Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Edit custom filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 2
1948 3
1950 8
1951 6
1952 11
1953 9
1954 7
1955 12
1956 10
1957 10
1958 16
1959 18
1960 30
1961 41
1962 60
1963 103
1964 188
1965 113
1966 108
1967 131
1968 158
1969 165
1970 156
1971 132
1972 150
1973 163
1974 151
1975 117
1976 121
1977 111
1978 104
1979 108
1980 100
1981 116
1982 103
1983 98
1984 102
1985 92
1986 89
1987 83
1988 70
1989 93
1990 96
1991 83
1992 91
1993 65
1994 75
1995 83
1996 77
1997 57
1998 62
1999 81
2000 63
2001 60
2002 73
2003 77
2004 80
2005 97
2006 83
2007 94
2008 97
2009 91
2010 104
2011 100
2012 117
2013 131
2014 148
2015 130
2016 139
2017 158
2018 144
2019 149
2020 204
2021 168
2022 191
2023 164
2024 165
2025 172
2026 128
2027 1

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

7,249 results

Results by year

Filters applied: . Clear all
Page 1
The severity of acute viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency: a case-control study.
Ali M, Ayaz O, Ghos Z, Parkash O. Ali M, et al. J Pak Med Assoc. 2026 Jul;76(7):1011-1014. doi: 10.47391/JPMA.21107. J Pak Med Assoc. 2026. PMID: 42444206
OBJECTIVE: To compare outcomes and severity parameters in patients with acute viral hepatitis and those with acute viral hepatitis and glucose-6-phosphate dehydrogenase deficiency. METHODS: The retrospective, case-control study was conducted at Aga Khan University H …
OBJECTIVE: To compare outcomes and severity parameters in patients with acute viral hepatitis and those with acute viral hepatitis and gluco …
Management of Uncomplicated Plasmodium vivax Malaria in a Pregnant Patient With G6PD Deficiency.
Patel RY, Ngo JM, Maknojiya AN, Meza A. Patel RY, et al. Cureus. 2026 Jun 6;18(6):e110364. doi: 10.7759/cureus.110364. eCollection 2026 Jun. Cureus. 2026. PMID: 42441108 Free PMC article.
Radical cure of Plasmodium as well as with P. ovale requires the use of 8-aminoquinolines to clear both blood and liver parasites; however, they are contraindicated in glucose-6-phosphate dehydrogenase (G6PD) deficiency due to the risk of causing hemolysis an …
Radical cure of Plasmodium as well as with P. ovale requires the use of 8-aminoquinolines to clear both blood and liver parasites; however, …
Use of the "STANDARD G6PDTM" quantitative point-of-care test in neonates and infants.
Gornsawun G, Moo E, Htoo K, Chalermvisutkul S, Gilder ME, Moo PK, Archusuksan L, Prins TJ, Hanboonkunupakarn B, McGready R, Nosten F, Bancone G. Gornsawun G, et al. PLoS One. 2026 Jul 10;21(7):e0346837. doi: 10.1371/journal.pone.0346837. eCollection 2026. PLoS One. 2026. PMID: 42430419 Free PMC article.
The primary aim of the study was to assess equivalency of cord blood and neonatal capillary blood for diagnosis of G6PD deficiency using the quantitative point-of-care "STANDARD G6PDTM" test (SD Biosensor, Korea). ...The study demonstrated that the "STANDARD G6PDTM" …
The primary aim of the study was to assess equivalency of cord blood and neonatal capillary blood for diagnosis of G6PD deficiency …
Screening of glucose-6-phosphate dehydrogenase deficiency in a cohort of 215,137 newborns: an epidemiological and pathogenic variant spectrum study in Yueyang, China.
Cao N, Xie D, Zhou X, Mu H, Yuan Y, Wan L, Sun A, Hu C. Cao N, et al. Front Genet. 2026 Jun 25;17:1810076. doi: 10.3389/fgene.2026.1810076. eCollection 2026. Front Genet. 2026. PMID: 42422491 Free PMC article.
BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a prevalent inherited metabolic disorder, affecting approximately 500 million individuals worldwide. ...CONCLUSION: Stratified by gestational age and seasonal variation, cut-off value optimiza …
BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a prevalent inherited metabolic disorder, affecting …
Silent Risks in the Blood Supply: Co-Inherited Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Trait Among Donors at the Cape Coast Teaching Hospital, Ghana: A Cross-Sectional Study.
Essel BKM, Quarm W, Fynn C, Storph RP, Duah E, Adela EM, Ofori E, Aidoo NB, Adu P. Essel BKM, et al. Health Sci Rep. 2026 Jul 7;9(7):e72785. doi: 10.1002/hsr2.72785. eCollection 2026 Jul. Health Sci Rep. 2026. PMID: 42422163 Free PMC article.
