Heba Amin Hassan (Heba Hassan)

Scopus Author ID ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 8

Top Venues

Hormones (Athens, Greece)

American journal of medical genetics. Part A

Journal of pediatric endocrinology & metabolism : JPEM

National Research Centre

Al-Azhar University (PHD)

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

Affiliation History

National Research Centre

Egypt

Researcher / Dr :: Medical Molecular Genetics Dept.

Education History

Al-Azhar University

Egypt

PHD :: Faculty of Pharmacy

Cairo University

Egypt

MSC :: Faculty of Pharmacy

Cairo University

Egypt

BSC :: Faculty of Pharmacy

Publications

Heba Amin Hassan, Inas Mazen, Aya Elaidy, Alaa K Kamel, Noura R Eissa, Mona L Essawi
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II. Hormones (Athens, Greece) (2024)
Heba Amin Hassan, Inas Mazen, Aya Elaidy, Alaa K Kamel, Noura R Eissa, Mona L Essawi
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II. Hormones (Athens, Greece) 23 (2) (2024)
Heba Amin Hassan, Inas Mazen, Aya Elaidy, Alaa K Kamel, Noura R Eissa, Mona L Essawi
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II. Hormones (Athens, Greece) 23 (2) (2024)
Heba Amin Hassan, Inas Mazen, Aya Elaidy, Alaa K Kamel, Noura R Eissa, Mona L Essawi
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II. Hormones (Athens, Greece) 23 (2) (2024)
Heba Amin Hassan, Inas Mazen, Aya Elaidy, Alaa K Kamel, Noura R Eissa, Mona L Essawi
Expanding the phenotypic spectrum of LHCGR signal peptide insertion variant: novel clinical and allelic findings causing Leydig cell hypoplasia type II. Hormones (Athens, Greece) 23 (2) (2024)
Mona Essawi, Inas Mazen, Lubna Fawaz, Heba Amin Hassan, Nagham ElBagoury, Michael Peter, Khadiga Gaafar, Mahmoud Amer, Wajeet Nabil, Gisela Hohmann, Hala Soliman, Wolfgang Sippell
Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from Egypt. Journal of pediatric endocrinology & metabolism : JPEM 33 (7) (2021)
Inas Mazen, Mona Mekkawy, Alaa Kamel, Mona Essawi, Heba Amin Hassan, Mohamed S Abdel-Hamid, Khalda Sayed Amr, Hala Soliman, Mona El-Ruby, Ahmed Torky, Mona El Gammal, Aya Elaidy, Anu Bashamboo, Kenneth McElreavey
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. American journal of medical genetics. Part A 185 (6) (2021)
Heba Amin Hassan, M L Essawi, M K Mekkawy, I Mazen
Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I. Hormones (Athens, Greece) 19 (4) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Heba Amin Hassan (Heba Hassan)