about
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung diseaseLong-term results of the transmanubrial osteomuscular-sparing approach for pediatric tumors.Immature cryopreserved ovary restores puberty and fertility in mice without alteration of epigenetic marksIdentification of a human splenic marginal zone B cell precursor with NOTCH2-dependent differentiation properties.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.Comprehensive study of the intestinal stage of listeriosis in a rat ligated ileal loop system.A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors.Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.Laparoscopic resection of abdominal neuroblastoma.Prenatal intestinal obstruction affects the myenteric plexus and causes functional bowel impairment in fetal rat experimental model of intestinal atresiaDissection of the MYCN locus in Feingold syndrome and isolated oesophageal atresia.Decreased expression of the interleukin 2 receptor on CD8 recipient lymphocytes in intestinal grafts rendered tolerant by liver transplantation in rats.Liver-induced immune tolerance in recipients of combined liver-intestine transplants.Abdominal desmoplastic small round cell tumor without extraperitoneal metastases: Is there a benefit for HIPEC after macroscopically complete cytoreductive surgery?Assessment of Primary Site Response in Children With High-Risk Neuroblastoma: An International Multicenter Study.Preserving fertility in prepubertal children.Tracheal and bronchial tumorsValidation of the French versions of the Hirschsprung's disease and Anorectal malformations Quality of Life (HAQL) questionnaires for adolescents and adults.Surgery of ovarian tumors in children.Guidelines for imaging and staging of neuroblastic tumors: consensus report from the International Neuroblastoma Risk Group Project.Ovarian transposition in prepubescent and adolescent girls with cancer.Neonatal cancer.Impact of spinal dysraphism on urinary and faecal prognosis in 25 cases of cloacal malformation.Surgical management of thymic epithelial tumors in children: lessons from the French Society of Pediatric Oncology and review of the literature.Prenatal counselling and the role of the paediatric surgeon.Minimally invasive resection of adrenal masses in infants and children: results of a European multi-center survey.Pediatric Patient With Renal Cell Carcinoma Treated by Successive Antiangiogenics Drugs: A Case Report and Review of the Literature.Recurrence of Solid Pseudopapillary Neoplasms of the Pancreas: Results of a Nationwide Study of Risk Factors and Treatment Modalities.Host response to a dam mutant of Salmonella enterica serovar enteritidis with a temperature-sensitive phenotype.Image-defined risk factors in unresectable neuroblastoma: SIOPEN study on incidence, chemotherapy-induced variation, and impact on surgical outcomes.Laparoscopic Splenectomy in Children: A Modified Technique with Joint Sealing of Segmental Splenic Arteries and Veins Favorably Compared with the Classic Technique.Radiogenomics of neuroblastomas: Relationships between imaging phenotypes, tumor genomic profile and survival.EFTUD2 haploinsufficiency leads to syndromic oesophageal atresia.Is laparoscopic management suitable for solid pseudo-papillary tumors of the pancreas?Seventeen years after successful small bowel transplantation: long term graft acceptance without immune tolerance.[Anorectal malformations].The impact of anorectal malformations on anorectal function and social integration in adulthood: report from a national database.Outcome of suprarenal localized masses diagnosed during the perinatal period: a retrospective multicenter study.Changes in WT1 splicing are associated with a specific gene expression profile in Wilms' tumour.WNT/beta-catenin pathway activation in Wilms tumors: a unifying mechanism with multiple entries?
P50
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P50
description
French researcher and pediatric physician
@en
praticien hospitalier en chirurgie pédiatrique
@fr
wetenschapper
@nl
name
Sabine Sarnacki
@ast
Sabine Sarnacki
@en
Sabine Sarnacki
@es
Sabine Sarnacki
@fr
Sabine Sarnacki
@nl
Sabine Sarnacki
@sl
type
label
Sabine Sarnacki
@ast
Sabine Sarnacki
@en
Sabine Sarnacki
@es
Sabine Sarnacki
@fr
Sabine Sarnacki
@nl
Sabine Sarnacki
@sl
altLabel
Sabine Sarnacki-Féray
@en
Sabine Sarnacki-Féray
@fr
prefLabel
Sabine Sarnacki
@ast
Sabine Sarnacki
@en
Sabine Sarnacki
@es
Sabine Sarnacki
@fr
Sabine Sarnacki
@nl
Sabine Sarnacki
@sl
P214
P1053
I-2692-2017
P106
P1477
Sabine Sarnacki
@fr
P21
P213
0000 0000 5759 826X
P214
P31
P3829
P496
0000-0003-4304-5578
P734
P735
P7859
viaf-79240072