Prevalence of Mediterranean Mutation of Glucose 6 Phosphate Dehydrogenase in Children of Malak Din Khel Subtribe of Afridi by Mohammad Amjid, Nazish Farooq

Subjects: “…anemic, enzymopathy, hemoglobinopathy, hemolysis, hemoglobin…”
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Clinical case of chronic hepatitis in a domestic dog by T. P. Lokes-Krupka, I. Yu. Vlokh, A. S. Baklytska, N. S. Kanivets, L. P. Karysheva

Subjects: “…hepatopathy, enzymopathy, metabolic disorders, animal…”
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Glucose-6-Phosphate Dehydrogenase Deficiency among Male Blood Donors inSana’a City, Yemen by Molham AL-Habori, Rashad Al-Absi, Fakiha A. Bazara, Hafiz A. Al-Nood

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Exercise and Redox Status Responses Following Alpha-Lipoic Acid Supplementation in G6PD Deficient Individuals by Kalliopi Georgakouli, Ioannis G. Fatouros, Apostolos Fragkos, Theofanis Tzatzakis, Chariklia K. Deli, Konstantinos Papanikolaou, Yiannis Koutedakis, Athanasios Z. Jamurtas

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Serum microRNAs as new biomarkers for detecting subclinical hemolysis in the nonacute phase of G6PD deficiency by Kanyarat Boonpeng, Tatsuki Shibuta, Yoshitaka Hirooka, Kasem Kulkeaw, Duangdao Palasuwan, Tsukuru Umemura

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Hsp70- and Hsp90-mediated proteasomal degradation underlies TPIsugarkill pathogenesis in Drosophila by Stacy L. Hrizo, Michael J. Palladino

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Early mitochondrial dysfunction leads to altered redox chemistry underlying pathogenesis of TPI deficiency by Stacy L. Hrizo, Isaac J. Fisher, Daniel R. Long, Joshua A. Hutton, Zhaohui Liu, Michael J. Palladino

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Protective effect of Mediterranean-type glucose-6-phosphate dehydrogenase deficiency against Plasmodium vivax malaria by Ghulam R Awab, Fahima Aaram, Natsuda Jamornthanyawat, Kanokon Suwannasin, Watcharee Pagornrat, James A Watson, Charles J Woodrow, Arjen M Dondorp, Nicholas PJ Day, Mallika Imwong, Nicholas J White

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A rare mutation (p.F149del) of the NT5C3A gene is associated with pyrimidine 5′-nucleotidase deficiency by Dżamila M. Bogusławska, Michał Skulski, Rafał Bartoszewski, Beata Machnicka, Elżbieta Heger, Kazimierz Kuliczkowski, Aleksander F. Sikorski

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Haematological profile of malaria patients with G6PD and PKLR variants (erythrocytic enzymopathies): a cross-sectional study in Thailand by Punchalee Mungkalasut, Patcharakorn Kiatamornrak, Watcharapong Jugnam-Ang, Srivicha Krudsood, Poonlarp Cheepsunthorn, Chalisa Louicharoen Cheepsunthorn

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Rare red cell enzymopathies in the Indian population: A comprehensive review by Prabhakar Kedar, Rashmi Dongerdiye, Ritika Khurana, Sangeeta Mudaliar

Subjects: “…Red cell enzymopathies…”
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Acquired glucose‐6‐phosphate dehydrogenase deficiency after allogeneic stem‐cell transplantation by Quentin Vô, Mehdi Khourssaji, Alaa Beshir, Elodie Collinge

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Squeezing for Life – Properties of Red Blood Cell Deformability by Rick Huisjes, Anna Bogdanova, Wouter W. van Solinge, Raymond M. Schiffelers, Lars Kaestner, Lars Kaestner, Richard van Wijk

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SARS-CoV-2 Infection and Anemia—A Focus on RBC Deformability and Membrane Proteomics—Integrated Observational Prospective Study by Angelo D’Alessandro, Elena Krisnevskaya, Valentina Leguizamon, Ines Hernández, Carolina de la Torre, Joan-Josep Bech, Josep-Tomàs Navarro, Joan-Lluis Vives-Corrons

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Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family by Rashmi Dongerdiye, Abhilasha Sampagar, Rati Devendra, Prashant Warang, Prabhakar Kedar

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Coupling between Protein Stability and Catalytic Activity Determines Pathogenicity of G6PD Variants by Anna D. Cunningham, Alexandre Colavin, Kerwyn Casey Huang, Daria Mochly-Rosen

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DAHEAN: A Danish nationwide study ensuring quality assurance through real-world data for suspected hereditary anemia patients by 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

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GENETIC DISORDERS OF RED CELL GLYCOLYSIS : A REVIEW FROM THE MOLECULAR TO CLINICAL AND THERAPEUTIC APROACHES by SOPHIA DELICOU, THEONI KANELLOPOULOU, CHRYSSANTHI KONTAXI, ARGIRI VLACHOPOULOU, ZOI PALANTZA, KONSTANTINOS MARAGKOS

Subjects: “…glycolytic enzymopathies…”
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Resultados relevantes en biología molecular, enzimopatías y citogenética en el período 1996-2010 Relevant results in molecular Biology, enzymopathies and citogenetics during 1996-2... by Ana María Amor-Vigil, Gisela Martínez-Antuña, Kalia Lavaut-Sánchez, Graciela Pérez-Diez de los Ríos, Ana Hernández-Martínez, Marianela Estrada-del Cueto

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