C. Crétolle

发表

Dissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia

A. Munnich, N. Philip, A. Verloes, 2011, European Journal of Human Genetics.

ERNICA guidelines for the management of rectosigmoid Hirschsprung’s disease

J. Hugot, D. Cavalieri, R. Hofstra, 2020, Orphanet Journal of Rare Diseases.

The impact of anorectal malformations on anorectal function and social integration in adulthood: report from a national database

S. Sarnacki, J. Hardouin, G. Meurette, 2013, Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland.

Transition of care in patients with anorectal malformations: Consensus by the ARM-net consortium.

C. Grano, S. Giuliani, G. Brisighelli, 2017, Journal of pediatric surgery.

Currarino syndrome as an etiology of a neonatal Escherichia coli meningitis

J. Rozé, J. Caillon, G. Picherot, 2007, Journal of Perinatology.

1-Serological methods: description of LIPS assay

D. Kariyawasam, C. Huon, I. Sermet-Gaudelus, 2021 .

Prior infection by seasonal coronaviruses does not prevent SARS-CoV-2 infection and associated Multisystem Inflammatory Syndrome in children

D. Kariyawasam, C. Huon, B. Bader-Meunier, 2020, medRxiv.

Spinal dysraphism as a new entity in V.A.C.TE.R.L syndrome, resulting in a novel acronym V.A.C.TE.R.L.S

S. Sarnacki, M. Zérah, M. Catala, 2020, European Journal of Pediatrics.

The Currarino syndrome: a syndromic form of anorectal malformation. Clinical, genetic and therapeutic aspects.

C. Crétolle, 2015 .

New clinical and therapeutic perspectives in Currarino syndrome (study of 29 cases).

Y. Révillon, S. Lyonnet, S. Sarnacki, 2006, Journal of pediatric surgery.

Currarino syndrome shown by prenatal onset ventriculomegaly and spinal dysraphism

S. Lyonnet, S. Sarnacki, F. Encha-Razavi, 2007, American journal of medical genetics. Part A.

Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype–phenotype correlation

A. Munnich, Y. Révillon, S. Lyonnet, 2008, Human mutation.

How to Explore Fetal Sacral Agenesis Without Open Dysraphism: Key Prenatal Imaging and Clinical Implications

A. Benachi, N. Mottet, F. Guimiot, 2018, Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine.

Blockade of the integrin αLβ2 but not of integrins α4 and/or β7 significantly prolongs intestinal allograft survival in mice

Y. Révillon, N. Brousse, M. Cavazzana‐Calvo, 2000 .

Consensus Review of Best Practice of Transanal Irrigation in Children

M. Benninga, U. Rolle, G. Mosiello, 2017, Journal of pediatric gastroenterology and nutrition.

A low Anorectal Malformation Exposing a Complete Colorectal Duplication : A Case Report

S. Sarnacki, S. Beaudoin, A. Pire, 2016 .

Value of 18F-fluoro-L-dopa PET in the preoperative localization of focal lesions in congenital hyperinsulinism.

F. Brunelle, M. Ribeiro, Y. Aigrain, 2009, Radiology.

Think of the Conus Medullaris at the Time of Diagnosis of Fetal Sacral Agenesis

A. Benachi, N. Mottet, J. Martinovic, 2016, Fetal Diagnosis and Therapy.

Multicentric evaluation of the adherence to Peristeen® transanal irrigation system in children.

P. Lallemant-Dudek, V. Forin, F. Hameury, 2019, Annals of physical and rehabilitation medicine.

Long-Term Functional Outcomes of an Anorectal Malformation French National Cohort

S. Sarnacki, N. Kalfa, P. Buisson, 2022, Journal of pediatric gastroenterology and nutrition.

Towards the perfect ARM center: the European Union’s criteria for centers of expertise and their implementation in the member states. A report from the ARM-Net

M. Lacher, S. Sarnacki, E. Jenetzky, 2015, Pediatric Surgery International.

European consensus meeting of ARM-Net members concerning diagnosis and early management of newborns with anorectal malformations

I. V. van Rooij, M. Lacher, E. Jenetzky, 2015, Techniques in Coloproctology.

Long-term Outcome of Hirschsprung Disease: Impact on Quality of Life and Social Condition at Adult Age

G. Meurette, P. Lehur, V. Wyart, 2019, Diseases of the colon and rectum.

Research perspectives in the etiology of congenital anorectal malformations using data of the International Consortium on Anorectal Malformations: evidence for risk factors across different populations

I. V. van Rooij, H. Brunner, M. Clementi, 2010, Pediatric Surgery International.

Impact of spinal dysraphism on urinary and faecal prognosis in 25 cases of cloacal malformation.

J. Jais, S. Sarnacki, Y. Aigrain, 2014, Journal of pediatric urology.

Validation of the French versions of the Hirschsprung’s disease and Anorectal malformations Quality of Life (HAQL) questionnaires for adolescents and adults

S. Sarnacki, J. Hardouin, F. Feuillet, 2017, Health and Quality of Life Outcomes.

Prior infection by seasonal coronaviruses, as assessed by serology, does not prevent SARS-CoV-2 infection and disease in children, France, April to June 2020

D. Kariyawasam, C. Huon, I. Sermet-Gaudelus, 2021, Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin.

The challenge of measuring quality of life in children with Hirschsprung's disease or anorectal malformation.

S. Sarnacki, J. Hardouin, G. Podevin, 2013, Journal of pediatric surgery.

[Anorectal malformations].

S. Sarnacki, Y. Aigrain, H. Lottmann, 2013, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.

Anti-LFA-1 Antibody Postpones T-cell Receptor Triggering While Preserving Generation of Regulatory T Cells in T-cell Receptor Anti-HY Transgenic Mice

N. Brousse, O. Lantz, S. Sarnacki, 2006, Transplantation.

Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000.

F. Brunelle, J. Saudubray, J. Rahier, 2002, Journal of pediatric surgery.

Variations in the Detection of Anorectal Anomalies at Birth among European Cities

S. Eaton, S. Sarnacki, P. de Coppi, 2019, European Journal of Pediatric Surgery.

Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32‐q27.2

H. Engels, H. Reutter, M. Ludwig, 2017, Clinical genetics.