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Turgay Coskun
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50
Ozalp, Imran
39
Tokatli, Aysegul
16
Kalkanoglu, Serap
15
Dursun, Ali
12
Ozgüç, Meral
7
Erdem, Hayat
6
Tekinalp, Gülsevin
6
Yüce, Aysel
5
Yurdakök, Murat
5
ayter, sükriye
5
Topçu, Meral
5
Büyükpamukçu, Münevver
5
Gögüs, Safiye
5
Besbas, Nesrin
5
Haliloglu, Göknur
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All Publications
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2009: Aydogdu Sultan Durmus; Kirel Birgul; Coskun Turgay; Kose Suna
Prevalence of cystinuria among elementary schoolchildren in Eskisehir, Turkey.
Scandinavian journal of urology and nephrology 2009;43(2):138-41.
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2008: Topaloglu Rezan; Lebre Anne S; Demirkaya Erkan; Kuskonmaz Baris; Coskun Turgay; Orhan Diclehan; Gürgey Aytemiz; Gümrük Fatma
Two new cases with Pearson syndrome and review of Hacettepe experience.
The Turkish journal of pediatrics 2008;50(6):572-6.
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2008: Kuskonmaz Baris; Unal Sule; Cördükcü Emine; Aydin Halil; Coskun Turgay; Gurgey Aytemiz; Gumruk Fatma
Lymphocytic vacuolization in sialic acid storage disease.
American journal of hematology 2008;83(10):821.
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2008: Haliloglu G; Jobard F; Oguz K K; Anlar B; Akalan N; Coskun T; Sass J O; Fischer J; Topcu M
L-2-hydroxyglutaric aciduria and brain tumors in children with mutations in the L2HGDH gene: neuroimaging findings.
Neuropediatrics 2008;39(2):119-22.
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2008: Bora Gamze; Ozkan Behzat; Dayangaç-Erden Didem; Erdem-Yurter Hayat; Coskun Turgay
Vitamin D receptor gene polymorphisms in Turkish children with vitamin D deficient rickets.
The Turkish journal of pediatrics 2008;50(1):30-3.
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2007: Aliefendioglu Didem; Dursun Ali; Coskun Turgay; Akçören Zuhal; Wanders Ronald J A; Waterham Hans R
A newborn with VLCAD deficiency. Clinical, biochemical, and histopathological findings.
European journal of pediatrics 2007;166(10):1077-80.
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2007: Yetgin Sevgi; Aytac Selin; Kalkanoglu Serap; Coskun Turgay; Ortmann Christina; Kratz Christian; Niemeyer Charlotte
Biotinidase deficiency and juvenile myelomonocytic leukemia in a Turkish infant of consanguineous parents.
Pediatric hematology and oncology 2007;24(6):453-5.
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2007: Olmez Akgün; Yalçin S Songül; Yurdakök Kadriye; Coskun Turgay
Serum zinc levels in children with acute gastroenteritis.
Pediatrics international : official journal of the Japan Pediatric Society 2007;49(3):314-7.
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2007: Sivri Hatice Serap Kalkanoglu; Genç Gülsüm Aydan; Tokatli Aysegül; Dursun Ali; Coskun Turgay; Aydin Halil Ibrahim; Sennaroglu Levent; Belgin Erol; Jensen Kevin; Wolf Barry
Hearing loss in biotinidase deficiency: genotype-phenotype correlation.
The Journal of pediatrics 2007;150(4):439-42.
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2007: Genc G A; Sivri-Kalkanoglu H S; Dursun A; Aydin H I; Tokatli A; Sennaroglu L; Belgin E; Wolf B; Coskun T
Audiologic findings in children with biotinidase deficiency in Turkey.
International journal of pediatric otorhinolaryngology 2007;71(2):333-9.
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2007: Tokatli Aysegül; Kalkanoglu-Sivri H Serap; Yüce Aysel; Coskun Turgay
Acetaminophen-induced hepatotoxicity in a glutathione synthetase-deficient patient.
The Turkish journal of pediatrics 2007;49(1):75-6.
