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Wyszukujesz frazę ""Anemia, Hypochromic"" wg kryterium: Temat


Tytuł :
Inoculum reduction and vector control on the temporal progress of citrus variegated chlorosis incidence.
Autorzy :
Bassanezi RB; Research & Development Department, Fund for Citrus Protection - Fundecitrus, Araraquara, Brazil.
Primiano IV; Research & Development Department, Fund for Citrus Protection - Fundecitrus, Araraquara, Brazil.
Moreira AS; Embrapa Cassava & Fruits, Cruz das Almas, Brazil.
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Źródło :
Pest management science [Pest Manag Sci] 2021 Jul; Vol. 77 (7), pp. 3333-3340. Date of Electronic Publication: 2021 Apr 05.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Citrus*
Incidence ; Plant Diseases/prevention & control ; Xylella
SCR Organism :
Xylella fastidiosa
Czasopismo naukowe
Tytuł :
Utilization of Discriminant Formulas in the Differentiation of Alpha Thalassemia, Beta Thalassemia, and Iron Deficiency in Premarital Setting.
Autorzy :
Saboor M
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Źródło :
Clinical laboratory [Clin Lab] 2021 Apr 01; Vol. 67 (4).
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Anemia, Iron-Deficiency*/diagnosis
alpha-Thalassemia*/diagnosis
alpha-Thalassemia*/genetics
beta-Thalassemia*/diagnosis
Diagnosis, Differential ; Erythrocyte Indices ; Female ; Humans ; Iron
Czasopismo naukowe
Tytuł :
Gibberellic acid decreases Melanocallis caryaefoliae (Hemiptera: Aphididae) population density and chlorotic feeding injury to foliage in pecan orchards.
Autorzy :
Cottrell TE; Agricultural Research Service, Southeastern Fruit and Tree Nut Research Laboratory, USDA, Byron, GA, USA.
Wood BW; Agricultural Research Service, Southeastern Fruit and Tree Nut Research Laboratory, USDA, Byron, GA, USA.
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Źródło :
Pest management science [Pest Manag Sci] 2021 Mar; Vol. 77 (3), pp. 1512-1519. Date of Electronic Publication: 2020 Nov 22.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Aphids*
Carya*
Animals ; Gibberellins ; Population Density
Czasopismo naukowe
Tytuł :
Dizygotic twins with prolonged jaundice and microcytic, hypochromic, hemolytic anemia with pyropoikilocytosis.
Autorzy :
Bahr TM; Division of Neonatology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT, United States of America. Electronic address: .
Lozano-Chinga M; Division of Hematology/Oncology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT, United States of America.
Agarwal AM; Division of Hematopathology, Department of Pathology, University of Utah Health, Salt Lake City, UT, United States of America; ARUP Laboratories, Salt Lake City, UT, United States of America.
Meznarich JA; Division of Hematology/Oncology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT, United States of America.
Gerday E; Department of Pediatrics, Division of Neonatology, Utah Valley Hospital, Provo, UT, United States of America.
Smoot JL; Department of Pediatrics, Division of Neonatology, Utah Valley Hospital, Provo, UT, United States of America.
Taylor A; Department of Pathology, Utah Valley Hospital, Provo, UT, United States of America.
Christensen RD; Division of Neonatology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT, United States of America; Division of Hematology/Oncology, Department of Pediatrics, University of Utah Health, Salt Lake City, UT, United States of America.
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Źródło :
Blood cells, molecules & diseases [Blood Cells Mol Dis] 2020 Nov; Vol. 85, pp. 102462. Date of Electronic Publication: 2020 Jun 25.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Anemia, Hemolytic/*complications
Anemia, Hypochromic/*complications
Elliptocytosis, Hereditary/*complications
Jaundice/*complications
Anemia, Hemolytic/blood ; Anemia, Hemolytic/genetics ; Anemia, Hypochromic/blood ; Anemia, Hypochromic/genetics ; Elliptocytosis, Hereditary/blood ; Elliptocytosis, Hereditary/genetics ; Humans ; Infant, Newborn ; Jaundice/blood ; Jaundice/genetics ; Male ; Point Mutation ; Spectrin/genetics ; Twins, Dizygotic/genetics
SCR Disease Name :
Anemia, hypochromic microcytic; Pyropoikilocytosis, Hereditary
Czasopismo naukowe
Tytuł :
[A case with α-thalassemia caused by novel start codon variant in conjunct with right deletion variant of α2-globin gene].
