Publications by authors named "Eminoglu T"

Claim this Profile
A
A Rare Pitfall in Bone Mineral Densitometry: Gaucher Disease.
Mine Araz, Gizem Sutcu, Llknur Surucu Kara, Tuba Eminoglu, Elgin Ozkan

Clin Nucl Med· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genotype-Phenotype Correlation of the Childhood-Onset Bethlem Myopathy in the Mediterranean Region of Turkey.
Muhammet G Kutluk, Naz Kadem, Omer Bektas, Nadide C Randa, Gökcen O Tuncer

Ann Indian Acad Neurol· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Novel Variant of COL6A2 Gene Causing Bethlem Myopathy and Evaluation of Essential Hypertension.
M Gultekin Kutluk, Naz Kadem, Omer Bektas, Nadide Cemre Randa, Gökcen Oz Tuncer

Ann Indian Acad Neurol· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG.
Silvia Radenkovic, Matthew J Bird, Tim L Emmerzaal, Sunnie Y Wong, Catarina Felgueira

Am J Hum Genet· May 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A NEONATE PRESENTING WITH GRACILE SYNDROME AND BJORNSTAD PHENOTYPE ASSOCIATED WITH BCS1L MUTATION.
H Akduman, T Eminoglu, E Okulu, O Erdeve, B Atasay

Genet Couns· October 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Galactosialidosis in a Newborn with a Novel Mutation in the Gene Presenting with Transient Hyperparathyroidism.
Okulu E, Tunc G, Eminoglu T, Erdeve O, Atasay B

Balkan J Med Genet· December 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Janus-faced manifestations of homozygous familial hypobetalipoproteinemia due to apolipoprotein B truncations.
Enza Di Leo, Tuba Eminoglu, Lucia Magnolo, Musa Gökalp Bolkent, Leyla Tümer

J Clin Lipidol· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel homozygous YARS2 mutation causes severe myopathy, lactic acidosis, and sideroblastic anemia 2.
Junya Nakajima, Tuba F Eminoglu, Goksel Vatansever, Mitsuko Nakashima, Yoshinori Tsurusaki

J Hum Genet· April 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Transient neonatal hyperparathyroidism: a presenting feature of sialidosis type II.
Tuba Fatma Eminoglu, Mehpare Ozkan, Suleiman Igdoura, Arzu Dursun, Ayşegül Zenciroğlu

J Pediatr Endocrinol Metab· December 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
Q
Quality of life in children treated with restrictive diet for inherited metabolic disease.
Tuba F Eminoglu, Sebnem A Soysal, Leyla Tumer, Ilyas Okur, Alev Hasanoglu

Pediatr Int· August 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cystic fibrosis presenting with neonatal cholestasis simulating biliary atresia in a patient with a novel mutation.
Tuba Fatma Eminoglu, Emine Polat, Selim Gökçe, Fatih Süheyl Ezgü, Saliha Senel

Indian J Pediatr· June 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rapid screening of 12 common mutations in Turkish GSD 1a patients using electronic DNA microarray.
Tuba Fatma Eminoglu, Fatih Süheyl Ezgu, Alev Hasanoglu, Leyla Tumer

Gene· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hypercalcemia in glycogen storage disease type I patients of Turkish origin.
Ciğdem Seher Kasapkara, Leyla Tümer, Ilyas Okur, Tuba Eminoğlu, Fatih Süheyl Ezgü

Turk J Pediatr· April 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An infantile case of Zellweger syndrome presented with Kabuki-like phenotype.
F Ezgu, T Eminoglu, I Okur, M Gunduz, L Tumer

Genet Couns· October 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
V
Very long-chain acyl CoA dehydrogenase deficiency which was accepted as infanticide.
Tuba F Eminoglu, Leyla Tumer, Ilyas Okur, Fatih S Ezgu, Gursel Biberoglu

Forensic Sci Int· July 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): case report with a new mutation.
Zeren Bariş, Tuba Eminoğlu, Buket Dalgiç, Leyla Tümer, Alev Hasanoğlu

Eur J Pediatr· November 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multisystem involvement in a patient due to accumulation of amylopectin-like material with diminished branching enzyme activity.
T F Eminoglu, L Tumer, I Okur, R Olgunturk, A Hasanoglu

J Inherit Metab Dis· December 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Lipid apheresis applications in childhood: experience in the University Hospital of Gazi.
Tuba F Eminoglu, Idil Yenicesu, Leyla Tumer, Ilyas Okur, Günter Dilsiz

Transfus Apher Sci· December 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Factors related to non-alcoholic fatty liver disease in obese children.
Tuba F Eminoğlu, Orhun M Camurdan, Suna O Oktar, Aysun Bideci, Buket Dalgiç

Turk J Gastroenterol· June 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
Rapid screening of 10 common mutations in Turkish Gaucher patients using electronic DNA microarray.
Fatih Ezgu, Alev Hasanoglu, Ilyas Okur, Gursel Biberoglu, Leyla Tumer

Blood Cells Mol Dis· May 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis