المؤلفون: Andreas Glenthøj, Andreas Ørslev Rasmussen, Selma Kofoed Bendtsen, Henrik Hasle, Marianne Hoffmann, Klaus Rieneck, Morten Hanefeld Dziegiel, Lene Dissing Sjö, Henrik Frederiksen, Dennis Lund Hansen, Daniel El Fassi, Mathias Rathe, Peter-Diedrich Matthias Jensen, Anne Winther-Larsen, Christian Nielsen, Marianne Olsen, Nina Toft, Mads Okkels Birk Lorenzen, Lise Heilmann Jensen, Sif Gudbrandsdottir, Jens Helby, Maria Rossing, Richard van Wijk, Jesper Petersen

المصدر: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)

مصطلحات موضوعية: Hereditary anemia, Hemoglobinopathies, Membranopathies, Enzymopathies, Whole genome sequencing, Precision diagnostics, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/571fe371a8f54ba6b50bfb5757c53faf

المؤلفون: Lebedev, A. S.^{Aff1, Aff2, Aff3}, Kotova, M. M., Kolesnikova, T. O., Galstyan, D. S.^{Aff1, Aff3, Aff4}, Kalueff, A. V.^{Aff1, Aff2, Aff3, Aff4, Aff5, IDS0022093023060145_cor5}

المصدر: Journal of Evolutionary Biochemistry and Physiology. 59(6):2072-2085

المؤلفون: Glenthøj, Andreas^{Aff1, Aff2, IDs13023024032984_cor1}, Rasmussen, Andreas Ørslev, Bendtsen, Selma Kofoed, Hasle, Henrik, Hoffmann, Marianne, Rieneck, Klaus, Dziegiel, Morten Hanefeld^{Aff2, Aff6}, Sjö, Lene Dissing, Frederiksen, Henrik^{Aff8, Aff9}, Hansen, Dennis Lund, Fassi, Daniel El^{Aff1, Aff2}, Rathe, Mathias^{Aff9, Aff10}, Jensen, Peter-Diedrich Matthias, Winther-Larsen, Anne, Nielsen, Christian, Olsen, Marianne, Toft, Nina, Lorenzen, Mads Okkels Birk, Jensen, Lise Heilmann, Gudbrandsdottir, Sif, Helby, Jens, Rossing, Maria^{Aff2, Aff3}, van Wijk, Richard, Petersen, Jesper

المصدر: Orphanet Journal of Rare Diseases. 19(1)

المؤلفون: Angelo D’Alessandro, Elena Krisnevskaya, Valentina Leguizamon, Ines Hernández, Carolina de la Torre, Joan-Josep Bech, Josep-Tomàs Navarro, Joan-Lluis Vives-Corrons

المصدر: Microorganisms, Vol 12, Iss 3, p 453 (2024)

مصطلحات موضوعية: COVID-19, anemia, red blood cells, membranopathies, enzymopathies, ektacytometry, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2076-2607/12/3/453; https://doaj.org/toc/2076-2607

URL الوصول: https://doaj.org/article/e412f4b292c14de1a181516af8831a97

المؤلفون: Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar Kedar

المصدر: BMC Medical Genomics, Vol 14, Iss 1, Pp 1-7 (2021)

مصطلحات موضوعية: Adenylate kinase deficiency, Enzymopathies, Prenatal diagnosis, Congenital hemolytic anemia, Internal medicine, RC31-1245, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1755-8794

URL الوصول: https://doaj.org/article/ee4ee9f765ef45d3a13594a0a32fc152

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المؤلفون: Dongerdiye, Rashmi, Sampagar, Abhilasha, Devendra, Rati, Warang, Prashant, Kedar, Prabhakar^Aff1

المصدر: BMC Medical Genomics. 14(1)

المؤلفون: Richard van Wijk, Paola Bianchi

المصدر: Frontiers in Physiology, Vol 11 (2020)

مصطلحات موضوعية: red blood cell, hemolytic anemia, enzymopathies, membranopathies, congenital dyserythropoetic anemia, Physiology, QP1-981

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fphys.2020.601746/full; https://doaj.org/toc/1664-042X

URL الوصول: https://doaj.org/article/4318d1cb316b4266a134a336d383ce85

المؤلفون: Rick Huisjes, Anna Bogdanova, Wouter W. van Solinge, Raymond M. Schiffelers, Lars Kaestner, Richard van Wijk

المصدر: Frontiers in Physiology, Vol 9 (2018)

مصطلحات موضوعية: deformability, vesiculation, sickle cell anemia, thalassemia, hereditary spherocytosis, enzymopathies, Physiology, QP1-981

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fphys.2018.00656/full; https://doaj.org/toc/1664-042X

URL الوصول: https://doaj.org/article/c41aa2ddbc964becaa1ba2f223210ec6

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