Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Joaquin Brintrup"'
Autor:
Amanda S. Wendt, Joaquin Brintrup, Jillian L. Waid, Abdul Kader, Nathalie J. Lambrecht, Sabine Gabrysch
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-11 (2023)
Abstract Background Inherited blood disorders affect 7% of the population worldwide, with higher prevalences in countries in the “thalassemia belt,” which includes Bangladesh. Clinical management options for severely affected individuals are expe
Externí odkaz:
https://doaj.org/article/96821e39f9cb4e93bb1376a882a97b60
Autor:
Nora Kießling, Joaquin Brintrup, Ahmed Zeynudin, Nuredin Abduselam, Sylvia Götz, Margith Mack, Michael Pritsch, Andreas Wieser, Elisabeth Kohne, Nicole Berens-Riha
Publikováno v:
Malaria Journal, Vol 17, Iss 1, Pp 1-10 (2018)
Abstract Background The study aimed to gain first data on the prevalence of G6PD enzyme deficiency measured by spectrophotometry and associated genetic variants in Jimma and surroundings, Ethiopia. The area is a Plasmodium vivax endemic region, but 8
Externí odkaz:
https://doaj.org/article/995904eeabe94787a0e79a957cc55437
Autor:
Georgia Lahr, Joaquin Brintrup, Stefan Over, Gerhard E. Feurle, Klaus-Michel Debatin, Elisabeth Kohne
Publikováno v:
Haematologica, Vol 92, Iss 9 (2007)
Codon 104(−G), a heterozygous frameshift mutation in exon 2 of HBB, resulted in a dominantly inherited β0-phenotype with mild anemia in a German kindred, and thalassemia intermedia in the index patient. A co-inherited α gene triplication, long-te
Externí odkaz:
https://doaj.org/article/73d9485f3232416e8ba1e9d2bfb92306
Autor:
Kießling, Nora, Joaquin Brintrup, Zeynudin, Ahmed, Abduselam, Nuredin, Götz, Sylvia, Mack, Margith, Pritsch, Michael, Wieser, Andreas, Kohne, Elisabeth, Berens-Riha, Nicole
Additional file 2. G6PD Card (Englisch).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::312057ef8db65128be23cd93a1c8e4fa
Autor:
Usama El-Safy, Ahmed Al-Akhras, Mohamed Hosam Mourad, Joaquin Brintrup, Tamer Hassan, Marwa Zakaria, Elisabeth Kohne, Hadeel M. Abdelrahman, M. A. Badr
Publikováno v:
Biomedical reports. 4(6)
In β-thalassemia, certain mutations cause a complete absence of β-globin chain synthesis, termed β 0 -thalassemia, while others may allow certain β-globin production and are termed β + - or β ++ -thalassemia. The homozygous state results in sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::469ed41d3db9f6d4a5993a790a30fe48
https://pubmed.ncbi.nlm.nih.gov/27284414
https://pubmed.ncbi.nlm.nih.gov/27284414
Autor:
Hubert Hug, Klaus-Michael Debatin, Marianne Krause, Joaquin Brintrup, Weidong Du, Flavio Ortigao, Elisabeth Kohne
Publikováno v:
Biotechnology(Faisalabad). 2:121-130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7416f3d5fb44016f2b6553ce36b5749b
https://doi.org/10.3923/biotech.2003.121.130
https://doi.org/10.3923/biotech.2003.121.130
Autor:
Gerhard E. Feurle, Klaus-Michel Debatin, Joaquin Brintrup, Georgia Lahr, Elisabeth Kohne, Stefan Over
Publikováno v:
Haematologica. 92:1264-1265
Codon 104(-G), a heterozygous frameshift mutation in exon 2 of HBB, resulted in a dominantly inherited beta0-phenotype with mild anemia in a German kindred, and thalassemia intermedia in the index patient. A co-inherited a gene triplication, long-ter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18741d125785f651788be7804c7680e8
https://doi.org/10.3324/haematol.11383
https://doi.org/10.3324/haematol.11383