Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Theodoros Georgiou

Showing results (1-10 of 15) with videos related to

Pageof 2
Sort By:
Clinical Biochemistry|May 1, 2016
Chitotriosidase deficiency in the Cypriot population: Identification of a novel deletion in the CHIT1 geneGavriella Mavrikiou, Petros Petrou, Theodoros Georgiou, et al.
JMIR Rehabilitation and Assistive Technologies|September 14, 2020
Rhythmic Haptic Cueing Using Wearable Devices as Physiotherapy for Huntington Disease: Case StudyTheodoros Georgiou, Riasat Islam, Simon Holland, et al.
Journal of Child Neurology|March 29, 2005
Magnetic resonance imaging findings and novel mutations in GM1 gangliosidosisAithala Gururaj, László Sztriha, Josef Hertecant, et al.
Genetic Testing and Molecular Biomarkers|September 1, 2009
Maple syrup urine disease in Cypriot families: identification of three novel mutations and biochemical characterization of the p.Thr211Met mutation in the E1alpha subunitTheodoros Georgiou, Jacinta L Chuang, R Max Wynn, et al.
Genetic Testing|June 10, 2005
The Arg482His mutation in the beta-galactosidase gene is responsible for a high frequency of GM1 gangliosidosis carriers in a Cypriot villageTheodoros Georgiou, Goula Stylianidou, Violetta Anastasiadou, et al.
Meta Gene|January 22, 2015
The first family with Tay-Sachs disease in Cyprus: Genetic analysis reveals a nonsense (c.78G>A) and a silent (c.1305C>T) mutation and allows preimplantation genetic diagnosisTheodoros Georgiou, George Christopoulos, Violetta Anastasiadou, et al.
Molecular Genetics & Genomic Medicine|January 17, 2020
A novel mutation deep within intron 7 of the GBA gene causes Gaucher diseaseAnna Malekkou, Ioanna Sevastou, Gavriella Mavrikiou, et al.
IEEE Transactions on Pattern Analysis and Machine Intelligence|November 1, 2022
Deep Learning for Instance Retrieval: A SurveyWei Chen, Yu Liu, Weiping Wang, et al.
Clinical Biochemistry|June 29, 2014
Molecular analysis of Cypriot patients with Glutaric aciduria type I: identification of two novel mutationsTheodoros Georgiou, Paola Nicolaidou, Anastasia Hadjichristou, et al.
Clinical Biochemistry|February 15, 2012
The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screeningTheodoros Georgiou, Gladys Ho, Marios Vogazianos, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Clinical Biochemistry|May 1, 2016
Chitotriosidase deficiency in the Cypriot population: Identification of a novel deletion in the CHIT1 geneGavriella Mavrikiou, Petros Petrou, Theodoros Georgiou, et al.
JMIR Rehabilitation and Assistive Technologies|September 14, 2020
Rhythmic Haptic Cueing Using Wearable Devices as Physiotherapy for Huntington Disease: Case StudyTheodoros Georgiou, Riasat Islam, Simon Holland, et al.
Journal of Child Neurology|March 29, 2005
Magnetic resonance imaging findings and novel mutations in GM1 gangliosidosisAithala Gururaj, László Sztriha, Josef Hertecant, et al.
Genetic Testing and Molecular Biomarkers|September 1, 2009
Maple syrup urine disease in Cypriot families: identification of three novel mutations and biochemical characterization of the p.Thr211Met mutation in the E1alpha subunitTheodoros Georgiou, Jacinta L Chuang, R Max Wynn, et al.
Genetic Testing|June 10, 2005
The Arg482His mutation in the beta-galactosidase gene is responsible for a high frequency of GM1 gangliosidosis carriers in a Cypriot villageTheodoros Georgiou, Goula Stylianidou, Violetta Anastasiadou, et al.
Meta Gene|January 22, 2015
The first family with Tay-Sachs disease in Cyprus: Genetic analysis reveals a nonsense (c.78G>A) and a silent (c.1305C>T) mutation and allows preimplantation genetic diagnosisTheodoros Georgiou, George Christopoulos, Violetta Anastasiadou, et al.
Molecular Genetics & Genomic Medicine|January 17, 2020
A novel mutation deep within intron 7 of the GBA gene causes Gaucher diseaseAnna Malekkou, Ioanna Sevastou, Gavriella Mavrikiou, et al.
IEEE Transactions on Pattern Analysis and Machine Intelligence|November 1, 2022
Deep Learning for Instance Retrieval: A SurveyWei Chen, Yu Liu, Weiping Wang, et al.
Clinical Biochemistry|June 29, 2014
Molecular analysis of Cypriot patients with Glutaric aciduria type I: identification of two novel mutationsTheodoros Georgiou, Paola Nicolaidou, Anastasia Hadjichristou, et al.
Clinical Biochemistry|February 15, 2012
The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screeningTheodoros Georgiou, Gladys Ho, Marios Vogazianos, et al.
Pageof 2