Publications by authors named "Steve Courel"

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Nationwide Outcomes After Thoracoscopic Versus Open Resection of Congenital Pulmonary Airway Malformations in Newborns.
Carlos Theodore Huerta, Walter A Ramsey, Steve C Courel, Gareth P Gilna, Rebecca A Saberi

J Laparoendosc Adv Surg Tech A· September 2023

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Nationwide management of perforated pediatric appendicitis: Interval versus same-admission appendectomy.
Carlos Theodore Huerta, Steve C Courel, Walter A Ramsey, Rebecca A Saberi, Gareth P Gilna

J Pediatr Surg· April 2023

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Difference between SARS-CoV-2, seasonal coronavirus, influenza, and respiratory syncytial virus infection in solid organ transplant recipients.
Maria A Mendoza, Gabriel Motoa, Mohammed A Raja, Paola Frattaroli, Anmary Fernandez, Steve C Courel

Transpl Infect Dis· February 2023

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Outcomes of Gastrostomy Tubes in Newborns With Congenital Heart Disease and Comparison of Techniques.
Carlos Theodore Huerta, Walter A Ramsey, Steve C Courel, Rebecca A Saberi, Gareth P Gilna

J Surg Res· December 2022

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Reinfection with SARS-CoV-2 in solid-organ transplant recipients: Incidence density and convalescent immunity prior to reinfection.
Stephen Morris, Shweta Anjan, Suresh Pallikkuth, Paola Frattaroli, Steve Courel

Transpl Infect Dis· June 2022

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Erratum to: A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement.
Adriana P Rebelo, Andrea Cortese, Amit Abraham, Yael Eshed-Eisenbach, Gal Shner, Steve Courel

Brain· August 2021

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A CADM3 variant causes Charcot-Marie-Tooth disease with marked upper limb involvement.
Adriana P Rebelo, Andrea Cortese, Amit Abraham, Yael Eshed-Eisenbach, Gal Shner, Steve Courel

Brain· May 2021

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Assessing non-Mendelian inheritance in inherited axonopathies.
Dana M Bis-Brewer, Ziv Gan-Or, Patrick Sleiman, , Hakon Hakonarson, Steve Courel

Genet Med· December 2020

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Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Andrea Cortese, Yi Zhu, Adriana P Rebelo, Sara Negri, Steve Courel

Nat Genet· June 2020

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes.
Andrea Cortese, Yi Zhu, Adriana P Rebelo, Sara Negri, Steve Courel

Nat Genet· May 2020

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POLG mutations presenting as Charcot-Marie-Tooth disease.
Jade Phillips, Steve Courel, Adriana P Rebelo, Dana M Bis-Brewer, Tanya Bardakjian

J Peripher Nerv Syst· June 2019

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Mohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Steve Courel

Am J Hum Genet· June 2019

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.
Mohammad Ali Farazi Fard, Adriana P Rebelo, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Steve Courel

Am J Hum Genet· April 2019

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A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family.
Lois Dankwa, Jessica Richardson, William W Motley, Mena Scavina, Steve Courel

Neuromuscul Disord· February 2019

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Identification of a new SYT2 variant validates an unusual distal motor neuropathy phenotype.
Nataly I Montes-Chinea, Zhuo Guan, Marcella Coutts, Cecilia Vidal, Steve Courel

Neurol Genet· December 2018

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Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2.
Petra Lassuthova, Adriana P Rebelo, Gianina Ravenscroft, Phillipa J Lamont, Mark R Davis, Steve Courel

Am J Hum Genet· March 2018

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