Čájehuvvojit 1 - 20 oktiibuot 22 bohtosis ohcui Fuad Al Mutairi', ohcanáigi: 0,08s
Aiddostahte ozu
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1
Hyperhomocysteinemia: Clinical Insights Dahkki Fuad Al Mutairi
Almmustuhtton 2020-10-01
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2
Heterozygous mutation in SLC36A2 gene causing hyperglycinuria and nephrolithiasis Dahkki Maha Al Harbi, Fuad Al Mutairi
Almmustuhtton 2019-06-01
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3
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Dilated cardiomyopathy in a child with truncating mutation in NRAP gene Dahkki Hind Abdelrahman Ahmed, Saleh Al-ghamdi, Fuad Al Mutairi
Almmustuhtton 2018-12-01
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5
Continuous supernumerary teeth development in cleidocranial dysplasia post-surgical extraction – A novel case report Dahkki Faisal Joueidi, Ahmad Joueidi, Yanal Nusair, Fuad Al Mutairi, Samar Al Hayek
Almmustuhtton 2023-12-01
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Outcomes of cases with elevated 3-hydroxyisovaleryl carnitine report from the newborn screening program Dahkki Fuad Al Mutairi, Randa Alkhalaf, Abdul Rafiq Khan, Ali Al Othaim, Majid Alfadhel
Almmustuhtton 2024-12-01
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8
Coexistence of atopic dermatitis and thrombocytosis: diagnostic odyssey: a case report Dahkki Fuad Al Mutairi, Meshal Alberreet, Lara Alkuhaimi, Khalid Aleisa, Rana Almana, Asma Awadalla
Almmustuhtton 2023-06-01
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9
HMG-CoA Lyase Deficiency: A Retrospective Study of 62 Saudi Patients Dahkki Majid Alfadhel, Majid Alfadhel, Basma Abadel, Hind Almaghthawi, Muhammad Umair, Zuhair Rahbeeni, Eissa Faqeih, Mohammed Almannai, Ali Alasmari, Mohammed Saleh, Wafaa Eyaid, Wafaa Eyaid, Ahmed Alfares, Ahmed Alfares, Fuad Al Mutairi, Fuad Al Mutairi
Almmustuhtton 2022-05-01
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10
The phenotypic spectrum of dihydrolipoamide dehydrogenase deficiency in Saudi Arabia Dahkki Anar Alfarsi, Majid Alfadhel, Seham Alameer, Amal Alhashem, Brahim Tabarki, Faroug Ababneh, Ahmed Al Fares, Fuad Al Mutairi
Almmustuhtton 2021-12-01
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11
Genetic carrier screening for disorders included in newborn screening in the Saudi population Dahkki Mariam Al Eissa, Taghrid Aloraini, Lamia Alsubaie, Abdulrahman Alswaid, Wafaa Eyiad, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, Ahmed Alfares
Almmustuhtton 2021-12-01
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12
Novel mutation of the FHL1 gene associated with congenital myopathy and early respiratory muscles involvement: a case report Dahkki Rana Almutairi, Sara Alrashidi, Muhammed Umair, Maha Alshalan, Lamia Alsubaie, Taghrid Aloraini, Ahmed Al Ahmad, Ahmed Alfares, Fuad Al Mutairi
Almmustuhtton 2020-06-01
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13
Genetic impact of non-consanguineous marriages in Saudi Arabia. Dahkki Mohammed Alyahya, Taghrid Aloraini, Youseef Al-Harbi, Lamia Alsubaie, Abdulrahman Alswaid, Wafaa Eyaid, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, Ahmed Alfares
Almmustuhtton 2022-12-01
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14
