Relevant bibliographies by topics / Acanthocytes

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Acanthocytes'

Author: Grafiati
Published: 4 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Acanthocytes"

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Bayreuther, C., M. Borg, C. Ferrero-Vacher, A. Chaussenot, and C. Lebrun. "Choréo-acanthocytose sans acanthocytes." Revue Neurologique 166, no. 1 (2010): 100–103. http://dx.doi.org/10.1016/j.neurol.2009.03.005.

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Darras, Alexis, Kevin Peikert, Antonia Rabe, et al. "Acanthocyte Sedimentation Rate as a Diagnostic Biomarker for Neuroacanthocytosis Syndromes: Experimental Evidence and Physical Justification." Cells 10, no. 4 (2021): 788. http://dx.doi.org/10.3390/cells10040788.

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(1) Background: Chorea-acanthocytosis and McLeod syndrome are the core diseases among the group of rare neurodegenerative disorders called neuroacanthocytosis syndromes (NASs). NAS patients have a variable number of irregularly spiky erythrocytes, so-called acanthocytes. Their detection is a crucial but error-prone parameter in the diagnosis of NASs, often leading to misdiagnoses. (2) Methods: We measured the standard Westergren erythrocyte sedimentation rate (ESR) of various blood samples from NAS patients and healthy controls. Furthermore, we manipulated the ESR by swapping the erythrocytes
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Doll, D. C., A. F. List, D. A. Dayhoff, T. S. Loy, Q. S. Ringenberg, and J. W. Yarbro. "Acanthocytosis associated with myelodysplasia." Journal of Clinical Oncology 7, no. 10 (1989): 1569–72. http://dx.doi.org/10.1200/jco.1989.7.10.1569.

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Dysplastic hematopoiesis associated with erythrocyte macrocytosis is a morphologic hallmark of myelodysplasia. We report the cases of six patients with myelodysplasia in which acanthocytosis was the predominant red blood cell (RBC) abnormality. In each case acanthocytes represented 5% to 10% of circulating RBC forms and was the primary reason for referral in two cases. None of the patients had comorbid conditions known to be associated with acanthocyte formation. Myelodysplasia should be considered in the differential diagnosis of acanthocytosis, particularly in the anemic, elderly individual.
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De Franceschi, Lucia, Carlo Tomelleri, Alessandro Matte, et al. "Erythrocyte membrane changes of chorea-acanthocytosis are the result of altered Lyn kinase activity." Blood 118, no. 20 (2011): 5652–63. http://dx.doi.org/10.1182/blood-2011-05-355339.

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Abstract Acanthocytic RBCs are a peculiar diagnostic feature of chorea-acanthocytosis (ChAc), a rare autosomal recessive neurodegenerative disorder. Although recent years have witnessed some progress in the molecular characterization of ChAc, the mechanism(s) responsible for generation of acanthocytes in ChAc is largely unknown. As the membrane protein composition of ChAc RBCs is similar to that of normal RBCs, we evaluated the tyrosine (Tyr)–phosphorylation profile of RBCs using comparative proteomics. Increased Tyr phosphorylation state of several membrane proteins, including band 3, β-spect
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Redman, CM, T. Huima, E. Robbins, S. Lee, and WL Marsh. "Effect of phosphatidylserine on the shape of McLeod red cell acanthocytes." Blood 74, no. 5 (1989): 1826–35. http://dx.doi.org/10.1182/blood.v74.5.1826.1826.

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Abstract The rare McLeod blood group phenotype is characterized by weak Kell antigens, lack of the common Kx antigen, and acanthocytic morphology. Previous studies that did not detect membrane or cytoskeletal protein abnormalities suggested a lipid disturbance. In normal red cells, dimyristoyl phosphatidylserine (DMPS) is transported across the membrane by an enzymatic process and accumulates in the inner leaflet of the membrane bilayer causing discocyte to stomatocyte shape changes. Scanning electron microscopy of McLeod red cells shows a mixture comprised of 15% discocytes, 51% with irregula
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Redman, CM, T. Huima, E. Robbins, S. Lee, and WL Marsh. "Effect of phosphatidylserine on the shape of McLeod red cell acanthocytes." Blood 74, no. 5 (1989): 1826–35. http://dx.doi.org/10.1182/blood.v74.5.1826.bloodjournal7451826.

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The rare McLeod blood group phenotype is characterized by weak Kell antigens, lack of the common Kx antigen, and acanthocytic morphology. Previous studies that did not detect membrane or cytoskeletal protein abnormalities suggested a lipid disturbance. In normal red cells, dimyristoyl phosphatidylserine (DMPS) is transported across the membrane by an enzymatic process and accumulates in the inner leaflet of the membrane bilayer causing discocyte to stomatocyte shape changes. Scanning electron microscopy of McLeod red cells shows a mixture comprised of 15% discocytes, 51% with irregular surface
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7

Oner, Ozge Gonul, and Asuman Orhan Varoglu. "Phenotypic variability in sisters with VPS13A disease (chorea-acanthocytosis)." Ideggyógyászati szemle 78, no. 1-2 (2025): 69–72. https://doi.org/10.18071/isz.78.0069.

