glutamine and HbS Disease

glutamine has been researched along with HbS Disease in 48 studies

Research

Studies (48)

TimeframeStudies, this research(%)All Research%
pre-19902 (4.17)18.7374
1990's4 (8.33)18.2507
2000's3 (6.25)29.6817
2010's19 (39.58)24.3611
2020's20 (41.67)2.80

Authors

AuthorsStudies
Alkindi, S; Estepp, J; Ezzat, H; Lam, H; Minniti, CP; Shah, N; Zaidi, AU1
Cimpeanu, E; Dutta, D; Jafri, F; Leibovitch, JN; Lim, SH; Poplawska, M; Tambe, AV1
Hagar, R; Kuypers, FA; Larkin, S; Lavrisha, L; Morris, CR; Saulys, A; Suh, JH; Vichinsky, EP1
Cimpeanu, E; Dutta, D; Jafri, F; Jang, T; Lim, SH; Poplawska, M; Seong, G1
Fasipe, TA; Kavanagh, PL; Wun, T1
Hagar, R; Hohman, LS; Kuypers, FA; Lavrisha, L; Lum, JJ; Morris, CR; Rokeby, A; Saulys, A; Vichinsky, E; Walter, PB1
Gannon, M; Hsu, LL; Wu, HW1
Lee, MT; Ogu, UO1
Ataga, KI; Desai, PC; Rai, P1
Adel, AM; Al-Okka, R; Elenga, N; Etienne-Julan, M; Loko, G; Yassin, MA1
Cappellini, MD; Ferraresi, M; Kattamis, A; Leoni, S; Motta, I; Panzieri, DL1
Jonassaint, CR; Kane-Gill, SL; Newman, TV; Novelli, EM; Suh, K; Yang, J1
Carden, MA; Little, J1
Howell, CM; Monus, T1
Burns, BN; Cieri-Hutcherson, NE; Conway-Habes, EE; Hutcherson, TC; White, NA1
Quinn, CT; Sadaf, A1
Cox, SE; Hart, E; Kirkham, FJ; Stotesbury, H1
Gordeuk, VR; Han, J; Saraf, SL1
Adams, CD1
Hehre, RJ1
Ashley-Koch, AE; Bartolucci, P; Brugnara, C; Clish, CB; Galactéros, F; Garrett, ME; Hirschhorn, JN; Ilboudo, Y; Lettre, G; Telen, MJ1
Chan, F; Crouch, A; Minniti, CP; Ogu, UO; Sebastian, G; Thomas, M; Vattappally, L; You, S1
Rungkitwattanakul, D; Singh, D; Weaver, SB1
Wilmore, DW1
Aschenbrenner, DS1
Ortiz de Montellano, PR1
Ansari, J; Gavins, FNE; Moufarrej, YE; Pawlinski, R1
Akhter, R; Ali, SI; Khan, A1
Quinn, CT1
Minniti, CP1
Bellevue, R; Blake, OA; Gordeuk, VR; Guillaume, E; Hsu, LL; Kanter, J; Lanzkron, S; Lasky, JL; Miller, ST; Neumayr, LD; New, TN; Niihara, Y; Osunkwo, I; Panosyan, EH; Razon, RL; Sadanandan, S; Sarnaik, S; Sieger, L; Smith, WR; Stark, CW; Tran, LT; Vichinsky, EP; Viswanathan, K1
Ataga, KI1
Niihara, Y; Smith, WR; Stark, CW1
Guddati, AK; Kota, V1
Anker, MS; Anker, SD; Haverkamp, W1
Hoppe, C; Neumayr, L1
Simpson, S1
Cremer, L; Li, CS; Mackert, P; Olivi, S; Storm, M; Wang, W; Williams, R1
Ames, B; Bland, DA; Hagar, W; Klings, ES; Kuypers, FA; Larkin, S; Morris, CR; Shigenaga, M; Steinberg, MH; Suh, JH; Vichinsky, EP1
Leboulch, P; London, IM; Oh, YH; Takekoshi, KJ; Westerman, KW1
Bayne, E; Darmaun, D; Haymond, MW; Pitel, P; Sager, BK; Salman, EK; Wiisanen, A1
Akiyama, DS; Niihara, Y; Tanaka, KR; Zerez, CR2
Ellory, JC; Gibson, JS; Kiessling, K; Roberts, N1
Rumen, NM1
Cawein, MJ; Gleason, EM; Mackenzie, RD; Schatzman, GL1

