF]

Int J Mol Sci
Chatzis D, Banos A, Fanouriakis A, Karampitsakos T, Tzilas V.   +4 more
europepmc   +1 more source

Extracellular Matrix Remodeling: The Common Denominator in Connective Tissue Diseases Possibilities for Evaluation and Current Understanding of the Matrix as More Than a Passive Architecture, but a Key Player in Tissue Failure

, 2012
M.A. Karsdal, Mette Juul Nielsen, Jannie Marie Bülow Sand, Kim Henriksen, Federica Genovese, Anne‐Christine Bay‐Jensen, Victoria Smith, Joanne I. Adamkewicz, Claus Christiansen, Diana Julie Leeming   +9 more
openalex   +2 more sources

Melkersson–Rosenthal syndrome as an early manifestation of mixed connective tissue disease [PDF]

, 2015
Dorota Jasińska, Jerzy Boczon
openalex   +1 more source