Publications by authors named "Stephane Romano"

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Safety and Efficacy of Percutaneous Morton Neuroma Cryoneurolysis Under Ultrasound Guidance.
Benjamin Moulin, Giorgio Angelopoulos, Jean Luc Sarrazin, Stephane Romano, Olivier Vignaux

Cardiovasc Intervent Radiol· June 2024

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Radiolunate arthrodesis and scaphoidectomy combined to Sauvé-Kapandji procedure as treatment of wrist osteoarthritis: Clinical and radiological results.
Rémy Pichard, Marc Juvenspan, Patrick Houvet, Stéphane Romano

Hand Surg Rehabil· October 2023

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Perianesthetic concerns for the non-COVID-19 patients requiring surgery during the COVID-19 pandemic outbreak: An observational study.
Gilles Boccara, David Cassagnol, Laurent Bargues, Thierry Guenoun, Benjamin Aubier, Stéphane Romano

J Clin Anesth· November 2020

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An Erased Physical Marking from the Holocaust.
Amir Oron, Yehuda David, Stéphane Romano

Isr Med Assoc J· April 2020

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Multiple sources of metabolic disturbance in ETHE1-related ethylmalonic encephalopathy.
Magalie Barth, Chris Ottolenghi, Laurence Hubert, Dominique Chrétien, Valérie Serre, Stéphane Romano

J Inherit Metab Dis· December 2010

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Cardiomyopathies in propionic aciduria are reversible after liver transplantation.
Stéphane Romano, Vassili Valayannopoulos, Guy Touati, Jean-Pierre Jais, Daniel Rabier

J Pediatr· January 2010

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CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation.
Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker, Sophie Audollent, Nadia Elkhartoufi, Stéphane Romano

Hum Mutat· November 2009

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Structural insights on pathogenic effects of novel mutations causing pyruvate carboxylase deficiency.
Sophie Monnot, Valérie Serre, Bernadette Chadefaux-Vekemans, Joelle Aupetit, Stéphane Romano

Hum Mutat· May 2009

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What's new in metabolic and genetic hypoglycaemias: diagnosis and management.
Vassili Valayannopoulos, Stéphane Romano, Karine Mention, Anne Vassault, Daniel Rabier

Eur J Pediatr· March 2008

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CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders.
Francesco Brancati, Giuseppe Barrano, Jennifer L Silhavy, Sarah E Marsh, Lorena Travaglini, Stephane Romano

Am J Hum Genet· July 2007

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The Meckel-Gruber syndrome gene, MKS3, is mutated in Joubert syndrome.
Lekbir Baala, Stephane Romano, Rana Khaddour, Sophie Saunier, Ursula M Smith

Am J Hum Genet· January 2007

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