Autorzy :
Chen Y; Central Laboratory, the Affiliated Haikou Hospital of Xiangya Medical College, Central South University, Haikou, Hainan 570208, China. .
Wang J
Wang C
Chen S
Feng N
Liu H
Tang X
Zhang S
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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. 12-14.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Anemia, Hypochromic*/genetics
Codon, Initiator*/genetics
alpha-Globins*/genetics
alpha-Thalassemia*/genetics
Female ; Genetic Counseling ; Genetic Variation ; Genotype ; Humans ; Male ; Mutation ; Pregnancy ; Prenatal Diagnosis
Czasopismo naukowe
Tytuł :
Frequency and types of haemoglobinopathies in children with microcytic anaemia.
Autorzy :
Khan SA; Department of Pediatrics, Shifa College of Medicine, Shifa international Hospital, Islamabad, Pakistan.
Aaraj S; Department of Pediatrics, Shifa College of Medicne, Islamabad, Pakistan.
Hussain SNF; Final Year Student, Shifa College of Medicine, Islamabad, Pakistan.
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Źródło :
JPMA. The Journal of the Pakistan Medical Association [J Pak Med Assoc] 2021 Jan; Vol. 71 (1(A)), pp. 78-80.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Anemia, Iron-Deficiency*/epidemiology
Hemoglobinopathies*/complications
Hemoglobinopathies*/epidemiology
Child ; Female ; Humans ; Pakistan/epidemiology ; Pregnancy ; Prospective Studies
Czasopismo naukowe
Tytuł :
[Iron deficiency in adults : to understand what biological evaluation should be carried out].
Autorzy :
Manckoundia P; Pôle Personnes Âgées, CHU Dijon-Bourgogne, France.; UMR Inserm/U1093 Cognition, Action, Plasticité sensorimotrice, Université Bourgogne Franche-Comté, Dijon, France.
Barben J; Pôle Personnes Âgées, CHU Dijon-Bourgogne, France.
Asgassou S; Pôle Personnes Âgées, CHU Dijon-Bourgogne, France.
Putot A; Pôle Personnes Âgées, CHU Dijon-Bourgogne, France.
Konaté A; Unité de DIAGnostic et d'Orientation RApide (DIAGORA), Département de Médecine interne, CHU, Montpellier, France.
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Transliterated Title :
Déficit en fer chez l’adulte : comprendre quel bilan biologique réaliser.
Źródło :
Revue medicale de Liege [Rev Med Liege] 2020 Dec; Vol. 75 (12), pp. 791-796.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Anemia, Iron-Deficiency*/diagnosis
Biological Products*
Adult ; Biomarkers ; Humans ; Iron
Czasopismo naukowe
Tytuł :
[Hematological Analysis and Diagnosis of Two Rare Abnormal Hemoglobin].
Autorzy :
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.
Guo H; 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.
Yuan TL; 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.
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.
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,E-mail: .
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Źródło :
Zhongguo shi yan xue ye xue za zhi [Zhongguo Shi Yan Xue Ye Xue Za Zhi] 2020 Dec; Vol. 28 (6), pp. 2028-2032.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Hemoglobins, Abnormal*/genetics
alpha-Thalassemia*/diagnosis
alpha-Thalassemia*/genetics
beta-Thalassemia*
Heterozygote ; Humans
Czasopismo naukowe
Tytuł :
Leaf chlorosis in Arabidopsis thaliana hybrids is associated with transgenerational decline and imbalanced ribosome number.
Autorzy :
Vaid N; Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
Ishihara H; Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
Plötner B; Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
Sageman-Furnas K; Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
Wiszniewski A; Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
Laitinen RAE; Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476, Potsdam-Golm, Germany.
