Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Genetic spectrum and clinical early natural history of glucose-6-phosphate dehydrogenase deficiency in Mexican children detected through newborn screening ; volume:16 ; number:1 ; day:26 ; month:2 ; year:2021 ; pages:1-11 ; date:12.2021
Orphanet journal of rare diseases ; 16, Heft 1 (26.2.2021), 1-11, 12.2021
- Creator
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Vela-Amieva, Marcela
Alcántara-Ortigoza, Miguel Angel
González-del Angel, Ariadna
Belmont-Martínez, Leticia
López-Candiani, Carlos
Ibarra-González, Isabel
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s13023-021-01693-9
- URN
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urn:nbn:de:101:1-2021041322260187424433
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:50 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vela-Amieva, Marcela
- Alcántara-Ortigoza, Miguel Angel
- González-del Angel, Ariadna
- Belmont-Martínez, Leticia
- López-Candiani, Carlos
- Ibarra-González, Isabel
- SpringerLink (Online service)
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Reduced glutathione and glutathione disulfide in the blood of glucose-6-phosphate dehydrogenase-deficient newborns
Glyceraldehyde-3-phosphate dehydrogenase, GAP DH 2
Glyceraldehyde-3-phosphate dehydrogenase, GAP DH 1
Methionine adenosyltransferase I/III deficiency detected by newborn screening
Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency
In vitro and in vivo regulation of glyceraldehyde-3-phosphate dehydrogenase isozymes [glyceraldehyde-phosphate-dehydrogenase-isozymes] from chenopodium rubrum L.
Implications of differential peroxyl radical-induced inactivation of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase for the pentose phosphate pathway
Testis-specific glyceraldehyde-3-phosphate dehydrogenase: origin and evolution
Mitochondrial glycerol 3‐phosphate dehydrogenase promotes skeletal muscle regeneration
Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates
Genetic determinants of glucose-6-phosphate dehydrogenase activity in Kenya
Glyceraldehyde-3-phosphate dehydrogenase is overexpressed in colorectal cancer onset
Reduced glutathione and glutathione disulfide in the blood of glucose-6-phosphate dehydrogenase-deficient newborns
Glyceraldehyde-3-phosphate dehydrogenase, GAP DH 2
Glyceraldehyde-3-phosphate dehydrogenase, GAP DH 1
Methionine adenosyltransferase I/III deficiency detected by newborn screening
Enhanced Eryptosis in Glucose-6-Phosphate Dehydrogenase Deficiency
In vitro and in vivo regulation of glyceraldehyde-3-phosphate dehydrogenase isozymes [glyceraldehyde-phosphate-dehydrogenase-isozymes] from chenopodium rubrum L.
Implications of differential peroxyl radical-induced inactivation of glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase for the pentose phosphate pathway
Testis-specific glyceraldehyde-3-phosphate dehydrogenase: origin and evolution
Mitochondrial glycerol 3‐phosphate dehydrogenase promotes skeletal muscle regeneration
Newborn screening of glucose-6-phosphate dehydrogenase deficiency in Guangxi, China: determination of optimal cutoff value to identify heterozygous female neonates
Genetic determinants of glucose-6-phosphate dehydrogenase activity in Kenya