<?xml version="1.0" encoding="utf-8" ?> <rss version="2.0" xmlns:opensearch="http://a9.com/-/spec/opensearch/1.1/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:atom="http://www.w3.org/2005/Atom"> <channel> <title> <![CDATA[Cairo University Libraries portal Search for 'au:&quot;Hamdi Mahmoud Hassaneen &quot;'with limit(s): 'suppress:false']]> </title> <!-- prettier-ignore-start --> <link> https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-search.pl?idx=&#38;q=au%3A%22Hamdi%20Mahmoud%20Hassaneen%20%22&#38;sort_by=relevance&#38;format=rss </link> <!-- prettier-ignore-end --> <atom:link rel="self" type="application/rss+xml" href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-search.pl?idx=&#38;q=au%3A%22Hamdi%20Mahmoud%20Hassaneen%20%22&#38;sort_by=relevance&#38;format=rss" /> <description> Search results for 'au:&quot;Hamdi Mahmoud Hassaneen &quot;'with limit(s): 'suppress:false' at Cairo University Libraries portal </description> <opensearch:totalResults>22</opensearch:totalResults> <opensearch:startIndex>0</opensearch:startIndex> <opensearch:itemsPerPage>50</opensearch:itemsPerPage> <atom:link rel="search" type="application/opensearchdescription+xml" href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-search.pl?idx=&#38;q=au%3A%22Hamdi%20Mahmoud%20Hassaneen%20%22&#38;sort_by=relevance&#38;format=opensearchdescription" /> <opensearch:Query role="request" searchTerms="idx%3D%26q%3Dau%253A%2522Hamdi%2520Mahmoud%2520Hassaneen%2520%2522suppress%3Afalse" startPage="" /> <item> <title> synthesis of heterocyclic compounds incorporating indane - 1 , 3 - Dione moiety / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=11918</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 105Leaves ; 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=11918">Place hold on <em>synthesis of heterocyclic compounds incorporating indane - 1 , 3 - Dione moiety / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=11918</guid> </item> <item> <title> Microbiological and biochemical studies on the production of natamycin / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=11175</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 171Leaves : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=11175">Place hold on <em>Microbiological and biochemical studies on the production of natamycin / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=11175</guid> </item> <item> <title> A Biochemical Study of some Neurotransmitter Substances and Neuroprotecting Enzymes in Newborns with No Visible CongenitalAnomalies / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=4537</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 197P : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=4537">Place hold on <em>A Biochemical Study of some Neurotransmitter Substances and Neuroprotecting Enzymes in Newborns with No Visible CongenitalAnomalies / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=4537</guid> </item> <item> <title> Molecular basis of influenza a virus sensitivity to commercial drugs : Screening for novel antiviral compounds / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=61353</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 119 P. : 25cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=61353">Place hold on <em>Molecular basis of influenza a virus sensitivity to commercial drugs : </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=61353</guid> </item> <item> <title> Molecular study of human leucocyte antigen and ctyokine receptor expressions in hepatitis C virus infected patients / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=16734</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 125Leaves : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=16734">Place hold on <em>Molecular study of human leucocyte antigen and ctyokine receptor expressions in hepatitis C virus infected patients / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=16734</guid> </item> <item> <title> Novel synthesis and reactions of some nitrogen and sulfur heterocyclic systems / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=43966</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 83p : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=43966">Place hold on <em>Novel synthesis and reactions of some nitrogen and sulfur heterocyclic systems / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=43966</guid> </item> <item> <title> Synthesis of fused heterocyclic compounds / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=64000</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 84P ; 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=64000">Place hold on <em>Synthesis of fused heterocyclic compounds / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=64000</guid> </item> <item> <title> Determination Of Residues Of Carbamate Pesticides In Vegetables / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=180046</link> <!-- prettier-ignore-end --> <description> <p> 1994 .<br /> 106 Leaves : 30 cm. + .<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=180046">Place hold on <em>Determination Of Residues Of Carbamate Pesticides In Vegetables / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=180046</guid> </item> <item> <title> New approaches for the synthesis of derivatives of some extracted naturally occurring materials together with their cytotoxic evaluation / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=57247</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 189 P. : 25cm .