Reviews

16 review(s) available for glutamine and HbS Disease

ArticleYear
l-glutamine, crizanlizumab, voxelotor, and cell-based therapy for adult sickle cell disease: Hype or hope?
    Blood reviews, 2022, Volume: 53

    Topics: Adult; Anemia, Sickle Cell; Antibodies, Monoclonal, Humanized; Benzaldehydes; Glutamine; Hematopoietic Stem Cell Transplantation; Humans; Pyrazines; Pyrazoles

2022
L-glutamine for sickle cell disease: more than reducing redox.
    Annals of hematology, 2022, Volume: 101, Issue:8

    Topics: Anemia, Sickle Cell; Glutamine; Hemoglobinopathies; Humans; NAD; Oxidation-Reduction; Volatile Organic Compounds

2022
Sickle Cell Disease: A Review.
    JAMA, 2022, 07-05, Volume: 328, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Antibodies, Monoclonal, Humanized; Antisickling Agents; Benzaldehydes; Child; Glutamine; Hematologic Agents; Hematopoietic Stem Cell Transplantation; Humans; Hydroxyurea; Infant, Newborn; Neonatal Screening; Pain; Pyrazines; Pyrazoles; Transition to Adult Care; United States

2022
Sickle cell disease in the new era: advances in drug treatment.
    Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis, 2022, Volume: 61, Issue:5

    Topics: Anemia, Sickle Cell; Fetal Hemoglobin; Glutamine; Hemoglobin, Sickle; Hemoglobins; Humans; Hydroxyurea; Nitric Oxide; Oxidants; Oxygen; United States

2022
The Evolving Landscape of Drug Therapies for Sickle Cell Disease.
    Hematology/oncology clinics of North America, 2022, Volume: 36, Issue:6

    Topics: Anemia, Sickle Cell; Genetic Therapy; Glutamine; Hematopoietic Stem Cell Transplantation; Humans; Hydroxyurea

2022
Therapeutic perspective for children and young adults living with thalassemia and sickle cell disease.
    European journal of pediatrics, 2023, Volume: 182, Issue:6

    Topics: Anemia, Sickle Cell; Child; Child, Preschool; Glutamine; Hemoglobinopathies; Humans; Infant; Thalassemia; Young Adult

2023
Emerging disease-modifying therapies for sickle cell disease.
    Haematologica, 2019, Volume: 104, Issue:9

    Topics: Anemia, Sickle Cell; Antioxidants; Antisickling Agents; Blood Coagulation; Clinical Trials as Topic; Drug Approval; Erythrocytes; Fetal Hemoglobin; Glutamine; Hematopoietic Stem Cell Transplantation; Hemoglobin, Sickle; Humans; Hydroxyurea; Inflammation; Platelet Activation; Polymers; United States; United States Food and Drug Administration

2019
Current and emerging treatments for sickle cell disease.
    JAAPA : official journal of the American Academy of Physician Assistants, 2019, Volume: 32, Issue:9

    Topics: Acute Chest Syndrome; Acute Disease; Analgesics, Opioid; Anemia, Sickle Cell; Anti-Bacterial Agents; Antisickling Agents; Chronic Disease; Disease Progression; Erythrocyte Transfusion; Fluid Therapy; Genetic Therapy; Glutamine; Hematopoietic Stem Cell Transplantation; Humans; Hydroxyurea; Infant, Newborn; Infection Control; Infections; Mesenteric Ischemia; Neonatal Screening; Oxygen Inhalation Therapy; Pain Management; Patient Education as Topic; Pneumococcal Infections; Pneumococcal Vaccines; Stroke

