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Michal Witt

Showing results (1-10 of 11) with videos related to

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International Journal of Molecular Sciences|April 23, 2022
Perspectives for Primary Ciliary DyskinesiaZuzanna Bukowy-Bieryllo, Michal Witt, Ewa Zietkiewicz
BMC Blood Disorders|January 12, 2005
Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridizationJustyna Jólkowska, Anna Pieczonka, Tomasz Strabel, et al.
European Journal of Human Genetics : EJHG|February 14, 2008
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15qMaciej Geremek, Frederieke Schoenmaker, Ewa Zietkiewicz, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 27, 2003
Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 testJaroslaw Walkowiak, Sanda Nousia-Arvanitakis, Christina Agguridaki, et al.
Journal of Medical Genetics|August 2, 2019
Truncating mutations in exons 20 and 21 of <i>OFD1</i> can cause primary ciliary dyskinesia without associated syndromic symptomsZuzanna Bukowy-Bieryllo, Alicja Rabiasz, Maciej Dabrowski, et al.
American Journal of Respiratory Cell and Molecular Biology|March 28, 2019
<i>CFAP300</i>: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms TraffickingEwa Zietkiewicz, Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, et al.
European Journal of Human Genetics : EJHG|August 8, 2008
Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendationsEls Dequeker, Manfred Stuhrmann, Michael A Morris, et al.
The European Respiratory Journal|December 15, 2015
An international registry for primary ciliary dyskinesiaClaudius Werner, Martin Lablans, Maximilian Ataian, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
ERJ Open Research|September 23, 2020
Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesiaSuzanne Crowley, Inês Azevedo, Mieke Boon, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
International Journal of Molecular Sciences|April 23, 2022
Perspectives for Primary Ciliary DyskinesiaZuzanna Bukowy-Bieryllo, Michal Witt, Ewa Zietkiewicz
BMC Blood Disorders|January 12, 2005
Hematopoietic chimerism after allogeneic stem cell transplantation: a comparison of quantitative analysis by automated DNA sizing and fluorescent in situ hybridizationJustyna Jólkowska, Anna Pieczonka, Tomasz Strabel, et al.
European Journal of Human Genetics : EJHG|February 14, 2008
Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15qMaciej Geremek, Frederieke Schoenmaker, Ewa Zietkiewicz, et al.
Journal of Pediatric Gastroenterology and Nutrition|March 27, 2003
Longitudinal follow-up of exocrine pancreatic function in pancreatic sufficient cystic fibrosis patients using the fecal elastase-1 testJaroslaw Walkowiak, Sanda Nousia-Arvanitakis, Christina Agguridaki, et al.
Journal of Medical Genetics|August 2, 2019
Truncating mutations in exons 20 and 21 of <i>OFD1</i> can cause primary ciliary dyskinesia without associated syndromic symptomsZuzanna Bukowy-Bieryllo, Alicja Rabiasz, Maciej Dabrowski, et al.
American Journal of Respiratory Cell and Molecular Biology|March 28, 2019
<i>CFAP300</i>: Mutations in Slavic Patients with Primary Ciliary Dyskinesia and a Role in Ciliary Dynein Arms TraffickingEwa Zietkiewicz, Zuzanna Bukowy-Bieryllo, Alicja Rabiasz, et al.
European Journal of Human Genetics : EJHG|August 8, 2008
Best practice guidelines for molecular genetic diagnosis of cystic fibrosis and CFTR-related disorders--updated European recommendationsEls Dequeker, Manfred Stuhrmann, Michael A Morris, et al.
The European Respiratory Journal|December 15, 2015
An international registry for primary ciliary dyskinesiaClaudius Werner, Martin Lablans, Maximilian Ataian, et al.
American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.
ERJ Open Research|September 23, 2020
Access to medicines for rare diseases: beating the drum for primary ciliary dyskinesiaSuzanne Crowley, Inês Azevedo, Mieke Boon, et al.
Pageof 2