<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=57247">Place hold on <em>New approaches for the synthesis of derivatives of some extracted naturally occurring materials together with their cytotoxic evaluation / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=57247</guid> </item> <item> <title> Utility of hydrazonoyl halides in the synthesis of azoloazines with expected biological activities / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=64213</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 174 P. ; 25cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=64213">Place hold on <em>Utility of hydrazonoyl halides in the synthesis of azoloazines with expected biological activities / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=64213</guid> </item> <item> <title> Novel routes to azoles and azines and this condensed derivatives utilizing enamine and amidrazon precursors / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=29150</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 49Leaves ; 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=29150">Place hold on <em>Novel routes to azoles and azines and this condensed derivatives utilizing enamine and amidrazon precursors / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=29150</guid> </item> <item> <title> Study the expression of DYRK1B Gene and Its Association with Metabolic Syndrome Among The Egyptians / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=164730</link> <!-- prettier-ignore-end --> <description> <p> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=164730">Place hold on <em>Study the expression of DYRK1B Gene and Its Association with Metabolic Syndrome Among The Egyptians /</em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=164730</guid> </item> <item> <title> Synthesis of heterocyclic compounds containing and derived from furochromones with expected biological activity / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=4020</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 112Leaves : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=4020">Place hold on <em>Synthesis of heterocyclic compounds containing and derived from furochromones with expected biological activity / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=4020</guid> </item> <item> <title> Synthesis of heterocyclic compounds containing nitrogen and / or sulfur / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=37819</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 56 P. : 25cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=37819">Place hold on <em>Synthesis of heterocyclic compounds containing nitrogen and / or sulfur / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=37819</guid> </item> <item> <title> Synthesis of heterocyclic compounds containing nitrogen and / or sulfur with expected biological activity / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=35622</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 103 P. : 25cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=35622">Place hold on <em>Synthesis of heterocyclic compounds containing nitrogen and / or sulfur with expected biological activity / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=35622</guid> </item> <item> <title> Utility of some isoquinoline derivatives in the synthesis of fused heterocyclic compounds with expected biological activities / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=47303</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 137 P. ; 25cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=47303">Place hold on <em>Utility of some isoquinoline derivatives in the synthesis of fused heterocyclic compounds with expected biological activities / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=47303</guid> </item> <item> <title> Palladium-catalyzed cross-coupling reaction of terminal alkynes with aryl halides / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=40479</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 198 P. : 25cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=40479">Place hold on <em>Palladium-catalyzed cross-coupling reaction of terminal alkynes with aryl halides / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=40479</guid> </item> <item> <title> Synthesis of some fused azines with expected biological activity / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=4542</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 139P. ; 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=4542">Place hold on <em>Synthesis of some fused azines with expected biological activity / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=4542</guid> </item> <item> <title> Reactivity of azaenamines towards electrophilic reagents : novel routs to arylazoazoles / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=78689</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 129P : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=78689">Place hold on <em>Reactivity of azaenamines towards electrophilic reagents : novel routs to arylazoazoles / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=78689</guid> </item> <item> <title> Synthesis of Some New Heterocycles With Anticipated Biological Activities / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=165143</link> <!-- prettier-ignore-end --> <description> <p> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=165143">Place hold on <em>Synthesis of Some New Heterocycles With Anticipated Biological Activities /</em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=165143</guid> </item> <item> <title> Identification and characterization of bacterially expressed structural protein of hepatitis C virus genotype 4 / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=29639</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 78 Leaves : 30cm.<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=29639">Place hold on <em>Identification and characterization of bacterially expressed structural protein of hepatitis C virus genotype 4 / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=29639</guid> </item> <item> <title> Synthesis, reactions and biological evaluation of some chalcones and schiff bases incorporating heterocyclic compounds / </title> <dc:identifier>ردمك: </dc:identifier> <!-- prettier-ignore-start --> <link>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=83530</link> <!-- prettier-ignore-end --> <description> <p> .<br /> 137 P. : 25cm .<br /> </p> <p> <a href="https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-reserve.pl?biblionumber=83530">Place hold on <em>Synthesis, reactions and biological evaluation of some chalcones and schiff bases incorporating heterocyclic compounds / </em></a> </p> </description> <guid>https://lis.cl.cu.edu.eg/cgi-bin/koha/opac-detail.pl?biblionumber=83530</guid> </item> </channel> </rss>
