Results 51 to 60 of about 357,975 (161)

Early‐life stasis in partial seasonal migration is underpinned by among‐cohort variation in migratory plasticity and selective disappearance

Journal of Animal Ecology, Volume 95, Issue 3, Page 538-552, March 2026.
Changes to mean early‐life phenotypes are fundamentally driven by joint dynamics of plasticity and selection, but such effects are rarely quantified. We show that cross‐cohort stasis in the degree of partial migration is underpinned by substantial within‐ and among‐cohort variation in plasticity and selection on migration, indicating high environmental
Cassandra R. Ugland, Paul Acker, Sarah J. Burthe, Rita Fortuna, Carrie Gunn, Michael P. Harris, Josie H. Hewitt, Timothy I. Morley, Mark A. Newell, Robert L. Swann, Erin A. Taylor, Sarah Wanless, Francis Daunt, Jane M. Reid   +13 more
wiley   +1 more source

Reply re: "Management of Marcus Gunn jaw winking synkinesis"

, 2004
Purpose: To report the outcomes of a management protocol for Marcus Gunn jaw winking ...
Bowyer, JD, Sullivan, TJ
core   +1 more source

Optic neuritis with secondary retinal venous stasis in a case of abdominal tuberculosis

Oman Journal of Ophthalmology, 2016
The authors report a case of unilateral optic neuritis along with secondary retinal venous stasis in a patient diagnosed with abdominal tuberculosis. Patient presented with diminished visual acuity, colour perception and Marcus Gunn pupillary response ...
Harshika Chawla, Vishal Vohra, Praveen Malik   +2 more
doaj   +1 more source

For an inviting anthropology Pour une anthropologie accueillante

Journal of the Royal Anthropological Institute, Volume 32, Issue 1, Page 7-26, March 2026.
Anthropologists have recently become inspired, captivated even, by the practices of the arts, design, and architecture in efforts to renew anthropology's modes of engagement and understandings of its relevance, particularly affecting how we approach ethnographic fieldwork.
Tomás Criado, Francisco Martínez, Eeva Berglund   +2 more
wiley   +1 more source

Sydrome de Marcus-Gunn: à propos d'un cas

The Pan African Medical Journal, 2016
Le syndrome de Marcus Gunn est un syndrome qui associe un ptosis congénital et une syncinésie mandibulo-palpébrale lors de certains mouvements mandibulaires.
Rajaa Elhannati, Meriem Abdellaoui, Idriss Andalloussi Benatiya, Hicham Tahri   +3 more
doaj   +1 more source

Fluoride and Neurodevelopmental Hazard Modelling: An Assessment of Concentration‐Response Analysis

Community Dentistry and Oral Epidemiology, Volume 54, Issue 1, Page 101-111, February 2026.
ABSTRACT Objectives A National Academies Consensus Study report concluded that the evidence did not support an assessment that fluoride is a neurodevelopmental hazard. However, some researchers have undertaken benchmark dose modelling to determine a safe fluoride concentration level in water.
Jayanth V. Kumar, Mark E. Moss, Honghu Liu, Susan Fisher‐Owens, Andrew Rugg‐Gunn, Julia Kuring   +5 more
wiley   +1 more source

RISK FACTORS FOR DEVELOPMENT OF NEOVASCULAR GLAUCOMA AFTER MINIINVASIVE DIABETIC VITRECTOMY IN PATIENTS WITH POLIFERATIVE DIABETIC RETINOPATHY

Medična Informatika ta Inženerìâ, 2015
The article presents the risk factors for neovascular glaucoma in patients after miniinvasive diabetic vitrectomy. This was a retrospective study of 237 eyes (237 patients) who underwent combined sutureless vitrectomy 23/25G for the complications of ...
A. N. Ruban
doaj   +1 more source

Thank You to Our 2025 Reviewers

Water Resources Research, Volume 62, Issue 4, April 2026.
Georgia Destouni, Andrea Castelletti, Simone Fatichi, Shafiqul Islam, Madan Kumar Jha, Stefan Kollet, Di Long, Chiyuan Miao, Hamid Moradkhani, Audrey Sawyer, Chaopeng Shen, Kamini Singha, Kerstin Stahl, Ellen Wohl, Yi Zheng   +14 more
wiley   +1 more source

Marcus Gunn phenomena

, 2016
Tato bakalářská je zaměřena na problematiku Marcus Gunn syndromu, především na jeho příčiny, projevy, léčbu a jeho souvislosti s ostatními vadami.
Tomandlová Eliška
core  

Speech and Language Disorders Associated With 7q31 Deletions Implicating FOXP2

American Journal of Medical Genetics Part A, Volume 197, Issue 12, December 2025.
ABSTRACT Some 7q31 deletions encompass FOXP2, a gene long associated with speech and language disorders. Intragenic pathogenic FOXP2 variants cause FOXP2‐related speech and language disorder, which has been well characterized in the literature. Conversely, the phenotype associated with 7q31 deletions is neglected.
Lottie D. Morison, Ruth Braden, David J. Amor, Angela T. Morgan   +3 more
wiley   +1 more source