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Chorea-acanthocytosis (VPS13A disease) is a rare multisystem neurodegenerative disorder with a broad phenotypic spectrum. It is characterized by neuropsychiatric symptoms and the presence of acanthocytes. However, the relationship between acanthocytes and disease severity remains unclear. Diagnosis is established through genetic testing. We present two sisters with VPS13A disease, each exhibiting distinct clinical presentations. The younger presents with severe symptoms including drug-resistant epilepsy, neuropsychiatric issues, chorea, and self-mutilation, along with the presence of acanthocy
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8

Luo, Hong, Xuan Li, Guohong Li, Yanbo Pan, and Keqin Zhang. "Acanthocytes of Stropharia rugosoannulata Function as a Nematode-Attacking Device." Applied and Environmental Microbiology 72, no. 4 (2006): 2982–87. http://dx.doi.org/10.1128/aem.72.4.2982-2987.2006.

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ABSTRACT Efficient killing of nematodes by Stropharia rugosoannulata Farlow ex Murrill cultures was observed. This fungus showed the ability to immobilize the free-living nematode Panagrellus redivivus Goodey within minutes and to immobilize the pine wilt nematode Bursaphelenchus xylophilus (Steiner & Buhrer) Nickle within hours on agar plates. Moreover, P. redivivus worms were completely degraded by the fungus within 24 to 48 h. The cultures of S. rugosoannulata studied shared the characteristic of abundantly producing cells with finger-like projections called acanthocytes. We showed that
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Klempíř, Jiří, Jan Roth, Kateřina Zárubová, Martin Písačka, Nataša Špačková, and Louise Tilley. "The McLeod syndrome without acanthocytes." Parkinsonism & Related Disorders 14, no. 4 (2008): 364–66. http://dx.doi.org/10.1016/j.parkreldis.2007.07.011.

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Khodadad, Jena K., Ronald S. Weinstein, Laurence W. Marsh, and Theodore L. Steck. "Shape determinants of McLeod acanthocytes." Journal of Membrane Biology 107, no. 3 (1989): 213–18. http://dx.doi.org/10.1007/bf01871936.

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Dissertations / Theses on the topic "Acanthocytes"

1

Choppe, Olivier Weber Michel. "La chorée-acanthocytose à propos d'un cas observé à l'île de la Réunion /." [S.l.] : [s.n.], 2003. http://www.scd.uhp-nancy.fr/docnum/SCDMED_T_2003_CHOPPE_OLIVIER.pdf.

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Brisard, Luc. "Association d'une chorée et d'une acanthocytose : à propos d'une observation, revue de la littérature et discussion." Bordeaux 2, 1994. http://www.theses.fr/1994BOR2M210.

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Cuissard, Laurent. "Evaluation précise du pronostic des cirrhoses compliquées d'acanthocytose." Montpellier 1, 1992. http://www.theses.fr/1992MON11043.

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Lindner, Kamila [Verfasser], and Artur [Akademischer Betreuer] Pfitzner. "Wirt-Virus Wechselwirkungen bei der Infektion durch Acanthocystis turfacea Chlorella Virus 1 : Regulation der Genexpression früher Gene und des Ubiquitin-Systems / Kamila Lindner ; Betreuer: Artur Pfitzner." Hohenheim : Kommunikations-, Informations- und Medienzentrum der Universität Hohenheim, 2021. http://d-nb.info/1236630173/34.

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TOMELLERI, Carlo. "Integrated analysis of novel signal transduction pathways in red cells from patients with neuroacanthocytosis." Doctoral thesis, 2012. http://hdl.handle.net/11562/395336.

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Il termine neuroacantocitosi (NA) raggruppa diverse malattie genetiche rare che condividono manifestazioni neurologiche simili e la presenza di globuli rossi stellati nella circolazione periferica, gli acantociti. Le due principali malattie classificate come NA sono Corea acantocitosi (ChAc) e sindrome di McLeod (MLS). Poiché la presenza di acantociti è una caratteristica comune di questi disordini, lo studio dei meccanismi alla base della loro formazione può aiutare a comprendere la patogenesi delle NA. In questa tesi viene presentata una serie di studi sui meccanismi di signaling e sulle mo
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Book chapters on the topic "Acanthocytes"

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"Acanthocytes." In Clinical Veterinary Advisor. Elsevier, 2012. http://dx.doi.org/10.1016/b978-1-4160-9979-6.00348-2.

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"acanthocyte, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/3717413741.

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Conference papers on the topic "Acanthocytes"

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Saito, Monalisa Moura, Dhyego Ferreira Moreira de Lacerda, Ana Claudia Marque Gouveia de Melo, Lucas Monteiro Barros Nunes, Luana Cristina Rodrigues de Oliveira Costa, and Eduarda Silvestre Ribeiro da Costa Gomes. "Neurodegeneration with cerebral iron accumulation: a case report." In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.145.

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Introduction: NBIA is a rare disease, with a prevalence of 1/1,000,000.It is characterized by abnormal iron accumulation. Clinical findings may include progressive extrapyramidal disorders, involvement of the pyramidal, peripheral, autonomic nervous systems, superior cortical, visual and cerebellar functions. The diagnosis is made through the association of clinical findings and complementary exams. Currently, the treatment is only symptomatic, with no specific therapy. Case report: 5-year-old female, reporting involuntary movements and difficulty walking a day ago. Presented agitation and del
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