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Wyszukujesz frazę ""Sickle cell trait"" wg kryterium: Temat


Tytuł :
Prevalence of Hemoglobinopathies (β-Thalassemia and Sickle Cell Trait) in the Adult Population of Al Majma'ah, Saudi Arabia.
Autorzy :
Mir SA; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Al Majma'ah, Riyadh Province, Saudi Arabia.
Alshehri BM; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Al Majma'ah, Riyadh Province, Saudi Arabia.
Alaidarous M; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Al Majma'ah, Riyadh Province, Saudi Arabia.
Banawas SS; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Al Majma'ah, Riyadh Province, Saudi Arabia.
Dukhyil AAAB; Department of Medical Laboratory Sciences, College of Applied Medical Sciences, Majmaah University, Al Majma'ah, Riyadh Province, Saudi Arabia.
Alturki MK; Premarital Screening Center, King Khaled General Hospital, Al Majma'ah, Riyadh Province, Saudi Arabia.
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Źródło :
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 47-50. Date of Electronic Publication: 2020 Feb 24.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation*
Hemoglobin, Sickle/*genetics
Sickle Cell Trait/*epidemiology
beta-Globins/*genetics
beta-Thalassemia/*epidemiology
Adult ; Chromatography, High Pressure Liquid ; Female ; Gene Expression ; Genetic Counseling ; Genetic Testing ; Humans ; Male ; Premarital Examinations ; Prevalence ; Retrospective Studies ; Saudi Arabia/epidemiology ; Sickle Cell Trait/blood ; Sickle Cell Trait/diagnosis ; Sickle Cell Trait/genetics ; beta-Globins/deficiency ; beta-Thalassemia/blood ; beta-Thalassemia/diagnosis ; beta-Thalassemia/genetics
Czasopismo naukowe
Tytuł :
Impact of COVID-19 Infection on 24 Patients with Sickle Cell Disease. One Center Urban Experience, Detroit, MI, USA.
Autorzy :
Balanchivadze N; Department of Hematology and Oncology, Henry Ford Health System, Detroit, MI, USA.
Kudirka AA; Department of Internal Medicine, Henry Ford Health System, Detroit, MI, USA.
Askar S; Department of Internal Medicine, Henry Ford Health System, Detroit, MI, USA.
Almadhoun K; Department of Internal Medicine, Henry Ford Health System, Detroit, MI, USA.
Kuriakose P; Department of Hematology and Oncology, Henry Ford Health System, Detroit, MI, USA.
Fadel R; Department of Internal Medicine, Henry Ford Health System, Detroit, MI, USA.
Dabak V; Department of Hematology and Oncology, Henry Ford Health System, Detroit, MI, USA.
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Źródło :
Hemoglobin [Hemoglobin] 2020 Jul; Vol. 44 (4), pp. 284-289. Date of Electronic Publication: 2020 Jul 28.
Typ publikacji :
Journal Article
MeSH Terms :
Betacoronavirus*
Pandemics*
Anemia, Sickle Cell/*complications
Coronavirus Infections/*complications
Pneumonia, Viral/*complications
Acute Disease ; Adult ; Aged ; Aged, 80 and over ; Anemia, Sickle Cell/therapy ; COVID-19 ; Comorbidity ; Coronavirus Infections/blood ; Coronavirus Infections/epidemiology ; Coronavirus Infections/physiopathology ; Erythrocyte Transfusion ; Female ; Humans ; Hypertension/complications ; Length of Stay ; Male ; Michigan/epidemiology ; Middle Aged ; Obesity/complications ; Pain/etiology ; Pneumonia, Viral/blood ; Pneumonia, Viral/epidemiology ; Pneumonia, Viral/physiopathology ; Pulmonary Embolism/etiology ; Retrospective Studies ; SARS-CoV-2 ; Sickle Cell Trait/complications ; Symptom Assessment ; Urban Population ; Young Adult
Czasopismo naukowe
Tytuł :
α-Thalassemia does not seem to influence erythrocyte deformability in sickle cell trait carriers.
Autorzy :
Vayá A; Haemorheology and Haemostasis Unit, Service of Clinical Pathology, La Fe University Hospital , Valencia , Spain .
Collado S
Alis R
Vera B
Romagnoli M
Barragán E
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Źródło :
Hemoglobin [Hemoglobin] 2014; Vol. 38 (3), pp. 165-8. Date of Electronic Publication: 2014 Mar 07.
Typ publikacji :
Clinical Trial; Comparative Study; Journal Article
MeSH Terms :
Erythrocyte Deformability*
Erythrocytes/*metabolism
Sickle Cell Trait/*metabolism
alpha-Thalassemia/*metabolism
Adult ; Amino Acid Substitution ; Erythrocyte Indices ; Erythrocytes/pathology ; Female ; Hemoglobin, Sickle/genetics ; Hemoglobin, Sickle/metabolism ; Humans ; Male ; Middle Aged ; Mutation, Missense ; Sickle Cell Trait/genetics ; Sickle Cell Trait/pathology ; alpha-Thalassemia/genetics ; alpha-Thalassemia/pathology
Czasopismo naukowe
Tytuł :
Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.
Autorzy :
Akinbami AO; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
Campbell AD; b Department of Pediatrics , University of Michigan , Ann Arbor , Michigan , USA.
Han ZJ; c Quest Diagnostics Nichols Institute , Chantilly , Virginia , USA.
Luo HY; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
Chui DH; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
Steinberg MH; a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.
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Źródło :
Hemoglobin [Hemoglobin] 2016; Vol. 40 (1), pp. 64-5. Date of Electronic Publication: 2015 Sep 15.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Point Mutation*
Fetal Hemoglobin/*genetics
Hemoglobin SC Disease/*genetics
Hemoglobin, Sickle/*genetics
Sickle Cell Trait/*genetics
gamma-Globins/*genetics
Adult ; Female ; Hemoglobin C/genetics ; Heterozygote ; Humans ; Infant ; Male ; Promoter Regions, Genetic
Czasopismo naukowe
Tytuł :
Hydroxyurea promotes the reduction of spontaneous BFU-e to normal levels in SS and S/beta thalassemic patients.
Autorzy :
Bincoletto C; Department of Pharmacology, Hemocentre, State University of Campinas, UNICAMP, São Paulo, Brazil.
Perlingeiro RC
Saad ST
Costa FF
Queiroz ML
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Źródło :
Hemoglobin [Hemoglobin] 2001 Feb; Vol. 25 (1), pp. 1-7.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Anemia, Sickle Cell/*blood
Antisickling Agents/*pharmacology
Erythroid Precursor Cells/*drug effects
Hydroxyurea/*pharmacology
Sickle Cell Trait/*blood
beta-Thalassemia/*blood
Anemia, Sickle Cell/drug therapy ; Anemia, Sickle Cell/pathology ; Antisickling Agents/therapeutic use ; Blood Cell Count ; Cell Differentiation/drug effects ; Cell Division/drug effects ; Cells, Cultured/drug effects ; Culture Media, Conditioned/pharmacology ; Erythropoietin/pharmacology ; Heterozygote ; Humans ; Hydroxyurea/therapeutic use ; Sickle Cell Trait/drug therapy ; Sickle Cell Trait/pathology ; beta-Thalassemia/drug therapy ; beta-Thalassemia/pathology
Czasopismo naukowe
Tytuł :
Clinical and hematological responses to hydroxyurea in Sicilian patients with Hb S/beta-thalassemia.
Autorzy :
Rigano P; Thalassemia Centre, Research Unit P. Cutino, V. Cervello Hospital, Palermo, Italy. />Rodgers GP
Renda D
Renda MC
Aquino A
Maggio A
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Źródło :
Hemoglobin [Hemoglobin] 2001 Feb; Vol. 25 (1), pp. 9-17.
Typ publikacji :
Clinical Trial; Journal Article
MeSH Terms :
Antisickling Agents/*therapeutic use
Hydroxyurea/*therapeutic use
Sickle Cell Trait/*drug therapy
Thalassemia/*drug therapy
Adult ; Antisickling Agents/adverse effects ; Antisickling Agents/blood ; Blood Cell Count ; Bone Marrow Diseases/chemically induced ; Female ; Heterozygote ; Hospitalization/statistics & numerical data ; Humans ; Hydroxyurea/adverse effects ; Hydroxyurea/blood ; Male ; Middle Aged ; Phenotype ; Sicily ; Sickle Cell Trait/blood ; Thalassemia/blood ; Treatment Outcome
Czasopismo naukowe
Tytuł :
HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.
Autorzy :
Sweeting I; Medical Research Council Laboratories (Jamaica), University of the West Indies, Mona, Kingston.
Serjeant BE
Serjeant GR
Kulozik AE
Vetter B
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Źródło :
Hemoglobin [Hemoglobin] 1998 Mar; Vol. 22 (2), pp. 153-6.
Typ publikacji :
Journal Article
MeSH Terms :
Globins/*genetics
Hemoglobin, Sickle/*analysis
Hemoglobins, Abnormal/*analysis
Sickle Cell Trait/*genetics
beta-Thalassemia/*genetics
Adolescent ; Adult ; African Continental Ancestry Group/genetics ; Blood Protein Electrophoresis ; Child ; Chromatography, High Pressure Liquid ; Codon/genetics ; Female ; Hemoglobin, Sickle/genetics ; Hemoglobins, Abnormal/genetics ; Heterozygote ; Humans ; Isoelectric Focusing ; Jamaica/epidemiology ; Male ; Sickle Cell Trait/complications ; beta-Thalassemia/complications
Czasopismo naukowe
Tytuł :
Pneumococcal septicemia and meningitis in an infant with Hb S/D-Los Angeles disease: a failure of neonatal hemoglobinopathy screening.
Autorzy :
Abhyankar SH; Department of Pediatrics, SUNY-Health Science Center, Brooklyn 11203.
Miller ST
Rao SP
Brown AB
Pass KA
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Źródło :
Hemoglobin [Hemoglobin] 1991; Vol. 15 (1-2), pp. 119-23.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Hemoglobinometry*
Hemoglobinopathies/*diagnosis
Hemoglobins, Abnormal/*genetics
Mass Screening/*methods
Meningitis, Pneumococcal/*complications
Pneumococcal Infections/*complications
Sepsis/*complications
Sickle Cell Trait/*diagnosis
Blood Protein Electrophoresis ; Diagnostic Errors ; Electrophoresis, Agar Gel ; Electrophoresis, Cellulose Acetate ; Female ; Fetal Blood/chemistry ; Fetal Hemoglobin/analysis ; Genetic Predisposition to Disease ; Hemoglobin A/analysis ; Hemoglobin, Sickle/analysis ; Hemoglobinopathies/complications ; Humans ; Infant ; Isoelectric Focusing ; Male ; Maternal-Fetal Exchange ; New York ; Pregnancy ; Sickle Cell Trait/complications
Czasopismo naukowe
Tytuł :
The risk of potential thromboembolic, renal and cardiac complications of sickle cell trait.
Autorzy :
Bucknor MD; Department of Radiology and Biomedical Imaging; University of California San Francisco, San Francisco , California , USA.
Goo JS
Coppolino ML
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Źródło :
Hemoglobin [Hemoglobin] 2014; Vol. 38 (1), pp. 28-32. Date of Electronic Publication: 2013 Oct 07.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Heart Diseases/*etiology
Kidney Diseases/*etiology
Sickle Cell Trait/*complications
Thromboembolism/*etiology
Adult ; Anemia, Sickle Cell/complications ; Databases, Factual ; Heart Diseases/epidemiology ; Humans ; Kidney Diseases/epidemiology ; Male ; Middle Aged ; Patient Outcome Assessment ; Retrospective Studies ; Risk ; Thromboembolism/epidemiology ; Young Adult
Czasopismo naukowe
Tytuł :
Prevalence of the β(S) gene among scheduled castes, scheduled tribes and other backward class groups in Central India.
Autorzy :
Shrikhande AV; Department of Pathology, Indira Gandhi Government Medical College , Nagpur, Maharashtra , India .
Arjunan A
Agarwal A
Dani A
Tijare J
Gettig E
Krishnamurti L
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Źródło :
Hemoglobin [Hemoglobin] 2014; Vol. 38 (4), pp. 230-5.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation*
Social Class*
Anemia, Sickle Cell/*epidemiology
Anemia, Sickle Cell/*genetics
Ethnic Groups/*genetics
beta-Globins/*genetics
Adolescent ; Adult ; Child ; Child, Preschool ; Genetic Counseling ; Genetic Testing ; Genotype ; Geography ; Humans ; India/epidemiology ; Infant ; Middle Aged ; Prevalence ; Sickle Cell Trait ; Young Adult
Czasopismo naukowe
Tytuł :
Effects of a Single Sickling Event on the Mechanical Fragility of Sickle Cell Trait Erythrocytes.
Autorzy :
Presley, Tennille D. (AUTHOR)
Perlegas, Andreas S. (AUTHOR)
Bain, Lauren E. (AUTHOR)
Ballas, Samir K. (AUTHOR)
Nichols, James S. (AUTHOR)
Sabio, Hernan (AUTHOR)
Gladwin, Mark T. (AUTHOR)
Kato, Gregory J. (AUTHOR)
Kim-Shapiro, Daniel B. (AUTHOR)
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Źródło :
Hemoglobin. Feb2010, Vol. 34 Issue 1, p24-36. 13p. 1 Black and White Photograph, 1 Chart, 3 Graphs.
Czasopismo naukowe
Tytuł :
A De Novo Heterozygous Variant (HBB: c.379delG, p.Val127Cysfs*32) Associated with a Mild β-Thalassemia Intermedia Phenotype in a Turkish Child.
Autorzy :
Gürlek-Gökçebay, Dilek
Akpinar-Tekgunduz, Sibel
Erdem, Haktan B.
Yarali, Nese
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Temat :
FETAL hemoglobin
ERYTHROCYTES
PHENOTYPES
BLOOD cells
CELL membranes
HEMOLYSIS & hemolysins
SICKLE cell trait
HYDROPS fetalis
Źródło :
Hemoglobin; Jul-Sep2019, Vol. 43 Issue 4/5, p277-279, 3p
Czasopismo naukowe
Tytuł :
Awareness and Attitude of University Students About Screening and Testing for Hemoglobinopathies: Case Study of the Aseer Region, Saudi Arabia.
Autorzy :
Eissa, Mohamed
Patel, Ayyub A.
Farag, Shehata
Babiker, Nashwa H.
Al-Shahrani, Malak S.
Al-Nahari, Albatool M.
Al Sahmaa, Ali M.
Al-Shraim, Mubarak
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Temat :
GENETIC disorders
COLLEGE students
ATTITUDE change (Psychology)
SICKLE cell trait
BLOOD testing
BLOOD sampling
Źródło :
Hemoglobin; Jul2018, Vol. 42 Issue 4, p264-268, 5p
Terminy geograficzne :
SAUDI Arabia
Czasopismo naukowe
Tytuł :
Haplotypes linked to three rare beta-thalassemia mutations, originally reported in Tunisia.
Autorzy :
Bibi A; Laboratoire de Biochimie et de Biologie Moléculaire, Hôpital d'Enfants, Tunisie.
Messaoud T
Fattoum S
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Źródło :
Hemoglobin [Hemoglobin] 2006; Vol. 30 (2), pp. 175-81.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Mutation*
Globins/*genetics
Haplotypes/*genetics
beta-Thalassemia/*genetics
Codon/genetics ; DNA Mutational Analysis ; Ethnic Groups/genetics ; Female ; Heterozygote ; Homozygote ; Humans ; Male ; Mutagenesis, Insertional ; Mutation, Missense ; Pedigree ; Phenotype ; Point Mutation ; Polymerase Chain Reaction ; Polymorphism, Restriction Fragment Length ; Sickle Cell Trait/complications ; Sickle Cell Trait/genetics ; Tunisia ; beta-Thalassemia/complications
Czasopismo naukowe
Tytuł :
Association of Hb H disease with sickle-trait.
Autorzy :
Martinez G
Ferreira R
Hernandez A
Di Rienzo A
Colombo B
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Źródło :
Hemoglobin [Hemoglobin] 1986; Vol. 10 (4), pp. 421-5.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Anemia, Sickle Cell/*complications
Sickle Cell Trait/*complications
Thalassemia/*complications
Adolescent ; African Continental Ancestry Group ; Asian Continental Ancestry Group ; Genotype ; Globins/genetics ; Hemoglobin, Sickle/genetics ; Humans ; Male ; Sickle Cell Trait/blood ; Sickle Cell Trait/genetics ; Thalassemia/blood ; Thalassemia/genetics
Czasopismo naukowe
Tytuł :
Molecular basis of beta-thalassemia in the Maldives.
Autorzy :
Furuumi H; Institute of Genetic Information, Kyushu University, Fukuoka, Japan.
Firdous N
Inoue T
Ohta H
Winichagoon P
Fucharoen S
Fukumaki Y
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Źródło :
Hemoglobin [Hemoglobin] 1998 Mar; Vol. 22 (2), pp. 141-51.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Globins/*genetics
beta-Thalassemia/*genetics
Algeria/ethnology ; Codon/genetics ; DNA Mutational Analysis ; Ethnic Groups/genetics ; Genotype ; Haplotypes/genetics ; Hemoglobin E/genetics ; Hemoglobin, Sickle/genetics ; Hemoglobinuria/complications ; Hemoglobinuria/genetics ; Humans ; India/ethnology ; Indian Ocean Islands/epidemiology ; Indonesia/ethnology ; Malaria/epidemiology ; Malaysia/ethnology ; Polymerase Chain Reaction ; Portugal/ethnology ; Sickle Cell Trait/complications ; Sickle Cell Trait/genetics ; beta-Thalassemia/complications ; beta-Thalassemia/epidemiology ; beta-Thalassemia/ethnology
Czasopismo naukowe
Tytuł :
Hb O-Tibesti [beta121(GH4)Glu-->Lys; beta11(A8)Val-->Ile], a hemoglobin variant carrying in the same beta chain the substitutions of Hb O-Arab and Hb Hamilton, found in combination with Hb S [beta6(A3)Glu-->Val].
Autorzy :
Préhu C; INSERM U 468 and Department of Biochemistry, Hôpital Henri Mondor, Créteil, France.
Riou J
Sartelet I
Promé D
Claparols C
Denier M
Motte J
Galactéros F
Wajcman H
Pokaż więcej
Źródło :
Hemoglobin [Hemoglobin] 2002 Feb; Vol. 26 (1), pp. 13-20.
Typ publikacji :
Case Reports; Comparative Study; Journal Article
MeSH Terms :
Amino Acid Substitution*
Globins/*genetics
Hemoglobin, Sickle/*genetics
Hemoglobins, Abnormal/*chemistry
Hemoglobins, Abnormal/*isolation & purification
Sickle Cell Trait/*genetics
Blood Protein Electrophoresis ; Chad/ethnology ; Child ; Chromatography, High Pressure Liquid ; France ; Globins/chemistry ; Hemoglobins, Abnormal/genetics ; Heterozygote ; Humans ; Hydrophobic and Hydrophilic Interactions ; Male ; Sudan/ethnology
Czasopismo naukowe

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