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Tytuł:
Analysis of Mean Corpuscular Volume and Red Cell Distribution Width in Patients with Aplastic Anemia.
Autorzy:
Liu L; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Fu Q; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Zhang D; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Chen D; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Wang F; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Guo R; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Xie X; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Jiang Z; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Yu J; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Li Y; Department of Hematology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
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Źródło:
Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 31-35. Date of Electronic Publication: 2023 May 10.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Aplastic*/diagnosis
Anemia, Macrocytic*
Humans ; Erythrocyte Indices ; Bone Marrow ; Hemoglobins
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Case Fatality Rate and Severity of COVID-19 among Patients with Sickle Cell Disease: A Systematic Review and Meta-Analysis.
Autorzy:
Silva Borborema T; Faculdade Dinâmica do Vale do Piranga, Ponte Nova, Minas Gerais, Brazil.; Hospital Infantil João Paulo II, Belo Horizonte, MG, Brazil.
Moreira Brito JC; Fundação Ezequiel Dias (FUNED), Belo Horizonte, MG, Brazil.
Lima Batista EM; Santa Casa-Belo Horizonte: Instituto de Ensino e Pesquisa, Belo Horizonte, Minas Gerais, Brazil.
Siqueira Batista R; Faculdade Dinâmica do Vale do Piranga, Ponte Nova, Minas Gerais, Brazil.; Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil.
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Źródło:
Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 85-96. Date of Electronic Publication: 2023 Jun 16.
Typ publikacji:
Meta-Analysis; Systematic Review; Journal Article; Review
MeSH Terms:
COVID-19*
Influenza A Virus, H1N1 Subtype*
Anemia, Sickle Cell*/complications
Humans ; Adult ; SARS-CoV-2 ; Pandemics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Novel Insights into the Pathophysiology and Treatment of Sickle Cell Disease.
Autorzy:
Araújo ADS; Department of Hematology, Fundação de Hematologia e Hemoterapia de Pernambucol, Brazi.
Silva Pinto AC; Department of Medical Imaging, Hematology and Oncology, Hemocentro de Ribeirão Preto, Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto - USP, Brazil.
Lobo CLC; Department of Clinical Research, Instituto Estadual de Hematologia Arthur de Siqueira Cavalcanti (HEMORIO), Brazil.
Figueiredo MS; Department of Clinical and Experimental Oncology, Escola Paulista de Medicina da Universidade Federal de São Paulo (UNIFESP), Brazil.
Menosi Gualandro SF; Department of Hematology, Hospital das Clínicas da Faculdade de Medicina da USP, Brazi.
Olalla Saad ST; Department of Internal Medicine, Faculdade de Ciências Médicas - UNICAMP, Brazil.
Cancado RD; Department of Hematology and Oncology, Faculdade de Ciências Médicas da Santa Casa de São Paulo, Brazil.
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Źródło:
Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 71-79. Date of Electronic Publication: 2023 Jun 12.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Hemoglobin, Sickle*
Anemia, Sickle Cell*/drug therapy
Humans ; Erythrocytes ; Hemoglobins ; Erythrocytes, Abnormal
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Hb Ryazan: An Elongated C-Terminal β-Chain Due to a New Frameshift Mutation, HBB: c.396delG p.Val133Trpfs*25.
Autorzy:
Demidova E; Laboratory of Genetic Engineering, National Medical Research Center for Hematology, Moscow, Russia.
Salomashkina V; Laboratory of Genetic Engineering, National Medical Research Center for Hematology, Moscow, Russia.
Selivanova D; Laboratory of Genetic Engineering, National Medical Research Center for Hematology, Moscow, Russia.
Litvin E; Applied and Fundamental Pharmacology Laboratory, Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Karamyan N; Clinical Diagnostics Laboratory, Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Mann S; Molecular Biology Laboratory, Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Dvirnyk V; Clinical Diagnostics Laboratory, National Medical Research Center for Hematology, Moscow, Russia.
Maryina S; Clinical Diagnostics Laboratory, National Medical Research Center for Hematology, Moscow, Russia.
Petrova N; Clinical Diagnostics Laboratory, National Medical Research Center for Hematology, Moscow, Russia.
Gorgidze L; Resuscitation and Intensive Care Department, National Medical Research Center for Hematology, Moscow, Russia.
