Kor, Yılmaz : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (36)
Les plus populaires
Liste
- Liste
- Tableau

1

The effect of feeding system on fattening performance, slaughter, and carcass characteristics of Norduz male kids

Irfan Daskiran, Mehmet Bingol, Serhat Karaca, Ayhan Yilmaz, Ayse Ozge Cetin, Askin Kor

Journal:

Tropical Animal Health and Production

Année:

2010

Langue:

english

Fichier:

PDF, 222 KB

english, 2010

2

Preliminary study: Evaluation of melatonin secretion in children and adolescents with type 1 diabetes mellitus

Kor, Yilmaz, Geyikli, Iclal, Keskin, Mehmet, Akan, Muslum

Journal:

Indian Journal of Endocrinology and Metabolism

Année:

2014

Langue:

english

Fichier:

PDF, 577 KB

english, 2014

3

Homozygous familial hypobetalipoproteinemia: A Turkish case carrying a missense mutation in apolipoprotein B

Yilmaz, Berna Seker, Mungan, Neslihan Onenli, Di Leo, Enza, Magnolo, Lucia, Artuso, Lucia, Bernardis, Isabella, Tumgor, Gokhan, Kor, Deniz, Tarugi, Patrizia

Journal:

Clinica Chimica Acta

Année:

2016

Langue:

english

Fichier:

PDF, 419 KB

english, 2016

4

Unusual presentation: Pulmonary hemosiderosis with celiac disease and retinitis pigmentosa in a child

Ozlem Keskin, Mehmet Keskin, Elif Guler, Ediz Tutar, Oguzhan Saygili, Ercan Kucukosmanoglu, Yilmaz Kor, Haydar Celik, Enes Coskun

Journal:

Pediatric Pulmonology

Année:

2011

Langue:

english

Fichier:

PDF, 616 KB

english, 2011

5

Statin administration did not influence the progression of lung injury or associated organ failures in a cohort of patients with acute lung injury

Daryl J. Kor, Remzi Iscimen, Murat Yilmaz, Michael J. Brown, Daniel R. Brown, Ognjen Gajic

Journal:

Intensive Care Medicine

Année:

2009

Langue:

english

Fichier:

PDF, 196 KB

english, 2009

6

Prevalence and correlates of restless legs syndrome in adolescents

KUTLUHAN YILMAZ, AYSE KILINCASLAN, NERIMAN AYDIN, DENIZ KOR

Journal:

Developmental Medicine & Child Neurology

Année:

2011

Langue:

english

Fichier:

PDF, 217 KB

english, 2011

7

Hemorrhagic cardiac tamponade and successful pericardiocentesis in a one-day newborn

Osman Baspinar, Yilmaz Kor, Ziya Bayraktaroglu

Journal:

Acta Paediatrica

Année:

2006

Langue:

english

Fichier:

PDF, 102 KB

english, 2006

8

Bartter syndrome and growth hormone deficiency: three cases

Buyukcelik, Mithat, Keskin, Mehmet, Kilic, Beltinge Demircioglu, Kor, Yilmaz, Balat, Ayse

Journal:

Pediatric Nephrology

Année:

2012

Langue:

english

Fichier:

PDF, 147 KB

english, 2012

9

Gaucher disease type II or type III: a case report of an intermediate form with a new mutation

Yilmaz, Berna Seker, Kor, Deniz, Incecik, Faruk, Ozkinay, Ferda, Herguner, Ozlem Mihriban, Onenli-Mungan, Neslihan

Journal:

Molecular Genetics and Metabolism

Année:

2014

Langue:

english

Fichier:

PDF, 57 KB

english, 2014

10

Transfusion from male-only vs female donors in critically ill recipients of high plasma volume components

O Gajic,M Yilmaz,R Iscimen,D Kor,J Winters,B Afessa,J Farmer

Journal:

Critical Care (BioMed Central)

Année:

2007

Langue:

english

Fichier:

PDF, 12.65 MB

english, 2007

11

Two Novel Missense Mutations in Nonketotic Hyperglycinemia

Yilmaz, B. S., Kor, D., Ceylaner, S., Mert, G. G., Incecik, F., Kartal, E., Mungan, N. O.

Journal:

Journal of Child Neurology

Année:

2015

Langue:

english

Fichier:

PDF, 279 KB

english, 2015

12

The first report of cabergoline-induced immune hemolytic anemia in an adolescent with prolactinoma

Gürbüz, Fatih, Yağcı-Küpeli, Begül, Kör, Yılmaz, Yüksel, Bilgin, Zorludemir, Suzan, Gürbüz, Berrak Bilginer, Küpeli, Serhan

Journal:

Journal of Pediatric Endocrinology and Metabolism

Année:

2014

Langue:

english

Fichier:

PDF, 2.18 MB

english, 2014

13

Screening Frequency of Celiac Disease and Autoimmune Thyroiditis in Children and Adolescents With Type 1 Diabetes Mellitus in Turkey and Comparison With Last Surveys

