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  <title>OAR@UM Collection:</title>
  <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/27466" />
  <subtitle />
  <id>https://www.um.edu.mt/library/oar/handle/123456789/27466</id>
  <updated>2026-04-28T21:05:12Z</updated>
  <dc:date>2026-04-28T21:05:12Z</dc:date>
  <entry>
    <title>Publishing on the WWW : part 4 : pubmed central : a publishing paradigm shift</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3855" />
    <author>
      <name>Grech, Victor E.</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3855</id>
    <updated>2018-03-23T07:02:27Z</updated>
    <published>2001-01-01T00:00:00Z</published>
    <summary type="text">Title: Publishing on the WWW : part 4 : pubmed central : a publishing paradigm shift
Authors: Grech, Victor E.
Abstract: This article discusses the environment leading to the founding of the Pubmed Central&#xD;
database, and its likely effects on publishing as we know it.</summary>
    <dc:date>2001-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Prenatal diagnosis of congenital anomalies</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3796" />
    <author>
      <name>Todros, Tullia</name>
    </author>
    <author>
      <name>Capuzzo, E.</name>
    </author>
    <author>
      <name>Gaglioti, Pietro</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3796</id>
    <updated>2019-02-11T14:41:23Z</updated>
    <published>2001-01-01T00:00:00Z</published>
    <summary type="text">Title: Prenatal diagnosis of congenital anomalies
Authors: Todros, Tullia; Capuzzo, E.; Gaglioti, Pietro
Abstract: Up till the early 1970s, prenatal diagnosis of congenital anomalies was primarily&#xD;
aimed at detecting chromosomal abnormalities by amniocentesis. Over the last two decades, prenatal diagnosis has greatly benefited from advances in ultrasound technology and in our ability to detect microscopic and submicroscopic chromosome abnormalities as well as single gene disorders, leading to substantive improvements&#xD;
in detection of such congenital anomalies. At present, invasive prenatal diagnosis&#xD;
continues to be the gold standard for pregnancies at increased risk for chromosomal&#xD;
anomaly or other genetic disease, with chorionic villus sampling being the procedure&#xD;
of choice for the first trimester whereas mid-trimester amniocentesis continues to be&#xD;
the most common form of invasive procedure for prenatal diagnosis. Still, invasive&#xD;
techniques are restricted to subgroups at risk for anomalies, for whom such time-consuming procedures are believed to be cost-effective, also accounting for&#xD;
procedure-related abortive risks. In the low-risk population prenatal diagnosis&#xD;
generally consists of screening procedures by means of ultrasound and maternal&#xD;
serum biochemistry.</summary>
    <dc:date>2001-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Clinical manifestations of Noonan syndrome</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3793" />
    <author>
      <name>Digilio, Maria Cristina</name>
    </author>
    <author>
      <name>Marino, Bonnie</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3793</id>
    <updated>2017-12-14T14:57:23Z</updated>
    <published>2001-01-01T00:00:00Z</published>
    <summary type="text">Title: Clinical manifestations of Noonan syndrome
Authors: Digilio, Maria Cristina; Marino, Bonnie
Abstract: Noonan syndrome is a common genetic disorder characterized by facial anomalies,&#xD;
congenital heart defect, short stature, webbed neck, chest deformities and&#xD;
undescended testes. The phenotypic expression of Noonan syndrome is extremely&#xD;
variable, with some affected subjects showing only minor features of the syndrome.&#xD;
Cardiac malformations are also heterogeneous. Pulmonary stenosis, with or without&#xD;
dysplastic pulmonary valve and hypertrophic cardiomyopathy, are the “classic”&#xD;
cardiac defects reported in Noonan syndrome. However, atrial septal defect,&#xD;
atrioventricular septal defect, left-sided obstructive lesions, tetralogy of Fallot and&#xD;
patent ductus arteriosus have also been described. Autosomal dominant inheritance&#xD;
has been documented in some families, although many cases appear to be sporadic.&#xD;
The diagnosis of Noonan syndrome is at present purely clinical, because a&#xD;
“diagnostic” test is not available. Indeed, although a gene for Noonan syndrome has&#xD;
been recently mapped by linkage analysis to chromosome 12q, the gene or genes of&#xD;
the syndrome have not been yet cloned.</summary>
    <dc:date>2001-01-01T00:00:00Z</dc:date>
  </entry>
  <entry>
    <title>Paediatrics in the XX century</title>
    <link rel="alternate" href="https://www.um.edu.mt/library/oar/handle/123456789/3787" />
    <author>
      <name>Vassallo Agius, Paul</name>
    </author>
    <id>https://www.um.edu.mt/library/oar/handle/123456789/3787</id>
    <updated>2015-07-02T01:04:38Z</updated>
    <published>2001-01-01T00:00:00Z</published>
    <summary type="text">Title: Paediatrics in the XX century
Authors: Vassallo Agius, Paul
Abstract: This is an editorial about the end of the twentieth century, with its seamless merging into the twenty first century, and a new millennium, is an excellent opportunity to reflect on the&#xD;
achievements in pediatrics over the last hundred years or so, and also perhaps&#xD;
hazard a guess at the expected developments in the twenty first century.&#xD;
The foundations of medical sciences were mainly laid during the preceding century or&#xD;
two, and after millennia of care of children by doctors who also cared for adults, the&#xD;
special needs of children were slowly but surely recognised, especially during the&#xD;
latter half of the nineteenth century. The emphasis has been on regarding the problems in the care of the child, especially the newborn baby, as needing special care and attention.</summary>
    <dc:date>2001-01-01T00:00:00Z</dc:date>
  </entry>
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