Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Nermine Salah"'
Autor:
Maha Mohamed Sayed, Nagia Aly Fahmy, Mahmoud Mamdouh Mohamed El Habiby, Nermine Salah Eldin Elsayed, Sara Mohamed Kamal Mohamed El Bukhari, Rehab Mohamed Naguib
Publikováno v:
Middle East Current Psychiatry, Vol 29, Iss 1, Pp 1-9 (2022)
Abstract Background Children with Duchenne muscular dystrophy report a higher rate of cognitive and psychiatric disorders relative to general population. This study will describe and compare the psychiatric and cognitive problems in DMD patients with
Externí odkaz:
https://doaj.org/article/a49b48a409ea4239b9b943aa18f7e0b5
Autor:
Azza M. Kamel, Marwa F. Mira, Gamal T. A. Ebid, Samar H. Kassem, Eman R. Radwan, Mona Mamdouh, Maha Amin, Nora Badawy, Hafez Bazaraa, Amani Ibrahim, Nermine Salah
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Abstract Background Type1 diabetes mellitus (T1DM) has a multi-factorial pathogenesis; the interplay between genetic susceptibility and environmental factors is thought to provide the fundamental element for the disease. Apart from HLA, more than 50
Externí odkaz:
https://doaj.org/article/4e645fbd4ccb41e58b52b77f83d8a1b1
Autor:
Azza M. Kamel, Marwa F. Mira, Ghada I. Mossallam, Gamal T.A. Ebid, Eman R. Radwan, Nelly H. Aly Eldin, Mona Mamdouh, Maha Amin, Nora Badawy, Hafez Bazaraa, Amani Ibrahim, Nermine Salah, John Hansen
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 1, Pp 25-30 (2014)
Background: Type 1 diabetes is one of the most common chronic childhood illnesses. Interplay between genetic susceptibility and environmental factors is thought to provide the fundamental element for the disease. Apart from the Major Histocompatibili
Externí odkaz:
https://doaj.org/article/8eca1d3f359049c88a610141adf094fc
Autor:
Amani S. Ibrahim, Samar H. Kassem, Mona Mamdouh, Eman R. Radwan, Hafez M. Bazaraa, Gamal T. A. Ebid, Nermine Salah, Marwa F Mira, Nora Badawy, Azza M. Kamel, Maha M. Amin
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 20, Iss 1, Pp 1-6 (2019)
Background Type1 diabetes mellitus (T1DM) has a multi-factorial pathogenesis; the interplay between genetic susceptibility and environmental factors is thought to provide the fundamental element for the disease. Apart from HLA, more than 50 genetic v
Autor:
Sayed, Maha Mohamed, Fahmy, Nagia Aly, El Habiby, Mahmoud Mamdouh Mohamed, Elsayed, Nermine Salah Eldin, El Bukhari, Sara Mohamed Kamal Mohamed, Naguib, Rehab Mohamed
Publikováno v:
Middle East Current Psychiatry; 10/6/2022, Vol. 29 Issue 1, p1-9, 9p
Autor:
Hanan M. Fouad, Ghada M. Anwar, Faten Ahmed Mahmoud, Amal Abd El-Hamid, Nermine Salah, Noha Musa, Hala M. Lotfi
Publikováno v:
European Journal of Medical Genetics. 58:31-34
Background/Aims An association of type 1 DM and familial Mediterranean fever (FMF) has been newly reported in the medical literature. The aim of the present work was to investigate frequency of MEFV gene mutations in Egyptian children with type 1 dia
Autor:
Amani S. Ibrahim, Gamal T. A. Ebid, Azza M. Kamel, Maha M. Amin, Nora Badawy, Eman R. Radwan, Nelly H. Aly El-Din, Mona Mamdouh, Hafez M. Bazaraa, John A. Hansen, Marwa F Mira, Nermine Salah, Ghada I. Mossallam
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 15, Iss 1, Pp 25-30 (2014)
Background: Type 1 diabetes is one of the most common chronic childhood illnesses. Interplay between genetic susceptibility and environmental factors is thought to provide the fundamental element for the disease. Apart from the Major Histocompatibili
Autor:
Jing Tian, Bruno Reversade, Mona Aglan, Gamal Ahmed Hosny, Mustafa Herdem, Bernd Wollnik, Khalda Amr, Mohammad Shboul, A. Kemal Topaloglu, Tarek H. El-Badry, Nermine Salah Eldin, Samia A. Temtamy, Junxian Ong
Publikováno v:
Middle East Journal of Medical Genetics. 1:64-70
Autor:
Pierre Bougnères, Michel Goossens, Cécile Teinturier, Jean-Louis Chaussain, Mona Hafez, Philippe Duquesnoy, Serge Amselem, Florence Dastot, Anne Roy, Nermine Salah, Irene Netchine, Valère Cacheux, Isis Ghali
Publikováno v:
FEBS Letters. 437:216-220
Prop-1 is a newly isolated pituitary-specific paired-like homeodomain transcription factor whose cDNA sequence is well known in mouse. To study its involvement in human combined pituitary hormone deficiency (CPHD), we have isolated the human cDNA ort
Autor:
Temtamy, Samia, Aglan, Mona, Topaloglu, A. Kemal, Wollnik, Bernd, Amr, Khalda, El-Badry, Tarek H., Hosny, Gamal A., Eldin, Nermine Salah, Shboul, Mohammad, Herdem, Mustafa, Ong, Junxian, Reversade, Bruno, Tian, Jing
Publikováno v:
Middle East Journal of Medical Genetics; Jul2012, Vol. 1 Issue 2, p64-70, 7p