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Źródło :
The New phytologist [New Phytol] 2020 Nov; Vol. 228 (3), pp. 989-1000. Date of Electronic Publication: 2020 Jul 15.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Anemia, Hypochromic*
Arabidopsis*/genetics
Epigenesis, Genetic ; Gene Expression Regulation, Plant ; Plant Leaves/genetics ; Ribosomes/genetics
Czasopismo naukowe
Tytuł :
Application of HbA 2 levels and red cell indices-based new model in the differentiation of thalassemia traits from iron deficiency in hypochromic microcytic anemia Cases.
Autorzy :
Zhou Y; The First People's Hospital of Changde, Changde, China.
Zhang J; The First People's Hospital of Changde, Changde, China.
Wang C; The First People's Hospital of Changde, Changde, China.
Zhou L; The First People's Hospital of Changde, Changde, China.
Zhou L; The First People's Hospital of Changde, Changde, China.
Ou D; Changde Hospital of University of South China, Changde, China.
Peng D; The First People's Hospital of Changde, Changde, China.; Changde Hospital of University of South China, Changde, China.
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Źródło :
International journal of laboratory hematology [Int J Lab Hematol] 2020 Oct; Vol. 42 (5), pp. 526-532. Date of Electronic Publication: 2020 Jun 21.
Typ publikacji :
Journal Article
MeSH Terms :
Hemoglobin A2*/genetics
Anemia, Hypochromic/*blood
Anemia, Hypochromic/*diagnosis
Anemia, Iron-Deficiency/*blood
Anemia, Iron-Deficiency/*diagnosis
Thalassemia/*blood
Thalassemia/*diagnosis
Adolescent ; Adult ; Alleles ; Anemia, Hypochromic/etiology ; Diagnosis, Differential ; Erythrocyte Indices ; Female ; Gene Frequency ; Genotype ; Humans ; Male ; Mutation ; ROC Curve ; Sensitivity and Specificity ; Young Adult
SCR Disease Name :
Anemia, hypochromic microcytic
Czasopismo naukowe
Tytuł :
Prochlorococcus Cells Rely on Microbial Interactions Rather than on Chlorotic Resting Stages To Survive Long-Term Nutrient Starvation.
Autorzy :
Roth-Rosenberg D; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Aharonovich D; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Luzzatto-Knaan T; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Vogts A; Department of Biological Oceanography, Leibniz-Institute for Baltic Sea Research, Warnemuende, Germany.
Zoccarato L; Department of Experimental Limnology, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Stechlin, Germany.
Eigemann F; Department of Biological Oceanography, Leibniz-Institute for Baltic Sea Research, Warnemuende, Germany.
Nago N; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel.
Grossart HP; Department of Experimental Limnology, Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Stechlin, Germany.; Potsdam University, Institute of Biochemistry and Biology, Potsdam, Germany.
Voss M; Department of Biological Oceanography, Leibniz-Institute for Baltic Sea Research, Warnemuende, Germany.
Sher D; Department of Marine Biology, Leon H. Charney School of Marine Sciences, University of Haifa, Haifa, Israel .
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Źródło :
MBio [mBio] 2020 Aug 11; Vol. 11 (4). Date of Electronic Publication: 2020 Aug 11.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Anemia, Hypochromic*
Microbial Interactions*
Nutrients*
Prochlorococcus/*metabolism
Alteromonas/metabolism ; Axenic Culture ; Genome, Bacterial ; Heterotrophic Processes ; Microbial Viability ; Phylogeny ; Prochlorococcus/growth & development ; Seawater/microbiology
SCR Organism :
Alteromonas macleodii
Czasopismo naukowe
Tytuł :
Bone pain, splenomegaly and microcytic anemia in a young woman.
Autorzy :
Mahtat EM; Clinical Hematology Department, Mohammed V Military Teaching Hospital, Rabat, Morocco; Université Mohamed V, Rabat, Morocco. Electronic address: .
Hasnaoui N; Clinical Hematology Department, Mohammed V Military Teaching Hospital, Rabat, Morocco.
Zahid H; Université Mohamed V, Rabat, Morocco; Hematology Laboratory, Mohammed V Military Teaching Hospital, Rabat, Morocco.
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Źródło :
European journal of internal medicine [Eur J Intern Med] 2020 Aug; Vol. 78, pp. 129-130. Date of Electronic Publication: 2020 Jul 01.
