Results 61 to 70 of about 1,134,664 (163)
International Journal of Osteoarchaeology, Volume 35, Issue 2, March/April 2025.ABSTRACT Pellagra is a disease caused by a nutritional deficiency, with fatal outcome due to multiple‐organ failure, that affected European rural areas until the early decades of the 20th century, especially Veneto region (Italy). At the skeletal level, previous studies pointed out that pathological signs left by the disease are generic and typical of ...
Nicola Carrara +8 more
wiley +1 more source
, 1999 OBJECTIVE: To investigate the effect of parity on Down syndrome (DS). METHODS: The study was conducted on data from Northeast Italy (NEI) (1981-1996) and Sicily (ISMAC) (1991-1996) Congenital Malformation Registries.
Working Group on Down Syndrome +4 more
core +1 more source
The experience of humour in Asperger’s syndrome [PDF]
, 2010 A Thesis submitted in fulfilment of the requirements of the University of Wolverhampton for the degree of Doctor of Counselling Psychology.This study investigated the experience of humour of people with Asperger’s syndrome.
Ruggeri, Susan
core +3 more sources
Ortner's syndrome: a rare case of cardiovocal hoarseness
Italian Journal of Medicine, 2013 Introduction Ortner's syndrome, also known as cardiovocal syndrome, is a rare clinical entity with hoarseness due to left recurrent laryngeal nerve (RLN) palsy owing to a cardiovascular disease.
Gelorma Belmonte +7 more
doaj +1 more source
British Journal of Pharmacology, Volume 182, Issue 1, Page 181-197, January 2025.Abstract Background and Purpose Pathogenic gain‐of‐function mutations in Cav1.3 L‐type voltage‐gated Ca2+‐channels (CACNA1D) cause neurodevelopmental disorders with or without endocrine symptoms. We aimed to confirm a pathogenic gain‐of function phenotype of CACNA1D de novo missense mutations A749T and L271H, and investigated the molecular mechanism ...
Ferenc Török +5 more
wiley +1 more source
Exploring face perception in disorders of development: evidence from Williams syndrome and autism [PDF]
, 2008 Individuals with Williams syndrome (WS) and autism are characterized by different social phenotypes but have been said to show similar atypicalities of face-processing style.
Riby, Deborah +2 more
core +1 more source
Collaborative practice with parents in occupational therapy for children: A scoping review
Australian Occupational Therapy Journal, Volume 71, Issue 5, Page 833-850, October 2024.Abstract Introduction In childhood intervention, parent–therapist collaboration is central to the family‐centred approach. Despite long‐standing discussion in occupational therapy literature, the field faces challenges, including inconsistent terminology and difficulties in translating theory into practice.
Carla R. Lage +4 more
wiley +1 more source
Ortner's syndrome secondary to a thoracic thrombosed aortic aneurysm: Case report
Radiology Case ReportsOrtner's syndrome refers to vocal cord paralysis resulting from compression of the left recurrent laryngeal nerve by abnormal mediastinal vascular structures.
Mohammed Leknani +6 more
doaj +1 more source
A Leadership of Refusal: Remaking the Narrative of the Falling Leader
British Journal of Management, Volume 35, Issue 4, Page 2137-2154, October 2024.Abstract The metaphor of the glass cliff is used to describe patterns whereby women are more likely to be selected for challenging leadership positions that have a higher risk of failure. This paper explores how the glass cliff metaphor contributes to a narrative of woman's fall that individualizes a leader's responsibility to avoid risks that may lead
Emma Bell +2 more
wiley +1 more source
Reversible Ortner’s syndrome in a woman with decompensated rheumatic heart disease: a case report
Journal of Medical Case ReportsBackground Ortner’s syndrome, or cardiovocal syndrome, is a rare form of left recurrent laryngeal nerve palsy caused by cardiovascular pathology. Historically associated with massive left atrial enlargement from rheumatic heart disease (RHD), it is now ...
Prabhat Sharma +5 more
doaj +1 more source