2019
Systematic Review of l-glutamine for Prevention of Vaso-occlusive Pain Crisis in Patients with Sickle Cell Disease.
    Pharmacotherapy, 2019, Volume: 39, Issue:11

    Topics: Anemia, Sickle Cell; Glutamine; Hospitalization; Humans; Pain; Randomized Controlled Trials as Topic

2019
L-glutamine for sickle cell disease: Knight or pawn?
    Experimental biology and medicine (Maywood, N.J.), 2020, Volume: 245, Issue:2

    Topics: Anemia, Sickle Cell; Animals; Clinical Trials as Topic; Glutamine; Glutathione; Humans; Intestines; Nitric Oxide

2020
Systematic Review of Crizanlizumab: A New Parenteral Option to Reduce Vaso-occlusive Pain Crises in Patients with Sickle Cell Disease.
    Pharmacotherapy, 2020, Volume: 40, Issue:6

    Topics: Anemia, Sickle Cell; Animals; Antibodies, Monoclonal, Humanized; Glutamine; Humans; Hydroxyurea; P-Selectin; Pain; Randomized Controlled Trials as Topic

2020
Managing patients with sickle cell disease in primary care.
    JAAPA : official journal of the American Academy of Physician Assistants, 2020, Volume: 33, Issue:10

    Topics: Administration, Oral; Anemia, Sickle Cell; Antibodies, Monoclonal, Humanized; Antisickling Agents; Blood Transfusion; Evidence-Based Medicine; Female; Glutamine; Hematopoietic Stem Cell Transplantation; Humans; Hydroxyurea; Iodine Isotopes; Maintenance Chemotherapy; Male; Monitoring, Physiologic; Practice Guidelines as Topic; Primary Health Care

2020
Contemporary Management and Prevention of Vaso-Occlusive Crises (VOCs) in Adults With Sickle Cell Disease.
    Journal of pharmacy practice, 2023, Volume: 36, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Glutamine; Hospitalization; Humans; Hydroxyurea

2023
Sickle cell disease: a malady beyond a hemoglobin defect in cerebrovascular disease.
    Expert review of hematology, 2018, Volume: 11, Issue:1

    Topics: Anemia, Sickle Cell; Antisickling Agents; Cell Communication; Cerebrovascular Disorders; Disease Progression; Glutamine; Hemoglobins; Humans; Hydroxyurea; Inflammation; Mutation; Neutrophils; Quality of Life

2018
l-Glutamine for sickle cell anemia: more questions than answers.
    Blood, 2018, 08-16, Volume: 132, Issue:7

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Child; Child, Preschool; Drug Approval; Female; Glutamine; Humans; Hydroxyurea; Male; United States; United States Food and Drug Administration

2018
Sickle Cell Disease: Monitoring, Current Treatment, and Therapeutics Under Development.
    Hematology/oncology clinics of North America, 2019, Volume: 33, Issue:3

    Topics: Anemia, Sickle Cell; Antisickling Agents; Child; Clinical Trials as Topic; Erythrocyte Transfusion; Glutamine; Humans; Hydroxyurea; Monitoring, Physiologic; Stem Cell Transplantation

2019

Trials

4 trial(s) available for glutamine and HbS Disease

ArticleYear
The effects of glutamine supplementation on markers of apoptosis and autophagy in sickle cell disease peripheral blood mononuclear cells.
    Complementary therapies in medicine, 2022, Volume: 70

    Topics: Adult; Anemia, Sickle Cell; Apoptosis; Autophagy; bcl-2-Associated X Protein; Biomarkers; Dietary Supplements; Female; Glutamine; Humans; Leukocytes, Mononuclear; Male; Middle Aged; Prospective Studies; Tricuspid Valve Insufficiency

