Results 131 to 140 of about 5,131 (194)

Curing the “Incurable”: First Successful Hematopoietic Stem Cell Transplantation in Severe Hereditary Spherocytosis with Homozygous <i>SPTA1</i> Variant and Hepatic Fibrosis [PDF]

Turk J Haematol
Koçak Göl D, Işık E, Gök V, Özcan A, Yılmaz E, Ünal E, Karakükcü M.   +6 more
europepmc   +1 more source

Splenic Artery Embolization as a Primary Treatment for Hereditary Spherocytosis: A Case Report. [PDF]

Cureus
Mahamat HA, Alamin SM, Alrawi A, Al Mohammad OA, Alsaadi A, Balila S.   +5 more
europepmc   +1 more source

Three novel heterozygous ANK1 loss-of-function variants cause hereditary spherocytosis in Chinese families. [PDF]

Ann Hematol
Wang Y, Liu T, Wang W, Li Y, Xiao L, Xiang Y, Huang L, Zhang Y, Yu J.   +8 more
europepmc   +1 more source

Genetic screening strategy for children with hereditary spherocytosis in Jiangxi Province of China. [PDF]

Front Pediatr
Wu C, Xu Z, Wan Q, Chen F, Ye Y, Wang H.
europepmc   +1 more source

Transcatheter edge-to-edge repair for post-surgical recurrent mitral regurgitation in hereditary spherocytosis: a case report. [PDF]

Eur Heart J Case Rep
Yagasaki H, Umeda Y, Suzuki T, Watanabe R, Noda T.   +4 more
europepmc   +1 more source

Clinical characteristics of hereditary spherocytosis with red blood cell membrane protein gene variants. [PDF]

Front Pediatr
Cheng J, Zhang L, Yao J, Zhao S, Jiang J.   +4 more
europepmc   +1 more source

Drug-induced liver injury from Deferasirox in a pediatric patient with hereditary spherocytosis: A case report. [PDF]

JPGN Rep
Talwar S, Rosenthal B, Vissa M, Cort K, Byers J, Ali S.   +5 more
europepmc   +1 more source

Red cell shape regulation by band 3-ankyrin-spectrin linkage: implications for clinical severity of bovine hereditary spherocytosis. [PDF]

Blood Red Cells Iron
Miyazono K, Tomihari M, Arashiki N, Koshino I, Otsuka-Yamasaki Y, Kizaki K, Tsukamoto T, Inanami O, Deguchi A, Kitaguchi E, Demura M, Mohandas N, Takakuwa Y, Inaba M.   +13 more
europepmc   +1 more source

Case Report: Identification and functional characterization of a novel heterozygous splice-donor (c.647+1G>A) site mutation in the <i>SPTB</i> gene that causes hereditary spherocytosis with hemolytic anemia. [PDF]

Front Genet
Cao K, Luo X, Liu L, Mao X, Liu R, Chen Y, Banerjee S.   +6 more
europepmc   +1 more source

Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in Türkiye [PDF]

Turk J Haematol
Doğru Ö, Alavanda C, Demir Ş, Koç A, Ata P.   +4 more
europepmc   +1 more source