Teams
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Sabine Sarnacki
>> Associated Lab
IMAG2 - Computational anatomy for image-guided minimally invasive surgery in pe… -
Yves Ville
>> Associated Lab
Impact@Imagine – innovative multidisciplinary prenatal approach of congenital d… -
Véronique Abadie
>> Reference center for rare diseases
Pierre Robin sequence and congenital feeding and swallowing disorders -
Jeanne Amiel
>> Reference center for rare diseases
Developmental abnormalities and malformation syndromes in the Ile-de-France reg… -
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Michel Zérah
>> Reference center for rare diseases
Rares vertebral and spinal malformations (C-MAVEM)
Filière Neurosphinx
Associated with the European Reference Network (ERN) eUROGEN -
Michel Zérah
Reference center for rare diseases
Craniosynostosis and craniofacial malformations (CRANIOST)
Filière TETE COU
Associated with the European Reference Network (ERN) Craniofacial anomalies and ENT disorders
Imagine's Offers
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Enteric nervous system diseases
Hirschprung DiseaseGenotype Phenotype-
Cohorts
> 100 patients
TargetsTherapeuticsClinical trialsCongenital central hypoventilation syndrome (Ondine's curse)Genotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsPigmentary anomalies
Waardenburg syndromeGenotype Phenotype-
Cohorts
35 patients
TargetsTherapeuticsClinical trials -
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CHARGE syndrome
CHARGE SyndromeGenotype Phenotype-
Cohorts
> 100 pediatric and adult patients
TargetsTherapeuticsClinical trialsPosterior cleft palate
Pierre Robin syndromeGenotype Phenotype-
Cohorts
> 400 pediatric and adult patients
TargetsTherapeuticsClinical trials22q11 microdeletion syndromeGenotype Phenotype-
Cohorts
> 500 pediatric and adult patients
TargetsTherapeuticsClinical trialsCongenital sucking, swallowing, and feeding disorders due to rare syndromesGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCongenital sucking, swallowing, and feeding disorders due to neurodevelopmental disordersGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsFeeding behaviour disorders post traumatic or due to developmental malformationsGenotype PhenotypeTargetsTherapeuticsClinical trialsFeeding problems in normal populationsGenotype PhenotypeTargetsTherapeuticsClinical trialsSecondary velopharyngial insufficiencyGenotype PhenotypeTargetsTherapeuticsClinical trialsCysts and fistulas
Cleft lip/palateGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCysts and fistulas of the first branchial cleftGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCysts and fistulas of the second branchial cleftGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCysts and fistulas of fourth branchial pouchGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsThyroglossal duct cystsGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsNasal tip and dorsum cysts and fistulasGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsDermoid cysts of all head and neck locationsGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsBranchial anomalies and fibrochondromasGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsAtypical cysts and fistulasGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsPrimary Velopharyngeal insuffiency
Primary Velopharyngeal insuffiencyGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsLarynx and trachea
Hypoplasia, laryngeal atresiaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsLaryngo-tracheal cleftsGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsTracheal hypoplasiaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsLarynx mobility anomaliesGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsLaryngomalaciaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsTracheoesophageal fistulaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsTracheomalaciaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsInfantile hemangiomaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsRecurrent respiratoryl papillomatosisGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsLaryngeal-tracheal papillomatosisGenotype Phenotype-
Cohorts
Constitution of a national cohort
TargetsTherapeuticsClinical trialsNose sinuses and skull base
