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Seite 2 für „Globin“ · Literaturverweise aus öffentlichen Artikeln
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Sulfhemoglobinemia in a 53-Year-Old With a History of Phenazopyridine Misuse
pubmed · 37496545
Literaturverweis öffnenA Mass Spectrometry-Based Multiplexed Targeted Assay for Detection of Hemoglobinopathies from Dried Blood Spots
pubmed · 40998492
Literaturverweis öffnenParoxysmale nächtliche Hämoglobinurie – Folgen eines fehlenden Ankers
pubmed · 16450736
Literaturverweis öffnenGenetics of Hb F/F Cell Variance in Adults and Heterocellular Hereditary Persistence of Fetal Hemoglobin
pubmed · 9859924
Literaturverweis öffnenAnesthetic management of congenital methemoglobinemia in emergency caesarean delivery: a case report
pubmed · 41175461
Literaturverweis öffnenSevere Methemoglobinemia Due to Accidental Ingestion of Nitrite-Containing Nail Polish Remover: A Case Report
pubmed · 42143736
Literaturverweis öffnenGlycated Hemoglobin, Lifestyle, and Sarcopenia in Rural Older Adults: A Cross-Sectional Analysis
pubmed · 42457571
Literaturverweis öffnen[G-6-PD deficiency with hemoglobinopathy and alpha-thalassemia].
pubmed · 4970086
Literaturverweis öffnenMolecular and Clinical Characterization of the Hb Tübingen [β106(G8) Leu→ Gln, HBB: c.320 T>A] Associated With Congenital Methemoglobinemia in a Chinese Family
pubmed · 41918241
Literaturverweis öffnenEmerging Technologies and Advanced Strategies in Hemoglobin Defect Screening
pubmed · 40869515
Literaturverweis öffnenHemoglobin Mass as a Determinant of Inter-Individual Susceptibility to Carbon Monoxide Poisoning
doi · 10.20944/preprints202605.0815.v1
Literaturverweis öffnenHereditary methemoglobinemia diagnosed in adulthood: Type 1 cytochrome B5 reductase deficiency
pubmed · 42319687
Literaturverweis öffnenDie paroxysmale nächtliche Hämoglobinurie - ein erworbener genetischer Defekt der hämatopoietischen Stammzelle<sup>*</sup>
pubmed · 7821202
Literaturverweis öffnenFamilial erythrocytosis and phenotypic heterogeneity associated with different defects in alpha globin genes: a significant new case of Hb Wroclaw (α88(F9) Ala>Glu; HBA1: c.266C>A)
pubmed · 41622866
Literaturverweis öffnenNeonatal cyanosis: exploring the complexity of coexisting congenital methemoglobinaemia and pulmonary hypertension
pubmed · 42156105
Literaturverweis öffnenMolecular Basis of Hereditary Persistence of Fetal Hemoglobin
pubmed · 9668525
Literaturverweis öffnenCongenital Methemoglobinemia: A Cause of Polycythemia
pubmed · 39794672
Literaturverweis öffnenDetecting muscle strain in professional football players through plasma myoglobin levels
pubmed · 40742786
Literaturverweis öffnenAssociation of immunonutrition-based indices (Hemoglobin-Albumin-Lymphocyte-Platelet, prognostic nutritional index, and C-reactive protein-albumin-lymphocyte) with the latency period in preterm prelabor rupture of membranes
pubmed · 42385041
Literaturverweis öffnen[Paroxysmal nocturnal hemoglobinuria. Strübing-Marchiafava-Micheli anemia].
pubmed · 5331732
Literaturverweis öffnenHb F-SickKids (HBG2: C.308A > G): A Novel γ-Globin Variant Associated with Transient Neonatal Cyanosis
pubmed · 42267386
Literaturverweis öffnenCase report: neonatal cyanosis secondary to congenital methemoglobinemia, a cause to consider in newborn cyanosis
pubmed · 40225075
Literaturverweis öffnenIdentification of a novel hereditary spherocytosis gene mutation in a Chinese child with α-globin gene triplication
pubmed · 42467362
Literaturverweis öffnenCase Report: A case report and literature review of hemoglobin variation associated with neonatal cyanosis
pubmed · 38415208
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