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Daniela Gueraldi

Showing results (1-10 of 32) with videos related to

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Handbook of Clinical Neurology|September 25, 2024
Lysosomal storage diseasesAlessandro P Burlina, Renzo Manara, Daniela Gueraldi
Metabolites|June 25, 2025
The Hidden Burden: Gastrointestinal Involvement in Lysosomal Storage DisordersVincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi, et al.
Frontiers in Pediatrics|June 26, 2025
Case Report: Novel treatment approach for severe interstitial lung disease in type 3 Gaucher diseaseVincenza Gragnaniello, Silvia Carraro, Tiziana Zangardi, et al.
Springerplus|March 2, 2013
An unusual case report on the possible role of Warfarin in migraine prophylaxisAngelo Russo, Sara Santi, Daniela Gueraldi, et al.
Nutrients|July 18, 2020
The Impact of a Slow-Release Large Neutral Amino Acids Supplement on Treatment Adherence in Adult Patients with PhenylketonuriaAlessandro P Burlina, Chiara Cazzorla, Pamela Massa, et al.
Reports (MDPI)|February 20, 2026
Short-Term Intensive Avalglucosidase Alfa Regimen in Late-Diagnosed Infantile Pompe Disease: A Case ReportVincenza Gragnaniello, Alice Pozza, Chiara Cazzorla, et al.
Nutrients|October 24, 2019
Large Neutral Amino Acid Therapy Increases Tyrosine Levels in Adult Patients with Phenylketonuria: A Long-Term StudyAlessandro P Burlina, Chiara Cazzorla, Pamela Massa, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
A new strategy of desensitization in mucopolysaccharidosis type II disease treated with idursulfase therapy: A case report and review of the literatureVincenza Gragnaniello, Silvia Carraro, Laura Rubert, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 10, 2023
Variant in the allosteric domain of CPS1 protein associated with effectiveness of N-carbamoyl glutamate therapy in neonatal onset CPS1 deficiencyVincenza Gragnaniello, Daniela Gueraldi, Andrea Puma, et al.
American Journal of Medical Genetics. Part A|July 10, 2025
Early Enzyme Replacement Therapy Does Not Prevent the Protein Losing Enteropathy Syndrome in Neurovisceral Gaucher DiseaseVincenza Gragnaniello, Mara Cananzi, Annachiara Cavaliere, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 4
Handbook of Clinical Neurology|September 25, 2024
Lysosomal storage diseasesAlessandro P Burlina, Renzo Manara, Daniela Gueraldi
Metabolites|June 25, 2025
The Hidden Burden: Gastrointestinal Involvement in Lysosomal Storage DisordersVincenza Gragnaniello, Chiara Cazzorla, Daniela Gueraldi, et al.
Frontiers in Pediatrics|June 26, 2025
Case Report: Novel treatment approach for severe interstitial lung disease in type 3 Gaucher diseaseVincenza Gragnaniello, Silvia Carraro, Tiziana Zangardi, et al.
Springerplus|March 2, 2013
An unusual case report on the possible role of Warfarin in migraine prophylaxisAngelo Russo, Sara Santi, Daniela Gueraldi, et al.
Nutrients|July 18, 2020
The Impact of a Slow-Release Large Neutral Amino Acids Supplement on Treatment Adherence in Adult Patients with PhenylketonuriaAlessandro P Burlina, Chiara Cazzorla, Pamela Massa, et al.
Reports (MDPI)|February 20, 2026
Short-Term Intensive Avalglucosidase Alfa Regimen in Late-Diagnosed Infantile Pompe Disease: A Case ReportVincenza Gragnaniello, Alice Pozza, Chiara Cazzorla, et al.
Nutrients|October 24, 2019
Large Neutral Amino Acid Therapy Increases Tyrosine Levels in Adult Patients with Phenylketonuria: A Long-Term StudyAlessandro P Burlina, Chiara Cazzorla, Pamela Massa, et al.
Molecular Genetics and Metabolism Reports|July 5, 2022
A new strategy of desensitization in mucopolysaccharidosis type II disease treated with idursulfase therapy: A case report and review of the literatureVincenza Gragnaniello, Silvia Carraro, Laura Rubert, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 10, 2023
Variant in the allosteric domain of CPS1 protein associated with effectiveness of N-carbamoyl glutamate therapy in neonatal onset CPS1 deficiencyVincenza Gragnaniello, Daniela Gueraldi, Andrea Puma, et al.
American Journal of Medical Genetics. Part A|July 10, 2025
Early Enzyme Replacement Therapy Does Not Prevent the Protein Losing Enteropathy Syndrome in Neurovisceral Gaucher DiseaseVincenza Gragnaniello, Mara Cananzi, Annachiara Cavaliere, et al.
Pageof 4