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 PhenotypeTargetsTherapeuticsClinical trialsCongenital central hypoventilation syndrome (Ondine's curse)Genotype PhenotypeTargetsTherapeuticsClinical trialsPigmentary anomalies
Waardenburg syndromeGenotype PhenotypeTargetsTherapeuticsClinical trials -
CHARGE syndrome
CHARGE SyndromeGenotype PhenotypeTargetsTherapeuticsClinical trialsPosterior cleft palate
Pierre Robin syndromeGenotype PhenotypeTargetsTherapeuticsClinical trials22q11 microdeletion syndromeGenotype PhenotypeTargetsTherapeuticsClinical trialsCongenital sucking, swallowing, and feeding disorders due to rare syndromesGenotype PhenotypeTargetsTherapeuticsClinical trialsCongenital sucking, swallowing, and feeding disorders due to neurodevelopmental disordersGenotype PhenotypeTargetsTherapeuticsClinical 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 PhenotypeTargetsTherapeuticsClinical trialsCysts and fistulas of the first branchial cleftGenotype PhenotypeTargetsTherapeuticsClinical trialsCysts and fistulas of the second branchial cleftGenotype PhenotypeTargetsTherapeuticsClinical trialsCysts and fistulas of fourth branchial pouchGenotype PhenotypeTargetsTherapeuticsClinical trialsThyroglossal duct cystsGenotype PhenotypeTargetsTherapeuticsClinical trialsNasal tip and dorsum cysts and fistulasGenotype PhenotypeTargetsTherapeuticsClinical trialsDermoid cysts of all head and neck locationsGenotype PhenotypeTargetsTherapeuticsClinical trialsBranchial anomalies and fibrochondromasGenotype PhenotypeTargetsTherapeuticsClinical trialsAtypical cysts and fistulasGenotype PhenotypeTargetsTherapeuticsClinical trialsPrimary Velopharyngeal insuffiency
Primary Velopharyngeal insuffiencyGenotype PhenotypeTargetsTherapeuticsClinical trialsLarynx and trachea
Hypoplasia, laryngeal atresiaGenotype PhenotypeTargetsTherapeuticsClinical trialsLaryngo-tracheal cleftsGenotype PhenotypeTargetsTherapeuticsClinical trialsTracheal hypoplasiaGenotype PhenotypeTargetsTherapeuticsClinical trialsLarynx mobility anomaliesGenotype PhenotypeTargetsTherapeuticsClinical trialsLaryngomalaciaGenotype PhenotypeTargetsTherapeuticsClinical trialsTracheoesophageal fistulaGenotype PhenotypeTargetsTherapeuticsClinical trialsTracheomalaciaGenotype PhenotypeTargetsTherapeuticsClinical trialsInfantile hemangiomaGenotype PhenotypeTargetsTherapeuticsClinical trialsRecurrent respiratoryl papillomatosisGenotype PhenotypeTargetsTherapeuticsClinical trialsLaryngeal-tracheal papillomatosisGenotype PhenotypeTargetsTherapeuticsClinical trialsNose sinuses and skull base
Choanal atresiaGenotype PhenotypeTargetsTherapeuticsClinical trialsCongenital nasal pyriform aperture stenosisGenotype PhenotypeTargetsTherapeuticsClinical trialsCongenital meningocele and meningocephaloceleGenotype PhenotypeTargetsTherapeuticsClinical trialsNasolacrimal duct cystGenotype PhenotypeTargetsTherapeuticsClinical trials -
Transmission deafness
Outer ear malformationsGenotype PhenotypeTargetsTherapeuticsClinical trialsOssicles malformations - minor aplasiaGenotype PhenotypeTargetsTherapeuticsClinical trialsOuter ear and duct malformations
Major aplasiaGenotype PhenotypeTargetsTherapeuticsClinical trialsCongenital stenosis of external auditory canals (notably 18q deletion)Genotype PhenotypeTargetsTherapeuticsClinical trials -
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Heterotaxia
Atrio Ventricular Canal Defect (AVCD)Genotype PhenotypeTargetsTherapeuticsClinical trialsDouble Outlet Right Ventricle (DORV)Genotype PhenotypeTargetsTherapeuticsClinical trialsTransposition of the great arteries (TGA)Genotype PhenotypeTargetsTherapeuticsClinical trials -
Spina bifida or myelomeningoceleGenotype PhenotypeTargetsTherapeuticsClinical trialsAortic valve stenosisGenotype PhenotypeTargetsTherapeuticsClinical trialsDiaphragmatic herniaGenotype PhenotypeTargetsTherapeuticsClinical trialsLower Urinary Tract Obstruction (LUTO)Genotype PhenotypeTargetsTherapeuticsClinical trialsMonochorionic pregnancy or twin-to-twin transfusion syndromeGenotype PhenotypeTargetsTherapeuticsClinical trialsCytomegalovirus (CMV)Genotype PhenotypeTargetsTherapeuticsClinical trialsHydrocephalusGenotype PhenotypeTargetsTherapeuticsClinical trials
Specific 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 PhenotypeTargetsTherapeuticsClinical trialsOther dysraphismsGenotype PhenotypeTargetsTherapeuticsClinical trials
Contacts
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Thibaut PERCHET
Business development manager
- nicolas.doulet@institutimagine.org
- +33 1 42 75 42 55