Peredel'skaya A; Department of Orphan Diseases, National Medical Research Center for Hematology, Moscow, Russia.
Tsvetaeva N; Department of Orphan Diseases, National Medical Research Center for Hematology, Moscow, Russia.
Smetanina N; Department of Pediatric Hematology and Oncology, Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Moscow, Russia.
Surin V; Laboratory of Genetic Engineering, National Medical Research Center for Hematology, Moscow, Russia.
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Źródło:
Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 97-101. Date of Electronic Publication: 2023 May 17.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Anemia, Hemolytic*/genetics
Hemoglobins, Abnormal*/genetics
Hemoglobins, Abnormal*/chemistry
Female ; Humans ; beta-Globins/genetics ; beta-Globins/chemistry ; Codon, Terminator ; Exons ; Frameshift Mutation ; Mutation
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Effect of α Thalassemia on the Severity of Plasmodium falciparum Malaria in Different Sickle Cell Genotypes in Indian Adults: A Hospital-Based Study.
Autorzy:
Purohit P; Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Sciences and Research (VIMSAR), Burla, Sambalpur, India.; Multidisciplinary Research Unit, M.K.C.G. Medical College, Berhampur, India.
Mohanty PK; Department of Medicine, Veer Surendra Sai Institute of Medical Sciences and Research (VIMSAR), Burla, Sambalpur, India.
Panigrahi J; Department of Biotechnology, Berhampur University, Berhampur, Ganjam, India.
Das K; Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Sciences and Research (VIMSAR), Burla, Sambalpur, India.
Patel S; Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Sciences and Research (VIMSAR), Burla, Sambalpur, India.
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Źródło:
Hemoglobin [Hemoglobin] 2023 Jan; Vol. 47 (1), pp. 11-18. Date of Electronic Publication: 2023 Apr 26.
Typ publikacji:
Journal Article
MeSH Terms:
Malaria, Falciparum*/epidemiology
Malaria*/epidemiology
Malaria*/genetics
Anemia, Sickle Cell*/epidemiology
Anemia, Sickle Cell*/genetics
alpha-Thalassemia*/epidemiology
alpha-Thalassemia*/genetics
Sickle Cell Trait*/genetics
Humans ; Adult ; Hemoglobins/genetics ; Hemoglobin, Sickle/genetics ; Genotype ; Hospitals ; Plasmodium falciparum/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Severe Hb H Disease Caused by Hb Zürich-Albisrieden ( HBA1 : c.178G>C): Another Case Report.
Autorzy:
Wu SM; Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong Province, People's Republic of China.
Huang SR; Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong Province, People's Republic of China.
Li C; Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong Province, People's Republic of China.
Chen GL; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China.
Li DZ; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China.
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Źródło:
Hemoglobin [Hemoglobin] 2022 Nov; Vol. 46 (6), pp. 341-343. Date of Electronic Publication: 2023 Feb 23.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
alpha-Thalassemia*/genetics
Hemoglobins, Abnormal*/genetics
Anemia*
Humans ; Glycated Hemoglobin ; Mutation ; alpha-Globins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Anemia in Sri Lanka: A Literature Review.
Autorzy:
Amarasingha AADS; Department of Medical Laboratory Science, Faculty of Allied Health Sciences, University of Ruhuna, Galle, Sri Lanka.
Silva HJRL; Department of Biochemistry and Clinical Chemistry, Faculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.
Perera PS; Department of Biochemistry and Clinical Chemistry, Faculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.
Premawardhena AP; Department of Medicine, Faculty of Medicine, University of Kelaniya, Kelaniya, Sri Lanka.
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Źródło:
Hemoglobin [Hemoglobin] 2022 Jul; Vol. 46 (4), pp. 214-224. Date of Electronic Publication: 2022 Aug 24.
Typ publikacji:
Journal Article; Review
MeSH Terms:
Anemia*/epidemiology
Anemia*/etiology
Pregnancy ; Child ; Humans ; Female ; Aged ; Sri Lanka/epidemiology ; Prevalence ; Surveys and Questionnaires
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease.
