Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Francesco Emma

Showing results (141-150 of 225) with videos related to

Pageof 23
Sort By:
Kidney International|March 21, 2016
Activation of the transcription factor EB rescues lysosomal abnormalities in cystinotic kidney cellsLaura R Rega, Elena Polishchuk, Sandro Montefusco, et al.
Pediatric Nephrology (Berlin, Germany)|July 8, 2009
Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutationsEnrica Tosetto, Maria Addis, Gianluca Caridi, et al.
Kidney International|January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular DisordersMartin Konrad, Tom Nijenhuis, Gema Ariceta, et al.
Kidney International|July 10, 2019
Atypical IgM on T cells predict relapse and steroid dependence in idiopathic nephrotic syndromeManuela Colucci, Rita Carsetti, Maria Manuela Rosado, et al.
Human Molecular Genetics|February 9, 2022
Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosisPatrick Krohn, Laura Rita Rega, Marianne Harvent, et al.
Clinical Kidney Journal|August 25, 2022
Expert guidance on the multidisciplinary management of cystinosis in adolescent and adult patientsElena Levtchenko, Aude Servais, Sally A Hulton, et al.
Journal of the American Society of Nephrology : JASN|September 15, 2007
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvementFrancesca Diomedi-Camassei, Silvia Di Giandomenico, Filippo M Santorelli, et al.
Pediatric Nephrology (Berlin, Germany)|September 5, 2014
Short-term survival of hyperammonemic neonates treated with dialysisStefano Picca, Carlo Dionisi-Vici, Andrea Bartuli, et al.
Journal of the American Society of Nephrology : JASN|February 1, 2014
Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndromePiero Ruggenenti, Barbara Ruggiero, Paolo Cravedi, et al.
Human Mutation|August 21, 2015
A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal DysplasiaGinevra Zanni, Vera M Kalscheuer, Andreas Friedrich, et al.
Pageof 23

Showing results (141-150 of 225) with videos related to

Sort By:
Pageof 23
Kidney International|March 21, 2016
Activation of the transcription factor EB rescues lysosomal abnormalities in cystinotic kidney cellsLaura R Rega, Elena Polishchuk, Sandro Montefusco, et al.
Pediatric Nephrology (Berlin, Germany)|July 8, 2009
Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutationsEnrica Tosetto, Maria Addis, Gianluca Caridi, et al.
Kidney International|January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular DisordersMartin Konrad, Tom Nijenhuis, Gema Ariceta, et al.
Kidney International|July 10, 2019
Atypical IgM on T cells predict relapse and steroid dependence in idiopathic nephrotic syndromeManuela Colucci, Rita Carsetti, Maria Manuela Rosado, et al.
Human Molecular Genetics|February 9, 2022
Multisystem involvement, defective lysosomes and impaired autophagy in a novel rat model of nephropathic cystinosisPatrick Krohn, Laura Rita Rega, Marianne Harvent, et al.
Clinical Kidney Journal|August 25, 2022
Expert guidance on the multidisciplinary management of cystinosis in adolescent and adult patientsElena Levtchenko, Aude Servais, Sally A Hulton, et al.
Journal of the American Society of Nephrology : JASN|September 15, 2007
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvementFrancesca Diomedi-Camassei, Silvia Di Giandomenico, Filippo M Santorelli, et al.
Pediatric Nephrology (Berlin, Germany)|September 5, 2014
Short-term survival of hyperammonemic neonates treated with dialysisStefano Picca, Carlo Dionisi-Vici, Andrea Bartuli, et al.
Journal of the American Society of Nephrology : JASN|February 1, 2014
Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndromePiero Ruggenenti, Barbara Ruggiero, Paolo Cravedi, et al.
Human Mutation|August 21, 2015
A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal DysplasiaGinevra Zanni, Vera M Kalscheuer, Andreas Friedrich, et al.
Pageof 23