Splenic sequestration crisis as an index manifestation of heterozygous hemoglobinopathy in an adult [PDF]
, 2019 Eseosa Edo-Osagie +6 more
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Intervention and Prevention of Hereditary Hemolytic Disorders in Two Ethnic Communities of Sundargarh District of Orissa, India: An Experience from KAP Studies [PDF]
, 2010 Hereditary hemolytic disorders are important public health challenges in India. They cause a high degree of morbidity, mortality and fetal wastage in vulnerable communities.
Balgir, RS
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Dissecting the role of genetic modifiers of hemoglobinopathies: A futuristic approach towards precision medicine [PDF]
, 2021 Priya Hariharan +4 more
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Italian patients with hemoglobinopathies exhibit a 5‐fold increase in age‐standardized lethality due to SARS‐CoV‐2 infection [PDF]
, 2021 Filomena Longo +53 more
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The New Hemoglobinopathies [PDF]
, 1970 The clinical explorations which have resulted from studies of mutant hemoglobin have allowed definition of a variety of syndromes whose manifestations require explanation in terms of the effects of molecular distortion on physiological processes.
Cooper, Robert M.
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Case Reports in Clinical PracticeSo far, different types of SOX5 variants have been reported in patients with LAMSHF syndrome, which are mainly clustered in the HMG domain. The LAMSHF syndrome has a broad variety of clinical manifestations such as developmental delay, speech delay ...
Akbar Amirfiroozy +4 more
doaj +1 more source
Heart Involvement in Hemoglobinopathies: Two Case Reports and Brief Review of Literature
, 2022 openalex +1 more source
Electron Transfer Dissociation Mass Spectrometry of Hemoglobin on Clinical Samples [PDF]
, 2018 A mass spectrometry-based assay combining the specificity of selected reaction monitoring and the protein ion activation capabilities of electron transfer dissociation was developed and employed for the rapid identification of hemoglobin variants from ...
Clerici, Lorella +8 more
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Comparative efficacy of deferiprone, deferoxamine and combination of deferiprone and deferoxamine on serum ferritin value in Beta-Thalassemia patients [PDF]
, 2015 Background: Iron overload is a predictable and life-threatening complication in patients with thalassemia. Effective and convenient iron chelation remains one of the main targets of clinical management of thalassemia major.
Amlashi, H.M. +3 more
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