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Silverio Perrotta

Showing results (21-30 of 200) with videos related to

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Haematologica|March 7, 2007
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease geneEwa Zdebska, Achille Iolascon, Justyna Spychalska, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 15, 2014
Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidusMilena Brugnara, Rossella Gaudino, Silvana Tedeschi, et al.
Journal of Clinical Medicine|January 11, 2022
Hearing Loss in Beta-Thalassemia: Systematic ReviewImmacolata Tartaglione, Roberta Carfora, Davide Brotto, et al.
Oncotarget|October 18, 2016
Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functionsAdriana Borriello, Ilaria Caldarelli, Debora Bencivenga, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|January 14, 2015
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of NaplesAngela Belsito, Dario Costa, Carmela Fiorito, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 9, 2023
Response letter to: Halo-like phenomenon in neurofibromatosis type 1: A potential new diagnostic criterionCamilo Arias-Rodriguez, Julia Nowowiejska, Claudia Santoro, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 23, 2019
Report on a child with neurofibromatosis type 2 and unilateral moyamoya: further evidence of cerebral vasculopathy in NF2Claudia Santoro, Federica Palladino, Pia Bernardo, et al.
Hemoglobin|September 26, 2018
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on PolypharmacyMaddalena Casale, Stefania Picariello, Felice Corvino, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 10, 2025
Severe cervical kyphosis in a complex child with NF1, case report and literature reviewLuigi Aurelio Nasto, Ferruccio De Prisco, Enrico Pola, et al.
Frontiers in Genetics|December 8, 2018
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil DeformityDomenico Roberti, Renata Conforti, Teresa Giugliano, et al.
Pageof 20

Showing results (21-30 of 200) with videos related to

Sort By:
Pageof 20
Haematologica|March 7, 2007
Abnormalities of erythrocyte glycoconjugates are identical in two families with congenital dyserythropoietic anemia type II with different chromosomal localizations of the disease geneEwa Zdebska, Achille Iolascon, Justyna Spychalska, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|May 15, 2014
Type III Bartter-like syndrome in an infant boy with Gitelman syndrome and autosomal dominant familial neurohypophyseal diabetes insipidusMilena Brugnara, Rossella Gaudino, Silvana Tedeschi, et al.
Journal of Clinical Medicine|January 11, 2022
Hearing Loss in Beta-Thalassemia: Systematic ReviewImmacolata Tartaglione, Roberta Carfora, Davide Brotto, et al.
Oncotarget|October 18, 2016
Tyrosine kinase inhibitors and mesenchymal stromal cells: effects on self-renewal, commitment and functionsAdriana Borriello, Ilaria Caldarelli, Debora Bencivenga, et al.
Transfusion and Apheresis Science : Official Journal of the World Apheresis Association : Official Journal of the European Society for Haemapheresis|January 14, 2015
Erythrocyte genotyping for transfusion-dependent patients at the Azienda Universitaria Policlinico of NaplesAngela Belsito, Dario Costa, Carmela Fiorito, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 9, 2023
Response letter to: Halo-like phenomenon in neurofibromatosis type 1: A potential new diagnostic criterionCamilo Arias-Rodriguez, Julia Nowowiejska, Claudia Santoro, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 23, 2019
Report on a child with neurofibromatosis type 2 and unilateral moyamoya: further evidence of cerebral vasculopathy in NF2Claudia Santoro, Federica Palladino, Pia Bernardo, et al.
Hemoglobin|September 26, 2018
Life-Threatening Drug-Induced Liver Injury in a Patient with β-Thalassemia Major and Severe Iron Overload on PolypharmacyMaddalena Casale, Stefania Picariello, Felice Corvino, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 10, 2025
Severe cervical kyphosis in a complex child with NF1, case report and literature reviewLuigi Aurelio Nasto, Ferruccio De Prisco, Enrico Pola, et al.
Frontiers in Genetics|December 8, 2018
A Novel 12q13.2-q13.3 Microdeletion Syndrome With Combined Features of Diamond Blackfan Anemia, Pierre Robin Sequence and Klippel Feil DeformityDomenico Roberti, Renata Conforti, Teresa Giugliano, et al.
Pageof 20