2022
A Phase 3 Trial of l-Glutamine in Sickle Cell Disease.
    The New England journal of medicine, 2018, Jul-19, Volume: 379, Issue:3

    Topics: Administration, Oral; Adolescent; Adult; Anemia, Sickle Cell; Antisickling Agents; beta-Thalassemia; Child; Child, Preschool; Double-Blind Method; Drug Therapy, Combination; Female; Glutamine; Humans; Hydroxyurea; Intention to Treat Analysis; Male; Middle Aged; Pain; Pain Management; Young Adult

2018
Oral glutamine supplementation decreases resting energy expenditure in children and adolescents with sickle cell anemia.
    Journal of pediatric hematology/oncology, 2004, Volume: 26, Issue:10

    Topics: Administration, Oral; Adolescent; Amino Acids; Anemia, Sickle Cell; Basal Metabolism; Body Composition; Child; Child, Preschool; Female; Glutamine; Growth; Humans; Male; Nutritional Status; Patient Compliance; Treatment Outcome; Tryptophan; Weight Gain

2004
Oral L-glutamine therapy for sickle cell anemia: I. Subjective clinical improvement and favorable change in red cell NAD redox potential.
    American journal of hematology, 1998, Volume: 58, Issue:2

    Topics: Administration, Oral; Adult; Anemia, Sickle Cell; Dietary Supplements; Erythrocytes; Glutamine; Humans; Middle Aged; NAD; Oxidation-Reduction; Pilot Projects; Treatment Outcome

1998

Other Studies

28 other study(ies) available for glutamine and HbS Disease

ArticleYear
A reanalysis of pain crises data from the pivotal l-glutamine in sickle cell disease trial.
    Contemporary clinical trials, 2021, Volume: 110

    Topics: Anemia, Sickle Cell; Communication; Glutamine; Humans; Pain

2021
Implications for the metabolic fate of oral glutamine supplementation within plasma and erythrocytes of patients with sickle cell disease: A pharmacokinetics study.
    Complementary therapies in medicine, 2022, Volume: 64

    Topics: Amino Acids; Anemia, Sickle Cell; Dietary Supplements; Erythrocytes; Female; Glutamine; Humans; Middle Aged

2022
Evaluation of Glutamine Utilization in Patients With Sickle Cell Disease.
    Journal of pediatric hematology/oncology, 2023, 01-01, Volume: 45, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Child; Glutamine; Humans; Medication Adherence; Retrospective Studies

2023
"Long-term efficacy and safety of L-glutamine in preventing sickle cell disease-related acute complications and hemolysis in pediatric and adult patients-Real-world, observational study".
    European journal of haematology, 2023, Volume: 110, Issue:6

    Topics: Adult; Anemia, Sickle Cell; Child; Glutamine; Hemolysis; Humans; Pain

2023
Use of Disease-Modifying Treatments in Patients With Sickle Cell Disease.
    JAMA network open, 2023, Nov-01, Volume: 6, Issue:11

    Topics: Acute Chest Syndrome; Adult; Anemia, Sickle Cell; Child; Cross-Sectional Studies; Female; Glutamine; Humans; Hydroxyurea; Inpatients; Male

2023
L-Glutamine in sickle cell disease.
    Drugs of today (Barcelona, Spain : 1998), 2020, Volume: 56, Issue:4

    Topics: Adult; Anemia, Sickle Cell; Animals; Child; Clinical Trials, Phase II as Topic; Clinical Trials, Phase III as Topic; Double-Blind Method; Erythrocytes; Glutamine; Humans; Mice; NAD; Randomized Controlled Trials as Topic

2020
A Mendelian randomization study of circulating glutamine and red blood cell traits.
    Pediatric blood & cancer, 2020, Volume: 67, Issue:9

