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Items: 5

1.

Three New Mutations and Mild, Asymmetrical Phenotype in the Highly Distinctive LAMM Syndrome: A Report of Eight Further Cases.

Al Yassin A, D'Arco F, Morín M, Pagarkar W, Harrop-Griffiths K, Shaida A, Fernández E, Cullup T, De-Souza B, Moreno-Pelayo MA, Bitner-Glindzicz M.

Genes (Basel). 2019 Jul 12;10(7). pii: E529. doi: 10.3390/genes10070529.

2.

Consensus Statement of the Indian Academy of Pediatrics on Newborn Hearing Screening.

From National Consultation Meeting for Developing IAP Guidelines on Neurodevelopmental Disorders under the aegis of IAP Childhood Disability Group and the Committee on Child Development and Neurodevelopmental Disorders, Paul A, Prasad C, Kamath SS, Dalwai S, C Nair MK, Pagarkar W.

Indian Pediatr. 2017 Aug 15;54(8):647-651. Epub 2017 Jun 4.

3.

The bony cochlear nerve canal in children with absent or hypoplastic cochlear nerves.

Pagarkar W, Gunny R, Saunders DE, Yung W, Rajput K.

Int J Pediatr Otorhinolaryngol. 2011 Jun;75(6):764-73. doi: 10.1016/j.ijporl.2011.02.017. Epub 2011 Apr 16.

PMID:
21497917
4.

Subjective visual vertical and horizontal: effect of the preset angle.

Pagarkar W, Bamiou DE, Ridout D, Luxon LM.

Arch Otolaryngol Head Neck Surg. 2008 Apr;134(4):394-401. doi: 10.1001/archotol.134.4.394.

PMID:
18427005
5.

Late postnatal onset of hearing loss due to GJB2 mutations.

Pagarkar W, Bitner-Glindzicz M, Knight J, Sirimanna T.

Int J Pediatr Otorhinolaryngol. 2006 Jun;70(6):1119-24. Epub 2006 Feb 15.

PMID:
16469394

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