A controlled retrospective follow-up study of the impact of genetic counselling on parental reproduction following the birth of a Down syndrome child

1982 ◽  
Vol 4 (1) ◽  
pp. 54
Keyword(s):  
Down Syndrome ◽  
Genetic Counselling ◽  
Follow Up Study ◽  
Down Syndrome Child ◽  
The Impact ◽  
Syndrome Child

An overview of body weight of older persons, including the impact on mortality The national health and nutrition examination survey i-epidemiologic follow-up study

1991 ◽  
Vol 44 (8) ◽  
pp. 743-753 ◽  
Author(s):  
Joan C. Cornoni-Huntley ◽  
Tamara B. Harris ◽  
Donald F. Everett ◽  
Demetrius Albanes ◽  
Marc S. Micozzi ◽  
...  
Keyword(s):  
Body Weight ◽  
National Health ◽  
Older Persons ◽  
Nutrition Examination Survey ◽  
Follow Up Study ◽  
Health And Nutrition ◽  
The Impact

scholarly journals Keeping the Flame Lit: The Value of the Long-Term Permanence of a Science Club

2018 ◽  
Vol 41 (1) ◽  
pp. 132-143
Author(s):  
Miguel García-Guerrero ◽  
Bertha Michel-Sandoval ◽  
Viridiana Esparza-Manrique ◽  
Amelia Rodríguez-Pinedo ◽  
Vianey Raudales-Hernández ◽  
...  
Keyword(s):  
Public Communication ◽  
Children And Young People ◽  
Follow Up Study ◽  
School Programs ◽  
Science Clubs ◽  
The Impact ◽  
Science Club ◽  
Science Activities

Science clubs are programs that allow people (especially children and youngsters) to meet regularly outside of school programs and engage with science and technology activities. Clubs encourage participants to foster attitudes, capabilities, and knowledge related to STEM fields with the goal of promoting interest and passion about science. As such programs provide big opportunities to improve the impact of public communication of science activities, it is really important to look at the impacts of such programs. Quark Group runs the Children Science Club since 2002, and up to 2016, it developed science recreation activities with 711 children and young people. In order to establish the influence the club had on its participants, we conducted a survey that provided 244 answers. This article presents the findings of this follow-up study.

Shifts in Fear of Success in Men and Women from 1968 to 1987

1987 ◽  
Vol 61 (1) ◽  
pp. 36-38 ◽  
Author(s):  
Darhl M. Pedersen ◽  
Tracy Conlin
Keyword(s):  
Women's Liberation ◽  
Fear Of Success ◽  
Cultural Changes ◽  
Men And Women ◽  
Follow Up Study ◽  
Women’S Liberation ◽  
Societal Changes ◽  
The Impact

A follow-up study on feat of success was completed 19 years after Horner collected her data in 1968. It was hypothesized that cultural changes relating to women's liberation would result in fewer women and more men exhibiting fear of success compared to Horner's findings. 25 men and 25 women were tested using Horner's procedures to facilitate comparisons. A higher percentage of men exhibited fear of success than Horner reported; however, the percentage of women remained about the same. Apparently, the impact of societal changes on men has been greater than on women.

The impact of cardiovascular diseases on hearing deterioration: a 13-year follow-up study

2021 ◽  
pp. 1-6
Author(s):  
Venla Lohi ◽  
Pasi Ohtonen ◽  
Martti Sorri ◽  
Elina Mäki-Torkko ◽  
Samuli Hannula
Keyword(s):  
Cardiovascular Diseases ◽  
Follow Up Study ◽  
The Impact

scholarly journals Partial Syndrome of Myotonic Dystrophy: Clinical Presentation and Follow-up

1989 ◽  
Vol 16 (1) ◽  
pp. 99-103 ◽  
Author(s):  
Jean Mathieu ◽  
Marcel Simard ◽  
Marc De Braekeleer ◽  
Camil Boily ◽  
Aurèle Deschênes
Keyword(s):  
Myotonic Dystrophy ◽  
Genetic Counselling ◽  
Clinical Presentation ◽  
Dna Probes ◽  
Average Period ◽  
Reliable Identification ◽  
Follow Up Study ◽  
Gene Carriers ◽  
Typical Form

ABSTRACT:The neurological and ophthalmological investigation of 602 members of 88 Saguenay kindreds affected by myotonic dystrophy (MyD) revealed 130 persons with a partial syndrome. These patients, whose average age was 34.1 years, showed different abnormalities such as particular ophthalmic and/or neuro-muscular signs, suggesting MyD in the absence of myotonia or typical lens abnormalities. After an average period of 2,4 years, 44 of these 130 patients were reassessed by the same neurologists and ophthalmologists. Thirty still had a partial syndrome, 8 showed a typical form of MyD and 6 no longer presented any identifiable anomaly. This preliminary follow-up study of the partial MyD syndrome did not allow us to identify any clinical anomaly from which the presence of the MyD gene could be predicted in a significant way. It furthermore suggested that the identification of equivocal or unspecific signs among these patients can sometimes lead to misdiagnosis. This must be taken into account when providing genetic counselling. It furthermore indicates that the use of DNA probes is essential for a reliable identification of asymptomatic MyD gene carriers.

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