Results 91 to 100 of about 53,574 (237)

How I manage aplastic anaemia in children

Aplastic anaemia (AA) is a rare heterogeneous condition in children. 1520% of cases are constitutional and correct diagnosis of these inherited causes of AA is important for appropriate management.
Samarasinghe S, Webb DKH
core   +4 more sources

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes

Molecular Cytogenetics, 2012
Background Chromosome changes in the bone marrow (BM) of patients with persistent cytopenia are often considered diagnostic for a myelodysplastic syndrome (MDS).
Marletta Cristina, Valli Roberto, Pressato Barbara, Mare Lydia, Montalbano Giuseppe, Menna Giuseppe, Loffredo Giuseppe, Bernardo Maria, Vinti Luciana, Ferrari Simona, Di Cesare-Merlone Alessandra, Zecca Marco, Lo Curto Francesco, Locatelli Franco, Pasquali Francesco, Maserati Emanuela   +15 more
doaj   +1 more source

Thymostimulin in Aplastic Anaemia [PDF]

Acta Haematologica, 2009
Giustolisi R, Guglielmo P, Cacciola E, CACCIOLA, Rossella Rosaria   +3 more
openaire   +3 more sources

Oral Lichenoid Lesions in Patients With Dyskeratosis Congenita: A Retrospective Case Series

Oral Diseases, EarlyView.
ABSTRACT Background Dyskeratosis congenita (DKC) is a rare inherited multisystem disorder primarily affecting the mucocutaneous and hematopoietic systems. Classically, it presents with the ectodermal triad of reticulate skin pigmentation, nail dystrophy, and oral leukoplakia.
Yehuda Zadik, Ori Finfter, Tevel Amiel, Amina Massarwa, Refael Cohen, Jawad Abu Tair, Anna Novikov, Polina Stepensky, Irina Zaidman, Ehud Even‐Or   +9 more
wiley   +1 more source

Differences in Disease Severity but Similar Telomere Lengths in Genetic Subgroups of Patients with Telomerase and Shelterin Mutations [PDF]

, 2011
This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are ...
Anna Ratcliffe, Tom J Vulliamy, Vulliamy Tom J., Kirwan, MJ, Hossain, U, Ratcliffe Anna, Vulliamy, Tom J., Baqai Charlotte, Kirwan Michael J., Baqai, Charlotte, Michael J. Kirwan, Baqai, C, Ratcliffe, A, Beswick, Richard, Marsh, Judith, Walne, Amanda, Beswick, R, Inderjeet Dokal, Dokal, Inderjeet, Walne Amanda, Kirwan, Michael J., Marsh, J, Charlotte Baqai, Judith Marsh, Marsh Judith, Tom J. Vulliamy, Beswick Richard, Dokal, I, Hossain, Upal, Vulliamy, TJ, Upal Hossain, Amanda Walne, Dokal Inderjeet, Richard Beswick, Michael J Kirwan, Ratcliffe, Anna, Hossain Upal, Walne, A   +37 more
core   +2 more sources

Genotyping of human parvovirus B19 in clinical samples from Brazil and Paraguay using heteroduplex mobility assay, single-stranded conformation polymorphism and nucleotide sequencing

Memorias do Instituto Oswaldo Cruz, 2011
Heteroduplex mobility assay, single-stranded conformation polymorphism and nucleotide sequencing were utilised to genotype human parvovirus B19 samples from Brazil and Paraguay.
Marcos César Lima de Mendonça, Ana Maria de Amorim Ferreira, Marta Gonçalves Matos dos Santos, Elva Cristina Oviedo, Maria Sônia Dal Bello, Marilda Mendonça Siqueira, Juan Manuel Piñeiro Maceira, Maria Genoveva von Hubinger, José Nelson dos Santos Silva Couceiro   +8 more
doaj   +1 more source

Understanding extracellular vesicles in antiaging

Periodontology 2000, EarlyView.
Abstract Background Aging is a multifactorial process marked by gradual cellular dysregulation, regulated by hallmarks, including genomic instability, mitochondrial dysregulation, and chronic inflammation. Extracellular vesicles (EVs), especially exosomes, have emerged as pivotal mediators of cell‐to‐cell communication with potential roles in both ...
Paras Ahmad, Nathan E. Estrin, Anton Sculean, Richard J. Miron   +3 more
wiley   +1 more source

Cyclosporin in aplastic anaemia : failure and success stories

, 1993
Two patients aged twelve and ten years who fulfilled the criteria of severe aplastic anaemia as defined by the International Aplastic Anaemia Group\u27 were treated with cyclosporin for six months.
Husna Zayadi
core  

Gut microbial dysbiosis: The hidden culprit behind Aplastic anaemia?

The Microbe
Aplastic anaemia (AA) is an autoimmune haematological disorder characterized by pancytopenia and hypocellular bone marrow. Several environmental factors are associated with the aetiology of this disorder.
Rojina Yasmin, Paramita Mandal
doaj   +1 more source

Challenges of Dengue in Hematological Disease Patients: Descriptive Analysis From the DANGO Registry During the 2023–2024 Outbreak in Argentina

Transplant Infectious Disease, EarlyView.
During the 2023–2024 Argentine dengue outbreak, 33 patients with hematological disease showed high complication rates, frequent hospitalization (64%), severe thrombocytopenia (90%), and 6% dengue‐attributable mortality. Transfusion‐associated cases were documented.
Gustavo Adolfo Méndez, Carla Niveyro, Pedro Andrés Villalba Apestegui, Victoria Isabel Martin, Lucila María Compañy Kec, María Cynthia Tomasino, Mariana del Carmen del Marull, Haydee Ingrid Bernard, Claudia Patricia Lorena Fernández, Flavia Marcela Pelech, Maria Fernanda Tosin, María Fernanda González‐Hobecker, Karen Beatrice Duranona, Angela Daiana Jara, Justus Cornely, Oliver A. Cornely, Jon Salmanton‐García   +16 more
wiley   +1 more source