Results 101 to 110 of about 2,574,835 (312)

Medication‐Related Osteonecrosis of the Jaws in Patients on Antiresorptive Medication With Dental Implants. A Scoping Review

Clinical Oral Implants Research, EarlyView.
ABSTRACT Objectives Patients receiving antiresorptive medication (AR) for osteoporosis or cancer are at risk of medication‐related osteonecrosis of the jaws (MRONJ), especially after surgical procedures. Dental implant (DI) placement in high‐dose AR (HDAR) patients is widely discouraged, and thorough counseling is recommended for low‐dose AR (LDAR ...
Sanne Werner Moeller Andersen, Nishma Vandvig Hindocha, Iben Poulsen, Henning Schliephake, Simon Storgård Jensen   +4 more
wiley   +1 more source

POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome

Human Mutation, 2015
Segmental progeroid syndromes are rare, heterogeneous disorders characterized by signs of premature aging affecting more than one tissue or organ. A prototypic example is the Werner syndrome (WS), caused by biallelic germline mutations in the Werner ...
D. Lessel, F. Hisama, K. Szakszon, Bidisha Saha, Alexander Barrios Sanjuanelo, B. Salbert, Pamela D. Steele, J. Baldwin, W. Brown, C. Piussan, H. Plauchu, J. Szilvássy, E. Horkay, J. Högel, G. Martin, A. Herr, J. Oshima, C. Kubisch   +17 more
semanticscholar   +1 more source

Androgen-responsive non-coding small RNAs extend the potential of HCG stimulation to act as a bioassay of androgen sufficiency [PDF]

, 2017
Background: It is unclear whether a short-term change in circulating androgens is associated with changes in the transcriptome of the peripheral blood mononuclear cells (PBMC).
Ahmed, S.F., Boroujerdi, M., Chudleigh, S., Herzyk, P., McMillan, M., Mudaliar, M.A.V., Rodie, M.E., Tobias, E.S.   +7 more
core   +1 more source

How Do I Diagnose Multiple System Atrophy—A Videolibrary on Clinical and Imaging Features

Movement Disorders Clinical Practice, EarlyView.
Victoria Sidoroff, Luca Baldelli, Nathaniel Bendahan, Giovanna Calandra‐Buonaura, Nicole Campese, Gustavo Da Prat, Margherita Fabbri, Alessandra Fanciulli, Joaquim J. Ferreira, Florin Gandor, Emilia Gatto, Gabriela S. Gilmour, Sabrina Katzdobler, Horacio Kaufmann, Vladimir Kostic, Florian Krismer, Vikram Khurana, Anthony Lang, Johannes Levin, Patricio Millar Vernetti, Maria Teresa Pellecchia, Igor Petrovic, Werner Poewe, Cecilia Raccagni, Rita Moiron Simões, Wolfgang Singer, Michael Strupp, Thilo van Eimeren, Maria Stamelou, Günter Höglinger, Gregor Wenning, Iva Stankovic, on behalf of the MDS MSA Study group   +32 more
wiley   +1 more source

The Experience of Stigma in People Affected by Fibromyalgia: A Metasynthesis

Journal of Advanced Nursing, EarlyView.
ABSTRACT Aim To review the qualitative literature regarding how people with fibromyalgia experience and are impacted by stigma. Design A systematic review and metasynthesis of qualitative studies was conducted following the Thomas and Harden method. Methods The electronic databases PubMed, CINAHL, PsycInfo, Embase and Scopus were queried (September ...
Benedetta Colombo, Eleonora Zanella, Alessandro Galazzi, Paola Arcadi   +3 more
wiley   +1 more source

Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming

Frontiers in Genetics, 2015
Werner syndrome (WS) is a rare human autosomal recessive premature aging disorder characterized by early onset of aging-associated diseases, chromosomal instability, and cancer predisposition.
A. Shimamoto, K. Yokote, H. Tahara
semanticscholar   +1 more source

Genomic instability and DNA replication defects in progeroid syndromes [PDF]

, 2018
Progeroid syndromes induced by mutations in lamin A or in its interactors – named progeroid laminopathies – are model systems for the dissection of the molecular pathways causing physio- logical and premature aging.
Chiara Merigliano, Fiammetta Vernì, Isabella Saggio, Mattia La Torre, Romina Burla   +4 more
core   +1 more source

European Guideline (EuroGuiDerm) on atopic eczema: Living update

Journal of the European Academy of Dermatology and Venereology, EarlyView.
The updated guideline includes a new evidence‐based recommendation for the IL‐13 inhibitor lebrikizumab. In addition, the Janus kinase inhibitors baricitinib and abrocitinib, which were initially only approved for adult patients, are now also recommended for children from the age of 2 and adolescents from the age of 12, respectively.
A. Wollenberg, M. Kinberger, B. Arents, N. Aszodi, S. Barbarot, T. Bieber, H. A. Brough, P. Calzavara‐Pinton, S. Christen‐Zaech, M. Deleuran, M. Dittmann, N. Fosse, K. Gáspár, L. A. A. Gerbens, U. Gieler, G. Girolomoni, S. Gregoriou, S. Holland, C. G. Mortz, A. Nast, U. Nygaard, E. M. Rehbinder, J. Ring, M. Rossi, E. Serra‐Baldrich, D. Simon, Z. Z. Szalai, J. C. Szepietowski, A. Torrelo, T. Werfel, R. N. Werner, C. Flohr   +31 more
wiley   +1 more source

Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice

PLoS ONE, 2015
Werner syndrome (WS) is a premature aging disorder caused by mutations in a RecQ-family DNA helicase, WRN. Mice lacking part of the helicase domain of the WRN orthologue exhibit many phenotypic features of WS, including metabolic abnormalities and a ...
Lucie Aumailley, C. Garand, M. Dubois, F. Johnson, A. Marette, M. Lebel   +5 more
semanticscholar   +1 more source

Herlyn-Werner-Wunderlich syndrome presenting with dysmenorrhea: a case report

Journal of Medical Case Reports, 2019
Background Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. The most common presentation is abdominal pain, dysmenorrhea, and abdominal mass secondary
Dilruba Sharmen Nishu, Md. Monir Uddin, Khadija Akter, Shameema Akter, Monira Sarmin, Sartaj Begum   +5 more
doaj   +1 more source