In sub-Saharan Africa, blood donors are not routinely screened for glucose-6-phosphate dehydrogenase (G6PD) deficiency or sickle cell trait (SCT). Evidence on co-inheritance in donors is limited, despite possible harm to vulnerable recipients such as neonates …
In sub-Saharan Africa, blood donors are not routinely screened for glucose-6-phosphate dehydrogenase (G6PD) deficiency …
Prevalence of G6PD candidate variants in malaria-endemic populations of northern Brazil.
Landeira LFL, da Silva DSP, Velozo CA, Fernandes Dos Santos VC, Lima KO, Evangelista MVP, Martorano RM, Banic DM, Cardoso CC. Landeira LFL, et al. Braz J Infect Dis. 2026 Jul 8;30(4):105893. doi: 10.1016/j.bjid.2026.105893. Online ahead of print. Braz J Infect Dis. 2026. PMID: 42419048 Free PMC article.
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PDd) is the most prevalent enzymopathy worldwide and is particularly frequent in malaria-endemic regions. ...This study demonstrates that multiplex SNaPshot genotyping is a viable approach for targeted screening of th …
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PDd) is the most prevalent enzymopathy worldwide and is particularly frequent …
Poppers, A Potential Trigger for Hemolytic Anemia: A Case Report.
Ugarte AT, Baldero DA, Lasa-Berasain P, García AL. Ugarte AT, et al. J Clin Pract Res. 2026 May 4;48(3):325-327. doi: 10.14744/cpr.2026.38231. eCollection 2026 Jun. J Clin Pract Res. 2026. PMID: 42416121 Free PMC article.
BACKGROUND: Hemolytic anemia is a rare but possible complication of inhaled nitrite use, particularly among patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. This occurs when the oxidative effect of nitrites exceeds the enzymatic reducing cap …
BACKGROUND: Hemolytic anemia is a rare but possible complication of inhaled nitrite use, particularly among patients with glucose-6-phosphat …
G6PD deficiency and the exportome of plasmodium falciparum FCB-2: a comparative analysis utilizing one-dimensional blue-native electrophoresis and timstof mass spectrometry.
De la Rosa Cogollo I, Hernáez ML, Clemente LF, Marrugo-Padilla A, Rodríguez-Cavallo E, Méndez-Cuadro D. De la Rosa Cogollo I, et al. Parasitol Res. 2026 Jul 2. doi: 10.1007/s00436-026-08717-y. Online ahead of print. Parasitol Res. 2026. PMID: 42390622
However, there is limited understanding of its behavior in cells harboring protective polymorphisms against severe malaria, such as those associated with glucose-6-phosphate dehydrogenase (G6PD) deficiency, where reduced adhesion and early phagocytosis have b …
However, there is limited understanding of its behavior in cells harboring protective polymorphisms against severe malaria, such as those as …
Philippine Clinical Practice Guidelines for Periodic Health Examination: Screening for Congenital and Developmental Disorders.
Abacan MAR, Baltazar-Braganza KR, Cabaluna ITG, Ocampo IS; Philippine Periodic Health Examination Task Force on Screening for Congenital and Developmental Disorders. Abacan MAR, et al. Acta Med Philipp. 2026 May 30;60(10):28-41. doi: 10.47895/amp.v60i10.10675. eCollection 2026. Acta Med Philipp. 2026. PMID: 42382931 Free PMC article.
This CPG contains recommendations for the screening for critical congenital heart disease, thalassemia, Glucose-6-phosphate dehydrogenase (G6PD) deficiency, developmental delay, and autism spectrum disorder. Recommendations against routine screening of cystic …
This CPG contains recommendations for the screening for critical congenital heart disease, thalassemia, Glucose-6-phosphate dehydrogenase …
Parental Knowledge, Attitude, and Practice toward Glucose 6 Phosphate Dehydrogenase Deficiency: A Cross-sectional Study.
Alshamsi MA, Al Teneiji MT, Kar SS, Dube R, Patni MM. Alshamsi MA, et al. Ann Afr Med. 2026 Jun 30. doi: 10.4103/aam.aam_264_26. Online ahead of print. Ann Afr Med. 2026. PMID: 42381385 Free article. English, French.
BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common inherited enzymatic disorder that may result in acute hemolytic anemia when affected individuals are exposed to specific triggers. ...Data were collected at a single point in time usi …
BACKGROUND: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common inherited enzymatic disorder that may resul …
7,249 results