Gabriella Ana Horvath (G Horvath, Gabriella Horvath, Gabriella A Horvath)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 9

Top Topics

Intellectual Disability

Autism Spectrum Disorder

Molecular Docking

Top Venues

Journal of inherited metabolic disease

Neuropediatrics

Molecular genetics & genomic medicine

The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

This page only lists publications with an associated author ORCID identifier.

Publications

Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Ana Horvath, Thomas Lücke, Cheuk Wing Fung, Suet-Na Wong, Elisenda Cortés-Saladelafont, M Mar Rovira-Remisa, Yılmaz Yıldız, Saadet Mercimek-Mahmutoglu, Birgit Assmann, Galina Stevanović, Filippo Manti, Heiko Brennenstuhl, Sabine Jung-Klawitter, Kathrin Jeltsch, Hatice Serap Sivri, Sven F Garbade, Àngels García-Cazorla, Thomas Opladen
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Ana Horvath, Thomas Lücke, Cheuk Wing Fung, Suet-Na Wong, Elisenda Cortés-Saladelafont, M Mar Rovira-Remisa, Yılmaz Yıldız, Saadet Mercimek-Mahmutoglu, Birgit Assmann, Galina Stevanović, Filippo Manti, Heiko Brennenstuhl, Sabine Jung-Klawitter, Kathrin Jeltsch, Hatice Serap Sivri, Sven F Garbade, Àngels García-Cazorla, Thomas Opladen
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease 47 (3) (2024)
Natalia Alexandra Julia-Palacios, Oya Kuseyri Hübschmann, Mireia Olivella, Roser Pons, Gabriella Ana Horvath, Thomas Lücke, Cheuk Wing Fung, Suet-Na Wong, Elisenda Cortés-Saladelafont, M Mar Rovira-Remisa, Yılmaz Yıldız, Saadet Mercimek-Mahmutoglu, Birgit Assmann, Galina Stevanović, Filippo Manti, Heiko Brennenstuhl, Sabine Jung-Klawitter, Kathrin Jeltsch, Hatice Serap Sivri, Sven F Garbade, Àngels García-Cazorla, Thomas Opladen
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency. Journal of inherited metabolic disease (2024)
Maksim Parfyonov, Robin Friedlander, Brian Banno, Dean Elbe, Gabriella Ana Horvath
Psychiatric Manifestations in Patients with Biopterin Defects. Neuropediatrics 53 (3) (2022)
Csilla Egri, Mary Dunbar, Gabriella Ana Horvath
Correlation Between Salivary, Platelet and Central Serotonin Levels in Children. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 47 (2) (2021)
J Micallef, S Stockler-Ipsiroglu, C D van Karnebeek, R Salvarinova-Zivkovic, Gabriella Ana Horvath
Recurrent Dystonic Crisis and Rhabdomyolysis Treated with Dantrolene in Two Patients with Aromatic L-Amino Acid Decarboxylase Deficiency. Neuropediatrics 51 (3) (2020)
Liza Douiev, Ruth Sheffer, Gabriella Ana Horvath, Ann Saada
Bezafibrate Improves Mitochondrial Fission and Function in DNM1L-Deficient Patient Cells. Cells 9 (2) (2020)
Maja Tarailo-Graovac, Farah R Zahir, Irena Zivkovic, Michelle Moksa, Kathryn Selby, Sunita Sinha, Corey Nislow, Sylvia G Stockler-Ipsiroglu, Ruth Sheffer, Ann Saada-Reisch, Jan M Friedman, Clara D M van Karnebeek, Gabriella Ana Horvath
De novo pathogenic DNM1L variant in a patient diagnosed with atypical hereditary sensory and autonomic neuropathy. Molecular genetics & genomic medicine 7 (10) (2019)
Gabriella Ana Horvath, Maja Tarailo-Graovac, Tanja Bartel, Simone Race, Margot I Van Allen, Ingrid Blydt-Hansen, Colin J Ross, Wyeth W Wasserman, Mary B Connolly, Clara D M van Karnebeek
Improvement of Self-Injury With Dopamine and Serotonin Replacement Therapy in a Patient With a Hemizygous PAK3 Mutation: A New Therapeutic Strategy for Neuropsychiatric Features of an Intellectual Disability Syndrome. Journal of child neurology 33 (1) (2018)