Works by Hartley, Louise

Results: 12

Cardiovascular events and risk in patients with systemic lupus erythematosus: Systematic literature review and meta-analysis.

Published in:

Lupus, 2023, v. 32, n. 3, p. 325, doi. 10.1177/09612033221147471

By:

Bello, Natalia;
Meyers, Kristin J;
Workman, Jennifer;
Hartley, Louise;
McMahon, Maureen

Publication type:

Article

Newborn bloodspot screening for Duchenne Muscular Dystrophy: 21 years experience in Wales (UK).

Published in:

European Journal of Human Genetics, 2013, v. 21, n. 10, p. 1049, doi. 10.1038/ejhg.2012.301

By:

Moat, Stuart J;
Bradley, Donald M;
Salmon, Rachel;
Clarke, Angus;
Hartley, Louise

Publication type:

Article

Examining the impact of web-based mindfulness on undergraduate student's quality of life: a randomized controlled trial.

Published in:

BMC Digital Health, 2023, v. 1, n. 1, p. 1, doi. 10.1186/s44247-023-00023-2

By:

Ahmad, Farah;
El Morr, Christo;
Ritvo, Paul;
MVC Team;
Abbas, Sahir;
Bohr, Yvonne;
Ferrari, Manuela;
Alan Fung, Wai Lun;
Hartley, Louise;
Mawani, Amin;
McKenzie, Kwame;
Odai, Jan E.

Publication type:

Article

Update on leukodystrophies and developing trials.

Published in:

Journal of Neurology, 2024, v. 271, n. 1, p. 593, doi. 10.1007/s00415-023-11996-5

By:

Ceravolo, Giorgia;
Zhelcheska, Kristina;
Squadrito, Violetta;
Pellerin, David;
Gitto, Eloisa;
Hartley, Louise;
Houlden, Henry

Publication type:

Article

Exploring links between early adversities and later outcomes for children adopted from care: Implications for planning post adoption support.

Published in:

Developmental Child Welfare, 2020, v. 2, n. 1, p. 52, doi. 10.1177/2516103220908043

By:

Neil, Elsbeth;
Morciano, Marcello;
Young, Julie;
Hartley, Louise

Publication type:

Article

Adult vaccination coverage in the United States: A database analysis and literature review of improvement strategies.

Published in:

Human Vaccines & Immunotherapeutics, 2024, v. 20, n. 1, p. 1, doi. 10.1080/21645515.2024.2381283

By:

Eiden, Amanda L.;
Hartley, Louise;
Garbinsky, Diana;
Saande, Cassondra;
Russo, Jon;
Hufstader Gabriel, Meghan;
Price, Mark;
Bhatti, Alexandra

Publication type:

Article

Appearance concerns and smoking in young men and women: Going beyond weight control.

Published in:

Drugs: Education, Prevention & Policy, 2010, v. 17, n. 3, p. 261, doi. 10.3109/09687630802422019

By:

Grogan, Sarah;
Hartley, Louise;
Conner, Mark;
Fry, Gary;
Gough, Brendan

Publication type:

Article

Resilience learning from the COVID-19 pandemic and its relevance for routine immunization programs.

Published in:

2022

By:

Falope, Oluyemisi;
Nyaku, Mawuli K.;
O'Rourke, Ciara;
Hermany, Lindsay V.;
Plavchak, Brittany;
Mauskopf, Josephine;
Hartley, Louise;
Kruk, Margaret E.

Publication type:

Literature Review

New horizons in systems engineering and thinking to improve health and social care for older people.

Published in:

Age & Ageing, 2024, v. 53, n. 10, p. 1, doi. 10.1093/ageing/afae238

By:

Aujla, Navneet;
Tooman, Tricia;
Arakelyan, Stella;
Kerby, Tim;
Hartley, Louise;
O'Donnell, Amy;
Guthrie, Bruce;
Underwood, Ian;
Jacko, Julie A;
Anand, Atul

Publication type:

Article

Loss-of-function mutations in SCN4A cause severe foetal hypokinesia or 'classical' congenital myopathy.

Published in:

2016

By:

Zaharieva, Irina T.;
Thor, Michael G.;
Oates, Emily C.;
Karnebeek, Clara van;
Hendson, Glenda;
Blom, Eveline;
Witting, Nanna;
Rasmussen, Magnhild;
Gabbett, Michael T.;
Ravenscroft, Gianina;
Sframeli, Maria;
Suetterlin, Karen;
Sarkozy, Anna;
D'Argenzio, Luigi;
Hartley, Louise;
Matthews, Emma;
Pitt, Matthew;
Vissing, John;
Ballegaard, Martin;
Krarup, Christian

Publication type:

journal article

Prolonged respiratory failure responds to conventional therapy in isolated homocysteine remethylation defects.

Published in:

2023

By:

Whitehouse, Abigail;
Rehsi, Preeya;
Hartley, Louise;
Grunewald, Stephanie;
Yilmaz, Berna Seker;
Pegoretti Baruteau, Kelly;
Yaman, Ayhan;
Thavagnanam, Suren;
Baruteau, Julien

Publication type:

Case Study

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy.

Published in:

BMC Medical Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12881-016-0294-2

By:

Fry, Andrew E.;
Rees, Elliott;
Thompson, Rose;
Mantripragada, Kiran;
Blake, Penny;
Jones, Glyn;
Morgan, Sian;
Jose, Sian;
Mugalaasi, Hood;
Archer, Hayley;
McCann, Emma;
Clarke, Angus;
Taylor, Clare;
Davies, Sally;
Gibbon, Frances;
Te Water Naude, Johann;
Hartley, Louise;
Thomas, Gareth;
White, Catharine;
Natarajan, Jaya

Publication type:

Article