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Wyszukujesz frazę ""THALASSEMIA"" wg kryterium: Temat


Tytuł :
Development of a genomic DNA reference material panel for thalassemia genetic testing.
Autorzy :
Yin Z; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Qu S; Division of In Vitro Diagnostics for Non-Infectious Diseases, National Institutes for Food and Drug Control, Beijing, China.
Huang C; Division of In Vitro Diagnostics for Non-Infectious Diseases, National Institutes for Food and Drug Control, Beijing, China.
Chen F; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.; MGI-Shenzhen, BGI-Shenzhen, Shenzhen, China.
Li J; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Chen S; BGI-Shenzhen, Shenzhen, China.; Clinical Laboratory of BGI Health, BGI-Shenzhen, Shenzhen, China.
Ye J; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Yang Y; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Zheng Y; BGI-Shenzhen, Shenzhen, China.; Clinical Laboratory of BGI Health, BGI-Shenzhen, Shenzhen, China.
Zhang X; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Yang X; School of Laboratory Medicine and Biotechnology, Southern Medical University, Guangzhou, China.
Xie L; Hybribio Limited, Sino-Singapore Guangzhou Knowledge City, Guangzhou, China.
Wei J; Research and Development Department, Yaneng BIOscience (Shenzhen) Co. Ltd, Shenzhen, China.
Wei F; The Genetics Laboratory, Shenzhen Longgang District Maternity and Child Healthcare Hospital, Shenzhen, China.
Guo J; BGI-Shenzhen, Shenzhen, China.; China National GeneBank, BGI-Shenzhen, Shenzhen, China.
Huang J; Division of In Vitro Diagnostics for Non-Infectious Diseases, National Institutes for Food and Drug Control, Beijing, China.
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Źródło :
International journal of laboratory hematology [Int J Lab Hematol] 2020 Oct; Vol. 42 (5), pp. 510-517. Date of Electronic Publication: 2020 Apr 16.
Typ publikacji :
Journal Article
MeSH Terms :
Genetic Markers*
Genomics*/methods
Genomics*/standards
Genetic Testing/*methods
Thalassemia/*diagnosis
Thalassemia/*genetics
Alleles ; Cell Line ; China ; Genetic Testing/standards ; Genotype ; Humans ; Reference Standards ; Reproducibility of Results ; alpha-Globins/genetics ; beta-Globins/genetics ; beta-Thalassemia/diagnosis ; beta-Thalassemia/genetics
Czasopismo naukowe
Tytuł :
[Diagnostic Value of HBA 2 in Different Types of Thalassemia].
Autorzy :
Peng R; Department of Women's Health, Chongqing Maternal and Child Health Hospital, Chongqing 401147,China.
Gu HY; Department of Women's Health, Chongqing Maternal and Child Health Hospital, Chongqing 401147,China.
Qin M; Department of Women's Health, Chongqing Maternal and Child Health Hospital, Chongqing 401147,China.
Zhang HY; Department of Women's Health, Chongqing Maternal and Child Health Hospital, Chongqing 401147,China,E-mail: .
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 217-220.
Typ publikacji :
Journal Article
MeSH Terms :
alpha-Thalassemia*/diagnosis
alpha-Thalassemia*/genetics
beta-Thalassemia*/diagnosis
Child ; Female ; Hematologic Tests ; Hemoglobin A2/analysis ; Humans ; Mass Screening ; Pregnancy
Czasopismo naukowe
Tytuł :
[Clinical value of PCR-flow Fluorescence Hybridization in Prenatal Genetic Diagnosis of Thalassemia].
Autorzy :
Liu CL; Department of Laboratory Medicine, The Second Hospital of Yunnan Province/Affiliated Hospital of Yunnan University, Kunming 650021, Yunnan Province, China.
Chen PS; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China,E-mail: .
He XH; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China.
Yu XG; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China.
Huang H; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China.
Huang B; Department of Laboratory Medicine, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, Guangdong Province, China.
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 221-227.
