Gika AD - Search Results

1

Counseling in isolated mild fetal ventriculomegaly.

Melchiorre K, Bhide A, Gika AD, Pilu G, Papageorghiou AT. Melchiorre K, et al. Among authors: gika ad. Ultrasound Obstet Gynecol. 2009 Aug;34(2):212-24. doi: 10.1002/uog.7307. Ultrasound Obstet Gynecol. 2009. PMID: 19644944 Free article. Review.

2

Recurrent acute necrotizing encephalopathy following influenza A in a genetically predisposed family.

Gika AD, Rich P, Gupta S, Neilson DE, Clarke A. Gika AD, et al. Dev Med Child Neurol. 2010 Jan;52(1):99-102. doi: 10.1111/j.1469-8749.2009.03405.x. Epub 2009 Oct 7. Dev Med Child Neurol. 2010. PMID: 19811512 Free article.

3

White matter abnormalities and dystonic motor disorder associated with mutations in the SLC16A2 gene.

Gika AD, Siddiqui A, Hulse AJ, Edward S, Fallon P, McEntagart ME, Jan W, Josifova D, Lerman-Sagie T, Drummond J, Thompson E, Refetoff S, Bönnemann CG, Jungbluth H. Gika AD, et al. Dev Med Child Neurol. 2010 May;52(5):475-82. doi: 10.1111/j.1469-8749.2009.03471.x. Epub 2009 Oct 7. Dev Med Child Neurol. 2010. PMID: 19811520 Free PMC article.

4

A novel GLRA1 mutation in a recessive hyperekplexia pedigree.

Forsyth RJ, Gika AD, Ginjaar I, Tijssen MA. Forsyth RJ, et al. Among authors: gika ad. Mov Disord. 2007 Aug 15;22(11):1643-5. doi: 10.1002/mds.21574. Mov Disord. 2007. PMID: 17534957

5

Infection-triggered familial or recurrent cases of acute necrotizing encephalopathy caused by mutations in a component of the nuclear pore, RANBP2.

Neilson DE, Adams MD, Orr CM, Schelling DK, Eiben RM, Kerr DS, Anderson J, Bassuk AG, Bye AM, Childs AM, Clarke A, Crow YJ, Di Rocco M, Dohna-Schwake C, Dueckers G, Fasano AE, Gika AD, Gionnis D, Gorman MP, Grattan-Smith PJ, Hackenberg A, Kuster A, Lentschig MG, Lopez-Laso E, Marco EJ, Mastroyianni S, Perrier J, Schmitt-Mechelke T, Servidei S, Skardoutsou A, Uldall P, van der Knaap MS, Goglin KC, Tefft DL, Aubin C, de Jager P, Hafler D, Warman ML. Neilson DE, et al. Among authors: gika ad. Am J Hum Genet. 2009 Jan;84(1):44-51. doi: 10.1016/j.ajhg.2008.12.009. Am J Hum Genet. 2009. PMID: 19118815 Free PMC article.

6

Trihexyphenidyl for acute life-threatening episodes due to a dystonic movement disorder in Rett syndrome.

Gika AD, Hughes E, Goyal S, Sparkes M, Lin JP. Gika AD, et al. Mov Disord. 2010 Feb 15;25(3):385-9. doi: 10.1002/mds.22926. Mov Disord. 2010. PMID: 20063434

7

A series of Greek children with pure hereditary spastic paraplegia: clinical features and genetic findings.

Polymeris AA, Tessa A, Anagnostopoulou K, Rubegni A, Galatolo D, Dinopoulos A, Gika AD, Youroukos S, Skouteli E, Santorelli FM, Pons R. Polymeris AA, et al. Among authors: gika ad. J Neurol. 2016 Aug;263(8):1604-11. doi: 10.1007/s00415-016-8179-z. Epub 2016 Jun 3. J Neurol. 2016. PMID: 27260292

8

Childhood optic neuritis clinical features and outcome.

Absoud M, Cummins C, Desai N, Gika A, McSweeney N, Munot P, Hemingway C, Lim M, Nischal KK, Wassmer E. Absoud M, et al. Arch Dis Child. 2011 Sep;96(9):860-2. doi: 10.1136/adc.2009.175422. Epub 2010 Jun 16. Arch Dis Child. 2011. PMID: 20554767

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