Typ publikacji :
Journal Article
MeSH Terms :
Anemia, Hypochromic*
Gaucher Disease*
Female ; Humans ; Pain ; Splenomegaly/diagnostic imaging ; Splenomegaly/etiology
Czasopismo naukowe
Tytuł :
Parenteral iron therapy and phosphorus homeostasis: A review.
Autorzy :
Kalantar-Zadeh K; Division of Nephrology and Hypertension and Kidney Transplantation, University of California Irvine, Orange, California, USA.
Ganz T; David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, California, USA.
Trumbo H; St. Mary Medical Center, Langhorne, Pennsylvania, USA.
Seid MH; Department of Obstetrics and Gynecology, University of Southern California Verdugo Hills Hospital, Glendale, California, USA.
Goodnough LT; Department of Pathology and Medicine, Stanford University, Stanford, California, USA.
Levine MA; Center for Bone Health and Division of Endocrinology and Diabetes, Children's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
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Źródło :
American journal of hematology [Am J Hematol] 2021 May 01; Vol. 96 (5), pp. 606-616. Date of Electronic Publication: 2021 Feb 09.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Review
MeSH Terms :
Hypophosphatemia/*etiology
Iron/*adverse effects
Phosphorus/*metabolism
Anemia, Hypochromic/drug therapy ; Calcitriol/physiology ; Ferric Compounds/administration & dosage ; Ferric Compounds/adverse effects ; Ferric Compounds/pharmacology ; Fibroblast Growth Factors/biosynthesis ; Fibroblast Growth Factors/genetics ; Fibroblast Growth Factors/physiology ; Homeostasis/drug effects ; Homeostasis/physiology ; Humans ; Hypophosphatemia/chemically induced ; Hypophosphatemia/diagnosis ; Hypophosphatemia/therapy ; Infusions, Parenteral ; Iron/administration & dosage ; Iron/deficiency ; Kidney/metabolism ; Malabsorption Syndromes/complications ; Maltose/administration & dosage ; Maltose/adverse effects ; Maltose/analogs & derivatives ; Maltose/pharmacology ; Osteomalacia/etiology ; Parathyroid Hormone/physiology ; Phosphorus, Dietary/pharmacokinetics
Czasopismo naukowe
Tytuł :
Novel mechanism of hereditary pyropoikilocytosis phenotype due to co-inheritance of β globin and α spectrin mutations.
Autorzy :
Kim SJ; Hematology, University of Utah & Huntsman Cancer Center, Salt Lake City, Utah.
Song J; Hematology, University of Utah & Huntsman Cancer Center, Salt Lake City, Utah.
Reading NS; Department of Pathology, ARUP Laboratories, Salt Lake City, Utah.
Lautersztain J; Florida Cancer Specialists and Research Institute, Tampa, Florida.
Kutlar A; Medical College of Georgia, Augusta, Georgia.
Agarwal AM; Department of Pathology, ARUP Laboratories, Salt Lake City, Utah.
Coetzer TL; Department of Molecular Medicine and Haematology, School of Pathology, University of the Witwatersrand, Johannesburg, South Africa.
Prchal JT; Hematology, University of Utah & Huntsman Cancer Center, Salt Lake City, Utah.
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Źródło :
American journal of hematology [Am J Hematol] 2021 May 01; Vol. 96 (5), pp. E150-E154. Date of Electronic Publication: 2021 Feb 25.
Typ publikacji :
Case Reports; Letter; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Frameshift Mutation*
Point Mutation*
Elliptocytosis, Hereditary/*genetics
Spectrin/*genetics
beta-Globins/*genetics
Anemia, Hypochromic/genetics ; Cells, Cultured ; Child ; Elliptocytosis, Hereditary/complications ; Exons/genetics ; Female ; Genetic Association Studies ; Heterozygote ; Humans ; Jaundice/etiology ; Male ; Middle Aged ; Myelodysplastic Syndromes/blood ; Myelodysplastic Syndromes/complications ; Protein Conformation ; Sickle Cell Trait/genetics
SCR Disease Name :
Pyropoikilocytosis, Hereditary
Raport
Tytuł :
Lower white matter volume in beta-thalassemia associated with anemia and cognitive performance.
