Results 21 to 30 of about 25,914 (218)

Parkinson's Syndrome Secondary to Congenital Absence of the Left Internal Carotid Artery: a Case Report and Review of the Literature [PDF]

open access: yesZhongguo quanke yixue, 2023
Congenital absence of the internal carotid artery (ICA) is a rare congenital developmental anomaly, which is often associated with carotid canal atresia and structural abnormalities of the ICA. It may be asymptomatic, or shows noticeable symptoms such as
SUN Xiaoling, LI Zhijun
doaj   +1 more source

Unusual case of persistent Horner′s syndrome following epidural anaesthesia and caesarean section

open access: yesIndian Journal of Ophthalmology, 2011
This is a rare case of persistent Horner′s syndrome following epidural anesthesia and Caesarean section. A 33-year-old female presented with persistent ptosis and miosis following epidural anesthesia and Caesarian section several months prior.
Shubhra Goel, Cat Nguyen Burkat
doaj   +1 more source

The motivating operation and negatively reinforced problem behavior. A systematic review. [PDF]

open access: yes, 2014
The concept of motivational operations exerts an increasing influence on the understanding and assessment of problem behavior in people with intellectual and developmental disability. In this systematic review of 59 methodologically robust studies of the
Borthwick-Duffy S. A.   +7 more
core   +1 more source

Cultural syndromes: Socially learned but real [PDF]

open access: yes, 2016
While some of mental disorders due to emotional distress occur cross-culturally, others seem to be much more bound to particular cultures. In this paper, I propose that many of these “cultural syndromes” are culturally sanctioned responses to ...
Godman, Marion
core   +2 more sources

Acquired Horner′s syndrome in an infant: A case report

open access: yesMuller Journal of Medical Sciences and Research, 2014
Horner′s syndrome has varied etiology. We report a case of acquired Horner′s syndrome in an infant. A 3-month-old female child was referred for drooping of right eye upper lid on the second postoperative day following neck surgery.
Sumana J Kamath   +2 more
doaj   +1 more source

Regulation of the G2/M Transition in Rodent Oocytes [PDF]

open access: yes, 2010
Regulation of maturation in meiotically competent mammalian oocytes is a complex process involving the carefully coordinated exchange of signals between the somatic and germ cell compartments of the ovarian follicle via paracrine and cell–cell coupling ...
Downs, Stephen
core   +2 more sources

Training verbal working memory in children with mild intellectual disabilities: effects on problem-solving [PDF]

open access: yes, 2018
This multiple case study explores the effects of a cognitive training program in children with mild to borderline intellectual disability. Experimental training effects were evaluated comparing pre-post-test changes after (a) a baseline phase versus a ...
Caira, Simona   +6 more
core   +3 more sources

Pourfour du Petit Syndrome in a Patient with Thyroid Carcinoma

open access: yesCase Reports in Neurology, 2010
The clinical presentation of Pourfour du Petit syndrome (PdPs) is the opposite of Horner syndrome. Although all disorders underlying Horner syndrome may potentially present as PdPs, very few cases of the latter have been described in the literature.
Sergi Martinez-Ramirez   +2 more
doaj   +1 more source

Raeder's syndrome caused by a dissecant carotid aneurysm [PDF]

open access: yes, 1988
Os autores descrevem um caso de síndrome paratrigeminal de Raeder causada por aneurisma dissecante da carótida interna e tecem comentários sobre aspectos do diagnóstico.The authors report a case of Raeder's paratrigeminal syndrome and make some comments ...
Henriques, Fernando Guilhon   +1 more
core   +1 more source

Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome [PDF]

open access: yes, 2010
Background The introduction of molecular karyotyping technologies facilitated the identification of specific genetic disorders associated with imbalances of certain genomic regions.
Bena, F   +23 more
core   +2 more sources

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