    Topics: Acute Pain; Anemia, Sickle Cell; Erythrocytes; Glutamine; Humans; Mendelian Randomization Analysis; Oxidative Stress

2020
Potential causal role of l-glutamine in sickle cell disease painful crises: A Mendelian randomization analysis.
    Blood cells, molecules & diseases, 2021, Volume: 86

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Child; Child, Preschool; Female; Glutamine; Humans; Male; Mendelian Randomization Analysis; Middle Aged; Pain; Young Adult

2021
L-glutamine use in adults with sickle cell disease: Clinical trials where success meets reality.
    American journal of hematology, 2021, Volume: 96, Issue:1

    Topics: Adult; Aged; Anemia, Sickle Cell; Clinical Trials as Topic; Female; Follow-Up Studies; Glutamine; Humans; Male; Middle Aged; Retrospective Studies

2021
Food and Drug Administration Approval of Glutamine for Sickle Cell Disease: Success and Precautions in Glutamine Research.
    JPEN. Journal of parenteral and enteral nutrition, 2017, Volume: 41, Issue:6

    Topics: Anemia, Sickle Cell; Drug Approval; Enteral Nutrition; Glutamine; Humans; Outcome Assessment, Health Care; Parenteral Nutrition; Research; United States; United States Food and Drug Administration

2017
New Drug for Sickle Cell Disease.
    The American journal of nursing, 2017, Volume: 117, Issue:11

    Topics: Administration, Oral; Anemia, Sickle Cell; Drug Approval; Glutamine; Humans

2017
A New Step in the Treatment of Sickle Cell Disease
    Biochemistry, 2018, 02-06, Volume: 57, Issue:5

    Topics: Amide Synthases; Ammonia; Anemia, Sickle Cell; Animals; Antisickling Agents; Drug Discovery; Glutaminase; Glutamine; Humans; NAD

2018
L-glutamine (Endari) for sickle cell disease.
    The Medical letter on drugs and therapeutics, 2018, 01-29, Volume: 60, Issue:1539

    Topics: Anemia, Sickle Cell; Antisickling Agents; Drug Costs; Drug Interactions; Glutamine; Humans; Treatment Outcome

2018
Challenges and new horizons for sickle cell disease.
    The Lancet. Haematology, 2018, Volume: 5, Issue:2

    Topics: Adult; Anemia, Sickle Cell; Clinical Trials as Topic; Glutamine; Humans

2018
L-Glutamine approved for use in patients with sickle cell disease.
    JPMA. The Journal of the Pakistan Medical Association, 2018, Volume: 68, Issue:3

    Topics: Acute Chest Syndrome; Anemia, Sickle Cell; Drug Approval; Glutamine; Hospitalization; Humans

2018
l-Glutamine and the Dawn of Combination Therapy for Sickle Cell Disease.
    The New England journal of medicine, 2018, 07-19, Volume: 379, Issue:3

    Topics: Anemia, Sickle Cell; Combined Modality Therapy; Glutamine; Humans

2018
New and experimental agents for sickle cell disease.
    Clinical advances in hematology & oncology : H&O, 2018, Volume: 16, Issue:7

    Topics: Anemia, Sickle Cell; Antisickling Agents; Combined Modality Therapy; Drug Discovery; Erythrocyte Transfusion; Glutamine; Humans; Hydroxyurea

2018
A Phase 3 Trial of l-Glutamine in Sickle Cell Disease.
    The New England journal of medicine, 2018, 11-08, Volume: 379, Issue:19

    Topics: Anemia, Sickle Cell; Glutamine; Humans

2018
A Phase 3 Trial of l-Glutamine in Sickle Cell Disease.
    The New England journal of medicine, 2018, 11-08, Volume: 379, Issue:19

    Topics: Anemia, Sickle Cell; Glutamine; Humans

2018
A Phase 3 Trial of l-Glutamine in Sickle Cell Disease.
    The New England journal of medicine, 2018, 11-08, Volume: 379, Issue:19

