Results 251 to 260 of about 13,953,274 (395)

Traditional Reproductive Health and Family Planning Practices among the Dagomba

, 1970
Abukari Kwame, Pammla Petrucka
openalex   +2 more sources

Guidelines for Family-Centered Care in the Neonatal, Pediatric, and Adult ICU

Critical Care Medicine, 2017
J. Davidson, Rebecca A. Aslakson, Ann C. Long, K. Puntillo, Erin K Kross, J. Hart, C. Cox, H. Wunsch, Mary A. Wickline, M. Nunnally, G. Netzer, N. Kentish-Barnes, C. Sprung, C. Hartog, M. Coombs, R. Gerritsen, R. Hopkins, L. Franck, Y. Skrobik, A. Kon, E. Scruth, M. Harvey, M. Lewis-Newby, D. White, S. Swoboda, C. Cooke, M. Levy, É. Azoulay, J. Curtis   +28 more
semanticscholar   +1 more source

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

Establishing a standing patient advisory board in family practice research: A qualitative evaluation from patients' and researchers' perspectives. [PDF]

Health Expect
Engler J, Engler F, Gerber M, Brosse F, Voigt K, Mergenthal K.   +5 more
europepmc   +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

Gender Disparities in Adverse Events Resulting From Low-Value Practices in Family Practice in Spain: A Retrospective Cohort Study. [PDF]

Int J Public Health
Mira JJ, Carratala-Munuera C, Vicente MA, Astier-Peña MP, García-Torres D, Soriano C, Sánchez-García A, Chilet-Rosell E, Gil-Guillén VF, López-Pineda A, Pérez-Jover V.   +10 more
europepmc   +1 more source

Mood responses to COVID-19: Implications for family practice in South Africa. [PDF]

S Afr Fam Pract (2004), 2021
Van Wijk C, Majola PZ.
europepmc   +1 more source

Does higher quality of diabetes management in family practice reduce unplanned hospital admissions?

Health Services Research, 2011
M. Dusheiko, T. Doran, H. Gravelle, C. Fullwood, M. Roland   +4 more
semanticscholar   +1 more source

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

Retraction: Unicentric Castleman Disease With Systemic Symptoms: A Rare Case From Family Practice. [PDF]

Cureus
Aljuaid AK, Iskandar MN, Almalki AA, Alsuqayh KS, Almufarrih YA, Alosaimi SG, Aljamaan LF, Aldaihani SF, Alghamdi SA, Alaamree MA, Fageeh LM, Almagrafi SA, Al Halbub AY, Alghamdi ZS, Al-Hawaj F.   +14 more
europepmc   +1 more source