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Turgay Coskun

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Turkey

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TOP 3
Sahin Takci; Sule Yigit; Turgay Coskun; Sibel Kadayifcilar; Burcu Hismi
A rare galactosemia complication: vitreous hemorrhage.
M Kilic; Turgay Coskun; A Dursun; Figen Gürakan; S Schmitt; H S Sivri; M Taskesen; Aysegul Tokatli; S Küry
A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene.
Rezan Topaloglu; Lambert van den Heuvel; Thierry Vilboux; Aysin Bakkaloglu; Nesrin Besbas; Turgay Coskun; Meral Gunay-Aygun; Robert Kleta; Fatih Ozaltin; Brad Tinloy; William A Gahl
Genetic basis of cystinosis in Turkish patients: a single-center experience.

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All Publications

2012: Sahin Takci; Sule Yigit; Turgay Coskun; Sibel Kadayifcilar; Burcu Hismi
A rare galactosemia complication: vitreous hemorrhage.
JIMD reports 2012;5():89-93.
2012: M Kilic; Turgay Coskun; A Dursun; Figen Gürakan; S Schmitt; H S Sivri; M Taskesen; Aysegul Tokatli; S Küry
A Zinc Sulphate-Resistant Acrodermatitis Enteropathica Patient with a Novel Mutation in SLC39A4 Gene.
JIMD reports 2012;2():25-8.
2012: Rezan Topaloglu; Lambert van den Heuvel; Thierry Vilboux; Aysin Bakkaloglu; Nesrin Besbas; Turgay Coskun; Meral Gunay-Aygun; Robert Kleta; Fatih Ozaltin; Brad Tinloy; William A Gahl
Genetic basis of cystinosis in Turkish patients: a single-center experience.
Pediatric nephrology (Berlin, Germany) 2012;27(1):115-21.
2009: Göknur Haliloglu; Kader Karli Oguz; J O Sass; C M Temucin; A Celiker; Turgay Coskun; Judith Fischer; Meral Topcu
Peripheral neuropathy in a patient with D-2-hydroxyglutaric aciduria.
Journal of inherited metabolic disease 2009;32 Suppl 1():S21-5.
2009: Sultan Durmus Aydogdu; Birgul Kirel; Turgay Coskun; Suna Kose
Prevalence of cystinuria among elementary schoolchildren in Eskisehir, Turkey.
Scandinavian journal of urology and nephrology 2009;43(2):138-41.
2008: Baris Kuskonmaz; Sule Unal; Emine Cördükcü; Halil Aydin; Turgay Coskun; Aytemiz Gurgey; Fatma Gumruk
Lymphocytic vacuolization in sialic acid storage disease.
American journal of hematology 2008;83(10):821.
2008: Göknur Haliloglu; Florence Jobard; Kader Karli Oguz; Banu Anlar; Nejat Akalan; Turgay Coskun; J O Sass; Judith Fischer; Meral Topcu
L-2-hydroxyglutaric aciduria and brain tumors in children with mutations in the L2HGDH gene: neuroimaging findings.
Neuropediatrics 2008;39(2):119-22.
2007: Sevgi Yetgin; Selin Aytac; Serap Kalkanoglu; Turgay Coskun; Christina Ortmann; Christian Kratz; Charlotte Niemeyer
Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents.
Pediatric hematology and oncology 2007;24(6):453-5.
2007: Akgün Olmez; S Songül Yalçin; Kadriye Yurdakök; Turgay Coskun
Serum zinc levels in children with acute gastroenteritis.
Pediatrics international : official journal of the Japan Pediatric Society 2007;49(3):314-7.
2006: Betul Tavil; Hatice Serapl Kalkanoglu Sivri; Turgay Coskun; Aytemiz Gurgey; Emel Ozyurek; Ali Dursun; Aysegul Tokatli; Cigdem Altay; Fatma Gumruk
Haematological findings in children with inborn errors of metabolism.
Journal of inherited metabolic disease 2006;29(5):607-11.
