Mahmoud M Noureldeen

ORCID

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 7

Top Venues

Clinical genetics

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

Publications

Mohammed Almannai, Dana Marafi, Maha Saad Zaki, Reza Maroofian, Stephanie Efthymiou, Nebal Waill Saadi, Bilal Filimban, Hormos Salimi Dafsari, Fatima Rahman, Shazia Maqbool, Eissa Faqeih, Fuad Al Mutairi, Hind Alsharhan, Omar Abdelaty, Saadoun Bin-Hasan, Ruizhi Duan, Mahmoud M Noureldeen, Alaa Alqattan, Henry Houlden, Jill V Hunter, Jennifer E Posey, James R Lupski, Ayman W. El-Hattab
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder. Clinical genetics (2024)
Mohammed Almannai, Dana Marafi, Maha Saad Zaki, Reza Maroofian, Stephanie Efthymiou, Nebal Waill Saadi, Bilal Filimban, Hormos Salimi Dafsari, Fatima Rahman, Shazia Maqbool, Eissa Faqeih, Fuad Al Mutairi, Hind Alsharhan, Omar Abdelaty, Saadoun Bin-Hasan, Ruizhi Duan, Mahmoud M Noureldeen, Alaa Alqattan, Henry Houlden, Jill V Hunter, Jennifer E Posey, James R Lupski, Ayman W. El-Hattab
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder. Clinical genetics 105 (6) (2024)
Mohammed Almannai, Dana Marafi, Maha Saad Zaki, Reza Maroofian, Stephanie Efthymiou, Nebal Waill Saadi, Bilal Filimban, Hormos Salimi Dafsari, Fatima Rahman, Shazia Maqbool, Eissa Faqeih, Fuad Al Mutairi, Hind Alsharhan, Omar Abdelaty, Saadoun Bin-Hasan, Ruizhi Duan, Mahmoud M Noureldeen, Alaa Alqattan, Henry Houlden, Jill V Hunter, Jennifer E Posey, James R Lupski, Ayman W. El-Hattab
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder. Clinical genetics 105 (6) (2024)
Mohammed Almannai, Dana Marafi, Maha Saad Zaki, Reza Maroofian, Stephanie Efthymiou, Nebal Waill Saadi, Bilal Filimban, Hormos Salimi Dafsari, Fatima Rahman, Shazia Maqbool, Eissa Faqeih, Fuad Al Mutairi, Hind Alsharhan, Omar Abdelaty, Saadoun Bin-Hasan, Ruizhi Duan, Mahmoud M Noureldeen, Alaa Alqattan, Henry Houlden, Jill V Hunter, Jennifer E Posey, James R Lupski, Ayman W. El-Hattab
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder. Clinical genetics 105 (6) (2024)
Mohammed Almannai, Dana Marafi, Maha Saad Zaki, Reza Maroofian, Stephanie Efthymiou, Nebal Waill Saadi, Bilal Filimban, Hormos Salimi Dafsari, Fatima Rahman, Shazia Maqbool, Eissa Faqeih, Fuad Al Mutairi, Hind Alsharhan, Omar Abdelaty, Saadoun Bin-Hasan, Ruizhi Duan, Mahmoud M Noureldeen, Alaa Alqattan, Henry Houlden, Jill V Hunter, Jennifer E Posey, James R Lupski, Ayman W. El-Hattab
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder. Clinical genetics 105 (6) (2024)
Mohammed Almannai, Dana Marafi, Maha Saad Zaki, Reza Maroofian, Stephanie Efthymiou, Nebal Waill Saadi, Bilal Filimban, Hormos Salimi Dafsari, Fatima Rahman, Shazia Maqbool, Eissa Faqeih, Fuad Al Mutairi, Hind Alsharhan, Omar Abdelaty, Saadoun Bin-Hasan, Ruizhi Duan, Mahmoud M Noureldeen, Alaa Alqattan, Henry Houlden, Jill V Hunter, Jennifer E Posey, James R Lupski, Ayman W. El-Hattab
Expanding the phenotype of PPP1R21-related neurodevelopmental disorder. Clinical genetics 105 (6) (2024)
Maha Saad Zaki, Wessam E Sharaf-Eldin, Karima Rafat, Hasnaa M Elbendary, Mona Kamel, Nour Elkhateeb, Mahmoud M Noureldeen, Mohamed A Abdeltawab, Abdelrahim A Sadek, Mona L Essawi, Tracy Lau, David Murphy, Mohamed S Abdel-Hamid, Henry Holuden, Mahmoud Y Issa, Joseph G Gleeson
Clinical and molecular spectrum of a large Egyptian cohort with ALS2-related disorders of infantile-onset of clinical continuum IAHSP/JPLS. Clinical genetics (2023)

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Publication Activity (10 Years)

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Mahmoud M Noureldeen