Publications by authors named "Muhammet Ensar Dogan"

Claim this Profile
A
A Rare Cause of Primary Microcephaly: 4 New Variants in CDK5RAP2 Gene and Review of the Literature.
Murat Erdogan, Aysel Unal, Muhammet Ensar Dogan, Sumeyra Oguz, Burhan Balta

Am J Med Genet A· September 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders.
Veysel Gök, Alper Ozcan, Fatma Türkan Mutlu, Ebru Yılmaz, Deniz Kocak Göl, Muhammet Ensar Dogan

Res Pract Thromb Haemost· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The clinical presentation and genetic diagnosis of Tangier disease in the pediatric age group.
Selcan Öztürk, Muhammet Ensar Doğan, Banu Kadıoğlu Yılmaz, Ayten Güleç, Pembe Soylu Üstkoyuncu

J Pediatr Endocrinol Metab· March 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel loss of function mutation in the HAVCR2 gene in a patient diagnosed with Hodgkin's lymphoma.
Serife Erdem, Ebru Yilmaz, Alper Ozcan, Ahmed Nazim Canatan, Atil Bisgin, Muhammet Ensar Dogan

Immunol Res· March 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Pyruvate kinase deficiency in 29 Turkish patients with two novel intronic variants.
Veysel Gök, Göksel Leblebisatan, Dilek Gürlek Gökçebay, Salih Güler, Muhammet Ensar Doğan

Br J Haematol· July 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Novel Variant in Gene, a Controversial Gene, in Long QT Syndrome.
Murat Erdogan, Suleyman Sunkak, Oguzhan Bahadır, Muhammet Ensar Doğan, Yasin Ada

Mol Syndromol· March 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
EVs vs. EVs: MSCs and Tregs as a source of invisible possibilities.
Zahra Heydari, Maria Peshkova, Zeynep Burcin Gonen, Ianos Coretchi, Ahmet Eken, Muhammet Ensar Dogan

J Mol Med (Berl)· February 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel MTX2 gene splice site variant resulting in exon skipping, causing the recently described mandibuloacral dysplasia progeroid syndrome.
Burcu Yeter Doğan, Neslihan Günay, Yasin Ada, Muhammet Ensar Doğan

Am J Med Genet A· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A teenager boy with a novel variant of Sitosterolemia presented with pancytopenia.
Veysel Gok, Hayato Tada, Muhammet Ensar Dogan, Ummü Alakus Sari, Kübra Aslan

Clin Chim Acta· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Questions.
Neslihan Günay, Ayşe Seda Pınarbaşı, Muhammet Ensar Doğan, Sibel Yel, Aynur Gencer Balaban

Pediatr Nephrol· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A rare cause of membranoproliferative patterns of injury in siblings with steroid-resistant nephrotic syndrome: Answers.
Neslihan Günay, Ayşe Seda Pınarbaşı, Muhammet Ensar Doğan, Sibel Yel, Aynur Gencer Balaban

Pediatr Nephrol· December 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Varied phenotypic spectrum presenting of paroxysmal exercise-induced dyskinesia: a Turkish family with SLC2A1 mutation.
Murat Gultekin, Muhammet Ensar Dogan, Gulsah Simsir, Ayse Nazlı Basak

Neurol Sci· November 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Change in gene expression levels of GABA, glutamate and neurosteroid pathways due to acoustic trauma in the cochlea.
Meltem Cerrah Gunes, Murat Salih Gunes, Alperen Vural, Fatma Aybuga, Arslan Bayram, Muhammet Ensar Dogan

J Neurogenet· March 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
Effects of thymoquinone in prevention of experimental contrast-induced nephropathy in rats.
Ulaş Serkan Topaloğlu, Murat Hayri Sipahioğlu, İnayet Güntürk, Hülya Akgün, Muhammet Ensar Doğan

Iran J Basic Med Sci· December 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Increased vitamin D receptor gene expression and rs11568820 and rs4516035 promoter polymorphisms in autistic disorder.
Burhan Balta, Hakan Gumus, Ruslan Bayramov, Keziban Korkmaz Bayramov, Murat Erdogan, Muhammet Ensar Dogan

Mol Biol Rep· August 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prenatal diagnosis of upper extremity malformations with ultrasonography: Diagnostic features and perinatal outcome.
Mehmet Serdar Kutuk, Ozguc Altun, Sadan Tutus, Muhammet Ensar Dogan, Mahmut Tuncay Ozgun

J Clin Ultrasound· June 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis