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	1.	Idursulfatase therapy in mucopolysaccharidosis type II: after 2.5 years of treatment--no benefit for older patients with multisystem involvement. [electronic resource] by Gucev, Zoran S Tasic, Velibor Producer: 20120705 In: Pediatric neurology vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Greenberg dysplasia (hydrops-ectopic calcification-moth-eaten skeletal dysplasia): prenatal ultrasound diagnosis and review of literature. [electronic resource] by Trajkovski, Zoran Vrcakovski, Miodrag Saveski, Jordan Gucev, Zoran S Producer: 20030210 In: American journal of medical genetics vol. 111 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	The degree of H19 hypomethylation in children with Silver-Russel syndrome (SRS) is not associated with the severity of phenotype and the clinical severity score (CSS). [electronic resource] by Gucev, Zoran S Saranac, Ljiljana Jancevska, Aleksandra Tasic, Velibor Producer: 20160408 In: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki) vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	4.	A case of Silver-Russell syndrome (SRS): multiple pituitary hormone deficiency, lack of H19 hypomethylation and favourable growth hormone (GH) treatment response. [electronic resource] by Gucev, Zoran S Tasic, Velibor Jancevska, Aleksandra Kirovski, Ilija Producer: 20091109 In: Journal of genetics vol. 88 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Papillorenal syndrome after Beta-interferon treatment in pregnancy. [electronic resource] by Gucev, Zoran S Kirovski, Ilija Jancevska, Aleksandra Popjordanova, Nada Tasic, Velibor Producer: 20100118 In: Renal failure vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Distinguishing deficiencies in the steroidogenic acute regulatory protein and the cholesterol side chain cleavage enzyme causing neonatal adrenal failure. [electronic resource] by Gucev, Zoran S Tee, Meng Kian Chitayat, David Wherrett, Diane K Miller, Walter L Producer: 20130516 In: The Journal of pediatrics vol. 162 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Arthrogryposis multiplex congenital (AMC) in a three year old boy: differential diagnosis with distal arthrogryposis: a case report. [electronic resource] by Gucev, Zoran S Pop-Jordanova, Nada Dumalovska, Gordana Stomnaroska, Orhideja Zafirovski, Gorgji Tasic, Velibor B Producer: 20110714 In: Cases journal vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Congenital lipomatous overgrowth, vascular malformations, and epidermal nevi (CLOVE) syndrome: CNS malformations and seizures may be a component of this disorder. [electronic resource] by Gucev, Zoran S Tasic, Velibor Jancevska, Aleksandra Konstantinova, Marina Krstevska Pop-Jordanova, Nada Trajkovski, Zoran Biesecker, Leslie G Producer: 20081112 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Mutational analysis of TAC and TACR3 in idiopathic central precocious puberty. [electronic resource] by Krstevska-Konstantinova, Marina Tasic, Velibor B Montenegro, Luciana Ribeiro Dervisov, Donco Beneduzzi, Daiane Gontijo Silveira, Leticia F Gucev, Zoran S Producer: 20160324 In: Prilozi (Makedonska akademija na naukite i umetnostite. Oddelenie za medicinski nauki) vol. 35 Availability: No items available. Save to lists Add to cart (remove)
	10.	Mutational analysis of KISS1 and KISS1R in idiopathic central precocious puberty. [electronic resource] by Krstevska-Konstantinova, Marina Jovanovska, Jana Tasic, Velibor B Montenegro, Luciana Ribeiro Beneduzzi, Daiane Silveira, Leticia F G Gucev, Zoran S Producer: 20160728 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Childhood craniopharyngioma in Macedonia: incidence and outcome after subtotal resection and cranial irradiation. [electronic resource] by Gucev, Zoran S Danilovski, Dragan Tasic, Velibor Ugrinovski, Jovica Nastova, Vesna Jancevska, Aleksandra Krstevska-Konstantinova, Marina Pop-Jordanova, Nada Kirovski, Ilija Producer: 20110513 In: World journal of pediatrics : WJP vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Autosomal dominant spondylocostal dysostosis in three generations of a Macedonian family: Negative mutation analysis of DLL3, MESP2, HES7, and LFNG. [electronic resource] by Gucev, Zoran S Tasic, Velibor Pop-Jordanova, Nada Sparrow, Duncan B Dunwoodie, Sally L Ellard, Sian Young, Elizabeth Turnpenny, Peter D Producer: 20100830 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Novel beta-galactosidase gene mutation p.W273R in a woman with mucopolysaccharidosis type IVB (Morquio B) and lack of response to in vitro chaperone treatment of her skin fibroblasts. [electronic resource] by Gucev, Zoran S Tasic, Velibor Jancevska, Aleksandra Zafirovski, Georgi Kremensky, Ivo Sinigerska, Ivanka Nanba, Eiji Higaki, Katsumi Gucev, Filip Suzuki, Yoshiyuki Producer: 20080820 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Autosomal dominant spondylocostal dysostosis is caused by mutation in TBX6. [electronic resource] by Sparrow, Duncan B McInerney-Leo, Aideen Gucev, Zoran S Gardiner, Brooke Marshall, Mhairi Leo, Paul J Chapman, Deborah L Tasic, Velibor Shishko, Abduhadi Brown, Matthew A Duncan, Emma L Dunwoodie, Sally L Producer: 20130903 In: Human molecular genetics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis. [electronic resource] by Halbritter, Jan Baum, Michelle Hynes, Ann Marie Rice, Sarah J Thwaites, David T Gucev, Zoran S Fisher, Brittany Spaneas, Leslie Porath, Jonathan D Braun, Daniela A Wassner, Ari J Nelson, Caleb P Tasic, Velibor Sayer, John A Hildebrandt, Friedhelm Producer: 20150428 In: Journal of the American Society of Nephrology : JASN vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)