Autorzy:
Warang PP; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Shinde NS; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Umare VD; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Deshmukh PV; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Ghosh K; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Madkaikar MR; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Colah RB; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
Mukherjee MB; Department of Haematogenetics, Indian Council of Medical Research, National Institute of Immunohaematology, Mumbai, Maharashtra, India.
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Źródło:
Hemoglobin [Hemoglobin] 2022 Jul; Vol. 46 (4), pp. 260-264. Date of Electronic Publication: 2022 Sep 08.
Typ publikacji:
Journal Article
MeSH Terms:
Carica*/chemistry
Carica*/metabolism
Anemia, Sickle Cell*/drug therapy
Humans ; Quality of Life ; Fermentation ; Oxidative Stress ; Antioxidants/pharmacology ; Antioxidants/therapeutic use
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Bringing Sickle Cell Disease Care Closer to Home: Feasibility and Efficacy of a Quality Improvement Initiative at a Community Hospital.
Autorzy:
Binding A; Department of Medicine, William Osler Health System, Brampton, ON, Canada.; University Health Network, University of Toronto, Toronto, ON, Canada.
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Źródło:
Hemoglobin [Hemoglobin] 2022 Mar; Vol. 46 (2), pp. 91-94. Date of Electronic Publication: 2022 May 13.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/epidemiology
Anemia, Sickle Cell*/therapy
Hydroxyurea*/therapeutic use
Adult ; Antisickling Agents ; Child ; Feasibility Studies ; Hospitals, Community ; Humans ; Quality Improvement
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Iron Chelators, Such as Deferasirox, When Combined With Hydroxyurea, Provide an Additional Benefit of Iron Chelation in Patients Receiving Chronic Transfusion Therapy.
Autorzy:
Manganas K; Thalassaemia and Sickle Cell Department, Hippokration General Hospital, Athens, Greece.
Delicou S; Thalassaemia and Sickle Cell Department, Hippokration General Hospital, Athens, Greece.
Xydaki A; Thalassaemia and Sickle Cell Department, Hippokration General Hospital, Athens, Greece.
Koskinas J; Department of Internal Medicine, Hippokration General Hospital, National and Kapodistrian University of Athens Medical School, Athens, Greece.
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Źródło:
Hemoglobin [Hemoglobin] 2022 Mar; Vol. 46 (2), pp. 114-117. Date of Electronic Publication: 2022 Sep 07.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/complications
Anemia, Sickle Cell*/therapy
Iron Chelating Agents*/therapeutic use
Iron Overload*/drug therapy
Iron Overload*/etiology
Alanine Transaminase/therapeutic use ; Aspartate Aminotransferases/therapeutic use ; Chelation Therapy ; Creatinine/therapeutic use ; Deferasirox/therapeutic use ; Ferritins ; Humans ; Hydroxyurea/therapeutic use ; Iron ; Lactate Dehydrogenases
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Haptoglobin Genotypes Associated with Vaso-Occlusive Crisis in Sickle Cell Anemia Patients of Eastern India.
Autorzy:
Meher S; Odisha Sickle Cell Project (NHM), Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.; Department of Bioscience and Biotechnology, Fakir Mohan University, Balasore, Odisha, India.
Mohanty PK; Odisha Sickle Cell Project (NHM), Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.; Department of Medicine, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Patel S; Odisha Sickle Cell Project (NHM), Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Das K; Odisha Sickle Cell Project (NHM), Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Sahoo S; Odisha Sickle Cell Project (NHM), Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Dehury S; Odisha Sickle Cell Project (NHM), Sickle Cell Clinic and Molecular Biology Laboratory, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Mohapatra MK; Department of Medicine, Veer Surendra Sai Institute of Medical Science & Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Jit BP; School of Life Sciences, AIPH University, Bhubaneswar, Odisha, India.
Das P; School of Life Sciences, AIPH University, Bhubaneswar, Odisha, India.
Dash BP; Department of Bioscience and Biotechnology, Fakir Mohan University, Balasore, Odisha, India.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Nov; Vol. 45 (6), pp. 358-364. Date of Electronic Publication: 2021 Jan 03.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/complications
Anemia, Sickle Cell*/genetics
Haptoglobins*/genetics
Bilirubin ; Chromosomal Proteins, Non-Histone/genetics ; Genotype ; Hemoglobins/genetics ; Hemolysis ; Humans ; India ; L-Lactate Dehydrogenase
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Hb S ( HBB : c.20A>T) Characteristics by High Performance Liquid Chromatography in Patients with Sickle Cell Disease Receiving the Novel Agent Voxelotor.