Typ publikacji :
Journal Article
MeSH Terms :
alpha-Thalassemia*/diagnosis
alpha-Thalassemia*/genetics
beta-Thalassemia*/diagnosis
beta-Thalassemia*/genetics
China ; Female ; Genotype ; Humans ; Mutation ; Polymerase Chain Reaction ; Pregnancy ; Prenatal Diagnosis
Czasopismo naukowe
Tytuł :
[The Clinical Value of Combined Detection of RBC, Ret-He and HbA2 for Thalassemia].
Autorzy :
Yuan QR; Department of Clinical Laboratory Examination,The Seventh Affiliated Hospital of Sun Yat-sen University,Shenzhen 518000,Guanghdong Province, China.
Niu SQ; Department of Clinical Laboratory Examination,The Seventh Affiliated Hospital of Sun Yat-sen University,Shenzhen 518000,Guanghdong Province, China.
Lin XP; Department of Clinical Laboratory Examination,The Seventh Affiliated Hospital of Sun Yat-sen University,Shenzhen 518000,Guanghdong Province, China.
Luo ZF; Department of Clinical Laboratory Examination,The Seventh Affiliated Hospital of Sun Yat-sen University,Shenzhen 518000,Guanghdong Province, China,E-mail: .
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 203-206.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Iron-Deficiency*
alpha-Thalassemia*
beta-Thalassemia*/diagnosis
Erythrocyte Indices ; Humans ; Proto-Oncogene Proteins c-ret ; ROC Curve
Czasopismo naukowe
Tytuł :
[The Value of Umbilical Cord Blood Erythrocyte Index in the Screening of Neonatal Thalassemia].
Autorzy :
Zhuang CJ; Department of Clinical Laboratory Examination, Boai Hospital of Zhongshan Affiliated with Southern Medical University, Zhongshan 528400, Guangdong Province, China.
Wu XW; Prenatal Diagnosis Center, Boai Hospital of Zhongshan Affiliated with Southern Medical University, Zhongshan 528400, Guangdong Province, China.
Wan ZD; Prenatal Diagnosis Center, Boai Hospital of Zhongshan Affiliated with Southern Medical University, Zhongshan 528400, Guangdong Province, China.
Huang X; Department of Clinical Laboratory Examination, Boai Hospital of Zhongshan Affiliated with Southern Medical University, Zhongshan 528400, Guangdong Province, China,,E-mail:.
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 193-197.
Typ publikacji :
Journal Article
MeSH Terms :
alpha-Thalassemia*/diagnosis
beta-Thalassemia*
Child ; Erythrocyte Indices ; Fetal Blood ; Humans ; Infant, Newborn ; Mass Screening
Czasopismo naukowe
Tytuł :
[Application of Next-Generation Sequencing in Screening of Thalassemia Gene in 11212 Pregnant Women in Suxian and Beihu Districts of Chenzhou City, Hunan Province].
Autorzy :
Yang M; Chenzhou Hospital Affiliated to University of South China,Chenzhou 423000,Hunan Province, China.
Li CY; Center of Prenatal Diagnosis, Chenzhou No.1 People's Hospital, Chenzhou 423000,Hunan Province, China.
Lei DZ; Chenzhou Hospital Affiliated to University of South China,Chenzhou 423000,Hunan Province, China,Center of Prenatal Diagnosis, Chenzhou No.1 People's Hospital, Chenzhou 423000,Hunan Province, China.
Zhang HQ; Center of Prenatal Diagnosis, Chenzhou No.1 People's Hospital, Chenzhou 423000,Hunan Province, China,E-mail: .
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 188-192.
Typ publikacji :
Journal Article
MeSH Terms :
Hemoglobins, Abnormal*
alpha-Thalassemia*/genetics
beta-Thalassemia*/genetics
China ; Female ; Genotype ; High-Throughput Nucleotide Sequencing ; Humans ; Mutation ; Pregnancy ; Pregnant Women
Czasopismo naukowe
Tytuł :
[β-Thalassemia among Newborns in Wuhan Region and Its Influence Factors].
