نتائج البحث - "Zidovska, Jana"

1

Academic Journal

Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers

المؤلفون: Tesner, Pavel, Vlckova, Marketa, Drabova, Jana, Vseticka, Jan, Klimova, Anna, Lastuvkova, Jana, Zidovska, Jana, Kremlikova Pourova, Radka, Hancarova, Miroslava, Sedlacek, Zdenek, Kocarek, Eduard

المصدر: Cytogenetic and Genome Research ; volume 154, issue 4, page 187-195 ; ISSN 1424-8581 1424-859X

الاتاحة: http://dx.doi.org/10.1159/000488790
https://karger.com/cgr/article-pdf/154/4/187/3926574/000488790.pdf

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2

Academic Journal

The impact of Huntington disease on garegivers: the Czech experience

المؤلفون: Roth, Jan, Uhrová, Teresa, Doubek, Pavel, Preiss, Marek, Zidovska, Jana, Havrdová, Eva, Ruzicka, Evzen

المصدر: Revista de Neuro-Psiquiatria; Vol 65 No 3-4 (2002): Revista de Neuro-Psiquiatría; 168-173 ; Revista de Neuro-Psiquiatria; Vol. 65 Núm. 3-4 (2002): Revista de Neuro-Psiquiatría; 168-173 ; 1609-7394 ; 0034-8597

وصف الملف: application/pdf

Relation: https://revistas.upch.edu.pe/index.php/RNP/article/view/1520/1548; https://revistas.upch.edu.pe/index.php/RNP/article/view/1520

الاتاحة: https://revistas.upch.edu.pe/index.php/RNP/article/view/1520
https://doi.org/10.20453/rnp.v65i3-4.1520

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3

Academic Journal

High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague area

المؤلفون: Pohlreich, Petr, Zikan, Michal, Stribrna, Jana, Kleibl, Zdenek, Janatova, Marketa, Kotlas, Jaroslav, Zidovska, Jana, Novotny, Jan, Petruzelka, Lubos, Szabo, Csilla, Matous, Bohuslav

المصدر: Breast Cancer Research ; volume 7, issue 5 ; ISSN 1465-542X

الاتاحة: http://dx.doi.org/10.1186/bcr1282
http://link.springer.com/article/10.1186/bcr1282/fulltext.html
http://link.springer.com/content/pdf/10.1186/bcr1282.pdf

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4

Academic Journal

The number of CAG repeats within the normal allele does not influence the age of onset in Huntington's disease

المؤلفون: Klempíř, Jiří, Židovská, Jana, Štochl, Jan, Ing, Věra Kebrdlová, Uhrová, Tereza, Roth, Jan

المساهمون: Czech Ministry of Education Research Programs

المصدر: Movement Disorders ; volume 26, issue 1, page 125-129 ; ISSN 0885-3185 1531-8257

الاتاحة: http://dx.doi.org/10.1002/mds.23436
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmds.23436
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.23436/fullpdf

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5

Academic Journal

Variation of selective gray and white matter atrophy in Huntington's disease

المؤلفون: Jech, Robert, Klempíř, Jiří, Vymazal, Josef, Židovská, Jana, Klempířová, Olga, Růžička, Evžen, Roth, Jan

المصدر: Movement Disorders ; volume 22, issue 12, page 1783-1789 ; ISSN 0885-3185 1531-8257

الاتاحة: http://dx.doi.org/10.1002/mds.21620
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmds.21620
https://onlinelibrary.wiley.com/doi/full/10.1002/mds.21620

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6

Academic Journal

MR relaxometry in Huntington's disease: Correlation between imaging, genetic and clinical parameters

المؤلفون: Vymazal, Josef, Klempíř, Jiří, Jech, Robert, Židovská, Jana, Syka, Michael, Růžička, Evžen, Roth, Jan

المصدر: Journal of the Neurological Sciences ; volume 263, issue 1-2, page 20-25 ; ISSN 0022-510X

الاتاحة: http://dx.doi.org/10.1016/j.jns.2007.05.018
https://api.elsevier.com/content/article/PII:S0022510X07003772?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0022510X07003772?httpAccept=text/plain

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7

Academic Journal

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease

مصطلحات موضوعية: 570 Biowissenschaften, Biologie, ddc:570, 610 Medizin, ddc:610

وصف الملف: application/pdf

Relation: https://epub.uni-regensburg.de/1000/1/metzger.pdf; Metzger, Silke, Bauer, Peter, Tomiuk, Juergen, Laccone, Franco, Didonato, Stefano, Gellera, Cinzia, Soliveri, Paola, Lange, Herwig W., Weirich-Schwaiger, Helga, Wenning, Gregor K., Melegh, Bela, Havasi, Victoria, Balikó, Lazlo, Wieczorek, Stefan, Arning, Larissa, Zaremba, Jacek, Sulek, Anna, Hoffman-Zacharska, Dorota, Basak, A. Nazli, Ersoy, Nagehan, Zidovska, Jana, Kebrdlova, Vera, Pandolfo, Massimo, Ribaï, Pascale, Kadasi, Ludovit, Kvasnicova, Marta, Weber, Bernhard H. F., Kreuz, Friedmar, Dose, Matthias, Stuhrmann, Manfred und Riess, Olaf (2006) The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease. Neurogenetics 7 (1), S. 27-30.

الاتاحة: https://epub.uni-regensburg.de/1000/
https://epub.uni-regensburg.de/1000/1/metzger.pdf
https://doi.org/10.1007/s10048-005-0023-z
https://doi.org/10.5283/epub.1000

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8

Academic Journal

Genetic analysis of candidate genes modifying the age-at-onset in Huntington's disease.

المصدر: Human genetics, 120 (2

مصطلحات موضوعية: Sciences bio-médicales et agricoles, Acyltransferases, Adaptor Proteins, Signal Transducing, Adolescent, Adult, Age of Onset, Aged, 80 and over, Brain-Derived Neurotrophic Factor -- genetics, Brain-Derived Neurotrophic Factor -- metabolism, Carrier Proteins -- genetics, Carrier Proteins -- metabolism, Child, Preschool, DNA-Binding Proteins -- genetics, DNA-Binding Proteins -- metabolism, Humans, Huntington Disease -- epidemiology, Huntington Disease -- genetics, Huntington Disease -- metabolism, Middle Aged, Nerve Tissue Proteins -- genetics, Nerve Tissue Proteins -- metabolism, Nuclear Proteins -- metabolism, Polymorphism, Genetic, Receptors, Kainic Acid -- genetics, TATA-Box Binding Protein -- genetics

وصف الملف: No full-text files

Relation: uri/info:doi/10.1007/s00439-006-0221-2; uri/info:pmid/16847693; uri/info:scp/33746961204; http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51418

الاتاحة: http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/51418

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