Results 101 to 110 of about 5,131 (194)

Congenital dyserythropoietic anemia masquerading as hereditary spherocytosis

open access: yes
Background: Congenital dyserythropoietic anemias (CDA) type II is a rare hereditary chronic hemolytic anemia due to a defect in the SEC23B gene which shows varying degrees of ineffective erythropoiesis and is often misdiagnosed as a red blood cell (RBC ...
Kaninika Sanyal   +4 more
core   +1 more source

A novel <i>ANK1</i> gene mutation associated with hereditary spherocytosis: a case report. [PDF]

open access: yesFront Pediatr
Lai M   +7 more
europepmc   +1 more source

Comorbidity of Dengue and Hereditary Spherocytosis in an 18-Year-Old Patient: A Case Report. [PDF]

open access: yesCureus
Becerra-Carrillo RI   +4 more
europepmc   +1 more source

Marked reduction of spectrinin hereditary spherocytosis in the common house mouse.

open access: yes, 1978
In contrast to the disease in humans, hereditary spherocytosis in the common house mouse produces an extreme spherocytosis. The cells show a broad distribution in size ranging from microcytic to macrocytic.
Shohet, S B   +2 more
core  

Clinical Characteristics and Gene Mutations of Hereditary Spherocytosis in 59 Chinese Children. [PDF]

open access: yesMol Genet Genomic Med
Li Y   +7 more
europepmc   +1 more source

Cognitive impairment in hereditary spherocytosis. [PDF]

open access: yesBr J Haematol
Tartaglione I   +12 more
europepmc   +1 more source

Hereditary Spherocytosis: Review of Presentation at Birth. [PDF]

open access: yesChildren (Basel)
Achenjang NS   +3 more
europepmc   +1 more source

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