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2007: Yildirim Sükran; Tokatli Aysegül; Yilmaz Engin; Coskun Turgay
Assessment of tetrahydrobiopterin responsiveness in Turkish hyperphenylalaninemic patients.
The Turkish journal of pediatrics 2007;49(1):1-6.
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2006: Kocabas Can Naci; Adalioglu Gönül; Coskun Turgay; Tuncer Ayfer; Sekerel Bülent Enis
The relationship between serum selenium levels and frequent wheeze in children.
The Turkish journal of pediatrics 2006;48(4):308-12.
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2006: Tavil Betul; Sivri Hatice Serapl Kalkanoglu; Coskun Turgay; Gurgey Aytemiz; Ozyurek Emel; Dursun Ali; Tokatli Aysegul; Altay Cigdem; Gumruk Fatma
Haematological findings in children with inborn errors of metabolism.
Journal of inherited metabolic disease 2006;29(5):607-11.
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2006: Büyükpamukçu Münevver; Varan Ali; Haberal Mehmet; Büyükpamukçu Nebil; Köksal Yavuz; Coskun Turgay; Yüce Aysel; Kale Gülsev; Akyüz Canan; Kutluk Tezer
The efficacy of liver transplantation in malignant liver tumors associated with tyrosinemia: clinical and laboratory findings of five cases.
Pediatric transplantation 2006;10(4):517-20.
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2006: Kölker Stefan; Garbade Sven F; Greenberg Cheryl R; Leonard James V; Saudubray Jean-Marie; Ribes Antonia; Kalkanoglu H Serap; Lund Allan M; Merinero Begoña; Wajner Moacir; Troncoso Mónica; Williams Monique; Walter John H; Campistol Jaume; Martí-Herrero Milagros; Caswill Melissa; Burlina Alberto B; Lagler Florian; Maier Esther M; Schwahn Bernd; Tokatli Aysegul; Dursun Ali; Coskun Turgay; Chalmers Ronald A; Koeller David M; Zschocke Johannes; Christensen Ernst; Burgard Peter; Hoffmann Georg F
Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency.
Pediatric research 2006;59(6):840-7.
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2006: Ichida K; Aydin H Ibrahim; Hosoyamada M; Kalkanoglu H Serap; Dursun A; Ohno I; Coskun T; Tokatli A; Shibasaki T; Hosoya T
A Turkish case with molybdenum cofactor deficiency.
Nucleosides, nucleotides & nucleic acids 2006;25(9-11):1087-91.
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2005: Bayrakci Umut Selda; Besbas Nesrin; Ozcebe Osman; Coskun Turgay; Akgul Ergan; Kutluk Tezer; Bakkaloglu Aysin
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.
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2005: Günes B; Yalçin S S; Kalkanoglu H S; Onol S; Dursun A; Coskun T
The effect of oral L-carnitine supplementation on the lipid profiles of hyperlipidaemic children.
Acta paediatrica (Oslo, Norway : 1992) 2005;94(6):711-6.
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2005: Ozyürek Hamit; Turanli Güzide; Aliefendioglu Didem; Coskun Turgay
Repetitive EEG recordings are necessary for the diagnosis of early myoclonic encephalopathy.
Neurology India 2005;53(2):235-7.
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2005: Sözen M Mert; Whittall Ros; Oner Cihan; Tokatli Aysegül; Kalkanoglu H Serap; Dursun Ali; Coskun Turgay; Oner Reyhan; Humphries Steve E
The molecular basis of familial hypercholesterolaemia in Turkish patients.
Atherosclerosis 2005;180(1):63-71.
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2005: Saltik-Temizel Inci Nur; Coskun Turgay; Yüce Aysel; Koçak Nurten
Fanconi-Bickel syndrome in three Turkish patients with different homozygous mutations.
The Turkish journal of pediatrics 2005;47(2):167-9.
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2005: Yalnizoglu Dilek; Sari Neriman; Turanli Güzide; Coskun Turgay; Topçu Meral
Neurophysiologic features in glutaric aciduria type I.
