Kiraz, Aslihan: search on Z-Library

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1

A rare disorder: Hutchinson–Gilford Progeria Syndrome

Aslihan Kiraz, Samim Ozen

Journal:

Current Opinion in Biotechnology

Year:

2011

Language:

english

File:

PDF, 86 KB

english, 2011

2

A case with ring chromosome 6: Very rare chromosomal abnormalities

Erdogan, Murat, Balta, Burhan, Kiraz, Aslihan, Bahadir, Oguzhan

Journal:

Journal of Biotechnology

Year:

2014

Language:

english

File:

PDF, 83 KB

english, 2014

3

The role of TNF-α and PAI-1 gene polymorphisms in familial Mediterranean fever

Munis Dundar,Aslihan Kiraz,Burhan Balta,Elif Funda Emirogullari…

Journal:

Modern Rheumatology

Year:

2013

Language:

english

File:

PDF, 210 KB

english, 2013

4

The role of TNF-α and PAI-1 gene polymorphisms in familial Mediterranean fever

Dundar, Munis, Kiraz, Aslihan, Balta, Burhan, Emirogullari, Elif Funda, Zararsiz, Gokmen, Yurci, Alper, Aslan, Duran, Baskol, Mevlut

Journal:

Modern Rheumatology

Year:

2013

Language:

english

File:

PDF, 236 KB

english, 2013

5

Thyroid Hypoplasia as a Cause of Congenital Hypothyroidism in Monozygotic Twins Concordant for Rubinstein-Taybi Syndrome

Akın, Mustafa Ali, Güneş, Tamer, Akın, Leyla, Çoban, Dilek, Kara Oncu, Sena, Kiraz, Aslıhan, Kurtoğlu, Selim

Journal:

Journal of Clinical Research in Pediatric Endocrinology

Year:

2011

Language:

english

File:

PDF, 581 KB

english, 2011

6

A Rare Cause of Neonatal Hemolytic Anemia

Soylu Ustkoyuncu, Pembe, Mutlu, Fatma Türkan, Kiraz, Aslihan, Tag Balkis, Zuhal, Yel, Sibel

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2017

Language:

english

File:

PDF, 186 KB

english, 2017

7

Decreased disulphide/thiol ratio in patients with autosomal recessive non-syndromic hearing loss

Balta, Burhan, Gundogdu, Ramazan, Erdogan, Murat, Alisik, Murat, Kiraz, Aslihan, Ozcan, Ibrahim, Erel, Ozcan

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2018

Language:

english

File:

PDF, 198 KB

english, 2018

8

Points to be noted on Poland syndrome

Kiraz, Aslihan, Balta, Burhan, Erdogan, Murat, Bahadir, Oguzhan

Journal:

Journal of Biotechnology

Year:

2014

Language:

english

File:

PDF, 62 KB

english, 2014

9

Wiedemann–Rautenstrauch syndrome report of the patient with premature delivery

Erdogan, Murat, Kiraz, Aslihan, Balta, Burhan, Bahadir, Oguzhan, Sahin, Ozlem

Journal:

Journal of Biotechnology

Year:

2014

Language:

english

File:

PDF, 69 KB

english, 2014

10

Asymmetric Crying Face in a Newborn with Isotretinoin Embryopathy

Sarici, Dilek, Akin, Mustafa Ali, Kurtoglu, Selim, Uzum, Kazim, Kiraz, Aslihan

Journal:

Pediatric Dermatology

Year:

2013

Language:

english

File:

PDF, 173 KB

english, 2013

11

Unbalanced 3;22 translocation with 22q11 and 3p deletion syndrome

Munis Dundar, Aslihan Kiraz, Sener Tasdemir, Hilal Akalin, Selim Kurtoglu, Filiz Hafo, Naci Cine, Hakan Savli

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 144 KB

english, 2010

12

Three patients resembling Teebi-Shaltout syndrome

Aldemir, Ozgur, Ozen, Samim, Erdem, Sevcan, Kiraz, Aslihan, Akarsu, Nurten, Alanay, Yasemin

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 183 KB

english, 2013

13

Wiedemann–Rautenstrauch syndrome: Report of a variant case

Aslihan Kiraz, Samim Ozen, Filiz Tubas, Yusuf Usta, Ozgur Aldemir, Yasemin Alanay

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 100 KB

english, 2012

14

Does thiol–disulphide balance show oxidative stress in different MEFV mutations?

Balta, Burhan, Erdogan, Murat, Alisik, Murat, Kiraz, Aslihan, Akalin, Tayfun, Bastug, Funda, Erel, Ozcan

Journal:

Rheumatology International

Year:

2017

Language:

english

File:

PDF, 710 KB

english, 2017

15

Cytogenetic damage of radiotherapy in long-term head and neck cancer survivors

Unal, Dilek, Kiraz, Aslihan, Avci, Deniz, Tasdemir, Arzu, Unal, Tuba Dilay, Cagli, Sedat, Eroglu, Celalettin, Yuce, Imdat, Ozcan, Ibrahim, Kaplan, Bunyamin

Journal:

International Journal of Radiation Biology

Year:

2016

Language:

english

File:

PDF, 790 KB

english, 2016

16

Common Familial Mediterranean Fever gene mutations in a Turkish cohort

Munis Dundar, Elif Funda Emirogullari, Aslihan Kiraz, Serpil Taheri, Mevlut Baskol

Journal:

Molecular Biology Reports

Year:

2011

Language:

english

File:

PDF, 1.56 MB

english, 2011

17

A patient with hyperphalangism

Kiraz, Aslihan, Tubas, Filiz, Ekinci, Yakup, Dögen, Mehmet E., Varli, Muhiddin

Journal:

Clinical Dysmorphology

Year:

2013

Language:

english

File:

PDF, 199 KB

english, 2013

18

Combination of two different homozygote mutations in Pompe disease

Arslan, Alev, Poyrazoğlu, Hatice Gamze, Kiraz, Aslihan, Özcan, Alper, Işık, Halid, Ergul, Ayse Betül, Mungan, Neslihan Önenli, Streubel, Berthold, Ceylaner, Serdar, Altuner Torun, Yasemin

Journal:

Pediatrics International

Year:

2016

Language:

english

File:

PDF, 779 KB

english, 2016

19

A short-rib polydactyly syndrome: Ellis–van Creveld syndrome

Kiraz, Aslihan, Erdogan, Murat, Balta, Burhan, Bahadir, Oguzhan, Akın, Mehmet Ali

Journal:

Journal of Biotechnology

Year:

2014

Language:

english

File:

PDF, 76 KB

english, 2014

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