Keskin, Mehmet, Keskin, Ozlem, Temel, Levent, Dai, Alper, Güler, Elif, Kor, Yilmaz, Coskun, Yavuz

Journal:

The Endocrinologist

Année:

2010

Langue:

english

Fichier:

PDF, 127 KB

english, 2010

14

An asymptomatic mother diagnosed with 3-methylcrotonyl-CoA carboxylase deficiency after newborn screening

Kör, Deniz, Mungan, Neslihan Önenli, Yılmaz, Berna Şeker, Öktem, Murat

Journal:

Journal of Pediatric Endocrinology and Metabolism

Année:

2015

Langue:

english

Fichier:

PDF, 377 KB

english, 2015

15

The domestic livestock resources of Turkey: goat breeds and types and their conservation status

Yilmaz, Orhan, Kor, Askin, Ertugrul, Mehmet, Wilson, R. Trevor

Journal:

Animal Genetic Resources/Ressources génétiques animales/Recursos genéticos animales

Année:

2012

Fichier:

PDF, 596 KB

2012

16

Autoimmune Polyglandular Syndrome Type 3c with Ectodermal Dysplasia, Immune Deficiency and Hemolytic-Uremic Syndrome

Büyükçelik, Mithat, Keskin, Mehmet, Keskin, Özlem, Bay, Ali, Demircioğlu Kılıç, Beltinge, Kor, Yılmaz, Kılınç, M. Arda, Balat, Ayşe

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Année:

2014

Langue:

english

Fichier:

PDF, 105 KB

english, 2014

17

Trends in the Frequency of HLA DR-DQ Haplotypes Among Children and Adolescents with Type 1 Diabetes Mellitus in the Southeast Region of Turkey

Keskin, Mehmet, Aygün, Ayşe, Pehlivan, Sacide, Keskin, Özlem, Kor, Yılmaz, Balat, Ayşe, Coşkun, Yavuz

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Année:

2012

Langue:

english

Fichier:

PDF, 76 KB

english, 2012

18

Increased Resistin Serum Concentrations in Patients with Type 1 Diabetes Mellitus

İclal, Geyikli, Mehmet, Keskin, Yılmaz, Kör, Müslüm, Akan

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Année:

2013

Langue:

english

Fichier:

PDF, 185 KB

english, 2013

19

Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up

Yilmaz, Berna Seker, Kor, Deniz, Mungan, Neslihan Onenli, Erdem, Sevcan, Ceylaner, Serdar

Journal:

Journal of Pediatric Endocrinology and Metabolism

Année:

2015

Langue:

english

Fichier:

PDF, 531 KB

english, 2015

20

Chanarin-Dorfman syndrome: A case report

Mungan, Neslihan Onenli, Tuncez, Ebru, Yilmaz, Berna Seker, Leblebisatan, Goksel, Kunt, Zeynep, Bulut, Derya, Kor, Deniz

Journal:

Molecular Genetics and Metabolism

Année:

2016

Langue:

english

Fichier:

PDF, 70 KB

english, 2016

21

Transfusion from male-only versus female donors in critically ill recipients of high plasma volume components*

Gajic, Ognjen, Yilmaz, Murat, Iscimen, Remzi, Kor, Daryl J., Winters, Jeffrey L., Moore, S Breanndan, Afessa, Bekele

Journal:

Critical Care Medicine

Année:

2007

Langue:

english

Fichier:

PDF, 167 KB

english, 2007

22

Successful cardiovascular surgery experience and enzyme replacement therapy in type 3C Gaucher disease

Mungan, Neslihan, Bulut, Derya, Salih, Orhan, Gulcan, Oner, Deniz, Ali, Erdem, Sevcan, Kor, Deniz, Yılmaz, Berna, Acar, Sebile, Ozbarlas, Nazan

Journal:

Molecular Genetics and Metabolism

Année:

2017

Langue:

english

Fichier:

PDF, 44 KB

english, 2017

23

Mutational Analysis of PHEX , FGF23 and CLCN5 in Patients with Hypophosphataemic Rickets

Guven, Ayla, Al-Rijjal, Roua A., BinEssa, Huda, Dogan, Durmuş, Kor, Yılmaz, Zou, Minjing, Kaya, Namik, Al-Enazi, Anwar F., Hancili, Suna, Tarım, Ömer, Baitei, Essa Y., Kattan, Walaa E, Meyer, Brian F.

