Skip Nav Destination
Close Modal
Update search
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
All
- All
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Subjects
Journal
Article Type
Date
Availability
1-9 of 9
Keywords: Prevention
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
Diagnosis of Familial Hypercholesterolemia in General Practice Using Clinical Diagnostic Criteria or Genetic Testing as Part of Cascade Genetic Screening
Available to Purchase
Journal:
Community Genetics
Community Genetics (2008) 11 (1): 26–35.
Published Online: 15 January 2008
... or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Familial hypercholesterolemia Genetics Lipoproteins Mutation Prevention Screening Familial hypercholesterolemia (FH) is an autosomal dominantly inherited disorder of lipid...
Journal Articles
Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran
Available to PurchaseHossein Najmabadi, Alireza Ghamari, Farhad Sahebjam, Roxana Kariminejad, Valeh Hadavi, Talayeh Khatibi, Ashraf Samavat, Elaheh Mehdipour, Bernadette Modell, Mohammand Hassan Kariminejad
Journal:
Community Genetics
Community Genetics (2006) 9 (2): 93–97.
Published Online: 06 April 2006
...Hossein Najmabadi; Alireza Ghamari; Farhad Sahebjam; Roxana Kariminejad; Valeh Hadavi; Talayeh Khatibi; Ashraf Samavat; Elaheh Mehdipour; Bernadette Modell; Mohammand Hassan Kariminejad For 14 years, Iranian scientists have worked to develop a national thalassemia prevention program. Although...
Journal Articles
Community Diagnosis of Maternal Exposure to Risk Factors for Congenital Defects
Available to Purchase
Journal:
Community Genetics
Community Genetics (2003) 6 (2): 96–103.
Published Online: 17 October 2003
... age, alcohol ingestion and smoking), social and economic factors (family income and type of work), and welfare factors (prenatal care, illnesses during pregnancy, drug therapy, and vaccinations). These factors were matched up with the Decalogue for Prevention of Congenital Defects recommended...
Journal Articles
From Knowledge to Implementation
Available to Purchase
Journal:
Community Genetics
Community Genetics (2002) 5 (1): 5–7.
Published Online: 27 September 2002
... to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements. Congenital anomalies Genetic diseases Prevention Policy Implementation Every year some 3–9 million infants (2–6% of newborns) are born worldwide with major...
Journal Articles
Preventing Congenital Anomalies in Developing Countries
Available to Purchase
Journal:
Community Genetics
Community Genetics (2002) 5 (1): 61–69.
Published Online: 27 September 2002
... of exposures to infections and malnutrition. A number of successful measures for the prevention of congenital anomalies are being taken in a number of developing nations. Primary prevention programs are based on public education about preconceptional and prenatal risks. Prevention based on reproduction options...
Journal Articles
Teratology Information Services in Europe and Their Contribution to the Prevention of Congenital Anomalies
Available to Purchase
Journal:
Community Genetics
Community Genetics (2002) 5 (1): 8–12.
Published Online: 27 September 2002
...Maurizio Clementi; Elena Di Gianantonio; Asher Ornoy Objectives: To inform on Teratology Information Services (TIS) in Europe, their history, function and activity in preventing congenital malformations. Conclusions: Clinical teratology tries to identify human teratogens. TIS play an important role...
Journal Articles
Antiepileptic Drugs in Pregnancy: Options for the Prevention of Congenital Abnormalities
Available to Purchase
Journal:
Community Genetics
Community Genetics (2002) 5 (1): 40–49.
Published Online: 27 September 2002
...K. ten Berg; D. Lindhout Maternal antiepileptic drug use during pregnancy is associated with an increased prevalence of congenital malformations in the offspring. This article describes the commonly known teratogenic effects of antiepileptic drugs. Options for primary and secondary prevention...
Journal Articles
Prenatal Screening and the Reduction of Birth Defects in Populations
Available to Purchase
Journal:
Community Genetics
Community Genetics (1999) 2 (1): 9–17.
Published Online: 20 October 1999
.... Birth defects Prenatal screening Prevention Ultrasound screening Population screening It is not easy to define precisely a birth defect, but a working definition is a gross anatomic developmental anomaly present at birth or found during the first year of life. Under this definition...
Journal Articles
The Molecular Spectrum of Beta-Thalassemia and Abnormal Hemoglobins in the Allochthonous and Autochthonous Dutch Population
Available to PurchasePiero C. Giordano, Cees L. Harteveld, Angelien J.G.M. Heister, Desirée Batelaan, Peter van Delft, Rob Plug, Monique Losekoot, Luigi F. Bernini
Journal:
Community Genetics
Community Genetics (1999) 1 (4): 243–251.
Published Online: 17 June 1999
..., and the number of homozygous children is rising. Prevention by prenatal diagnosis requires a suitable protocol and knowledge about the molecular defects present in the country. Therefore we have analyzed a large number of patients and carriers, both at the hematological and at the DNA level. Our survey revealed...