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	1.	Molecular analysis of Turkish mucopolysaccharidosis IVA (Morquio A) patients: identification of novel mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene. [electronic resource] by Terzioglu, Mugen Tokatli, Aysegul Coskun, Turgay Emre, Serap Producer: 20021223 In: Human mutation vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Lipid Droplets in Health and Disease. [electronic resource] by Onal, Gizem Kutlu, Ozlem Gozuacik, Devrim Dokmeci Emre, Serap Producer: 20180430 In: Lipids in health and disease vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Molecular analysis of Turkish Gaucher disease patients: identification of novel mutations in glucocerebrosidase (GBA) gene. [electronic resource] by Emre, Serap Gürakan, Figen Yüce, Aysel Rolf, Arnold Scott, Ronald Ozen, Hasan Producer: 20081014 In: European journal of medical genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Chanarin-Dorfman syndrome: Genotype-Phenotype Correlation. [electronic resource] by Nur, Banu Guzel Gencpinar, Pinar Yuzbasıoglu, Ayse Emre, Serap Dokmeci Mihci, Ercan Producer: 20160128 In: European journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Multiple endocrine neoplasia type 2b associated with lichen nitidus. [electronic resource] by Altaykan, Asli Ersoy-Evans, Sibel Emre, Serap Orhan, Diclehan Güçer, Safak Erkin, Gül Producer: 20071119 In: European journal of dermatology : EJD vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Impairment of lipophagy by PNPLA1 mutations causes lipid droplet accumulation in primary fibroblasts of Autosomal Recessive Congenital Ichthyosis patients. [electronic resource] by Onal, Gizem Kutlu, Ozlem Ozer, Ebru Gozuacik, Devrim Karaduman, Aysen Dokmeci Emre, Serap Producer: 20190826 In: Journal of dermatological science vol. 93 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Biochemical and molecular analysis of mucopolysaccharidoses in Turkey. [electronic resource] by Emre, Serap Terzioğlu, Mügen Coşkun, Turgay Tokath, Ayşegül Ozalp, Imran Müller, Vivien Hopwood, John Producer: 20020306 In: The Turkish journal of pediatrics vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	8.	Outcome of enzyme replacement therapy in Turkish patients with Gaucher disease: does late intervention affect the response? [electronic resource] by Arikan-Ayyildiz, Zeynep Yüce, Aysel Emre, Serap Baysoy, Gökhan Saltik-Temizel, Inci Nur Gürakan, Figen Producer: 20120216 In: The Turkish journal of pediatrics vol. 53 Availability: No items available. Save to lists Add to cart (remove)
	9.	Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B. [electronic resource] by Emre, Serap Terzioglu, Mugen Tokatli, Aysegul Coskun, Turgay Ozalp, Imran Weber, Birgit Hopwood, John J Producer: 20020305 In: Human mutation vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. [electronic resource] by Emre, Serap Unver, Neşe Evans, Sibel Ersoy Yüzbaşioğlu, Ayşe Gürakan, Figen Gümrük, Fatma Karaduman, Ayşen Producer: 20101012 In: European journal of medical genetics vol. 53 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Application of Fourier transform infrared spectroscopy to biomolecular profiling of cultured fibroblast cells from Gaucher disease patients: A preliminary investigation. [electronic resource] by Igci, Nasit Sharafi, Parisa Demiralp, Duygu Ozel Demiralp, Cemil Ozerk Yuce, Aysel Emre, Serap Dokmeci Producer: 20180313 In: Advances in clinical and experimental medicine : official organ Wroclaw Medical University vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Identification of two novel PNPLA1 mutations in Turkish families with autosomal recessive congenital ichthyosis. [electronic resource] by Dökmeci-Emre, Serap Taşkıran, Zihni Ekim Yüzbaşıoğlu, Ayşe Önal, Gizem Akarsu, Ayşe Nurten Karaduman, Ayşen Özgüç, Meral Producer: 20181219 In: The Turkish journal of pediatrics vol. 59 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1. [electronic resource] by Jobard, Florence Lefèvre, Caroline Karaduman, Aysen Blanchet-Bardon, Claudine Emre, Serap Weissenbach, Jean Ozgüc, Meral Lathrop, Mark Prud'homme, Jean-François Fischer, Judith Producer: 20020319 In: Human molecular genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. [electronic resource] by Lesueur, Fabienne Bouadjar, Bakar Lefèvre, Caroline Jobard, Florence Audebert, Stéphanie Lakhdar, Hakima Martin, Ludovic Tadini, Gianluca Karaduman, Aysen Emre, Serap Saker, Safa Lathrop, Mark Fischer, Judith Producer: 20070405 In: The Journal of investigative dermatology vol. 127 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)