Autorzy:
Tsitsikas DA; Haemoglobinopathy Service, Department of Haematology, Homerton University Hospital, National Health Service Foundation Trust, London, UK.
Kamal M; Haemoglobinopathy Service, Department of Haematology, Homerton University Hospital, National Health Service Foundation Trust, London, UK.
Braimoh A; Haemoglobinopathy Service, Department of Haematology, Homerton University Hospital, National Health Service Foundation Trust, London, UK.
Benson S; Haemoglobinopathy Service, Department of Haematology, Homerton University Hospital, National Health Service Foundation Trust, London, UK.
Abukar J; Haemoglobinopathy Service, Department of Haematology, Homerton University Hospital, National Health Service Foundation Trust, London, UK.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Nov; Vol. 45 (6), pp. 355-357. Date of Electronic Publication: 2021 Feb 24.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/diagnosis
Anemia, Sickle Cell*/drug therapy
Hemoglobin, Sickle*/analysis
Benzaldehydes/adverse effects ; Chromatography, High Pressure Liquid ; Humans ; Pyrazines ; Pyrazoles
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Incidence Rate of COVID-19 Infection in Hemoglobinopathies: A Systematic Review and Meta-analysis.
Autorzy:
Haghpanah S; Hematology Research Center, Shiraz, University of Medical Sciences, Shiraz, Iran.
Hosseini-Bensenjan M; Hematology Research Center, Shiraz, University of Medical Sciences, Shiraz, Iran.
Sayadi M; Cardiovascular Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Karimi M; Hematology Research Center, Shiraz, University of Medical Sciences, Shiraz, Iran.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Nov; Vol. 45 (6), pp. 371-379. Date of Electronic Publication: 2021 May 24.
Typ publikacji:
Journal Article; Meta-Analysis; Review; Systematic Review
MeSH Terms:
Anemia, Sickle Cell*/complications
Anemia, Sickle Cell*/epidemiology
COVID-19*/epidemiology
Hemoglobinopathies*/epidemiology
beta-Thalassemia*/epidemiology
Humans ; Incidence
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Hb Mizuho ( HBB : c.206T>C): Pitfalls of Screening Tests in an Unstable Hemoglobin Variant Diagnosed after Targeted Next-Generation Sequencing.
Autorzy:
Yadav DD; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Jamwal M; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Singh N; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Sharma R; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Das R; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Trehan A; Department of Pediatric Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Bansal D; Department of Pediatric Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Chhabra S; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Sharma P; Department of Hematology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Sep; Vol. 45 (5), pp. 338-340. Date of Electronic Publication: 2022 Feb 10.
Typ publikacji:
Case Reports; Journal Article
MeSH Terms:
Anemia, Hemolytic*/diagnosis
Anemia, Hemolytic*/genetics
Hemoglobins, Abnormal*/genetics
Asian People ; Child, Preschool ; High-Throughput Nucleotide Sequencing ; Humans ; Male
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Profiling of 35 Cases of Hb S/Hb E ( HBB : c.20A>T/ HBB : c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India.
Autorzy:
Dehury S; Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India.; School of Life Sciences, Sambalpur University, Jyoti Vihar, Burla, Sambalpur, Odisha, India.
Mohanty PK; Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India.; Department of Medicine, VIMSAR, Burla, Sambalpur, Odisha, India.
Patel S; Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Meher S; Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Das K; Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Purohit P; Multi-Disciplinary Research Unit, Maharaja Krishna Chandra Gajapati (MKCG) Medical College, Berhampur, Odisha, India.
Sahoo S; Sickle Cell Institute, Sickle Cell Project (National Health Mission Odisha), Veer Surendra Sai Institute of Medical Science and Research (VIMSAR), Burla, Sambalpur, Odisha, India.
