ÇOĞULU, Özgür: search on Z-Library

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

Don't use scam websites

51

A Novel Homozygous Ala529Val LMNA Mutation in Turkish Patients with Mandibuloacral Dysplasia

Garg, Abhimanyu, Cogulu, Ozgur, Ozkinay, Ferda, Onay, Huseyin, Agarwal, Anil K.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2005

Language:

english

File:

PDF, 322 KB

english, 2005

52

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

53

Trigonocephaly and Wilson??s disease in two siblings

Cogulu, Ozgur, Onay, Huseyin, Ozgenc, Funda, Karaca, Emin, Gunduz, Cumhur, Tzetis, Maria, Cankaya, Tufan, Kanavakis, Emmanuel, Ozkinay, Ferda

Journal:

Clinical Dysmorphology

Year:

2005

Language:

english

File:

PDF, 111 KB

english, 2005

54

A new patient with LACHT syndrome (Mardini-Nyhan association)

Atik, Tahir, Torun, Huseyin Ozan, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

American Journal of Medical Genetics Part A

Year:

2015

Language:

english

File:

PDF, 305 KB

english, 2015

55

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

56

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

57

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

58

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

59

Seckel syndrome with Morgagni hernia

Onder, Asan, Cogulu, Ozgur, Ekmekci, Aslihan, Pariltay, Erhan, Kirbiyik, Ozgur, Ozkinay, Ferda

Journal:

Clinical Dysmorphology

Year:

2007

Language:

english

File:

PDF, 100 KB

english, 2007

60

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

61

Evaluation of the miRNA profiling and effectiveness of the propolis on B-cell acute lymphoblastic leukemia cell line

Yilmaz, Ugur Cem, Bagca, Bakiye Goker, Karaca, Emin, Durmaz, Asude, Durmaz, Burak, Aykut, Ayca, Kayalar, Husniye, Avci, Cigir Biray, Susluer, Sunde Yilmaz, Gunduz, Cumhur, Cogulu, Ozgur

Journal:

Biomedicine & Pharmacotherapy

Year:

2016

Language:

english

File:

PDF, 2.68 MB

english, 2016

62

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

63

Evaluation of the effects of miRNAs in familial Mediterranean fever

Hortu, Hacer Orsdemir, Karaca, Emin, Sozeri, Betul, Gulez, Nesrin, Makay, Balahan, Gunduz, Cumhur, Atik, Tahir, Tekin, Ismihan Merve, Unsal, Sevket Erbil, Ozgur, Cogulu

Journal:

Clinical Rheumatology

Year:

2018

Language:

english

File:

PDF, 779 KB

english, 2018

64

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

65

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

66

Laboratory Genetic Testing in Clinical Practice

Cogulu, Ozgur, Alanay, Yasemin, Toruner, Gokce A.

Journal:

BioMed Research International

Year:

2013

Language:

english

File:

PDF, 1.03 MB

english, 2013

67

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

68

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

69

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

70

A rare sex chromosome aneuploidy: 48,XXYY syndrome

Atik, Tahir, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

Türk Pediatri Arşivi

Year:

2016

Language:

english

File:

PDF, 456 KB

english, 2016

71

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

72

An X-Linked Hyper-IgM Patient Followed Successfully for 23 Years without Hematopoietic Stem Cell Transplantation

Kutukculer, Necil, Karaca, Neslihan Edeer, Aksu, Guzide, Aykut, Ayca, Pariltay, Erhan, Cogulu, Ozgur

Journal:

Case Reports in Immunology

Year:

2018

Language:

english

File:

PDF, 2.01 MB

english, 2018

73

Chronic granulamatous disease: two decades of experience from a pediatric immunology unit in a country with high rate of consangineous marriages

Kutukculer, Necil, Aykut, Ayca, Karaca, Neslihan E., Durmaz, Asude, Aksu, Guzide, Genel, Ferah, Pariltay, Erhan, Cogulu, Özgür, Azarsız, Elif

Journal:

Scandinavian Journal of Immunology

Year:

2018

Language:

english

File:

PDF, 403 KB

english, 2018

74

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

75

Correction to: Evaluation of the effects of miRNAs in familial Mediterranean fever

Hortu, Hacer Orsdemir, Karaca, Emin, Sozeri, Betul, Gulez, Nesrin, Makay, Balahan, Gunduz, Cumhur, Atik, Tahir, Tekin, Ismihan Merve, Unsal, Sevket Erbil, Cogulu, Ozgur

Journal:

Clinical Rheumatology

Year:

2019

Language:

english

File:

PDF, 282 KB

english, 2019

76

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

Language:

english

File:

PDF, 1.90 MB

english, 2018

77

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

78

Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure

Karaca, Yasemin, Pariltay, Erhan, Mardan, Lamiya, Karaca, Emin, Durmaz, Asude, Durmaz, Burak, Aykut, Ayca, Akin, Haluk, Cogulu, Ozgur

Journal:

Reproductive Biology

Year:

2019

File:

PDF, 341 KB

2019

79

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

80

Clinical and molecular aspects of PTEN mutations in 10 pediatric patients

Isik, Esra, Simsir, Ozguc Semih, Solmaz, Asli Ece, Onay, Huseyin, Atik, Tahir, Aykut, Ayca, Durmaz, Asude, Cogulu, Ozgur, Ozkinay, Ferda

Journal:

Annals of Human Genetics

Year:

2020

Language:

english

File:

PDF, 633 KB

english, 2020

81

Human immune disorder associated with homozygous hypomorphic mutation affecting MALT1B splice variant

Kutukculer, Necil, Seeholzer, Thomas, OâNeill, Thomas J., GraÃ, Carina, Aykut, Ayca, Karaca, Neslihan Edeer, Durmaz, Asude, Cogulu, Ozgur, Aksu, Guzide, Gehring, Torben, Gewies, Andreas, Krappmann,

Journal:

Journal of Allergy and Clinical Immunology

Year:

2020

File:

PDF, 7.19 MB

2020

82

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

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@z-lib.do

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