Cargando…

Severe congenital neutropenia associated with the ELANE gene in Chinese children: case report

Detalles Bibliográficos
Autores principales:	Gao, Liwei, He, Jianxin, Wu, Runhui
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2018
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331322/ https://www.ncbi.nlm.nih.gov/pubmed/32851234 http://dx.doi.org/10.1002/ped4.12027

Ejemplares similares

Novel ELANE Gene Mutation in a Korean Girl with Severe Congenital Neutropenia
por: Shim, Ye Jee, et al.
Publicado: (2011)

Different Clinical Phenotypes in Familial Severe Congenital Neutropenia Cases with Same Mutation of the ELANE Gene
por: Cho, Hye-Kyung, et al.
Publicado: (2014)

Severe congenital neutropenia caused by the ELANE gene mutation in a Vietnamese boy with misdiagnosis of tuberculosis and autoimmune neutropenia: a case report
por: Vu, Quang Van, et al.
Publicado: (2015)

Severe congenital neutropenia caused by ELANE gene mutation: A case report and literature review
por: Wang, Jing, et al.
Publicado: (2022)

Mutations in the ELANE Gene are Associated with Development of Periodontitis in Patients with Severe Congenital Neutropenia
por: Ye, Ying, et al.
Publicado: (2011)

Functional characteristics of circulating granulocytes in severe congenital neutropenia caused by ELANE mutations
por: Liu, Qiao, et al.
Publicado: (2019)

Screening for ELANE, HAX1 and GFI1 gene mutations in children with neutropenia and clinical characterization of two novel mutations in ELANE gene
por: Komvilaisak, Patcharee, et al.
Publicado: (2023)

Severe congenital neutropenia in a multigenerational family with a novel neutrophil elastase (ELANE) mutation
por: van de Vosse, Esther, et al.
Publicado: (2010)

HSCT may lower leukemia risk in ELANE neutropenia: a before–after study from the French Severe Congenital Neutropenia Registry
por: Rotulo, Gioacchino Andrea, et al.
Publicado: (2020)

Paediatric autoimmune diseases with ELANE mutations associated with neutropenia
por: Zhang, Dan, et al.
Publicado: (2023)

CRISPR-Cas9-Mediated ELANE Mutation Correction in Hematopoietic Stem and Progenitor Cells to Treat Severe Congenital Neutropenia
por: Tran, Ngoc Tung, et al.
Publicado: (2020)

Allogeneic Transplant in ELANE and MEFV Mutation Positive Severe Cyclic Neutropenia: Review of Prognostic Factors for Secondary Severe Events
por: Okolo, Onyemaechi N., et al.
Publicado: (2017)

Severe congenital neutropenia mimicking chronic idiopathic neutropenia: a case report
por: Kim, Juhyung, et al.
Publicado: (2022)

Management of tooth extraction in a patient with ELANE gene mutation-induced cyclic neutropenia: A case report
por: Aota, Keiko, et al.
Publicado: (2019)

ELANE gene mutation-induced cyclic neutropenia manifesting as recurrent fever with oral mucosal ulcer: A case report
por: Chen, Xin, et al.
Publicado: (2018)

Severe congenital cyclic neutropenia: A case report
por: Patil, Vidyavathi H, et al.
Publicado: (2016)

Severe congenital neutropenia: case report
por: Gomes, Luiz Carlos Bandoli
Publicado: (2015)

P1357: MILESTONE (MODIFYING ELANE GOLDBERG–HOGNES BOX TO INHIBIT EXPRESSION), A UNIVERSAL, SAFE AND EFFECTIVE CRISPR/CAS9N-MEDIATED GENOME EDITING STRATEGY FOR ELANE RELATED SEVERE CONGENITAL NEUTROPENIA
por: Nasri, Masoud, et al.
Publicado: (2023)

Comparison of Gene Editing versus a Neutrophil Elastase Inhibitor as Potential Therapies for ELANE Neutropenia
por: Makaryan, Vahagn, et al.
Publicado: (2022)

P458: HIPSC DISEASE MODELING TO STUDY LEUKEMIA DEVELOPMENT IN HAX1 VS ELANE ASSOCIATED CONGENITAL NEUTROPENIA
por: Dannenmann, Benjamin, et al.
Publicado: (2023)

Mutant allele knockout with novel CRISPR nuclease promotes myelopoiesis in ELANE neutropenia
por: Sabo, Peter, et al.
Publicado: (2022)

Manifestation of severe congenital neutropenia in the oral cavity. Case report
por: Krasuska-Sławińska, Ewa, et al.
Publicado: (2023)

Case report: Five-year periodontal management of a patient with two novel mutation sites in ELANE-induced cyclic neutropenia
por: Lao, Zhentao, et al.
Publicado: (2022)

Case Report: Characterization of known (c.607G>C) and novel (c.416C>G) ELANE mutations in two Mexican families with congenital neutropenia
por: Núñez-Núñez, María Enriqueta, et al.
Publicado: (2023)

Annual Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2005)

Annual Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2006)

Annual Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2007)

Annual Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2008)

Pyoderma Gangrenosum Secondary to Severe Congenital Neutropenia
por: Wakabayashi, Nao, et al.
Publicado: (2018)

CRISPR/Cas9-mediated ELANE knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells of severe congenital neutropenia patients
por: Nasri, Masoud, et al.
Publicado: (2020)

Second Quarterly Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2004)

Clinical, Laboratory, and Molecular Characteristics and Remission Status in Children With Severe Congenital and Non-congenital Neutropenia
por: Gong, Ruo-Lan, et al.
Publicado: (2018)

First 2005 Intermediate Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2005)

Second 2005 Intermediate Report of the ELAN Collaboration
por: Richard, F, et al.
Publicado: (2005)

First intermediate report of the ELAN Collaboration: 2006
por: Richard, F
Publicado: (2006)

Status Report for the LTECSC Work Package within ELAN: A summary of the Workshop session at the first ELAN Workshop in Frascati
por: Lilje, L
Publicado: (2004)

Cardiac and Renal Malformations in a Patient with Sepsis and Severe Congenital Neutropenia
por: Eghbali, Aziz, et al.
Publicado: (2010)

Identification of biallelic germline variants of SRP68 in a sporadic case with severe congenital neutropenia
por: Schmaltz-Panneau, Barbara, et al.
Publicado: (2021)

Periodontal Disease in Two Siblings with VPS45-associated Severe Congenital Neutropenia Type V: A Case Report
por: Alotaibi, Faris A, et al.
Publicado: (2020)

Severe congenital neutropenia and liver abscess: Surgical treatment breaks the vicious cycle
por: Lao, Jing, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_su4kh3vgvlr9s49vdfjpdmuupd