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List of works by Heba Amin Hassan

A novel nonsense mutation in exon 1 of HSD17B3 gene in an Egyptian 46,XY adult female presenting with primary amenorrhea.

scientific article published on 18 June 2013

Assessment of the most common CYP21A2 point mutations in a cohort of congenital adrenal hyperplasia patients from Egypt

scientific article published on 03 July 2020

Biochemical Analysis of Four Missense Mutations in the HSD17B3 Gene Associated With 46,XY Disorders of Sex Development in Egyptian Patients

scientific article published in September 2017

Circulating miRNAs 21 and 221 as biomarkers for early diagnosis of prostate cancer.

scientific article published on 5 September 2014

Extracellular miR-145, miR-223 and miR-326 expression signature allow for differential diagnosis of immune-mediated neuroinflammatory diseases.

scientific article published on 15 November 2017

Mutational Profile of 10 Afflicted Egyptian Families with 17-β-HSD-3 Deficiency.

scientific article

Novel mutations of the LHCGR gene in two families with 46,XY DSD causing Leydig cell hypoplasia I

scientific article published on 14 July 2020

Unique karyotype: mos 46,X,dic(X;Y)(p22.33;p11.32)/ 45,X/45,dic(X;Y)(p22.33;p11.32) in an Egyptian patient with Ovotesticular disorder of sexual development.

scientific article published on 09 May 2013

WT1 Gene Mutation, p.R462W, in a 46,XY DSD Patient from Egypt with Gonadoblastoma and Review of the Literature

scientific article published on 11 January 2018

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