User profiles for C. Bruno
Christopher C BrunoPhD Candidate - Management, The Wharton School - University of Pennsylvania Verified email at wharton.upenn.edu Cited by 170 |
Prenatal identification of invasive placentation using magnetic resonance imaging: systematic review and meta‐analysis
…, J Palacios‐Jaraquemada, CH Bruno… - … in Obstetrics & …, 2014 - Wiley Online Library
Objective To assess systematically the performance of prenatal magnetic resonance
imaging ( MRI ) in diagnosing the presence, degree and topography of disorders of invasive …
imaging ( MRI ) in diagnosing the presence, degree and topography of disorders of invasive …
[HTML][HTML] Caveolinopathies: from the biology of caveolin-3 to human diseases
In muscle tissue the protein caveolin-3 forms caveolae–flask-shaped invaginations localized
on the cytoplasmic surface of the sarcolemmal membrane. Caveolae have a key role in the …
on the cytoplasmic surface of the sarcolemmal membrane. Caveolae have a key role in the …
Does sustainability generate better financial performance? review, meta-analysis, and propositions
Sustainability in business and ESG (environmental, social, and governance) in finance have
exploded in popularity among researchers and practitioners. We surveyed 1,141 primary …
exploded in popularity among researchers and practitioners. We surveyed 1,141 primary …
GMES Sentinel-1 mission
…, B Duesmann, B Rosich, N Miranda, C Bruno… - Remote sensing of …, 2012 - Elsevier
… This ensured the continuation of C-band data and added enhanced capabilities such as
wide swaths and dual polarisation, features that have since rapidly been integrated into and …
wide swaths and dual polarisation, features that have since rapidly been integrated into and …
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
… 1 c). Quantitative analysis by immunohistochemistry and immunoblotting showed that
caveolin-3 expression in patients was reduced by 92% and 95%, respectively, compared with …
caveolin-3 expression in patients was reduced by 92% and 95%, respectively, compared with …
[HTML][HTML] Respiratory complex III is required to maintain complex I in mammalian mitochondria
…, R Moreno-Loshuertos, A Pérez-Martos, C Bruno… - Molecular cell, 2004 - cell.com
… from A22 cells was analyzed separately by second dimension in (C): faster migrating band
(C Ii) and slower migrating band (C Is). The remaining symbols are as indicated in Figure 4. …
(C Ii) and slower migrating band (C Is). The remaining symbols are as indicated in Figure 4. …
[HTML][HTML] Exercise Intolerance Due to Mutations in the Cytochrome b Gene of Mitochondrial DNA
…, MG Hanna, H Reichmann, C Bruno… - … England Journal of …, 1999 - Mass Medical Soc
Background The mitochondrial myopathies typically affect many organ systems and are
associated with mutations in mitochondrial DNA (mtDNA) that are maternally inherited. However, …
associated with mutations in mitochondrial DNA (mtDNA) that are maternally inherited. However, …
Assessment of 135 794 pediatric patients tested for severe acute respiratory syndrome coronavirus 2 across the United States
…, D Ranade, S Rao, O Sofela, J Zahner, C Bruno… - JAMA …, 2021 - jamanetwork.com
Importance There is limited information on severe acute respiratory syndrome coronavirus 2
(SARS-CoV-2) testing and infection among pediatric patients across the United States. …
(SARS-CoV-2) testing and infection among pediatric patients across the United States. …
[HTML][HTML] Risdiplam-treated infants with type 1 spinal muscular atrophy versus historical controls
…, E Zanoteli, G Baranello, C Bruno… - … England Journal of …, 2021 - Mass Medical Soc
Background Type 1 spinal muscular atrophy (SMA) is a progressive neuromuscular disease
characterized by an onset at 6 months of age or younger, an inability to sit without support, …
characterized by an onset at 6 months of age or younger, an inability to sit without support, …
Onasemnogene abeparvovec gene therapy for symptomatic infantile-onset spinal muscular atrophy type 1 (STR1VE-EU): an open-label, single-arm, multicentre …
…, R Masson, O Boespflug-Tanguy, C Bruno… - The Lancet …, 2021 - thelancet.com
Background Spinal muscular atrophy is a rare, autosomal recessive, neuromuscular disease
caused by biallelic loss of the survival motor neuron 1 (SMN1) gene, resulting in motor …
caused by biallelic loss of the survival motor neuron 1 (SMN1) gene, resulting in motor …