Results 131 to 140 of about 312,696 (257)

Hereditary hypochromic microcytic anemia associated with loss‐of‐function DMT1 gene mutations and absence of liver iron overload

open access: yesAmerican journal of hematology/oncology, 2018
M. Casale   +10 more
semanticscholar   +1 more source

Alpha-thalassemia due to novel deletions and complex rearrangements in the subtelomeric region of chromosome 16p [PDF]

open access: yes, 2017
2º Dia do Jovem Investigador do Instituto Nacional de Saúde Doutor Ricardo Jorge, INSA, 8 maio 2017Introduction: Inherited deletions removing the α-globin genes and/or their upstream regulatory elements (MCSs) give rise to alpha-thalassemia, one of the ...
Batalha Reis, Ana   +18 more
core   +1 more source

Clinical and radiological recurrence after childhood arterial ischemic stroke [PDF]

open access: yes, 2006
Background: Data on rates and risk factors for clinical and radiological recurrence of childhood arterial ischemic stroke (AIS) might inform secondary prevention strategies.
Ganesan, V.   +3 more
core  

Terapêutica com doses profiláticas de sulfato ferroso como medida de intervenção no combate à carência de ferro em crianças atendidas em unidades básicas de saúde

open access: yesRevista de Saúde Pública
Objetivou-se testar a terapêutica com doses profiláticas de sulfato ferroso no combate à anemia carencial ferropriva, em 620 crianças de 4 a 36 meses de idade, atendidas em duas unidades de saúde do Município de São Paulo, Brasil.
Marco A. A. Torres   +3 more
doaj  

A Study of Anemia in Hospitalized Infants at A Tertiary Care Hospital

open access: yesNational Journal of Community Medicine, 2015
Background: Anemia is a significant public health problem that occurs worldwide with higher prevalence noted in children less than 3 years. Objective of the study was to determine the occur- rence, pattern and severity of anemia among hospitalized ...
KS Sahana   +3 more
doaj  

Etude D'une Famille Atteinte D'alpha Thalassemie en Iran

open access: yesActa Medica Iranica, 1965
This a case report of an Iranien jewish young women, who had hypochromic anemia inspitc of incrcscd medullary Iron..
Esther Aghai
doaj  

Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin

open access: yesEuropean Journal of Human Genetics, 2015
Ji-wei Huang   +8 more
semanticscholar   +1 more source

Systemic inflammation impairs recovery from hookworm-associated anemia in a wild marine mammal host. [PDF]

open access: yesFront Immunol
Zaitseva V   +11 more
europepmc   +1 more source

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