Results 21 to 30 of about 1,301 (49)

Bone marrow mesenchymal stem cells from patients with aplastic anemia maintain functional and immune properties and do not contribute to the pathogenesis of the disease

open access: yesHaematologica, 2014
Aplastic anemia is a life-threatening bone marrow failure disorder characterized by peripheral pancytopenia and marrow hypoplasia. The majority of cases of aplastic anemia remain idiopathic, although hematopoietic stem cell deficiency and impaired immune
Clara Bueno   +13 more
doaj   +1 more source

Clinical utility of hematological parameters in aplastic anemia

open access: yesScientific Reports
Hematological parameters available on automated hematology analyzers have been shown to be useful indicators for hematological disorders. However, extensive studies especially in aplastic anemia for these indices are sparse.
Lizhong Zhang   +4 more
doaj   +1 more source

Bilateral Spontaneous Hyphemas in a Patient with Aplastic Anemia

open access: yesCase Reports in Ophthalmology, 2018
Bilateral spontaneous hyphemas are a rare ophthalmic event. Aplastic anemia is a hematologic condition with well-documented manifestations in the posterior segment but not the anterior segment.
Mohammad Z. Siddiqui   +4 more
doaj   +1 more source

Scurvy: A treatable forgotten fatal differential diagnosis and potential etiology of leukemia and aplastic anemia in pediatric population

open access: yesHealth Science Reports, 2023
Scurvy is a rare nutritional deficiency disease which is less likely to be suspected and it mostly lead to delayed diagnosis. It can present with features which can mislead clinicians to misdiagnose the condition as leukemia or aplastic anemia.
Harold L. Mashauri
doaj   +1 more source

Response of Paroxysmal Nocturnal Hemoglobinuria Clone with Aplastic Anemia to Rituximab

open access: yesCase Reports in Hematology, 2012
Paroxysmal nocturnal hemoglobinuria is caused by expansion of a hematopoietic stem cell clone with an acquired somatic mutation in the PIG-A gene. This mutation aborts the synthesis and expression of the glycosylphosphatidylinositol anchor proteins CD55
Radha Raghupathy, Olga Derman
doaj   +1 more source

Spontaneously resolved severe retinopathy associated with aplastic anemia

open access: yesOman Journal of Ophthalmology, 2021
Aplastic anemia is a rare, usually autoimmune disorder of bone marrow stem cells leading to pancytopenia and hypoplastic marrow that presents with anemia, infection or bleeding which can be potentially sight and life-threatening.
Washoo Mal, Mohamed Al-Abri
doaj   +1 more source

APLASTIC ANEMIA ET CAUSA OF SUSPECT VIRAL HEPATITIS INFECTION: A CASE REPORT

open access: yese-Jurnal Medika Udayana, 2014
Aplastic anemia is anemia that occurs because of a failure of hematopoiesis is relatively rarebut can be life threatening. The cause of aplastic anemia itself is still largely unknown oridiopathic.
I Wayan Wawan Lismana
doaj  

Aplastic anemia: a new complication in the recent mysterious hepatitis outbreak among children worldwide: two case reports

open access: yesJournal of Medical Case Reports, 2022
Background Recently, an unknown hepatitis outbreak among children has concerned many individuals worldwide. These cases are frequently reported, mainly from Europe and other countries.
Ali Ghanei-Shahmirzadi   +8 more
doaj   +1 more source

Therapeutic effect of androgen therapy in a mouse model of aplastic anemia produced by short telomeres

open access: yesHaematologica, 2015
Aplastic anemia is a rare but life-threatening disorder characterized by cytopenia in at least two of the three blood lineages. A frequent feature of patients with aplastic anemia is that they have shorter telomeres than those of age-matched controls ...
Christian Bär   +3 more
doaj   +1 more source

Successful treatment of severe aplastic anemia with syngeneic stem cell transplantation in the setting of active disseminated mucormycosis

open access: yesMedical Mycology Case Reports, 2019
Severe aplastic anemia (SAA) is a hematological disease resulting in pancytopenia due to bone marrow failure. Treatment consists of immunosppressive therapy, or allo-SCT.
Jean El-Cheikh   +6 more
doaj  

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