Autorzy :
Zhou B; Wuhan Children's Hospital(Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology,Wuhan 430016,Hubei Province, China.
Xiong Q; Wuhan Children's Hospital(Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology,Wuhan 430016,Hubei Province, China.
Cai WQ; Wuhan Children's Hospital(Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology,Wuhan 430016,Hubei Province, China.
Hu XJ; Wuhan Children's Hospital(Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology,Wuhan 430016,Hubei Province, China,E-mail:.
Shen SS; Wuhan Children's Hospital(Wuhan Maternal and Child Healthcare Hospital), Tongji Medical College, Huazhong University of Science & Technology,Wuhan 430016,Hubei Province, China.
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 198-202.
Typ publikacji :
Journal Article
MeSH Terms :
Thalassemia*
beta-Thalassemia*/epidemiology
beta-Thalassemia*/genetics
Electrophoresis, Capillary ; Humans ; Infant, Newborn ; Mass Screening ; Mutation
Czasopismo naukowe
Tytuł :
Splenic sequestration in the adult: cross sectional imaging appearance of an uncommon diagnosis.
Autorzy :
Esterson YB; Russell H. Morgan Department of Radiology, Johns Hopkins University School of Medicine, 601 N Caroline Street, Baltimore, MD 21287, USA. Electronic address: .
Sheth S; Russell H. Morgan Department of Radiology, Johns Hopkins University School of Medicine, 601 N Caroline Street, Baltimore, MD 21287, USA.
Kawamoto S; Russell H. Morgan Department of Radiology, Johns Hopkins University School of Medicine, 601 N Caroline Street, Baltimore, MD 21287, USA.
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Źródło :
Clinical imaging [Clin Imaging] 2021 Jan; Vol. 69, pp. 369-373. Date of Electronic Publication: 2020 Oct 12.
Typ publikacji :
Case Reports; Journal Article; Review
MeSH Terms :
Anemia, Sickle Cell*
Hypersplenism*
Splenic Diseases*/diagnostic imaging
beta-Thalassemia*/complications
beta-Thalassemia*/diagnostic imaging
Adult ; Child ; Humans ; Male ; Splenomegaly/diagnostic imaging ; Splenomegaly/etiology
Czasopismo naukowe
Tytuł :
The impact of COVID-19 on transfusion-dependent thalassemia patients of Karachi, Pakistan: A single-center experience.
Autorzy :
Arshad Ali S; Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan. Electronic address: .
Azim D; Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan.
Hassan HM; Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan.
Iqbal A; Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan.
Ahmed N; Department of Pathology, Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan.
Kumar S; Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan.
Nasim S; Dow Medical College, Dow University of Health Sciences, Baba-e-Urdu Road, 74200 Karachi, Pakistan.
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Źródło :
Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine [Transfus Clin Biol] 2021 Feb; Vol. 28 (1), pp. 60-67. Date of Electronic Publication: 2020 Oct 19.
Typ publikacji :
Journal Article
MeSH Terms :
COVID-19*
Continuity of Patient Care*
Pandemics*
SARS-CoV-2*
Blood Donors/*supply & distribution
Blood Transfusion/*statistics & numerical data
beta-Thalassemia/*therapy
Adolescent ; Blood Grouping and Crossmatching ; Child ; Child, Preschool ; Cross-Sectional Studies ; Female ; Health Services Accessibility ; Humans ; Male ; Pakistan/epidemiology ; Patient Acceptance of Health Care ; Patient Compliance ; Procedures and Techniques Utilization ; Retrospective Studies ; Rural Population ; beta-Thalassemia/epidemiology
Czasopismo naukowe
Tytuł :
Revisiting the non-transfusion-dependent (NTDT) vs. transfusion-dependent (TDT) thalassemia classification 10 years later.
Autorzy :
Musallam KM; International Network of Hematology, London, UK.
Cappellini MD; Department of Clinical Sciences and Community, University of Milan, Milan, Italy.
Viprakasit V; Department of Pediatrics & Thalassemia Center, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Kattamis A; First Department of Pediatrics, National and Kapodistrian University of Athens, Athens, Greece.
