Výsledky vyhledávání - "Alorainy Ibrahim"

Akademický článek

Pictorial Essay: Infants of diabetic mothers

Autor: Alorainy Ibrahim, Barlas Nauman, Al-Boukai Amer

Publikováno v: Indian Journal of Radiology and Imaging, Vol 20, Iss 3, Pp 174-181 (2010)

About 3 to 10% of pregnancies are complicated by glycemic control abnormalities. Maternal diabetes results in significantly greater risk for antenatal, perinatal, and neonatal morbidity and mortality, as well as congenital malformations. The number o

Externí odkaz: https://doaj.org/article/70d6351dea5445acb7bdd43be625f300

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Akademický článek

Attitude towards MRI safety during pregnancy

Autor: Alorainy Ibrahim, Albadr Fahad, Abujamea Abdullah

Publikováno v: Annals of Saudi Medicine, Vol 26, Iss 4, Pp 306-309 (2006)

Externí odkaz: https://doaj.org/article/d7d30c81a2bf4c05ad3877ebbaebb338

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Akademický článek

Pattern of congenital brain malformations at a referral hospital in Saudi Arabia : An MRI study

Autor: Alorainy Ibrahim

Publikováno v: Annals of Saudi Medicine, Vol 26, Iss 1, Pp 28-37 (2006)

Background: More than 2000 different congenital cerebral malformations have been described in the literature, for which several classification systems have been proposed. With the help of these classification systems, it is now possible, with neuroim

Externí odkaz: https://doaj.org/article/d32fbd185fe941d8b614167549b564d6

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Akademický článek

A novel syndrome of lethal familial hyperekplexia associated with brain malformation

Autor: Seidahmed Mohammed, Salih Mustafa A, Abdulbasit Omer B, Shaheed Meeralebbae, Al Hussein Khalid, Miqdad Abeer M, Al Rasheed Abdullah K, Alazami Anas M, Alorainy Ibrahim A, Alkuraya Fowzan S

Publikováno v: BMC Neurology, Vol 12, Iss 1, p 125 (2012)

Abstract Background Hyperekplexia (HPX) is a rare non-epileptic disorder manifesting immediately after birth with exaggerated persistent startle reaction to unexpected auditory, somatosensory and visual stimuli, and non-habituating generalized flexor

Externí odkaz: https://doaj.org/article/34aaba7ffc234162b9b3d83627678e7b

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Akademický článek

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

Autor: Al-Fakey Yasser H, Van Maldergem Lionel, McGrath John A, Liu Lu, Alorainy Ibrahim A, Alrasheed Saleh, Abu-Amero Khaled K, Salih Mustafa A, AlSuhaibani Adel H, Oystreck Darren T, Bosley Thomas M

Publikováno v: BMC Medical Genetics, Vol 12, Iss 1, p 31 (2011)

Abstract Background Lipoid proteinosis is a rare autosomal recessive disease characterized by cutaneous and mucosal lesions and hoarseness appearing in early childhood. It is caused by homozygous or compound heterozygous mutations in the ECM1 gene. T

Externí odkaz: https://doaj.org/article/67c1e507338140d2a5d1c152bdbde22d

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