The Turkish journal of pediatrics 2005;47(2):153-8.
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2005: Teksam Ozlem; Yurdakok Murat; Coskun Turgay
Molybdenum cofactor deficiency presenting with severe metabolic acidosis and intracranial hemorrhage.
Journal of child neurology 2005;20(2):155-7.
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2005: Korkmaz Ayse; Tekinalp Gulsevin; Coskun Turgay; Yigit Sule; Yurdakok Murat
Plasma carnitine levels in preterm infants with respiratory distress syndrome.
Pediatrics international : official journal of the Japan Pediatric Society 2005;47(1):49-52.
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2005: Topçu Meral; Aydin Omer Faruk; Yalçinkaya Cengiz; Haliloglu Göknur; Aysun Sabiha; Anlar Banu; Topaloglu Haluk; Turanli Güzide; Yalnizoglu Dilek; Kesimer Mehmet; Coskun Turgay
L-2-hydroxyglutaric aciduria: a report of 29 patients.
The Turkish journal of pediatrics 2005;47(1):1-7.
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2005: Unal Sule; Kalkanoglu H Serap; Kocaefe Cetin; Gucer Safak; Ozen Seza; Turanli Guzide; Coskun Turgay
Four-month-old infant with focal segmental glomerulosclerosis and mitochondrial DNA deletion.
Journal of child neurology 2005;20(1):83-4.
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2005: Ozçelik U; Dogru D; Akçören Z; Coskun T; Kaya S; Göçmen A
Xanthoma disseminatum: a child with respiratory system involvement and bronchiectasis.
Pediatric pulmonology 2005;39(1):84-7.
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2004: Topçu Meral; Jobard Florence; Halliez Sophie; Coskun Turgay; Yalçinkayal Cengiz; Gerceker Filiz Ozbas; Wanders Ronald J A; Prud'homme Jean-François; Lathrop Mark; Ozguc Meral; Fischer Judith
L-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1.
Human molecular genetics 2004;13(22):2803-11.
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2004: Kalkanoglu H Serap; Dursun Ali; Tokatli Aysegül; Coskun Turgay; Karasimav Defne; Topaloglu Haluk
A boy with spastic paraparesis and dyspnea.
Journal of child neurology 2004;19(5):397-8.
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2004: Olmez Akgün; Yalçin Songül; Yurdakök Kadriye; Coskun Turgay
Serum selenium levels in acute gastroenteritis of possible viral origin.
Journal of tropical pediatrics 2004;50(2):78-81.
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2004: Ozer Suzan; Ulusahin Aylin; Ulusoy Semra; Okur Hamza; Coskun Turgay; Tuncali Timur; Gögüs Ahmet; Akarsu A Nurten
Is vitamin D hypothesis for schizophrenia valid? Independent segregation of psychosis in a family with vitamin-D-dependent rickets type IIA.
Progress in neuro-psychopharmacology & biological psychiatry 2004;28(2):255-66.
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2004: Derman Orhan; Kanbur Nuray O; Coskun Turgay; Pehlivantürk Berna
Refeeding problems in a severe anorexia nervosa case.
International journal of adolescent medicine and health 2004;16(1):65-9.
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2004: Topçu Meral; Yalnizoglu Dilek; Saatçi Isil; Haliloglu Göknur; Topaloglu Haluk; Senbil Nesrin; Onol Saniye; Coskun Turgay
Effect of topiramate on enlargement of head in Canavan disease: a new option for treatment of megalencephaly.
The Turkish journal of pediatrics 2004;46(1):67-71.
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2003: Besbas Nesrin; Ozaltin Fatih; Coskun Turgay; Ozalp Sila; Saatçi Umit; Bakkaloglu Aysin; El Nahas A Meguid
Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children.
Pediatric nephrology (Berlin, Germany) 2003;18(12):1255-9.
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2003: Karagoz Tevfik; Coskun Turgay; Ozalp Imran; Ozkaya Ethem; Ersoy Fugen
Immune function in children with classical phenylketonuria and tetrahydrobiopterin deficiencies.
