Results 51 to 60 of about 5,131 (199)

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

Red blood cell membrane proteome as a reporter of disease severity, transfusion impact and genetic background in transfusion‐dependent β‐thalassaemia

British Journal of Haematology, Volume 208, Issue 6, Page 1980-1992, June 2026.
Summary Omics technologies have transformed research in haemoglobinopathies, yet the proteome of RBCs remains largely unexplored in transfusion‐dependent thalassaemia (TDT). In this proteomic analysis, Red blood cell (RBC) membranes from 48 adults with TDT were compared with healthy controls.
Konstantina Theocharaki, Sophia Delicou, Aikaterini Ntzoura‐Kani, Nikolaos Simantiris, Marianna Politou, Veroniki Komninaka, Martina Samiotaki, Jerome Zoidakis, Marianna H. Antonelou   +8 more
wiley   +1 more source

Hold on to your units: Quality of red cell concentrates is only affected after multiple transient warming events

Transfusion, Volume 66, Issue 6, Page 1180-1191, June 2026.
Abstract Background Cryopreserved red cell concentrates (RCCs) glycerolized using a high glycerol (40%) method can be stored below −65°C for up to 30 years; however, units may be inadvertently warmed above −65°C due to freezer failures, human errors, or routine inventory management.
Jayme Kurach, Mackenzie Brandon‐Coatham, Nishaka William, Carly Olafson, Tracey R. Turner, Anika Tahsin Rahman, Behrouz Ehsani‐Moghaddam, Gwen Clarke, Jason P. Acker   +8 more
wiley   +1 more source