Camelia Alkhzouz

5PUBLICATIONS
24CO-AUTHORS
Regenerative medicine (incl. stem cells)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Medical biochemistry - proteins and peptides (incl. medical proteomics)Gene expression (incl. microarray and other genome-wide approaches)
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Publications (5)

|May 04, 2026
Molecular Diagnosis and Phenotypic Variability of Noonan Syndrome: Experience from a Romanian Multicenter Study.

|Nov 13, 2025
Clinical and Genetic Characterization of Noonan Syndrome in a Romanian Cohort from Transylvania: Details on PTPN11 c.922A>G Variant and Phenotypic Spectrum.

Florina Victoria Nazarie, Diana Miclea, Crina Șufană

|Aug 01, 2025
Telomere Biology, Erosion, and Age-Related Conditions: Insights from Down Syndrome and Other Telomere-Associated Disorders.

Enikő Kutasi, Adina Chis, Mihaela Adela Vintan

|Mar 28, 2025
Salivary Proteome Insights: Evaluation of Saliva Preparation Methods in Mucopolysaccharidoses Research.

Maria-Andreea Soporan, Ioana-Ecaterina Pralea, Maria Iacobescu

|Jan 21, 2023
Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene.

Anca-Lelia Riza, Camelia Alkhzouz, Marius Farcaș

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Frequent Collaborators

3 joint publications

Romana Vulturar

2 joint publications

Simona Bucerzan

2 joint publications

Cecilia Lazea

2 joint publications

Călin Lazăr