Publications by authors named "Alice Dica"

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Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective Study.
Maria Nedelcu, Dana Craiu, Elena Neagu, Carmen Magdalena Burloiu, Catrinel Mihaela Iliescu, Alice Dica

Eur J Paediatr Neurol· November 2025

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Disease-Modifying Treatment Options in Very Early Onset Multiple Sclerosis-What Choices Are There for Onset Under 5 Years of Age? A Systematic Review.
Dana Craiu, Alice Denisa Dica, Cristina Pomeran, George Pescaru, Shay Menascu

J Clin Med· November 2025

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Age-Onset-Related Particularities of Pediatric MS-Understanding the Spectrum: A Tertiary Center Experience.
Alice Denisa Dică, Dana Craiu, Florentina Ionela Linca, Magdalena Budișteanu, Catrinel Iliescu

Diseases· June 2025

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Overtime Challenges of Diagnosis and Treatment in Two Pediatric Patients with Extensive Cerebral Tumefactive Lesions Indicative of Baló's Type Multiple Sclerosis.
Alice Denisa Dică, Dana Craiu, Catrinel Iliescu, Marcel-Alexandru Găină, Carmen Sandu

Children (Basel)· May 2025

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Pediatric-Onset Multiple Sclerosis (POMS) and Epilepsy: Exploring Etiological Complexity-Outcomes from a Single-Center Experience.
Alice Denisa Dică, Dana Craiu, Catrinel Iliescu, Marcel-Alexandru Găină, Carmen Sandu

Children (Basel)· May 2025

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Mapping variants in thyroid hormone transporter MCT8 to disease severity by genomic, phenotypic, functional, structural and deep learning integration.
Stefan Groeneweg, Ferdy S van Geest, Mariano Martín, Mafalda Dias, Jonathan Frazer, Alice Dica

Nat Commun· March 2025

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Endocrine Disorders in a Newborn with Heterozygous Galactosemia, Down Syndrome and Complex Cardiac Malformation: Case Report.
Ioana Rosca, Alina Turenschi, Alin Nicolescu, Andreea Teodora Constantin, Adina Maria Canciu, Alice Denisa Dica

Medicina (Kaunas)· April 2023

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Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study.
Ferdy S van Geest, Stefan Groeneweg, Erica L T van den Akker, Iuliu Bacos, Diana Barca, Alice Dica

J Clin Endocrinol Metab· February 2022

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Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from Romania.
Magdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, Catrinel Iliescu, Maria Dobre, Alice Dica

Exp Ther Med· January 2022

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Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study.
Stefan Groeneweg, Ferdy S van Geest, Ayhan Abacı, Alberto Alcantud, Gautem P Ambegaonkar, Alice Dica

Lancet Diabetes Endocrinol· July 2020

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Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial.
Stefan Groeneweg, Robin P Peeters, Carla Moran, Athanasia Stoupa, Françoise Auriol, Alice Dica

Lancet Diabetes Endocrinol· September 2019

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Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations.
Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, Laura Vandervore, Alice Dica

Eur J Med Genet· December 2018

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Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy.
Gabrielle Rudolf, Gaetan Lesca, Mana M Mehrjouy, Audrey Labalme, Manal Salmi, Alice Dica

Eur J Hum Genet· December 2016

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Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs.
Dana Craiu, Octavia Dragostin, Alice Dica, Dorota Hoffman-Zacharska, Monika Gos

Eur J Paediatr Neurol· January 2015

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Intellectual disability and epilepsy in down syndrome.
Diana Barca, Oana Tarta-Arsene, Alice Dica, Catrinel Iliescu, Magdalena Budisteanu

Maedica (Bucur)· December 2014

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