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Dora Angelicheva

Showing results (11-20 of 19) with videos related to

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Brain : a Journal of Neurology|March 16, 2007
Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutationVioleta Mihaylova, Janina Hantke, Ivanka Sinigerska, et al.
Neurobiology of Disease|February 10, 2011
Ndrg1 in development and maintenance of the myelin sheathRosalind H M King, David Chandler, Sash Lopaticki, et al.
American Journal of Human Genetics|August 21, 2012
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1Velina Guergueltcheva, Dimitar N Azmanov, Dora Angelicheva, et al.
Epilepsia|April 30, 2009
Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32Dora Angelicheva, Ivailo Tournev, Velina Guergueltcheva, et al.
European Journal of Human Genetics : EJHG|December 25, 2021
Correction to: Origins, admixture and founder lineages in European RomaBegoña Martínez-Cruz, Isabel Mendizabal, Christine Harmant, et al.
European Journal of Human Genetics : EJHG|September 17, 2015
Origins, admixture and founder lineages in European RomaBegoña Martínez-Cruz, Isabel Mendizabal, Christine Harmant, et al.
Pediatric Research|April 30, 2002
The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across EuropeMichael Hunter, Evelyne Heyer, Frederic Austerlitz, et al.
American Journal of Human Genetics|August 24, 2004
Mutation history of the roma/gypsiesBharti Morar, David Gresham, Dora Angelicheva, et al.
Nature Genetics|October 1, 2003
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndromeRaymonda Varon, Rebecca Gooding, Christina Steglich, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Brain : a Journal of Neurology|March 16, 2007
Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutationVioleta Mihaylova, Janina Hantke, Ivanka Sinigerska, et al.
Neurobiology of Disease|February 10, 2011
Ndrg1 in development and maintenance of the myelin sheathRosalind H M King, David Chandler, Sash Lopaticki, et al.
American Journal of Human Genetics|August 21, 2012
Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1Velina Guergueltcheva, Dimitar N Azmanov, Dora Angelicheva, et al.
Epilepsia|April 30, 2009
Partial epilepsy syndrome in a Gypsy family linked to 5q31.3-q32Dora Angelicheva, Ivailo Tournev, Velina Guergueltcheva, et al.
European Journal of Human Genetics : EJHG|December 25, 2021
Correction to: Origins, admixture and founder lineages in European RomaBegoña Martínez-Cruz, Isabel Mendizabal, Christine Harmant, et al.
European Journal of Human Genetics : EJHG|September 17, 2015
Origins, admixture and founder lineages in European RomaBegoña Martínez-Cruz, Isabel Mendizabal, Christine Harmant, et al.
Pediatric Research|April 30, 2002
The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across EuropeMichael Hunter, Evelyne Heyer, Frederic Austerlitz, et al.
American Journal of Human Genetics|August 24, 2004
Mutation history of the roma/gypsiesBharti Morar, David Gresham, Dora Angelicheva, et al.
Nature Genetics|October 1, 2003
Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndromeRaymonda Varon, Rebecca Gooding, Christina Steglich, et al.
Pageof 2