Publications by authors named "Aditi Parikh"

9Publications

Heterotopic Quadruplet Pregnancy After ICSI Conception.

J Obstet Gynaecol India 2018 Dec 12;68(6):505-507. Epub 2017 Sep 12.

Department of Obstetrics and Gynecology, KEM Hospital, Pune, India.

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http://dx.doi.org/10.1007/s13224-017-1049-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6207550PMC
December 2018

Reply to "Early resolution of subretinal fluid without high-dose corticosteroids in a pregnant patient with Vogt-Koyanagi Harada disease" by Sugita et al.

J Ophthalmic Inflamm Infect 2016 Dec 3;6(1):13. Epub 2016 May 3.

Vittala International Institute of Ophthalmology & Prabha Eye Clinic and Research Center, 504, 40th Cross, Jayanagar 8th block, Bangalore, 560070, India.

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http://dx.doi.org/10.1186/s12348-016-0080-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854856PMC
December 2016

The prevalence of congenital hearing loss in neonates with Down syndrome.

J Pediatr 2015 Jan 18;166(1):168-71. Epub 2014 Oct 18.

Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, OH.

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http://dx.doi.org/10.1016/j.jpeds.2014.09.005DOI Listing
January 2015

De novo microduplication of the FMR1 gene in a patient with developmental delay, epilepsy and hyperactivity.

Eur J Hum Genet 2012 Nov 2;20(11):1197-200. Epub 2012 May 2.

Center for Human Genetics, University Hospitals Case Medical Center, Cleveland, OH 44106, USA.

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http://www.nature.com/articles/ejhg201278
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http://dx.doi.org/10.1038/ejhg.2012.78DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476717PMC
November 2012

8p21 microdeletion in a patient with intellectual disability and behavioral abnormalities.

Am J Med Genet A 2011 Dec 7;155A(12):3148-52. Epub 2011 Nov 7.

Center for Human Genetics, University Hospitals Case Medical Center, Cleveland, Ohio, USA.

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http://doi.wiley.com/10.1002/ajmg.a.34317
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.34317DOI Listing
December 2011

Late manifestations of tricho-rhino-pharangeal syndrome in a patient: Expanded skeletal phenotype in adulthood.

Am J Med Genet A 2010 Aug;152A(8):2115-9

Center for Human Genetics, University Hospitals Case Medical Center, Cleveland, Ohio, USA.

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http://dx.doi.org/10.1002/ajmg.a.33511DOI Listing
August 2010