Autorzy :
Choi S; Neuroscience Graduate Program, University of Southern California, Los Angeles, California, USA.; Signal and Image Processing Institute, University of Southern California, Los Angeles, California, USA.; Division of Hematology, Oncology and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Los Angeles, California, USA.
Leahy RM; Neuroscience Graduate Program, University of Southern California, Los Angeles, California, USA.; Signal and Image Processing Institute, University of Southern California, Los Angeles, California, USA.
Wood JC; Division of Hematology, Oncology and Blood and Marrow Transplantation, Children's Hospital Los Angeles, Los Angeles, California, USA.; Department of Pediatrics, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
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Źródło :
American journal of hematology [Am J Hematol] 2020 Jun; Vol. 95 (6), pp. E144-E146. Date of Electronic Publication: 2020 Apr 07.
Typ publikacji :
Letter; Research Support, N.I.H., Extramural; Comment
MeSH Terms :
Anemia, Hypochromic*
Anemia, Sickle Cell*
White Matter*
beta-Thalassemia*
Cognition ; Humans
Raport
Tytuł :
The hematological effects of copper deficiency.
Autorzy :
Al-Bubseree B; West of Scotland Cancer Centre, Gartnavel General Hospital, Glasgow, UK.
Leach M; West of Scotland Cancer Centre, Gartnavel General Hospital, Glasgow, UK.
Jones R; Borders General Hospital, Melrose, UK.
Bain BJ; Centre for Haematology, St Mary's Hospital campus of Imperial College Faculty of Medicine, St Mary's Hospital, London, UK.
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Źródło :
American journal of hematology [Am J Hematol] 2020 Apr; Vol. 95 (4), pp. 446. Date of Electronic Publication: 2020 Feb 05.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Anemia, Hypochromic/*etiology
Copper/*deficiency
Enteral Nutrition/*adverse effects
Neutropenia/*etiology
Adult ; Anemia, Hypochromic/diagnosis ; Cerebral Palsy/complications ; Copper/blood ; Diagnosis, Differential ; Epilepsy/complications ; Humans ; Male ; Myelodysplastic Syndromes/diagnosis ; Pneumonia, Aspiration/etiology ; Pneumonia, Aspiration/prevention & control
Czasopismo naukowe
Tytuł :
Prevalence of 3.7 and 4.2 deletions in Sudanese patients with red cells hypochromia and microcytosis.
Autorzy :
Osman HA; Department of Biotechnology, School of Pharmacy, Ahafad University for Women, Omdurman, Sudan. .
Hamid MMA; Institute of Endemic Diseases, Medical Campus, University of Khartoum, Khartoum, Sudan.
Ahmad RB; Hematology Unit, Cancer Research Centre Institute for Medical Research Jalan Pahang, 50588, Kuala Lumpur, Malaysia.
Saleem M; Advanced Genomics SDN BHD (GenomixLAB), Kota Damansara, Malaysia.
Abdallah SA; Department of Pathology, Faculty of Medicine, Alneelain University, Khartoum, Sudan.
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Źródło :
BMC research notes [BMC Res Notes] 2020 Feb 10; Vol. 13 (1), pp. 65. Date of Electronic Publication: 2020 Feb 10.
Typ publikacji :
Journal Article
MeSH Terms :
Genetic Testing*
Anemia, Hypochromic/*genetics
Chromosomes, Human, Pair 3/*genetics
Chromosomes, Human, Pair 4/*genetics
alpha-Thalassemia/*diagnosis
alpha-Thalassemia/*genetics
Adolescent ; Adult ; Anemia, Hypochromic/epidemiology ; Child ; Female ; Humans ; Male ; Middle Aged ; Prevalence ; Sequence Deletion ; Sudan/epidemiology ; Young Adult ; alpha-Thalassemia/epidemiology
Czasopismo naukowe
Tytuł :
Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
Autorzy :
Sajadpour Z; Genetic Division, Biology Department, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Amini-Farsani Z; Young Researchers and Elites Club, Shahrekord Branch, Islamic Azad University, Shahrekord, Iran.
