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    <title>Meurs-van Woezik, H. van</title>
    <link>http://repub.eur.nl/res/aut/3722/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
    <item>
      <title>Coronary artery changes 3 years after reimplantation of an anomalous right coronary artery (Article)</title>
      <link>http://repub.eur.nl/res/pub/4115/</link>
      <pubDate>1984-01-01T00:00:00Z</pubDate>
      <description>In this paper we report the sequelae of a patient with an anomalous right coronary artery (RCA) originating from the pulmonary artery (PA) in association with a normal heart, operated upon at the age of 13 years. Three years after the end-to-side reimplantation of the RCA, with a rim of the PA, into the aorta, the surgical result has been evaluated by cineangiography. Before operation both coronary arteries were tortuous and increased in size. Afterwards the left coronary artery showed a normalized calibre, although the RCA remained tortuous with no decrease of the internal diameter. The notable postoperative changes in shape and size of the LCA may be due to the disappearance of the steal phenomenon. The lack of involutive changes in the RCA could be explained by its thinner wall. Left ventricular wall motion, evaluated under resting conditions and during an atrial pacing stress test, was found to be normal.</description>
    </item> <item>
      <title>Congenital arteriovenous fistula between the internal mammary artery and the pulmonary artery (Article)</title>
      <link>http://repub.eur.nl/res/pub/4116/</link>
      <pubDate>1984-01-01T00:00:00Z</pubDate>
      <description>This is the fourth reported case of congenital arteriovenous fistula between the internal mammary artery and pulmonary artery. Precise and complete diagnostic evaluation is required to localize, delineate and appreciate the haemodynamic significance of this type of arteriovenous shunt. A brief review of the literature is given with suggestions for diagnosis.</description>
    </item> <item>
      <title>The great arteries in normal and some congenitally malformed hearts their internal calibres and tunica media in relation to blood flow  (Doctoral Thesis)</title>
      <link>http://repub.eur.nl/res/pub/25781/</link>
      <pubDate>1979-06-27T00:00:00Z</pubDate>
      <description>The road from fertilized egg to newborn baby is a fascinating
and complicated one. What happens to eggs that actually come in contact
with spenns has been stuclied by many authors and has been summarized
by Witschi in 1969. About 16% of the eggs do not cleave, either because
they are not penetrated by sperms or because the mitotic mechanism
does not function. Another 15% are lost during the first week, at various
preimplantation stages ( cleavage and blastocyst stages ). The stage of
early implantation and development during the second week brings a
further lossof 27%. In the third to sixth week there is a loss of 8%
and the late abortion loss is about 3%. Live births will then amount to
only 31%. It has been shown that 1-12% of all these newborn children
carry some major congenital malformation recognizable at or shortly
after birth ( Yerushalmy, 1969; Lilienfeld, 1969 ), Reports of congenital
malformations show congenital heart malformations in about 0.8% of total
births ( Kerrebijn, 1964; Hoffman and Christianson, 1978 ). In the
Netherlands with 177.090 newborns in 1976 this will be about 1400 per
year of which 123 were surgically corrected and 416 died in the first
year of life ( Centraal Bureau voor Statistiek, 1976, 1978 ).
The majority of congenital he'art malfonnations are of rmknown
etiology and are believed to be the result of the interaction of
environmental and genetic influences ( Nora, 1968 ). The risk for
recurrence of the same lesion in cases with an affected parent or
sibling is small but exceeds the expectation risk for the same lesion
in the general population. Vertical transmission of atrial septal
defects through four generations has been described (Lynch et al.,
1978 ) .
These children bom with congenital heart malfonnations are of
special interest to the paediatric cardiologist and cardiovascular
surgeon.</description>
    </item> <item>
      <title>The great arteries in normal and some congenitally malformed hearts their internal calibres and tunica media in relation to blood flow  (Doctoral Thesis)</title>
      <link>http://repub.eur.nl/res/pub/25782/</link>
      <pubDate>1979-06-27T00:00:00Z</pubDate>
      <description>The road from fertilized egg to newborn baby is a fascinating
and complicated one. What happens to eggs that actually come in contact
with spenns has been stuclied by many authors and has been summarized
by Witschi in 1969. About 16% of the eggs do not cleave, either because
they are not penetrated by sperms or because the mitotic mechanism
does not function. Another 15% are lost during the first week, at various
preimplantation stages ( cleavage and blastocyst stages ). The stage of
early implantation and development during the second week brings a
further lossof 27%. In the third to sixth week there is a loss of 8%
and the late abortion loss is about 3%. Live births will then amount to
only 31%. It has been shown that 1-12% of all these newborn children
carry some major congenital malformation recognizable at or shortly
after birth ( Yerushalmy, 1969; Lilienfeld, 1969 ), Reports of congenital
malformations show congenital heart malformations in about 0.8% of total
births ( Kerrebijn, 1964; Hoffman and Christianson, 1978 ). In the
Netherlands with 177.090 newborns in 1976 this will be about 1400 per
year of which 123 were surgically corrected and 416 died in the first
year of life ( Centraal Bureau voor Statistiek, 1976, 1978 ).
The majority of congenital he'art malfonnations are of rmknown
etiology and are believed to be the result of the interaction of
environmental and genetic influences ( Nora, 1968 ). The risk for
recurrence of the same lesion in cases with an affected parent or
sibling is small but exceeds the expectation risk for the same lesion
in the general population. Vertical transmission of atrial septal
defects through four generations has been described (Lynch et al.,
1978 ) .
These children bom with congenital heart malfonnations are of
special interest to the paediatric cardiologist and cardiovascular
surgeon.</description>
    </item>
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