Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Adeel G. Chaudhary"'
Autor:
Shatha Alharazy, Eman Alissa, Susan Lanham-New, Muhammad Imran Naseer, Adeel G. Chaudhary, M Denise Robertson
Publikováno v:
BMC Endocrine Disorders, Vol 21, Iss 1, Pp 1-10 (2021)
Abstract Background The relationship between vitamin D (VitD) and insulin sensitivity and secretion in type 2 diabetes mellitus (T2D) has been shown to be different amongst different ethnic populations. In Saudi Arabia, where both T2D and VitD defici
Externí odkaz:
https://doaj.org/article/bfddfdd69fd146cfa49800e19ce22ac1
Autor:
Shatha Alharazy, Muhammad Imran Naseer, Eman Alissa, Margaret Denise Robertson, Susan Lanham-New, Adeel G. Chaudhary
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
BackgroundNumerous research studies have found an association between vitamin D (vitD) status and single-nucleotide polymorphisms (SNPs) in genes involved in vitD metabolism. It is notable that the influence of these SNPs on 25-hydroxyvitamin D [25(O
Externí odkaz:
https://doaj.org/article/4a2842a2b004402e895beca2b0068522
Autor:
Asma A. Batarfi, Najlaa Filimban, Osama S. Bajouh, Ashraf Dallol, Adeel G. Chaudhary, Sherin Bakhashab
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-7 (2019)
Abstract Background Polycystic ovary syndrome (PCOS) is a common endocrine disorder causing infertility in reproductive-age women. The cause of PCOS is not fully understood but it is thought to be influenced by environmental and genetic factors. Obes
Externí odkaz:
https://doaj.org/article/19193c52d2ff45209c215dac9e0ffe69
Autor:
Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Osama Yousef Muthaffar, Sameera Sogaty, Hiba Alkhatabi, Sarah Almaghrabi, Adeel G. Chaudhary
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Autosomal recessive primary microcephaly (MCPH) is a neurodevelopmental defect that is characterized by reduced head circumference at birth along with non-progressive intellectual disability. Till date, 25 genes related to MCPH have been reported so
Externí odkaz:
https://doaj.org/article/6a65631b3f314ae18ee7a9b60daf7005
Autor:
Walaa F. Alsanie, Majid Alhomrani, Ahmed Gaber, Hamza Habeeballah, Heba A. Alkhatabi, Raed I. Felimban, Sherin Abdelrahman, Charlotte A. E. Hauser, Adeel G. Chaudhary, Abdulhakeem S. Alamri, Bassem M. Raafat, Abdulwahab Alamri, Sirajudheen Anwar, Khaled A. Alswat, Yusuf S. Althobaiti, Yousif A. Asiri
Publikováno v:
Cells, Vol 11, Iss 5, p 852 (2022)
Pregabalin is widely used as a treatment for multiple neurological disorders; however, it has been reported to have the potential for misuse. Due to a lack of safety studies in pregnancy, pregabalin is considered the last treatment option for various
Externí odkaz:
https://doaj.org/article/7fd0e3a0ad94482a83114eae6dacc38e
Autor:
Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Francisco J. Guzmán-Vega, Stefan T. Arold, Peter Natesan Pushparaj, Adeel G. Chaudhary, Mohammad H. AlQahtani
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Intellectual developmental disorder with dysmorphic facies and ptosis is an autosomal dominant condition characterized by delayed psychomotor development, intellectual disability, delayed speech, and dysmorphic facial features, mostly ptosis. Heteroz
Externí odkaz:
https://doaj.org/article/f57cfc2f8f7e42ee95dad64dd5c15fe5
Autor:
Muhammad Imran Naseer, Angham Abdulrahman Abdulkareem, Peter Natesan Pushparaj, Fehmida Bibi, Adeel G. Chaudhary
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Hereditary spastic paraplegias (HSPs) is a rare heterogeneous group of neurodegenerative diseases, with upper and lower limb spasticity motor neuron disintegration leading to paraplegias. NT5C2 gene (OMIM: 600417) encode a hydrolase enzyme 5'-nucleot
Externí odkaz:
https://doaj.org/article/45d69397197e481db89ce931fb539def
Autor:
Hans-Juergen Schulten, Mohammed Bangash, Sajjad Karim, Ashraf Dallol, Deema Hussein, Adnan Merdad, Fatma K. Al-Thoubaity, Jaudah Al-Maghrabi, Awatif Jamal, Fahad Al-Ghamdi, Hani Choudhry, Saleh S. Baeesa, Adeel G. Chaudhary, Mohammed H. Al-Qahtani
Publikováno v:
Journal of Translational Medicine, Vol 15, Iss 1, Pp 1-20 (2017)
Abstract Background Breast cancer brain metastases (BCBM) develop in about 20–30% of breast cancer (BC) patients. BCBM are associated with dismal prognosis not at least due to lack of valuable molecular therapeutic targets. The aim of the study was
Externí odkaz:
https://doaj.org/article/e86e8296aa2f4abca58df44680a0ab14
Autor:
Muhammad Imran Naseer, Mahmood Rasool, Sameera Sogaty, Rukhaa Adeel Chaudhary, Haifa Mansour Mansour, Adeel G. Chaudhary, Adel M. Abuzenadah, Mohammad H. Al-Qahtani
Publikováno v:
Annals of Saudi Medicine, Vol 37, Iss 2, Pp 148-153 (2017)
BACKGROUND: Primary microcephaly (MCPH) is a rare developmental defect characterized by impaired cognitive functions, retarded neurodevelopment and reduced brain size. It is genetically heterogeneous and more than 17 genes so far have been identified
Externí odkaz:
https://doaj.org/article/68fcde9db8c847658ba7baff514cdeaa
Autor:
Muhammad I. Naseer, Adeel G. Chaudhary, Mahmood Rasool, Gauthaman Kalamegam, Fai T. Ashgan, Mourad Assidi, Farid Ahmed, Shakeel A. Ansari, Syed Kashif Zaidi, Mohammed M. Jan, Mohammad H. Al-Qahtani
Publikováno v:
BMC Genomics, Vol 17, Iss S9, Pp 61-69 (2016)
Abstract Background Epilepsy is genetically complex but common brain disorder of the world affecting millions of people with almost of all age groups. Novel Copy number variations (CNVs) are considered as important reason for the numerous neurodevelo
Externí odkaz:
https://doaj.org/article/81f5e322f424411cb593722614e6b144