Indian pediatrics 2003;40(9):822-33.
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2003: Celiker Reyhan; Bal Serpil; Bakkaloglu Aysin; Ozaydin Eda; Coskun Turgay; Cetin Alp; Dinçer Fitnat
Factors playing a role in the development of decreased bone mineral density in juvenile chronic arthritis.
Rheumatology international 2003;23(3):127-9.
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2003: Kocabas Can Naci; Coskun Turgay; Yurdakök Murat; Haziroglu Rifki
The effects of aflatoxin B1 on the development of kwashiorkor in mice.
Human & experimental toxicology 2003;22(3):155-8.
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2003: Aliefendioglu Didem; Tana Aslan A yse; Coskun Turgay; Dursun Ali; Cakmak Fatma Nur; Kesimer Mehmet
Transient nonketotic hyperglycinemia: two case reports and literature review.
Pediatric neurology 2003;28(2):151-5.
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2003: Olmez Akgün; Nilssen Oivind; Coskun Turgay; Klenow Helle
Alpha-mannosidosis and mutational analysis in a Turkish patient.
The Turkish journal of pediatrics 2003;45(1):46-50.
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2002: Terzioglu Mugen; Tokatli Aysegul; Coskun Turgay; Emre Serap
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.
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2002: Yaris N; Ceviz N; Coskun T; Akytüz C; Büyükpamukçu M
Serum carnitine levels during the doxorubicin therapy. Its role in cardiotoxicity.
Journal of experimental & clinical cancer research : CR 2002;21(2):165-70.
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2002: Dursun A; Henneke M; Ozgül K; Gartner J; Coskun T; Tokatli A; Kalkanoglu H S; Demirkol M; Wendel U; Ozalp I
Maple syrup urine disease: mutation analysis in Turkish patients.
Journal of inherited metabolic disease 2002;25(2):89-97.
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2002: Topcu M; Saatci I; Haliloglu G; Kesimer M; Coskun T
D-glyceric aciduria in a six-month-old boy presenting with West syndrome and autistic behaviour.
Neuropediatrics 2002;33(1):47-50.
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2002: Emre Serap; Terzioglu Mugen; Tokatli Aysegul; Coskun Turgay; Ozalp Imran; Weber Birgit; Hopwood John J
Sanfilippo syndrome in Turkey: Identification of novel mutations in subtypes A and B.
Human mutation 2002;19(2):184-5.
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2002: Yaris Nilgün; Akyüz Canan; Coskun Turgay; Kutluk Tezer; Büyükpamukçu Münevver
Nutritional status of children with cancer and its effects on survival.
The Turkish journal of pediatrics 2002;44(1):35-9.
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2002: Emre Serap; Terzioglu Mügen; Coskun Turgay; Tokath Aysegül; Ozalp Imran; Müller Vivien; Hopwood John
Biochemical and molecular analysis of mucopolysaccharidoses in Turkey.
The Turkish journal of pediatrics 2002;44(1):13-7.
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2002: Yaris Nilgun; Akyüz Canan; Coskun Turgay; Büyükpamukçu Münevver
Serum carnitine levels of pediatric cancer patients.
Pediatric hematology and oncology 2002;19(1):1-8.
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2001: Dursun A; Kalkanoglu H S; Coskun T; Tokatli A; Bittner R; Koçak N; Yüce A; Ozalp I; Boehme H J
Mutation analysis in Turkish patients with hereditary fructose intolerance.
Journal of inherited metabolic disease 2001;24(5):523-6.
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2001: Kalkanoglu H S; Romstad A; Coskun T; Güttler F
Evaluation of a fetus at risk for dihydropteridine reductase deficiency by direct mutation analysis using denaturing gradient gel electrophoresis.
Prenatal diagnosis 2001;21(10):868-70.
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2001: Kalkanoglu H S; Coskun T; Aydogdu S D; Tokatli A; Gürgey A
Factor V Leiden mutation in Turkish patients with homozygous cystathionine beta-synthase deficiency.
