Ozgur, Cogulu: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

1

Highest heterogeneity for cystic fibrosis: 36 mutations account for 75% of all CF chromosomes in Turkish patients

Mehmet Okyay Kılınç, Vasiliki Ninidu Ninis, Elif Dağlı, Mübeccel Demirkol, Ferda Özkınay, Zeliha Arıkan, Özgür Çoğulu, Gülden Hüner, Fazilet Karakoç, Aslıhan Tolun

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 168 KB

english, 2002

2

The relationship between ACTN3 R577X gene polymorphism and physical performance in amateur soccer players and sedentary individuals

Koku, Fatma E., Karamızrak, Süleyman O., Çiftçi, Aynur S., Taşlıdere, Hasan, Durmaz, Burak, Çoğulu, Özgür

Journal:

Biology of Sport

Year:

2019

Language:

english

File:

PDF, 239 KB

english, 2019

3

Genetic factors associated with the predisposition to late onset Alzheimer's disease

Durmaz, Asude, Kumral, Emre, Durmaz, Burak, Onay, Huseyin, Aslan, Gulcin Itirli, Ozkinay, Ferda, Pehlivan, Sacide, Orman, Mehmet, Cogulu, Ozgur

Journal:

Year:

2019

Language:

english

File:

PDF, 592 KB

english, 2019

4

The Association of minor congenital anomalies and childhood cancer

Asude Durmaz, Burak Durmaz, Bengu Kadioglu, Serap Aksoylar, Deniz Karapinar, Guldane Koturoglu, Mehmet N. Orman, Ferda Ozkinay, Ozgur Cogulu

Journal:

Pediatric Blood & Cancer

Year:

2011

Language:

english

File:

PDF, 117 KB

english, 2011

5

Laboratory Genetic Testing in Clinical Practice 2016

Cogulu, Ozgur, Schoumans, Jacqueline, Toruner, Gokce, Demkow, Urszula, Karaca, Emin, Durmaz, Asude Alpman

Journal:

BioMed Research International

Year:

2017

Language:

english

File:

PDF, 1.06 MB

english, 2017

6

Evolution of Genetic Techniques: Past, Present, and Beyond

Durmaz, Asude Alpman, Karaca, Emin, Demkow, Urszula, Toruner, Gokce, Schoumans, Jacqueline, Cogulu, Ozgur

Journal:

BioMed Research International

Year:

2015

Language:

english

File:

PDF, 2.20 MB

english, 2015

7

Evaluation of Telomerase mRNA (hTERT) in Childhood Acute Leukemia

Cogulu, Ozgur, Kosova, Buket, Karaca, Emin, Gunduz, Cumhur, Ozkinay, Ferda, Aksoylar, Serap, Gulen, Huseyin, Kantar, Mehmet, On&#x0130, z, Haldun, Karapinar, Deniz, Cetingul, Nazan, Erbay, Ay&#x0015F, e

Journal:

Leukemia and Lymphoma

Year:

2004

Language:

english

File:

PDF, 123 KB

english, 2004

8

MicroRNA expression profiling in children with different asthma phenotypes

Midyat, Levent, Gulen, Figen, Karaca, Emin, Ozkinay, Ferda, Tanac, Remziye, Demir, Esen, Cogulu, Ozgur, Aslan, Asli, Ozkinay, Cihangir, Onay, Huseyin, Atasever, Mesude

Journal:

Pediatric Pulmonology

Year:

2016

File:

PDF, 288 KB

2016

9

Clinical and Genetic Features of L1 Syndrome Patients: Definition of Two Novel Mutations

Isik, Esra, Onay, Huseyin, Atik, Tahir, Akgun, Bilcag, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

Clinical Neurology and Neurosurgery

Year:

2018

Language:

english

File:

PDF, 340 KB

english, 2018

10

A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow

Durmaz, Burak, Alpman Durmaz, Asude, Karaca, Emin, Saydam, Guray, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

Turkish Journal of Hematology

Year:

2010

Language:

english

File:

PDF, 61 KB

english, 2010

11

Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndrome

Eren Akarcan, Sanem, Edeer Karaca, Neslihan, Aksu, Guzide, Aykut, Ayca, Yilmaz Karapinar, Deniz, Cetin, Funda, Aydinok, Yesim, Azarsiz, Elif, Gambineri, Eleonora, Cogulu, Ozgur, Ulusoy Severcan, Ezgi,

Journal:

JMM Case Reports

Year:

2018

File:

PDF, 1.90 MB

2018

12

Pediatrik cerrahide sık karşılaşılan konjenital anomalilere genetik yaklaşım

Durmaz, Asude, Durmaz, Burak, Karaca, Emin, Ergün, Orkan, Çoğulu, Özgür

Journal:

Bakirkoy Tip Dergisi / Medical Journal of Bakirkoy

Year:

2013

File:

PDF, 13.10 MB

2013

13

Laboratory Genetic Testing in Clinical Practice 2014

Cogulu, Ozgur, Schoumans, Jacqueline, Toruner, Gokce, Demkow, Urszula, Karaca, Emin, Durmaz, Asude Alpman

Journal:

BioMed Research International

Year:

2015

Language:

english

File:

PDF, 1.05 MB

english, 2015

14

Evaluation of Manisa propolis effect on leukemia cell line by telomerase activity

Cumhur Gunduz, Cigir Biray, Buket Kosova, Berna Yilmaz, Zuhal Eroglu, Fahri Şahin, Serdar Bedii Omay, Ozgur Cogulu

Journal:

Leukemia Research

Year:

2005

Language:

english

File:

PDF, 125 KB

english, 2005

15

Multiple cutaneous hemangiomas in a patient with combined pituitary hormone deficiency

Aykut, Ayca, Ozen, Samim, Sımsek, Damla Gokşen, Onay, Huseyin, Cogulu, Ozgur, Darcan, Sukran, Ozkinay, Ferda

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2014

Language:

english

File:

PDF, 1.61 MB

english, 2014

16

A novel mutation in two families with pycnodysostosis

Ozdemir, Taha R., Atik, Tahir, Karaca, Emin, Onay, Huseyin, Ozkinay, Ferda, Cogulu, Ozgur

Journal:

Clinical Dysmorphology

Year:

2013

Language:

english

File:

PDF, 283 KB

english, 2013

17

Clinical Applications for Next-Generation Sequencing || Next Generation Sequencing as a Tool for Noninvasive Prenatal Tests

Year:

2016

Language:

english

File:

PDF, 669 KB

english, 2016

18

Primary Cutaneous Nocardiosis in an Adolescent with Crohn Disease

Svoboda, Steven A., Eikenberg, Joshua D., Cogulu, Ozgur

Journal:

Case Reports in Pediatrics

Year:

2020

File:

PDF, 1.38 MB

2020

19

Pachyonychia congenita type 2, N92S mutation of keratin 17 gene: clinical features, mutation analysis and pathological view

Ozgur Cogulu, Huseyin Onay, Ayca Aykut, Neil J. Wilson, Frances J. D. Smith, Tugrul Dereli, Ferda Ozkinay

Journal:

European Journal of Pediatrics

Year:

2009

Language:

english

File:

PDF, 207 KB

english, 2009

20

The Correlation between miRNA (miR: microribonucleic acid) Levels and Clinical Endpoints in Heart Failure

Sayın, Ahmet, Zihni, Burcu, Alkan, Mustafa Beyazıt, Bilgin, Murat, Yıldız, Berkir Serhat, Gül, İlker, Çoğulu, Muhsin Özgür, Karaca, Emin, Zoghi, Mehdi

Journal:

Journal of the American College of Cardiology

Year:

2013

Language:

english

File:

PDF, 109 KB

english, 2013

21

A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion

Durmaz, Asude Alpman, Akin, Haluk, Ekmekci, Aslihan Yilmaz, Onay, Huseyin, Durmaz, Burak, Cogulu, Ozgur, Aydinok, Yesim, Ozkinay, Ferda

