E-LIB Suche - Ergebnisse für: Kiraz, Aslihan

1

A Case Series of Three Patients with Cleidocranial Dysplasi..:

Berber, Uğur ; Gül Şıraz, Ülkü ; Yakubi, Mustafa...
The Cleft Palate Craniofacial Journal. , 2024

Link: https://doi.org/10.1177/..

2

Recurrent symptomatic urolithiasis in a patient with cystic..:

Yel, Sibel ; Dursun, Ismail ; Köse, Mehmet...
Pediatric Nephrology. , 2024

Link: https://doi.org/10.1007/..

3

Evaluation of chromosomal abnormalities in the postnatal co..:

Akalin, Hilal ; Sahin, Izem Olcay ; Paskal, Seyma Aktas...
Journal of Clinical Laboratory Analysis. 38 (2023) 1-2 - p. , 2023

Link: https://doi.org/10.1002/..

4

Contribution of genotypes in Prothrombin and Factor V Leide..:

Kiraz, Aslıhan ; Sezer, Ozlem ; Alemdar, Adem...
Journal of Medical Virology. 95 (2023) 2 - p. , 2023

Link: https://doi.org/10.1002/..

5

Osteopontin as an early predictor of atherosclerosis in att..:

Baspinar, Osman ; Kocer, Derya ; Kiraz, Aslihan..
Medicine. 102 (2023) 39 - p. e35137 , 2023

Link: https://doi.org/10.1097/..

6

A truncating variant in the THOC6 gene with new findings in..:

Kiraz, Aslıhan ; Tubaş, Filiz ; Seber, Turgut
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1568-1571 , 2022

Link: https://doi.org/10.1002/..

7

Analysis of ACE2 and TMPRSS2 coding variants as a risk fact..:

Duman, Nilgun ; Tuncel, Gulten ; Bisgin, Atil...
Journal of Medical Virology. 94 (2022) 11 - p. 5225-5243 , 2022

Link: https://doi.org/10.1002/..

8

Two Pathogenic Variants in Two Ultra Rare Syndromes; Smith-..:

Ozdemir, Yesim ; Cag, Murat ; Dundar, Munis..
International Journal of Innovative Research in Medical Science. 7 (2022) 2 - p. 100-106 , 2022

Link: https://doi.org/10.23958..

9

Tubulopathy and hepatomegaly in a 2-year-old boy: Questions:

Ustkoyuncu, Pembe Soylu ; Bastug, Funda ; Kiraz, Aslıhan...
Pediatric Nephrology. , 2021

Link: https://doi.org/10.1007/..

10

Tubulopathy and hepatomegaly in a 2-year-old boy: Answers:

Ustkoyuncu, Pembe Soylu ; Bastug, Funda ; Kiraz, Aslıhan...
Pediatric Nephrology. , 2021

Link: https://doi.org/10.1007/..

11

A comprehensive molecular analysis and genotype–phenotype c..:

Balta, Burhan ; Erdogan, Murat ; Kiraz, Aslıhan...
Molecular Biology Reports. 47 (2020) 3 - p. 1835-1843 , 2020

Link: https://doi.org/10.1007/..

12

A Frequent Mutation in the FTL Gene Causing Hyperferritinem..:

Balta, Burhan ; Erdoğan, Murat ; Kiraz, Aslıhan..
Turkish Journal of Hematology. 36 (2019) 1 - p. 25-28 , 2019

Link: https://doi.org/10.4274/..

13

Frequent Mutation in the FTL Gene Causing Hyperferritinemia..:

Balta, Burhan ; Erdoğan, Murat ; Kiraz, Aslıhan..
Turkish Journal of Hematology. , 2018

Link: https://doi.org/10.4274/..

14

Decreased disulphide/thiol ratio in patients with autosomal..:

Balta, Burhan ; Gundogdu, Ramazan ; Erdogan, Murat...
International Journal of Pediatric Otorhinolaryngology. 112 (2018) - p. 188-192 , 2018

Link: https://doi.org/10.1016/..

15

Does thiol–disulphide balance show oxidative stress in diff..:

Balta, Burhan ; Erdogan, Murat ; Alisik, Murat...
Rheumatology International. 38 (2017) 1 - p. 97-104 , 2017

Link: https://doi.org/10.1007/..