Literature DB >> 28800659

Neonatal-Onset Recurrent Guillain-Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency.

Didem Ardicli1, Ekim Z Taskiran2, Can Kosukcu2, Cagri Temucin3, Kader K Oguz4, Goknur Haliloglu1, Mehmet Alikasifoglu2, Haluk Topaloglu1.   

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Year:  2017        PMID： 28800659     DOI： 10.1055/s-0037-1604483

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN： 0174-304X            Impact factor:   1.947


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  8 in total

Review 1.  Association of Blood Group Antigen CD59 with Disease.

Authors:  Christof Weinstock
Journal:  Transfus Med Hemother       Date:  2022-01-13       Impact factor: 3.747

2.  Recurrent angioedema, Guillain-Barré, and myelitis in a girl with systemic lupus erythematosus and CD59 deficiency syndrome.

Authors:  Vadood Javadi Parvaneh; Leila Ghasemi; Khosro Rahmani; Reza Shiari; Mahbobeh Mesdaghi; Zahra Chavoshzadeh; Seyed Hassan Tonekaboni
Journal:  Auto Immun Highlights       Date:  2020-06-29

3.  Molecular pathogenesis of human CD59 deficiency.

Authors:  Netanel Karbian; Yael Eshed-Eisenbach; Adi Tabib; Hila Hoizman; B Paul Morgan; Ora Schueler-Furman; Elior Peles; Dror Mevorach
Journal:  Neurol Genet       Date:  2018-10-26

4.  Absence of pathogenic mutations in CD59 in chronic inflammatory demyelinating polyradiculoneuropathy.

Authors:  Lena Duchateau; Lorena Martín-Aguilar; Cinta Lleixà; Andrea Cortese; Oriol Dols-Icardo; Laura Cervera-Carles; Elba Pascual-Goñi; Jordi Diaz-Manera; Ilaria Calegari; Diego Franciotta; Ricard Rojas-Garcia; Isabel Illa; Jordi Clarimon; Luis Querol
Journal:  PLoS One       Date:  2019-02-22       Impact factor: 3.240

5.  Astrocyte- and Neuron-Derived Extracellular Vesicles from Alzheimer's Disease Patients Effect Complement-Mediated Neurotoxicity.

Authors:  Carlos J Nogueras-Ortiz; Vasiliki Mahairaki; Francheska Delgado-Peraza; Debamitra Das; Konstantinos Avgerinos; Erden Eren; Matthew Hentschel; Edward J Goetzl; Mark P Mattson; Dimitrios Kapogiannis
Journal:  Cells       Date:  2020-07-04       Impact factor: 6.600

6.  A Splice Site Mutation Associated with Congenital CD59 Deficiency.

Authors:  Jiani N Chai; Abul Kalam Azad; Kevin Kuan; Xiaoling Guo; Yanhua Wang
Journal:  Hematol Rep       Date:  2022-05-27

Review 7.  Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature.

Authors:  Hadley Stevens Smith; J Michael Swint; Seema R Lalani; Jose-Miguel Yamal; Marcia C de Oliveira Otto; Stephan Castellanos; Amy Taylor; Brendan H Lee; Heidi V Russell
Journal:  Genet Med       Date:  2018-05-14       Impact factor: 8.822

8.  European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management.

Authors:  Nicholas Brodszki; Ashley Frazer-Abel; Anete S Grumach; Michael Kirschfink; Jiri Litzman; Elena Perez; Mikko R J Seppänen; Kathleen E Sullivan; Stephen Jolles
Journal:  J Clin Immunol       Date:  2020-02-17       Impact factor: 8.317
  8 in total

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