Results 101 to 110 of about 1,160,233 (174)

Hereditary disorders of ineffective erythropoiesis. [PDF]

Blood Cells Mol Dis
King RA, Khoriaty R.
europepmc   +1 more source

A 9-year-old child presenting with anemia accompanied by abnormal red blood cell morphology. [PDF]

Pract Lab Med
Qin H, He Y, Xie Z.
europepmc   +1 more source

NETosis and Neutrophil Activity Quantification in Pediatric Patients with Essential Thrombocythemia. [PDF]

Int J Mol Sci
Adamanskaya EA, Korobkin JD, Pshonkin AV, Bogdanov AV, Galkina SV, Podoplelova NA, Yushkova EV, Panteleev MA, Novichkova GA, Smetanina NS, Sveshnikova AN.   +10 more
europepmc   +1 more source

Identification of a novel truncated pathogenic variant in PUS1 gene in two siblings of consanguineous Tunisian family: intrafamilial phenotypic variability related to mtDNA copy number. [PDF]

Ann Hematol
Ammar M, Kmiha S, Maalej M, Felhi R, Kharrat M, Alila-Fersi O, Chouchen J, Maaloul I, Mkaouar-Rebai E, Kammoun T, Tlili A, Fakhfakh F.   +11 more
europepmc   +1 more source

Acquired Primary Sideroblastic Anemiaの1例

Rinsho Ketsueki, 1967
TSUKADA, Toshiyasu, SHIMIZU, Masaru, MIWA, Shiro, ASAI, Ichitaro, ITO, Umeo   +4 more
openaire   +1 more source

Luspatercept for the treatment of transfusion-dependent non-severe aplastic anemia. [PDF]

Ann Hematol
Jia X, Zheng R, Hong Y, Ge H, Shen Y, Zhou Y, Yang X, Wu D.   +7 more
europepmc   +1 more source

Longstanding Microcytosis with a Thalassaemia-Like Phenotype and Inconclusive Molecular Testing: A Case Report. [PDF]

J Blood Med
Kuriri FA.
europepmc   +1 more source

Prevalence and factors associated with anemia among people living with HIV taking dolutegravir-based antiretroviral therapy at debre markos compressive specialized hospital, debre markos, northwest Ethiopia, 2024: A cross-sectional study. [PDF]

Ther Adv Hematol
Jemal M, Yesuf HA, Asfaw MS, Abebe G, Alem A, Geto Z, Kassaw AB, Adugna A, Abebaw D, Malik T, Abera MB, Seid MA.   +11 more
europepmc   +1 more source

X-Linked Sideroblastic Anaemia Caused by Intronic <i>ALAS2</i> Variant Resulting in Highly Variable Expressive Phenotype in Male Siblings, a Case Report. [PDF]

EJHaem
O'Connor J, Mannion N, McKenna C, Sweeney K, Niblock A.   +4 more
europepmc   +1 more source