Likaa Fasih Y Al-Kzayer
Overview
Explore the profile of Likaa Fasih Y Al-Kzayer including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
19
Citations
88
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Zhao J, Cui Y, Zhou H, Zhou D, Che Z, Zhang N, et al.
Transl Cancer Res
. 2024 Dec;
13(11):6255-6272.
PMID: 39697705
Background: The use of FMS-like tyrosine kinase 3 () as a crucial target for kinase inhibitors is well established, but its association with immune infiltration remains unclear. This study aimed...
2.
SARS-CoV-2-Associated Multisystem Inflammatory Syndrome in Children (MIS-C): A Case Report from Iraq
Al-Simaani R, Al-Kzayer L, Ali K, Al-Ani M, Nakazawa Y
Pediatr Rep
. 2023 Sep;
15(3):532-540.
PMID: 37755408
The novel coronavirus disease (COVID-19) continues to evolve. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2)-associated multisystem inflammatory syndrome in children (MIS-C) is a rare post-COVID-19 complication that affects children with critical...
3.
Al-Kzayer L, Saeed R, Habeeb Ghali H, Tanaka M, Al-Jadiry M, Faraj S, et al.
Transl Pediatr
. 2023 Jun;
12(5):827-844.
PMID: 37305720
Background: Molecular analyses in hematological malignancies provide insights about genetic makeup. Probable etiological factors in leukemogenesis could also be disclosed. Since genetic analyses are still primitive in Iraq, a country...
4.
Hanna H, Baz H, Al-Kzayer L, El Haddad H, El-Mougy F
J Appl Biomed
. 2023 Jan;
20(4):141-145.
PMID: 36708719
Background: Dysmetabolic iron overload syndrome (DIOS) is characterized by hyperferritinemia and normal transferrin saturation level with components of metabolic syndrome (MS). Among cases of MS, we determined those with DIOS...
5.
Liu T, Al-Kzayer L, Sarsam S, Chen L, Saeed R, Ali K, et al.
Transl Pediatr
. 2022 Mar;
11(1):163-173.
PMID: 35242663
Congenital mesoblastic nephroma (CMN) is a rare tumor, yet it is the most frequently diagnosed renal neoplasm in the first 3 months of life. CMN reports with prenatal magnetic resonance...
6.
Thanh Nha Uyen L, Amano Y, Al-Kzayer L, Kubota N, Kobayashi J, Nakazawa Y, et al.
Int J Hematol
. 2019 Dec;
111(3):451-462.
PMID: 31865541
We recently reported that methylation of PCDH17 gene is found in 30% of children with B-cell precursor acute lymphoblastic leukemia (ALL), and is significantly correlated to event-free or overall survival....
7.
Al-Kzayer L, Al-Aradi H, Shigemura T, Sano K, Tanaka M, Hamada M, et al.
BMC Med Genet
. 2019 Jun;
20(1):114.
PMID: 31242861
Background: Dedicator of cytokinesis 8 (DOCK8) deficiency (MIM #243700) is a rare disease, leads to a combined primary immunodeficiency (PID), and accounts for the autosomal recessive-hyper immunoglobulin E syndrome (AR-HIES)....
8.
Chen L, Zhai L, Al-Kzayer L, Sarsam S, Liu T, Alzakar R, et al.
Front Neurol
. 2019 Feb;
10:79.
PMID: 30792691
Melanocytic nevi present at birth, or within the first few months of life, are defined as congenital melanocytic nevi (CMN). Neurocutaneous melanosis (NCM) is a rare disorder, represents pigment cell...
9.
Al-Kzayer L, Yassin A, Salih K, Shigemura T, Sano K, Al-Simaani R, et al.
Front Immunol
. 2019 Feb;
10:58.
PMID: 30740107
Mendelian susceptibility to mycobacterial diseases (MSMD) is a rare condition of primary immunodeficiency disorder. Interleukin-12 receptor β1 (IL12RB1) deficiency, is the most common genetic etiology of MSMD, which is characterized...
10.
Al-Kzayer L, Sarsam S, Alhur N, Liu T, Nakazawa Y
Oncotarget
. 2018 Feb;
9(2):2962-2968.
PMID: 29416828
Goldenhar´s syndrome (GS) also known as oculo-auriculo-vertebral spectrum (OAVS) is a relatively rare condition. GS is of multifactorial etiology that includes environmental and/or genetic factors, in addition to teratogens that...