2006: Stefan Kölker; Sven F Garbade; Cheryl R Greenberg; James V Leonard; Jean-Marie Saudubray; Antonia Ribes; H Serap Kalkanoglu; Allan M Lund; Begoña Merinero; Moacir Wajner; Mónica Troncoso; Monique Williams; John H Walter; Jaume Campistol; Milagros Martí-Herrero; Melissa Caswill; Alberto Burlina; Florian Lagler; Esther M Maier; Bernd Schwahn; Aysegul Tokatli; Ali Dursun; Turgay Coskun; Ronald A Chalmers; David M Koeller; Johannes Zschocke; Ernst Christensen; Peter Burgard; Georg F Hoffmann
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency.
Pediatric research 2006;59(6):840-7.
2006: Kimiyoshi Ichida; Halil Ibrahim Aydin; Makoto Hosoyamada; H Serap Kalkanoglu; A Dursun; Iwao Ohno; Turgay Coskun; Aysegul Tokatli; Toshiaki Shibasaki; Tatsuo Hosoya
A Turkish case with molybdenum cofactor deficiency.
Nucleosides, nucleotides & nucleic acids 2006;25(9-11):1087-91.
2005: Umut Selda Bayrakci; Nesrin Besbas; Osman Ozcebe; Turgay Coskun; Ergan Akgul; Tezer Kutluk; Aysin Bakkaloglu
Direct adsorption of lipoproteins from whole blood by direct adsorption of lipoprotein apheresis: first experience in two hypercholesterolemic children.
Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy 2005;9(6):469-72.
2005: Hamit Ozyürek; Güzide Turanli; Didem Aliefendioglu; Turgay Coskun
Repetitive EEG recordings are necessary for the diagnosis of early myoclonic encephalopathy.
Neurology India 2005;53(2):235-7.
2005: Ozlem Teksam; Murat Yurdakok; Turgay Coskun
Molybdenum cofactor deficiency presenting with severe metabolic acidosis and intracranial hemorrhage.
Journal of child neurology 2005;20(2):155-7.
2005: Ayse Korkmaz; Gülsevin Tekinalp; Turgay Coskun; Sule Yigit; Murat Yurdakok
Plasma carnitine levels in preterm infants with respiratory distress syndrome.
Pediatrics international : official journal of the Japan Pediatric Society 2005;47(1):49-52.
2005: Sule Unal; H Serap Kalkanoğlu; Cetin Kocaefe; Safak Gucer; Seza Ozen; Güzide Turanli; Turgay Coskun
Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletion.
Journal of child neurology 2005;20(1):83-4.
2004: Meral Topçu; Florence Jobard; Sophie Halliez; Turgay Coskun; Cengiz Yalçinkayal; Filiz Ozbas Gerceker; Ronald J A Wanders; Jean-François Prud'homme; Mark Lathrop; Meral Ozguc; Judith Fischer
L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1.
Human molecular genetics 2004;13(22):2803-11.
2003: Tevfik Karagoz; Turgay Coskun; Imran Ozalp; Ethem Ozkaya; Fügen Ersoy
Immune function in children with classical phenylketonuria and tetrahydrobiopterin deficiencies.
Indian pediatrics 2003;40(9):822-33.
2003: Reyhan Celiker; Serpil Bal; Aysin Bakkaloğlu; Eda Ozaydin; Turgay Coskun; Alp Cetin; Fitnat Dinçer
Factors playing a role in the development of decreased bone mineral density in juvenile chronic arthritis.
Rheumatology international 2003;23(3):127-9.
2002: Mügen Terzioglu; Aysegul Tokatli; Turgay Coskun; Serap Emre
Molecular analysis of Turkish mucopolysaccharidosis IVA (Morquio A) patients: identification of novel mutations in the N-acetylgalactosamine-6-sulfate sulfatase (GALNS) gene.
Human mutation 2002;20(6):477-8.
2002: Nilgün Yaris; Naci Ceviz; Turgay Coskun; C Akytüz; Münevver Büyükpamukçu
Serum carnitine levels during the doxorubicin therapy. Its role in cardiotoxicity.
