Results 101 to 110 of about 5,131 (199)

Feasibility of Intensive Chemotherapy in Hereditary Spherocytosis

Background: This study presents a young man with hereditary spherocytosis (HS) who underwent intensive chemotherapy for newly diagnosed diffuse large B-cell lymphoma (DLBCL) and achieved complete remission.
Giubbilei Cristina, Puccini Benedetta, Vannucchi Alessandro Maria, Nassi Luca, Sordi Benedetta, D’Angelo Simona, Ciceri Manuel, Carrai Valentina   +7 more
core   +1 more source

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

Iron overload in hereditary spherocytosis: Are genetic factors the cause?

International audienceSummary Non‐transfusional iron overload (IOL) in hereditary spherocytosis (HS) is poorly documented compared with other red blood cell disorders.
Giansily-Blaizot, Muriel, Aguilar Martinez, Patricia, Cunat, Séverine, Azoury, Vincent, Bertchansky, Ivan, Mahe, Perrine, Donaty, Lucie   +6 more
core   +1 more source

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

, 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, Bernstein, S E, Greenquist, A C   +2 more
core  

Pediatric laparoscopic splenectomy using a repurposed sterile diathermy pouch as a retrieval bag: preliminary experience. [PDF]

BMC Surg
Zain M.
europepmc   +1 more source

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

Cureus
Becerra-Carrillo RI, Mendoza-Maldonado C, Rendón-Aguilar H, Torres-Hernández M, Ochoa-Ramírez L.   +4 more
europepmc   +1 more source

Diagnostic Utility of Next-Generation Sequencing for Unconjugated Hyperbilirubinemia in Children. [PDF]

Pediatr Gastroenterol Hepatol Nutr
Kim HJ.
europepmc   +1 more source

A novel heterozygous mutation in ANK1 solves a mystery of a patient with hyperbilirubinemia and splenomegaly. [PDF]

Pak J Med Sci
Shi Y, Ou Y, Wu H.
europepmc   +1 more source

Correction: Identification of a novel <i>ANK1</i> gene variant c.1504-9G>A and its mechanism of intron retention in hereditary spherocytosis. [PDF]

Front Genet
Xiong T, Xu Z, Wan Q, Chen F, Ye Y, Wang H, Wu C.   +6 more
europepmc   +1 more source

Ganglioneuroma in a child with hereditary spherocytosis

, 2012
Hereditary spherocytosis (HS) is the most frequent cause of congenital hemolytic anemia. Extramedullary hematopoiesis (EMH) mimicking a mass may develop in the lymph nodes, kidneys, pleura, mediastinum, adrenal gland, and in particular the spleen and ...
Bahattin Tunç, Ayper Kaçar, Haci Ahmet Demir, Suna Emir, Emrah Senel, Semanur Ozdel   +5 more
core