Ghada Y El-Kamah (Ghada El-Kamah)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 7

Top Venues

Genes

Molecular genetics & genomic medicine

Archives of dermatological research

National Research Centre

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Research Centre

Egypt

Professor :: Clinical Genetics department

Publications

Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Ghada Y El-Kamah, Mennat I Mehrez, Mohamed B Taher, Hala T El-Bassyouni, Khaled R Gaber, Khalda S Amr
Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families. Genes 14 (4) (2023)
Khalda Amr, Hala T El-Bassyouni, Samira Ismail, Eman Youness, Sherien M El-Daly, Abeer Y Ebrahim, Ghada Y El-Kamah
Genetic assessment of ten Egyptian patients with Sjögren-Larsson syndrome: expanding the clinical spectrum and reporting a novel ALDH3A2 mutation. Archives of dermatological research 311 (9) (2019)
Khalda Amr, Patrycja Pawlikowska, Said Aoufouchi, Filippo Rosselli, Ghada Y El-Kamah
Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine-responsive megaloblastic anemia in an Egyptian family. Molecular genetics & genomic medicine 7 (7) (2019)

Ghada Y El-Kamah.css-eqlu8i{font-size:small;padding-left:4px;} (Ghada El-Kamah)

Publication Activity (10 Years)

Top Topics

Top Venues

Ghada Y El-Kamah (Ghada El-Kamah)