Journal of inherited metabolic disease 2001;24(3):367-9.
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2001: Ozalp I; Coskun T; Tokatli A; Kalkanoglu H S; Dursun A; Tokol S; Köksal G; Ozgüc M; Köse R
Newborn PKU screening in Turkey: at present and organization for future.
The Turkish journal of pediatrics 2001;43(2):97-101.
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2001: Dayangaç D; Kalkanoglu H S; Durmus-Aydogdu S; Erdem H; Besbas N; Coskun T
Molecular genetic analyses of cystinuria type 1 in 24 Turkish patients.
The Turkish journal of pediatrics 2001;43(2):110-3.
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2001: Topcu M; Coskun T; Haliloglu G; Saatci I
Molybdenum cofactor deficiency: report of three cases presenting as hypoxic-ischemic encephalopathy.
Journal of child neurology 2001;16(4):264-70.
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2000: Dursun A; Yilma Y; Ozsari M; Kandemir N; Coskun T
Neuroleptic malignant syndrome in a patient with citrullinaemia.
Journal of inherited metabolic disease 2000;23(8):841-2.
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2000: Romstad A; Kalkanoglu H S; Coskun T; Demirkol M; Tokatli A; Dursun A; Baykal T; Ozalp I; Guldberg P; Güttler F
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE).
Human genetics 2000;107(6):546-53.
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2000: Dursun A; Aliefendioglu D; Ozkan B; Coskun T
Carnitinuria in rickets due to vitamin D deficiency.
The Turkish journal of pediatrics 2000;42(4):278-80.
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2000: Yilmaz E; Cali F; Roman V; Ozalp I; Coskun T; Tokatli A; Kalkanoglu H S; Ozgüç M
Molecular basis of mild hyperphenylalaninaemia in Turkey.
Journal of inherited metabolic disease 2000;23(5):523-5.
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2000: Pomponio R J; Coskun T; Demirkol M; Tokatli A; Ozalp I; Hüner G; Baykal T; Wolf B
Novel mutations cause biotinidase deficiency in Turkish children.
Journal of inherited metabolic disease 2000;23(2):120-8.
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2000: Blanton S H; Pandya A; Landa B L; Javaheri R; Xia X; Nance W E; Pomponio R J; Norrgard K J; Swango K L; Demirkol M; Gülden H; Coskun T; Tokatli A; Ozalp I; Wolf B
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations.
Human heredity 2000;50(2):102-11.
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2000: Kalkanoglu H S; Anadol D; Yilmaz E; Coskun T
Phenylketonuria and cystic fibrosis in the same patient.
Pediatrics international : official journal of the Japan Pediatric Society 2000;42(1):92-3.
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1999: Kalkanoglu H S; Coskun T
Neurological crisis mimicking acute pancreatitis in tyrosinemia type I.
The Turkish journal of pediatrics 1999;41(4):501-4.
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1999: Coskun T; Karagöz T; Kalkanoglu S; Tokatli A; Ozalp I; Thöny B; Blau N
Guanosine triphosphate cyclohydrolase I deficiency: a rare cause of hyperphenylalaninemia.
The Turkish journal of pediatrics 1999;41(2):231-7.
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1999: Yurdakök K; Ozmert E; Yalçin S S; Coskun T
Rehydration of moderately dehydrated children with transient glucose intolerance using rice oral rehydration solution.
Acta paediatrica (Oslo, Norway : 1992) 1999;88(1):34-7.
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1999: Seyrantepe V; Ozguc M; Coskun T; Ozalp I; Reichardt J K
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.
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1998: Olcay L; Gümrük F; Boduroglu K; Coskun T; Tunçbilek E
Anaemia and thrombocytopenia due to haemophagocytosis in a 7-month-old boy with galactosialidosis.
Journal of inherited metabolic disease 1998;21(6):679-80.
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1998: Yalçin S S; Yurdakök K; Ozalp I; Coskun T
The effect of live measles vaccines on serum vitamin A levels in healthy children.
Acta paediatrica Japonica; Overseas edition 1998;40(4):345-9.