Choanal atresiaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCongenital nasal pyriform aperture stenosisGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCongenital meningocele and meningocephaloceleGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsNasolacrimal duct cystGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trials -
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Transmission deafness
Outer ear malformationsGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsOssicles malformations - minor aplasiaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsOuter ear and duct malformations
Major aplasiaGenotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsCongenital stenosis of external auditory canals (notably 18q deletion)Genotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trials -
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Heterotaxia
Atrio Ventricular Canal Defect (AVCD)Genotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsDouble Outlet Right Ventricle (DORV)Genotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsTransposition of the great arteries (TGA)Genotype Phenotype-
Cohorts
Please, contact us
TargetsTherapeuticsClinical trials -
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Spina bifida or myelomeningoceleGenotype PhenotypeTargetsTherapeutics
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Protocols/Technics
Endoscopic fetal surgery
Clinical trials-
NCT
ENDOSPIN (NCT02390895) Prenatal Endoscopic Repair of Fetal Spina Bifida
Aortic valve stenosisGenotype PhenotypeTargetsTherapeutics-
Protocols/Technics
Fetal aortic valvuloplasty
Clinical trialsDiaphragmatic herniaGenotype PhenotypeTargetsTherapeutics-
Protocols/Technics
Endotracheal foetoscopy PLUG (Plug the Lung Until it Grows)
Clinical trialsLower Urinary Tract Obstruction (LUTO)Genotype PhenotypeTargetsTherapeuticsClinical trialsMonochorionic pregnancy or twin-to-twin transfusion syndromeGenotype PhenotypeTargetsTherapeutics-
Protocols/Technics
Fetoscopic laser ablation of placental anastomoses
Clinical trialsCytomegalovirus (CMV)Genotype PhenotypeTargetsTherapeutics-
Specific therapeutic approaches
Valaciclovir (ZELITREX)
Clinical trialsHydrocephalusGenotype PhenotypeTargetsTherapeutics-
Specific therapeutic approaches
In neonates:
- Ventriculoperitoneal shunting
- Ventriculocisternostomy
Fetal treatment:
- Ventriculo-amniotic shunting
- Endoscopic ventriculocisternostomy
Clinical trialsSpecific technics
Diagnostic:
- Amniocentesis
- Trophoblast biopsy
- Fetal blood sampling
Fetal therapy:
- Endoscopic fetal surgery
- Fetal aortic valvuloplasty
- Endotracheal foetoscopy PLUG (Plug the Lung Until it Grows)
- Fetoscopic laser ablation of placental anastomoses
- Ventriculo-amniotic shunting
- Endoscopic ventriculocisternostomy
- Fetal anaesthesia
- Ex utero intrapartum treatment (EXIT procedure)
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Brain malformations
Joubert syndrome (JS)Genotype PhenotypeTargetsTherapeuticsClinical trialsMeckel syndrome (MKS)Genotype PhenotypeTargetsTherapeuticsClinical trialsHydrolethalus syndrome (HLS)Genotype PhenotypeTargetsTherapeuticsClinical trialsCorpus Callosum malformationsGenotype PhenotypeTargetsTherapeuticsClinical trialsMalformations of cortical developmentGenotype PhenotypeTargetsTherapeuticsClinical trialsCardiac ciliopathies
HeterotaxiaGenotype PhenotypeTargetsTherapeuticsClinical trialsSitus inversusGenotype PhenotypeTargetsTherapeuticsClinical trialsRenal ciliopathies
NephronophthisisGenotype PhenotypeTargetsTherapeuticsClinical trialsOcular ciliopathies
Leber Congenital Amaurosis (LCA)Genotype PhenotypeTargetsTherapeuticsClinical trialsX-linked retinitis pigmentosa (XLRP)Genotype PhenotypeTargetsTherapeuticsClinical trialsSkeletal ciliopathies
Short-rib polydactylyGenotype PhenotypeTargetsTherapeuticsClinical trialsEllis Van Creveld syndromeGenotype PhenotypeTargetsTherapeuticsClinical trialsJeune asphyxiating thoracic dystrophyGenotype PhenotypeTargetsTherapeuticsClinical trials -
Spina bifida (or myelomeningocele)Genotype Phenotype
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Cohorts
Please, contact us
TargetsTherapeuticsClinical trialsOther dysraphismsGenotype PhenotypeTargetsTherapeuticsClinical trials -
Contacts
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Thibaut PERCHET
Business development manager
- nicolas.doulet@institutimagine.org
- +33 1 42 75 42 55