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	1.	Pyloric stenosis in a boy with non-ketotic hyperglycinaemia. [electronic resource] by al-Essa, M Ozand, P T Producer: 19990528 In: Journal of inherited metabolic disease vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	[Genetic encephalopathies in a newborn]. [electronic resource] by Chaves-Carballo, E al-Essa, M A Producer: 20000614 In: Revista de neurologia vol. 29 Availability: No items available. Save to lists Add to cart (remove)
	3.	Anticipation in a family with autosomal dominant spinocerebellar ataxia. [electronic resource] by Al-Essa, M Dabbagh, O Ozand, P T Producer: 20121002 In: Annals of Saudi medicine vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Retinopathy of prematurity in infants with birth weight above 1500 grams. [electronic resource] by Al-Essa, M Rashwan, N Al-Ajmi, M Producer: 20030815 In: East African medical journal vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	3-Hydroxy-3-methylglutaryl-CoA lyase deficiency in a boy with VATER association. [electronic resource] by al-Essa, M Rashed, M Ozand, P T Producer: 19981130 In: Journal of inherited metabolic disease vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Tyrosinemia type II: Report of the first four cases in Saudi Arabia. [electronic resource] by Al-Essa, M Rashed, M Ozand, P T Producer: 20121002 In: Annals of Saudi medicine vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Saudi experience with classic homocystinuria. [electronic resource] by Al-Essa, M Rashed, M Ozand, P T Producer: 20121002 In: Annals of Saudi medicine vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Threshold stage of retinopathy of prematurity: maternal and neonatal risk factors. [electronic resource] by Al-Essa, M Azad, R V Rashwan, N Producer: 20070517 In: Annals of Saudi medicine vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	2-[fluorine-18] fluoro-2-deoxy-D-glucose PET scan of the brain in maple syrup urine disease. [electronic resource] by al-Essa, M al-Hussein, K Ozand, P T Producer: 19991026 In: Clinical nuclear medicine vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Hyperpipecolic acidemia: clinical, biochemical, and radiologic observations. [electronic resource] by Al-Essa, M A Chaves-Carballo, E Ozand, P T Producer: 20000104 In: Pediatric neurology vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Classic homocystinuria: clinical, biochemical and radiological observations, and therapeutic outcome of 24 Saudi patients. [electronic resource] by al-Essa, M A Rashed, M S Ozand, P T Producer: 20020417 In: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	12.	Parental awareness of liver disease among children in Saudi Arabia. [electronic resource] by Al-Essa, M A Al-Mehaidib, A Al-Gain, S Producer: 20121002 In: Annals of Saudi medicine vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Lipoprotein A profiles in Arab newborns. [electronic resource] by Alsaeid, M al-Essa, M Alsaeid, K Sharma, P N Producer: 19990422 In: Pediatrics international : official journal of the Japan Pediatric Society vol. 41 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Awareness of inborn errors of metabolism among parents in Saudi Arabia. [electronic resource] by Al Essa, M Ozand, P T Al-Gain, S I Producer: 20121002 In: Annals of Saudi medicine vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Tyrosinaemia type II: an easily diagnosed metabolic disorder with a rewarding therapeutic response. [electronic resource] by al-Essa, M A Rashed, M S Ozand, P T Producer: 20020417 In: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	16.	Impaired DNA synthesis in dermal fibroblasts from Zellweger syndrome patients. [electronic resource] by Dhaunsi, G S Rahbeeni, Z al-Essa, M Ozand, P T Producer: 19980611 In: Journal of inherited metabolic disease vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Biotinidase deficiency: a treatable genetic disorder in the Saudi population. [electronic resource] by Joshi, S al-Essa, M A Archibald, A Ozand, P T Producer: 20020417 In: Eastern Mediterranean health journal = La revue de sante de la Mediterranee orientale = al-Majallah al-sihhiyah li-sharq al-mutawassit vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	18.	Comparing REM- and NREM-Related Obstructive Sleep Apnea in Jordan: A Cross-Sectional Study. [electronic resource] by Al Oweidat, K AlRyalat, S A Al-Essa, M Obeidat, N Producer: 20190403 In: Canadian respiratory journal vol. 2018 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	Novel mutations in children with profound biotinidase deficiency from Saudi Arabia. [electronic resource] by Pomponio, R J Ozand, P T Al Essa, M Wolf, B Producer: 20000725 In: Journal of inherited metabolic disease vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Angiotensin-converting enzyme gene insertion/deletion polymorphism in Kuwaiti children with retinopathy of prematurity. [electronic resource] by Haider, M Z Devarajan, L V Al-Essa, M Kumar, H Producer: 20030318 In: Biology of the neonate vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 57 results.