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1998: Besbas N; Ozdemir S; Saatçi U; Coskun T; Ozen S; Topaloglu R; Bakkaloglu A; El Nahas A M
Nutritional assessment of children on haemodialysis: value of IGF-I, TNF-alpha and IL-1beta.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 1998;13(6):1484-8.
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1998: Tokatli A; Coskun T; Ozalp I
Citrullinemia. Clinical experience with 23 cases.
The Turkish journal of pediatrics 1998;40(2):185-93.
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1998: Wolf B; Pomponio R J; Norrgard K J; Lott I T; Baumgartner E R; Suormala T; Ramaekers V T; Coskun T; Tokatli A; Ozalp I; Hymes J
Delayed-onset profound biotinidase deficiency.
The Journal of pediatrics 1998;132(2):362-5.
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1998: Kiliç I; Ozalp I; Coskun T; Tokatli A; Emre S; Saldamli I; Köksel H; Ozboy O
The effect of zinc-supplemented bread consumption on school children with asymptomatic zinc deficiency.
Journal of pediatric gastroenterology and nutrition 1998;26(2):167-71.
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1998: Andiran N; Coskun T; Ozaydin E; Seçmeer G
Recurrent meningitis associated with congenital paravertebral dermal sinus tract.
The Turkish journal of pediatrics 1998;40(1):121-5.
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1998: Tokatli A; Coskun T; Ozalp I
Isovaleric acidemia. Clinical presentation of 6 cases.
The Turkish journal of pediatrics 1998;40(1):111-9.
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1997: Tokatli A; Coskun T; Ozalp I
Biotinidase deficiency with neurological features resembling multiple sclerosis.
Journal of inherited metabolic disease 1997;20(5):707-8.
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1997: Gürgey A; Gögüs S; Saatçi U; Bilginturan N; Yordam N; Coskun T; Ozkutlu S; Sahin N
Leprechaunism in two Turkish patients.
The Turkish journal of pediatrics 1997;39(3):387-93.
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1997: Coskun T; Gögüs S; Akçören Z; Tokatli A; Ozalp I
Acute pancreatitis in a patient with glutaric acidemia type II.
The Turkish journal of pediatrics 1997;39(3):379-85.
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1997: Tokatli A; Coskun T; Ozalp I
Hypophosphatemic vitamin-D resistant rickets associated with epidermal nevus syndrome. A case report.
The Turkish journal of pediatrics 1997;39(2):247-51.
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1996: Tatar G; Coskun T; Simsek H
Superior mesenteric artery syndrome. A case report.
The Turkish journal of pediatrics 1996;38(3):367-70.
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1996: Gungor N; Tokath A; Coskun T; Ozguc M; Ozalp I
Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia.
European journal of pediatrics 1996;155(3):257-8.
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1995: Yurdakök M; Coskun T; Erdem G; Göktogan S; Ozalp I; Tekinalp G
Cerebrospinal fluid amino acid levels in newborn infants with intracranial hemorrhage.
Acta paediatrica Japonica; Overseas edition 1995;37(6):694-6.
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1995: Yilmaz E; Erdem H; Ozgüç M; Coskun T; Ozçelik U; Göçmen A; Ozalp I
Study of 12 mutations in Turkish cystic fibrosis patients.
Human heredity 1995;45(3):175-7.
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1995: Camur S; Coskun T; Kiper N
Alpha-mannosidosis: the first Turkish case.
Acta paediatrica Japonica; Overseas edition 1995;37(2):230-2.
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1995: Tekinalp G; Yükselen A; Balkanci F; Coskun T; Yurdakök M
Hypophosphatasia in a newborn infant.
The Turkish journal of pediatrics 1995;37(1):61-5.
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1995: Tekinalp G; Coskun T; Oran O; Ozalp I; Figen G; Ergin H
Nonketotic hyperglycinemia in a newborn infant.
The Turkish journal of pediatrics 1995;37(1):57-60.
