Sepiapterin Reductase Deficiency: Two Indian Siblings with Unusual Clinical Features
Identifieur interne : 002428 ( Main/Merge ); précédent : 002427; suivant : 002429Sepiapterin Reductase Deficiency: Two Indian Siblings with Unusual Clinical Features
Auteurs : Gurusidheshwar M. Wali [Inde] ; Beat Thony [Suisse] ; Nenad Blau [Suisse]Source :
- Movement disorders [ 0885-3185 ] ; 2010.
Descripteurs français
- Pascal (Inist)
- Wicri :
- topic : Déficit.
English descriptors
Links toward previous steps (curation, corpus...)
- to stream PascalFrancis, to step Corpus: 000B06
- to stream PascalFrancis, to step Curation: 002213
- to stream PascalFrancis, to step Checkpoint: 000841
Links to Exploration step
Pascal:10-0288358Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en" level="a">Sepiapterin Reductase Deficiency: Two Indian Siblings with Unusual Clinical Features</title>
<author><name sortKey="Wali, Gurusidheshwar M" sort="Wali, Gurusidheshwar M" uniqKey="Wali G" first="Gurusidheshwar M." last="Wali">Gurusidheshwar M. Wali</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Neurospecialities Centre Belgaum, Karnataka State</s1>
<s3>IND</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
<country>Inde</country>
<wicri:noRegion>Neurospecialities Centre Belgaum, Karnataka State</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Thony, Beat" sort="Thony, Beat" uniqKey="Thony B" first="Beat" last="Thony">Beat Thony</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</s1>
<s2>Zurich</s2>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Suisse</country>
<wicri:noRegion>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Blau, Nenad" sort="Blau, Nenad" uniqKey="Blau N" first="Nenad" last="Blau">Nenad Blau</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</s1>
<s2>Zurich</s2>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Suisse</country>
<wicri:noRegion>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</wicri:noRegion>
</affiliation>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">INIST</idno>
<idno type="inist">10-0288358</idno>
<date when="2010">2010</date>
<idno type="stanalyst">PASCAL 10-0288358 INIST</idno>
<idno type="RBID">Pascal:10-0288358</idno>
<idno type="wicri:Area/PascalFrancis/Corpus">000B06</idno>
<idno type="wicri:Area/PascalFrancis/Curation">002213</idno>
<idno type="wicri:Area/PascalFrancis/Checkpoint">000841</idno>
<idno type="wicri:doubleKey">0885-3185:2010:Wali G:sepiapterin:reductase:deficiency</idno>
<idno type="wicri:Area/Main/Merge">002428</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en" level="a">Sepiapterin Reductase Deficiency: Two Indian Siblings with Unusual Clinical Features</title>
<author><name sortKey="Wali, Gurusidheshwar M" sort="Wali, Gurusidheshwar M" uniqKey="Wali G" first="Gurusidheshwar M." last="Wali">Gurusidheshwar M. Wali</name>
<affiliation wicri:level="1"><inist:fA14 i1="01"><s1>Neurospecialities Centre Belgaum, Karnataka State</s1>
<s3>IND</s3>
<sZ>1 aut.</sZ>
</inist:fA14>
<country>Inde</country>
<wicri:noRegion>Neurospecialities Centre Belgaum, Karnataka State</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Thony, Beat" sort="Thony, Beat" uniqKey="Thony B" first="Beat" last="Thony">Beat Thony</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</s1>
<s2>Zurich</s2>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Suisse</country>
<wicri:noRegion>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Blau, Nenad" sort="Blau, Nenad" uniqKey="Blau N" first="Nenad" last="Blau">Nenad Blau</name>
<affiliation wicri:level="1"><inist:fA14 i1="02"><s1>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</s1>
<s2>Zurich</s2>
<s3>CHE</s3>
<sZ>2 aut.</sZ>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>Suisse</country>
<wicri:noRegion>Laboratory of Clinical Chemistry ana Biochemistry University Children's Hospital</wicri:noRegion>
</affiliation>
</author>
</analytic>
<series><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2010">2010</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
<seriesStmt><title level="j" type="main">Movement disorders</title>
<title level="j" type="abbreviated">Mov. disord.</title>
<idno type="ISSN">0885-3185</idno>
</seriesStmt>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Deficiency</term>
<term>Indian</term>
<term>Nervous system diseases</term>
<term>Sepiapterin reductase</term>
<term>Sibling</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr"><term>Déficit</term>
<term>Pathologie du système nerveux</term>
<term>Sepiapterin reductase</term>
<term>Indien</term>
<term>Fratrie</term>
</keywords>
<keywords scheme="Wicri" type="topic" xml:lang="fr"><term>Déficit</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
</TEI>
<affiliations><list><country><li>Inde</li>
<li>Suisse</li>
</country>
</list>
<tree><country name="Inde"><noRegion><name sortKey="Wali, Gurusidheshwar M" sort="Wali, Gurusidheshwar M" uniqKey="Wali G" first="Gurusidheshwar M." last="Wali">Gurusidheshwar M. Wali</name>
</noRegion>
</country>
<country name="Suisse"><noRegion><name sortKey="Thony, Beat" sort="Thony, Beat" uniqKey="Thony B" first="Beat" last="Thony">Beat Thony</name>
</noRegion>
<name sortKey="Blau, Nenad" sort="Blau, Nenad" uniqKey="Blau N" first="Nenad" last="Blau">Nenad Blau</name>
</country>
</tree>
</affiliations>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Main/Merge
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 002428 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Merge/biblio.hfd -nk 002428 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Wicri/Santé |area= MovDisordV3 |flux= Main |étape= Merge |type= RBID |clé= Pascal:10-0288358 |texte= Sepiapterin Reductase Deficiency: Two Indian Siblings with Unusual Clinical Features }}
![]() | This area was generated with Dilib version V0.6.23. | ![]() |