Rivella S; Department of Pediatrics, Division of Hematology, Raymond G. Perelman Center for Cellular and Molecular Therapeutics; Abramson Research Center at The Children's Hospital of Philadelphia (CHOP); Cell and Molecular Biology Affinity Group (CAMB), Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Taher AT; Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon.
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Źródło :
American journal of hematology [Am J Hematol] 2021 Feb 01; Vol. 96 (2), pp. E54-E56. Date of Electronic Publication: 2020 Dec 09.
Typ publikacji :
Letter; Review
MeSH Terms :
Blood Transfusion*
Iron Overload*/classification
Iron Overload*/etiology
Iron Overload*/therapy
Thalassemia*/classification
Thalassemia*/therapy
Humans
Recenzja
Tytuł :
Global loss of Tfr2 with concomitant induced iron deficiency greatly ameliorates the phenotype of a murine thalassemia intermedia model.
Autorzy :
Schmidt PJ; Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Fitzgerald K; Alnylam Pharmaceuticals, Inc., Cambridge, Massachusetts, USA.
Butler JS; Alnylam Pharmaceuticals, Inc., Cambridge, Massachusetts, USA.; Current: Intellia Therapeutics, Inc., Cambridge, Massachusetts, USA.
Fleming MD; Department of Pathology, Boston Children's Hospital and Harvard Medical School, Boston, Massachusetts, USA.
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Źródło :
American journal of hematology [Am J Hematol] 2021 Feb 01; Vol. 96 (2), pp. 251-257. Date of Electronic Publication: 2020 Nov 27.
Typ publikacji :
Journal Article
MeSH Terms :
Hemochromatosis/*metabolism
Iron/*deficiency
Receptors, Transferrin/*deficiency
beta-Thalassemia/*metabolism
Amino Acid Substitution ; Animals ; Disease Models, Animal ; GPI-Linked Proteins/genetics ; GPI-Linked Proteins/metabolism ; Hemochromatosis/genetics ; Hemochromatosis/pathology ; Hemochromatosis Protein/genetics ; Hemochromatosis Protein/metabolism ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Mice ; Mice, Transgenic ; Mutation, Missense ; Receptors, Transferrin/metabolism ; Serine Endopeptidases/genetics ; Serine Endopeptidases/metabolism ; beta-Thalassemia/genetics ; beta-Thalassemia/pathology
Czasopismo naukowe
Tytuł :
[Analysis of phenotypes of Hb J-Bangkok and concomitant thalassemia].
Autorzy :
Li Y; Department of Laboratory Medicine, Luohu District People's Hospital, Shenzhen, Guangdong 518001, China. .
Cai Q
Jin X
Qin J
Chen Y
Li R
Mo Y
Zhang X
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan 10; Vol. 38 (1), pp. 7-11.
Typ publikacji :
Journal Article
MeSH Terms :
Hemoglobins, Abnormal*/genetics
beta-Thalassemia*/complications
beta-Thalassemia*/genetics
Female ; Heterozygote ; Humans ; Male ; Phenotype ; Thailand
Czasopismo naukowe
Tytuł :
[Research progress of iron metabolism in phenotype modification of β-thalassemia].
Autorzy :
Chen D; Department of Laboratory, Institute of Obstetrics and Gynecology, the Third Affiliated Hospital of Guangzhou Medical University, Guangdong Provincial Key Laboratory for Major Obstetric Diseases, Guangdong Provincial Key Laboratory for Reproduction and Genetics in General Universities, Guangzhou, Guangdong 510150, China. .
Sun X
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Źródło :
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2021 Jan 10; Vol. 38 (1), pp. 27-31.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Iron*/metabolism
beta-Thalassemia*/genetics
beta-Thalassemia*/physiopathology
Humans ; Iron Overload/genetics ; Phenotype ; Research/trends
Czasopismo naukowe
Tytuł :
Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
Autorzy :
Giardine BM; The Pennsylvania State University, Center for Computational Biology and Bioinformatics, University Park, PA, USA.