Journal:

Clinical Endocrinology

Année:

2017

Langue:

english

Fichier:

PDF, 3.09 MB

english, 2017

24

Severe cardiac involvement in Gaucher type IIIC: a case report and review of the literature

Kör, Yılmaz, Keskin, Mehmet, Başpınar, Osman

Journal:

Cardiology in the Young

Année:

2017

Langue:

english

Fichier:

PDF, 287 KB

english, 2017

25

Improved metabolic control in tetrahydrobiopterin (BH4), responsive phenylketonuria with sapropterin administered in two divided doses vs. a single daily dose

Kör, Deniz, Yılmaz, Berna Şeker, Bulut, Fatma Derya, Ceylaner, Serdar, Mungan, Neslihan Önenli

Journal:

Journal of Pediatric Endocrinology and Metabolism

Année:

2017

Langue:

english

Fichier:

PDF, 116 KB

english, 2017

26

Turkish case of ethylmalonic encephalopathy misdiagnosed as short chain acyl-CoA dehydrogenase deficiency

Bulut, Fatma Derya, Kör, Deniz, Şeker-Yılmaz, Berna, Gül-Mert, Gülen, Kılavuz, Sebile, Önenli-Mungan, Neslihan

Journal:

Metabolic Brain Disease

Année:

2017

Langue:

english

Fichier:

PDF, 494 KB

english, 2017

27

Mucopolysaccharidosis type VI, 9 sibling pairs and 1 set of three siblings: single center experience from Turkey

Mungan, Neslihan, Bulut, Fatma Derya, Kör, Deniz, Seker-Yılmaz, Berna, Kılavuz, Sebile, Onan, Bilen, Başaran, Sibel, Beşen, Şeyda, Dağkıran, Muhammed, Demir, Fadli, Ekinci, Faruk, Tolunay, İlknur

Journal:

Molecular Genetics and Metabolism

Année:

2018

Langue:

english

Fichier:

PDF, 50 KB

english, 2018

28

Cukurova University experience of lysosomal diseases in adulthood: Report of 57 patients

Mungan, Neslihan, Bulut, Fatma Derya, Şeker-Yılmaz, Berna, Kılavuz, Sebile, Kör, Deniz, Koç, Filiz, Gürkan, Emel, Paydaş, Saime, Güvenç, Birol, Atmış, Bahriye, Deniz, Ali

Journal:

Molecular Genetics and Metabolism

Année:

2018

Langue:

english

Fichier:

PDF, 52 KB

english, 2018

29

Twenty-seven mutations with three novel pathologenic variants causing biotinidase deficiency: a report of 203 patients from the southeastern part of Turkey

Seker Yilmaz, Berna, Mungan, Neslihan Onenli, Kor, Deniz, Bulut, Derya, Seydaoglu, Gülşah, Öktem, Murat, Ceylaner, Serdar

Journal:

Journal of Pediatric Endocrinology and Metabolism

Année:

2018

Langue:

english

Fichier:

PDF, 114 KB

english, 2018

30

Four Gaucher disease type II patients with three novel mutations: a single centre experience from Turkey

Bulut, Fatma Derya, Kör, Deniz, Şeker-Yılmaz, Berna, Hergüner, Özlem, Ceylaner, Serdar, Özkınay, Ferda, Kılavuz, Sebile, Önenli-Mungan, Neslihan

Journal:

Metabolic Brain Disease

Année:

2018

Langue:

english

Fichier:

PDF, 487 KB

english, 2018

31

Central precocious puberty in a case of late-diagnosed familial testotoxicosis and long-term treatment monitoring

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 363 KB

english, 2018

32

Current status of the congenital hypothyroidism neonatal screening program in Adana Province, Turkey

Kor, Yılmaz, Kor, Deniz

Journal:

Journal of Pediatric Endocrinology and Metabolism

Année:

2018

Langue:

english

Fichier:

PDF, 278 KB

english, 2018

33

Early onset alpha-mannosidosis: A Turkish case

Mungan, Neslihan, Yilmaz, Berna Seker, Kor, Deniz, Bulut, Derya, Kılavuz, Sebile, Erdem, Sevcan

Journal:

Molecular Genetics and Metabolism

Année:

2018

Langue:

english

Fichier:

PDF, 68 KB

english, 2018

34

Phenotype heterogeneity of congenital adrenal hyperplasia due to genetic mosaicism and concomitant nephrogenic diabetes insipidus in a sibling

Kor, Yılmaz, Zou, Minjing, Al-Rijjal, Roua A., Monies, Dorota, Meyer, Brian F., Shi, Yufei

Journal:

BMC Medical Genetics

Année:

2018

Langue:

english

Fichier:

PDF, 1.25 MB

english, 2018

35

A case with Pallister-Killian syndrome misdiagnosed as mucopolysaccharidosis

Mungan, Neslihan, Kılavuz, Sebile, Bulut, Derya, Kör, Deniz, Yılmaz, Berna, Ceylaner, Serdar

Journal:

Molecular Genetics and Metabolism

Année:

2018

Fichier:

PDF, 52 KB

2018

36

Autoimmune thyroiditis in children and adolescents with type 1 diabetes mellitus is associated with elevated IgG4 but not with low vitamin D

Demir, Korcan, Keskin, Mehmet, Kör, Yιlmaz, Karaoglan, Murat, Gümüstekin Bülbül, Özlem

Journal:

Année:

2014

Fichier:

PDF, 281 KB

2014