Daniel Grinberg
Grinberg, Daniel, 1985-....
VIAF ID: 315736924 (Personal)
Permalink: http://viaf.org/viaf/315736924
Preferred Forms
- 100 0 _ ‡a Daniel Grinberg
- 100 1 _ ‡a Grinberg, Daniel, ‡d 1985-....
4xx's: Alternate Name Forms (3)
Works
Title | Sources |
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Antisense oligonucleotide treatment for a pseudoexon-generating mutation in the NPC1 gene causing Niemann-Pick type C disease | |
Approche multi-physique pour l'évaluation des conséquences objectives de la réparation de la valve mitrale. | |
Artificial mitral chordae: When length matters | |
Ascending aortic aneurysm: Update to existing guidelines | |
The association between common vitamin D receptor gene variations and osteoporosis: a participant-level meta-analysis | |
Cardiopulmonary Bypass Priming with Hydroxyethyl Starch 6% 130/0.4 or Sodium Chloride 0.9%: A Preliminary Double-Blind Randomized Controlled Study in Cardiac Surgery | |
Chirurgie mitrale par voie mini-invasive et sans clampage aortique : à propos de 37 cas de patients à haut risque | |
Combined Minimally Invasive Redo Mitral Surgery and Pectus Excavatum Correction | |
Description of extreme longevity in the Balearic Islands: Exploring a potential Blue Zone in Menorca, Spain | |
Design and evaluation of a transesophageal HIFU probe for ultrasound-guided cardiac ablation: simulation of a HIFU mini-maze procedure and preliminary ex vivo trials | |
Erratum to: The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America | |
Extending the phenotypic spectrum of Bohring-Opitz syndrome: Mild case confirmed by functional studies | |
Five new cases of syndromic intellectual disability due to KAT6A mutations: widening the molecular and clinical spectrum | |
Functional characterization of the C7ORF76 genomic region, a prominent GWAS signal for osteoporosis in 7q21.3. | |
Functional relevance of the BMD-associated polymorphism rs312009: novel involvement of RUNX2 in LRP5 transcriptional regulation | |
Gaucher disease: Biochemical and molecular findings in 141 patients diagnosed in Greece | |
Generation of a human neuronal stable cell model for niemann-pick C disease by RNA interference | |
Generation of two compound heterozygous HGSNAT-mutated lines from healthy induced pluripotent stem cells using CRISPR/Cas9 to model Sanfilippo C syndrome | |
Genetic determinants of aromatase inhibitor-related arthralgia: the B-ABLE cohort study | |
Homozygosity for the double D409H+H255Q allele in type II Gaucher disease. | |
Hypertrophic cardiomyopathy: the edge-to-edge secures the correction of the systolic anterior motion. | |
Identification and functional analyses of CBS alleles in Spanish and Argentinian homocystinuric patients. | |
In vitro functional assay of alleles and haplotypes of two COL1A1-promoter SNPs | |
Influence of trends in hospital volume over time on patient outcomes for high-risk surgery | |
Maroteaux-Lamy syndrome: functional characterization of pathogenic mutations and polymorphisms in the arylsulfatase B gene | |
Measuring chordae tension during transapical neochordae implantation: Toward understanding objective consequences of mitral valve repair | |
Minithoracotomy and Beating Heart Strategy for Mitral Surgery in Secondary Mitral Regurgitation | |
Mitral valve repair based on intraoperative objective measurement | |
Mitral valve repair based on physical characterization of coaptation forces | |
A mutation within the saposin D domain in a Gaucher disease patient with normal glucocerebrosidase activity. | |
Mutational spectrum by phenotype: panel-based NGS testing of patients with clinical suspicion of RASopathy and children with multiple café-au-lait macules | |
Outcomes after extracorporeal life support for postcardiotomy cardiogenic shock | |
Perinatal lethal phenotype with generalized ichthyosis in a type 2 Gaucher disease patient with the [L444P;E326K]/P182L genotype: effect of the E326K change in neonatal and classic forms of the disease | |
Perspective of the GEMSTONE Consortium on Current and Future Approaches to Functional Validation for Skeletal Genetic Disease Using Cellular, Molecular and Animal-Modeling Techniques | |
Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7 | |
Polymorphisms of genes involved in homocysteine metabolism in preeclampsia and in uncomplicated pregnancies | |
Present and future of antisense therapy for splicing modulation in inherited metabolic disease | |
Promising results of the chaperone effect caused by imino sugars and aminocyclitol derivatives on mutant glucocerebrosidases causing Gaucher disease | |
Quality Assessment of Reporting of Economic Evaluation in Cardiac Sugery: Has it Improved? | |
Recent patents relating to siRNAs and therapeutic strategies for genetic diseases | |
Risk factors and prognostic impact of left ventricular assist device-associated infections | |
A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders | |
Simvastatin and atorvastatin enhance gene expression of collagen type 1 and osteocalcin in primary human osteoblasts and MG-63 cultures | |
Stereodivergent synthesis of right- and left-handed iminoxylitol heterodimers and monomers. Study of their impact on β-glucocerebrosidase activity | |
Sutureless 3f Enable valve implantation concomitant with mitral valve surgery. | |
A tensed Tendyne | |
Total percutaneous femoral vessels cannulation for minimally invasive mitral valve surgery. | |
Totally endoscopic aortic valve replacement (TEAVR). | |
Tracing Toxic Legacies: GIS and the Dispersed Violence of Agent Orange | |
Transcatheter aortic valve implantation using the left transcarotid approach in patients with previous ipsilateral carotid endarterectomy. | |
Two novel (1098insA and Y313H) and one rare (R359Q) mutations detected in exon 8 of the β‐glucocerebrosidase gene in Gaucher's disease patients | |
Veno-arterial extracorporeal membrane oxygenation for cardiogenic shock due to myocarditis in adult patients | |
What do MITRA-FR and COAPT teach us about the percutaneous treatment of secondary mitral regurgitation? | |
Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture |