Autori: Potic Ana D
Naslov | Developmental delay can precede neurologic regression in early onset metachromatic leukodystrophy (Article) |
Autori | Adang Laura Ann ... Potic Ana D ... (broj koautora 48) |
Info | MOLECULAR GENETICS AND METABOLISM, (2024), vol. 142 br. 4, str. - |
Projekat | Global Leukodystrophy Initiative Clinical Trials Network (PI: Vanderver) [GLIA-CTN U54TR002823]; Lysosomal Disease Network (LDN) [U54NS065768]; RDCRN Data Management and Coordinating Center (DMCC) [U2CTR002818]; NCATS; NINDS; NIDDK [K23NS114113]; CURE grant [DFG GR 4688/2-1, EPCD000034]; FRQS; CIHR |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
Naslov | Hypomyelination caused by a novel homozygous pathogenic variant in FOLR1: complete clinical and radiological recovery with oral folinic acid therapy and review of the literature (Review) |
Autori | Potic Ana D Perrier Stefanie Radovic Tijana Gavrilovic Svetlana Ostojic Jelena V Tran Luan T Thiffault Isabelle Pastinen Tomi Schiffmann Raphael Bernard Genevieve |
Info | ORPHANET JOURNAL OF RARE DISEASES, (2023), vol. 18 br. 1, str. - |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa |
Naslov | Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C (Article) |
Autori | Pelletier Felixe ... Potic Ana D ... Pekic Sandra R ... Popovic Vera P ... (broj koautora 119) |
Info | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, (2021), vol. 106 br. 2, str. E660-E674 |
Projekat | Canadian Institutes of Health Research [201610PJT-377869, MOP-G2-341146-159133-BRIDG]; Fondation Les Amis d'Elliot; Leuco-Action; Fondation Lueur d'Espoir pour Ayden; Fondation le Tout pour Loo; Reseau de Medecine Genetique Appliquee of the Fonds de Recherche du Quebec-Sante; Compute Canada; Fonds de Recherche du Quebec en Sante (FRQS) Doctoral Scholarship; Fondation du Grand defi Pierre Lavoie Doctoral Scholarship; McGill Faculty of Medicine F. S.B. Miller Fellowship; Research Institute of the McGill University Health Centre Desjardins Studentship in Child Health Research; Directorate of Higher Education Overseas Scholarship-Dikti Scholarship, Ministry of National Education, Republic of Indonesia; CIHR [201603PJT-148695]; BC Children's Hospital Foundation through its intramural Investigator Grant Award Program (IGAP); National Institute for Neurological Disorders and Stroke [R01NS082094]; Jakob Kamens Chair in Translational Neurotherapeutics; Fonds de Recherche du Quebec-Sante (FRQS); Canadian Institutes of Health Research; European Reference Network for Rare Neurological Disorders (ERN-RND) [739510] |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C (Article) |
Autori | Pelletier Felixe ... Potic Ana D ... Pekic Sandra R ... Popovic Vera P ... (broj koautora 119) |
Info | JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, (2021), vol. 106 br. 2, str. E660-E674 |
Projekat | Canadian Institutes of Health Research (CIHR) [201610PJT-377869, MOP-G2-341146-159133-BRIDG]; Fondation Les Amis d'Elliot; Leuco-Action; Fondation Lueur d'Espoir pour Ayden; Fondation le Tout pour Loo; Reseau de Medec |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Cardiac phenotype in ATP1A3-related syndromes A multicenter cohort study (Article) |
Autori | Balestrini Simona ... Brankovic Vesna ... Potic Ana D ... (broj koautora 54) |
Info | NEUROLOGY, (2020), vol. 95 br. 21, str. E2866-E2879 |
Projekat | Epilepsy Society, UK; National Institute for Health Research Biomedical Research Centres funding scheme; Muir Maxwell Trust; National Institute of Neurological Disorders and Stroke [R01NS058949]; National Institute for Health Research Biomedical Centre at Great Ormond Street Hospital for Children NHS Foundation Trust; University College London; DFG-Grant [TR-128]; Duke Institute of Brain Sciences, Duke Research and discretionary funds; National Health and Medical Research Council of Australia; National Heart, Lung, and Blood Institute grant [F30 HL131217]; British Heart Foundation [RG/15/15/31742]; AHC UK; Max's Foundation (via the Great Ormond Street Hospital Children's Charity); MRC [MR/T024062/1] Funding Source: UKRI |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Cardiac Phenotype In ATP1A3 Related-Syndromes: A Multicentre Study (Meeting Abstract) |
Autori | Balestrini Simona ... Brankovic Vesna ... Potic Ana D ... (broj koautora 49) |
Info | EPILEPSIA, (2019), vol. 60 br. , Suppl. 2, str. 173-173 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Pure myopathy with enlarged mitochondria associated to a new mutation in MTND2 gene (Article) |
Autori | Zanolini Alice Potic Ana D Carrara Franco Lamantea Eleonora Diodato Daria Blasevich Flavia Marchet Silvia Marina Mora Pallotti Francesco Morandi Lucia Zeviani Massimo Lamperti Costanza |
Info | MOLECULAR GENETICS AND METABOLISM REPORTS, (2017), vol. 10 br. , str. 24-27 |
Projekat | Fondazione Pierfranco e Luisa Mariani [CM23]; Italian Association of Mitochondrial Disease Patients and Families (Mitocon ONLUS); Cell line and DNA Bank of Genetic Movement Disorders and Mitochondrial Diseases of Telethon Network of Genetics BiobanksFonda |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | From chronic recurrent headache to leukodystrophies (Meeting Abstract) |
Autori | Potic Ana D Di Bella Daniela Salsano E Taroni Franco |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2017), vol. 24 br. , Suppl. 1, str. 373-373 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | Phenotypic variability in 4H leukodystrophy caused by POLR3A mutations (Meeting Abstract) |
Autori | Potic Ana D Pekic Sandra R |
Info | EUROPEAN JOURNAL OF NEUROLOGY, (2016), vol. 23 br. , Suppl. 2, str. 148-148 |
Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | CAPOS syndrome and hemiplegic migraine in a novel pedigree with the specific ATP1A3 mutation (Article) |
Autori | Potic Ana D Nmezi Bruce Padiath Quasar S |
Info | JOURNAL OF THE NEUROLOGICAL SCIENCES, (2015), vol. 358 br. 1-2, str. 453-456 |
Projekat | University of Pittsburgh |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |