Results 1 to 10 of about 3,031 (182)

Glucose-6-phosphate dehydrogenase deficiency as a cause for nonimmune hydrops fetalis and severe fetal anemia: A systematic review. [PDF]

Mol Genet Genomic Med
Glucose‐6‐phosphate dehydrogenase (G6PD) deficiency is a rare cause of nonimmune hydrops fetalis and most cases require fetal or neonatal transfusion. Although G6PD deficiency is an X‐linked recessive condition, female fetuses can be affected. Testing should be considered if parental history indicates.
Iyer NS, Mossayebi MH, Gao TJ, Haizler-Cohen L, Di Mascio D, McLaren RA, Al-Kouatly HB.   +6 more
europepmc   +5 more sources

Glucosephosphate isomerase and isocltrate dehydrogenase polymorphisms in the hake,Merluccius australis [PDF]

New Zealand Journal of Marine and Freshwater Research, 1979
As part of a stock separation programme on the hake, Merluccius australis (Hutton), two polymorphic proteins — glucosephosphate isomerase and isocitrate dehydrogenase — were examined in four samples of fish from around the South Island of New Zealand and the waters to the south.
P. J. Smith, G. J. Patchell, P. G. Benson   +2 more
openaire   +2 more sources

Pediatric Mixed Plasmodium vivax–P. falciparum Infection with Disparate Parasitemias: Diagnostic and Surveillance Challenges [PDF]

Children
Background and Clinical Significance: Malaria remains a significant public health issue in Latin America, where Plasmodium vivax predominates but P. falciparum continues to circulate.
Jose Luis Estela-Zape
doaj   +2 more sources

Glucosephosphate isomerase and α‐glycerophosphate dehydrogenase electromorph frequencies in groperPolyprion oxygeneiosisfrom central New Zealand [PDF]

New Zealand Journal of Marine and Freshwater Research, 1985
Abstract Liver samples from groper Polyprion oxygeneiosis collected around the coasts of central New Zealand, were tested for two polymorphic enzymes, glucosephosphate isomerase and α‐glycerophosphate dehydrogenase. Repeat samples from Cook Strait and off the Wairarapa coast showed that variation in electromorph frequencies was as great within as ...
P. J. Smith, A. D. Johnston
openaire   +2 more sources

Concurrent measurements of carcinoembryonic antigen, glucosephosphate isomerase, gamma-glutamyltransferase, and lactate dehydrogenase in malignant, normal adult, and fetal colon tissues.

Clinical Chemistry, 1980
Abstract Carcinoembryonic antigen and activities of glucosephosphate isomerase (EC 5.3.1.9), γ-glutamyltransferase (EC 2.3.2.2), and lactate dehydrogenase (EC 1.1.1.27) were measured in aqueous extracts of fetal, normal adult, and malignant human colon tissues.
D. Munjal
openaire   +3 more sources

[Various genetic and clinical aspects of patients with hemolytic anemia caused by glucosephosphate dehydrogenase deficiency (DG6F)].

Boletin medico del Hospital Infantil de Mexico, 1975
Five families with DG6F deficiency were studied. Out of the first family, neinatal hyperbilirubinemia was evident in 3 children. Exchange transfusion was given to the first two. Possibly, the hemolytic crisis was subsequent to the application of vitamin K.
A H, Toro, R, Soto Allande, A, Bello González   +2 more
openaire   +2 more sources

[Lactate dehydrogenase, glucosephosphate dehydrogenase, glutathione reductase and adenosine triphosphatase activities in the erythrocytes of patients with acute viral hepatitis].

Terapevticheskii arkhiv, 1987
Some indices of erythrocyte metabolism (EM): activity of lactate dehydrogenase (LDH), glucose-6-phosphate dehydrogenase (G-6-PD), glutathione reductase (GR) and common adenosinetriphosphatase (ATPase) activity were studied in 102 patients with acute viral hepatitis (AVH). The suppression of erythrocyte enzymatic activity (EE) was revealed.
V A, Martynov, V I, Kolobaev
openaire   +2 more sources

Molecular Characterization of Glucose-6-phosphate Dehydrogenase Deficiency in Oman

Oman Medical Journal, 2023
Objectives: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most encountered abnormality of red blood cell metabolism worldwide and has a high prevalence in Oman.
Ammar Al-Sheryani1, , Hajer Al-Gheithi, Muntadhar Al Moosawi, Shaoib Al-Zadjali, Yasser Wali, Murtadha Al-Khabori   +5 more
doaj   +1 more source

Dental Management of a Patient with Pulmonary Atresia and Ventricular Septal Defect

Frontiers in Dentistry, 2021
Pulmonary atresia with ventricular septal defect (PA/VSD) is one of the congenital heart diseases that results in cyanosis, susceptibility to bacterial endocarditis, and increased risk of complications during general anesthesia.
Ghassem Ansari, Mahsa Mansouri, Leila Eftekhar   +2 more
doaj   +1 more source

Population screening for glucose-6-phosphate dehydrogenase deficiency using quantitative point-of-care tests: a systematic review

Frontiers in Genetics, 2023
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked hereditary disorder and a global public health concern that is most prevalent in malaria-endemic regions including Asia, Africa, and the Mediterranean.
Mohamed Afiq Hidayat Zailani, Raja Zahratul Azma Raja Sabudin, Azlin Ithnin, Hafiza Alauddin, Siti Aishah Sulaiman, Endom Ismail, Ainoon Othman   +6 more
doaj   +1 more source