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1995: Coskun T; Erkul E; Seyrantepe V; Ozgüç M; Tokatli A; Ozalp I
Mutational analysis of Turkish galactosaemia patients.
Journal of inherited metabolic disease 1995;18(3):368-9.
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1994: Onur M A; Vural I; Basçi N; Pamir R; Coskun T; Isimer A; Kas H S; Beksaç S; Hincal A A; Tümer A
Effect of encapsulation of chloramphenicol in albumin microspheres on its in vitro transfer across the human placenta.
Journal of microencapsulation 1994;11(6):657-62.
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1994: Ozçelik U; Göçmen A; Kiper N; Coskun T; Yilmaz E; Ozgüç M
Sodium chloride deficiency in cystic fibrosis patients.
European journal of pediatrics 1994;153(11):829-31.
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1994: Coskun T; Tokatli A; Ozalp I
Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases.
The Turkish journal of pediatrics 1994;36(4):267-78.
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1994: Yetgin S; Balci S; Irken G; Coskun T; Say B
Aase-Smith syndrome: report of a new case with unusual features.
The Turkish journal of pediatrics 1994;36(3):239-42.
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1994: Ozgüç M; Yilmaz E; Erdem H; Coskun T; Ozçelik U; Togan I; Göçmen A; Ayter S; Ozalp I
Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families.
Clinical genetics 1994;45(5):266-8.
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1994: Ozgüç M; Tekin A; Erdem H; Yilmaz E; Ayter S; Coskun T; Can A; Gögüs S; Caglar M; Kale G
Analysis of delta F508 mutation in cystic fibrosis pathology specimens.
Pediatric pathology / affiliated with the International Paediatric Pathology Association 1994;14(3):491-6.
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1994: Tokatli A; Coskun T; Kocabas C N; Ozalp I; Balci S
Classical phenylketonuria associated with Goldenhar's syndrome. A case report.
The Turkish journal of pediatrics 1994;36(2):153-6.
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1994: Güngör N; Coskun T; Akçören Z; Caglar M
I-cell disease. A case report and review of the literature.
The Turkish journal of pediatrics 1994;36(2):145-52.
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1994: Kalayci O; Coskun T; Tokatli A; Demir E; Erdem G; Güngör C; Yükselen A; Ozalp I
Infantile spasms as the initial symptom of biotinidase deficiency.
The Journal of pediatrics 1994;124(1):103-4.
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1994: Ozgüç M; Yilmaz E; Erdem H; Coskun T; Tokatli A; Ozalp I
Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients.
Journal of inherited metabolic disease 1994;17(3):373-4.
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1994: Ozalp I; Coskun T; Ozgüç M; Tokatli A; Yalaz K; Vanli L; Yilmaz E; Erbay A
Genetic and neurological evaluation of untreated and late-treated patients with phenylketonuria.
Journal of inherited metabolic disease 1994;17(3):371.
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1993: Yurdakök M; Haziroglu R; Coskun T
Is L-carnitine protective in hypoxic cerebral edema in newborn mice?
The Turkish journal of pediatrics 1993;35(4):267-70.
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1993: Onur M A; Vural I; Kas H S; Hincal A A; Coskun T; Kanra G; Tümer A
Decrease in the placental transfer of chloramphenicol when administered in albumin microspheres into rats.
Journal of microencapsulation 1993;10(3):367-74.
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1993: Yüce A; Coskun T; Koçak N; Ozsoylu S; Ozalp I; Gögüs S
Type I glycogenosis with renal tubular dysfunction (presentation of two cases).
The Turkish journal of pediatrics 1993;35(3):201-4.
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1993: Coskun T; Ozalp I; Tokatli A
Iminoglycinuria: a benign type of inherited aminoaciduria.
The Turkish journal of pediatrics 1993;35(2):121-5.
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1993: Ozgüç M; Ozalp I; Coskun T; Yilmaz E; Erdem H; Ayter S
Mutation analysis in Turkish phenylketonuria patients.
Journal of medical genetics 1993;30(2):129-30.