Ratha J; School of Life Sciences, Sambalpur University, Jyoti Vihar, Burla, Sambalpur, Odisha, India.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Nov; Vol. 45 (6), pp. 380-386. Date of Electronic Publication: 2022 Mar 04.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/genetics
alpha-Thalassemia*/genetics
beta-Thalassemia*/genetics
Haplotypes ; Humans ; Multigene Family ; beta-Globins/genetics
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Acute Chest Syndrome in Sickle Cell Disease: Clinical Presentation and Outcomes. The Experience of a Single Thalassemia and Sickle Cell Unit in a University Hospital.
Autorzy:
Delicou S; Thalassemia and Sickle Cell Unit, Hippocration General Hospital, Athens, Greece.
Aggeli K; First Department of Cardiology, National and Kapodistrian University of Athens School of Medicine, Athens, Greece.; First Department of Cardiology, Hippocration General Hospital Athens, University of Athens, Athens, Greece.
Magganas K; Thalassemia and Sickle Cell Unit, Hippocration General Hospital, Athens, Greece.
Patsourakos D; Thalassemia and Sickle Cell Unit, Hippocration General Hospital, Athens, Greece.
Xydaki A; Thalassemia and Sickle Cell Unit, Hippocration General Hospital, Athens, Greece.
Koskinas J; Second Department of Internal Medicine, National and Kapodistrian University of Athens School of Medicine, Athens, Greece.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Sep; Vol. 45 (5), pp. 303-308. Date of Electronic Publication: 2021 Nov 24.
Typ publikacji:
Journal Article
MeSH Terms:
Acute Chest Syndrome*/diagnosis
Acute Chest Syndrome*/etiology
Acute Chest Syndrome*/therapy
Anemia, Sickle Cell*/complications
Anemia, Sickle Cell*/therapy
Pulmonary Embolism*
Thalassemia*/complications
Acute Disease ; Adult ; Hospitals ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy.
Autorzy:
Idris IM; Department of Hematology and Blood Transfusion, Aminu Kano Teaching Hospital, Kano, Nigeria.
Yusuf AA; Department of Hematology and Blood Transfusion, Aminu Kano Teaching Hospital, Kano, Nigeria.; College of Health Sciences, Bayero University Kano, Kano, Nigeria.
Gwarzo DH; Department of Hematology and Blood Transfusion, Aminu Kano Teaching Hospital, Kano, Nigeria.; College of Health Sciences, Bayero University Kano, Kano, Nigeria.
Kurawa MS; College of Health Sciences, Bayero University Kano, Kano, Nigeria.; Department of Ophthalmology, Aminu Kano Teaching Hospital, Kano, Nigeria.
Shuaib A; College of Health Sciences, Bayero University Kano, Kano, Nigeria.; Department of Ophthalmology, Aminu Kano Teaching Hospital, Kano, Nigeria.
Galadanci AA; Department of Hematology and Blood Transfusion, Aminu Kano Teaching Hospital, Kano, Nigeria.; College of Health Sciences, Bayero University Kano, Kano, Nigeria.
Ibrahim H; Department of Hematology, Murtala Mohammed Specialist Hospital, Kano, Nigeria.
Borodo AM; Department of Hematology, Murtala Mohammed Specialist Hospital, Kano, Nigeria.
Jobbi YD; Department of Hematology and Blood Transfusion, Aminu Kano Teaching Hospital, Kano, Nigeria.
Danagundi MB; Department of Ophthalmology, Aminu Kano Teaching Hospital, Kano, Nigeria.
Borodo SB; Department of Ophthalmology, Aminu Kano Teaching Hospital, Kano, Nigeria.
Mohammed IY; College of Health Sciences, Bayero University Kano, Kano, Nigeria.; Department of Chemical Pathology, Aminu Kano Teaching Hospital, Kano, Nigeria.
Galadanci NA; Department of Epidemiology, University of Alabama at Birmingham, School of Public Health, Birmingham, AL, USA.
Kuliya-Gwarzo A; Department of Hematology and Blood Transfusion, Aminu Kano Teaching Hospital, Kano, Nigeria.; College of Health Sciences, Bayero University Kano, Kano, Nigeria.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Jul; Vol. 45 (4), pp. 228-233. Date of Electronic Publication: 2021 Aug 06.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/complications
Anemia, Sickle Cell*/diagnosis
Anemia, Sickle Cell*/genetics
Retinal Diseases*/diagnosis
Retinal Diseases*/epidemiology
Retinal Diseases*/etiology
Adolescent ; Adult ; Blood Pressure ; Cross-Sectional Studies ; Humans ; Vision Disorders/complications ; Young Adult
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Prolonged QTc Interval in Nigerian Children with Sickle Cell Anemia.