Supplementary testing after negative or inconclusive exome sequencing results Dahkki Balsam AlMaarik, Taghrid Aloraini, Roselyn Paclejan, Mohammed Balwi, Lamia Alsubaie, Abdulrahman Alswaid, Wafaa Eyiad, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, Ahmed A. Alfares
Almmustuhtton 2023-06-01
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15
Biallelic HMGXB4 loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features Dahkki Fuad Al Mutairi, Faisal Joueidi, Maha Alshalan, Essra Aloyouni, Mariam Ballow, Mohammed Aldrees, Abdulkareem Al Abdulrahman, Abeer Al Tuwaijri, Safdar Abbas, Muhammad Umair, Majid Alfadhel
Almmustuhtton 2024-08-01
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16
Common disease-associated gene variants in a Saudi Arabian population Dahkki Mariam Aleissa, Taghrid Aloraini, Lamia Fahad Alsubaie, Madawi Hassoun, Ghada Abdulrahman, Abdulrahman Swaid, Wafa Al Eyaid, Fuad Al Mutairi, Faroug Ababneh, Majid Alfadhel, Ahmed Alfares
Almmustuhtton 2022-01-01
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17
Homozygous truncating NEK10 mutation, associated with primary ciliary dyskinesia: a case report Dahkki Fuad Al Mutairi, Randa Alkhalaf, Abdullah Alkhorayyef, Fayhan Alroqi, Alyafee Yusra, Muhammad Umair, Fetaini Nouf, Amjad Khan, Alharbi Meshael, Aleidi Hamad, Alaujan Monira, Abdulaziz Asiri, Kheloud M. Alhamoudi, Majid Alfadhel
Almmustuhtton 2020-05-01
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18
Evaluation of long-term effectiveness of the use of carglumic acid in patients with propionic acidemia (PA) or methylmalonic acidemia (MMA): study protocol for a randomized control... Dahkki Marwan Nashabat, Abdulrahman Obaid, Fuad Al Mutairi, Mohammed Saleh, Mohammed Elamin, Hind Ahmed, Faroug Ababneh, Wafaa Eyaid, Abdulrahman Alswaid, Lina Alohali, Eissa Faqeih, Majed Aljeraisy, Mohamed A. Hussein, Ali Alasmari, Majid Alfadhel
Almmustuhtton 2019-06-01
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19
Long-term effectiveness of carglumic acid in patients with propionic acidemia (PA) and methylmalonic acidemia (MMA): a randomized clinical trial Dahkki Majid Alfadhel, Marwan Nashabat, Mohammed Saleh, Mohammed Elamin, Ahmed Alfares, Ali Al Othaim, Muhammad Umair, Hind Ahmed, Faroug Ababneh, Fuad Al Mutairi, Wafaa Eyaid, Abdulrahman Alswaid, Lina Alohali, Eissa Faqeih, Mohammed Almannai, Majed Aljeraisy, Bayan Albdah, Mohamed A. Hussein, Zuhair Rahbeeni, Ali Alasmari
Almmustuhtton 2021-10-01
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20
The Leukodystrophy Spectrum in Saudi Arabia: Epidemiological, Clinical, Radiological, and Genetic Data Dahkki Majid Alfadhel, Majid Alfadhel, Majid Alfadhel, Mohammed Almuqbil, Mohammed Almuqbil, Fuad Al Mutairi, Fuad Al Mutairi, Muhammad Umair, Mohammed Almannai, Malak Alghamdi, Hamad Althiyab, Rayyan Albarakati, Fahad A. Bashiri, Walaa Alshuaibi, Duaa Ba-Armah, Duaa Ba-Armah, Mohammed A. Saleh, Ali Al-Asmari, Eissa Faqeih, Waleed Altuwaijri, Waleed Altuwaijri, Ahmed Al-Rumayyan, Ahmed Al-Rumayyan, Mohammed Ali Balwi, Mohammed Ali Balwi, Faroug Ababneh, Abdulrahman Faiz Alswaid, Abdulrahman Faiz Alswaid, Wafaa M. Eyaid, Wafaa M. Eyaid, Naif A. M. Almontashiri, Naif A. M. Almontashiri, Amal Alhashem, Amal Alhashem, Khalid Hundallah, Aida Bertoli-Avella, Peter Bauer, Christian Beetz, Muhammad Talal Alrifai, Muhammad Talal Alrifai, Ahmed Alfares, Ahmed Alfares, Brahim Tabarki
Almmustuhtton 2021-05-01
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