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1993: Coskun T; Topçu M; Ustündag I; Ozalp I; Renda Y; Ciger A; Nurlu G
Neurophysiological studies of patients with classical phenylketonuria: evaluation of results of IQ scores, EEG and evoked potentials.
The Turkish journal of pediatrics 1993;35(1):1-10.
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1993: Ozgüç M; Ozalp I; Coskun T; Yilmaz E; Erdem H; Ayter S
Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients.
The Turkish journal of pediatrics 1993;35(1):11-4.
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1993: Günel M; Coskun T; Tokatli A; Ozalp I
3-Hydroxy-3-methylglutaryl coenzyme A lyase deficiency.
Journal of inherited metabolic disease 1993;16(6):1062-3.
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1993: Coskun T; Ozalp I; Tokatli A; Blau N; Niederwieser A
Hyperphenylalaninaemia due to tetrahydrobiopterin deficiency: a report of 16 cases.
Journal of inherited metabolic disease 1993;16(3):605-7.
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1992: Yurdakök M; Göktogan S; Erdem G; Ozalp I; Tekinalp G; Coskun T; Caglar M
Cerebrospinal fluid glutamine level in the differential diagnosis of a "bloody tap" in newborn infants.
Brain & development 1992;14(6):428-9.
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1992: Salman B; Besbas N; Coskun T; Yilmazbayhan D; Sarialioglu F
Intussusception due to ectopic pancreatic tissue in a nine-month-old child.
The Turkish journal of pediatrics 1992;34(4):255-8.
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1992: Coskun T; Ozen H; Büyükpamukçu M; Kale G
Neuroblastoma presenting as protein-losing enteropathy.
The Turkish journal of pediatrics 1992;34(2):107-9.
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1992: Tokatli A; Coskun T; Ozalp I; Günay M
The major presenting symptom in a biotinidase-deficient patient: laryngeal stridor.
Journal of inherited metabolic disease 1992;15(2):281-2.
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1991: Coskun T; Ozalp I; Tekinalp G
Hereditary fructose intolerance in a patient with phenylketonuria.
The Turkish journal of pediatrics 1991;33(3):181-4.
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1991: Yilmaz E; Ozgüç M; Coskun T; Beksaç S; Cakar N; Ayter S; Ozalp I
Prenatal diagnosis of cystic fibrosis in a Turkish family.
The Turkish journal of pediatrics 1991;33(2):79-84.
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1991: Tokatli A; Coskun T; Cataltepe S; Ozalp I
Valproate-induced lethal hyperammonaemic coma in a carrier of ornithine carbamoyltransferase deficiency.
Journal of inherited metabolic disease 1991;14(5):836-7.
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1991: Tokatli A; Coskun T; Ozalp I
Fifteen years' experience with 212 hyperammonaemic cases at a metabolic unit.
Journal of inherited metabolic disease 1991;14(5):698-706.
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1991: Coskun T; Ozalp I; Koçak N; Yüce A; Caglar M; Berger R
Type I hereditary tyrosinaemia: presentation of 11 cases.
Journal of inherited metabolic disease 1991;14(5):765-70.
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1990: Coskun T; Ozalp I; Kale G; Gögüs S
Scleroderma-like skin lesions in two patients with phenylketonuria.
European journal of pediatrics 1990;150(2):109-10.
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1990: Coskun T; Besim A; Ozalp I; Eryilmaz M
Intracranial calcification in dihydropteridine reductase deficiency.
The Turkish journal of pediatrics 1990;32(4):259-64.
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1990: Ozalp I; Coskun T; Tokol S; Demircin G; Mönch E
Inherited metabolic disorders in Turkey.
Journal of inherited metabolic disease 1990;13(5):732-8.
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1989: Lichter-Konecki U; Schlotter M; Yaylak C; Ozgüç M; Coskun T; Ozalp I; Wendel U; Batzler U; Trefz F K; Konecki D
DNA haplotype analysis at the phenylalanine hydroxylase locus in the Turkish population.
Human genetics 1989;81(4):373-6.
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1987: Coskun T; Ozalp I; Mönch S; Kneer J
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.
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