APROVADOS - Pôster
NÚMERO | TÍTULO | AUTOR |
01 | WHOLE EXOME SEQUENCING FOR ASSESSMENT OF UNCLASSIFIED GLYCOGEN STORAGE DISEASES AND DISORDERS OF ENERGY METABOLISM | Corbinian N. Wanner, Uyen T. Doan, Monika Dambska, Kathryn R. Dahlberg, Ana Estrella, Young Mok Lee, Patrick T. Ryan, David A. Weinstein |
02 |
NATURAL HISTORY OF PAEDIATRIC PATIENTS WITH GLYCOGEN STORAGE DISEASE TYPE 1B IN ENGLAND: RESULTS OF A MULTI-SITE SURVEY |
Rebecca Kylie Halligan, Fiona White, Nazreen Banu Kamarus Jaman, M McSweeney, Steven Kitchen, Bernd Schwahn, Helen Mundy, Saikat Santra |
03 | Interventions and outcomes in Adult GSD III: a three centre study in collaboration with Association for Glycogen Storage Disease (AGSD-UK) | Alison Woodall, Louise V Robertson, Charlotte Dawson, Rahda Ramachandran, Diane Green, Allan Muir, Reena Sharma |
04 | FREQUENCY OF RS2229611 SNP IN 3’UTR OF G6PC IN BRAZILIAN PATIENTS WITH GLYCOGENOSIS TYPE IA. | Franciele Cabral Pinheiro, Fernanda Sperb-Ludwig, Carolina Fishinger Moura De Souza, Ida Vanessa Doederlein Schwartz |
05 | CRISPR/CAS9-MEDIATED EDITING OF HEPATIC G6PC IN MICE ALLOWS TO INVESTIGATE THE CLINICAL SPECTRUM OF GLYCOGEN STORAGE DISEASE TYPE IA | Martijn GS Rutten, Nicolette CA Huijkman, Trijnie Bos, Niels J Kloosterhuis, Rachel Thomas, Alain de Bruin, Bart van de Sluis, Maaike H Oosterveer |
06 | DISEASE BURDEN AND UNMET NEEDS IN POMPE DISEASE: RESULTS FROM A PATIENT SURVEY IN THE UNITED KINGDOM | Jacqueline Adam, Allan Muir, Nina Patel, Jenny Wilson |
07 | CLINICAL AND MOLECULAR CHARACTERISTICS OF FRUCTOSE 1,6 BISPHOSPHATASE DEFICIENCY (FBP1D) PATIENTS IN ISRAEL- for poster presentation | Zehavi Yoav, Avraham Zeharia, Galit Tal, Hanna Mandel, Ben Pode-Shakked, Ronen Spiegel |
08 | Fibroblast growth factor 21 (FGF21) is a novel sensitive biomarker for the diagnosis and control of hepatic glycogenoses- for poster presentation | Yoav Zehavi, Nachshon Buchsetav, Ann Saada, Ronen Spiegel |
09 | LIVER TRANSPLANT FOR GLYCOGEN STORAGE DISEASE TYPE IIIA: A CASE REPORT | Tatiele Nalin, Bibiana Mello de Oliveira, Karina Colonetti, Rafael de Marchi, Vaneisse L Monteiro, Matheus T Michalczuk, Carolina F M de Souza, Mario R A da Silva, Ida V D Schwartz |
10 | HEPATIC NON-GSD-IB: IS THE IMMUNE SYSTEM CHALLENGED BY THE METABOLIC DEFECT? | Karina Colonetti, Filippo Pinto Vairo, Marina Siebert, Tatiele Nalin, Soraia Poloni, Luiz Fernando Wurdig Roesch, Carolina F M de Souza, Ida Vanessa Doederlein Schwartz |
11 | PRECLINICAL DEVELOPMENT OF SPK-3006, AN INVESTIGATIONAL LIVER-DIRECTED AAV GENE THERAPY FOR THE TREATMENT OF POMPE DISEASE | Sean M Armour, Jayme ML Nordin, Helena Costa Verdera, Daniel M Cohen, Pauline Sellier, Marco Crosariol, Fanny Collaud, Christopher Riling, William J Quinn III, Hayely Hanby, Umut Cagin , Francesco Puzzo, Virginia Haurigot, Giuseppe Ronzitti, Pasqualina Colelle, Xavier M Anguela, Federico Mingozzi |
12 | HEPCIDIN, INTERLEUKIN-6 LEVELS AND IRON METABOLISM PARAMETERS IN PATIENTS WITH HEPATIC GLYCOGEN STORAGE DISEASES | Tatiele Nalin, Tatiele Nalin, Fernanda Sperb-Ludwig, Fernanda Sperb-Ludwig, Marina Siebert, David A Weinstein, David A Weinstein, Terry G J Derks, Terry G J Derks, Carolina FM de Souza , Carolina FM de Souza, Ida V D Schwartz, Ida V D Schwartz |
13 | THE COEXISTENCE OF GLYCOGEN STORAGE DISEASE TYPE 0 AND LIMB-GIRDLE MUSCULAR DYSTROPHY IN A PATIENT | Jokasta Sousa Rocha, Isadora Moraes Mundim Prado, Luiz Roberto da Silva |