    Topics: Anemia, Sickle Cell; Glutamine; Humans

2018
Sickle cell disease: a new era.
    The Lancet. Haematology, 2019, Volume: 6, Issue:8

    Topics: Anemia, Sickle Cell; Child; Cost of Illness; Global Health; Glutamine; Humans

2019
Erythrocyte glutamine depletion, altered redox environment, and pulmonary hypertension in sickle cell disease.
    Blood, 2008, Jan-01, Volume: 111, Issue:1

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Echinococcosis, Pulmonary; Erythrocytes; Female; Glutamic Acid; Glutamine; Hemolysis; Humans; Hydrogen-Ion Concentration; Male; NADP; Nitric Oxide; Oxidation-Reduction; Tricuspid Valve Insufficiency

2008
Retroviral transfer of a human beta-globin/delta-globin hybrid gene linked to beta locus control region hypersensitive site 2 aimed at the gene therapy of sickle cell disease.
    Proceedings of the National Academy of Sciences of the United States of America, 1995, Mar-28, Volume: 92, Issue:7

    Topics: 3T3 Cells; Alanine; Amino Acid Sequence; Anemia, Sickle Cell; Animals; Base Sequence; Conserved Sequence; Gene Transfer Techniques; Genetic Therapy; Genetic Vectors; Globins; Glutamine; Hemoglobin, Sickle; Humans; Introns; Macromolecular Substances; Mice; Models, Structural; Molecular Sequence Data; Phosphoglycerate Kinase; Protein Multimerization; Recombination, Genetic; Retroviridae; Sequence Homology, Amino Acid

1995
Protein and energy metabolism in prepubertal children with sickle cell anemia.
    Pediatric research, 1996, Volume: 40, Issue:1

    Topics: Amino Acids; Anemia, Sickle Cell; Basal Metabolism; Calorimetry, Indirect; Case-Control Studies; Child; Energy Metabolism; Female; Glutamine; Humans; Infusions, Intravenous; Male; Proteins; Puberty; Reticulocytes

1996
Increased red cell glutamine availability in sickle cell anemia: demonstration of increased active transport, affinity, and increased glutamate level in intact red cells.
    The Journal of laboratory and clinical medicine, 1997, Volume: 130, Issue:1

    Topics: Anemia, Sickle Cell; Biological Transport, Active; Erythrocytes; Glutamic Acid; Glutamine; Humans; Kinetics; NAD

1997
A comparison in normal individuals and sickle cell patients of reduced glutathione precursors and their transport between plasma and red cells.
    The hematology journal : the official journal of the European Haematology Association, 2000, Volume: 1, Issue:4

    Topics: Adult; Amino Acid Transport System ASC; Amino Acid Transport System L; Anemia, Sickle Cell; Biological Transport; Carbon Monoxide; Cysteine; Enzyme Inhibitors; Erythrocytes; Female; Glutamic Acid; Glutamine; Glutathione; Glycine; Humans; Male; Middle Aged; Oxygen; Protein Kinase Inhibitors; Protein Kinases; Serine; Staurosporine

2000
Inhibition of sickling in erythrocytes by amino acids.
    Blood, 1975, Volume: 45, Issue:1

    Topics: Amino Acids; Anemia, Sickle Cell; Asparagine; Erythrocytes; Glutamine; Hemoglobin, Sickle; Homoserine; Humans

1975
An in vitro method for screening compounds for the effect on the rate of sickling of erythrocytes.
    The Journal of international medical research, 1976, Volume: 4, Issue:6

    Topics: 2-Hydroxyphenethylamine; Anemia, Sickle Cell; Aniline Compounds; Antisickling Agents; Calcium; Erythrocyte Membrane; Erythrocytes; Ethanolamines; Glutamine; Humans; Methods; Oxygen; Procaine

1976