Results 191 to 200 of about 3,550,881 (351)

Clinical and Radiographic Evaluation of Molar Root-Incisor Malformation (MRIM): A Case Series. [PDF]

Case Rep Dent
Karahan A, Mısır M, Koruyucu M.
europepmc   +1 more source

On permanents of circulants [PDF]

Pacific Journal of Mathematics, 1972
openaire   +4 more sources

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam, Ali Laith, Aslihan Gunel, Melda Yilmaz, Nazli Basak, Halil Idrisoglu, P. Hande Ozdinler   +6 more
wiley   +1 more source

A Retrospective Study of Replacement Resorption and Its Risk Factors After Replantation of Avulsed Young Permanent Teeth. [PDF]

Clin Exp Dent Res
Min G, Jianyan Q, Chenxing C, Suyu G.
europepmc   +1 more source

Design and Multi-Objective Optimization for Improving Torque Performance of a Permanent Magnet-Assisted Synchronous Reluctance Motor [PDF]

Jiajia Zhang, Feng Xing, Lipeng Kang, Caiyan Qin   +3 more
openalex   +1 more source

Permanent Members [PDF]

The American Journal of Nursing, 1913
openaire   +1 more source

Interleukin‐6 as a Key Biomarker in Facioscapulohumeral Dystrophy: Evidence From Longitudinal Analyses

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini, Emanuela Martinuzzi, Sandra Dhifallah, Abderhmane Slioui, Angela Puma, Luisa Villa, Michele Cavalli, Andra Ezaru, Jérémy Garcia, Manuela Gambella, Federico Torre, Luca Jacopo Pavan, Nicolas Glaichenhaus, Sabrina Sacconi   +13 more
wiley   +1 more source

Real-World Outcomes of Spinal Cord Stimulation: A Consecutive Institutional Experience with 505 Trials, Trial-to-Implant Ratio, Long-Term Efficacy, and Explantation Risk Factors. [PDF]

J Pain Res
Gheith R, Wortmann M, Najjar M, Oliver C, Whitlow B, Raterman B, Shackelford KR.   +6 more
europepmc   +1 more source

Design and Implementation of a Low Power Wind Turbine Emulator Through the Induction Motor-Permanent Magnet Generator Arrangement

, 2020
David Felipe Bajonero-Sandoval, Jeyson Sanabria-Vargas, César Leonardo Trujillo Rodríguez   +2 more
openalex   +2 more sources

SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas, Pablo Iruzubieta, Alberto Damborenea, Laura Pérez‐Fernández, Inmaculada Azorín, Juan Carlos Jiménez García, Ana Töpf, Pilar Martí, Lorena Fores‐Toribio, María Manterola, Rosana Blanco‐Mañez, Oihane Pikatza‐Menoio, Sonia Alonso‐Martín, Volker Straub, Aitziber L. Cortajarena, Adolfo López de Munain, David De Sancho, Lorea Blázquez, Juan J. Vilchez   +18 more
wiley   +1 more source