14 | INFLAMMATORY BOWEL DISEASE IN NON-IB HEPATIC GLYCOGEN STORAGE DISEASES: A CASE SERIES | BIBIANA MELLO OLIVEIRA, VANEISSE LIMA MONTEIRO, MARIANA SCORTEGAGNA, FERNANDA SPERB-LUDWIG, KARINA COLONETTI, BRUNA BENTO dos SANTOS, LILIA FARRET REFOSCO, RODRIGO REZENDE ARANTES, JOSÉ SIMON CAMELO, CAROLINA FISCHINGER MOURA de SOUZA, IDA VANESSA DOEDERLEIN SCHWARTZ |
15 | HEPATIC GLYCOGEN STORAGE DISEASES: ANTHROPOMETRIC CHARACTERIZATION AT BIRTH AND AT THE BEGINNING OF TREATMENT | Vaneisse Cristina Lima Monteiro, Bibiana Mello de Oliveira, Mariana L Scortegagna, Soraia Poloni, Bruna Bento dos Santos, Fernanda Sperb-Ludwig, Lilia Farret Refosco, Carolina Fischinger Moura de Souza, Ida Vanessa Doederlein Schwartz |
16 | FANCONI BICKEL SYNDROME. FIRST CASE REPORTED IN URUGUAY. | Aida Lemes, Cristina Zabala, Mariana Castro, Maria Laura Fernández, Andrea Ponce de León |
17 | BONE MINERAL DENSITY AND BONE TURNOVER MARKERS IN PATIENTS WITH HEPATIC GLYCOGEN STORAGE DISEASES | Jésica Tamara Jacoby, Bruna Bento Santos, Tatiéle Nalin, Lilia Farret Refosco, Carolina Fischinger Souza, Poli Mara Spritzer, Soraia Polini, Roberta Hack Mendes, Ida Vanessa Doederlein Schwartz |
18 | PSEUDODEFICIENCY IN GLYCOGEN STORAGE DISEASE TYPE II: THE NEED OF ALLELE FREQUENCY STUDIES IN BRAZILIAN POPULATION | Diana Málaga, Ana Carolina Brusius-Facchin, Ana Karolina Andrade, Bibiana Mello Oliveira, Temis Maria Félix, Kristiane Michelin-Tirelli, Jaqueline Schulte, Jamile Pereira, Eurico Camargo Neto, Carolina Fischinger Moura de Souza, Roberto Giugliani |
19 | A RETROSPECTIVE COHORT STUDY ON B12 LEVELS IN HEPATIC GLYCOGEN STORAGE DISEASES | Vaneisse Cristina Lima Monteiro, Bibiana Mello Oliveira, Mariana L Scortegagna, Soraia Poloni, Fernanda Sperb-Ludwig, Bruna Bento dos Santos, Lilia Farret Refosco, Carolina Fischinger Moura de Souza, Ida Vanessa Doederlein Schwartz |
20 | ASYMPTOMATIC FAMILY WITH LATE ONSET POMPE DISEASE: AN UNEXPECTED DIAGNOSIS | Márcia Gonçalves Ribeiro |
21 | ALGLUCOSIDASE ALFA ENZYME REPLACEMENT THERAPY IN EARLY AND LATE-ONSET POMPE DISEASE: A SYSTEMATIC LITERATURE REVIEW | Ana Paula Pedroso Junges, Alícia Dorneles Dornelles, Ida Vanessa Doederlein Schwartz, Haliton Alves de Oliveira Júnior, Bárbara Krug, Candice Gonçalves, Luciana Rizzon |
22 | GLIOMA IN GLYCOGEN STORAGE DISEASE TYPE IA: CORRELATION OR SPURIOUS ASSOCIATION? | Mariana Lima Scortegagna, Bibiana Mello de Oliveira, Vaneisse Cristina Lima Monteiro, Sperb-Ludwig Fernanda, Lília Farret Refosco, Carolina Fischinger Moura de Souza, Ida Vanessa Doederlein Schwartz |
23 | GLYCOGEN STORAGE DISEASE DIAGNOSIS OF TWO PATIENTS BY NEXT GENERATION SEQUENCING | Louise Lapagesse Camargo Pinto, Marileise Santos Obelar, Gisele Rosone Luca, Francisca Ligia Cirilo Carvalho, Izabella Zacarias, Ida Vanessa Doederlein Schwartz, Carolina Fischinger Moura Souza, Fernanda Sperb-Ludwig |
24 | LIVER TRANSPLANTATION IN HEPATIC GLYCOGEN STORAGE DISEASES: CASE SERIES STUDY FROM A REFERENCE CENTRE FOR RARE DISEASES IN SOUTHERN BRAZIL | MARIANA SCORTEGAGNA, BIBIANA MELLO OLIVEIRA, VANEISSE LIMA MONTEIRO, LILIA FARRET REFOSCO, CAROLINA FISCHINGER MOURA de SOUZA, IDA VANESSA DOEDERLEIN SCHWARTZ |
25 | NON-VIRAL AGL GENE DELIVERY AS A POSSIBLE THERAPEUTIC APPROACH FOR GLYCOGEN STORAGE DISEASE TYPE III (GSDIII) | Doriana Triggiani |
26 | LYSINURIC PROTEIN INTOLERANCE AS A DIFFERENTIAL DIAGNOSIS OF GLYCOGEN STORAGE DISEASES: AN ILLUSTRATIVE CASE REPORT | BIBIANA M OLIVEIRA, VANEISSE L MONTEIRO, BRUNA B DOS SANTOS, LILIA F REFOSCO, IDA V D SCHWARTZ, CAROLINA FISCHINGER MOURA de SOUZA |