Motovali-Bashi M; Genetic Division, Biology Department, Faculty of Sciences, University of Isfahan, Isfahan, Iran.
Yadollahi M; Department of Operative Dentistry, School of Dentistry, Shahrekord University of Medical Sciences, Shahrekord, Iran.
Khosravi-Farsani N; Department of Biology, University of Kharazmi, Tehran, Iran.
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Źródło :
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 27-30. Date of Electronic Publication: 2020 Jan 03.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation*
Anemia, Hypochromic/*genetics
Fetal Hemoglobin/*genetics
Hemoglobins, Abnormal/*genetics
alpha-Globins/*genetics
beta-Globins/*genetics
beta-Thalassemia/*genetics
Adult ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/pathology ; Female ; Gene Expression ; Haplotypes ; Hepatomegaly/diagnosis ; Hepatomegaly/genetics ; Hepatomegaly/pathology ; Humans ; Iran ; Linkage Disequilibrium ; Male ; Phenotype ; Polymorphism, Restriction Fragment Length ; Sequence Analysis, DNA ; Splenomegaly/diagnosis ; Splenomegaly/genetics ; Splenomegaly/pathology ; alpha-Globins/deficiency ; beta-Globins/deficiency ; beta-Thalassemia/diagnosis ; beta-Thalassemia/pathology
Czasopismo naukowe
Tytuł :
α-Globin Genotypes Associated with Hb H Disease: A Report from Oman and a Review of the Literature from the Eastern Mediterranean Region.
Autorzy :
Al-Riyami AZ; Department of Hematology, Sultan Qaboos University Hospital, Muscat, Oman.
Daar S; Department of Hematology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Kindi SA; Department of Hematology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Madhani AA; Department of Medicine, Sohar Hospital, Ministry of Health, Muscat, Oman.
Wali Y; Department of Child Health, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.
Rawahi MA; Department of Hematology, Sultan Qaboos University Hospital, Muscat, Oman.
Zadjali SA; Department of Hematology, Sultan Qaboos University Hospital, Muscat, Oman.
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Źródło :
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 20-26. Date of Electronic Publication: 2020 Feb 05.
Typ publikacji :
Journal Article
MeSH Terms :
Mutation*
Anemia, Hypochromic/*genetics
Hemoglobin A2/*genetics
Hemoglobin H/*genetics
Hemoglobin, Sickle/*genetics
alpha-Globins/*genetics
alpha-Thalassemia/*genetics
Adolescent ; Adult ; Aged ; Aged, 80 and over ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/pathology ; Child ; Child, Preschool ; Erythrocyte Indices ; Female ; Gene Expression ; Genotype ; Humans ; Infant ; Male ; Mediterranean Region ; Middle Aged ; Oman ; Phenotype ; Retrospective Studies ; Sequence Analysis, DNA ; alpha-Globins/deficiency ; alpha-Thalassemia/diagnosis ; alpha-Thalassemia/pathology
Czasopismo naukowe
Tytuł :
A Novel β-Thalassemia Mutation [IVS-I-6 (T>G), HBB : c.92+6T>G] in a Chinese Family.
Autorzy :
Luo H; Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi Province, People's Republic of China.
Zou Y; Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi Province, People's Republic of China.
Liu Y; Department of Prenatal Diagnostic Center, Jiangxi Maternal and Child health Hospital, Nanchang, Jiangxi Province, People's Republic of China.
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Źródło :
Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 55-57. Date of Electronic Publication: 2020 Jan 15.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Mutation*
Anemia, Hypochromic/*genetics
Hemoglobins, Abnormal/*genetics
beta-Globins/*genetics
beta-Thalassemia/*genetics
Adult ; Alleles ; Anemia, Hypochromic/diagnosis ; Anemia, Hypochromic/ethnology ; Asian Continental Ancestry Group ; Child ; Family ; Female ; Gene Expression ; Genotype ; Hemoglobin A2/genetics ; Humans ; Middle Aged ; Pedigree ; Phenotype ; Polymerase Chain Reaction ; Sequence Analysis, DNA ; beta-Globins/deficiency ; beta-Thalassemia/diagnosis ; beta-Thalassemia/ethnology
Czasopismo naukowe

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