Results 51 to 60 of about 5,131 (194)

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

Br J Haematol
International audienceSummary Non‐transfusional iron overload (IOL) in hereditary spherocytosis (HS) is poorly documented compared with other red blood cell disorders.
Donaty L, Giansily-Blaizot M, Bertchansky I, Cunat S, Azoury V, Mahe P, Aguilar Martinez P.   +6 more
europepmc   +2 more sources

Integrative preimplantation genetic testing analysis for a Chinese family with hereditary spherocytosis caused by a novel splicing variant of SPTB

Frontiers in Genetics, 2023
Hereditary spherocytosis (HS), the most common inherited hemolytic anemia disorder, is characterized by osmotically fragile microspherocytic red cells with a reduced surface area on the peripheral blood smear.
Yafei Tian, Yao Wang, Jingmin Yang, Jingmin Yang, Jingmin Yang, Pengfei Gao, Pengfei Gao, Hui Xu, Yiming Wu, Mengru Li, Hongyan Chen, Daru Lu, Daru Lu, Hongli Yan   +13 more
doaj   +1 more source

Nutritional Potential, Phytochemical Content, In Vivo Antioxidant, and Antanemic Potential of Musa paradisiaca Flower

Food Chemistry International, Volume 2, Issue 2, Page 246-262, June 2026.
After collecting Musa paradisiaca leaves, some were dried and others were used to produce aqueous extracts. The extracts and powders were characterized and then administered to rats made anaemic by PHZ. After 14 days of administration of the two samples, the rats were euthanized and it was observed that after 9 days of treatment, the aqueous extract ...
Josée Rebeca Nombo, Jethro Roland Misse Ngangue Ekwala, Somon Régine Tuem, Stéphano Tene Tambo, Merlin Ngafon Nchoutpouen, Valery Jean François Nsoga, Jules Christophe Koule Manz, Jordan Mekui Nwotue, Mathieu Ndomou   +8 more
wiley   +1 more source

Hereditary Spherocytosis [PDF]

Blood, 1951
Abstract Clinical, hematologic and genetic data on 28 cases of hereditary spherocytosis are presented for the purpose of characterizing this disorder as completely as possible. On the basis of this experience it is recommended that the following typical laboratory findings be sought in establishing a diagnosis in suspected cases: (1 ...
LAWRENCE E. YOUNG, MARY JANE IZZO, RICHARD F. PLATZER   +2 more
openaire   +1 more source

Bilateral macular hemorrhage in a patient with COVID-19

American Journal of Ophthalmology Case Reports, 2020
Purpose: We report a case of a patient with a known hereditary spherocytosis who developed a bilateral macular hemorrhage in concurrence with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-related respiratory syndrome.
Rossella D'Aloisio, Vincenzo Nasillo, Matteo Gironi, Rodolfo Mastropasqua   +3 more
doaj   +1 more source

Microesferocitose hereditária: avaliação de 20 casos. [PDF]

, 1987
Trabalho de Conclusão de Curso - Universidade Federal de Santa Catarina, Centro de Ciências da Saúde, Departamento de Pediatria, Curso de Medicina, Florianópolis ...
Fiamoncini, Altair
core  

Pyoderma Gangrenosum in a Patient With Hereditary Spherocytosis

, 2016
Pyoderma gangrenosum (PG) is a rare, relapsing cutaneous disease with 4 distinctive clinical manifestations: ulcerative, bullous, pustular, and vegetative lesions.
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core   +1 more source

Identification of a De Novoc.1000delA ANK1 mutation associated to hereditary spherocytosis in a neonate with Coombs-negative hemolytic jaundice-case reports and review of the literature

BMC Medical Genomics, 2021
Background To strengthen the understanding of Hereditary Spherocytosis (HS) and determine the disease-causing mutation present with neonatal jaundice. HS is a hemolytic condition resulting from various erythrocyte membrane defects.
Lichun Xie, Zhihao Xing, Changgang Li, Si-xi Liu, Fei-qiu Wen   +4 more
doaj   +1 more source

Density, heterogeneity and deformability of red cells as markers of clinical severity in hereditary spherocytosis [PDF]

, 2020
Hereditary spherocytosis originates from defective anchoring of the cytoskeletal network to the transmembrane protein complexes of the red blood cell. Red cells in hereditary spherocytosis are characterized by membrane instability, reduced deformability ...
Rick Huisjes, van Wijk, Richard, Anna Bogdanova, van Solinge, Wouter W, Laura Hertz, Rab, Minke A E, Seiler, E, Mañú-Pereira, Maria, Vives-Corrons, J.-L., Wouter W. van Solinge, Bogdanova, Anna, Esther Llaudet-Planas, Verhagen, Liesbeth P, Bogdanova, Anna; https://orcid.org/, Verhagen, LP, Raymond M. Schiffelers, van Solinge, W.W., Schiffelers, Raymond M, Hertz, Laura, Lars Kaestner, Silvia Pignatelli, Mahkro, A, Maria Mañú-Pereira, Elena Seiler, Polina Petkova-Kirova, Petkova-Kirova, Polina, Kaestner, Lars, Hertz, L, Petkova-Kirova, P, Schiffelers, Raymond, Vives Corrons, Joan-Luis, Minke A.E. Rab, Seiler, Elena, Huisjes, Rick, Rab, MAE, Makhro, Asya, Pignatelli, Silvia, Llaudet-Planas, Esther, Mañu-Pereira, Maria del Mar, Asya Makhro, Liesbeth P. Verhagen, Joan-LLuis Vives Corrons, Richard van Wijk   +42 more
core   +1 more source

On‐Chip Evaluation of Red Blood Cell Deformability Through Transit Velocity Index in Hematological Diseases

Small, Volume 22, Issue 33, 12 June 2026.
The deformability of red blood cell is essential for smooth microcirculation. We propose a deformability index using a microfluidic platform with capillary‐like constrictions, based on the relationship between cell deformation and transit velocity through the constrictions. Its effectiveness and clinical potential have been demonstrated in applications
Kenji Kajitani, Chia‐Hung Dylan Tsai, Tomohito Ohtani, Shigeo Wada, Ivan Cimrák, Misato Chimura, Tatsunori Taniguchi, Yasutaka Ueda, Jun‐ichi Nishimura, Yasushi Sakata   +9 more
wiley   +1 more source