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2009

Language:

english

File:

PDF, 83 KB

english, 2009

22

Evaluation of 80 children with prolonged fever

Ozgur Cogulu, Guldane Koturoglu, Zafer Kurugol, Ferda Ozkinay, Fadil Vardar, Cihangir Ozkinay

Journal:

Pediatrics International

Year:

2003

Language:

english

File:

PDF, 94 KB

english, 2003

23

The genotoxic effect of radiofrequency waves on mouse brain

Emin Karaca, Burak Durmaz, Huseyin Altug, Teoman Yildiz, Candan Guducu, Melis Irgi, Mehtap Gulcihan Cinar Koksal, Ferda Ozkinay, Cumhur Gunduz, Ozgur Cogulu

Journal:

Journal of Neuro-Oncology

Year:

2012

Language:

english

File:

PDF, 358 KB

english, 2012

24

Role of angiotensin-converting enzyme gene polymorphisms in children with sepsis and septic shock

Ozgur Cogulu, Huseyin Onay, Demet Uzunkaya, Cumhur Gunduz, Sacide Pehlivan, Fadil Vardar, Fusun Atlihan, Cihangir Ozkinay, Ferda Ozkinay

Journal:

Pediatrics International

Year:

2008

Language:

english

File:

PDF, 63 KB

english, 2008

25

Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency

Driessen, Gertjan J., IJspeert, Hanna, Wentink, Marjolein, Yntema, Helger G., van Hagen, P. Martin, van Strien, Arthur, Bucciol, Giorgia, Cogulu, Ozgur, Trip, Margreet, Nillesen, Willy, Peeters, Els A

Journal:

Journal of Allergy and Clinical Immunology

Year:

2016

Language:

english

File:

PDF, 1.25 MB

english, 2016

26

UroVysion Fluorescence in situ hybridization (UroVysion FISH) assay for detecting Turkish bladder cancer patients in voided urine: A preliminary study

Dodurga, Yavuz, Avcı, ÇIğır Biray, Yılmaz, Sunde, NazIı, Oktay, Çoğulu, Özgür, Cankaya, Tufan, Gündüz, Cumhur

Journal:

Współczesna Onkologia

Year:

2013

Language:

english

File:

PDF, 123 KB

english, 2013

27

P-88 Relationships between ACE I/D gene polymorphism and maxvo2 in soccer players and sedentary individuals

Arslan, A Sevgi, Islegen, Çetin, Koku, Fatma E, Karamizrak, S Oguz, Çogulu, Özgür, Durmaz, Burak, Taslidere, Hasan

Journal:

British Journal of Sports Medicine

Year:

2016

Language:

english

File:

PDF, 73 KB

english, 2016

28

Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia

Kaan Kavakli, Ozgur Cogulu, Emin Karaca, Burak Durmaz, Ferda Ozkinay, Semih Aydogdu, Hayal Ozkilic, Can Balkan, Deniz Karapinar, Yılmaz Ay

Journal:

Annals of Nuclear Medicine

Year:

2012

Language:

english

File:

PDF, 219 KB

english, 2012

29

A case of epicanthus, telecanthus, high palate, transitional vertebra associated with vesicoureteral reflux

Ozgur Cogulu, Burak Durmaz, Cihangir Ozkinay, Ferda Ozkinay

Journal:

Acta Paediatrica

Year:

2007

Language:

english

File:

PDF, 141 KB

english, 2007

30

Psychiatric Approaches for Disorders of Sex Development: Experience of a Multidisciplinary Team

Burcu, Özbaran, Samim, Özen, Damla, Gökşen, Özlem, Korkmaz, Hüseyin, Onay, Ferda, Özkınay, Özgür, Çoğulu, Serpil, Erermiş, Sezen, Köse, Ali, Avanoğlu, İbrahim, Ulman, Şükran, Darcan

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Year:

2013

Language:

english

File:

PDF, 5.94 MB

english, 2013

31

Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome

Durmaz, Burak, Karaca, Emin, Vural, Filiz, Cogulu, Ozgur, Alpman, Asude, Tombuloglu, Murat, Ozkinay, Ferda

Journal:

Acta Oncologica

Year:

2008

Language:

english

File:

PDF, 87 KB

english, 2008

32

Reference values of anthropometric measurements in healthy late preterm and term infants

SİYAH BİLGİN, Betül, UYGUR, Özgün, TEREK, Demet, ALTUN KÖROĞLU, Özge, YALAZ, Mehmet, AKISÜ, Mete, ÇOĞULU, Özgür, KÜLTÜRSAY, Nilgün

Journal:

TURKISH JOURNAL OF MEDICAL SCIENCES

Year:

2018

Language:

english

File:

PDF, 1.24 MB

english, 2018

33

Oxidative stress biomarkers in four Bloom syndrome (BS) patients and in their parents suggest in vivo redox abnormalities in BS phenotype

Adriana Zatterale, Frank J. Kelly, Paolo Degan, Marco d'Ischia, Federico V. Pallardó, Rita Calzone, Christina Dunster, Ana Lloret, Paola Manini, Ozgur Coğulu, Kaan Kavaklı, Giovanni Pagano

Journal:

Clinical Biochemistry

Year:

2007

Language:

english

File:

PDF, 137 KB

english, 2007

34

Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven-Year Period

Ozgur Cogulu, Ferda Ozkinay, Haluk Akin, Huseyin Onay, Emin Karaca, Asude Alpman Durmaz, Burak Durmaz, Ayca Aykut, Erhan Pariltay, Ozgur Kirbiyik, Cumhur Gunduz, Cihangir Ozkinay

Journal:

Journal of Genetic Counseling

Year:

2011

Language:

english

File:

PDF, 128 KB

english, 2011

35

Evaluation of the SMN and NAIP Genes in a Family: Homozygous Deletion of the SMN2 Gene in the Fetus and Outcome of the Pregnancy

Cogulu, Ozgur, Durmaz, Burak, Pehlivan, Sacide, Alpman, Asude, Ozkinay, Ferda

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2009

Language:

english

File:

PDF, 40 KB

english, 2009

36

Prenatal detection of a pure trisomy 10p case

Cumhur Gunduz, Ozgur Cogulu, Sermet Sagol, Osman Zekioglu, Cihangir Ozkinay, Ferda Ozkinay

Journal:

Prenatal Diagnosis

Year:

2003

Language:

english

File:

PDF, 114 KB

english, 2003

37

A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies

Durmaz, Burak, Cogulu, Ozgur, Dizdarer, Ceyhun, Stobbe, Heike, Pfaeffle, Roland, Ozkinay, Ferda

Journal:

Journal of Pediatric Endocrinology and Metabolism

Year:

2011

Language:

english

File:

PDF, 421 KB

english, 2011

38

Molecular Basis of β -Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation

Ozkinay, Ferda, Onay, Huseyin, Karaca, Emin, Arslan, Esra, Erturk, Biray, Ece Solmaz, Asli, Tekin, Ismihan Merve, Cogulu, Ozgur, Aydinok, Yeşim, Vergin, Canan

Journal:

Year:

2015

Language:

english

File:

PDF, 355 KB

english, 2015

39

Two cases of macrocephaly and immune deficiency

Cogulu, Ozgur, Aykut, Ayca, Kutukculer, Necil, Ozkinay, Cihangir, Ozkinay, Ferda

Journal:

Clinical Dysmorphology

Year:

2007

Language:

english

File:

PDF, 132 KB

english, 2007

40

Prospective Evaluation of Whole Genome MicroRNA Expression Profiling in Childhood Acute Lymphoblastic Leukemia

Duyu, Muhterem, Durmaz, Burak, Gunduz, Cumhur, Vergin, Canan, Yilmaz Karapinar, Deniz, Aksoylar, Serap, Kavakli, Kaan, Cetingul, Nazan, Irken, Gulersu, Yaman, Yontem, Ozkinay, Ferda, Cogulu, Ozgur

