G. Bartoloni, V. Nizzo, 'Lazio protostorico e mondo greco: considerazioni sulla cronologia relativa ed assoluta della terza fase laziale', in G. Bartoloni, F. Delpino (a cura di), Oriente e Occidente: metodi e discipline a confronto. Riflessioni sulla cronologia dell’età del Ferro italiana, incontro di studio, Roma 30-31 ottobre 2003

Autor: Nizzo, Valentino, Bartoloni, Gilda

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3686::43ca4c4eff80dabaa6f68f790f162af3
http://hdl.handle.net/11573/339711

Beta Thalassemia in Children: Established Approaches, Old Issues, New Non-Curative Therapies, and Perspectives on Healing.

Autor: Origa, Raffaella¹ (AUTHOR) raffaella.origa@unica.it, Issa, Layal² (AUTHOR) layal.issa@karma-leb.org

Publikováno v: Journal of Clinical Medicine. Nov2024, Vol. 13 Issue 22, p6966. 23p.

Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders (vol 10, 164, 2015)

Autor: Cassis L, Cortés-Saladelafont E, Molero M, Yubero-Siles D, González MJ, Ormazabal-Herrero A, Fons-Estupina C, Jou-Munoz C, Sierra-March C, Castejón Ponce E, Ramos F, Armstrong-Moron J, O'Callaghan-Gordo M, Casado M, Montero-Sanchez R, Meavilla-Olivas SM, Artuch-Iriberri R, Baric I, Bartoloni F, Bellettato CM, Bonifazi F, Ceci A, Cvitanovic-Šojat L, Dali CI, D'Avanzo F, Fumic K, Giannuzzi V, Lampe C, Scarpa M, Garcia-Cazorla A

Publikováno v: ORPHANET JOURNAL OF RARE DISEASES
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::01afd7d0dc5482f54bb58a5be9c15a9f
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=10331

Review and evaluation of the methodological quality of the existing guidelines and recommendations for inherited neurometabolic disorders

Autor: Cassis L, Cortés-Saladelafont E, Molero M, Yubero-Siles D, González MJ, Ormazabal-Herrero A, Fons-Estupina C, Jou-Munoz C, Sierra-March C, Castejón Ponce E, Ramos F, Armstrong-Moron J, O'Callaghan-Gordo M, Casado M, Montero-Sanchez R, Meavilla-Olivas SM, Artuch-Iriberri R, Baric I, Bartoloni F, Bellettato CM, Bonifazi F, Ceci A, Cvitanovic-Šojat L, Dali CI, D'Avanzo F, Fumic K, Giannuzzi V, Lampe C, Scarpa M, Garcia-Cazorla A

Publikováno v: ORPHANET JOURNAL OF RARE DISEASES
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname

Background: Inherited neurometabolic disorders (iNMDs) represent a group of almost seven hundred rare diseases whose common manifestations are clinical neurologic or cognitive symptoms that can appear at any time, in the first months/years of age or

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::2f2219094e2ac29211943220def4c105
http://fundanet.fsjd.org/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=8618

The ethical framework for performing research with rare inherited neurometabolic disease patients.

Autor: Giannuzzi V; Fondazione Per la Ricerca Farmacologica Gianni Benzi Onlus, Via Abate Eustasio 30, 70010, Valenzano, BA, Italy. vg@benzifoundation.org., Devlieger H; Department of Development and Regeneration, University of Leuven, O&N IV Herestraat 49-box 805, 3000, Leuven, Belgium., Margari L; Department of Basic Medical Sciences, Neuroscience and Sense Organs, 'Aldo Moro' University of Bari, Piazza Giulio Cesare 11, 70124, Bari, Italy., Odlind VL; Department of Obstetrics and Gynaecology, Uppsala Universitet, 751 85, Uppsala, SE, Sweden., Ragab L; Cairo University, Al Orman Guiza, Giza, 12613, Egypt., Bellettato CM; Brains for Brain Foundation - onlus, Padova, Italy., D'Avanzo F; Brains for Brain Foundation - onlus, Padova, Italy., Lampe C; Brains for Brain Foundation - onlus, Padova, Italy.; Department of Pediatric and Adolescent Medicine, Centre for Rare Diseases, Horst Schmidt Klinik Wiesbaden, Wiesbaden, Germany., Cassis L; Neurology, Gastroenterology Pathology and Clinical Biochemistry Departments, IRP-HSJD and CIBERER, Barcelona, Spain., Cortès-Saladelafont E; Neurology, Gastroenterology Pathology and Clinical Biochemistry Departments, IRP-HSJD and CIBERER, Barcelona, Spain., Cazorla ÁG; Neurology, Gastroenterology Pathology and Clinical Biochemistry Departments, IRP-HSJD and CIBERER, Barcelona, Spain., Barić I; University Hospital Centre Zagreb, Zagreb, Croatia.; School of Medicine, University of Zagreb, Zagreb, Croatia., Cvitanović-Šojat L; School of Medicine, University of Zagreb, Zagreb, Croatia., Fumić K; University Hospital Centre Zagreb, Zagreb, Croatia., Dali CI; Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark., Bartoloni F; Fondazione Per la Ricerca Farmacologica Gianni Benzi Onlus, Via Abate Eustasio 30, 70010, Valenzano, BA, Italy., Bonifazi F; Fondazione Per la Ricerca Farmacologica Gianni Benzi Onlus, Via Abate Eustasio 30, 70010, Valenzano, BA, Italy., Scarpa M; Brains for Brain Foundation - onlus, Padova, Italy.; Department of Pediatric and Adolescent Medicine, Centre for Rare Diseases, Horst Schmidt Klinik Wiesbaden, Wiesbaden, Germany., Ceci A; Fondazione Per la Ricerca Farmacologica Gianni Benzi Onlus, Via Abate Eustasio 30, 70010, Valenzano, BA, Italy.

Publikováno v: European journal of pediatrics [Eur J Pediatr] 2017 Mar; Vol. 176 (3), pp. 395-405. Date of Electronic Publication: 2017 Jan 16.