Zobrazeno 1 - 10
of 48
pro vyhledávání: '"Ali Al-Mehaidib"'
Autor:
Khalid AlSaleem, Ali Al-Mehaidib, Mohammed Banemai, Ibrahim bin-Hussain, Mousa Faqih, Ahmed Al Mehmadi
Publikováno v:
Annals of Saudi Medicine, Vol 33, Iss 5, Pp 500-504 (2013)
Gastrointestinal basidiobolomycosis (GIB) is an unusual fungal infection that manifests in the skin and rarely involves other systems. All of the few cases of GIB reported so far were diagnosed with difficulty, necessitating laparotomy and resection
Externí odkaz:
https://doaj.org/article/6068fb92d90045bcad31c29c6786aac4
Autor:
Wael A. Bahbah, Mostafa ElHodhod, Mohamed Salah, Fawaz AlRefaee, Muath AlTuraiki, Samira Mousa, Ali Al Mehaidib, Wafaa Helmi Ayesh, Ahmed N. El-Bazzar, Joseph El Haddad, Heba Y. El Khashab, Amr El Zawahry, Mohammed Hasosah, Sanaa Youssef Shaaban, Yvan Vandenplas
Publikováno v:
Nutrients, Vol 14, Iss 5, p 1067 (2022)
Background: Cow’s milk allergy (CMA) and cow’s milk intolerance (CMI) are the major cow’s milk disorders observed in infants and young children. This study investigates, for the first time, physician knowledge regarding CMA and CMI prevalence,
Externí odkaz:
https://doaj.org/article/9abbb10025e447d9b8bec199edffb70f
Autor:
Omar I. Saadah, Mohammad El Mouzan, Mohammad Al Mofarreh, Ali Al Mehaidib, Mohammad Al Edreesi, Mohammed Hasosah, Abdulrahman Al-Hussaini, Khalid AlSaleem
Publikováno v:
Gastroenterology Research and Practice, Vol 2016 (2016)
Background and Aims. Crohn’s disease (CD) is an evolving disease in KSA. Little is known about its characteristics in the Saudi population. The aims of this study were to describe the characteristics of Saudi children with CD and to determine wheth
Externí odkaz:
https://doaj.org/article/b4027237e6c5460aa82f376c975cb7f5
Autor:
Khaled Al Saraf, Suleiman Al-Hammadi, Mehdi Adeli, Ahmed Hussein, Ali Al-Mehaidib, Hasan M Isa, Hala El Feghali, Maroun Sokhn, Mortada El-Shabrawi, Ebtsam Mohammed AlBassam, Ahmed AlBadi, Moustafa Abdel Aziz El-Hodhod, Basil Nasrallah, Pierre Hage, Najwa Mohammed Mousa Al-Sawi
Publikováno v:
World Journal of Pediatrics
Background This study aimed to develop an expert consensus regarding the epidemiology, diagnosis, and management of cow’s milk protein allergy (CMPA) in the Middle East. Methods A three-step modified Delphi method was utilized to develop the consen
Publikováno v:
Inflammatory bowel diseases. 27(5)
Autor:
Dorota Monies, Fowzan S. Alkuraya, Yousef Binamer, Zinab A. Sawan, Ali Al-Mehaidib, Mohammed Abanemai, Khalid Alsaleem, Wajeeh Aldekhail
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f058bea16904f2a5a139c798dc244346
https://doi.org/10.1111/cge.13919/v3/response1
https://doi.org/10.1111/cge.13919/v3/response1
Autor:
Yousef Binamer, Zinab A. Sawan, Khalid Alsaleem, Ali Al-Mehaidib, Mohammed Abanemai, Dorota Monies, Wajeeh Aldekhail, Fowzan S. Alkuraya
Publikováno v:
Clinical geneticsREFERENCES. 99(4)
We describe an 11-year-old girl with PLACK Syndrome (peeling skin, leukonychia, acral punctate keratosis, cheilitis, and knuckle pads), who was found to have a novel homozygous variant in CAST, the pathogenicity of which was confirmed using blood-der
Autor:
Hamdy Mulia, Ali Al Mehaidib, Mohammed Abanemai, Khalid Al Saleem, Haifa Al Awadhi, Wajeeh Al Dekhail
Publikováno v:
International Journal of Pediatrics & Adolescent Medicine
International Journal of Pediatrics and Adolescent Medicine, Vol 5, Iss 1, Pp 31-33 (2018)
International Journal of Pediatrics and Adolescent Medicine, Vol 5, Iss 1, Pp 31-33 (2018)
Aluminum toxicity affecting bone mineral density is a known complication of long-term parentral nutrition. In this report, we describe a similar patient who suffered from bone disease and had a favorable response to chelation therapy using deferoxami
Autor:
Manal Mohammed, Khalid Alsaleem, Ali Al-Mehaidib, Yasir Al-Suyufi, Mohammed Banemai, Wajeeh Aldekhail, Khushnooda Ramzan, Faiqa Imtiaz, Rabab Allam, Amani Jambi, Abdulhakim Almuhandes
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 66:250-252
Congenital glucose-galactose malabsorption (cGGM) is a rare autosomal recessive disorder, caused by mutations in the SLC5A1 gene, encoding the sodium/glucose cotransporter 1, which may result in severe life-threatening osmotic diarrhea due to the acc
Autor:
Ghassan A Sukkar, Mohammed Hasosah, Ahmed Matrafi, Wasil Jastaniah, Mohamed B Satti, Ali Al-Mehaidib, Ashraf F Alsahafi
Publikováno v:
Inflammatory Bowel Diseases. 22:E34-E37