E-LIB Suche - Ergebnisse für: Duzkale, Neslihan

1

Novel mutated Dubin–Johnson syndrome diagnosed during acute..:

Afacan Öztürk, Hacer Berna ; Albayrak, Murat ; Reis Aras, Merih..
memo - Magazine of European Medical Oncology. , 2024

2

Causal Variants of the GJB6 Gene are Associated with Hearin..:

Duzkale, Neslihan ; Aygar, Gamze Tas ; Keseroglu, Kemal..
International Journal of Dermatology and Venereology. 5 (2022) 3 - p. 166-168 , 2022

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

3

Illustration of a rare case of hereditary spastic paraplegi..:

Onder, Halil ; Vural, Atay ; Duzkale, Neslihan..
Journal of Neurology. 269 (2022) 6 - p. 3343-3346 , 2022

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

4

Variants in Mitochondrial ATP Synthase Cause Variable Neuro..:

Zech, Michael ; Kopajtich, Robert ; Steinbrücker, Katja...
Annals of Neurology. 91 (2022) 2 - p. 225-237 , 2022

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

5

Niemann–Pick disease type B and Parkinson's disease: a coex..:

Onder, Halil ; Kocer, Bilge ; Duzkale, Neslihan.
Neurological Sciences. 43 (2022) 4 - p. 2867-2869 , 2022

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

6

Molecular evaluation of mutations in acute myeloid leukemia..:

Merdin, Alparslan ; Dal, Mehmet Sinan ; Kizil Çakar, Merih...
Medicine. 100 (2021) 41 - p. e27458 , 2021

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

7

Novel BRCA2 pathogenic genotype and breast cancer phenotype..:

Duzkale, Neslihan ; Eyerci, Nilnur ; Oksuzoglu, Berna..
European Journal of Medical Genetics. 63 (2020) 4 - p. 103771 , 2020

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

8

Deletion of chromosome 8q22.1, a critical region for Nablus..:

Jamuar, Saumya S. ; Duzkale, Hatice ; Duzkale, Neslihan...
American Journal of Medical Genetics Part A. 167 (2015) 6 - p. 1400-1405 , 2015

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

9

Significant neuropsychiatric symptoms: three mucopolysaccha..:

Değerliyurt, Aydan ; Yayıcı Köken, Özlem ; Teker, Neslihan Düzkale.
Neurocase. 27 (2021) 4 - p. 366-371 , 2021

Link: https://doi.org/10.1080/..

10

Variants in Mitochondrial ATP Synthase Cause Variable Neuro..:

Zech, Michael ; Kopajtich, Robert ; Steinbrücker, Katja...
https://mediatum.ub.tum.de/1654760. , 2022

Link: https://mediatum.ub.tum...

11

Variants in mitochondrial ATP synthase cause variable neuro..:

Zech, Michael ; Kopajtich, Robert ; Steinbrücker, Katja...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939050/. , 2022

Link: http://www.ncbi.nlm.nih...

12

Molecular evaluation of mutations in acute myeloid leukemia..:

Merdin, Alparslan ; Dal, Mehmet Sinan ; Kizil Çakar, Merih...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519194/. , 2021

Link: http://www.ncbi.nlm.nih...

13

Investigation of mitochondrial DNA polymorphisms in patient..:

KİKİ, İLHAMİ ; DÜZKALE, NESLİHAN ; SİNCAN, GÜLDEN...
2cf39f75-4801-444a-924d-32c01dcd3427. , 2021

Link: https://doi.org/10.18663..

14

Novel BRCA2 pathogenic genotype and breast cancer phenotype..:

Duzkale, Neslihan ; EYERCİ, NİLNUR ; Oksuzoglu, Berna..
Duzkale N., EYERCİ N., Oksuzoglu B., Teker T., Kandemir O., "Novel BRCA2 pathogenic genotype and breast cancer phenotype discordance in monozygotic triplets", EUROPEAN JOURNAL OF MEDICAL GENETICS, cilt.63, 2020. , 2020

Link: https://hdl.handle.net/1..

15

Evaluation of FMR1 gene mutations in Turkish women newly di..:

Sarıkaya, Esma ; Tokmak, Aytekin ; Çakar, Esra Şükran...
https://www.ijrcog.org/index.php/ijrcog/article/view/5802/4212. , 2019

Link: https://www.ijrcog.org/i..