Results 191 to 200 of about 32,034 (248)

The challenges of eating out for young people with eating disorders: a thematic analysis of the perspectives of young people, parents and carers, and clinicians. [PDF]

J Eat Disord
Shackshaft L, Chapman L, Hook A, Biddle L, Yardley L, Ford T, Attwood A, Penton-Voak I, Slater M, Rothwell E, Reeves S, Grant A, Downs J, Combe G, Clark-Stone S, Govender T, Stewart A, Moran P, Bould H.   +18 more
europepmc   +1 more source

How do visual and conceptual factors predict the object content in typical scene drawings?

British Journal of Psychology, EarlyView.
Abstract Imagine you draw a typical bedroom, your choice of objects is likely to depend on visual occurrence statistics (i.e. the objects present in previously encountered bedrooms) and semantic relations between objects and scenes (i.e. the semantic relationship between the bedroom and its constituent objects).
Gongting Wang, Ilker Duymaz, Matthew J. Foxwell, Micha Engeser, David Pitcher, Radoslaw M. Cichy, Daniel Kaiser   +6 more
wiley   +1 more source

Research Priorities for Children With Food Allergy: A UK James Lind Alliance Priority Setting Partnership

Clinical &Experimental Allergy, EarlyView.
The UK childhood food allergy James Lind Alliance Priority Setting Partnership collaboratively identified the most important research priorities highlighting the breadth of research required to improve the prevention, diagnosis, treatment and broader impacts of food allergy on those directly impacted. These provide a clear, stakeholder‐driven agenda to
Roxanne M. Parslow, Farhad Shokraneh, Sara J. Brown, Mary Feeney, Graham Roberts, Hora Soltani, Joanne Walsh, Amy Dobson, Emma Vaughan, Deborah Marriage, Suzi Holland, Mary Kelly, Holly Shaw, Alicia Kennedy, Eden Byrne, Liliana Jackson, Gail Jackson, Lauren Gluyas, Jonathan Gower, Alyson Huntley, Matthew J. Ridd   +20 more
wiley   +1 more source

Ultrasonography for Surgical Planning and Follow-Up in Neurofibromatosis Type 1. [PDF]

Diagnostics (Basel)
Shen PY, Ho CJ, Wu WT, Chang KV, Özçakar L.   +4 more
europepmc   +1 more source

‘Fatherhood Under Suspicion’: The Experiences of Fathers of At‐Risk Children From East Jerusalem Following Out‐of‐Home Placement

Child &Family Social Work, EarlyView.
ABSTRACT Fathers, particularly in conservative patriarchal societies and politically complex contexts, are often underrepresented in research on child protection and out‐of‐home placements. Addressing this significant knowledge gap, this study focuses on Palestinian fathers from East Jerusalem whose young children were removed from their homes by court
Mayis Eissa
wiley   +1 more source

Exploring Healthy Ageing in Place for Roma Communities: Insights from Knowledge Café Workshops in the UK. [PDF]

J Cross Cult Gerontol
Woolrych R, Marinov A, Sixsmith J, Greenfields M, Cisneros R, Torak P, Hyde A, Morteanu C, Smolinska-Poffley G.   +8 more
europepmc   +1 more source

Clinical and Genetic Profile of One Molecularly Confirmed and One Clinically Suspected Case of LZTR1‐Related Noonan Syndrome

Clinical Genetics, EarlyView.
This study illustrates the phenotypic variability of LZTR1‐related Noonan syndrome type 10 in two pediatric patients, including presentations without congenital heart defects. The findings emphasize the importance of whole‐exome sequencing and longitudinal re‐evaluation of variants of uncertain significance in achieving accurate diagnosis.
Karolina Skrzyńska, Barbara Kalina‐Faska, Ewa Błaszczyk, Aneta Gawlik‐Starzyk   +3 more
wiley   +1 more source

Using social norms to reduce plate waste in corporate dining. [PDF]

Sci Rep
Daker RJ, Del Mar Rojas M, Rakhimov R, Heffner K, Paine N, Cacciola K, Hanson C, Upritchard J.   +7 more
europepmc   +1 more source

Genetic Spectrum of Non‐PTPN11 Variants in Noonan Syndrome and Related RASopathies: Findings From a Russian Cohort

Clinical Genetics, EarlyView.
Noonan syndrome and related conditions are caused by variants in multiple genes. We analyzed 456 Russian patients using a 23‐gene panel and found disease‐causing variants in non‐PTPN11 genes in 85 cases. NF1, SOS1, BRAF, and SHOC2 explained half of these diagnoses.
Anna Orlova, Olga Shatokhina, Daria Guseva, Nina Demina, Aleksander Polyakov, Oхana Ryzkova   +5 more
wiley   +1 more source