Autorzy:
Anah MU; Department of Paediatrics, University of Calabar Teaching Hospital, Calabar, Nigeria.
Nlemadim AC; Department of Paediatrics, University of Calabar Teaching Hospital, Calabar, Nigeria.
Uzomba CI; Department of Paediatrics, University of Calabar Teaching Hospital, Calabar, Nigeria.
Ineji EO; Department of Paediatrics, University of Calabar Teaching Hospital, Calabar, Nigeria.
Odey FA; Department of Paediatrics, University of Calabar Teaching Hospital, Calabar, Nigeria.
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Źródło:
Hemoglobin [Hemoglobin] 2021 May; Vol. 45 (3), pp. 191-196. Date of Electronic Publication: 2021 Jun 10.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/complications
Long QT Syndrome/*etiology
Child ; Electrocardiography ; Female ; Humans ; Male ; Nigeria ; Prospective Studies ; Risk Factors
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Total Annual Economic Burden of Patients with Sickle Cell Disease in Steady State in Greece.
Autorzy:
Tsolakidis V; Faculty of Health Sciences, Department of Pharmacology, Medical School, Aristotle University of Medical Sciences Thessaloniki, Thessaloniki, Greece.
Vlachaki E; Adult Thalassemia Unit, Hippokration Hospital, Thessaloniki, Greece.
Papaioannou M; First Department of Internal Medicine, Aristotle University of Thessaloniki, AHEPA Hospital, Thessaloniki, Greece.
Pantelidou D; Adult Thalassemia Unit, AHEPA Hospital, Thessaloniki, Greece.
Diamantidis M; Thalassemia and Sickle Cell Disease Unit, General Hospital of Larissa, Larissa, Greece.
Eleftheriou P; Department of Haematology, University College London, London, UK.
Kouvelas D; Faculty of Health Sciences, Department of Pharmacology, Medical School, Aristotle University of Medical Sciences Thessaloniki, Thessaloniki, Greece.
Pourzitaki C; Faculty of Health Sciences, Department of Pharmacology, Medical School, Aristotle University of Medical Sciences Thessaloniki, Thessaloniki, Greece.
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Źródło:
Hemoglobin [Hemoglobin] 2021 May; Vol. 45 (3), pp. 143-149. Date of Electronic Publication: 2021 Aug 02.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/economics
Anemia, Sickle Cell*/epidemiology
Financial Stress*
Drug Costs ; Greece/epidemiology ; Hospitalization ; Humans
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Tytuł:
Clinical Features and Outcome of Sickle Cell Disease in a Tertiary Center in Northern Lebanon: A Retrospective Cohort Study in a Local, Hospital-Associated Registry.
Autorzy:
Inati A; School of Medicine, Lebanese American University, Byblos, Lebanon.; Department of Pediatrics, Nini Hospital, Tripoli, Lebanon.
Al Alam C; Department of Pediatrics, Nini Hospital, Tripoli, Lebanon.
El Ojaimi C; Department of Pediatrics, Nini Hospital, Tripoli, Lebanon.
Hamad T; Department of Pediatrics, Nini Hospital, Tripoli, Lebanon.
Kanakamedala H; Genesis Research, Hoboken, NJ, USA.
Pilipovic V; Novartis Pharma AG, Basel, Switzerland.
Sabah R; Novartis Pharma Services Inc., Beirut, Lebanon.
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Źródło:
Hemoglobin [Hemoglobin] 2021 Mar; Vol. 45 (2), pp. 80-86. Date of Electronic Publication: 2021 May 13.
Typ publikacji:
Journal Article
MeSH Terms:
Anemia, Sickle Cell*/complications
Anemia, Sickle Cell*/epidemiology
Anemia, Sickle Cell*/therapy
Volatile Organic Compounds*
Cohort Studies ; Hospitals ; Humans ; Hydroxyurea ; Lebanon/epidemiology ; Pain ; Registries ; Retrospective Studies
Czasopismo naukowe
Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
Wyświetlanie 1-20 z 1525

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