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Ensar Dogan, Muhammet
34
results:
Search for persons
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Format
Online (34)
Mediatypes
Articles (Online) (27)
Bookchapter (Online) (2)
OpenAccess-fulltext (5)
Sorted by: Relevance
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?
1
A teenager boy with a novel variant of Sitosterolemia prese..:
Gok, Veysel
;
Tada, Hayato
;
Ensar Dogan, Muhammet
...
Clinica Chimica Acta. 529 (2022) - p. 61-66 , 2022
Link:
https://doi.org/10.1016/..
?
2
Pyruvate kinase deficiency in 29 Turkish patients with two ..:
Gök, Veysel
;
Leblebisatan, Göksel
;
Gürlek Gökçebay, Dilek
...
British Journal of Haematology. 205 (2024) 1 - p. 236-242 , 2024
Link:
https://doi.org/10.1111/..
?
3
A novel MTX2 gene splice site variant resulting in exon ski..:
Yeter Doğan, Burcu
;
Günay, Neslihan
;
Ada, Yasin
.
American Journal of Medical Genetics Part A. 191 (2022) 1 - p. 173-182 , 2022
Link:
https://doi.org/10.1002/..
?
4
EVs vs. EVs: MSCs and Tregs as a source of invisible possib..:
Heydari, Zahra
;
Peshkova, Maria
;
Gonen, Zeynep Burcin
...
Journal of Molecular Medicine. 101 (2022) 1-2 - p. 51-63 , 2022
Link:
https://doi.org/10.1007/..
?
5
Varied phenotypic spectrum presenting of paroxysmal exercis..:
Gultekin, Murat
;
Dogan, Muhammet Ensar
;
Simsir, Gulsah
.
Neurological Sciences. 42 (2021) 11 - p. 4751-4754 , 2021
Link:
https://doi.org/10.1007/..
?
6
A rare cause of membranoproliferative patterns of injury in..:
Günay, Neslihan
;
Pınarbaşı, Ayşe Seda
;
Doğan, Muhammet Ensar
...
Pediatric Nephrology. 36 (2021) 12 - p. 4029-4032 , 2021
Link:
https://doi.org/10.1007/..
?
7
A rare cause of membranoproliferative patterns of injury in..:
Günay, Neslihan
;
Pınarbaşı, Ayşe Seda
;
Doğan, Muhammet Ensar
...
Pediatric Nephrology. 36 (2021) 12 - p. 4027-4028 , 2021
Link:
https://doi.org/10.1007/..
?
8
Increased vitamin D receptor gene expression and rs11568820..:
Balta, Burhan
;
Gumus, Hakan
;
Bayramov, Ruslan
...
Molecular Biology Reports. 45 (2018) 4 - p. 541-546 , 2018
Link:
https://doi.org/10.1007/..
?
9
Two novel missense variants of FGFR2 gene in two patients w..:
Dogan, Muhammet Ensar
;
Dundar, Bilge
;
Gunes, Meltem Cerrah
...
Journal of Biotechnology. 280 (2018) - p. S19-S20 , 2018
Link:
https://doi.org/10.1016/..
?
10
Frequency of chromosome variants in families with recurrent..:
Gunsili, Beyzanur
;
Bayramov, Ruslan
;
Kenanoglu, Sercan
...
Journal of Biotechnology. 256 (2017) - p. S76 , 2017
Link:
https://doi.org/10.1016/..
?
11
Retrospective results of 18 years prenatal diagnosis cases ..:
Bayramov, Ruslan
;
Kutuk, Mehmet Serdar
;
Kenanoglu, Sercan
...
Journal of Biotechnology. 256 (2017) - p. S76 , 2017
Link:
https://doi.org/10.1016/..
?
12
NF1 gene variant allele frequencies comparison of Turkish p..:
Bayramov, Ruslan
;
Dogan, Muhammet Ensar
;
Gunes, Meltem Cerrah
...
Journal of Biotechnology. 256 (2017) - p. S80 , 2017
Link:
https://doi.org/10.1016/..
?
13
The correlation of genotype–phenotype of FMF disease and it..:
Yavuz, Fatih
;
Bayramov, Ruslan
;
Kenanoglu, Sercan
...
Journal of Biotechnology. 256 (2017) - p. S75-S76 , 2017
Link:
https://doi.org/10.1016/..
?
14
A novel nonsense mutation in GALNS gene in family with MPS4..:
Gunes, Meltem Cerrah
;
Bayramov, Ruslan
;
Boyukoglan, Ruksan
...
Journal of Biotechnology. 231 (2016) - p. S108 , 2016
Link:
https://doi.org/10.1016/..
?
15
A case of XYY male patient with micropenis:
Bayramov, Ruslan
;
Gunes, Meltem Cerrah
;
Dogan, Muhammet Ensar
...
Journal of Biotechnology. 231 (2016) - p. S109 , 2016
Link:
https://doi.org/10.1016/..
1-15