Joly P; Biochimie des pathologies érythrocytaires, Laboratoire de Biochimie et Biologie Moléculaire Grand-Est, Groupement hospitalier Est, Hospices Civils de Lyon, Bron, France.; Laboratoire Interuniversitaire de Biologie de la Motricité (LIBM) EA7424, Equipe 'Biologie vasculaire et du globule rouge'', Université Claude Bernard Lyon 1, COMUE Lyon, France.
Pissard S; Assistance Publique Hopitaux de Paris), Department of Genetics GHU (Groupe Hospitalier Universitaire Henri Mondor) H. Mondor and Institut Mondor de Recherche biomedicale - INSERM U955 eq2, Creteil France.
Wajcman H; INSERM U955, CHU Henri Mondor, Creteil, France.
K Chui DH; Boston University School of Medicine, Department of Medicine, Pathology and Laboratory Medicine, Boston, MA, USA.
Hardison RC; The Pennsylvania State University, Center for Computational Biology and Bioinformatics, University Park, PA, USA.; Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA, USA.
Patrinos GP; University of Patras, School of Health Sciences, Department of Pharmacy, Laboratory of Pharmacogenomics and Individualized Therapy, Patras, Greece.; Erasmus University Medical Center Rotterdam, Faculty of Medicine and Health Sciences, Department of Pathology, Bioinformatics Unit, Rotterdam, the Netherlands.; United Arab Emirates University, College of Medicine and Health Sciences, Department of Pathology, Al-Ain, UAE.; United Arab Emirates University, Zayed Center of Health Sciences, Al-Ain, UAE.
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Źródło :
Nucleic acids research [Nucleic Acids Res] 2021 Jan 08; Vol. 49 (D1), pp. D1192-D1196.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms :
Databases, Genetic*
Mutation*
Software*
Hemoglobins/*genetics
Thalassemia/*genetics
Gene Expression ; Genetic Loci ; Genome, Human ; Genomics/methods ; Genotype ; Hemoglobins/chemistry ; Hemoglobins/metabolism ; Heterozygote ; Humans ; Internet ; Phenotype ; Thalassemia/classification ; Thalassemia/pathology
Czasopismo naukowe
Tytuł :
Bone marrow necrosis and fat embolism syndrome: a near fatal complication in previously undiagnosed sickle beta + thalassaemia.
Autorzy :
Budhathoki N; Hematology and Oncology, NYU Langone Hospital-Long Island, Mineola, New York, USA .
Timilsina S; Geriatrics, NYU Langone Hospital-Long Island, Mineola, New York, USA.
Ram B; Pathology, NYU Langone Hospital-Long Island, Mineola, New York, USA.
Marks D; Hematology and Oncology, NYU Langone Hospital-Long Island, Mineola, New York, USA.
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Źródło :
BMJ case reports [BMJ Case Rep] 2021 Jan 06; Vol. 14 (1). Date of Electronic Publication: 2021 Jan 06.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Anemia, Sickle Cell/*complications
Bone Marrow/*pathology
Embolism, Fat/*etiology
beta-Thalassemia/*complications
Adult ; Anemia, Sickle Cell/diagnosis ; Anemia, Sickle Cell/therapy ; Biopsy ; Embolism, Fat/therapy ; Erythrocyte Transfusion ; Humans ; Male ; Necrosis/etiology ; Necrosis/pathology ; Necrosis/therapy ; Treatment Outcome ; Vitamin B 12/administration & dosage ; beta-Thalassemia/diagnosis ; beta-Thalassemia/therapy
Czasopismo naukowe
Tytuł :
An assessment of the continuing medical education needs of US physicians in the management of patients with beta thalassemia.
Autorzy :
Stacy S; CE Outcomes, LLC, Birmingham, AL, 35205, USA.
Sheth S; Division of Pediatric Hematology and Oncology, Weill Cornell Medical College, New York, NY, 10065, USA.
Coleman B; CE Outcomes, LLC, Birmingham, AL, 35205, USA.
Cerenzia W; CE Outcomes, LLC, Birmingham, AL, 35205, USA. .