Journal of experimental & clinical cancer research : CR 2002;21(2):165-70.
2002: Meral Topcu; Isil Saatci; Göknur Haliloglu; Mehmet Kesimer; Turgay Coskun
D-glyceric aciduria in a six-month-old boy presenting with West syndrome and autistic behaviour.
Neuropediatrics 2002;33(1):47-50.
2002: Serap Emre; Mügen Terzioglu; Aysegul Tokatli; Turgay Coskun; Imran Ozalp; Birgit Weber; John J Hopwood
Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B.
Human mutation 2002;19(2):184-5.
2001: Meral Topcu; Turgay Coskun; Göknur Haliloglu; Isil Saatci
Molybdenum cofactor deficiency: report of three cases presenting as hypoxic-ischemic encephalopathy.
Journal of child neurology 2001;16(4):264-70.
2000: RJ Pomponio; Turgay Coskun; Mübeccel Demirkol; Aysegul Tokatli; Imran Ozalp; Gülden Hüner; Tolunay Baykal; Barry Wolf
Novel mutations cause biotinidase deficiency in Turkish children.
Journal of inherited metabolic disease 2000;23(2):120-8.
2000: S Blanton; Arti Pandya; BL Landa; R Javaheri; X Xia; Walter E Nance; RJ Pomponio; KJ Norrgard; KL Swango; Mübeccel Demirkol; H Gülden; Turgay Coskun; Aysegul Tokatli; Imran Ozalp; Barry Wolf
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations.
Human heredity 2000;50(2):102-11.
1999: Volkan Seyrantepe; Meral Ozguc; Turgay Coskun; Imran Ozalp; J K Reichardt
Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. Online.
Human mutation 1999;13(4):339.
1998: Barry Wolf; RJ Pomponio; KJ Norrgard; Ira T Lott; E Regula Baumgartner; Terttu Suormala; V T Ramaekers; Turgay Coskun; Aysegul Tokatli; Imran Ozalp; Jeanne Hymes
Delayed-onset profound biotinidase deficiency.
The Journal of pediatrics 1998;132(2):362-5.
1996: N Gungor; A Tokath; Turgay Coskun; Meral Ozguc; Imran Ozalp
Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia.
European journal of pediatrics 1996;155(3):257-8.
1995: Turgay Coskun; E Erkul; Volkan Seyrantepe; Meral Ozgüç; Aysegul Tokatli; Imran Ozalp
Mutational analysis of Turkish galactosaemia patients.
Journal of inherited metabolic disease 1995;18(3):368-9.
1994: Omer Kalayci; Turgay Coskun; Aysegul Tokatli; E Demir; Gülsen Erdem; C Güngör; A Yükselen; Imran Ozalp
Infantile spasms as the initial symptom of biotinidase deficiency.
The Journal of pediatrics 1994;124(1):103-4.
1993: Turgay Coskun; Imran Ozalp; Aysegul Tokatli; N Blau; A Niederwieser
Hyperphenylalaninaemia due to tetrahydrobiopterin deficiency: a report of 16 cases.
Journal of inherited metabolic disease 1993;16(3):605-7.
1990: Imran Ozalp; Turgay Coskun; S Tokol; Gülay Demircin; E Mönch
Inherited metabolic disorders in Turkey.
Journal of inherited metabolic disease 1990;13(5):732-8.
1989: U Lichter-Konecki; M Schlotter; C Yaylak; Meral Ozgüç; Turgay Coskun; Imran Ozalp; U Wendel; U Batzler; Friedrich K Trefz; DS Konecki
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population.
Human genetics 1989;81(4):373-6.
1987: Turgay Coskun; Imran Ozalp; S Mönch; J Kneer
Lethal hyperammonaemic coma due to ornithine transcarbamylase deficiency presenting as brain stem encephalitis in a previously asymptomatic ten-year-old boy.
Journal of inherited metabolic disease 1987;10(3):271.