Amniotic fluid metabolomic and lipidomic alterations associated with hemoglobin Bart’s diseases

[1]  L. Atzori,et al.  Metabolomic Investigation of β-Thalassemia in Chorionic Villi Samples , 2019, Journal of clinical medicine.

[2]  Yang Xia,et al.  Metabolomic and molecular insights into sickle cell disease and innovative therapies. , 2019, Blood advances.

[3]  E. Katsantoni Omics Studies in Hemoglobinopathies , 2019, Molecular Diagnosis & Therapy.

[4]  Jianpei Fang,et al.  Iron Metabolism and Oxidative Status in Patients with Hb H Disease , 2019, Hemoglobin.

[5]  T. Northen,et al.  Microbial Ecology on Solar Panels in Berkeley, CA, United States , 2018, Front. Microbiol..

[6]  P. Pramstaller,et al.  Metabolic Signature of Dietary Iron Overload in a Mouse Model , 2018, Cells.

[7]  I. Khan,et al.  Hydroxyurea Treated β-Thalassemia Children Demonstrate a Shift in Metabolism Towards Healthy Pattern , 2018, Scientific Reports.

[8]  Scott T. Miller,et al.  A Phase 3 Trial of l‐Glutamine in Sickle Cell Disease , 2018, The New England journal of medicine.

[9]  X. Qin,et al.  Analysis of Glycosylation Profiles of Serum Glycoprotein from Iron Overload Thalassemia. , 2018, Clinical laboratory.

[10]  N. Verma,et al.  Hypertriglyceridemia thalassemia syndrome , 2018, Journal of pediatric endocrinology & metabolism : JPEM.

[11]  F. Qadri,et al.  Impaired acylcarnitine profile in transfusion-dependent beta-thalassemia major patients in Bangladesh , 2018, Journal of advanced research.

[12]  D. Higgs,et al.  Molecular Basis and Genetic Modifiers of Thalassemia. , 2018, Hematology/oncology clinics of North America.

[13]  D. Weatherall,et al.  Thalassaemia , 2018, The Lancet.

[14]  Bolan Yu,et al.  Application of the amniotic fluid metabolome to the study of fetal malformations, using Down syndrome as a specific model , 2017, Molecular medicine reports.

[15]  Yunyan He,et al.  The prevalence of thalassemia in mainland China: evidence from epidemiological surveys , 2017, Scientific Reports.

[16]  I. Khan,et al.  β-Thalassemia Patients Revealed a Significant Change of Untargeted Metabolites in Comparison to Healthy Individuals , 2017, Scientific Reports.

[17]  Xiaoyan He,et al.  A novel tandem mass spectrometry method for first-line screening of mainly beta-thalassemia from dried blood spots. , 2017, Journal of proteomics.

[18]  X. Hao,et al.  Synthesis of (6R,12R)-6,12-Dimethylpentadecan-2-one, the Female-Produced Sex Pheromone from Banded Cucumber Beetle Diabrotica balteata, Based on a Chiron Approach , 2015, Natural product communications.

[19]  M. Hachicha,et al.  Hemolytic Anemia and Metabolic Acidosis: Think about Glutathione Synthetase Deficiency , 2015, Fetal and pediatric pathology.

[20]  B. Djerdjouri,et al.  Oxidative Status and Plasma Lipid Profile in β-Thalassemia Patients , 2015, Hemoglobin.

[21]  D. Weatherall,et al.  The α-thalassemias. , 2014, The New England journal of medicine.

[22]  T. Ebbels,et al.  Identifying biochemical phenotypic differences between cryptic species , 2014, Biology Letters.

[23]  E. Vichinsky Clinical manifestations of α-thalassemia. , 2013, Cold Spring Harbor Perspectives in Medicine.

[24]  S. Awadallah Protein antioxidants in thalassemia. , 2013, Advances in clinical chemistry.

[25]  G. Stamatoyannopoulos,et al.  Thalassaemia , 2012, The Lancet.

[26]  G. Christian,et al.  Review on screening and analysis techniques for hemoglobin variants and thalassemia. , 2005, Talanta.

[27]  R. Munday,et al.  Induction of phase II detoxification enzymes in rats by plant-derived isothiocyanates: comparison of allyl isothiocyanate with sulforaphane and related compounds. , 2004, Journal of agricultural and food chemistry.

[28]  Ü. Günay,et al.  LIPID PEROXIDATION AND ANTIOXIDANT STATUS IN ß-THALASSEMIA , 2000 .

[29]  H. Watt,et al.  SERUM MARKERS FOR DOWN'S SYNDROME IN RELATION TO NUMBER OF PREVIOUS BIRTHS AND MATERNAL AGE , 1996, Prenatal diagnosis.

[30]  S. Miwa,et al.  Three Cases of Hereditary Nonspherocytic Hemolytic Anemia Associated With Red Blood Cell Glutathione Deficiency , 1996 .

[31]  H. Fujii,et al.  Three cases of hereditary nonspherocytic hemolytic anemia associated with red blood cell glutathione deficiency. , 1996, Blood.

[32]  M. Nath,et al.  Hypertriglyceridemia-thalassemia syndrome. , 1974, Indian pediatrics.

[33]  P. Tolentino,et al.  [Clinical manifestations of thalassemia]. , 1956, Archives francaises de pediatrie.