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Źródło :
Annals of hematology [Ann Hematol] 2021 Jan; Vol. 100 (1), pp. 27-35. Date of Electronic Publication: 2020 Sep 01.
Typ publikacji :
Journal Article
MeSH Terms :
Disease Management*
Physicians*/standards
Surveys and Questionnaires*
Education, Medical, Continuing/*methods
Hematology/*education
beta-Thalassemia/*therapy
Adolescent ; Adult ; Education, Medical, Continuing/standards ; Female ; Hematology/standards ; Humans ; Male ; Patient Education as Topic/methods ; Patient Education as Topic/standards ; Transition to Adult Care/standards ; United States/epidemiology ; Young Adult ; beta-Thalassemia/epidemiology
Czasopismo naukowe
Tytuł :
[Genetic Analysis, Prenatal Diagnosis and Preimplantation Genetic Diagnosis of Taiwanese Deletion β-Thalassemia].
Autorzy :
DU L; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Qin DQ; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Liu L; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Lu J; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Yao CZ; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Huang HJ; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China.
Wang JC; Medical Genetics Center, Key Laboratory of Metabolic and Genetic Disease in Women and Children, Guangdong Women and Children Hospital, Guangzhou 511442, Guangdong Province, China,E-mail:.
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2019 Oct; Vol. 27 (5), pp. 1585-1591.
Typ publikacji :
Journal Article
MeSH Terms :
Preimplantation Diagnosis*
beta-Thalassemia*/genetics
Female ; Genetic Testing ; Humans ; Pregnancy ; Prenatal Diagnosis ; alpha-Thalassemia
Czasopismo naukowe
Tytuł :
[Detection of Irregular Antibodies after Blood Transfusion for Children with Thalassemia in Hainan].
Autorzy :
Xu CL; Department of Blood Transfusion, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou 570311, Hainan Province, China.
Cai XQ; Department of Blood Transfusion, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou 570311, Hainan Province, China.
Chen DJ; Department of Blood Transfusion, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou 570311, Hainan Province, China.
Wu JF; Department of Blood Transfusion, Hainan General Hospital (Hainan Affiliated Hospital of Hainan Medical University), Haikou 570311, Hainan Province, China,E-mail:.
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2021 Feb; Vol. 29 (1), pp. 243-247.
Typ publikacji :
Journal Article
MeSH Terms :
Blood Transfusion*
beta-Thalassemia*
ABO Blood-Group System ; Blood Grouping and Crossmatching ; Child ; Female ; Humans ; Infant ; Male ; Rh-Hr Blood-Group System
Czasopismo naukowe
Tytuł :
A plethora of gene therapies for hemoglobinopathies.
Autorzy :
Dunbar CE; Translational Stem Cell Biology Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA. .
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Źródło :
Nature medicine [Nat Med] 2021 Feb; Vol. 27 (2), pp. 202-204.
Typ publikacji :
Journal Article; Research Support, N.I.H., Intramural; Comment
MeSH Terms :
Anemia, Sickle Cell*/genetics
Anemia, Sickle Cell*/therapy
Hemoglobinopathies*/genetics
Hemoglobinopathies*/therapy
beta-Thalassemia*
CRISPR-Cas Systems ; Gene Editing ; Humans
Czasopismo naukowe
Tytuł :
Induction of Fetal Hemoglobin by Gene Therapy.
Autorzy :
Walters MC; From the Blood and Marrow Transplant Program, University of California, San Francisco-Benioff Children's Hospital, Oakland.
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Źródło :
The New England journal of medicine [N Engl J Med] 2021 Jan 21; Vol. 384 (3), pp. 284-285.
Typ publikacji :
Editorial; Comment
MeSH Terms :
Anemia, Sickle Cell*/genetics
Anemia, Sickle Cell*/therapy
beta-Thalassemia*/genetics
CRISPR-Cas Systems ; Fetal Hemoglobin/genetics ; Gene Editing ; Genetic Therapy ; Humans
Opinia redakcyjna

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