PENGARUH KADAR FERITIN SERUM TERHADAP PERUBAHAN FRAKSI LIPID PADA PASIEN THALASEMIA DENGAN TRANSFUSI BERULANG DI RSUD DR. ZAINOEL ABIDIN BANDA ACEH [PDF]
, 2018 ABSTRAKThalasemia merupakan salah satu penyakit hemoglobinopati yang dapat mengancam jiwa karena terjadinya penurunan atau kegagalan memproduksi sel darah merah.
SHINTA ARMISDA PUTRI
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Splenic sequestration crisis as an index manifestation of heterozygous hemoglobinopathy in an adult [PDF]
, 2019 Eseosa Edo-Osagie +6 more
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Journal of Clinical Laboratory Analysis, Volume 39, Issue 23, December 2025.
Rachana Mehta, Ranjana Sah
wiley +1 more source
Health Care Challenges of Hereditary Common Hematological Disorders in Odisha, India [PDF]
, 2012 Medical Genetics over the past few decades have emerged as an important and powerful medical specialty with increasing appreciation of its role and function in the biomedical sciences.
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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Acta Médica Costarricense, 2010 La exposición a ciertos medicamentos puede provocar anemia hemolítica con presencia de cuerpos de Heinz en sangre periférica. Esta anemia puede presentarse por sobredosis de medicamentos, tanto en individuos sanos como en personas con deficiencias ...
Walter Cartín +7 more
doaj
Sickle cell disease affects more than 100,000 individuals in the United States, among whom disease severity varies considerably. One factor that influences disease severity is the sickle cell disease genotype.
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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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Simultaneous occurrence of advanced neuroblastoma and acute lymphoblastic leukemia: a case report [PDF]
, 2011 Neuroblastoma is the most common extracranial solid tumor in children. The cooccurrence of neuroblastoma and acute lymphoblastic leukemia is rare. We report a rare case of advanced-stage neuroblastoma in a 3.5-year-old girl that was accompanied by ...
Fekri, Kiavash. +4 more
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Bases moleculares de hemoglobinopatias na Argentina [PDF]
, 2017 Durante el desarrollo de un individuo se expresan distintas cadenas de globina de tipo α y no-α, que se combinan en tetrámeros para formar hemoglobina. Los genes que las codifican se organizan en familias.
Scheps, Karen, Varela, Viviana
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