Fateen, Ekram M.

Top Publications

Top Publications Authored or Co-Authored by "Fateen, Ekram M."

• PEX6 is expressed in photoreceptor cilia and mutated in deafblindness with enamel dysplasia and microcephaly

  Human Mutation, Volume 37, No. 2, Year 2016, Citations 39
• Outcome of enzyme replacement therapy in children with Gaucher disease: The Egyptian experience

  Egyptian Journal of Medical Human Genetics, Volume 12, No. 1, Year 2011, Citations 25
• Dyggve-Melchior-Clausen syndrome: Clinical, genetic, and radiological study of 15 Egyptian patients from nine unrelated families

  Journal of Children's Orthopaedics, Volume 3, No. 6, Year 2009, Citations 16
• A multicenter, open-label, phase III study of Abcertin in Gaucher disease

  Medicine (United States), Volume 96, No. 45, Article e8492, Year 2017, Citations 15
• Twenty- five years of biochemical diagnosis of Gaucher disease: the Egyptian experience

  Heliyon, Volume 5, No. 10, Article e02574, Year 2019, Citations 12