Journal:

BioMed Research International

Year:

2014

Language:

english

File:

PDF, 1.40 MB

english, 2014

41

Determination of Lymphocyte Cytokinesis-Block Micronucleus Values in Apparently Healthy Children by means of Age and Sex

Durmaz, Burak, Taslidere, Hasan, Koturoglu, Guldane, Gunduz, Cumhur, Orman, Mehmet, Cogulu, Ozgur

Journal:

BioMed Research International

Year:

2019

Language:

english

File:

PDF, 1.59 MB

english, 2019

42

Progressive pseudorheumatoid arthropathy of childhood

Ozgur Cogulu, Ferda Ozkinay, Cihangir Ozkinay, Gül Sapmaz, Osman Yalman, Helda Binnur Deveci

Journal:

Indian Journal of Pediatrics

Year:

1999

Language:

english

File:

PDF, 1.17 MB

english, 1999

43

Interview with Parents of Children with Down Syndrome: Their Perceptions and Feelings

Asude Durmaz, Tufan Cankaya, Burak Durmaz, Ali Vahabi, Cumhur Gunduz, Ozgur Cogulu, Ferda Ozkinay

Journal:

Indian Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 90 KB

english, 2011

44

SMOC1 Is Essential for Ocular and Limb Development in Humans and Mice

Ippei Okada, Haruka Hamanoue, Koji Terada, Takaya Tohma, Andre Megarbane, Eliane Chouery, Joelle Abou-Ghoch, Nadine Jalkh, Ozgur Cogulu, Ferda Ozkinay, Kyoji Horie, Junji Takeda, Tatsuya Furuichi, Shi

Journal:

The American Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 1.94 MB

english, 2011

45

The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation

Schreml, Julia, Durmaz, Burak, Cogulu, Ozgur, Keupp, Katharina, Beleggia, Filippo, Pohl, Esther, Milz, Esther, Coker, Mahmut, Ucar, Sema Kalkan, Nürnberg, Gudrun, Nürnberg, Peter, Kuhn, Joachim, Ozkin

Journal:

Year:

2014

Language:

english

File:

PDF, 718 KB

english, 2014

46

The Rate of Sex Chromosome Aneuploidies in Prenatal Diagnosis and Subsequent Decisions in Western Turkey

Ataman, Esra, Cogulu, Ozgur, Durmaz, Asude, Karaca, Emin, Durmaz, Burak, Akin, Haluk, Ozkinay, Ferda

Journal:

Genetic Testing and Molecular Biomarkers

Year:

2012

Language:

english

File:

PDF, 81 KB

english, 2012

47

MEFVmutations in patients with familial Mediterranean fever from the Aegean region of Turkey

Haluk Akin, Huseyin Onay, Emre Turker, Ozgur Cogulu, Ferda Ozkinay

Journal:

Molecular Biology Reports

Year:

2010

Language:

english

File:

PDF, 179 KB

english, 2010

48

Biallelic TOR1A mutations cause severe arthrogryposis: A case requiring reverse phenotyping

Isik, Esra, Aykut, Ayca, Atik, Tahir, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 1.16 MB

english, 2018

49

A further Turkish case of Griscelli syndrome with new RAB27A mutation

Huseyin Onay, Can Balkan, Ozgur Cogulu, Yesim Aydinok, Deniz Yılmaz Karapinar, Ferda Ozkinay

Journal:

Journal of the American Academy of Dermatology

Year:

2008

Language:

english

File:

PDF, 143 KB

english, 2008

50

A case of Brachman de Lange syndrome with cerebellar vermis hypoplasia

Ozkinay, Ferda, Cogulu, Ozgur, G??nd??z, Cumhur, Levent, Erturk, Ozkinay, Cihangir

Journal:

Clinical Dysmorphology

Year:

1998

File:

PDF, 154 KB

1998

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски