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Author/Creator Loundon, Natalie

1. An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature. Issue 12 (7th October 2016)

Authors:
Lerat, Justine; Jonard, Laurence; Loundon, Natalie; Christin‐Maitre, Sophie; Lacombe, Didier; Goizet, Cyril; Rouzier, Cécile; Van Maldergem, Lionel; Gherbi, Souad; Garabedian, Eréa‐Nöel; Bonnefont, Jean‐ Paul; Touraine, Philippe; Mosnier, Isabelle; Munnich, Arnold; Denoyelle, Françoise; Marlin, S...
Journal:
Human mutation
Issue:
Volume 37:Issue 12(2016)
Page Start:
1354
Record Type:
Journal Article
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2. Analysis of specific risk factors of neurodevelopmental disorder in hearing-impaired infants under ten months of age: "EnTNDre" an opening research stemming from a transdisciplinary partnership. (March 2023)

Authors:
Akrich, Salomé; Parlato de Oliveira, Erika; Favrot-Meunier, Claire; Rebichon, Caroline; de Clerck, Aurélie; Ettori, Sophie; Rouillon, Isabelle; Prang, Isabelle; Loundon, Natalie
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 166(2023)
Page Start:
Record Type:
Journal Article
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5. EDNRB mutations cause Waardenburg syndrome type II in the heterozygous state. Issue 5 (15th March 2017)

Authors:
Issa, Sarah; Bondurand, Nadege; Faubert, Emmanuelle; Poisson, Sylvain; Lecerf, Laure; Nitschke, Patrick; Deggouj, Naima; Loundon, Natalie; Jonard, Laurence; David, Albert; Sznajer, Yves; Blanchet, Patricia; Marlin, Sandrine; Pingault, Veronique
Journal:
Human mutation
Issue:
Volume 38:Issue 5(2017)
Page Start:
581
Record Type:
Journal Article
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6. Hearing rehabilitation with the closed skin bone-anchored implant Sophono Alpha1: Results of a prospective study in 15 children with ear atresia. Issue 3 (March 2015)

Authors:
Denoyelle, Françoise; Coudert, Cyrille; Thierry, Briac; Parodi, Marine; Mazzaschi, Olivia; Vicaut, Eric; Tessier, Natacha; Loundon, Natalie; Garabedian, Eréa-Noël
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 79:Issue 3(2015:Mar.)
Page Start:
382
Record Type:
Journal Article
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7. High prevalence of congenital deafness on Reunion Island is due to a founder variant of LHFPL5. Issue 1 (4th November 2018)

Authors:
Lerat, Justine; Bonnet, Crystel; Cartault, François; Loundon, Natalie; Jacquemont, Marie‐Line; Darcel, Françoise; Rouillon, Isabelle; Mezouaghi, Kheira; Guichet, Agnes; Litzler, Julie; Gesny, Roselyne; Gherbi, Souad; Aissa, Ines Ben; Digeon, Fabienne Saint James; Garabedian, Eréa‐Nöel; Bonnefont,...
Journal:
Clinical genetics
Issue:
Volume 95:Issue 1(2019)
Page Start:
177
Record Type:
Journal Article
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8. International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient. (November 2016)

Authors:
Liming, Bryan J.; Carter, John; Cheng, Alan; Choo, Daniel; Curotta, John; Carvalho, Daniela; Germiller, John A.; Hone, Stephen; Kenna, Margaret A.; Loundon, Natalie; Preciado, Diego; Schilder, Anne; Reilly, Brian J.; Roman, Stephane; Strychowsky, Julie; Triglia, Jean-Michel; Young, Nancy; Smith, ...
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 90(2016:Nov.)
Page Start:
251
Record Type:
Journal Article
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9. International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient. (November 2016)

Authors:
Liming, Bryan J.; Carter, John; Cheng, Alan; Choo, Daniel; Curotta, John; Carvalho, Daniela; Germiller, John A.; Hone, Stephen; Kenna, Margaret A.; Loundon, Natalie; Preciado, Diego; Schilder, Anne; Reilly, Brian K.; Roman, Stephane; Strychowsky, Julie; Triglia, Jean-Michel; Young, Nancy; Smith, ...
Journal:
International journal of pediatric otorhinolaryngology
Issue:
Volume 90(2016:Nov.)
Page Start:
251
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